电催化剂
材料科学
催化作用
钙钛矿(结构)
析氧
锶
化学工程
电化学
氧气
惰性
铱
氧化还原
无机化学
化学
电极
物理化学
冶金
有机化学
工程类
作者
Xiao Liang,Lei Shi,Rui Cao,Gang Wan,Wensheng Yan,Hui Chen,Yipu Liu,Xiaoxin Zou
标识
DOI:10.1002/adma.202001430
摘要
A trade-off between catalytic activity and structural stability generally exists in oxygen evolution electrocatalysis, especially in acidic environment. This dilemma limits the development of higher-performance electrocatalysts that are required by next-generation electrochemical technologies. Here it is demonstrated that the inverse catalytic activity-structural stability relation can be broken by alloying catalytically inert strontium zirconate with the other catalytically active perovskite, strontium iridate. This strategy results in an alloyed perovskite electrocatalyst with simultaneously improved iridium mass activity and structural stability, by about five times, for the oxygen evolution reaction under acidic conditions. The experimental and theoretical results suggest that the alloying strategy generates multiple positive effects, mainly including the reduction of catalyst size, the decrease of catalyst covalency, and the weakening of surface oxygen-binding ability. The synergistic optimization of bulk and surface properties, as a result, enhances the intrinsic activity and availability of surface iridium sites, whilst significantly inhibiting the surface cation corrosion during electrocatalysis.
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