Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis: Difference between revisions
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{{DOI|doi=10.1021/acs.jpcc.8b00950}} | |||
=== Abstract === | |||
==== | ==== Summary==== | ||
A photochemical reduction of CO<sub>2</sub> was achieved using an iron porphyrin catalyst and an iridium complex as the photosensitizer. Carbon monoxide, produced with a TON of 178 under optimized conditions, was the main product, methane was produced in a substantial amount with the TON of 32, while hydrogen was formed as a minor byproduct. The experiments were performed under irradiation with ''λ >'' 420 nm in acetonitrile and in the presence of various amines as sacrificial electron donors. | |||
==== | ==== Advances and special progress==== | ||
The catalytic reduction of CO<sub>2</sub> could also be realized under aqueous conditions (acetonitrile/water 3:7 v:v), yielding carbon monoxide as the main product while methane was produced with selectivity up to 10% (TON of 3). | |||
==== | ==== Additional remarks==== | ||
{{#moleculelink:|link= | Among the various amines employed as sacrificial electron donors, TEA appeared as the best choice to maximize CO<sub>2</sub> product formation. | ||
-INDIGO- | |||
=== Content of the published article in detail === | |||
The article contains results for the reduction of CO<sub>2</sub> to CO as the main product under visible-light irradiation using iron porphyrin complex Fe(pTMAPP)Cl<sub>5</sub> ({{#moleculelink:|link=LKNRTBVZMCBYCY-NGWNFTKISA-I|image=false|width=300|height=200}}) as the catalysts, an iridium complex as the photosensitizer and various amines as the sacrificial electron donor. The catalytic system performs best (referring to the TON of CO production) with Ir(ppy)<sub>3</sub> ({{#moleculelink: |link=NSABRUJKERBGOU-UHFFFAOYSA-N|image=false|width=300|height=200}}) as the photosensitizer and TEA as the sacrificial electron donor. | |||
==== Catalyst==== | |||
{{#moleculelink:|link=LKNRTBVZMCBYCY-NGWNFTKISA-I|image=true|width=300|height=200}} | |||
====Photosensitizer==== | |||
<chemform smiles="C1C=C[C-]2[Ir+3]3([C-]4C=CC=CC=4C4C=CC=CN=43)3(N4=CC=CC=C4C4C=CC=CN=43)N3=CC=CC=C3C=2C=1.[P-](F)(F)(F)(F)(F)F" inchi="1S/2C11H8N.C10H8N2.F6P.Ir/c2*1-2-6-10(7-3-1)11-8-4-5-9-12-11;1-3-7-11-9(5-1)10-6-2-4-8-12-10;1-7(2,3,4,5)6;/h2*1-6,8-9H;1-8H;;/q2*-1;;-1;+3" inchikey="RJJGJTKSOSSNNL-UHFFFAOYSA-N" height="200px" width="300px" float="none"> | |||
-INDIGO-08012317332D | |||
0 0 0 0 0 0 0 0 0 0 0 V3000 | 0 0 0 0 0 0 0 0 0 0 0 V3000 | ||
M V30 BEGIN CTAB | M V30 BEGIN CTAB | ||
M V30 COUNTS | M V30 COUNTS 44 51 0 0 0 | ||
M V30 BEGIN ATOM | M V30 BEGIN ATOM | ||
M V30 1 C 4. | M V30 1 C 4.03485 -3.90007 0.0 0 | ||
M V30 2 C 5. | M V30 2 C 5.76515 -3.89959 0.0 0 | ||
M V30 3 C | M V30 3 C 4.90164 -3.39997 0.0 0 | ||
M V30 4 | M V30 4 C 5.76515 -4.90053 0.0 0 CHG=-1 | ||
M V30 5 C 4. | M V30 5 C 4.03485 -4.90502 0.0 0 | ||
M V30 6 C | M V30 6 C 4.90382 -5.40003 0.0 0 | ||
M V30 7 C | M V30 7 C 6.63141 -3.39999 0.0 0 | ||
M V30 8 C | M V30 8 C 7.49583 -1.90109 0.0 0 | ||
M V30 9 C | M V30 9 C 6.63149 -2.39928 0.0 0 | ||
M V30 10 C | M V30 10 C 8.36278 -2.40138 0.0 0 | ||
M V30 11 | M V30 11 N 7.50182 -3.90229 0.0 0 | ||
M V30 12 C | M V30 12 C 8.3649 -3.39706 0.0 0 | ||
M V30 13 C | M V30 13 C 4.08485 -6.82507 0.0 0 | ||
M V30 14 C | M V30 14 C 5.81515 -6.82459 0.0 0 CHG=-1 | ||
M V30 15 C | M V30 15 C 4.95164 -6.32497 0.0 0 | ||
M V30 16 C | M V30 16 C 5.81515 -7.82553 0.0 0 | ||
M V30 17 C | M V30 17 C 4.08485 -7.83002 0.0 0 | ||
M V30 18 C | M V30 18 C 4.95382 -8.32503 0.0 0 | ||
M V30 19 | M V30 19 C 6.68166 -8.3247 0.0 0 | ||
