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			<title>MENGGALI INOVASI DAN KREATIVITAS DALAM DUNIA REKREASI DIGITAL KONTEMPORER</title>
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			<pubDate>Sun, 06 Sep 2026 15:00:06 GMT</pubDate>
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			<title>Category:The Mechanics of Editorial Link Insertion Outreach That Earns Permanent Coverage</title>
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			<title>Category:Slot Gacor: Panduan Memahami Informasi dan Klaim di Internet</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:31 GMT</pubDate>
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			<title>Menyibak Tirai Rekreasi Digital: Seni Menikmati Permainan Slot dan Kasino dengan Bijak</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:15 GMT</pubDate>
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			<title>Menjelajahi Keindahan Seni Digital Serta Sensasi Hiburan Slot dan Kasino Kontemporer</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:14 GMT</pubDate>
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			<title>Menikmati Dunia Rekreasi Digital dengan Perspektif yang Bijak</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:12 GMT</pubDate>
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			<title>Menemukan Pengalaman Terbaik dalam Dunia Hiburan Slot dan Kasino Daring</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:11 GMT</pubDate>
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			<title>Menemukan Kedamaian di Sela Kesibukan Melalui Hiburan Digital Modern</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:10 GMT</pubDate>
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			<title>MENYELAMI HARMONI ESTETIKA DAN KREATIVITAS MODERN DALAM DUNIA SLOT SERTA KASINO</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:09 GMT</pubDate>
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			<title>MENJELAJAHI SISI KREATIF DAN ESTETIKA DALAM DUNIA SLOT DAN KASINO DIGITAL</title>
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			<pubDate>Sat, 05 Sep 2026 15:00:08 GMT</pubDate>
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			<title>MENEMUKAN KESENANGAN HIBURAN BERKUALITAS DALAM DUNIA SLOT DAN KASINO DIGITAL</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/MENEMUKAN_KESENANGAN_HIBURAN_BERKUALITAS_DALAM_DUNIA_SLOT_DAN_KASINO_DIGITAL</link>
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			<pubDate>Sat, 05 Sep 2026 15:00:06 GMT</pubDate>
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			<title>10.1038 s41467-023-36784-7-4</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-4&amp;diff=11495&amp;oldid=0</link>
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&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;lt;div class=&amp;quot;ce_import_notice&amp;quot;&amp;gt;Imported from: &amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;/opt/downloadPDF/chemwiki_pubstore/88766a7e865699abcbdaf32099d9d904.pdf/41467_2023_36784_MOESM1_ESM_6a9ab958b5351.pdf&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;/opt/downloadPDF/chemwiki_pubstore/88766a7e865699abcbdaf32099d9d904.pdf/Lei et al. - 2023 - Photocatalytic CO2 reduction with aminoanthraquinone organic dyes_6a9ab958b6fd6.pdf&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{{DISPLAYTITLE: Photocatalytic CO2 reduction with aminoanthraquinone organic dyes - 2026.09.04 - 4 }}&lt;br /&gt;
{{DOI|doi=10.1038/s41467-023-36784-7-4}}&lt;br /&gt;
&lt;br /&gt;
== Abstract Summary ==&lt;br /&gt;
This study examines a molecular photocatalytic system for the light-driven reduction of CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to CO using aminoanthraquinone organic dyes as photosensitizers and an iron porphyrin as the CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-reduction catalyst. The system operates in CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-saturated DMF under visible light with BIH as a sacrificial electron donor. Among six related dyes, the brominated hydroxy-aminoanthraquinone photosensitizer labeled &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; gave the highest activity. The article reports high turnover numbers for both the catalyst and the photosensitizer, while maintaining very high selectivity for CO over H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. Mechanistic experiments support a reductive quenching pathway and suggest that hydroxyanthrone-type reduced dye intermediates participate in electron transfer to the iron catalyst.&lt;br /&gt;
&lt;br /&gt;
== Advances and Special Progress ==&lt;br /&gt;
A central advance is the use of simple aminoanthraquinone organic dyes as effective visible-light absorbers in a noble-metal-free molecular CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction system. The article emphasizes that this system achieves high turnover numbers for both the photosensitizer and the catalyst, which it identifies as an unmet challenge in current light-driven systems.&lt;br /&gt;
&lt;br /&gt;
The structure-function comparison across dyes &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039;-&amp;#039;&amp;#039;&amp;#039;6&amp;#039;&amp;#039;&amp;#039; is another important advance. By varying substituents on the anthraquinone framework, the study links photocatalytic performance to built-in donor-acceptor character within the dye. The best-performing dye, &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039;, combines substituents with distinct electronic effects and gives the highest reported activity in the series.&lt;br /&gt;
&lt;br /&gt;
The work also provides mechanistic progress. Spectroscopic, electrochemical, quenching, isotopic labeling, DLS, and mercury-poisoning experiments are used to support a homogeneous molecular system and a proposed reductive quenching pathway. The data further support the formation of reduced and protonated dye-derived intermediates that can reduce the iron catalyst to catalytically relevant states.&lt;br /&gt;
&lt;br /&gt;
The reported CO selectivity is also notable. Most systems based on dyes &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039;-&amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; gave CO selectivities above 99%, showing efficient suppression of H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; evolution under the reported conditions.&lt;br /&gt;
&lt;br /&gt;
== Additional Remarks ==&lt;br /&gt;
The chemistry is significant because photochemical conversion of CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; into CO stores solar energy in a chemically useful reduced carbon product. CO is also a valuable intermediate for further chemical synthesis. This makes selective CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-to-CO photoreduction a relevant model transformation in artificial photosynthesis.&lt;br /&gt;
&lt;br /&gt;
At the same time, the system remains a sacrificial photochemical system rather than a complete solar-fuel cycle. BIH is consumed as the electron donor, so the setup does not perform the oxidative half-reaction of water splitting. The solvent is DMF, and water compatibility was not reported for this photocatalytic system.&lt;br /&gt;
&lt;br /&gt;
The article also identifies catalyst stability as a limitation. Component-addition experiments indicate that the iron porphyrin catalyst decomposes faster than the anthraquinone dye during catalysis. Thus, strong activity does not remove the durability challenge.&lt;br /&gt;
&lt;br /&gt;
Competition from H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation is generally suppressed, but not absent. The sulfonyl-containing dye &amp;#039;&amp;#039;&amp;#039;6&amp;#039;&amp;#039;&amp;#039; gave lower CO selectivity than the other dyes in the series, which the article associates with enhanced proton transfer to the catalyst and increased H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; generation.&lt;br /&gt;
&lt;br /&gt;
== Content of the Published Article in Detail ==&lt;br /&gt;
The reported photocatalytic system contains three essential molecular components: an aminoanthraquinone dye photosensitizer, the iron porphyrin catalyst FeTDHPP, and BIH as the sacrificial electron donor. Experiments were carried out in CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-saturated DMF under irradiation with white LED light of λ &amp;gt; 400 nm. Product gases were analyzed by gas chromatography. CO was the major product, while H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation was strongly suppressed in most cases.&lt;br /&gt;
&lt;br /&gt;
The article compares six dyes, labeled &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039;-&amp;#039;&amp;#039;&amp;#039;6&amp;#039;&amp;#039;&amp;#039;. These dyes absorb strongly in the visible region, with maximum absorption bands ranging from 478 to 592 nm. They also emit in the red region, with fluorescence lifetimes in the nanosecond range. Electrochemical studies show two reduction events for each dye. These photophysical and redox properties are presented as the basis for using the dyes as molecular photosensitizers in CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction.&lt;br /&gt;
&lt;br /&gt;
For catalytic testing, two types of performance evaluation were highlighted. In one, catalyst turnover numbers were measured using 20 μM photosensitizer, 0.6 μM FeTDHPP, and 60 mM BIH. Under these conditions, dye &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; gave the best catalytic performance, with TON&amp;lt;sub&amp;gt;Fe&amp;lt;/sub&amp;gt; = 21,616 ± 2351 for CO and CO selectivity greater than 99.9%. In another set of conditions designed to evaluate photosensitizer performance, 5 μM photosensitizer, 20 μM FeTDHPP, and 60 mM BIH were used. Under those conditions, dye &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; gave TON&amp;lt;sub&amp;gt;PS&amp;lt;/sub&amp;gt; = 6012 ± 606. The article further reports that when dye &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; and FeTDHPP were used at the same concentration, the system achieved TON = 4978 ± 326 and a CO quantum efficiency of 11.1% ± 0.9% at 450 nm.&lt;br /&gt;
&lt;br /&gt;
Mechanistically, the article argues that two broad quenching pathways are possible in such systems: reductive quenching of the excited photosensitizer by BIH, and oxidative quenching of the excited photosensitizer by the catalyst. The data support reductive quenching as the dominant pathway. Fluorescence lifetime quenching by BIH gave quenching rate constants near the diffusion-controlled limit, above 10&amp;lt;sup&amp;gt;9&amp;lt;/sup&amp;gt; M&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt; s&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt;. By contrast, oxidative quenching constants with the catalyst could not be measured accurately because the dye and catalyst strongly overlap spectrally. The article also notes that the BIH concentration in catalysis is more than 3000 times greater than the FeTDHPP concentration in the main catalytic conditions, which further supports reductive quenching.&lt;br /&gt;
&lt;br /&gt;
Ground-state interactions were examined by UV/Vis and &amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR studies. These experiments indicated no reaction between the dyes and BIH or FeTDHPP before irradiation, ruling out a static quenching pathway according to the article.&lt;br /&gt;
&lt;br /&gt;
To understand the photochemical sequence, the article studied anthraquinone itself as a model. Upon irradiation of AQ in the presence of BIH, UV/Vis spectroscopy showed rapid formation of a species near 560 nm, assigned to a proton-coupled one-electron reduction product AQH•. Continued irradiation produced a species near 520 nm, assigned to AQH&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. The article then proposes further protonation to form a hydroxyanthrone species AQH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. Additional spectroscopic evidence suggested formation of another photoproduct near 400-407 nm during irradiation. By analogy with the dye systems, and based on follow-up experiments, this ~400 nm species was tentatively assigned as a reduced hydroxyanthrone-type intermediate, PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
The mechanistic proposal is that after the dye absorbs light, BIH reductively quenches the excited dye. Through sequential electron-transfer and proton-transfer steps, the dye is converted into reduced and protonated intermediates, culminating in PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and then photoexcited PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;*; reductive quenching of PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;* gives PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. The article proposes that this PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; intermediate is a key strong reductant that transfers electrons to the iron catalyst.&lt;br /&gt;
&lt;br /&gt;
