过电位
催化作用
电催化剂
磷化物
吸附
材料科学
分解水
电解水
氢
无机化学
化学
电解
物理化学
电化学
电极
光催化
电解质
生物化学
有机化学
作者
Tingwen Zhao,Shuhao Wang,Yibing Li,Chen Jia,Zhen Su,Derek Hao,Bing‐Jie Ni,Qiang Zhang,Chuan Zhao
出处
期刊:Small
[Wiley]
日期:2022-09-04
卷期号:18 (40)
被引量:52
标识
DOI:10.1002/smll.202204758
摘要
Regulating the electronic structure and intrinsic activity of catalysts' active sites with optimal hydrogen intermediates adsorption is crucial to enhancing the hydrogen evolution reaction (HER) in alkaline media. Herein, a heterostructured V-doped Ni2 P/Ni12 P5 (V-Ni2 P/Ni12 P5 ) electrocatalyst is fabricated through a hydrothermal treatment and controllable phosphidation process. In comparison with pure-phase V-Ni2 P, in/ex situ characterizations and theoretical calculations reveal a redistribution of electrons and active sites in V-Ni2 P/Ni12 P5 due to the V doping and heterointerfaces effect. The strong coupling between Ni2 P and Ni12 P5 at the interface leads to an increased electron density at interfacial Ni sites while depleting at P sites, with V-doping further promoting the electron accumulation at Ni sites. This is accompanied by the change of active sites from the anionic P sites to the interfacial Ni-V bridge sites in V-Ni2 P/Ni12 P5 . Benefiting from the interface electronic structure, increased number of active sites, and optimized H-adsorption energy, the V-Ni2 P/Ni12 P5 exhibits an overpotential of 62 mV to deliver 10 mA cm-2 and excellent long-term stability for HER. The V-Ni2 P/Ni12 P5 catalyst is applied for anion exchange membrane water electrolysis to deliver superior performance with a current density of 500 mA cm-2 at a cell voltage of 1.79 V and excellent durability.
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