Iron-Doped Nickel Phosphide Nanosheets InSitu Grown on Nickel Submicrowires as Efficient Electrocatalysts for Oxygen Evolution Reaction

被引:25
|
作者
Chen, Jiahui [1 ,2 ]
Li, Yunming [1 ,2 ]
Sheng, Guoqing [1 ]
Xu, Lu [1 ]
Ye, Huangqing [1 ,2 ]
Fu, Xian-Zhu [1 ,3 ]
Sun, Rong [1 ]
Wong, Ching-Ping [1 ,4 ,5 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
[2] Univ Chinese Acad Sci, Shenzhen Coll Adv Technol, Shenzhen 518055, Peoples R China
[3] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen 518055, Peoples R China
[4] Chinese Univ Hong Kong, Dept Elect Engn, Hong Kong 999077, Hong Kong, Peoples R China
[5] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
基金
中国国家自然科学基金;
关键词
doping; iron; nanostructures; nickel; water splitting; WATER OXIDATION; FACILE SYNTHESIS; NANOWIRE-ARRAY; NI; HYDROGEN; CATALYST; ALKALINE; CARBON; NANOPARTICLES; NANORODS;
D O I
10.1002/cctc.201800036
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
Tens of micrometers long metallic Ni submicrowires with a diameter of approximately 200 nm are prepared by a chemical reduction method under a magnetic field. Fe-doped Ni2P nanosheets are then insitu grown on Ni submicrowires by a simple wet-chemical reaction followed by a low-temperature phosphorization process. The (Ni0.87Fe0.13)(2)P-Ni composite exhibits the highest catalytic activity toward oxygen evolution reaction in alkaline solution among all the as-prepared (Ni1-xFex)(2)P-Ni catalysts, delivering a current density of 10 mAcm(-2) at an overpotential of only 257 mV and keeping high stability over 10 h electrolysis. These exceptional activities are attributed to the unique structure combining metallic Ni submicrowires as good electronically conductive substrate and the insitu grown Fe-doped Ni2P nanosheets. Specifically, Fe incorporation leads to strong electron interactions between Ni, Fe, and P, fast reaction kinetics, small charge-transfer resistance, and a large electrochemical surface area, which are responsible for the excellent catalytic performance.
引用
收藏
页码:2248 / 2253
页数:6
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