Electrochemical reasoning is central here. The article states that CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction by FeTDHPP occurs at an Fe(0) oxidation state at −1.55 V vs SCE. The directly reduced dye species PS&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;, PS&amp;lt;sup&amp;gt;2−&amp;lt;/sup&amp;gt;, and their protonated forms were considered insufficiently reducing for this step. In situ square-wave voltammetry after photolysis showed new reduction waves at potentials more negative than −1.90 V vs SCE, supporting the proposal that the photogenerated PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; species is sufficiently reducing to generate the required Fe(0) intermediate.&lt;br /&gt;
&lt;br /&gt;
The reduction sequence of the catalyst was monitored by UV/Vis spectroscopy. Under white LED irradiation, the Fe(III) catalyst was reported to convert rapidly to Fe(II), then to Fe(I), and the Fe(I) species decreased during ongoing CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction. The article interprets this as consistent with catalytically relevant stepwise reduction of the iron porphyrin.&lt;br /&gt;
&lt;br /&gt;
The role of BIH extends beyond the initial reductive quenching event. A peak attributed to BI• was observed electrochemically after irradiation. The article concludes that BIH donates two electrons in the overall CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction process under low-BIH conditions. However, the article also argues that direct reduction of the catalyst by BI• is slower than the pathway involving PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. This conclusion is supported by irradiation experiments at λ &amp;gt; 550 nm, which suppress formation of PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. Under these conditions, CO production became much slower and Fe(II) accumulated as the major catalyst-derived species, with less Fe(I) than under broadband visible irradiation.&lt;br /&gt;
&lt;br /&gt;
Several control experiments support the mechanistic interpretation and the homogeneous nature of the system. DLS measurements detected no nanoparticles before or after catalysis. Mercury poisoning had little effect on activity, arguing against catalysis by amalgam-forming metal impurities. Isotopic labeling under &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; gave exclusive &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;CO, showing that CO originates from CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
The article also compares dye structures. Dyes containing amino and hydroxyl substituents generally outperformed less favorably substituted analogues. The article interprets this in terms of internal donor-acceptor design on the anthraquinone framework, which promotes faster reductive quenching and higher catalytic rates. A generally linear relationship was reported between the initial TOF for CO production and the first reductive quenching rate constant across dyes &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039;-&amp;#039;&amp;#039;&amp;#039;6&amp;#039;&amp;#039;&amp;#039;.&lt;br /&gt;
&lt;br /&gt;
Stability tests showed that adding more BIH alone after rate decay did not restore activity, implying decomposition of the photosensitizer or catalyst rather than mere donor depletion. Adding catalyst and BIH restored significantly more activity than adding photosensitizer and BIH. The article therefore concludes that the iron porphyrin catalyst decomposes faster than the anthraquinone dye during photocatalysis.&lt;br /&gt;
&lt;br /&gt;
== Catalyst ==&lt;br /&gt;
The catalyst is &amp;#039;&amp;#039;&amp;#039;FeTDHPP&amp;#039;&amp;#039;&amp;#039;, an iron porphyrin complex used as the molecular CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-reduction catalyst. It is a homogeneous iron porphyrin system and serves as the site at which CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; is reduced to CO.&lt;br /&gt;
&lt;br /&gt;
The article discusses catalytically relevant Fe(III), Fe(II), Fe(I), and Fe(0) states. UV/Vis monitoring under irradiation showed conversion of Fe(III) to Fe(II) and then Fe(I). The article states that CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction occurs at an Fe(0) oxidation state. Thus, the catalyst functions through sequential reduction of the iron center.&lt;br /&gt;
&lt;br /&gt;
The catalyst gives high CO selectivity in this system, especially with the better-performing dyes. However, stability experiments indicate that FeTDHPP decomposes faster than the anthraquinone photosensitizer during catalysis, making catalyst durability a major limitation under the reported conditions.&lt;br /&gt;
&lt;br /&gt;
== Photosensitizer ==&lt;br /&gt;
The photosensitizers are a series of six aminoanthraquinone organic dyes labeled &amp;#039;&amp;#039;&amp;#039;1&amp;#039;&amp;#039;&amp;#039;-&amp;#039;&amp;#039;&amp;#039;6&amp;#039;&amp;#039;&amp;#039;. They are molecular organic dyes that absorb visible light and initiate the photochemical electron-transfer sequence. The main photosensitizer in the highest-performing system is &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039;.&lt;br /&gt;
&lt;br /&gt;
These dyes show visible absorption maxima from 478 to 592 nm and fluorescence in the 600-700 nm region. Their lifetimes are reported as 0.66-1.02 ns. Electrochemical studies showed two reduction events for each dye, supporting their ability to participate in sequential photoredox chemistry.&lt;br /&gt;
&lt;br /&gt;
The article proposes that the dyes operate mainly through &amp;#039;&amp;#039;&amp;#039;reductive quenching&amp;#039;&amp;#039;&amp;#039;. After excitation, BIH quenches the excited dye. The dye then undergoes further electron-transfer and proton-transfer chemistry to form reduced hydroxyanthrone-type intermediates such as PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and the proposed strongly reducing PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. This latter species is presented as a key reductant for the iron catalyst.&lt;br /&gt;
&lt;br /&gt;
Among the six dyes, &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; gave the highest activity. The article attributes the superior performance of dyes such as &amp;#039;&amp;#039;&amp;#039;4&amp;#039;&amp;#039;&amp;#039; and &amp;#039;&amp;#039;&amp;#039;5&amp;#039;&amp;#039;&amp;#039; to substituent-controlled donor-acceptor character on the anthraquinone scaffold. The dye series was also used to correlate reductive quenching kinetics with catalytic CO formation rates.&lt;br /&gt;
&lt;br /&gt;
The photosensitizer is more durable than the catalyst under the tested conditions, but light competition from decomposed species was suggested to limit complete recovery of activity after component re-addition experiments.&lt;br /&gt;
&lt;br /&gt;
== Investigation ==&lt;br /&gt;
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=inv0}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Photocatalytic CO2 conversion]]&lt;/div&gt;</description>
			<pubDate>Fri, 04 Sep 2026 12:30:07 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.1038_s41467-023-36784-7-4</comments>
		</item>
		<item>
			<title>10.1038 s41467-023-36784-7-4/inv0</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-4/inv0&amp;diff=11494&amp;oldid=0</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-4/inv0&amp;diff=11494&amp;oldid=0</guid>
			<description>&lt;p&gt;auto-generated&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Photocatalytic_CO2_conversion_experiments|experiments={{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=2395&lt;br /&gt;
|Turnover_frequency__CO=1510&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=2011&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=8.9&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=2738&lt;br /&gt;
|Turnover_frequency__CO=69&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=482&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=0.3&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=3551&lt;br /&gt;
|Turnover_frequency__CO=593&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=1523&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=3.0&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=8360&lt;br /&gt;
|Turnover_frequency__CO=1614&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=2849&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=8.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.0005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3174&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=19158&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=21616&lt;br /&gt;
|Turnover_frequency__CO=4028&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2576&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4028&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3942&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=1&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.001&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3587&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=1&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=17020&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=6012&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2325&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=11.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2134&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.002&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3817&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=8780&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.015&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=8772&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=5593&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=11250&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=50&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=891&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=5258&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4128&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=907&lt;br /&gt;
|Turnover_frequency__CO=93&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=1183&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=2.0&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
}}&lt;/div&gt;</description>
			<pubDate>Fri, 04 Sep 2026 12:30:06 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.1038_s41467-023-36784-7-4/inv0</comments>
		</item>
		<item>
			<title>10.1038 s41467-023-36784-7-3</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-3&amp;diff=11493&amp;oldid=0</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-3&amp;diff=11493&amp;oldid=0</guid>
			<description>&lt;p&gt;auto-generated&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;lt;div class=&amp;quot;ce_import_notice&amp;quot;&amp;gt;Imported from: &amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;/opt/downloadPDF/chemwiki_pubstore/7e9875d2bdb7974d9ffecb4b0a29f8f5.pdf/41467_2023_36784_MOESM1_ESM_6a9ab6d0777f3.pdf&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;/opt/downloadPDF/chemwiki_pubstore/7e9875d2bdb7974d9ffecb4b0a29f8f5.pdf/Lei et al. - 2023 - Photocatalytic CO2 reduction with aminoanthraquinone organic dyes_6a9ab6d079463.pdf&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{{DISPLAYTITLE: Photocatalytic CO2 reduction with aminoanthraquinone organic dyes - 2026.09.04 - 3 }}&lt;br /&gt;
{{DOI|doi=10.1038/s41467-023-36784-7-3}}&lt;br /&gt;
&lt;br /&gt;
== Abstract Summary ==&lt;br /&gt;
This article describes a molecular photocatalytic system for the reduction of CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to CO using an iron porphyrin catalyst together with aminoanthraquinone organic dyes as visible-light photosensitizers. The system operates in CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-saturated DMF with BIH as a sacrificial electron donor under visible irradiation. A series of six aminoanthraquinone dyes was compared, and the most active dye gave high activity together with very high CO selectivity. The work also presents mechanistic evidence that reductive quenching of the excited dye is the dominant photochemical entry step, and that reduced hydroxyanthrone-type dye species are important intermediates in delivering electrons to the iron catalyst.&lt;br /&gt;
&lt;br /&gt;
== Advances and Special Progress ==&lt;br /&gt;
A central advance is the use of simple aminoanthraquinone organic dyes as effective visible-light photosensitizers in a noble-metal-free molecular CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction system. The article emphasizes that both the catalyst and the photosensitizer can reach high turnover numbers, which it states had not been achieved in current light-driven systems of this type.&lt;br /&gt;
&lt;br /&gt;
The study also shows a clear structure–function relationship within a small, chemically related dye family. Changing substituents on the anthraquinone framework strongly changes photocatalytic activity. The article interprets this trend in terms of built-in donor–acceptor character within the dye, which promotes faster reductive quenching and better photocatalytic performance.&lt;br /&gt;
&lt;br /&gt;
Another advance is the mechanistic analysis. The article combines fluorescence quenching, lifetime measurements, UV/Vis monitoring during photolysis, electrochemical measurements, isotopic labeling, DLS, and mercury poisoning tests. These data support a homogeneous molecular system and provide evidence for reduced dye-derived intermediates that participate in catalyst reduction.&lt;br /&gt;
&lt;br /&gt;
