A Highly Active and Robust CoP/CoS2-Based Electrocatalyst Toward Overall Water Splitting

被引:22
作者
Pan, Yi [1 ]
Fang, Yini [1 ]
Jin, Haonan [1 ]
Zhang, Ming [1 ]
Wang, Lina [1 ]
Ma, Shijie [1 ]
Zhu, Han [2 ]
Du, Mingliang [2 ]
机构
[1] Zhejiang Sci Tech Univ, Coll Mat & Text, Hangzhou 310018, Zhejiang, Peoples R China
[2] Jiangnan Univ, Sch Chem & Mat Engn, Minist Educ, Key Lab Synthet & Biol Colloids, Wuxi 214122, Peoples R China
关键词
CoS2; CoP; Electrocatalysis; Hydrogen evolution reaction; Materials chemistry; HYDROGEN-EVOLUTION REACTION; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT ELECTROCATALYSTS; NANOSHEET ARRAYS; GRAPHENE FILMS; PHOSPHIDE; CATALYST; MOS2; ELECTRODES; NANOWIRES;
D O I
10.1007/s12678-019-00521-w
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
The development of low-cost, highly active, and robust electrocatalysts for catalyzing the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) holds a pivotal role in electrocatalytic water splitting. Herein, a two-step method was presented to synthesize CoS2/CoP heterostructures grown on carbon cloth (CoS2/CoP/CC). The precursor Co(OH)F/CC synthesized through the hydrothermal process can be successfully converted into CoS2/CoP/CC catalyst via gas-phase phosphorization and sulfurization. The as-obtained CoS2/CoP/CC exhibited promising performances for HER and OER with low overpotentials of 90 and 334mV at a current density of 10mAcm(-2) in 1.0M KOH, respectively. The improved electrocatalytic performance of the CoS2/CoP/CC can be attributed to the strong electron interactions and synergistic efforts between CoS2 and CoP, abundant active sites of the heterostructures, and enhanced smaller charge-transfer resistance.
引用
收藏
页码:253 / 261
页数:9
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