析氧
催化作用
电解水
尖晶石
电解
阳极
氧气
电子转移
化学
无机化学
材料科学
化学工程
浸出(土壤学)
电化学
光化学
冶金
电极
物理化学
地质学
有机化学
土壤科学
土壤水分
生物化学
工程类
电解质
作者
Yan Duan,Jun Yan Lee,Shibo Xi,Yuanmiao Sun,Jingjie Ge,Samuel Jun Hoong Ong,Yubo Chen,Shuo Dou,Fanxu Meng,Caozheng Diao,Adrian C. Fisher,Xin Wang,Günther G. Scherer,Alexis Grimaud,Zhichuan J. Xu
标识
DOI:10.1002/anie.202015060
摘要
Abstract A rational design for oxygen evolution reaction (OER) catalysts is pivotal to the overall efficiency of water electrolysis. Much work has been devoted to understanding cation leaching and surface reconstruction of very active electrocatalysts, but little on intentionally promoting the surface in a controlled fashion. We now report controllable anodic leaching of Cr in CoCr 2 O 4 by activating the pristine material at high potential, which enables the transformation of inactive spinel CoCr 2 O 4 into a highly active catalyst. The depletion of Cr and consumption of lattice oxygen facilitate surface defects and oxygen vacancies, exposing Co species to reconstruct into active Co oxyhydroxides differ from CoOOH. A novel mechanism with the evolution of tetrahedrally coordinated surface cation into octahedral configuration via non‐concerted proton‐electron transfer is proposed. This work shows the importance of controlled anodic potential in modifying the surface chemistry of electrocatalysts.
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