The reported product selectivity is also notable. CO is the major product in all tested systems, and for most dyes the selectivity for CO is above 99%. The most active dye–catalyst combination gives especially high CO formation while strongly suppressing H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; evolution.&lt;br /&gt;
&lt;br /&gt;
== Additional Remarks ==&lt;br /&gt;
The chemistry is relevant to solar-fuel research because CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-to-CO conversion stores reducing equivalents in a useful carbon-containing product. CO is an important two-electron reduction product and can serve as a feedstock for further chemical synthesis.&lt;br /&gt;
&lt;br /&gt;
At the same time, this is a sacrificial photochemical system rather than a fully closed artificial photosynthetic cycle. BIH is consumed as the electron donor, so the system does not perform complete sunlight-driven fuel formation from only CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and water. The solvent is DMF, not water, and the article does not report water compatibility as a feature of this system.&lt;br /&gt;
&lt;br /&gt;
The work shows strong catalytic activity, but durability remains limited by catalyst decomposition. The article reports that the iron porphyrin catalyst decomposes faster than the anthraquinone dye under the tested conditions. Thus, although the system is chemically informative and highly active, long-term operational stability is still a limitation.&lt;br /&gt;
&lt;br /&gt;
The mechanism is chemically elegant because the photosensitizer is not treated as a simple one-step electron shuttle. Instead, the article proposes sequential reduction and protonation chemistry of the anthraquinone scaffold, forming hydroxyanthrone-type intermediates that are then involved in catalyst reduction. This gives the study significance beyond performance alone, because it links dye structure to the detailed photochemical sequence.&lt;br /&gt;
&lt;br /&gt;
== Content of the Published Article in Detail ==&lt;br /&gt;
The molecular photocatalytic system contains three essential components: an iron porphyrin CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction catalyst, an aminoanthraquinone dye photosensitizer, and BIH as the sacrificial electron donor. The reactions are carried out in CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-saturated DMF under white LED irradiation with wavelengths above 400 nm. Gas products in the headspace are analyzed by gas chromatography. CO is the major product, while H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation is strongly suppressed.&lt;br /&gt;
&lt;br /&gt;
Six aminoanthraquinone dyes, labeled 1–6 in the article, were compared. They absorb in the visible region, with maximum absorption bands from 478 to 592 nm. They also emit red fluorescence in the 600–700 nm region, with lifetimes in the nanosecond range. Electrochemical measurements show two reduction events for each dye. These photophysical and redox properties support their use as photosensitizers in CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction.&lt;br /&gt;
&lt;br /&gt;
Under a standard catalyst-focused condition of 20 μM photosensitizer, 0.6 μM FeTDHPP, and 60 mM BIH, all six dyes support CO formation, but with strongly different activities. The article reports that dyes containing amino and hydroxy substituents are substantially more active than others, and that dye 5 is the best performer in the series. Under photosensitizer-focused conditions of 5 μM photosensitizer, 20 μM FeTDHPP, and 60 mM BIH, dye 5 again gives the highest photosensitizer turnover number. The article also reports that when dye 5 and FeTDHPP are used at the same concentration, the system can achieve high turnover numbers for both components simultaneously, together with a CO quantum efficiency of 11.1% at 450 nm based on two photons per CO.&lt;br /&gt;
&lt;br /&gt;
The article distinguishes observed data from mechanistic interpretation. Experimentally, fluorescence quenching and fluorescence lifetime measurements show rapid quenching of the excited photosensitizers by BIH, with quenching rate constants near the diffusion-controlled limit. Because there is strong overlap between dye absorption/emission and catalyst absorption, oxidative quenching by the catalyst could not be quantified accurately. However, the article reports no evidence for ground-state reaction between dye and BIH or between dye and FeTDHPP from UV/Vis and &amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR data. Together with the much higher concentration of BIH than FeTDHPP, these results support a &amp;#039;&amp;#039;proposed&amp;#039;&amp;#039; reductive quenching pathway as the dominant mechanism.&lt;br /&gt;
&lt;br /&gt;
In this proposed sequence, the dye first absorbs visible light to form an excited state. BIH then reduces the excited dye. The article further proposes that the anthraquinone scaffold undergoes sequential electron-transfer and proton-transfer steps, ultimately forming hydroxyanthrone-type species denoted PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and then PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. The article treats these as important intermediates in catalyst reduction. This interpretation is supported by UV/Vis studies of anthraquinone photolysis with BIH, where species assigned to protonated reduced anthraquinone intermediates appear over time, and by analogous spectral changes seen for dyes 1–6 during photocatalysis.&lt;br /&gt;
&lt;br /&gt;
More specifically, the article assigns an early photoproduct of anthraquinone near 560 nm to AQH• rather than AQ•&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; or AQ&amp;lt;sup&amp;gt;2−&amp;lt;/sup&amp;gt;, based on comparison with known spectra. A later intermediate near 520 nm is assigned to AQH&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. Continued reduction and protonation are proposed to generate 10-hydroxyanthrone-type species, described as AQH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. A further photoproduct near 400–407 nm is &amp;#039;&amp;#039;tentatively assigned&amp;#039;&amp;#039; to a more reduced hydroxyanthrone species analogous to PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. The article supports the importance of this species by showing that when it is generated photochemically from dye 5 and BIH, subsequent addition of FeTDHPP rapidly gives CO and an Fe(I) spectral signature. In a control experiment performed before generating this species, no CO is detected after catalyst addition.&lt;br /&gt;
&lt;br /&gt;
Electrochemical data are used to argue that the ordinary one- or two-electron reduced dye states are not reducing enough to generate the catalytically relevant Fe(0) state. The article states that CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction by FeTDHPP occurs at an Fe(0) oxidation state at −1.55 V vs SCE. In contrast, the measured reduction potentials of the dyes are much more positive. Therefore, the article proposes that the stronger reductant is the hydroxyanthrone-derived PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; photoproduct. In situ square-wave voltammetry after irradiation shows new reduction waves at more negative than −1.90 V vs SCE for systems containing dyes 1–6 with BIH, which supports the presence of more strongly reducing photoproducts.&lt;br /&gt;
&lt;br /&gt;
The catalyst redox sequence was followed by UV/Vis spectroscopy. Under white-light irradiation, the Fe(III) starting compound is converted rapidly to Fe(II), then to Fe(I), and the Fe(I) feature decreases during CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction. The article states that this observation is consistent with a previously reported mechanism for iron porphyrin CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction. When irradiation is restricted to wavelengths above 550 nm, the hydroxyanthrone-derived PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; pathway is shut down according to the article, and CO production becomes much slower. Under these conditions Fe(II) is the major observed catalyst species and Fe(I) accumulates to a lesser extent. Similar behavior is reported under 450 nm and 525 nm LED experiments. Irradiation of BIH and FeTDHPP without photosensitizer gives almost no Fe(I), only Fe(II). These observations support the article’s conclusion that BI• alone can reduce Fe(II) and Fe(I), but more slowly than the pathway involving PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
The article also discusses the role of proton transfer. Proton transfer is built into the proposed dye reduction chemistry, where reduced anthraquinone states are protonated to form hydroxyanthrone-type intermediates. The catalyst cycle also requires protons in the reduction of CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to CO. However, the detailed proton-transfer steps at the catalyst are not worked out beyond the proposed scheme. Competition with H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; evolution is low for most dyes. Dye 6, which contains a strongly acidic sulfonyl group, gives somewhat lower CO selectivity and the highest H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; selectivity in the series. The article proposes that this acidic group may promote proton transfer to the catalyst and thereby enhance H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation.&lt;br /&gt;
&lt;br /&gt;
Several control experiments support the molecular and homogeneous nature of the system. DLS detects no nanoparticles before or after catalysis. Mercury poisoning does not significantly change activity, arguing against amalgam-forming metal impurities as the source of catalysis. Isotopic labeling with &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; gives exclusively &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;CO, confirming CO formation from CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. Stability tests in which fresh components are added after activity loss show that catalyst decomposition is more important than photosensitizer decomposition under the tested conditions.&lt;br /&gt;
&lt;br /&gt;
Finally, the article correlates catalytic rate with reductive quenching rate across dyes 1–6. A generally linear trend is reported between the initial TOF for CO formation and the first reductive quenching rate constant. The article interprets this as evidence that faster reductive quenching promotes faster formation of the key reduced hydroxyanthrone-type intermediates and therefore higher catalytic activity.&lt;br /&gt;
&lt;br /&gt;
== Catalyst ==&lt;br /&gt;
The catalyst is FeTDHPP, an iron porphyrin complex. It is a molecular, porphyrinic CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction catalyst used in homogeneous solution. The article identifies it as the CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction catalyst throughout the photocatalytic system.&lt;br /&gt;
&lt;br /&gt;
Its redox chemistry is central to function. UV/Vis experiments show conversion of Fe(III) to Fe(II) and then Fe(I) under irradiation in the catalytic mixture. The article states that catalysis proceeds through an Fe(0) oxidation state for CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction. Electron transfer from reduced dye-derived intermediates is proposed to generate the required low-valent catalyst states.&lt;br /&gt;
&lt;br /&gt;
The catalyst is highly selective for CO formation in this system, especially when paired with the better-performing aminoanthraquinone dyes. However, the article reports that the catalyst decomposes faster than the photosensitizer during extended irradiation, and this is identified as a major cause of activity loss.&lt;br /&gt;
&lt;br /&gt;
== Photosensitizer ==&lt;br /&gt;
The photosensitizers are aminoanthraquinone organic dyes, specifically six dyes labeled 1–6. They are molecular organic chromophores that absorb visible light and initiate the photochemical electron-transfer sequence. Dye 5 is the main and best-performing photosensitizer in the study.&lt;br /&gt;
&lt;br /&gt;
These dyes show visible absorption maxima from 478 to 592 nm and emit in the 600–700 nm region. Their excited-state lifetimes are in the nanosecond range. Electrochemical measurements show two reduction events for each dye. The article uses these data to analyze how substituents alter light absorption, reduction potential, and catalytic behavior.&lt;br /&gt;
&lt;br /&gt;
Mechanistically, the excited photosensitizer is proposed to undergo predominantly reductive quenching by BIH rather than oxidative quenching by the iron catalyst. The article supports this conclusion using fluorescence lifetime quenching, lack of ground-state reaction by UV/Vis and NMR, and the large excess of BIH relative to catalyst. The dye is then proposed to pass through reduced and protonated anthraquinone-derived intermediates, including PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;, before transferring electrons to the catalyst.&lt;br /&gt;
&lt;br /&gt;
The substituent pattern is chemically important. The article proposes that internal donor–acceptor character within the anthraquinone framework improves activity. Dyes with amino and hydroxy substitution, especially dye 5, give the best results. The parent anthraquinone itself does not produce CO under the tested conditions, even though an AQH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;-type species is observed. This shows that substituent effects are essential for productive catalysis in this dye family.&lt;br /&gt;
