Crystalline MoP-amorphous MoS2 hybrid for superior hydrogen evolution reaction

被引:10
|
作者
Li, Xiaolin [1 ]
Zhang, Jialing [1 ]
Zhang, Chi [1 ]
Chen, Da [1 ]
Wang, Bolin [1 ]
Zhang, Rui [1 ]
Zhang, Yu [1 ]
Yan, Xinrong [1 ]
Gan, Qian [1 ]
Wang, Shentang [1 ]
Luo, Hong Qun [1 ]
Li, Nian Bing [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
关键词
Crystalline MoP; Amorphous MoS2; Surface engineering; Hydrogen evolution reaction; ACTIVE EDGE SITES; CATALYST; PERFORMANCE; GRAPHENE; ELECTROCATALYST; NANOPARTICLES; CHALLENGES; OXIDATION; DESIGN; FILMS;
D O I
10.1016/j.jssc.2020.121564
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Molybdenum disulfide (MoS2) is regarded as a perfect catalyst for electrochemical hydrogen evolution reaction (HER). However, the active sites are usually concealed due to the unique two dimensional structure of MoS2. Herein, we propose a facile surface engineering modus to improve the HER activity of MoS2. This strategy is demonstrated by in-situ growth of amorphous MoS2 layer on the molybdenum phosphide (MoP) nanoparticles anchored on the carbon nanotubes (MoS2/MoP/CNT). The HER activity is significantly promoted both through the defect engineering of amorphous MoS(2 )and the synergistic effect between the MoS2 and MoP phases. The MoS2/MoP/CNT sample presents significantly higher HER performance than the pure phase of MoP/CNT and MoS2/CNT samples, requiring overpotentials of 73 and 141 mV to drive a current density of 10 and 100 mA cm(-2).
引用
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页数:6
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