From Hydrogenases to Noble Metal–Free Catalytic Nanomaterials for H 2 Production and Uptake
Author(s) -
Alan Le Goff,
Vincent Artero,
Bruno Jousselme,
Phong D. Tran,
Nicolas Guillet,
Romain Metayé,
Aziz Fihri,
Serge Palacin,
Marc Fontecave
Publication year - 2009
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1179773
Subject(s) - hydrogenase , electrolysis , catalysis , electrolysis of water , nickel , hydrogen production , platinum , noble metal , chemistry , nanomaterials , nanotechnology , materials science , combinatorial chemistry , inorganic chemistry , organic chemistry , electrode , electrolyte
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.
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