&lt;br /&gt;
== Investigation ==&lt;br /&gt;
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=inv0}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Photocatalytic CO2 conversion]]&lt;/div&gt;</description>
			<pubDate>Fri, 04 Sep 2026 12:19:01 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.1038_s41467-023-36784-7-3</comments>
		</item>
		<item>
			<title>10.1038 s41467-023-36784-7-3/inv0</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-3/inv0&amp;diff=11492&amp;oldid=0</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7-3/inv0&amp;diff=11492&amp;oldid=0</guid>
			<description>&lt;p&gt;auto-generated&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Photocatalytic_CO2_conversion_experiments|experiments={{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=2395&lt;br /&gt;
|Turnover_frequency__CO=1510&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=2011&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=8.9&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=2738&lt;br /&gt;
|Turnover_frequency__CO=69&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=482&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=0.3&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=3551&lt;br /&gt;
|Turnover_frequency__CO=593&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=1523&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=3.0&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=8360&lt;br /&gt;
|Turnover_frequency__CO=1614&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=2849&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=8.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.0005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3174&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=19158&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=21616&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2576&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4028&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3942&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=1&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.001&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3587&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=1&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=17020&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=6012&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2325&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=11.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2134&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.002&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3817&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=8780&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.015&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=8772&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=5593&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=11250&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=50&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=891&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4978&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=11.1&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=25&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4128&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=907&lt;br /&gt;
|Turnover_frequency__CO=93&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=1183&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=not reported&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=2.0&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
}}&lt;/div&gt;</description>
			<pubDate>Fri, 04 Sep 2026 12:19:00 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.1038_s41467-023-36784-7-3/inv0</comments>
		</item>
		<item>
			<title>10.1038 s41467-023-36784-7</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7&amp;diff=11491&amp;oldid=0</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7&amp;diff=11491&amp;oldid=0</guid>
			<description>&lt;p&gt;auto-generated&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;lt;div class=&amp;quot;ce_import_notice&amp;quot;&amp;gt;Imported from: &amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;/opt/downloadPDF/chemwiki_pubstore/3367bc96dd5ea3f6f066a72bda21db9d.pdf/41467_2023_36784_MOESM1_ESM_6a9ab628c555c.pdf&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;/opt/downloadPDF/chemwiki_pubstore/3367bc96dd5ea3f6f066a72bda21db9d.pdf/Lei et al. - 2023 - Photocatalytic CO2 reduction with aminoanthraquinone organic dyes_6a9ab628c72a1.pdf&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{{DISPLAYTITLE: Photocatalytic CO2 reduction with aminoanthraquinone organic dyes - 2026.09.04 }}&lt;br /&gt;
{{DOI|doi=10.1038/s41467-023-36784-7}}&lt;br /&gt;
&lt;br /&gt;
== Abstract Summary ==&lt;br /&gt;
This article describes a homogeneous molecular photocatalytic system for reducing CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to CO under visible light using aminoanthraquinone organic dyes as photosensitizers and an iron porphyrin complex as the catalyst. The system uses a sacrificial organic electron donor in DMF solution under CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
The main finding is that aminoanthraquinone dyes can drive highly selective CO formation, and that one dye in particular, PS 5, gives especially high activity. The study reports high turnover numbers for both the photosensitizer and the catalyst in separate benchmark conditions, while mechanistic experiments support a reductive-quenching pathway and implicate reduced hydroxyanthrone-type dye intermediates in catalyst reduction.&lt;br /&gt;
&lt;br /&gt;
== Advances and Special Progress ==&lt;br /&gt;
A key advance is the use of simple aminoanthraquinone organic dyes as efficient visible-light absorbers for molecular CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; photoreduction. The article explicitly emphasizes that these systems avoid precious-metal photosensitizers and use commercially available organic dyes together with an iron porphyrin catalyst.&lt;br /&gt;
&lt;br /&gt;
Another important advance is the simultaneous demonstration of high activity metrics for both the catalyst and the photosensitizer, although these were established under different optimized concentration regimes. Under one condition, PS 5 with FeTDHPP gave a catalyst-based turnover number for CO of 21,616. Under another, the same dye gave a photosensitizer-based turnover number for CO of 6012. The article states that achieving high activity for both components has not been realized in current light-driven systems of this type.&lt;br /&gt;
&lt;br /&gt;
The work also provides mechanistic progress. Structure–function comparison across dyes 1–6 supports the idea that a built-in donor–acceptor character within the aminoanthraquinone framework promotes faster reductive quenching and higher catalytic rates. The study further proposes that hydroxyanthrone-derived reduced species formed after light-driven proton-coupled reduction of the dye are key intermediates for reducing the iron catalyst to catalytically relevant low-valent states.&lt;br /&gt;
&lt;br /&gt;
CO selectivity is another notable feature. The systems with PSs 1–5 gave CO as the major product with selectivities above 99%, while H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation was strongly suppressed. The reported quantum efficiency for CO production reached 11.1% at 450 nm for PS 5 under the stated conditions.&lt;br /&gt;
&lt;br /&gt;
== Additional Remarks ==&lt;br /&gt;
The chemistry is significant because it addresses solar-to-chemical conversion of CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; using molecular components made from earth-abundant elements at the catalytic center and organic dyes as light harvesters. The work is therefore relevant to the broader challenge of replacing noble-metal photosensitizers in artificial photosynthesis.&lt;br /&gt;
&lt;br /&gt;
At the same time, the study is a sacrificial photochemical system rather than a fully integrated sustainable fuel-forming device. It requires BIH as a sacrificial electron donor and uses DMF as the reaction medium. No water-compatible operating window is established as a main feature of this system, and the article does not present this work as a water-based photocatalytic platform.&lt;br /&gt;
&lt;br /&gt;
The system is chemically selective for CO over H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;, but durability remains limited by decomposition, especially of the iron porphyrin catalyst. Component-addition experiments showed that activity loss is associated mainly with catalyst decomposition rather than simple BIH depletion or rapid dye decomposition. This is mechanistically informative but also identifies a practical limitation.&lt;br /&gt;
&lt;br /&gt;
The article combines strong photocatalytic performance with detailed mechanistic analysis. Its strength lies in connecting substituent effects on the organic dyes with measurable quenching behavior, redox chemistry, photochemical intermediates, and catalytic output. Its limitations include reliance on a sacrificial donor, use of an aprotic organic solvent, and incomplete long-term stability.&lt;br /&gt;
&lt;br /&gt;
== Content of the Published Article in Detail ==&lt;br /&gt;
The photocatalytic system contains three essential molecular components: an aminoanthraquinone photosensitizer, the iron porphyrin catalyst FeTDHPP, and the sacrificial electron donor BIH. The reaction medium is CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;-saturated DMF, and irradiation is typically provided by white LED light with λ &amp;amp;gt; 400 nm. Gas products are analyzed from the headspace, and CO is reported as the main product.&lt;br /&gt;
&lt;br /&gt;
The article compares six aminoanthraquinone dyes, labeled 1–6. These dyes absorb across the visible region, with absorption maxima spanning 478–592 nm. They emit red fluorescence in the 600–700 nm region with lifetimes of 0.66–1.02 ns. Electrochemical measurements show two reduction events for each dye. The authors use these photophysical and electrochemical data to justify their use as reductively quenched organic photosensitizers.&lt;br /&gt;
&lt;br /&gt;
In the main catalytic comparison, the authors examined CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction with 20 μM photosensitizer, 0.6 μM FeTDHPP, and 60 mM BIH. Under these conditions, all six dyes gave CO as the major product, but their activities differed substantially. PS 5 was the most active, reaching a catalyst-based turnover number for CO of 21,616, while PS 4 was the next strongest at 8360. PSs 1–3 were less active, and PS 6 was markedly poorer. The article relates these differences to substituent effects within the anthraquinone framework.&lt;br /&gt;
&lt;br /&gt;
To evaluate photosensitizer endurance and efficiency separately, the authors also used conditions with high catalyst concentration and low dye concentration. With 20 μM FeTDHPP, 5 μM photosensitizer, and 60 mM BIH, PS 5 gave a photosensitizer-based turnover number for CO of 6012. PS 4 again performed strongly, while the others were lower.&lt;br /&gt;
&lt;br /&gt;
The article further reports experiments in which PS 5 and FeTDHPP were used at the same concentration. Under these matched conditions, the system achieved a CO turnover number of 4978 and a quantum efficiency of 11.1% at 450 nm, based on two photons per CO. This is presented as evidence that both light harvesting and catalytic reduction are efficient in this molecular combination.&lt;br /&gt;
&lt;br /&gt;
Mechanistically, the article argues that the system operates mainly through &amp;#039;&amp;#039;reductive quenching&amp;#039;&amp;#039; rather than oxidative quenching. The evidence includes the very high concentration of BIH relative to FeTDHPP, fluorescence lifetime quenching by BIH near the diffusion-controlled limit, and the lack of evidence for ground-state reaction between the dyes and either BIH or FeTDHPP in UV/Vis and &amp;lt;sup&amp;gt;1&amp;lt;/sup&amp;gt;H NMR studies. Because spectral overlap prevented accurate determination of oxidative quenching constants, the oxidative pathway is not completely excluded experimentally, but the data are interpreted in favor of reductive quenching as the dominant route.&lt;br /&gt;
&lt;br /&gt;
The authors also note that aminoanthraquinones can undergo excited-state intramolecular proton transfer, which complicated interpretation of steady-state emission quenching. For that reason, they relied on fluorescence lifetime measurements to determine quenching rate constants. These rate constants were all greater than 10&amp;lt;sup&amp;gt;9&amp;lt;/sup&amp;gt; M&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt; s&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt;, and the initial catalytic turnover frequencies showed a generally linear trend with these quenching constants.&lt;br /&gt;
&lt;br /&gt;
