Molecular engineered nanomaterials for catalytic hydrogen evolution and oxidation

被引:97
作者
Coutard, Nathan [1 ]
Kaeffer, Nicolas [1 ]
Artero, Vincent [1 ]
机构
[1] Univ Grenoble Alpes, Lab Chim & Biol Met, CNRS, UMR 5249,Commissariat Energie Atom & Energies Alt, 17 Rue Martyrs, F-38000 Grenoble, France
关键词
ELECTROCATALYTIC H-2 EVOLUTION; OXYGEN REDUCTION REACTIONS; DIIMINE-DIOXIME COMPLEXES; IRON-ONLY HYDROGENASE; MEMBRANE FUEL-CELLS; AQUEOUS-SOLUTION; CARBON ELECTRODES; CO2; REDUCTION; NIFE HYDROGENASE; PROTON REDUCTION;
D O I
10.1039/c6cc06311j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The active sites of hydrogenases have inspired the design of molecular catalysts for hydrogen evolution and oxidation. In this feature article, we showcase key elements of bio-inspiration before embarking on a tour of a representative series of molecular hydrogen evolving catalysts (HECs) and describing the toolbox available for benchmarking their performances. We then show how such catalysts can be immobilized on conducting substrates to prepare electrode materials active for hydrogen evolution and oxidation with a special emphasis on cobalt diimine-dioxime complexes and DuBois' nickel diphosphine compounds. We finally discuss the optimization required for implementing molecular-engineered materials into operational devices and illustrate how such molecular approaches can be expanded to other fuel-forming processes such as the electrochemical valorisation of carbon dioxide and the oxygen reduction or water oxidation reactions.
引用
收藏
页码:13728 / 13748
页数:21
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