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

• Published in: Science (American Association for the Advancement of Science) 2009-12, Vol.326 (5958), p.1384-1387
• Main Authors: Le Goff, Alan, Artero, Vincent, Jousselme, Bruno, Tran, Phong Dinh, Guillet, Nicolas, Métayé, Romain, Fihri, Aziz, Palacin, Serge, Fontecave, Marc
• Format: Article
• Language: English
• Subjects: Active sites; Applied sciences; Biomimetic Materials - chemistry; Carbon nanotubes; Catalysis; Catalysts; Catalytic Domain; Chemistry; Colloidal state and disperse state; Current density; Electric current; Electrochemical Techniques; Electrochemistry; Electrodes; Energy; Energy. Thermal use of fuels; Enzymes; Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc; Exact sciences and technology; Fuel cells; Fuel technology; General and physical chemistry; Hydrogen; Hydrogen - chemistry; Hydrogen-Ion Concentration; Hydrogenase - chemistry; Hydrogenases; Kinetics and mechanism of reactions; Ligands; Materials science; Membranes; Nanomaterials; nanotechnology; Nanotubes, Carbon - chemistry; Nickel; Nickel - chemistry; Overvoltage; Oxidation; Oxidation-Reduction; Phosphines - chemistry; Platinum; Protons; Q1; Sulfuric Acids - chemistry; Technology; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Wind energy
• ISSN: 0036-8075; 1095-9203
• DOI: 10.1126/science.1179773

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.