Constructing an Adaptive Heterojunction as a Highly Active Catalyst for the Oxygen Evolution Reaction

© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - 32(2020), 30 vom: 03. Juli, Seite e2001292
Auteur principal: Ren, Xiao (Auteur)
Autres auteurs: Wei, Chao, Sun, Yuanmiao, Liu, Xiaozhi, Meng, Fanqi, Meng, Xiaoxia, Sun, Shengnan, Xi, Shibo, Du, Yonghua, Bi, Zhuanfang, Shang, Guangyi, Fisher, Adrian C, Gu, Lin, Xu, Zhichuan J
Format: Article en ligne
Langue:English
Publié: 2020
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article adaptive junctions cycling delithiation oxygen evolution reconstruction
Description
Résumé:© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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 OO 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 (O2 )n - , commonly occurs in most highly active catalysts during the OER process. In this study, a highly active catalyst is designed: electrochemically delithiated LiNiO2 , which facilitates the formation of superoxo/peroxo-like (O2 )n - species, i.e., NiOO*, for enhancing OER activity. The OER-induced surface reconstruction builds an adaptive heterojunction, where NiOOH grows on delithiated LiNiO2 (delithiated-LiNiO2 /NiOOH). At this junction, the lithium vacancies within the delithiated LiNiO2 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 (O2 )n - for water oxidation
Description:Date Revised 16.11.2020
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202001292