A central mechanistic feature is the photochemical reduction and protonation sequence of the anthraquinone dyes. To probe this, the article studies anthraquinone itself as a model. Under irradiation in the presence of BIH, UV/Vis spectroscopy showed formation of transient species assigned by the authors to AQH•, AQH&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;, AQH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;, and eventually a more reduced species absorbing near 400 nm. By analogy, related intermediates are proposed for PSs 1–6.&lt;br /&gt;
&lt;br /&gt;
The article proposes that after reductive quenching and proton-coupled reduction, the photosensitizer forms a hydroxyanthrone-type intermediate PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;. Further excitation and reduction then generate PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. This reduced hydroxyanthrone-type species is proposed to be the key reductant that transfers electrons to the iron catalyst. This proposal is supported by several observations: a ~400 nm photoproduct accumulates during photolysis; adding FeTDHPP to a pre-irradiated solution of PS 5 and BIH caused rapid CO formation and formation of an Fe(I) species; and in situ square-wave voltammetry showed new reduction waves at potentials more negative than −1.90 V vs SCE after irradiation, consistent with a strongly reducing photoproduct.&lt;br /&gt;
&lt;br /&gt;
The iron catalyst undergoes stepwise photoreduction. UV/Vis experiments under white light showed conversion of Fe(III) to Fe(II) within minutes, followed by formation of Fe(I). The article notes that CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction by FeTDHPP is associated with an Fe(0) state, and proposes that PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; reduces Fe(II) or Fe(I) onward to Fe(0), from which CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction proceeds. Proton transfer is included in the proposed catalytic cycle, and the scheme presented by the authors includes 2 H&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; in the conversion of CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to CO.&lt;br /&gt;
&lt;br /&gt;
The role of BIH is twofold in the article’s interpretation. First, BIH reductively quenches the excited photosensitizer. Second, its one-electron oxidation product BI• is considered important in the photochemical sequence that generates PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;. Experiments under long-wavelength irradiation (&amp;amp;gt;550 nm), which suppress formation of PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt;, gave much slower CO production and mainly Fe(II) with less Fe(I), supporting the idea that direct BI• reduction of the catalyst is much less effective than reduction mediated by the reduced hydroxyanthrone-type dye intermediate.&lt;br /&gt;
&lt;br /&gt;
Several control and supporting experiments strengthen the chemical interpretation. Dynamic light scattering detected no nanoparticles before or after catalysis, and mercury poisoning did not significantly suppress activity, supporting a homogeneous molecular system rather than catalysis by metal particles. Isotopic labeling under &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; gave exclusive &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;CO, confirming CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; as the carbon source of the product. Stability tests in which additional components were added after activity decline showed that adding catalyst and BIH restored much more activity than adding BIH alone or photosensitizer plus BIH, indicating faster decomposition of the iron catalyst than the anthraquinone dye.&lt;br /&gt;
&lt;br /&gt;
Regarding side products, H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation was strongly suppressed in most systems. CO selectivity exceeded 99% for PSs 1–5 and was 98.5% for PS 6. The article attributes the poorer performance of PS 6 partly to its acidic sulfonyl group, which may facilitate proton transfer to the catalyst and thereby enhance H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; formation relative to the other dyes. CH&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt; and HCOOH are not reported as products for this aminoanthraquinone/FeTDHPP photocatalytic system.&lt;br /&gt;
&lt;br /&gt;
== Catalyst ==&lt;br /&gt;
The catalyst is FeTDHPP, an iron porphyrin complex. The article treats it as a molecular homogeneous CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction catalyst. It is used at low micromolar concentration in the main benchmarking experiments and is responsible for converting CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; to CO after receiving electrons from reduced photosensitizer-derived intermediates.&lt;br /&gt;
&lt;br /&gt;
The catalyst cycles through multiple oxidation states during operation. UV/Vis experiments support formation of Fe(II) and Fe(I) during photolysis, and the article states that CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; reduction by this catalyst occurs at an Fe(0) oxidation state. The proposed mechanism therefore involves sequential reduction of Fe(III) to Fe(II), Fe(I), and Fe(0).&lt;br /&gt;
&lt;br /&gt;
FeTDHPP is presented as highly selective for CO formation in this photocatalytic pairing, with H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; production largely suppressed under most conditions. However, its long-term stability is limited. Component-readdition experiments indicate that the catalyst decomposes faster than the anthraquinone dye, and this decomposition is an important cause of activity loss during prolonged irradiation.&lt;br /&gt;
&lt;br /&gt;
The catalyst remains molecular under the tested conditions according to the article’s control experiments. Dynamic light scattering did not reveal nanoparticle formation, and mercury poisoning did not materially change performance. These observations support homogeneous catalysis by the iron porphyrin complex rather than a heterogeneous impurity-derived pathway.&lt;br /&gt;
&lt;br /&gt;
== Photosensitizer ==&lt;br /&gt;
The photosensitizers are aminoanthraquinone organic dyes labeled 1–6. They act as visible-light absorbers and are the primary photoactive components responsible for initiating electron transfer from BIH to the catalyst. Their visible absorption maxima span from 478 to 592 nm, and they emit in the red region with nanosecond-scale lifetimes.&lt;br /&gt;
&lt;br /&gt;
The main photosensitizer highlighted by performance is PS 5. It gave the highest catalyst-based and photosensitizer-based turnover numbers for CO among the series and also delivered the highest reported quantum efficiency for CO production at 450 nm. PS 4 was the next strongest performer, while PS 6 was the least favorable among the hydroxy-containing derivatives.&lt;br /&gt;
&lt;br /&gt;
The article proposes that these dyes function mainly through reductive quenching of the excited state by BIH. Fluorescence lifetime quenching supports rapid electron transfer from BIH to excited PS. The reduced dyes then undergo proton-coupled transformations to hydroxyanthrone-type forms, and a further reduced species, written as PSH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;−&amp;lt;/sup&amp;gt; in the proposed mechanism, is suggested to be the active reductant for the iron catalyst.&lt;br /&gt;
&lt;br /&gt;
Structure matters strongly. The article explicitly interprets the substituent effects in terms of an internal donor–acceptor design within the anthraquinone framework. Amino groups are described as electron donating and hydroxyl groups as electron withdrawing on the anthraquinone core, and the best-performing dyes are those in which this asymmetry is thought to promote electron transfer. The poorer behavior of PS 6 is linked to its sulfonyl group and increased H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; selectivity.&lt;br /&gt;
&lt;br /&gt;
The dyes are relatively more persistent than the catalyst under reaction conditions, but they are not indefinitely stable. The system eventually loses activity, and although dye decomposition is not identified as the dominant failure pathway, the article does not claim unlimited photosensitizer durability.&lt;br /&gt;
&lt;br /&gt;
== Investigation ==&lt;br /&gt;
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=inv0}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Photocatalytic CO2 conversion]]&lt;/div&gt;</description>
			<pubDate>Fri, 04 Sep 2026 12:16:03 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.1038_s41467-023-36784-7</comments>
		</item>
		<item>
			<title>10.1038 s41467-023-36784-7/inv0</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7/inv0&amp;diff=11490&amp;oldid=0</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.1038_s41467-023-36784-7/inv0&amp;diff=11490&amp;oldid=0</guid>
			<description>&lt;p&gt;auto-generated&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Photocatalytic_CO2_conversion_experiments|experiments={{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=2395&lt;br /&gt;
|Turnover_frequency__CO=1510&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=2011&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=1&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=8.9&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=2738&lt;br /&gt;
|Turnover_frequency__CO=69&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=482&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=2&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=0.3&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=3551&lt;br /&gt;
|Turnover_frequency__CO=593&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=1523&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=3&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=3.0&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=8360&lt;br /&gt;
|Turnover_frequency__CO=1614&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=2849&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=4&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=8.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.0005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3174&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=19158&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=21616&lt;br /&gt;
|Turnover_frequency__CO=4028&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2576&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4028&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=10&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3942&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=1&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.001&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3587&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=1&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=17020&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=6012&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2325&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=11.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=2134&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.002&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=3817&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=8780&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.015&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=8772&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=5593&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=2&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=11250&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=50&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=891&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4978&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=11.1&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=5&lt;br /&gt;
|PS=5&lt;br /&gt;
|PS conc=0.01&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=not reported&lt;br /&gt;
|Turnover_number__CO=4128&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=0.6&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=48&lt;br /&gt;
|Turnover_number__CO=907&lt;br /&gt;
|Turnover_frequency__CO=93&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.005&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=&amp;gt;400&lt;br /&gt;
|irr time=72&lt;br /&gt;
|Turnover_number__CO=1183&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=100&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
{{Photocatalytic_CO2_conversion&lt;br /&gt;
|catalyst=FeTDHPP&lt;br /&gt;
|cat conc=20&lt;br /&gt;
|PS=6&lt;br /&gt;
|PS conc=0.02&lt;br /&gt;
|e-D=Molecule:100508&lt;br /&gt;
|e-D conc=0.06&lt;br /&gt;
|solvent A=Molecule:100529&lt;br /&gt;
|solvent B=&lt;br /&gt;
|solvent-ratio=&lt;br /&gt;
|feedstock gas=CO2&lt;br /&gt;
|Temperature=20&lt;br /&gt;
|λexc=450&lt;br /&gt;
|irr time=1&lt;br /&gt;
|Turnover_number__CO=not reported&lt;br /&gt;
|Turnover_frequency__CO=not reported&lt;br /&gt;
|Turnover_number__H2=not reported&lt;br /&gt;
|Turnover_frequency__H2=not reported&lt;br /&gt;
|additives=&lt;br /&gt;
|Turnover_number__HCOOH=not reported&lt;br /&gt;
|intensity=not reported&lt;br /&gt;
|Turnover_number__CH4=not reported&lt;br /&gt;
|additives conc=&lt;br /&gt;
|Quantum_yield__CO=2.0&lt;br /&gt;
|H-D=&lt;br /&gt;
|H-D conc=&lt;br /&gt;
|solvent C=&lt;br /&gt;
|Quantum_yield__HCOOH=&lt;br /&gt;
}}&lt;br /&gt;
