Photocatalytic CO2 conversion to HCOOH

CO₂ conversion to formic acid[Pro21][edit | edit source]

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.

Sacrificial electron donors[edit | edit source]

TEOA TEA BI(OH)H BIH BNAH

Ruthenium Catalysts[edit | edit source]

Ru(bpy)2CO3

Photosensitizers[edit | edit source]

Experiments[edit | edit source]

Table of all the experiments that have a turnover number for HCOOH greater than 100, sorted by catalyst and in descending order.

TON > 100

Table of all the experiments that have a turnover number for HCOOH lower than 100, sorted by catalyst and in descending order.

TON < 100

Cobalt Catalysts[edit | edit source]

Organic and semiconductor photosensitizer[edit | edit source]

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

Experiments[edit | edit source]

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

[VLP20] Visible-Light Photocatalytic Conversion of Carbon Dioxide by Ni(II) Complexes with N4S2 Coordination: Highly Efficient and Selective Production of Formate. Sung Eun Lee, Azam Nasirian, Ye Eun Kim, Pegah Tavakoli Fard, Youngmee Kim, Byeongmoon Jeong, Sung-Jin Kim, Jin-Ook Baeg, Jinheung Kim, Journal of the American Chemical Society 2020, Vol. 142, Pages 19142-19149. DOI2: 10.1021/jacs.0c08145
Publication: Visible-Light Photocatalytic Conversion of Carbon Dioxide by Ni(II) Complexes with N4S2 Coordination: Highly Efficient and Selective Production of Formate

[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

[AiR19] An integrated Re(i) photocatalyst/sensitizer that activates the formation of formic acid from reduction of CO₂. Yasmeen Hameed, Patrick Berro, Bulat Gabidullin, Darrin Richeson, Chemical Communications 2019, Vol. 55, Pages 11041-11044. DOI2: 10.1039/c9cc03943k
Publication: An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2

[PCR20] Photocatalytic CO₂ Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid. Kenji Kamada, Jieun Jung, Taku Wakabayashi, Keita Sekizawa, Shunsuke Sato, Takeshi Morikawa, Shunichi Fukuzumi, Susumu Saito, Journal of the American Chemical Society 2020, Vol. 142, Pages 10261-10266. DOI2: 10.1021/jacs.0c03097
Publication: Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid

[HEa16] Highly Efficient and Selective Photocatalytic CO₂ Reduction by Iron and Cobalt Quaterpyridine Complexes. Zhenguo Guo, Siwei Cheng, Claudio Cometto, Elodie Anxolabéhère-Mallart, Siu-Mui Ng, Chi-Chiu Ko, Guijian Liu, Lingjing Chen, Marc Robert, Tai-Chu Lau, Journal of the American Chemical Society 2016, Vol. 138, Pages 9413-9416. DOI2: 10.1021/jacs.6b06002
Publication: Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes

[PRo15] Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light. Alonso Rosas-Hernández, Henrik Junge, Matthias Beller, ChemCatChem 2015, Vol. 7, Pages 3316-3321. DOI2: 10.1002/cctc.201500494
Publication: Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light

[VLP19] Visible‐Light Photocatalytic Reduction of CO ₂ to Formic Acid with a Ru Catalyst Supported by N , N ′‐Bis(diphenylphosphino)‐2,6‐diaminopyridine Ligands. Yasmeen Hameed, Gyandshwar Kumar Rao, Jeffrey S. Ovens, Bulat Gabidullin, Darrin Richeson, ChemSusChem 2019, Vol. 12, Pages 3453-3457. DOI2: 10.1002/cssc.201901326
Publication: Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands

[Rtr16] Rhenium(i) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO₂ reduction. Jana Rohacova, Osamu Ishitani, Chemical Science 2016, Vol. 7, Pages 6728-6739. DOI2: 10.1039/c6sc01913g
Publication: Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction

[PCr14] Photocatalytic CO₂reduction using a Mn complex as a catalyst. Hiroyuki Takeda, Hiroki Koizumi, Kouhei Okamoto, Osamu Ishitani, Chem. Commun. 2014, Vol. 50, Pages 1491-1493. DOI2: 10.1039/c3cc48122k
Publication: Photocatalytic CO2 reduction using a Mn complex as a catalyst

