Surfactant-assisted hydrothermal synthesis of nitrogen doped Mo2C@C composites as highly efficient electrocatalysts for hydrogen evolution reaction

被引:54
|
作者
Liu, Yuchuan [1 ]
Huang, Baobing [1 ]
Hu, Xiang [1 ]
Xie, Zailai [1 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350016, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Mo2C@C; Electrocatalysts; Hydrogen evolution reaction; MOLYBDENUM CARBIDE NANOPARTICLES; HIGH-PERFORMANCE; BIFUNCTIONAL ELECTROCATALYST; MESOPOROUS CARBON; NANOWIRES; NANOSPHERES; NANOFIBERS; NANOTUBES; COBALT; GROWTH;
D O I
10.1016/j.ijhydene.2018.12.096
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
We describe a facile surfactant-assisted hydrothermal route to synthesize nitrogen doped Mo2C@C composites in the presence of cetyltrimethylammonium bromide (CTAB) as carbon source and structure guiding agent. The resulting Mo2C@C composites consist of Mo2C nanocrystals with sheet-like morphology and well-dispersed nitrogen element doping. Controllable experiments indicate that the additive amount of CTAB can efficiently tune porous structure and electrochemical activity of the as-prepared Mo2C@C materials. This unique nitrogen doped Mo2C@C composite provides several advantages for electrocatalytic applications: (1) nitrogen doped carbons can prevent the aggregation of Mo2C nanocrystals and render it high conductivity; (2) the homogeneous dispersion of Mo2C nanocrystals provides abundant active sites; (3) 2D morphology, the hierarchical porosity, and high surface areas allow large exposed field of active sites and facilitate mass transfer. As a result, the nitrogen doped Mo2C@C composites deliver superior HER electrocatalytic activities with a low overpotential of only 100 mV and also a low Tafel slope of 53 mV/dec in alkaline condition. Such CTAB-assisted strategy may open up an opportunity towards synthesis of low cost and high performance Mo-based electrocatalysts for various applications, such as water splitting. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3702 / 3710
页数:9
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