Category:Photocatalytic CO2 conversion to HCOOH

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CO2 conversion to formic acid[Pro21]

Formic acid (FA) is a simple chemical with many uses. Its applications include use as a preservative, in the leather and dyeing industry and chemical providing a C1 building block. It is also an important H2 carrier, because of its qualities as non-toxic, easily storable liquid. This also makes it directly usable in fuel cells.[Fas16] The global production is currently estimated at 870.000 metric tons in 2021 with a CAGR (Compound Annual Growth Report) of 3.87% in volume terms during the period 2022-2027.[https://www.mordorintelligence.com/industry-reports/formic-acid-market]

Industrial production of formic acid is done mainly by carbonylation of methanol and subsequent hydrolysation of methyl formate to formic acid.[FA00]

A direct approach of synthesis by hydrogenation of CO2 and using renewable energy, such as sunlight in photocatalysis, in a homogeneous environment, is the focus of this page.

Reaction

CO2 + H2 -> HCOOH

explanation

Sacrificial electron donors

TEOA TEA BI(OH)H BIH BNAH

Ruthenium Catalysts

100549 [Show R-Groups] 100481 [Show R-Groups] Ru(bpy)2CO3 100483 100551 [Show R-Groups] 100552 [Show R-Groups]

complexes ordered by metal

Photosensitizers

Ru(bpy)3Cl2 100832 100489 100533

photosensitizer compounds

Experiments

Entry CAT conc PS conc e-D conc Solvent λex [nm] irr time [h] Sel [%] TON QY [%] reference link to experiment
1 Ru(bpy)3Cl2 - TEOA DMF 400 1 69 4 [Pro85]
2 100549 Ru(bpy)3Cl2 TEOA DMF 400 2 - 326 [Pro90]
3 100550 Ru(bpy)3Cl2 TEOA DMF 400 2 - 255 [Pro90]
4 Ru(bpy)2CO3 Molecule with chemformId 100487 does not exist. TEOA NMP 400 5 78 21 [PRo15]
5 100551 Ru(bpy)3Cl2 TEOA DMF 405 24 99 380 [VLP19]
6 100552 100533 BI(OH)H/TEOA DMA 500 24 83 3269 [PCR20]

table with several experiments

Cobalt Catalysts

100553 [Show R-Groups] Co(MePP) tBuxant-(Co(qpy))2

Organic and semiconductor photosensitizer

3,7-Di((1,1'-biphenyl)-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine 100494 Tris-(1,10-phenanthroline)ruthenium

Experiments

Entry CAT conc PS conc e-D conc Solvent λex [nm] irr time [h] Sel [%] TON reference link to experiment
1 100553 - TEA MeCn 320 >80 245 [CPC98]
2 100553 - TEA MeCn 320 - 120 [CPC98]
3 100553 - TEA MeCn 320 - 120 [CPC98]
4 Co(MePP) - TEA MeCn 320 - 120 [CPC98]
5 Co(MePP) - TEA MeCn 320 - 120 [CPC98]
6 Co(MePP) - TEA MeCn 320 - 120 [CPC98]
7 tBuxant-(Co(qpy))2 Tris-(1,10-phenanthroline)ruthenium TEA MeCn 460 92 110 [Sco19]
8 tBuxant-(Co(qpy))2 Tris-(1,10-phenanthroline)ruthenium BIH/TEA MeCn 460 97 386 [Sco19]
9 tBuxant-(Co(qpy))2 Tris-(1,10-phenanthroline)ruthenium BIH/TEOA MeCn 460 76 821 [Sco19]
10 tBuxant-(Co(qpy))2 3,7-Di((1,1'-biphenyl)-4-yl)-10-(naphthalen-1-yl)-10H-phenoxazine BIH/TEOA MeCn 460 58 565 [Sco19]
11 tBuxant-(Co(qpy))2 100494 BIH/TEOA MeCn 460 91 493 [Sco19]

Literature

[Pro21] Photochemical reduction of carbon dioxide to formic acid. Robin Cauwenbergh, Shoubhik Das, Green Chemistry 2021, Vol. 23, Pages 2553-2574. DOI2: 10.1039/d0gc04040a
[Fas16] Formic acid synthesis using CO2 as raw material: Techno-economic and environmental evaluation and market potential. Mar Pérez-Fortes, Jan C. Schöneberger, Aikaterini Boulamanti, Gillian Harrison, Evangelos Tzimas, International Journal of Hydrogen Energy 2016, Vol. 41, Pages 16444-16462. DOI2: 10.1016/j.ijhydene.2016.05.199
[FA00] Formic Acid. Werner Reutemann, Heinz Kieczka, Ullmann's Encyclopedia of Industrial Chemistry 2000. DOI2: 10.1002/14356007.a12_013
[Pro85] Photochemical reduction of carbon dioxide to formate mediated by ruthenium bipyridine complexes as homogeneous catalysts. Jeannot Hawecker, Jean-Marie Lehn, Raymond Ziessel, Journal of the Chemical Society, Chemical Communications 1985, Pages 56. DOI2: 10.1039/c39850000056
[Pro90] Photochemical reduction of carbon dioxide to formate catalyzed by 2,2t́-bipyridine- or 1,10-phenanthroline-ruthenium(II) complexes. Jean-Marie Lehn, Raymond Ziessel, Journal of Organometallic Chemistry 1990, Vol. 382, Pages 157-173. DOI2: 10.1016/0022-328x(90)85224-m
[PCR20] Photocatalytic CO 2 Reduction under Visible‐Light Irradiation by Ruthenium CNC Pincer Complexes. Yasuhiro Arikawa, Itoe Tabata, Yukari Miura, Hiroki Tajiri, Yudai Seto, Shinnosuke Horiuchi, Eri Sakuda, Keisuke Umakoshi, Chemistry – A European Journal 2020, Vol. 26, Pages 5603-5606. DOI2: 10.1002/chem.201905840
Publication: Photocatalytic CO2 Reduction under Visible-Light Irradiation by Ruthenium CNC Pincer Complexes
[CPC98] Cobalt Porphyrin Catalyzed Reduction of CO2. Radiation Chemical, Photochemical, and Electrochemical Studies. D. Behar, T. Dhanasekaran, P. Neta, C. M. Hosten, D. Ejeh, P. Hambright, Etsuko Fujita, The Journal of Physical Chemistry A 1998, Vol. 102, Pages 2870-2877. DOI2: 10.1021/jp9807017
[Sco19] Selectivity control of CO versus HCOO− production in the visible-light-driven catalytic reduction of CO2 with two cooperative metal sites. Zhenguo Guo, Gui Chen, Claudio Cometto, Bing Ma, Hongyan Zhao, Thomas Groizard, Lingjing Chen, Hongbo Fan, Wai-Lun Man, Shek-Man Yiu, Kai-Chung Lau, Tai-Chu Lau, Marc Robert, Nature Catalysis 2019, Vol. 2, Pages 801-808. DOI2: 10.1038/s41929-019-0331-6