[HEa18] Highly Efficient and Robust Photocatalytic Systems for CO₂ Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts. Hiroyuki Takeda, Hiroko Kamiyama, Kouhei Okamoto, Mina Irimajiri, Toshihide Mizutani, Kazuhide Koike, Akiko Sekine, Osamu Ishitani, Journal of the American Chemical Society 2018, Vol. 140, Pages 17241-17254. DOI2: 10.1021/jacs.8b10619
Publication: Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts

[PRo16] Photocatalytic Reduction of Carbon Dioxide to CO and HCO₂H Using fac-Mn(CN)(bpy)(CO)₃. Po Ling Cheung, Charles W. Machan, Aramice Y. S. Malkhasian, Jay Agarwal, Clifford P. Kubiak, Inorganic Chemistry 2016, Vol. 55, Pages 3192-3198. DOI2: 10.1021/acs.inorgchem.6b00379
Publication: Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3

[PRD18] Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO ₂ Photoreduction. Thibault Fogeron, Pascal Retailleau, Lise‐Marie Chamoreau, Yun Li, Marc Fontecave, Angewandte Chemie International Edition 2018, Vol. 57, Pages 17033-17037. DOI2: 10.1002/anie.201809084
Publication: Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction

[Mcm17] Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH. Matthew Stanbury, Jean-Daniel Compain, Monica Trejo, Parker Smith, Eric Gouré, Sylvie Chardon-Noblat, Electrochimica Acta 2017, Vol. 240, Pages 288-299. DOI2: 10.1016/j.electacta.2017.04.080
Publication: Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH

[Itb17] [Ir(tpy)(bpy)Cl] as a Photocatalyst for CO₂ Reduction under Visible-Light Irradiation. Shunsuke Sato, Takeshi Morikawa, ChemPhotoChem 2017, Vol. 2, Pages 207-212. DOI2: 10.1002/cptc.201700133
Publication: Ir(tpy)(bpy)Cl as a Photocatalyst for CO2 Reduction under Visible-Light Irradiation

[Vld16] Visible light driven reduction of CO 2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer. Jun-Xiao Zhang, Chang-Ying Hu, Wei Wang, Hui Wang, Zhao-Yong Bian, Applied Catalysis A: General 2016, Vol. 522, Pages 145-151. DOI2: 10.1016/j.apcata.2016.04.035
Publication: Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer

[FIR18] Function-Integrated Ru Catalyst for Photochemical CO₂ Reduction. Sze Koon Lee, Mio Kondo, Masaya Okamura, Takafumi Enomoto, Go Nakamura, Shigeyuki Masaoka, Journal of the American Chemical Society 2018, Vol. 140, Pages 16899-16903. DOI2: 10.1021/jacs.8b09933
Publication: Function-Integrated Ru Catalyst for Photochemical CO2 Reduction

[MCo15] Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO₂ with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center. Lingjing Chen, Zhenguo Guo, Xi-Guang Wei, Charlotte Gallenkamp, Julien Bonin, Elodie Anxolabéhère-Mallart, Kai-Chung Lau, Tai-Chu Lau, Marc Robert, Journal of the American Chemical Society 2015, Vol. 137, Pages 10918-10921. DOI2: 10.1021/jacs.5b06535
Publication: Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center

