Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production: Difference between revisions
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==== Advances and special progress ==== | ==== Advances and special progress ==== | ||
A nickel catalyst inspired by the CODH enzyme was employed for the photocatalytic reduction of CO<sub>2</sub> with the back then highest reported TON values among nickel complexes in systems with [Ru(bpy)<sub>3</sub>]<sup>2+</sup>. | A nickel catalyst inspired by the CODH enzyme (carbon monoxide dehydrogenase) was employed for the photocatalytic reduction of CO<sub>2</sub> with the back then highest reported TON values among nickel complexes in systems with [Ru(bpy)<sub>3</sub>]<sup>2+</sup>. | ||
==== Additional remarks ==== | ==== Additional remarks ==== |
Revision as of 10:23, 11 January 2024
Abstract
Summary
A photochemical reduction of CO2 to CO was shown using the nickel complex [Ni(bpet)(MeCN)2][ClO4]2 as catalyst in combination with the ruthenium-based photosensitizer Ru(bpy)3Cl2. Turnover numbers (TONs) over 700 and a selectivity of >99% for CO were reached in dimethylacetamide/water. The experiments were conducted under visible-light irradiation (λ = 450 nm) using BIH as sacrificial reductants (see section SEDs below).
Advances and special progress
A nickel catalyst inspired by the CODH enzyme (carbon monoxide dehydrogenase) was employed for the photocatalytic reduction of CO2 with the back then highest reported TON values among nickel complexes in systems with [Ru(bpy)3]2+.
Additional remarks
The binding of CO2 to the nickel(0) species was identified as the potential rate-determining step of the reduction.
Content of the published article in detail
The article contains results for the reduction of CO2 to CO under visible-light catalysis using a nickel complex as a catalyst. The catalytic system performs best (referring to the TON of CO production) in dimethylacetamide/water.
Catalyst
Photosensitizer
Investigation
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | . | . | . | λexc [nm] | . | TON CO | . | TON H2 | . | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.03 | 0.5 | 0.1 | 450 | 713 | 6.9 | |||||||||||
2. | 0.03 | 0.5 | 0.1 | 450 | 159 | 11 | |||||||||||
3. | 0.03 | 0.5 | 0.1 | 450 | 67 | 3.4 | |||||||||||
4. | 0.03 | 0.5 | 0.1 | 450 | |||||||||||||
5. | 0.03 | 0.5 | 0.1 | 450 | |||||||||||||
6. | 0.03 | 0.5 | 0.1 | 450 | 2.6 | 25.5 |
Sacrificial electron donor
In this study, the experiments were done with the sacrificial electron donors TEOA (100507), BIH (100508), and TEA (100505).
Additives
In this study, no additives were tested.
Investigations
- Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)