Non-precious metal electrocatalysts with high activity for hydrogen oxidation reaction in alkaline electrolytes

被引:286
作者
Sheng, Wenchao [1 ,2 ]
Bivens, Adam P. [1 ,2 ]
Myint, MyatNoeZin [1 ,2 ]
Zhuang, Zhongbin [1 ,2 ]
Forest, Robert V. [1 ,2 ]
Fang, Qianrong [1 ,2 ]
Chen, Jingguang G. [3 ,4 ]
Yan, Yushan [1 ,2 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE 19716 USA
[2] Univ Delaware, Ctr Catalyt Sci & Technol, Newark, DE 19716 USA
[3] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[4] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
关键词
OXYGEN-REDUCTION ACTIVITY; RANEY-NICKEL CATALYST; FUEL-CELLS; WATER ELECTROLYSIS; EVOLUTION REACTION; COBALT-MOLYBDENUM; ELECTRODES; FUTURE; ALLOY; NI;
D O I
10.1039/c3ee43899f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A ternary metallic CoNiMo catalyst is electrochemically deposited on a polycrystalline gold (Au) disk electrode using pulse voltammetry, and characterized for hydrogen oxidation reaction (HOR) activity by temperature-controlled rotating disk electrode measurements in 0.1 M potassium hydroxide (KOH). The catalyst exhibits the highest HOR activity among all non-precious metal catalysts (e.g., 20 fold higher than Ni). At a sufficient loading, the CoNiMo catalyst is expected to outperform Pt and thus provides a promising low cost pathway for alkaline or alkaline membrane fuel cells. Density functional theory (DFT) calculations and parallel H-2-temperature programmed desorption (TPD) experiments on structurally much simpler model alloy systems show a trend that CoNiMo has a hydrogen binding energy (HBE) similar to Pt and much lower than Ni, suggesting that the formation of multi-metallic bonds modifies the HBE of Ni and is likely a significant contributing factor for the enhanced HOR activity.
引用
收藏
页码:1719 / 1724
页数:6
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