镝
析氧
钴
催化作用
氧气
材料科学
电化学
溶解
解吸
过渡金属
无机化学
吸附
化学
电极
物理化学
有机化学
生物化学
作者
Xuefeng Zhang,Honghong Zou,Li-Weng Ding,Xiao-Xiao Deng,Jiajun Zheng,Han-Feng Liu,Zi‐Ming Ye,Shengliang Zhong,Zi‐Yi Du,Jia Zhang,Chun‐Ting He
标识
DOI:10.1016/j.xcrp.2023.101571
摘要
Rare-earth doping is an efficient strategy to elevate the oxygen evolution reaction activity of transition-metal-based electrocatalysts, yet it often leads to deleterious electrochemical corrosion. Here, we introduce non-layered dysprosium oxysulfide (Dy2O2S) to a cobalt catalyst to address this issue. Benefiting from an electron-withdrawing Dy2O2S shell, the optimum chainmail-structured catalyst displays low overpotentials of 225 ± 1 and 299 ± 5 mV at 0.1 and 1.0 A·cm−2, respectively, for the oxygen evolution reaction under industrially relevant conditions. Moreover, Dy2O2S blocks the dissolution of dysprosium and cobalt, endowing the catalyst with almost 100% activity retention for at least 120 h at 1 A·cm−2. A variety of in situ/ex situ characterization techniques and theoretical calculations unveil the active sites and the interfacial electron redistribution, which facilitate the oxygen intermediate adsorption and oxygen desorption. This work provides a route to utilize rare-earth elements to optimize the performance of electrocatalysts.
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