过电位
钙钛矿(结构)
电催化剂
析氧
电化学
催化作用
氧化还原
材料科学
电解质
分解水
化学工程
纳米技术
无机化学
化学
电极
物理化学
光催化
生物化学
工程类
作者
Yonglong Huang,Huangwei Xiao,Beibei He,Wenjia Ma,Xueqin Liu,Zhuangzhuang Wu,Wenxin Wang,Ling Zhao,Qi Chen
标识
DOI:10.1016/j.jechem.2024.07.056
摘要
Developing efficient and stable electrocatalysts for the acidic oxygen evolution reaction (OER) is crucial yet challenging due to their sluggish kinetics and potential deactivation in harsh acidic environments. Herein, we propose an electronic regulation approach involving the incorporation of trace Pt into SrIrO3 perovskite to improve its activity and longevity for OER in acidic media. Both experimental and theoretical results reveal that trace Pt incorporation effectively regulates the electronic structure of SrIrO3, lowering the energy barrier of OER and mitigating the Ir overoxidation. The optimized 2%Pt-SrIrO3 electrocatalyst demonstrates an ultralow overpotential of 228 mV at 10 mA cm−2 and maintains stable over 50 h in 0.5 M H2SO4, rivaling most reported iridate perovskites. As a demonstration, the 2%Pt-SrIrO3||Pt/C based electrolytic cell exhibits high electrochemical performance and robustness for practical acidic water splitting. This protocol offers an attractive strategy for electronic structure manipulation in electrocatalysts towards electrocatalytic applications.
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