Turnover Number in Photoinduced Molecular Catalysis of Hydrogen Evolution: a Benchmarking for Catalysts?

被引:5
作者
Fortage, Jerome [1 ]
Collomb, Marie-Noelle [1 ]
Costentin, Cyrille [1 ]
机构
[1] Univ Grenoble Alpes, Dept Chim Mol, CNRS, F-38000 Grenoble, France
关键词
Hydrogen Evolution; Photocatalysis; Turnover Number; Photosensitizer; Catalysis; VISIBLE-LIGHT IRRADIATION; PHOTO-REDUCTION; POLYPYRIDINE COMPLEXES; HOMOGENEOUS CATALYSIS; AQUEOUS-SOLUTIONS; COBALT COMPLEXES; WATER; GENERATION; RUTHENIUM(II); MEDIATION;
D O I
10.1002/cssc.202400205
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of devices for production of H2 using light and a sustainable source of electrons may require the design of molecular systems combining a molecular catalyst and a photosensitizer. Evaluation of the efficiency of hydrogen production is commonly performed in homogeneous solution with a sacrificial electron donor and the report of the maximal turnover number vs catalyst ( TONcatlim ${TON_{cat}<^>{\lim } }$ ). This figure of merit is strongly dependent on deactivation pathways and does not by itself provide a benchmarking for catalysts. In particular, when the photosensitizer degradation is the primary source of limitation, a kinetic model, rationalizing literature data, shows that a decrease of the catalyst concentration leads to an increase of TONcatlim ${TON_{cat}<^>{\lim } }$ . It indicates that exceptionally high TONcatlim ${TON_{cat}<^>{\lim } }$ obtained at very low catalyst concentration shall not be considered as an indication of an exceptional catalytic system. We advocate for a systematic kinetic analysis in order to get a quantitative measure of the competitive pathways leading to TONcatlim ${TON_{cat}<^>{\lim } }$ values and to provide keys for performance improvement. Turnover numbers cannot be directly used as a benchmarking figure of merit for homogeneous molecular catalysts in photoinduced hydrogen production. However, kinetic analysis allows rationalization of the increase of turnover numbers as the concentration of catalyst is decreased in the context of limitation of the process by degradation of the photosensitizer. This provides a way for photocatalytic systems benchmarking. image
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页数:6
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共 39 条
[1]   Quantum Dot-Sensitized Photoreduction of CO2 in Water with Turnover Number &gt; 80,000 [J].
Arcudi, Francesca ;
Dordevic, Luka ;
Nagasing, Benjamin ;
Stupp, Samuel, I ;
Weiss, Emily A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2021, 143 (43) :18131-18138
[2]   The Hydrogen Issue [J].
Armaroli, Nicola ;
Balzani, Vincenzo .
CHEMSUSCHEM, 2011, 4 (01) :21-36
[3]   3d Element Complexes of Pentadentate Bipyridine-Pyridine-Based Ligand Scaffolds: Structures and Photocatalytic Activities [J].
Bachmann, Cyril ;
Guttentag, Miguel ;
Spingler, Bernhard ;
Alberto, Roger .
INORGANIC CHEMISTRY, 2013, 52 (10) :6055-6061
[4]   Best practices for experiments and reporting in photocatalytic CO2 reduction [J].
Bonchio, Marcella ;
Bonin, Julien ;
Ishitani, Osamu ;
Lu, Tong-Bu ;
Morikawa, Takeshi ;
Morris, Amanda J. ;
Reisner, Erwin ;
Sarkar, Debashrita ;
Toma, Francesca M. ;
Robert, Marc .
NATURE CATALYSIS, 2023, 6 (08) :657-665
[5]   Molecular catalysis of CO2reduction: recent advances and perspectives in electrochemical and light-driven processes with selected Fe, Ni and Co aza macrocyclic and polypyridine complexes [J].
Boutin, E. ;
Merakeb, L. ;
Ma, B. ;
Boudy, B. ;
Wang, M. ;
Bonin, J. ;
Anxolabehere-Mallart, E. ;
Robert, M. .
CHEMICAL SOCIETY REVIEWS, 2020, 49 (16) :5772-5809
[6]   HOMOGENEOUS CATALYSIS OF THE PHOTO-REDUCTION OF WATER BY VISIBLE-LIGHT - MEDIATION BY A TRIS(2,2'-BIPYRIDINE)RUTHENIUM(II)-COBALT(II) MACROCYCLE SYSTEM [J].
BROWN, GM ;
BRUNSCHWIG, BS ;
CREUTZ, C ;
ENDICOTT, JF ;
SUTIN, N .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (05) :1298-1300
[7]   MECHANISM OF THE FORMATION OF DIHYDROGEN FROM THE PHOTOINDUCED REACTIONS OF TRIS(BIPYRIDINE)RUTHENIUM(II) WITH TRIS(BIPYRIDINE)RHODIUM(III) [J].
BROWN, GM ;
CHAN, SF ;
CREUTZ, C ;
SCHWARZ, HA ;
SUTIN, N .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (25) :7638-7640
[8]   Electrochemical Properties of a Rhodium(III) Mono-Terpyridyl Complex and Use as a Catalyst for Light-Driven Hydrogen Evolution in Water [J].
Camara, Fakourou ;
Gavaggio, Thomas ;
Dautreppe, Baptiste ;
Chauvin, Jerome ;
Pecaut, Jacques ;
Aldakov, Dmitry ;
Collomb, Marie-Noelle ;
Fortage, Jerome .
MOLECULES, 2022, 27 (19)
[9]   Photoinduced Catalysis of Redox Reactions. Turnover Numbers, Turnover Frequency, and Limiting Processes: Kinetic Analysis and Application to Light-Driven Hydrogen Production [J].
Costentin, Cyrille ;
Camara, Fakourou ;
Fortage, Jerome ;
Collomb, Marie-Noelle .
ACS CATALYSIS, 2022, 12 (10) :6246-6254
[10]   Electro- and Solar-Driven Fuel Synthesis with First Row Transition Metal Complexes [J].
Dalle, Kristian E. ;
Warnan, Julien ;
Leung, Jane J. ;
Reuillard, Bertrand ;
Karmel, Isabell S. ;
Reisner, Erwin .
CHEMICAL REVIEWS, 2019, 119 (04) :2752-2875