Shrunken hollow Mo-N/Mo-C nanosphere structure for efficient hydrogen evolution in a broad pH range

被引:39
作者
Cheng, Ruilin [1 ]
He, Honglin [2 ]
Pu, Zonghua [1 ]
Amiinu, Ibrahim Saana [1 ]
Chen, Lei [1 ]
Wang, Zhe [1 ]
Li, Guoqiang [3 ]
Mu, Shichun [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[2] Guangzhou Mil Command, Wuhan Gen Hosp, Dept Radiol, Wuhan 430070, Hubei, Peoples R China
[3] South China Univ Technol, Dept Elect Mat, Guangzhou 510641, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Molybdenum carbide; Molybdenum nitride; Shrunken hollow sphere; Hydrogen evolution reaction; NITROGEN-DOPED CARBON; MOLYBDENUM PHOSPHIDE; ELECTROCATALYST; NANOPARTICLES; NANOSHEETS; GRAPHENE; CATALYSTS; SULFIDE;
D O I
10.1016/j.electacta.2018.12.128
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Finding a non-noble metal (NNM) electrocatalyst with comparative hydrogen evolution reaction (HER) activity in a broad pH range is essential but challenging. Here, we report a unique shrunken hollow spherical shell with Mo2N andMo(2)C dual active phases encapsulated by nitrogen-doped carbon (Mo-N/ C@N-C). As NNM electrocatalyst, it shows high HER activity and stability in a broad pH range. This material can be synthesized by pyrolysis of sulfonated polystyrene@polyaniline-MoOx sphere-like precursors using sulfonated polystyrene as template and polyaniline as carbon and nitrogen source. In an alkaline solution, the as-prepared Mo-N/C@N-C only needs an overpotential of 135mV to reach the current density of 10 mAcm(-2), and exhibits high electrochemical and structural durability. The catalyst also possesses similar performance in acidic and neutral media, making it a suitable candidate for hydrogen production in all pH media. Such excellent catalytic performance is mainly driven by the synergy of abundant Mo2N and Mo2C dual active centers, and shrunken hollow sphere structures with high packing density, as well as the N-C active site and protection of N-doped carbon frameworks. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:799 / 805
页数:7
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