钴
电催化剂
价(化学)
催化作用
化学
析氧
电化学
水溶液
八面体
无机化学
极化(电化学)
材料科学
结晶学
晶体结构
电极
物理化学
有机化学
作者
Jing Qi,Mingxing Chen,Wei Zhang,Rui Cao
标识
DOI:10.1016/s1872-2067(21)64035-4
摘要
Cobalt-based materials have been considered as promising candidates to electrocatalyze water oxidation. However, the structure-performance correlation remains largely elusive, due to the complex material structures and diverse performance-influencing factors in those Co-based catalysts. In this work, we designed two cobalt phosphates with distinct Co symmetry to explore the effect of coordination symmetry on electrocatalytic water oxidation. The two analogues have similar morphology, Co valence and 6-coordinated Co octahedron, but with different coordination symmetry. In contrast to symmetric Co3(PO4)2·8H2O, asymmetric NH4CoPO4·H2O exhibited enhanced electrocatalytic water oxidation activity in a neutral aqueous solution. It is proven that, by experimental and theoretical studies, the asymmetric Co coordination sites can facilitate the surface reconstruction under anodic polarization to boost the electrocatalysis. Based on this contrastive platform with distinct symmetry differences, the preferred configuration in cobalt-oxygen octahedrons for water oxidation has been straightforwardly assigned.
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