Mo-doped CoP nanosheets as high-performance electrocatalyst for HER and OER

被引:28
|
作者
Li, Shimin [1 ,2 ]
Bai, Lei [1 ,2 ]
Shi, Haibiao [1 ]
Hao, Xianfeng [1 ]
Chen, Ling [1 ]
Qin, Xiujuan [1 ,2 ]
Shao, Guangjie [1 ,2 ]
机构
[1] Yanshan Univ, Coll Environm & Chem Engn, Hebei Key Lab Heavy Met Deep Remediat Water & Res, Qinhuangdao 066004, Hebei, Peoples R China
[2] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Mo-CoP; Electrocatalyst; HER; OER; Overall water splitting; EFFICIENT BIFUNCTIONAL ELECTROCATALYST; HYDROGEN EVOLUTION; WATER; NANOWIRE; COBALT; CATALYST; ARRAY; NANOTUBES; NANOARRAY; ELECTRODE;
D O I
10.1007/s11581-021-04071-4
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
Transition-metal doping and structural improvement are facile and feasible strategies to obtain highly active catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Herein, we prepare Mo-CoP with a nanosheet structure via hydrothermal reactions and phosphorization. Taking advantage of the nanosheet array, the good electrocatalytic performance of Co-based materials for HER and excellent performance of Co-based phosphide for OER are fully demonstrated. Mo-CoP requires only 112 and 329.9 mV to achieve a current density of 100 mA/cm(2) for HER and OER in 1.0 M KOH, respectively. Furthermore, when it was used as bifunctional electrocatalyst, Mo-CoP could deliver 10 mA/cm(2) at a low cell voltage of 1.54 V. It was found that the activity of Mo-CoP could be ascribed to the structure of nanosheet and the synergistic role of two different metal phosphides. The most important is that the introduction of Mo improves the activity of the catalyst.
引用
收藏
页码:3109 / 3118
页数:10
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