析氧
尖晶石
催化作用
氧气
电负性
氧化还原
化学
氧化物
化学工程
无机化学
化学物理
电化学
材料科学
物理化学
电极
冶金
有机化学
工程类
作者
Kang Xiao,Yifan Wang,Peiyuan Wu,Liping Hou,Zhao‐Qing Liu
标识
DOI:10.1002/ange.202301408
摘要
Abstract The development of productive catalysts for the oxygen evolution reaction (OER) remains a major challenge requiring significant progress in both mechanism and material design. Conventionally, the thermodynamic barrier of lattice oxidation mechanism (LOM) is lower than that of absorbate evolution mechanism (AEM) because the former can overcome certain limitations. However, controlling the OER pathway from the AEM to the LOM by exploiting the intrinsic properties of the catalyst remains challenging. Herein, we incorporated F anions into the oxygen vacancies of spinel ZnCo 2 O 4 and established a link between the electronic structure and the OER catalytic mechanism. Theoretical density calculations revealed that F upshifts the O 2p center and activates the redox capability of lattice O, successfully triggering the LOM pathway. Moreover, the high electronegativity of F anions is favourable for balancing the residual protonation, which can stabilize the structure of the catalyst.
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