Hierarchical CoP@Ni2P catalysts for pH-universal hydrogen evolution at high current density

被引:74
|
作者
Jin, Mengtian [1 ]
Zhang, Xian [3 ,4 ]
Shi, Run [1 ]
Lian, Qing [1 ]
Niu, Shuzhang [1 ]
Peng, Ouwen [1 ]
Wang, Qun [1 ]
Cheng, Chun [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Peoples R China
[2] Guangdong Prov Key Lab Energy Mat Elect Power, Shenzhen 518055, Peoples R China
[3] Wuhan Univ Technol, Sch Resources & Environm Engn, Luoshi Rd 122, Wuhan 430070, Hubei, Peoples R China
[4] Wuhan Univ Technol, Hubei Key Lab Mineral Resources Proc & Environm, Luoshi Rd 122, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Hierarchical; Heterostructure; pH-universal; Hydrogen evolution reaction; High current density; EFFICIENT; ELECTROCATALYST; PHOSPHIDE; ARRAYS; NANOWIRE;
D O I
10.1016/j.apcatb.2021.120350
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
For large-scale implementation of electrochemical hydrogen production, it is essential to develop electrocatalysts that work well at high current densities over a wide pH range. Herein, we use a facile method to synthesize a hierarchical bimetal phosphide (CoP@Ni2P) on nickel foam, which requires very low overpotentials to achieve the benchmark 10 mA cm-2 (e.g., 16 mV in alkaline media). Furthermore, the CoP@Ni2P can deliver a high current density of 500 mA cm-2 at small overpotentials and show no obvious decay after the durability test for over 48 h at all pH levels. The outstanding catalytic performance is attributed to the superaerophobicity of the electrode surface, fast electron transport as well as the increased number of exposed active sites caused by the hierarchical structure and the synergistic effect of the heterostructures. Consequently, this work provides an advanced transition metal-based phosphide for large-scale hydrogen production in all pH ranges.
引用
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页数:10
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