过电位
分解水
催化作用
掺杂剂
材料科学
析氧
氧化物
兴奋剂
纳米结构
金属
密度泛函理论
纳米技术
过渡金属
化学工程
无机化学
化学
物理化学
电化学
冶金
计算化学
电极
生物化学
光催化
光电子学
工程类
作者
Haibin Ma,Jun Zhou,Yang Zhao,Shijie Wang,Zhiwei Hu,Jiwei Ma,Hongfei Cheng
出处
期刊:Small
[Wiley]
日期:2024-12-05
卷期号:21 (4): e2406353-e2406353
标识
DOI:10.1002/smll.202406353
摘要
Abstract The high overpotential and unsatisfactory stability of RuO 2 ‐based catalysts seriously hinder their application in acidic oxygen evolution reaction (OER). Herein, a Ru@RuO 2 core/shell catalyst doped with atomically dispersed Mn species, denoted as Ru@Mn‐RuO 2 , is reported, which is prepared by a facile one‐pot method. Detailed structural characterizations confirm that Mn is homogeneously and atomically distributed in RuO 2 shell, which causes lattice contraction of RuO 2 . The as‐prepared Ru@Mn‐RuO 2 exhibits a very low overpotential of 190 mV at the current density of 10 mA cm −2 and an excellent stability of 360 h, far surpassing the control samples Ru@RuO 2 without atomically dispersed Mn dopants and home‐made RuO 2 nanoparticles without metallic Ru core. With the further assistance of density functional theory calculations, the enhanced OER activity of Ru@Mn‐RuO 2 is attributed to multiple synergistic effects, including the MnO x ‐Ru (oxide shell) synergy, MnO x ‐Ru (metal core) synergy, and the Ru (core)‐RuO 2 (shell) synergy. Besides, the atomically dispersed Mn doping can increase the formation energy of soluble Ru cations, thus leading to the excellent stability of the Ru@Mn‐RuO 2 catalyst. This work shines light on the design of electrocatalysts with multiple synergistic effects towards efficient acid water splitting.
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