Construction of hetero-phase Mo2C-CoO@N-CNFs film as a self-supported Bi-functional catalyst towards overall water splitting

被引:51
作者
Gong, Tianyu [1 ]
Zhang, Jinyang [1 ]
Liu, Yang [1 ]
Hou, Linrui [1 ]
Deng, Jianlin [2 ]
Yuan, Changzhou [1 ]
机构
[1] Univ Jinan, Sch Mat Sci & Engn, Jinan 250022, Peoples R China
[2] Qilu Univ Technol, Adv Mat Inst, Shandong Acad Sci, Jinan 250014, Peoples R China
基金
中国国家自然科学基金;
关键词
Hetero-phaseMo2C-CoO; Self-supported catalyst; Synergistic effect; Electrospun film; Overall water splitting; N-DOPED CARBON; HYDROGEN EVOLUTION; MOLYBDENUM CARBIDE; HIGHLY EFFICIENT; BIFUNCTIONAL ELECTROCATALYST; HIGH-PERFORMANCE; NICKEL FOAM; NANOSHEETS; ELECTRODE; GRAPHENE;
D O I
10.1016/j.cej.2022.139025
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
It is an enormous challenge to develop low-cost non-noble metal bi-functional catalysts toward overall water splitting. The efficient water decomposition electrocatalysts need both intrinsic activities determined by electronic structure and superb mass transfer ability. For this, in the contribution, an efficient self-supported bi-functional catalyst, i.e., nanoscale hetero Mo2C-CoO encapsulated in N-doped carbon nanofibers (Mo2C-CoO@N- CNFs), is designed and fabricated with facile electrospinning avenue. Density functional theory and electro-chemical investigation manifest that the synergistic effect of bimetallic Mo/Co accelerates kinetics of hydrogen evolution reaction (HER) and lowers the energy barrier of oxygen evolution reaction (OER). Thanks to the structural and compositional merits, the optimized integrated Mo2C-CoO@N-CNFs film demonstrates remarkable catalytic activities in both OER and HER, and renders a current density of 10 mA cm(-2 )at 1.56 V when used for alkaline whole water cracking. The design concept here provides insights for future rational construction of advanced water decomposition catalysts.
引用
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页数:12
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