M V30 20 C | M V30 20 C 8.41196 -8.32139 0.0 0 | ||
M V30 21 | M V30 21 N 7.54763 -7.82318 0.0 0 | ||
M V30 22 C | M V30 22 C 8.41359 -9.32233 0.0 0 | ||
M V30 23 C | M V30 23 C 6.6833 -9.32964 0.0 0 | ||
M V30 24 C | M V30 24 C 7.55308 -9.82324 0.0 0 | ||
M V30 25 C | M V30 25 C 9.35985 -3.77507 0.0 0 | ||
M V30 26 C | M V30 26 C 11.0902 -3.77459 0.0 0 | ||
M V30 27 C | M V30 27 C 10.2266 -3.27497 0.0 0 | ||
M V30 28 C | M V30 28 C 11.0902 -4.77553 0.0 0 | ||
M V30 29 | M V30 29 N 9.35985 -4.78002 0.0 0 | ||
M V30 30 | M V30 30 C 10.2288 -5.27503 0.0 0 | ||
M V30 31 C | M V30 31 C 10.2327 -6.27503 0.0 0 | ||
M V30 32 C | M V30 32 C 11.105 -7.76933 0.0 0 | ||
M V30 33 C | M V30 33 C 11.1014 -6.7717 0.0 0 | ||
M V30 34 C 10. | M V30 34 C 10.2405 -8.27372 0.0 0 | ||
M V30 35 N 9. | M V30 35 N 9.36465 -6.78143 0.0 0 | ||
M V30 36 C | M V30 36 C 9.37498 -7.78146 0.0 0 | ||
M V30 37 Ir 7. | M V30 37 Ir 7.55 -5.775 0.0 0 CHG=3 | ||
M V30 38 P 13.517 -3.7 0.0 0 CHG=-1 | |||
M V30 39 F 14.383 -3.2 0.0 0 | |||
M V30 40 F 12.651 -3.2 0.0 0 | |||
M V30 41 F 13.517 -4.7 0.0 0 | |||
M V30 42 F 14.383 -4.2 0.0 0 | |||
M V30 43 F 13.517 -2.7 0.0 0 | |||
M V30 44 F 12.651 -4.2 0.0 0 | |||
M V30 END ATOM | M V30 END ATOM | ||
M V30 BEGIN BOND | M V30 BEGIN BOND | ||
Line 59: | Line 78: | ||
M V30 5 2 5 6 | M V30 5 2 5 6 | ||
M V30 6 1 6 4 | M V30 6 1 6 4 | ||
M V30 7 2 9 7 | M V30 7 1 2 7 | ||
M V30 | M V30 8 2 9 7 | ||
M V30 | M V30 9 2 10 8 | ||
M V30 | M V30 10 1 7 11 | ||
M V30 | M V30 11 1 8 9 | ||
M V30 | M V30 12 2 11 12 | ||
M V30 | M V30 13 1 12 10 | ||
M V30 | M V30 14 2 15 13 | ||
M V30 | M V30 15 2 16 14 | ||
M V30 | M V30 16 1 13 17 | ||
M V30 | M V30 17 1 14 15 | ||
M V30 | M V30 18 2 17 18 | ||
M V30 19 2 21 19 | M V30 19 1 18 16 | ||
M V30 | M V30 20 1 16 19 | ||
M V30 | M V30 21 2 21 19 | ||
M V30 | M V30 22 2 22 20 | ||
M V30 | M V30 23 1 19 23 | ||
M V30 | M V30 24 1 20 21 | ||
M V30 | M V30 25 2 23 24 | ||
M V30 | M V30 26 1 24 22 | ||
M V30 | M V30 27 2 27 25 | ||
M V30 | M V30 28 2 28 26 | ||
M V30 | M V30 29 1 25 29 | ||
M V30 | M V30 30 1 26 27 | ||
M V30 31 2 33 31 | M V30 31 2 29 30 | ||
M V30 | M V30 32 1 30 28 | ||
M V30 | M V30 33 1 30 31 | ||
M V30 | M V30 34 2 33 31 | ||
M V30 | M V30 35 2 34 32 | ||
M V30 | M V30 36 1 31 35 | ||
M V30 37 | M V30 37 1 32 33 | ||
M V30 | M V30 38 2 35 36 | ||
M V30 | M V30 39 1 36 34 | ||
M V30 | M V30 40 10 11 37 | ||
M V30 | M V30 41 10 37 29 | ||
M V30 | M V30 42 10 35 37 | ||
M V30 | M V30 43 10 37 21 | ||
M V30 | M V30 44 10 14 37 | ||
M V30 | M V30 45 10 37 4 | ||
M V30 46 1 38 39 | |||
M V30 47 1 38 40 | |||
M V30 48 1 38 41 | |||
M V30 49 1 38 42 | |||
M V30 50 1 38 43 | |||
M V30 51 1 38 44 | |||
M V30 END BOND | M V30 END BOND | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
</chemform> | </chemform> | ||
{{#moleculelink: |link=NSABRUJKERBGOU-UHFFFAOYSA-N|image=true}} | |||
====Investigation==== | |||
{{#experimentlist: |form=Photocatalytic_CO2_conversion_experiments|name=Photocatalytic reduction of CO2: conditions optimization}} | |||
{{#experimentlist: |form=Cyclic_Voltammetry_experiments|name=Cyclic voltammetry in various conditions}} | |||
====Sacrificial electron donor==== | |||
In this study, the experiments were conducted with TEA ({{#moleculelink:|link=ZMANZCXQSJIPKH-UHFFFAOYSA-N|image=false|width=300|height=200}}), TEOA ({{#moleculelink:|link=GSEJCLTVZPLZKY-UHFFFAOYSA-N|image=false|width=300|height=200}}), and DIPEA ({{#moleculelink:|link=JGFZNNIVVJXRND-UHFFFAOYSA-N|image=false|width=300|height=200}}) as sacrificial electron donors. | |||
==== | ====Additives==== | ||