}}&lt;/div&gt;</description>
			<pubDate>Fri, 04 Sep 2026 12:16:02 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.1038_s41467-023-36784-7/inv0</comments>
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			<title>Category:How to Choose a Better Online Casino Experience in 2026</title>
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			<title>Category:Exploring Better Online Casino Choices: What Modern Players Should Know</title>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
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				&lt;tr class=&quot;diff-title&quot; lang=&quot;en&quot;&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 17:35, 31 August 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l1&quot;&gt;Line 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[Category&lt;/del&gt;:&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Topic]][[Category:Publication]&lt;/del&gt;]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;The online casino industry has developed rapidly, giving players access to a wide range of games, payment options, promotional campaigns, and digital entertainment experiences. With so many platforms competing for attention, selecting the right casino requires more thought than simply choosing a website with an attractive advertisement.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;{{BaseTemplate}}&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Modern players are increasingly interested in convenience, variety, transparency, and dependable access. Understanding these factors can make the overall experience more organized and enjoyable.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Start With a Reliable Gaming Environment&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;A good online casino should make it easy for users to understand how the platform works. Important information about registration, deposits, withdrawals, bonuses, and available games should be presented in a straightforward way.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Players should also pay attention to website performance. A platform that loads properly on both desktop and mobile devices can provide a smoother experience. Simple navigation is another advantage because users can quickly find their preferred games without unnecessary steps.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;When researching the &lt;/ins&gt;[&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;https&lt;/ins&gt;:&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;//betsmovetr.com/ betsmove güncel adresi&lt;/ins&gt;]&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;, players should also be careful with outdated information. Online casino addresses can change, so relying on current and trustworthy access information is preferable to following random pages or unfamiliar advertisements.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Explore Different Game Categories&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Game selection remains one of the biggest reasons people choose one casino platform over another. Some players enjoy modern video slots with innovative themes, while others prefer classic table games such as roulette, blackjack, and baccarat.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Live casino games have also become increasingly popular because they combine online convenience with real-time dealer interaction. These games can provide a different atmosphere compared with traditional digital casino titles.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Instead of judging a platform only by the number of available games, players should consider whether the selection actually matches their interests. A smaller but well-organized catalogue can sometimes be more useful than an enormous collection that is difficult to navigate.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Read Promotional Conditions Carefully&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Bonuses can add extra value to an online casino experience, but promotional offers should never be judged by their headline amounts alone.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Players should check wagering requirements, eligible games, minimum deposits, maximum bonus values, expiration periods, and withdrawal restrictions before accepting an offer. These conditions determine how useful a promotion may actually be.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Taking time to understand the terms can prevent misunderstandings later. Players should also remember that promotional funds are not guaranteed winnings and should not encourage them to spend beyond their planned budget.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Consider Deposits and Withdrawals&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Financial transactions are another important part of choosing an online casino. Different platforms support different payment methods, and transaction times can vary depending on the option selected.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Before depositing, players should review the available methods and understand whether fees or minimum transaction amounts apply. Withdrawal procedures deserve equal attention because some platforms may require account verification before processing payments.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Keeping personal account information secure is equally important. Players should use strong passwords, avoid sharing login credentials, and be cautious when entering information on unfamiliar pages.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Why Current Website Information Matters&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Online services sometimes update their domains or access routes. As a result, players may encounter old addresses that no longer provide the expected service.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Anyone searching for the betsmove güncel adresi should verify that the information they find is current before entering account details. Search results can contain outdated pages, copied information, or unrelated websites, so careful checking is worthwhile.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Players should also avoid suspicious pages that request unnecessary personal information or attempt to redirect visitors through multiple unknown websites. Taking a few additional moments to confirm the destination can help create a safer browsing routine.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Mobile Gaming and Convenience&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Mobile compatibility has become an essential part of modern online gaming. Many users prefer playing from smartphones or tablets because these devices allow convenient access without requiring a desktop computer.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;A well-designed mobile experience should provide readable menus, responsive controls, fast loading times, and easy access to account functions. Players can test basic navigation before deciding whether a platform suits their preferences.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Mobile users should also keep their devices updated and avoid connecting through unsecured public networks when accessing accounts.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Practice Responsible Gaming&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Entertainment should remain the primary purpose of online casino activity. Players can establish personal limits for both time and spending before beginning a gaming session.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Setting a fixed budget can help prevent impulsive decisions. It is also useful to take regular breaks and avoid chasing losses. Gambling outcomes are unpredictable, and previous results do not guarantee future results.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;If gaming stops feeling recreational and begins interfering with everyday responsibilities, taking a break is an important step.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Conclusion&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Finding a suitable online casino involves looking beyond flashy promotions. Game variety, website usability, payment options, current access information, mobile performance, and responsible gaming practices all contribute to a better overall experience.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;For players researching the betsmove güncel adresi, checking current information carefully is an important part of the process. By comparing platforms thoughtfully and maintaining sensible limits, players can make more informed choices and keep online casino entertainment enjoyable.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Mon, 31 Aug 2026 15:35:00 GMT</pubDate>
			<dc:creator>110.39.39.26</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Exploring_Better_Online_Casino_Choices:_What_Modern_Players_Should_Know</comments>
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			<title>Category:Exploring Better Online Casino Choices: What Modern Players Should Know</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=Category:Exploring_Better_Online_Casino_Choices:_What_Modern_Players_Should_Know&amp;diff=11482&amp;oldid=0</link>
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			<pubDate>Mon, 31 Aug 2026 15:34:06 GMT</pubDate>
			<dc:creator>110.39.39.26</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Exploring_Better_Online_Casino_Choices:_What_Modern_Players_Should_Know</comments>
		</item>
		<item>
			<title>เส้นทางแห่งความก้าวหน้าและการปรับตัวของวงการเสี่ยงโชคในยุคไอที</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/%E0%B9%80%E0%B8%AA%E0%B9%89%E0%B8%99%E0%B8%97%E0%B8%B2%E0%B8%87%E0%B9%81%E0%B8%AB%E0%B9%88%E0%B8%87%E0%B8%84%E0%B8%A7%E0%B8%B2%E0%B8%A1%E0%B8%81%E0%B9%89%E0%B8%B2%E0%B8%A7%E0%B8%AB%E0%B8%99%E0%B9%89%E0%B8%B2%E0%B9%81%E0%B8%A5%E0%B8%B0%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B8%9B%E0%B8%A3%E0%B8%B1%E0%B8%9A%E0%B8%95%E0%B8%B1%E0%B8%A7%E0%B8%82%E0%B8%AD%E0%B8%87%E0%B8%A7%E0%B8%87%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B9%80%E0%B8%AA%E0%B8%B5%E0%B9%88%E0%B8%A2%E0%B8%87%E0%B9%82%E0%B8%8A%E0%B8%84%E0%B9%83%E0%B8%99%E0%B8%A2%E0%B8%B8%E0%B8%84%E0%B9%84%E0%B8%AD%E0%B8%97%E0%B8%B5</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=%E0%B9%80%E0%B8%AA%E0%B9%89%E0%B8%99%E0%B8%97%E0%B8%B2%E0%B8%87%E0%B9%81%E0%B8%AB%E0%B9%88%E0%B8%87%E0%B8%84%E0%B8%A7%E0%B8%B2%E0%B8%A1%E0%B8%81%E0%B9%89%E0%B8%B2%E0%B8%A7%E0%B8%AB%E0%B8%99%E0%B9%89%E0%B8%B2%E0%B9%81%E0%B8%A5%E0%B8%B0%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B8%9B%E0%B8%A3%E0%B8%B1%E0%B8%9A%E0%B8%95%E0%B8%B1%E0%B8%A7%E0%B8%82%E0%B8%AD%E0%B8%87%E0%B8%A7%E0%B8%87%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B9%80%E0%B8%AA%E0%B8%B5%E0%B9%88%E0%B8%A2%E0%B8%87%E0%B9%82%E0%B8%8A%E0%B8%84%E0%B9%83%E0%B8%99%E0%B8%A2%E0%B8%B8%E0%B8%84%E0%B9%84%E0%B8%AD%E0%B8%97%E0%B8%B5&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;เส้นทางแห่งความก้าวหน้าและการปรับตัวของวงการเสี่ยงโชคในยุคไอที (page does not exist)&quot;&gt;เส้นทางแห่งความก้าวหน้าและการปรับตัวของวงการเสี่ยงโชคในยุคไอที&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Mon, 31 Aug 2026 15:00:23 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:%E0%B9%80%E0%B8%AA%E0%B9%89%E0%B8%99%E0%B8%97%E0%B8%B2%E0%B8%87%E0%B9%81%E0%B8%AB%E0%B9%88%E0%B8%87%E0%B8%84%E0%B8%A7%E0%B8%B2%E0%B8%A1%E0%B8%81%E0%B9%89%E0%B8%B2%E0%B8%A7%E0%B8%AB%E0%B8%99%E0%B9%89%E0%B8%B2%E0%B9%81%E0%B8%A5%E0%B8%B0%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B8%9B%E0%B8%A3%E0%B8%B1%E0%B8%9A%E0%B8%95%E0%B8%B1%E0%B8%A7%E0%B8%82%E0%B8%AD%E0%B8%87%E0%B8%A7%E0%B8%87%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B9%80%E0%B8%AA%E0%B8%B5%E0%B9%88%E0%B8%A2%E0%B8%87%E0%B9%82%E0%B8%8A%E0%B8%84%E0%B9%83%E0%B8%99%E0%B8%A2%E0%B8%B8%E0%B8%84%E0%B9%84%E0%B8%AD%E0%B8%97%E0%B8%B5</comments>
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			<title>พลิกโฉมประสบการณ์การเสี่ยงโชคให้ล้ำสมัยและตอบโจทย์คนรุ่นใหม่</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/%E0%B8%9E%E0%B8%A5%E0%B8%B4%E0%B8%81%E0%B9%82%E0%B8%89%E0%B8%A1%E0%B8%9B%E0%B8%A3%E0%B8%B0%E0%B8%AA%E0%B8%9A%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B8%93%E0%B9%8C%E0%B8%81%E0%B8%B2%E0%B8%A3%E0%B9%80%E0%B8%AA%E0%B8%B5%E0%B9%88%E0%B8%A2%E0%B8%87%E0%B9%82%E0%B8%8A%E0%B8%84%E0%B9%83%E0%B8%AB%E0%B9%89%E0%B8%A5%E0%B9%89%E0%B8%B3%E0%B8%AA%E0%B8%A1%E0%B8%B1%E0%B8%A2%E0%B9%81%E0%B8%A5%E0%B8%B0%E0%B8%95%E0%B8%AD%E0%B8%9A%E0%B9%82%E0%B8%88%E0%B8%97%E0%B8%A2%E0%B9%8C%E0%B8%84%E0%B8%99%E0%B8%A3%E0%B8%B8%E0%B9%88%E0%B8%99%E0%B9%83%E0%B8%AB%E0%B8%A1%E0%B9%88</link>
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</description>
			<pubDate>Mon, 31 Aug 2026 15:00:22 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
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		</item>
		<item>
			<title>Menyusuri Keindahan Estetika dan Sensasi Permainan Kasino Digital</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menyusuri_Keindahan_Estetika_dan_Sensasi_Permainan_Kasino_Digital</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Menyusuri_Keindahan_Estetika_dan_Sensasi_Permainan_Kasino_Digital&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Menyusuri Keindahan Estetika dan Sensasi Permainan Kasino Digital (page does not exist)&quot;&gt;Menyusuri Keindahan Estetika dan Sensasi Permainan Kasino Digital&lt;/a&gt; Spam&lt;/p&gt;
