过电位
钴
催化作用
析氧
氧气
分解水
电催化剂
电解水
化学
氧化还原
材料科学
无机化学
化学工程
电解
物理化学
有机化学
电化学
电极
光催化
工程类
电解质
作者
Jiawei Zhao,Kaihang Yue,Hong Zhang,Shuyin Wei,Jiawei Zhu,Dongdong Wang,Junze Chen,V. Yu. Fominski,Gao‐Ren Li
标识
DOI:10.1038/s41467-024-46801-y
摘要
Abstract Electrocatalytic water splitting is a promising route for sustainable hydrogen production. However, the high overpotential of the anodic oxygen evolution reaction poses significant challenge. SrIrO 3 -based perovskite-type catalysts have shown great potential for acidic oxygen evolution reaction, but the origins of their high activity are still unclear. Herein, we develop a Co-doped SrIrO 3 system to enhance oxygen evolution reaction activity and elucidate the origin of catalytic activity. In situ experiments reveal Co activates surface lattice oxygen, rapidly exposing IrO x active sites, while bulk Co doping optimizes the adsorbate binding energy of IrO x . The Co-doped SrIrO 3 demonstrates high oxygen evolution reaction electrocatalytic activity, markedly surpassing the commercial IrO 2 catalysts in both conventional electrolyzer and proton exchange membrane water electrolyzer.
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