	cat	cat conc [µM]	PS	PS conc [mM]	e-D	e-D conc [M]	solvent A	additives	TON CO	TON H2	TON HCOOH	lit
1.	Ni(pbi)(pyS)2	0.004	Eosin Y	2	TEOA	0.4	H2O				14000	[VLP20]
2.	Ni(pbt)(pyS)2	0.004	Eosin Y	2	TEOA	0.4	H2O				13100	[VLP20]
3.	[Ru(bpy)(py)-(MeNHC)2CO][PF6]2	0.01	[Ru(dmb)3][PF6]2	0.05	BI(OH)H	0.1	DMA		300	1897	5634	[PCR20]
4.	[Ru(bpy)(py)-(MeNHC)2(MeCN)][PF6]2	0.01	[Ru(dmb)3][PF6]2	0.05	BI(OH)H	0.1	DMA		224	1438	4593	[PCR20]
5.	[Ru(bpy)(py)-(tBuNHC)2CO][PF6]2	0.01	[Ru(dmb)3][PF6]2	0.05	BI(OH)H	0.1	DMA		129	505	3792	[PCR20]
6.	[Ru(bpy)(py)-(tBuNHC)2(MeCN)][PF6]2	0.01	[Ru(dmb)3][PF6]2	0.05	BI(OH)H	0.1	DMA		129	556	3296	[PCR20]
7.	[Re(bpy)2(CO)2][OTf]	0.01	[Ru(bpy)3][PF6]	1	TEOA		DMA			375	2750	[AiR19]
8.	[Ir(mesbpy-(PCy2)2)][BPh4]	0.02			BIH	0.2	DMA		470	15	2080	[PCR20]
9.	[Re(bpy)2(CO)2][OTf]	0.02	[Ru(bpy)3][PF6]	1	TEOA		DMA			225	1480	[AiR19]
10.	[Re(bpy)2(CO)2][OTf]	0.05	[Ru(bpy)3][PF6]	1	TEOA		DMA			50	535	[AiR19]
11.	[Fe(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		3844	118	534	[HEa16]
12.	[Re(bpy)2(CO)2][OTf]	0.1	[Ru(bpy)3][PF6]	1	TEOA		DMA			38	428	[AiR19]
13.	[Ru(bpy)2ClCO][PF6]	1.6	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		40	67	419	[PRo15]
14.	[Ru(bpy)2ClCO][PF6]	0.0016	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		40	67	419	[PRo15]
15.	Ru(py)-(MeNdpp)2(CO)2Cl	0.025	[Ru(bpy)3][PF6]	0.025	TEOA		DMF				380	[VLP19]
16.	Ru(py)-(MeNdpp)2(CO)2Cl	0.1	[Ru(bpy)3][PF6]	0.1	TEOA		DMF			57.5	363	[VLP19]
17.	[Ru(bpy)(H2O)(CO)][PF6]	0.0016	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		45	65	335	[PRo15]
18.	[Ru(bpy)(H2O)(CO)][PF6]	1.6	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		45	65	335	[PRo15]
19.	[Ru(bpy)2ClCO][PF6]	0.0031	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		36	33	296	[PRo15]
20.	[Ru(bpy)2ClCO][PF6]	3.1	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		36	33	296	[PRo15]
21.	Ru(dtBubpy)(CO)2Cl2	0.05	Molecule:100877	0.05			DMF		20	72	290	[Rtr16]
22.	Ru(dtBubpy)(CO)2Cl2	0.05	Molecule:100877	0.05	BI(OH)H	0.03	DMF		16	49	280	[Rtr16]
23.	[Re(bpy)2(CO)2][OTf]	0.2	[Ru(bpy)3][PF6]	1	TEOA		DMA			24	275	[AiR19]
24.	[Ru(bpy)2HCO][PF6]	0.0016	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		25	62	225	[PRo15]
25.	[Ru(bpy)2HCO][PF6]	1.6	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		25	62	225	[PRo15]
26.	[Ru(bpy)(H2O)(CO)][PF6]	0.0031	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		34	28	211	[PRo15]
27.	[Ru(bpy)(H2O)(CO)][PF6]	3.1	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		34	28	211	[PRo15]
28.	Ru(py)-(MeNdpp)2(CO)2Cl	0.05	[Ru(bpy)3][PF6]	0.05	TEOA		DMF				210	[VLP19]
29.	[Co(qpy)(H2O)2][ClO4]2	0.005	purpurin	2	BIH	0.1	DMF	Argon atmosphere	0	226	167	[HEa16]
30.	Ru(py)-(MeNdpp)2(CO)2Cl	0.5	[Ru(bpy)3][PF6]	1	TEOA		DMF			14	162	[VLP19]
31.	Mn(bpy)(CO)3Br	0.05	Ru(bpy)3	0.05	BNAH	0.1	DMF		12	8	157	[PCr14]
32.	Mn(bpy)(CO)3Br	0.05	[Cu(phen)-(dPPh-Bu)2]2[PF6]2	0.25	BIH	0.01	MeCN		50	4	157	[HEa18]
33.	Mn(bpy)(CO)3Br	0.05	[Ru(dmb)3][PF6]2	0.05	BNAH	0.1	DMF		12	14	149	[PCr14]
34.	[Ru(bpy)2HCO][PF6]	0.0031	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		16	29	145	[PRo15]
35.	[Ru(bpy)2HCO][PF6]	3.1	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		16	29	145	[PRo15]
36.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	1	BNAH	0.1	DMF		7.1	1.6	130	[PRo16]
37.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF		9.1	1.2	130	[PRo16]
38.	[Ru(bpy)2ClCO][PF6]	0.0062	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		19	19	117	[PRo15]
39.	[Ru(bpy)2ClCO][PF6]	6.2	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		19	19	117	[PRo15]
40.	[Re(bpy)2(CO)2][OTf]	0.5	[Ru(bpy)3][PF6]	1	TEOA		DMA			15	115	[AiR19]
41.	[Fe(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.02	BIH	0.1	DMF		1365	0	115	[HEa16]
42.	[Ru(bpy)2HCO][PF6]	0.0062	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		21	16	107	[PRo15]
43.	[Ru(bpy)2HCO][PF6]	6.2	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		21	16	107	[PRo15]

