析氧
过电位
催化作用
电化学
材料科学
氧化还原
分解水
阳极
异质结
化学工程
光化学
氧气
无机化学
化学
电极
物理化学
有机化学
工程类
光催化
冶金
光电子学
作者
Xiao Ren,Chao Wei,Yuanmiao Sun,Xiaozhi Liu,Fanqi Meng,Xiaoxia Meng,Shengnan Sun,Shibo Xi,Yonghua Du,Zhuanfang Bi,Guangyi Shang,Adrian C. Fisher,Lin Gu,Zhichuan J. Xu
标识
DOI:10.1002/adma.202001292
摘要
Abstract Electrochemical water splitting is of prime importance to green energy technology. Particularly, the reaction at the anode side, namely the oxygen evolution reaction (OER), requires a high overpotential associated with OO bond formation, which dominates the energy‐efficiency of the whole process. Activating the anionic redox chemistry of oxygen in metal oxides, which involves the formation of superoxo/peroxo‐like (O 2 ) n − , commonly occurs in most highly active catalysts during the OER process. In this study, a highly active catalyst is designed: electrochemically delithiated LiNiO 2 , which facilitates the formation of superoxo/peroxo‐like (O 2 ) n − species, i.e., NiOO*, for enhancing OER activity. The OER‐induced surface reconstruction builds an adaptive heterojunction, where NiOOH grows on delithiated LiNiO 2 (delithiated‐LiNiO 2 /NiOOH). At this junction, the lithium vacancies within the delithiated LiNiO 2 optimize the electronic structure of the surface NiOOH to form stable NiOO* species, which enables better OER activity. This finding provides new insight for designing highly active catalysts with stable superoxo‐like/peroxo‐like (O 2 ) n − for water oxidation.
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