Electrospinning Hetero-Nanofibers of Fe3C-Mo2C/Nitrogen-Doped-Carbon as Efficient Electrocatalysts for Hydrogen Evolution

被引:112
作者
Lin, Huanlei [1 ]
Zhang, Wenbiao [1 ]
Shi, Zhangping [2 ,3 ]
Che, Minwei [1 ]
Yu, Xiang [1 ,4 ]
Tang, Yi [2 ,3 ]
Gao, Qingsheng [1 ]
机构
[1] Jinan Univ, Dept Chem, Coll Chem & Mat Sci, Guangzhou 510632, Guangdong, Peoples R China
[2] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Lab Adv Mat, Shanghai 200433, Peoples R China
[3] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Shanghai 200433, Peoples R China
[4] Jinan Univ, Analyt & Testing Ctr, Guangzhou 510632, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysts; heterostructures; hydrogen evolution reaction; metal carbides; synergic enhancement; METAL-ORGANIC FRAMEWORKS; MOLYBDENUM-CARBIDE; CARBON; NANOPARTICLES; NANOSHEETS; NANOTUBES; CATALYSTS; STRATEGY; TRENDS; MO2C;
D O I
10.1002/cssc.201700207
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heterostructured electrocatalysts with multiple active components are expected to synchronously address the two elementary steps in the hydrogen evolution reaction (HER), which require varied hydrogen-binding strength on the catalyst surface. Herein, electrospinning followed by a pyrolysis is introduced to design Fe3C-Mo2C/nitrogen-doped carbon (Fe3C-Mo2C/NC) hetero-nanofibers (HNFs) with tunable composition, leading to abundant Fe3C-Mo2C hetero-interfaces for synergy in electrocatalysis. Owing to the strong hydrogen binding on Mo2C and the relatively weak one on Fe3C, the hetero-interfaces of Fe3C-Mo2C remarkably promote HER kinetics and intrinsic activity. Additionally, the loose and porous N-doped carbon matrix, as a result of Fe-catalyzed carbonization, ensures the fast transport of electrolytes and electrons, thus minimizing diffusion limitation. As expected, the optimized Fe3C-Mo2C/NC HNFs afforded a low overpotential of 116 mV at a current density of -10 mA cm(-2) and striking kinetics metrics (onset overpotential: 42 mV, Tafel slope: 43 mVdec(-1)) in 0.5m H2SO4, outperforming most recently reported noble-metal-free electrocatalysts.
引用
收藏
页码:2597 / 2604
页数:8
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