Efficient NH3-Tolerant Nickel-Based Hydrogen Oxidation Catalyst for Anion Exchange Membrane Fuel Cells

被引:15
|
作者
Wang, Ye-Hua [1 ]
Gao, Fei-Yue [1 ]
Zhang, Xiao-Long [1 ]
Yang, Yu [1 ]
Liao, Jie [1 ]
Niu, Zhuang-Zhuang [1 ]
Qin, Shuai [1 ]
Yang, Peng-Peng [1 ]
Yu, Peng-Cheng [1 ]
Sun, Mei [1 ]
Gao, Min-Rui [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Div Nanomat & Chem, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
WORK FUNCTION; ADSORPTION; CO; ELECTRODES; AMMONIA; ELECTRONEGATIVITY; ELECTROCATALYSTS; SPECTROSCOPY; OCCUPANCY; STABILITY;
D O I
10.1021/jacs.3c06903
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Convertinghydrogen chemical energy into electrical energy by fuelcells offers high efficiencies and environmental advantages, but ultrapurehydrogen (over 99.97%) is required; otherwise, the electrode catalysts,typically platinum on carbon (Pt/C), will be poisoned by impuritygases such as ammonia (NH3). Here we demonstrate remarkableNH(3) resistivity over a nickel-molybdenum alloy (MoNi4) modulated by chromium (Cr) dopants. The resultant Cr-MoNi4 exhibits high activity toward alkaline hydrogen oxidationand can undergo 10,000 cycles without apparent activity decay in thepresence of 2 ppm of NH3. Furthermore, a fuel cell assembledwith this catalyst retains 95% of the initial peak power density evenwhen NH3 (10 ppm)/H-2 was fed, whereas the poweroutput reduces to 61% of the initial value for the Pt/C catalyst.Experimental and theoretical studies reveal that the Cr modifier notonly creates electron-rich states that restrain lone-pair electrondonation but also downshifts the d-band center to suppress d-electronback-donation, synergistically weakening NH3 adsorption.
引用
收藏
页码:17485 / 17494
页数:10
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