	cat	cat conc [µM]	PS	PS conc [mM]	e-D	e-D conc [M]	solvent A	additives	TON CO	TON H2	TON HCOOH	lit
1.	Mn(bpy)(CO)3Br	0.05	[Ru(dmb)3][PF6]2	0.05	BNAH	0.1	DMA		9	14	98	[PCr14]
2.	Ru(py)-(MeNdpp)2(CO)2Cl	1	[Ru(bpy)3][PF6]	1	TEOA		DMF			13.3	90.5	[VLP19]
3.	[Co(qpy)(H2O)2][ClO4]2	0	purpurin	2	BIH	0.1	DMF		0	0	90	[HEa16]
4.	[Fe(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.02	BIH	0.1	DMF	Argon atmosphere	0	52	88	[HEa16]
5.	[Mn(dtBubpy)(CO)3(MeCN)][PF6]	0.05	Molecule:100877	0.05			DMF		32		85	[Rtr16]
6.	[MoO(2Hqpdt)2][NBu4]	0.05	Ru(bpy)3Cl2	0.5	BIH	0.1	MeCN		40	89	83	[PRD18]
7.	[MoO(qpdt)2][NBu4]2	0.05	Ru(bpy)3Cl2	0.5	BIH	0.1	MeCN		73	670	80	[PRD18]
8.	Mn(bpy)(CO)3Br	0.05	[Ru(dmb)3][PF6]2	0.05	BNAH	0.1	MeCN		40	17	78	[PCr14]
9.	[Co(qpy)(H2O)2][ClO4]2	0.005	purpurin	2	BIH	0.1	DMF		790	11	78	[HEa16]
10.	[Ru(bpy)(H2O)(CO)][PF6]	6.2	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		21	14	75	[PRo15]
11.	[Ru(bpy)(H2O)(CO)][PF6]	0.0062	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		21	14	75	[PRo15]
12.	[Ru(bpy)(AcMe)2][PF6]	1.6	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		4	44	75	[PRo15]
13.	[Ru(bpy)(AcMe)2][PF6]	0.0016	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		4	44	75	[PRo15]
14.	Ru(py)-(HNdpp)2(CO)2Cl	0.5	[Ru(bpy)3][PF6]	1	TEOA		DMF			14	70.5	[VLP19]
15.	Mn(bpy)(CO)3Br	0.05	[Ru(dmb)3][PF6]2	0.05	BNAH	0.1	DMF		8	1	67	[PCr14]
16.	Molecule:100845	0.05	[Cu(phen)-(dPPh-Bu)2]2[PF6]2	0.25	BIH	0.01	MeCN		164	1	65	[HEa18]
17.	[Ru(bpy)(AcMe)2][PF6]	0.0062	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		4	12	64	[PRo15]
18.	[Ru(bpy)(AcMe)2][PF6]	6.2	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		4	12	64	[PRo15]
19.	[Ru(bpy)2ClCO][PF6]	0.025	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		13	8	62	[PRo15]
20.	[Ru(bpy)2ClCO][PF6]	25	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		13	8	62	[PRo15]
21.	[Mn(dtBubpy)(CO)3(MeCN)][PF6]	0.05	Molecule:100877	0.05	BI(OH)H	0.03	DMF		80		60	[Rtr16]
22.	Mn(phdk)(CO)3(MeCN)		Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		15		58	[Mcm17]
23.	Mn(phdk)(CO)3Br		Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		8		52	[Mcm17]
24.	Mn(phdk)(CO)3(MeCN)		Ru(bpy)3Cl2	200	BNAH	0.1	MeCN		8		52	[Mcm17]
25.	[Re(bpy)2(CO)2][OTf]	1	[Ru(bpy)3][PF6]	1	TEOA		DMA			1.5	52	[AiR19]
26.	[Fe(qpy)(H2O)2][ClO4]2	0.02	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		2660	29	51	[HEa16]
27.	Mn(phdk)(CO)3(MeCN)		Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		9		48	[Mcm17]
28.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		1879	15	48	[HEa16]
29.	Ru(py)-(HNdpp)2(CO)2Cl	1	[Ru(bpy)3][PF6]	1	TEOA		DMF			12	44.5	[VLP19]
30.	Ru(py)-(HNdpp)2(CO)2Cl	2	[Ru(bpy)3][PF6]	1	TEOA		DMF			9.3	41.5	[VLP19]
31.	Mn(phdk)(CO)3(MeCN)		Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		7		40	[Mcm17]
32.	[Ru(bpy)(H2O)(CO)][PF6]	0.025	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		7	9	40	[PRo15]
33.	[Ru(bpy)(H2O)(CO)][PF6]	25	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		7	9	40	[PRo15]
