双金属片
催化作用
析氧
材料科学
静电纺丝
分解水
化学工程
密度泛函理论
合理设计
电化学
碳纤维
纳米技术
化学
工程类
有机化学
物理化学
复合材料
电极
计算化学
复合数
聚合物
光催化
作者
Tianyu Gong,Jinyang Zhang,Yang Liu,Linrui Hou,Jianlin Deng,Changzhou Yuan
标识
DOI:10.1016/j.cej.2022.139025
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 electrochemical 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.
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