Bio-inspired noble metal-free nanomaterials approaching platinum performances for H2 evolution and uptake

被引:58
作者
Huan, Tran N. [1 ,2 ,3 ]
Jane, Reuben T. [1 ,2 ,3 ]
Benayad, Anass [1 ,4 ]
Guetaz, Laure [1 ,4 ]
Tran, Phong D. [1 ,2 ,3 ,5 ]
Artero, Vincent [1 ,2 ,3 ]
机构
[1] Univ Grenoble Alpes, F-38000 Grenoble, France
[2] CNRS, UMR 5249, Lab Chem & Biol Met, 17 Rue Martyrs, F-38054 Grenoble 9, France
[3] Commissariat Energie Atom & Energies Alternat CEA, Fundamental Res Div, F-38000 Grenoble, France
[4] Commissariat Energie Atom & Energies Alternat CEA, Inst Lab Innovat Technol Energies Nouvelles & Nan, F-38000 Grenoble, France
[5] Univ Sci & Technol Hanoi, Hanoi, Vietnam
关键词
HYDROGEN OXIDATION; OXYGEN REDUCTION; MOLECULAR ELECTROCATALYSTS; FUEL-CELLS; CATALYSTS; ELECTRODES; POTENTIALS; ACID;
D O I
10.1039/c5ee02739j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen/water interconversion is a key reaction in the context of new energy technologies, including hydrogen fuel cells, water electrolyzers, and water-splitting photoelectrochemical cells. Specifications differ for these technologies to meet economic viability but state-of-the-art prototypes all rely on the powerful catalytic properties of the platinum metal as a catalyst for hydrogen production and uptake. Yet, this scarce and expensive metal is not itself a sustainable resource and its replacement by low cost and readily available materials is a requisite for these technologies to become economically viable. Here we revisit the preparation of bioinspired nanomaterials for hydrogen evolution and uptake (Le Goff et al., Science, 2009, 326, 1384-1387) and show that molecular engineering combined with three dimensional structuring of the electrode material allows the preparation of stable materials based on nickel bisdiphosphine catalytic units with performances in a 0.5 M sulphuric acid aqueous electrolyte that approach those of commercial platinum-based materials (0.05 mg(Pt) cm(-2)) assessed under similar, technologically relevant, operational conditions.
引用
收藏
页码:940 / 947
页数:8
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