双金属片
过电位
塔菲尔方程
材料科学
多孔性
催化作用
化学工程
比表面积
电化学
兴奋剂
金属有机骨架
分解水
纳米技术
打赌理论
钼
无机化学
冶金
化学
电极
复合材料
物理化学
光电子学
金属
吸附
光催化
有机化学
工程类
作者
Ping Li,Dehua Zheng,Mengyou Gao,Xiaodong Zuo,Lei Sun,Qiannan Zhou,Jianjian Lin
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2021-08-23
卷期号:4 (9): 8875-8882
被引量:12
标识
DOI:10.1021/acsaem.1c01085
摘要
Non-noble metal electrocatalysts have attracted great attention on account of low cost, good stability, and excellent hydrogen evolution performance. One of the most efficient approaches to increase active sites is to enlarge the specific surface area. Herein, we prepared porous zinc, nitrogen co-doped molybdenum carbide (Zn, N co-doped Mo2C) with large specific surface area, which was derived from Zn, Mo bimetallic metal–organic frameworks (Zn, Mo bimetallic MOFs) via a two-step approach. Most of Zn formed a porous structure during the volatilizing process at high temperature and reduction condition. In addition, the N element from the MOF template was doped into Zn, N co-doped Mo2C. Benefitting from the co-doping of Zn and N, the porous structure with a large specific surface area (352.2 m2 g–1), and the electrochemical surface area (241.2 cm2), Zn, N co-doped Mo2C showed enhanced hydrogen evolution reaction activity in H2SO4 (0.5 mol L–1) with a low overpotential of 169.5 mV (10 mA cm–2), an onset potential of 56.3 mV (1 mA cm–2), a small Tafel slope (62.2 mV dec–1), and good stability. This work enlightens that the MOF template is beneficial to the preparation of porous catalysts with large specific surface area and thus displays efficient catalytic performance varying from energy storage to conversion.
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