34.	Ru(bpy)2CO3	6.2	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		3	11	39	[PRo15]
35.	Ru(bpy)2CO3	0.0062	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		3	11	39	[PRo15]
36.	Mn(bpy)(CO)3Br		Ru(bpy)3Cl2	100	BNAH	0.1	DMF		6		39	[Mcm17]
37.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	0.1	BNAH	0.1	DMF		3.9	0.64	36	[PRo16]
38.	[Fe(qpy)(H2O)2][ClO4]2	0.01	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		3087	121	35	[HEa16]
39.	[Co(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		2660	23	35	[HEa16]
40.	Mn(phdk)(CO)3(MeCN)		Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		7		34	[Mcm17]
41.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.05	BIH	0.1	MeCN		1336	10	34	[HEa16]
42.	[Ru(bpy)2HCO][PF6]	0.025	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		8	8	34	[PRo15]
43.	[Ru(bpy)2HCO][PF6]	25	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		8	8	34	[PRo15]
44.	[K]2[MoO(Hqpdt)2]	0.05	Ru(bpy)3Cl2	0.5	BIH	0.1	MeCN		13	51	31	[PRD18]
45.	[Ru(bpy)(AcMe)2][PF6]	0.025	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		3	4	27	[PRo15]
46.	[Ru(bpy)(AcMe)2][PF6]	25	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		3	4	27	[PRo15]
47.	[Co(qpy)(H2O)2][ClO4]2	0.005	purpurin	2			DMF	Argon atmosphere	0	0	26	[HEa16]
48.	Ru(bpy)2Cl2	6.2	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		3	9	26	[PRo15]
49.	Ru(bpy)2Cl2	0.0062	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		3	9	26	[PRo15]
50.	[Co(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.3			MeCN		114	25	25	[HEa16]
51.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0	BIH	0.1	DMF		0	0	24	[HEa16]
52.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.2	BIH	0.1	DMF		350	1	23	[HEa16]
53.	[Co(qpy)(H2O)2][ClO4]2	0.2	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		1262	7	23	[HEa16]
54.	Mn(phdk)(CO)3Br		Ru(bpy)3Cl2	100	BNAH	0.1	DMF		21		22	[Mcm17]
55.	[Fe(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.2			MeCN		160	8	22	[HEa16]
56.	[Co(qpy)(H2O)2][ClO4]2	0.1	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		466	2	22	[HEa16]
57.	Ru(bpy)2CO3	0.025	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		2	4	21	[PRo15]
58.	Ru(bpy)2CO3	25	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		2	4	21	[PRo15]
59.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF		3.2	0.45	21	[PRo16]
60.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.02	BIH	0.1	DMF	Argon atmosphere	0	3	21	[HEa16]
61.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.05	BIH	0.1	DMF		520	0	21	[HEa16]
62.	[Ir(bpy)(tpy)Cl][PF6]2	0.1			TEOA		MeCN		2	1	20	[Itb17]
63.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.2	BIH	0.1	DMF	Argon atmosphere	0	54	20	[HEa16]
64.	Mn(bpy)(CO)3Br	2	ZnTPP	0.5	TEA	0.1	MeCN		119		19	[Vld16]
65.	Mn(phdk)(CO)3(MeCN)	2	Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		5		18	[Mcm17]
66.	Mn(bpy)(CO)3Br	1.5	ZnTPP	0.5	TEA	0.1	MeCN		97		18	[Vld16]
67.	[Co(qpy)(H2O)2][ClO4]2	0.01	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		1875	11	18	[HEa16]
68.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	0.1	BNAH	0.1	DMF		2.8	0.2	16	[PRo16]
