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Binary Pd-Ni Nanoalloy Particles over Carbon Support with Superior Alkaline Formate Fuel Electrooxidation Performance
被引:30
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Anilkumar, Gopinathan M.
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Japan Sci & Technol Agcy JST CREST, Core Res Evolutionary Sci & Technol, Tokyo 1020076, Japan
Noritake Co Ltd, R&D Ctr, 300 Higashiyama, Miyochi, Miyoshi 4700293, Japan Tokyo Inst Technol, Lab Chem & Life Sci, Midori Ku, R1-17,4259 Nagatsuta, Yokohama, Kanagawa 226850, Japan

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[1] Tokyo Inst Technol, Lab Chem & Life Sci, Midori Ku, R1-17,4259 Nagatsuta, Yokohama, Kanagawa 226850, Japan
[2] Japan Sci & Technol Agcy JST CREST, Core Res Evolutionary Sci & Technol, Tokyo 1020076, Japan
[3] Noritake Co Ltd, R&D Ctr, 300 Higashiyama, Miyochi, Miyoshi 4700293, Japan
来源:
基金:
日本科学技术振兴机构;
关键词:
Carbon Support;
Electrocatalyst;
Fuel Cell;
Formate Oxidation Reaction;
Oxidation;
HEAT-TREATMENT;
OXIDATION;
ETHANOL;
PALLADIUM;
CATALYST;
ELECTROCATALYSTS;
REDUCTION;
CELLS;
NANOCRYSTALS;
OXIDE;
D O I:
10.1002/cctc.201900960
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Formate is the one legitimate carbon-neutral fuel that has the capability of being considered an alternative to alcohol fuels amidst the growing demand for efficient fuel-cell systems. In this manuscript, we demonstrate, for the first time, a class of binary Pd-Ni alloy nanoparticles over two different carbon supports showing exceptional enhancement of the formate oxidation reaction (FOR) performance in alkaline medium, compared to Pd/C. The synergistic effects of Pd and oxophilic Ni along with the electronic structure alteration of Pd induced through alloying resulted in an effective change in its catalytic ability, leading to a 5-time enhancement in the overall current density along with a lower overpotential during formate oxidation compared to Pd/C. The more active Pd catalytic sites of the nanoalloy helped to yield mass activities as high as 4.5 A mg(Pd)(-1) and 7.8 A mg(Pd)(-1) during FOR. The structural and electrochemical analysis justifies the synergistic effects and alterations in the Pd lattice ensuing a superior enhancement of electrochemically active Pd sites.
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页码:4731 / 4737
页数:7
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