Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts: Difference between revisions

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DOI 10.1021/jacs.8b10619
Authors Hiroyuki Takeda, Hiroko Kamiyama, Kouhei Okamoto, Mina Irimajiri, Toshihide Mizutani, Kazuhide Koike, Akiko Sekine, Osamu Ishitani,
Submitted 27.11.2018
Published online 27.11.2018
Licenses http://pubs.acs.org/page/policy/authorchoice_termsofuse.html,
Subjects Colloid and Surface Chemistry, Biochemistry, General Chemistry, Catalysis
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{{#doiinfobox: 10.1021/jacs.8b10619}}
{{DOI|doi=10.1021/jacs.8b10619}}
[[Category:Photocatalytic CO2 conversion to HCOOH]]
[[Category:Photocatalytic CO2 conversion to HCOOH]]
{{BaseTemplate}}
{{BaseTemplate}}
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A photochemical reduction of CO<sub>2</sub> to CO or formic acid was shown using the manganese complexes {{#moleculelink:|link=ZUZWBGQHMPVNDY-UHFFFAOYSA-M|image=false|width=300|height=200}}, {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}} or {{#moleculelink:|link=MMWVUSACGPQHBP-UHFFFAOYSA-M|image=false|width=300|height=200}} as catalyst in combination with the copper-based photosensitizer {{#moleculelink:|link=LRXMZDJKCHDVRC-UHFFFAOYSA-N|image=false|width=300|height=200}}. Turnover numbers (TONs) over 1300 for CO were reached in dimethylacetamide/TEOA for complex {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}}. The highest selectivity for CO (96%) was obtained for catalyst {{#moleculelink:|link=MMWVUSACGPQHBP-UHFFFAOYSA-M|image=false|width=300|height=200}} while catalyst {{#moleculelink:|link=ZUZWBGQHMPVNDY-UHFFFAOYSA-M|image=false|width=300|height=200}} allowed for the reduction of CO<sub>2</sub> to formic acid with a selectivity of 74%. The experiments were conducted under visible-light irradiation (λ = 436 nm) using BIH as sacrificial electron donor (see section SEDs below).
A photochemical reduction of CO<sub>2</sub> to CO or formic acid was shown using the manganese complexes {{#moleculelink:|link=ZUZWBGQHMPVNDY-UHFFFAOYSA-M|image=false|width=300|height=200}}, {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}} or {{#moleculelink:|link=MMWVUSACGPQHBP-UHFFFAOYSA-M|image=false|width=300|height=200}} as catalyst in combination with the copper-based photosensitizer {{#moleculelink:|link=LRXMZDJKCHDVRC-UHFFFAOYSA-N|image=false|width=300|height=200}}. Turnover numbers (TONs) over 1300 for CO were reached in dimethylacetamide/TEOA for complex {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}}. The highest selectivity for CO (96%) was obtained for catalyst {{#moleculelink:|link=MMWVUSACGPQHBP-UHFFFAOYSA-M|image=false|width=300|height=200}} while catalyst {{#moleculelink:|link=ZUZWBGQHMPVNDY-UHFFFAOYSA-M|image=false|width=300|height=200}} allowed for the reduction of CO<sub>2</sub> to formic acid with a selectivity of 74%. The experiments were conducted under visible-light irradiation (λ = 436 nm) using BIH as sacrificial electron donor (see section SEDs below).
==== Advances and special progress ====
==== Advances and special progress ====
Employing catalyst {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}}, the highest quantum yield for CO<sub>2</sub> reduction using abundant elements (57%) at that time was achieved.  
Employing catalyst {{#moleculelink:|link=AQJGHJDFPVIJPY-UHFFFAOYSA-M|image=false|width=300|height=200}}, the highest quantum yield for CO<sub>2</sub> reduction using abundant elements (57%) at that time was achieved. The authors also demonstrated the stability of their catalyst over a 36 h experiment, where it was shown that BIH was the limiting factor, even in large amounts.  


==== Additional remarks====
==== Additional remarks====
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====Investigation====
====Investigation====
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 1}}
{{#experimentlist: |form=Photocatalytic_CO2_conversion_experiments|name=Results for photocatalytic reduction of CO2}}
 
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Durability test|importFile=}}
 
====Sacrificial electron donor====
====Sacrificial electron donor====
In this study, the experiments were done with the sacrificial electron donors TEOA ([[Molecule:100507|100507]]) and BIH ([[Molecule:100508|100508]]).
In this study, the experiments were done with the sacrificial electron donors TEOA ([[Molecule:100507|100507]]) and BIH ([[Molecule:100508|100508]]).
====Additives====
====Additives====
In this study, no additives were tested.
In this study, no additives were tested.[[Category:Publication]]

Latest revision as of 10:37, 11 April 2024


Abstract[edit | edit source]

Summary[edit | edit source]

A photochemical reduction of CO2 to CO or formic acid was shown using the manganese complexes Mn(bpy)(CO)3Br, 100845 or Mn(oMesbpy)(CO)2Br as catalyst in combination with the copper-based photosensitizer [Cu(phen)-(dPPh-Bu)2]2[PF6]2. Turnover numbers (TONs) over 1300 for CO were reached in dimethylacetamide/TEOA for complex 100845. The highest selectivity for CO (96%) was obtained for catalyst Mn(oMesbpy)(CO)2Br while catalyst Mn(bpy)(CO)3Br allowed for the reduction of CO2 to formic acid with a selectivity of 74%. The experiments were conducted under visible-light irradiation (λ = 436 nm) using BIH as sacrificial electron donor (see section SEDs below).

Advances and special progress[edit | edit source]

Employing catalyst 100845, the highest quantum yield for CO2 reduction using abundant elements (57%) at that time was achieved. The authors also demonstrated the stability of their catalyst over a 36 h experiment, where it was shown that BIH was the limiting factor, even in large amounts.

Additional remarks[edit | edit source]

The authors could show that the substituents on the manganese complexes largely influenced the photocatalytic efficiency and product selectivity.

Content of the published article in detail[edit | edit source]

The article contains results for the reduction of CO2 to CO and formic acid under visible-light catalysis using manganese complexes as catalysts. The catalytic system performs best (referring to the TON of CO production) in DMA/TEOA.

Catalyst[edit | edit source]

100751 [Show R-Groups] Mn(oMesbpy)(CO)2Br

Photosensitizer[edit | edit source]

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

Investigation[edit | edit source]

catcat conc [µM]PSPS conc [mM]e-De-D conc [M]solvent A..λexc [nm].TON CO.TON H2TON HCOOH...
1.

Mn(bpy)(CO)3Br

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.01

MeCN

436504157
2.

Molecule:100845

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.01

MeCN

436164165
3.

Mn(oMesbpy)(CO)2Br

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.01

MeCN

4362080.55
catcat conc [µM]PSPS conc [mM]e-De-D conc [M]solvent A..λexc [nm].TON COTON H2TON HCOOH.
1.

Molecule:100845

0.05

[Cu(phen)-(dPPh-Bu)2]2[PF6]2

0.25

BIH

0.1

MeCN

436 nm100468310
Investigation-Name: Durability test

Sacrificial electron donor[edit | edit source]

In this study, the experiments were done with the sacrificial electron donors TEOA (100507) and BIH (100508).

Additives[edit | edit source]

In this study, no additives were tested.

Investigations