69.	Mn(bpy)(CO)3Br	0.5	ZnTPP	0.25	TEA	0.1	MeCN		64		16	[Vld16]
70.	Mn(bpy)(CO)3Br		Ru(bpy)3Cl2	100	BNAH	0.1	MeCN		47		15	[Mcm17]
71.	Ru(dppq)(tpy)(MeCN)	0.04			TEOA		DMA				14	[FIR18]
72.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.02	BIH	0.1	DMF		520	0	14	[HEa16]
73.	Mn(phdk)(CO)3Br		Ru(bpy)3Cl2	100			DMF		9		13	[Mcm17]
74.	Ru(bpy)2Cl2	0.025	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		1	2	13	[PRo15]
75.	Ru(bpy)2Cl2	25	[Ir(ppy)2(bpy)][PF6]	0.025	TEOA		NMP		1	2	13	[PRo15]
76.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF		0.92	0.25	11	[PRo16]
77.	[Co(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		182	0	11	[HEa16]
78.	[Re(bpy)2(CO)2][OTf]	1			TEOA		DMA				10.3	[AiR19]
79.	Mn(bpy)(CO)3Br	0.5	ZnTPP	0.5	TEA	0.1	MeCN		12		10	[Vld16]
80.	[Fe(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.05	BIH	0.1	DMF		0	0	10	[HEa16]
81.	Mn(CN)(bpy)(CO)3	1	[Ru(dmb)3][PF6]2	1	BNAH	0.1	DMF		2.3	0.37	9.5	[PRo16]
82.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	1	BNAH	0.1	MeCN		21	1.3	9	[PRo16]
83.	[Co(qpy)(H2O)2][ClO4]2	0.05	purpurin	2	BIH	0.1	DMF		197	1	9	[HEa16]
84.	[Ir(dmbpy)(tpy)Cl][PF6]2	0.1			TEOA		MeCN		5	3	9	[Itb17]
85.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	MeCN		19	1.4	8.1	[PRo16]
86.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.05	BIH	0.1	DMF	Argon atmosphere	0	0	8	[HEa16]
87.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.02	BIH	0.1	DMF		0	0	8	[HEa16]
88.	Molecule:100869	0.1			TEOA		MeCN		0	1	7	[Itb17]
89.	Mn(bpy)(CO)3Br	0.5	ZnTPP	1	TEA	0.1	MeCN		8		6	[Vld16]
90.	[Co(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.5	BIH	0.1	MeCN		521	49	6	[HEa16]
91.	[Co(qpy)(H2O)2][ClO4]2	0.05	purpurin	2	BIH	0.1	DMF	Argon atmosphere	0	78	6	[HEa16]
92.	Mn(CN)(bpy)(CO)3	1	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF		3	0.24	5.8	[PRo16]
93.	Mn(CN)(bpy)(CO)3		[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF		1.5	2.8	5.7	[PRo16]
94.	Mn(CN)(bpy)(CO)3	1	[Ru(dmb)3][PF6]2	1	BNAH	0.1	DMF		0.83	0.0073	5.2	[PRo16]
95.	Mn(oMesbpy)(CO)2Br	0.05	[Cu(phen)-(dPPh-Bu)2]2[PF6]2	0.25	BIH	0.01	MeCN		208	0.5	5	[HEa18]
96.	[Fe(pabop)Cl2][CLO4]	0.05	Ir(ppy)3	0.2	TEA		MeCN				5	[MCo15]
97.	[Co(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.5	BIH	0.1	MeCN		136	43	5	[HEa16]
98.	[Ir(dnbpy)(tpy)Cl][PF6]2	0.1			TEOA		MeCN		3	1	5	[Itb17]
99.	Mn(CN)(bpy)(CO)3	0.1	[Ru(dmb)3][PF6]2	0.1	BNAH	0.1	MeCN		7.9	0.56	4.5	[PRo16]
100.	Mn(phen)(CO)3Br		Ru(bpy)3Cl2	100	BNAH	0.1	DMF		17		4	[Mcm17]
101.	Mn(bpy)(CO)3Br	0.05	[Ru(dmb)3][PF6]2	0.05	BNAH	0.1	DMF	Argon gas	2	49	4	[PCr14]
102.	[Co(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		366	15	4	[HEa16]
103.	[Co(qpy)(H2O)2][ClO4]2	0.05	purpurin	0	BIH	0.1	DMF		27	0	4	[HEa16]
104.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF	Argon gas	1.5	7.8	3.8	[PRo16]
105.	Mn(CN)(bpy)(CO)3		[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF	Argon gas	0.87	1.3	3.2	[PRo16]
106.	Ru(dppq)(tpy)(MeCN)	0.04			BIH	0.1	DMA		58	1	3	[FIR18]
107.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN	Argon atmosphere	0	1	3	[HEa16]
