析氧
催化作用
钙钛矿(结构)
材料科学
化学工程
氧气
离子
纳米技术
无机化学
化学
电化学
物理化学
电极
有机化学
工程类
作者
Jing Zhang,Yuexiao Cui,Lichao Jia,Beibei He,Kun Zhang,Ling Zhao
标识
DOI:10.1016/j.ijhydene.2019.07.162
摘要
Development of cost-effective, highly-active and durable catalysts for oxygen evolution reaction (OER) is critical to sustainable energy conversion and storage devices. Perovskite oxides are exploited as a research frontier on OER, however, their activity and stability are still far from desirable. Herein, we highlight a paradigm shift in the design of highly efficient perovskite-type catalysts for OER by engineering anion defect. The Cl-doped LaFeO2.85Cl0.15 perovskite demonstrates an enhanced OER activity, which is attributed to the abundant surface oxygen vacancies and low adsorption energy of H2O molecule after Cl doping. Moreover, the LaFeO2.85Cl0.15 catalyst also delivers an improved electrocatalytic durability, in contrast to the pristine LaFeO3 catalyst.
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