{{#moleculelink:|link= | In some experiments described in this study, TFE ({{#moleculelink:|link=RHQDFWAXVIIEBN-UHFFFAOYSA-N|image=false|width=300|height=200}}) was used as an additive. | ||
[[Category:Photocatalytic conversion | [[Category:Photocatalytic CO2 conversion to CH4]][[Category:Publication]] |
Latest revision as of 14:36, 5 September 2024
Abstract[edit | edit source]
Summary[edit | edit source]
A photochemical reduction of CO2 was achieved using an iron porphyrin catalyst and an iridium complex as the photosensitizer. Carbon monoxide, produced with a TON of 178 under optimized conditions, was the main product, methane was produced in a substantial amount with the TON of 32, while hydrogen was formed as a minor byproduct. The experiments were performed under irradiation with λ > 420 nm in acetonitrile and in the presence of various amines as sacrificial electron donors.
Advances and special progress[edit | edit source]
The catalytic reduction of CO2 could also be realized under aqueous conditions (acetonitrile/water 3:7 v:v), yielding carbon monoxide as the main product while methane was produced with selectivity up to 10% (TON of 3).
Additional remarks[edit | edit source]
Among the various amines employed as sacrificial electron donors, TEA appeared as the best choice to maximize CO2 product formation.
Content of the published article in detail[edit | edit source]
The article contains results for the reduction of CO2 to CO as the main product under visible-light irradiation using iron porphyrin complex Fe(pTMAPP)Cl5 (Fe(pTMAPP)Cl5) as the catalysts, an iridium complex as the photosensitizer and various amines as the sacrificial electron donor. The catalytic system performs best (referring to the TON of CO production) with Ir(ppy)3 (Ir(ppy)3) as the photosensitizer and TEA as the sacrificial electron donor.
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 | . | additives | . | . | λexc [nm] | . | TON CO | TON CH4 | TON H2 | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.002 | 0.2 | 0.05 | > 420 | 178 | 32 | 103 | ||||||||||
2. | 0.002 | 0.2 | 0.05 | > 420 | 134 | 23 | 67 | ||||||||||
3. | 0.002 | 0.2 | 0.05 | > 420 | 151 | 24 | 77 | ||||||||||
4. | 0.002 | 0.2 | 0.05 | > 420 | 24 | 3 | 5 | ||||||||||
5. | 0.002 | 0.2 | 0.05 | > 420 | 19 | 3 | 4 | ||||||||||
6. | 0.002 | 0.2 | 0.05 | > 420 | 20 | 3 | 4 | ||||||||||
7. | 0.002 | 0.2 | 0.05 | > 420 | 198 | 31 | 24 | ||||||||||
8. | 0.002 | 0.2 | 0.05 | > 420 | 89 | 18 | |||||||||||
9. | 0.002 | 0.2 | 0.05 | TFE | > 420 | 100 | 19 | ||||||||||
10. | 0.002 | 0.2 | 0.05 | TFE | > 420 | 195 | 45 |
analyte | anl conc [mM] | reduction potential | solvent | electrolyte | . | . | gas | . | WE | . | . | RE | . | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1. | 0.5 | -2.0 , -1.4 | argon | glassy carbon | SCE | |||||||||
2. | 0.5 | -2.0, -1.4 | CO | glassy carbon | SCE | |||||||||
3. | 0.5 | -2.0, -1.4 | CO | glassy carbon | SCE | |||||||||
4. | 0.5 | -2.0, -1.4 | CO | glassy carbon | SCE | |||||||||
5. | 0.5 | -2.0 | CO | glassy carbon | SCE |
The results show an increase in current when the solution is irradiated and triethylamine (TEA) is added (see condition column).
Sacrificial electron donor[edit | edit source]
In this study, the experiments were conducted with TEA (TEA), TEOA (TEOA), and DIPEA (DIPEA) as sacrificial electron donors.
Additives[edit | edit source]
In some experiments described in this study, TFE (TFE) was used as an additive.
Investigations
- Cyclic voltammetry in various conditions (Assay, Cyclic Voltammetry experiments)
- Photocatalytic reduction of CO2: conditions optimization (Molecular process, Photocatalytic CO2 conversion experiments)