Light-Driven Reduction of CO2 to CO in Water with a Cobalt Molecular Catalyst and an Organic Sensitizer: Difference between revisions
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==== Summary ==== | ==== Summary ==== | ||
A photochemical reduction of | A photochemical reduction of CO<sub>2</sub> to CO was shown using the cobalt complex {{#moleculelink:|link=OZQYFMFOIFRRLI-UHFFFAOYSA-L|image=false|width=300|height=200}} as a catalyst in combination with the organic, water soluble triazatriangulenium photosensitizer {{#moleculelink:|link=DORDHQADTWICIT-UHFFFAOYSA-N|image=false|width=300|height=200}}. Turnover numbers (TONs) up to 19000 and selectivity of 93% for CO were reached in acetonitrile with 20% of water. The experiments were conducted under visible-light irradiation (λ > 450 nm) using tertiary amines or BIH as sacrificial reductants (see section SEDs below). The photoreduction could also be shown in 100% water. | ||
==== Advances and special progress ==== | ==== Advances and special progress ==== | ||
The photoreduction of | The photoreduction of CO<sub>2</sub> to CO could be shown in 100% water with a TON of 2600 and a selectivity of 94% without any noble metals or rare materials. | ||
==== Additional remarks ==== | ==== Additional remarks ==== | ||
In initial experiments, CO and formate were first produced with a total TON >3700 upon irradiation in CO<sub>2</sub>-saturated CH<sub>3</sub>CN solution with visible light. The addition of water enhanced the catalysis and directed it toward CO production (19,000 TON, 93% selectivity). | |||
=== Content of the published article in detail === | === Content of the published article in detail === | ||
The article contains results for the reduction of | The article contains results for the reduction of CO<sub>2</sub> to CO under visible-light catalysis using a cobalt complex as a catalyst. The catalytic system performs best (referring to the TON of CO production) in acetonitrile with 20% water using BIH and TEOA. | ||
==== Catalyst ==== | ==== Catalyst ==== | ||
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==== Sacrificial electron donor ==== | ==== Sacrificial electron donor ==== | ||
In this study, the experiments were done with the sacrificial reductants TEOA ([[Molecule:100507|100507]]), BIH ([[Molecule:100508|100508]]), and TEA ([[Molecule:100505|100505]]). | In this study, the experiments were done with the sacrificial reductants TEOA ([[Molecule:100507|100507]]), BIH ([[Molecule:100508|100508]]), and TEA ([[Molecule:100505|100505]]). | ||
==== Additives ==== | ==== Additives ==== | ||
In this study, some experiments were conducted under argon atmosphere or with the addition of Hg. |
Revision as of 13:44, 9 January 2024
Abstract
Summary
A photochemical reduction of CO2 to CO was shown using the cobalt complex [Co(qpy)(H2O)2][ClO4]2 as a catalyst in combination with the organic, water soluble triazatriangulenium photosensitizer 100797. Turnover numbers (TONs) up to 19000 and selectivity of 93% for CO were reached in acetonitrile with 20% of water. The experiments were conducted under visible-light irradiation (λ > 450 nm) using tertiary amines or BIH as sacrificial reductants (see section SEDs below). The photoreduction could also be shown in 100% water.
Advances and special progress
The photoreduction of CO2 to CO could be shown in 100% water with a TON of 2600 and a selectivity of 94% without any noble metals or rare materials.
Additional remarks
In initial experiments, CO and formate were first produced with a total TON >3700 upon irradiation in CO2-saturated CH3CN solution with visible light. The addition of water enhanced the catalysis and directed it toward CO production (19,000 TON, 93% selectivity).
Content of the published article in detail
The article contains results for the reduction of CO2 to CO under visible-light catalysis using a cobalt complex as a catalyst. The catalytic system performs best (referring to the TON of CO production) in acetonitrile with 20% water using BIH and TEOA.
Catalyst
Photosensitizer
Investigations
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | solvent A | . | . | additives | λexc [nm] | TON CO | TON H2 | TON HCOOH | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.002 | 0.2 | 0.1 | 450 | 2332 | 106 | 1370 | ||||||||
2. | 0.2 | 0.1 | 450 | 0 | 0 | 0 | |||||||||
3. | 0.002 | 0.1 | 450 | 0 | 0 | 0 | |||||||||
4. | 0.002 | 0.2 | 450 | 950 | 86 | 316 | |||||||||
5. | 0.002 | 0.2 | 0.1 | 450 | 107 | 7 | 5 | ||||||||
6. | 0.002 | 0.2 | 0.1 | Argon atmosphere | 450 | 0 | 7 | 0 | |||||||
7. | 0.005 | 0.2 | 0.1 | 450 | 0 | 159 | 0 | ||||||||
8. | 0.002 | 0.2 | 0.1 | Hg (0.1 mL) | 450 | 1880 | 255 | 1973 |
cat | cat conc [µM] | PS | PS conc [mM] | e-D | e-D conc [M] | . | . | solvent A | . | . | additives | λexc [nm] | TON CO | TON H2 | TON HCOOH | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.002 | 0.2 | 0.1 | 450 | 2332 | 106 | 1370 | ||||||||||
2. | 0.002 | 0.2 | 0.1 | 450 | 6228 | 304 | 2441 | ||||||||||
3. | 0.002 | 0.2 | 0.1 | 450 | 14691 | 283 | 1097 | ||||||||||
4. | 0.002 | 0.2 | 0.1 | 450 | 15822 | 220 | 1147 | ||||||||||
5. | 0.002 | 0.2 | 0.1 | 450 | 18989 | 227 | 1215 | ||||||||||
6. | 0.002 | 0.2 | 0.1 | Hg | 450 | 19646 | 226 | 415 | |||||||||
7. | 0.002 | 0.2 | 0.1 | 450 | 183 | 9 | 419 | ||||||||||
8. | 0.002 | 0.2 | 0.1 | 450 | 612 | 202 | 51 | ||||||||||
9. | 0.002 | 0.2 | 0.1 | 450 | 515 | 253 | 46 | ||||||||||
10. | 0.002 | 0.2 | 0.1 | 450 | 3171 | 498 | 179 | ||||||||||
11. | 0.002 | 0.2 | 0.1 | 450 | 6331 | 264 | 179 | ||||||||||
12. | 0.002 | 0.2 | 0.1 | Hg | 450 | 6286 | 304 | 97 |
Sacrificial electron donor
In this study, the experiments were done with the sacrificial reductants TEOA (100507), BIH (100508), and TEA (100505).
Additives
In this study, some experiments were conducted under argon atmosphere or with the addition of Hg.
Investigations
- Photocatalytic CO2 Reduction by 1 (2 μM) in CO2-Saturated Aqueous CH3CN Solutions (Molecular process, Photocatalytic CO2 conversion experiments)
- BIH + TEOA under Various Conditions (Molecular process, Photocatalytic CO2 conversion experiments)