From Hydrogenases to Noble Metal-Free Catalytic Nanomaterials for H2 Production and Uptake

被引:787
作者
Le Goff, Alan [2 ]
Artero, Vincent [1 ]
Jousselme, Bruno [2 ]
Tran, Phong Dinh [1 ]
Guillet, Nicolas [3 ]
Metaye, Romain [2 ]
Fihri, Aziz [1 ]
Palacin, Serge [2 ]
Fontecave, Marc [1 ,4 ]
机构
[1] Univ Grenoble 1, Lab Chim & Biol Met, CEA, CNRS UMR 5249,Inst Rech Technol & Sci Vivant, F-38054 Grenoble 9, France
[2] CEA, Inst Rayonnement Mat Saclay, Serv Phys & Chim Surfaces & Interfaces, Chem Surfaces & Interfaces Grp, F-91191 Gif Sur Yvette, France
[3] CEA, Inst Laboratoire Innovat Technol Energies Nouvell, Dept Technol Hydrogene, Lab Composants Pile Combustible Electrolyse & Mod, F-38054 Grenoble 9, France
[4] Coll France, F-75005 Paris, France
关键词
CARBON NANOTUBES; DIAZONIUM SALTS; CRYSTAL-STRUCTURE; ONLY HYDROGENASE; REDUCTION; COMPLEXES; OXIDATION; MODELS;
D O I
10.1126/science.1179773
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interconversion of water and hydrogen in unitized regenerative fuel cells is a promising energy storage framework for smoothing out the temporal fluctuations of solar and wind power. However, replacement of presently available platinum catalysts by lower-cost and more abundant materials is a requisite for this technology to become economically viable. Here, we show that the covalent attachment of a nickel bisdiphosphine-based mimic of the active site of hydrogenase enzymes onto multiwalled carbon nanotubes results in a high-surface area cathode material with high catalytic activity under the strongly acidic conditions required in proton exchange membrane technology. Hydrogen evolves from aqueous sulfuric acid solution with very low overvoltages (20 millivolts), and the catalyst exhibits exceptional stability ( more than 100,000 turnovers). The same catalyst is also very efficient for hydrogen oxidation in this environment, exhibiting current densities similar to those observed for hydrogenase-based materials.
引用
收藏
页码:1384 / 1387
页数:4
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