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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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==== | ||
Line 472: | Line 472: | ||
====Investigation==== | ====Investigation==== | ||
{{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 1}} | {{#experimentlist:|form=Photocatalytic_CO2_conversion_experiments|name=Table 1}} | ||
{{#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. |
Revision as of 12:32, 30 January 2024
Abstract
Summary
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
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
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
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
100751 [Show R-Groups] Mn(oMesbpy)(CO)2Br
Photosensitizer
Investigation
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | . | . | λexc [nm] | . | TON CO | TON H2 | TON HCOOH | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.05 | 0.25 | 0.1 | 436 nm | 1004 | 68 | 310 |
Sacrificial electron donor
In this study, the experiments were done with the sacrificial electron donors TEOA (100507) and BIH (100508).
Additives
In this study, no additives were tested.
Investigations
- Durability test (Molecular process, Photocatalytic CO2 conversion experiments)
- Results for photocatalytic reduction of CO2 (Molecular process, Photocatalytic CO2 conversion experiments)