过电位
析氧
催化作用
氧气
无定形固体
掺杂剂
电化学
材料科学
化学
化学工程
兴奋剂
纳米技术
无机化学
物理化学
结晶学
电极
光电子学
有机化学
工程类
作者
Yajing Mu,Dantong Zhang,Tianyi Gao,Lina Wang,Lei Zhang,Xiaoxin Zou,Weitao Zheng,Jinchang Fan,Xiaoqiang Cui
标识
DOI:10.1002/anie.202505908
摘要
Developing efficient Ru‐based catalysts is crucial in reducing reliance on costly Ir for the acidic oxygen evolution reaction (OER). However, these Ru‐based catalysts face a fundamental stability challenge due to the highly reactive nature of lattice oxygen. In this work, we propose an effective strategy to stabilize lattice oxygen in two‐dimensional amorphous RuOx through p‐p orbital hybridization by incorporating dopants such as Al, Ga, and In. Notably, Ga doping exhibits remarkable acidic OER performance, leads to a 137 mV reduction in overpotential at 10 mA cm‐2 and a 125‐fold improvement in stability compared to undoped RuOx. This also surpasses the performances of most reported Ru‐based catalysts. In contrast, doping with other elements from the same period, such as Mn, Co, or Cu, shows negligible improvements in catalytic performance. In‐situ electrochemical spectroscopic analysis, couples with theoretical calculations, reveals that the p‐p orbital hybridization in the Ga‐O coordination within Ga‐RuOx effectively reduces the reactivity of lattice oxygen, suppresses the overoxidation of Ru, and switches the reaction pathway from the lattice oxygen mechanism to the adsorbate evolution mechanism. This novel p‐p orbital hybridization strategy holds great potential for the development of efficient and robust electrocatalysts for OER and beyond.
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