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			<pubDate>Mon, 31 Aug 2026 15:00:21 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menyusuri_Keindahan_Estetika_dan_Sensasi_Permainan_Kasino_Digital</comments>
		</item>
		<item>
			<title>Menyelami Fenomena Hiburan Slot Kasino Digital di Era Kontemporer</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menyelami_Fenomena_Hiburan_Slot_Kasino_Digital_di_Era_Kontemporer</link>
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			<pubDate>Mon, 31 Aug 2026 15:00:20 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menyelami_Fenomena_Hiburan_Slot_Kasino_Digital_di_Era_Kontemporer</comments>
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		<item>
			<title>Menjelajahi Keunikan Kreatif dan Estetika dalam Lanskap Hiburan Digital Modern</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menjelajahi_Keunikan_Kreatif_dan_Estetika_dalam_Lanskap_Hiburan_Digital_Modern</link>
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			<pubDate>Mon, 31 Aug 2026 15:00:19 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menjelajahi_Keunikan_Kreatif_dan_Estetika_dalam_Lanskap_Hiburan_Digital_Modern</comments>
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			<title>Menikmati Pesona Seni Visual dan Inovasi dalam Lanskap Hiburan Virtual</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menikmati_Pesona_Seni_Visual_dan_Inovasi_dalam_Lanskap_Hiburan_Virtual</link>
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			<pubDate>Mon, 31 Aug 2026 15:00:17 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menikmati_Pesona_Seni_Visual_dan_Inovasi_dalam_Lanskap_Hiburan_Virtual</comments>
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		<item>
			<title>Menghadirkan Ruang Tenang di Tengah Hiruk-Pikuk Rutinitas</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menghadirkan_Ruang_Tenang_di_Tengah_Hiruk-Pikuk_Rutinitas</link>
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			<pubDate>Mon, 31 Aug 2026 15:00:12 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menghadirkan_Ruang_Tenang_di_Tengah_Hiruk-Pikuk_Rutinitas</comments>
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			<title>Menemukan Harmoni dan Hiburan Berkualitas dalam Dunia Kasino Daring</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menemukan_Harmoni_dan_Hiburan_Berkualitas_dalam_Dunia_Kasino_Daring</link>
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			<pubDate>Mon, 31 Aug 2026 15:00:09 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menemukan_Harmoni_dan_Hiburan_Berkualitas_dalam_Dunia_Kasino_Daring</comments>
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			<title>Category:A Simple Step-by-Step Overview of the Ufabet Login Process</title>
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			<pubDate>Mon, 31 Aug 2026 15:00:04 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:A_Simple_Step-by-Step_Overview_of_the_Ufabet_Login_Process</comments>
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		<item>
			<title>Category:Hello sir</title>
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 14:31, 31 August 2026&lt;/td&gt;
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			<pubDate>Mon, 31 Aug 2026 12:31:26 GMT</pubDate>
			<dc:creator>110.39.39.26</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Hello_sir</comments>
		</item>
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			<title>Category:Hello sir</title>
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			<pubDate>Mon, 31 Aug 2026 12:30:59 GMT</pubDate>
			<dc:creator>110.39.39.26</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Hello_sir</comments>
		</item>
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			<title>Category:Why Secure Credentials Matter When Using Ufabet Login for Online Access</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Category:Why_Secure_Credentials_Matter_When_Using_Ufabet_Login_for_Online_Access</link>
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			<pubDate>Sun, 30 Aug 2026 15:00:06 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Why_Secure_Credentials_Matter_When_Using_Ufabet_Login_for_Online_Access</comments>
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			<title>Category:Important Things to Consider Before Getting Started With Online Soccer Betting</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Category:Important_Things_to_Consider_Before_Getting_Started_With_Online_Soccer_Betting</link>
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			<pubDate>Sun, 30 Aug 2026 15:00:05 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Important_Things_to_Consider_Before_Getting_Started_With_Online_Soccer_Betting</comments>
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			<title>Category:What to Check Before Using Ufabet Login Access on a New Device</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Category:What_to_Check_Before_Using_Ufabet_Login_Access_on_a_New_Device</link>
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			<pubDate>Sat, 29 Aug 2026 15:00:19 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:What_to_Check_Before_Using_Ufabet_Login_Access_on_a_New_Device</comments>
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			<title>Merajut Kisah Dan Estetika Di Balik Layar Hiburan Kasino Daring Modern</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Merajut_Kisah_Dan_Estetika_Di_Balik_Layar_Hiburan_Kasino_Daring_Modern</link>
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			<pubDate>Sat, 29 Aug 2026 15:00:17 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Merajut_Kisah_Dan_Estetika_Di_Balik_Layar_Hiburan_Kasino_Daring_Modern</comments>
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			<title>Merajut Kembali Kebugaran Tubuh Lewat Seni Pijat Tradisional Berkualitas</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Merajut_Kembali_Kebugaran_Tubuh_Lewat_Seni_Pijat_Tradisional_Berkualitas</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Merajut_Kembali_Kebugaran_Tubuh_Lewat_Seni_Pijat_Tradisional_Berkualitas&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Merajut Kembali Kebugaran Tubuh Lewat Seni Pijat Tradisional Berkualitas (page does not exist)&quot;&gt;Merajut Kembali Kebugaran Tubuh Lewat Seni Pijat Tradisional Berkualitas&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Sat, 29 Aug 2026 15:00:16 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Merajut_Kembali_Kebugaran_Tubuh_Lewat_Seni_Pijat_Tradisional_Berkualitas</comments>
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		<item>
			<title>Menyongsong Era Baru Hiburan Digital Dalam Industri Slot Dan Kasino Daring</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menyongsong_Era_Baru_Hiburan_Digital_Dalam_Industri_Slot_Dan_Kasino_Daring</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Menyongsong_Era_Baru_Hiburan_Digital_Dalam_Industri_Slot_Dan_Kasino_Daring&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Menyongsong Era Baru Hiburan Digital Dalam Industri Slot Dan Kasino Daring (page does not exist)&quot;&gt;Menyongsong Era Baru Hiburan Digital Dalam Industri Slot Dan Kasino Daring&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Sat, 29 Aug 2026 15:00:15 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menyongsong_Era_Baru_Hiburan_Digital_Dalam_Industri_Slot_Dan_Kasino_Daring</comments>
		</item>
		<item>
			<title>Menyelami Daya Tarik dan Inovasi dalam Industri Hiburan Daring</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menyelami_Daya_Tarik_dan_Inovasi_dalam_Industri_Hiburan_Daring</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/Menyelami_Daya_Tarik_dan_Inovasi_dalam_Industri_Hiburan_Daring</guid>
			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Menyelami_Daya_Tarik_dan_Inovasi_dalam_Industri_Hiburan_Daring&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Menyelami Daya Tarik dan Inovasi dalam Industri Hiburan Daring (page does not exist)&quot;&gt;Menyelami Daya Tarik dan Inovasi dalam Industri Hiburan Daring&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Sat, 29 Aug 2026 15:00:14 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menyelami_Daya_Tarik_dan_Inovasi_dalam_Industri_Hiburan_Daring</comments>
		</item>
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			<title>Menjelajahi Panorama Estetika Dan Filosofi Rekreasi Dalam Ekosistem Kasino Digital</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menjelajahi_Panorama_Estetika_Dan_Filosofi_Rekreasi_Dalam_Ekosistem_Kasino_Digital</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Menjelajahi_Panorama_Estetika_Dan_Filosofi_Rekreasi_Dalam_Ekosistem_Kasino_Digital&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Menjelajahi Panorama Estetika Dan Filosofi Rekreasi Dalam Ekosistem Kasino Digital (page does not exist)&quot;&gt;Menjelajahi Panorama Estetika Dan Filosofi Rekreasi Dalam Ekosistem Kasino Digital&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Sat, 29 Aug 2026 15:00:12 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menjelajahi_Panorama_Estetika_Dan_Filosofi_Rekreasi_Dalam_Ekosistem_Kasino_Digital</comments>
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			<title>Menjelajahi Horizon Baru Hiburan Daring Dan Eksplorasi Seni Digital Kasino Modern</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Menjelajahi_Horizon_Baru_Hiburan_Daring_Dan_Eksplorasi_Seni_Digital_Kasino_Modern</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Menjelajahi_Horizon_Baru_Hiburan_Daring_Dan_Eksplorasi_Seni_Digital_Kasino_Modern&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Menjelajahi Horizon Baru Hiburan Daring Dan Eksplorasi Seni Digital Kasino Modern (page does not exist)&quot;&gt;Menjelajahi Horizon Baru Hiburan Daring Dan Eksplorasi Seni Digital Kasino Modern&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Sat, 29 Aug 2026 15:00:11 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:Menjelajahi_Horizon_Baru_Hiburan_Daring_Dan_Eksplorasi_Seni_Digital_Kasino_Modern</comments>
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			<title>EKSISTENSI REKREASI VIRTUAL DAN PENGARUHNYA TERHADAP GAYA HIDUP DIGITAL</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/EKSISTENSI_REKREASI_VIRTUAL_DAN_PENGARUHNYA_TERHADAP_GAYA_HIDUP_DIGITAL</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=EKSISTENSI_REKREASI_VIRTUAL_DAN_PENGARUHNYA_TERHADAP_GAYA_HIDUP_DIGITAL&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;EKSISTENSI REKREASI VIRTUAL DAN PENGARUHNYA TERHADAP GAYA HIDUP DIGITAL (page does not exist)&quot;&gt;EKSISTENSI REKREASI VIRTUAL DAN PENGARUHNYA TERHADAP GAYA HIDUP DIGITAL&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Sat, 29 Aug 2026 15:00:06 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:EKSISTENSI_REKREASI_VIRTUAL_DAN_PENGARUHNYA_TERHADAP_GAYA_HIDUP_DIGITAL</comments>
		</item>
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			<title>Category:What Beginners Should Check Before Using Ufabet Direct Website Access</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Category:What_Beginners_Should_Check_Before_Using_Ufabet_Direct_Website_Access</link>
			<guid isPermaLink="false">https://chemwiki.scc.kit.edu/main/mediawiki/Category:What_Beginners_Should_Check_Before_Using_Ufabet_Direct_Website_Access</guid>
			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Category:What_Beginners_Should_Check_Before_Using_Ufabet_Direct_Website_Access&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Category:What Beginners Should Check Before Using Ufabet Direct Website Access (page does not exist)&quot;&gt;Category:What Beginners Should Check Before Using Ufabet Direct Website Access&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Fri, 28 Aug 2026 15:00:22 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:What_Beginners_Should_Check_Before_Using_Ufabet_Direct_Website_Access</comments>
		</item>
		<item>
			<title>Category:777YK Slot: A Complete Guide to Making Better-Informed Game Choices</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/Category:777YK_Slot:_A_Complete_Guide_to_Making_Better-Informed_Game_Choices</link>
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			<description>&lt;p&gt;&lt;a href=&quot;/main/mediawiki/index.php?title=User:Maintenance_script&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new mw-userlink&quot; title=&quot;User:Maintenance script (page does not exist)&quot;&gt;&lt;bdi&gt;Maintenance script&lt;/bdi&gt;&lt;/a&gt; deleted page &lt;a href=&quot;/main/mediawiki/index.php?title=Category:777YK_Slot:_A_Complete_Guide_to_Making_Better-Informed_Game_Choices&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Category:777YK Slot: A Complete Guide to Making Better-Informed Game Choices (page does not exist)&quot;&gt;Category:777YK Slot: A Complete Guide to Making Better-Informed Game Choices&lt;/a&gt; Spam&lt;/p&gt;
</description>
			<pubDate>Fri, 28 Aug 2026 15:00:04 GMT</pubDate>
			<dc:creator>Maintenance script</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:777YK_Slot:_A_Complete_Guide_to_Making_Better-Informed_Game_Choices</comments>
		</item>
		<item>
