析氧
电催化剂
催化作用
钙钛矿(结构)
材料科学
掺杂剂
纳米技术
电化学
化学工程
化学物理
兴奋剂
化学
物理化学
电极
光电子学
结晶学
生物化学
工程类
作者
Xiaomin Xu,Yangli Pan,Yijun Zhong,Chenliang Shi,Daqin Guan,Lei Ge,Zhiwei Hu,Yi‐Ying Chin,Hong‐Ji Lin,Guangming Chen,Hao Wang,San Ping Jiang,Zongping Shao
标识
DOI:10.1002/advs.202200530
摘要
Abstract Oxygen evolution reaction (OER) is a key half‐reaction in many electrochemical transformations, and efficient electrocatalysts are critical to improve its kinetics which is typically sluggish due to its multielectron‐transfer nature. Perovskite oxides are a popular category of OER catalysts, while their activity remains insufficient under the conventional adsorbate evolution reaction scheme where scaling relations limit activity enhancement. The lattice oxygen‐mediated mechanism (LOM) has been recently reported to overcome such scaling relations and boost the OER catalysis over several doped perovskite catalysts. However, direct evidence supporting the LOM participation is still very little because the doping strategy applied would introduce additional active sites that may mask the real reaction mechanism. Herein, a dopant‐free, cation deficiency manipulation strategy to tailor the bulk diffusion properties of perovskites without affecting their surface properties is reported, providing a perfect platform for studying the contribution of LOM to OER catalysis. Further optimizing the A‐site deficiency achieves a perovskite candidate with excellent intrinsic OER activity, which also demonstrates outstanding performance in rechargeable Zn–air batteries and water electrolyzers. These findings not only corroborate the key role of LOM in OER electrocatalysis, but also provide an effective way for the rational design of better catalyst materials for clean energy technologies.
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