过电位
析氧
电化学
化学工程
材料科学
催化作用
分解水
电解
电解水
溶解
离子交换
密度泛函理论
电化学能量转换
无机化学
电极
离子
化学
物理化学
电解质
计算化学
生物化学
有机化学
工程类
光催化
作者
Fuli Wang,Jin‐Long Tan,Zheng‐Yang Jin,Chao‐Yue Gu,Qian‐Xi Lv,Yiwen Dong,Ren‐Qing Lv,Bin Dong,Yong‐Ming Chai
出处
期刊:Small
[Wiley]
日期:2024-04-12
卷期号:20 (33)
被引量:5
标识
DOI:10.1002/smll.202310064
摘要
Limited by the strong oxidation environment and sluggish reconstruction process in oxygen evolution reaction (OER), designing rapid self-reconstruction with high activity and stability electrocatalysts is crucial to promoting anion exchange membrane (AEM) water electrolyzer. Herein, trace Fe/S-modified Ni oxyhydroxide (Fe/S-NiOOH/NF) nanowires are constructed via a simple in situ electrochemical oxidation strategy based on precipitation-dissolution equilibrium. In situ characterization techniques reveal that the successful introduction of Fe and S leads to lattice disorder and boosts favorable hydroxyl capture, accelerating the formation of highly active γ-NiOOH. The Density Functional Theory (DFT) calculations have also verified that the incorporation of Fe and S optimizes the electrons redistribution and the d-band center, decreasing the energy barrier of the rate-determining step (
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