过电位
催化作用
分解水
材料科学
化学工程
可逆氢电极
电流密度
制氢
氢
电催化剂
吉布斯自由能
纳米技术
贵金属
析氧
电极
无机化学
金属
化学
电化学
物理化学
工作电极
热力学
冶金
有机化学
光催化
生物化学
量子力学
物理
工程类
作者
Lan Wang,Ning Gong,Zhou Zhou,Qicheng Zhang,Wenchao Peng,Yang Li,Fengbao Zhang,Wenchao Peng
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2022-02-28
卷期号:43 (4): 1176-1183
被引量:20
标识
DOI:10.1016/s1872-2067(21)63982-7
摘要
Hydrogen evolution reaction is a critical reaction in water splitting for hydrogen production. However, developing effective and stable non-noble-metal electrocatalysts which work well at high current densities demanded by industry still remain great challenge. Herein, taking advantage of the highly tunable metal-organic framework (MOF) templates, nitrogen doped binary transition metal phosphides electrocatalysts (N-CoPx/Ni2P) with three-dimensional (3D) conductive network structure were successfully synthesized. The 3D open porous channels could expose more catalytically active sites; nitrogen doping and the synergistic effect between CoP and Ni2P can increase the electron density of Co atoms at active sites, further optimizing the Gibbs free energy of hydrogen (ΔGH*) and water (ΔGH2O*). As a result, the obtained N-CoPx/Ni2P catalyst exhibits extraordinary electrocatalytic activity in a wide pH range. Especially, it requires an extremely low overpotential of 152 mV to deliver a high current density of 650 mA cm–2 in alkaline media. This work may shed some light on the rational design of cheap electrocatalysts and electrode materials that work well at high current densities.
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