108.	[Co(qpy)(H2O)2][ClO4]2	0.05	purpurin	2			DMF		0	0	3	[HEa16]
109.	[Co(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		497	5	3	[HEa16]
110.	Co(ClO4)2	0.05	purpurin	2	BIH	0.1	DMF		0	0	3	[HEa16]
111.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF	Argon gas			2.6	[PRo16]
112.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2		BNAH	0.1	DMF	Argon gas	2.3		2.2	[PRo16]
113.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	MeCN		5.9	0.24	2.1	[PRo16]
114.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2		BNAH	0.1	DMF		2.1		1.9	[PRo16]
115.	Mn(CN)(bpy)(CO)3	1	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	MeCN		4.2	0.8	1.4	[PRo16]
116.	Mn(CN)(bpy)(CO)3	1	[Ru(dmb)3][PF6]2	1	BNAH	0.1	MeCN		3.2	0.17	1.2	[PRo16]
117.	Mn(bpy)(CO)3Br	0.5			TEA	0.1	MeCN		2		1	[Vld16]
118.	[Co(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.3			MeCN		0	1	1	[HEa16]
119.	[Co(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN	Argon atmosphere	0	3	1	[HEa16]
120.	[Co(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		0	6	1	[HEa16]
121.	[Co(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		0	2	1	[HEa16]
122.	Co(ClO4)2	0.05	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN		33	11	1	[HEa16]
123.	Mn(CN)(bpy)(CO)3		[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF		0.6	1.2	0.72	[PRo16]
124.	Mn(CN)(bpy)(CO)3	0.5	[Ru(dmb)3][PF6]2	0.5	BNAH	0.1	DMF	Argon gas	2.2	4.4	0.55	[PRo16]
125.	[Fe(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.02	BIH	0.1	DMF		0	139	0	[HEa16]
126.	[Fe(qpy)(H2O)2][ClO4]2	0.01	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN	Argon atmosphere	0	0	0	[HEa16]
127.	[Fe(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN	Argon atmosphere	0	1	0	[HEa16]
128.	[Fe(qpy)(H2O)2][ClO4]2	0.05	Ru(bpy)3Cl2	0.05	BIH	0.1	MeCN		0	0	0	[HEa16]
129.	[Fe(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN		0	0	0	[HEa16]
130.	[Fe(qpy)(H2O)2][ClO4]2	0	Ru(bpy)3Cl2	0.05	BIH	0.1	MeCN		0	1	0	[HEa16]
131.	[Fe(qpy)(H2O)2][ClO4]2	0.02	Ru(bpy)3Cl2	0.2	BIH	0.1	MeCN	Argon atmosphere	0	0	0	[HEa16]
132.	[Co(qpy)(H2O)2][ClO4]2	0.005	Ru(bpy)3Cl2	0.3	BIH	0.1	MeCN	Argon atmosphere	0	33	0	[HEa16]

Photocatalytic CO2 conversion to HCOOH

Contents

CO₂ conversion to formic acid[Pro21][edit | edit source]

Sacrificial electron donors[edit | edit source]

Ruthenium Catalysts[edit | edit source]

Photosensitizers[edit | edit source]

Experiments[edit | edit source]

Cobalt Catalysts[edit | edit source]

Organic and semiconductor photosensitizer[edit | edit source]

Experiments[edit | edit source]

Literature

Topics

Photocatalytic CO2 conversion to HCOOH

CO2 conversion to formic acid[Pro21][edit | edit source]

Sacrificial electron donors[edit | edit source]

Ruthenium Catalysts[edit | edit source]

Photosensitizers[edit | edit source]

Experiments[edit | edit source]

Cobalt Catalysts[edit | edit source]

Organic and semiconductor photosensitizer[edit | edit source]

Experiments[edit | edit source]

Literature

Current site

Topics

CO₂ conversion to formic acid[Pro21][edit | edit source]