Facile preparation of carbon sphere supported molybdenum compounds (P, C and S) as hydrogen evolution electrocatalysts in acid and alkaline electrolytes

被引:143
作者
Wu, Zexing [1 ]
Wang, Jie [1 ]
Liu, Rong [1 ]
Xia, Kedong [1 ]
Xuan, Cuijuan [1 ]
Guo, Junpo [1 ]
Lei, Wen [1 ]
Wang, Deli [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Hubei Key Lab Mat Chem & Serv Failure, Key Lab Mat Chem Energy Convers & Storage,Minist, Wuhan 430074, Peoples R China
基金
国家教育部博士点专项基金资助;
关键词
Molybdenum compounds (P C and S); Hydrogen evolution reaction; Non-noble electrocatalysts; Carbon sphere; OXYGEN REDUCTION REACTION; HIGHLY EFFICIENT CATALYST; MOS2; NANOSHEETS; DOPED GRAPHENE; NANOPARTICLES; PHOSPHIDE; CARBIDE; NANOTUBES; NITROGEN; PERFORMANCE;
D O I
10.1016/j.nanoen.2017.01.014
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
Efficient electrocatalysts for hydrogen evolution reaction (HER) were developed based on the homogeneous dispersion of molybdenum composites (MoP, Mo2C, MoS2) on a glucose-derived carbon sphere matrix obtained by simply changing the precursors during the high temperature treatment. The potential composite materials showed different performance characteristics in different experimental designs. The as-synthesized MoP showed the best HER performance in acid medium with a low overpotential of 136 mV obtained at 10 mA cm(-2), while Mo2C-C showed the lowest overpotential for HER in alkaline medium, and for MoS2-C, which exhibited few layers structure (less than three layers), exhibiting favorable catalytic performance in both acid and alkaline electrolytes. Both MoP-C and Mo2C-C showed negligible overpotential loss after 5000 cycles in acid medium, but were relative unstable in alkaline medium. Moreover, the carbon sphere matrix improved the catalytic performance of molybdenum compounds by alleviating the aggregation of catalysts, providing sufficient area for electrolyte contact, and facilitating electron transfer. This work demonstrates a facile avenue to prepare cost-effective molybdenum compounds for HER. Furthermore, electrochemical performance of the catalysts was investigated in both acid and basic media.
引用
收藏
页码:511 / 519
页数:9
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