			<title>Category:Common Registration Mistakes to Avoid When Using Register with ufabet UFA168 Login</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=Category:Common_Registration_Mistakes_to_Avoid_When_Using_Register_with_ufabet_UFA168_Login&amp;diff=11440&amp;oldid=11439</link>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 16:34, 28 August 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l1&quot;&gt;Line 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[Category&lt;/del&gt;:&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Topic]][[Category:Publication]&lt;/del&gt;]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Introduction to Safer Account Registration&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;{{BaseTemplate}}&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Registering for an online betting account may appear to be a straightforward process, but small mistakes during registration can create unnecessary problems later. When dealing with services associated with ufabet or UFA168 login, beginners should pay attention to account details, security information, verification requirements, and the legitimacy of the website they are using. Rushing through registration simply to reach the betting interface can result in incorrect information, weak passwords, or confusion about account conditions. A better approach is to treat registration as an important security step. By understanding the most common mistakes and learning how to avoid them, newcomers can create an account more carefully and establish good habits from the beginning.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Using an Unverified Registration Website&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;One of the most serious mistakes is entering personal information into an unofficial or fraudulent registration page. Search engines, advertisements, social media posts, and private messages can sometimes direct users toward &lt;/ins&gt;[&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;https&lt;/ins&gt;:&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;//www.ufabet168.global/register/ สมัคร ufabet ufa168 ทางเข้า&lt;/ins&gt;] &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;websites that imitate legitimate services. These pages may look convincing while attempting to collect usernames, passwords, phone numbers, or financial information. Before registering, users should carefully verify the website address and rely on trusted official information when identifying the appropriate access point. Beginners should never assume that a page is legitimate simply because it uses familiar branding or appears in search results. If the source cannot be verified, it is safer to stop rather than submit sensitive information.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Entering Incorrect Personal Information&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Another common mistake is rushing through registration and entering inaccurate information. Depending on the service&#039;s requirements, users may need to provide contact details or other personal information that could later be used for account verification. Incorrect information can create difficulties when recovering an account or completing legitimate verification procedures. Users should carefully review every field before submitting the registration form and make sure that required information is accurate. They should also avoid creating an account using someone else&#039;s identity or allowing another person to register on their behalf. Account ownership should remain clear from the beginning.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Choosing a Weak or Reused Password&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;A password should not be treated as a minor part of registration. Using simple combinations such as a name, birthday, phone number, or sequential numbers can make an account easier to compromise. Reusing a password from another website creates another risk because a breach elsewhere could expose the same credentials. Beginners should create a strong, unique password specifically for their betting account. A password manager can be useful for generating and storing secure credentials. Most importantly, passwords should never be shared with friends, unofficial agents, strangers, or people claiming to provide technical support.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Skipping the Terms and Conditions&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Many users make the mistake of clicking through registration terms without reading them. However, these documents can contain important information about eligibility, account responsibilities, betting rules, payment procedures, withdrawals, promotions, verification, and restrictions. Beginners should take time to understand the conditions before accepting them. Promotional terms deserve particular attention because bonuses can include wagering requirements, expiry dates, eligible games, and withdrawal restrictions. Understanding these rules before registering or depositing money can help users avoid unpleasant surprises. If a condition is unclear, users should seek clarification through legitimate support resources before proceeding.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Ignoring Verification Requirements&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Verification can be an important part of maintaining an online account, particularly when financial transactions are involved. Some beginners may become frustrated if they discover that additional verification is required after registration. A better approach is to understand potential verification requirements in advance and follow official instructions carefully. Users should never send identity documents, passwords, or security codes to random individuals who claim they can complete verification on their behalf. Sensitive information should only be provided through legitimate account procedures. If a verification request seems suspicious, users should pause and confirm it through an official support channel.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Registering Multiple Accounts Without Understanding the Rules&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Another mistake is creating multiple accounts without first checking the applicable account policy. Some online services may restrict users to one account or impose specific conditions regarding duplicate registrations. Opening additional accounts without understanding these rules can create complications involving verification, promotions, balances, or account access. Beginners should therefore read the relevant terms before creating another account. If there is an existing account-access problem, using the official recovery process is generally more appropriate than immediately registering again with different details.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Depositing Money Too Quickly&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Registration does not mean that a user must immediately deposit money. Beginners sometimes become focused on promotional offers or the excitement of accessing the platform and add funds before understanding the payment and withdrawal procedures. Before making a deposit, users should review supported payment methods, transaction limits, verification requirements, processing conditions, and any applicable restrictions. They should also establish a personal entertainment budget. Money required for rent, bills, food, education, savings, or other essential expenses should never be used for betting. A thoughtful registration process should include financial planning rather than an automatic commitment to spend.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Sharing Login Details With Other People&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Allowing another person to use an account is another avoidable mistake. Sharing usernames, passwords, verification codes, or recovery information can make it difficult to determine who is responsible if an account is compromised or a transaction becomes disputed. Users should maintain personal control over their credentials and should never provide confidential information simply because someone claims to be helping. Legitimate support should be accessed through official channels and should not require users to surrender their passwords.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Conclusion&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt; &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;Avoiding common registration mistakes can make the experience of using ufabet or UFA168 login considerably more organized and secure. Beginners should verify the registration website, provide accurate information, create a unique password, read the terms, understand verification procedures, check account policies, and avoid depositing money before understanding the financial conditions. Protecting login credentials is equally important because account security continues long after registration is complete. Finally, users should remember that online betting involves financial risk and should only be approached within clearly defined personal limits. Taking a few extra minutes during registration can help prevent problems and provide a stronger foundation for responsible online account management.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Fri, 28 Aug 2026 14:34:18 GMT</pubDate>
			<dc:creator>110.39.39.26</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Common_Registration_Mistakes_to_Avoid_When_Using_Register_with_ufabet_UFA168_Login</comments>
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		<item>
			<title>Category:Common Registration Mistakes to Avoid When Using Register with ufabet UFA168 Login</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=Category:Common_Registration_Mistakes_to_Avoid_When_Using_Register_with_ufabet_UFA168_Login&amp;diff=11439&amp;oldid=0</link>
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			<pubDate>Fri, 28 Aug 2026 14:33:37 GMT</pubDate>
			<dc:creator>110.39.39.26</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Category_talk:Common_Registration_Mistakes_to_Avoid_When_Using_Register_with_ufabet_UFA168_Login</comments>
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			<title>10.3389 fchem.2026.1892359</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=10.3389_fchem.2026.1892359&amp;diff=11438&amp;oldid=11433</link>
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 11:12, 28 August 2026&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;4&quot; class=&quot;diff-multi&quot; lang=&quot;en&quot;&gt;(One intermediate revision by the same user not shown)&lt;/td&gt;&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l57&quot;&gt;Line 57:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 57:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=inv0}}&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=inv0}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category: Photocatalytic CO2 conversion&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;, &lt;/del&gt;Heterogeneous photocatalytic CO2 conversion&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;, &lt;/del&gt;Photocatalytic CO2 conversion to CO&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;, &lt;/del&gt;Photocatalytic CO2 conversion to CH4&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;, &lt;/del&gt;CO2 conversion]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category: Photocatalytic CO2 conversion&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;]] &lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[Category: &lt;/ins&gt;Heterogeneous photocatalytic CO2 conversion&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;]]&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[Category: &lt;/ins&gt;Photocatalytic CO2 conversion to CO&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;]]&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[Category: &lt;/ins&gt;Photocatalytic CO2 conversion to CH4&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;]]&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[Category: &lt;/ins&gt;CO2 conversion]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Fri, 28 Aug 2026 09:12:54 GMT</pubDate>
			<dc:creator>WikiSysop</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Talk:10.3389_fchem.2026.1892359</comments>
		</item>
		<item>
			<title>Author:Liqun Ye</title>
			<link>https://chemwiki.scc.kit.edu/main/mediawiki/index.php?title=Author:Liqun_Ye&amp;diff=11436&amp;oldid=0</link>
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&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;This author does not have an ORCID, so we show all publications with the name &amp;quot;Liqun Ye&amp;quot; &lt;br /&gt;
{{#ask:&lt;br /&gt;
[[Has subobject::&amp;lt;q&amp;gt;[[Author::Liqun Ye]][[Orcid::-]]&amp;lt;/q&amp;gt;]]&lt;br /&gt;
|?DOI&lt;br /&gt;
|?Journal&lt;br /&gt;
|?Publication date&lt;br /&gt;
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[[Category:Author]]&lt;/div&gt;</description>
			<pubDate>Fri, 28 Aug 2026 08:54:36 GMT</pubDate>
			<dc:creator>127.0.0.1</dc:creator>
			<comments>https://chemwiki.scc.kit.edu/main/mediawiki/Author_talk:Liqun_Ye</comments>
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