Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene–Isoquinoline Complex: Difference between revisions
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{{ | {{DOI|doi=10.1021/ja4074003}} | ||
=== Abstract === | |||
==== Summary ==== | |||
The synthesis and characterization of a new family of earth-abundant nickel complexes supported by ''N''-heterocyclic carbene-amine ligands for the highly-selective conversion of CO<sub>2</sub> to CO has been shown. Turnover number (TON) of 98,000 and turnover frequency of 3.9 s<sup>-1</sup> were achieved using the nickel catalyst {{#moleculelink:|link=CFQFJQWFSHKEAB-UHFFFAOYSA-N|image=false|width=300|height=200}} in combination with the iridium complex {{#moleculelink:|link=NSABRUJKERBGOU-UHFFFAOYSA-N|image=false|width=300|height=200}} as the photosensitizer under visible-light catalysis. The experiments were performed using a Xenon lamp as the visible-light source with triethylamine as sacrificial electron donor. | |||
==== Advances and special progress ==== | |||
The reported novel earth-abundant complexes also emerged as catalysts for the electrochemical CO<sub>2</sub> conversion to CO. Among them, the complex {{#moleculelink:|link=CFQFJQWFSHKEAB-UHFFFAOYSA-N|image=false|width=300|height=200}} had the lowest cathodic onset potential of ''E''cat = −1.2 V vs SCE. | |||
==== Additional remarks ==== | |||
Further studies have revealed that the overall efficiency of the developed solar-to-fuel cycle may be limited by the formation of the active Ni catalyst and/or the chemical reduction of CO<sub>2</sub> to CO at the reduced nickel center and provide a starting point for improved photoredox systems for sustainable carbon-neutral energy conversion | |||
=== Content of the published article in detail === | |||
The article contains results for the synthesis and characterization of novel earth-abundant nickel complexes, as well as for the photochemical reduction of CO<sub>2</sub> to CO. The catalytic system performed best (referring to the TON of CO production) using the complex {{#moleculelink:|link=CFQFJQWFSHKEAB-UHFFFAOYSA-N|image=false|width=300|height=200}} as the catalyst. | |||
==== Catalyst==== | ==== Catalyst==== | ||
{{#moleculelink:|link=CFQFJQWFSHKEAB-UHFFFAOYSA-N|image=true}} | {{#moleculelink:|link=CFQFJQWFSHKEAB-UHFFFAOYSA-N|image=true}} | ||
====Photosensitizer==== | ====Photosensitizer==== | ||
{{#moleculelink: |link= | {{#moleculelink: |link=NSABRUJKERBGOU-UHFFFAOYSA-N|image=true}} | ||
====Investigation==== | ====Investigation==== | ||
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====Sacrificial electron donor==== | ====Sacrificial electron donor==== | ||
{{#moleculelink: |link=ZMANZCXQSJIPKH-UHFFFAOYSA-N|image= | In this study, the experiments were done with the sacrificial electron donor triethylamine ({{#moleculelink:|link=ZMANZCXQSJIPKH-UHFFFAOYSA-N|image=false|width=300|height=200}}). | ||
[[Category:Photocatalytic CO2 conversion to CO]] | |||
==== Additives ==== | |||
In this study, no additives were used. | |||
[[Category:Photocatalytic CO2 conversion to CO]][[Category:Publication]] |
Latest revision as of 10:37, 11 April 2024
Abstract[edit | edit source]
Summary[edit | edit source]
The synthesis and characterization of a new family of earth-abundant nickel complexes supported by N-heterocyclic carbene-amine ligands for the highly-selective conversion of CO2 to CO has been shown. Turnover number (TON) of 98,000 and turnover frequency of 3.9 s-1 were achieved using the nickel catalyst [Ni(bimiqpr)][PF6]2 in combination with the iridium complex Ir(ppy)3 as the photosensitizer under visible-light catalysis. The experiments were performed using a Xenon lamp as the visible-light source with triethylamine as sacrificial electron donor.
Advances and special progress[edit | edit source]
The reported novel earth-abundant complexes also emerged as catalysts for the electrochemical CO2 conversion to CO. Among them, the complex [Ni(bimiqpr)][PF6]2 had the lowest cathodic onset potential of Ecat = −1.2 V vs SCE.
Additional remarks[edit | edit source]
Further studies have revealed that the overall efficiency of the developed solar-to-fuel cycle may be limited by the formation of the active Ni catalyst and/or the chemical reduction of CO2 to CO at the reduced nickel center and provide a starting point for improved photoredox systems for sustainable carbon-neutral energy conversion
Content of the published article in detail[edit | edit source]
The article contains results for the synthesis and characterization of novel earth-abundant nickel complexes, as well as for the photochemical reduction of CO2 to CO. The catalytic system performed best (referring to the TON of CO production) using the complex [Ni(bimiqpr)][PF6]2 as the catalyst.
Catalyst[edit | edit source]
Photosensitizer[edit | edit source]
Investigation[edit | edit source]
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | λexc [nm] | . | TON CO | . | . | . | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.000002 | 0.2 | 0.07 | solar spectrum | 98000 | |||||||||
2. | 0.00002 | 0.2 | 0.07 | solar spectrum | 9000 | |||||||||
3. | 0.0002 | 0.2 | 0.07 | solar spectrum | 1500 |
Sacrificial electron donor[edit | edit source]
In this study, the experiments were done with the sacrificial electron donor triethylamine (TEA).
Additives[edit | edit source]
In this study, no additives were used.
Investigations
- Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)