Covalency competition dominates the water oxidation structure–activity relationship on spinel oxides

尖晶石 析氧 竞赛(生物学) 八面体 催化作用 氧气 无机化学 化学工程 材料科学 化学 结晶学 物理化学 电化学 晶体结构 冶金 生态学 工程类 生物 生物化学 有机化学 电极
作者
Yuanmiao Sun,Hanbin Liao,Jiarui Wang,Bo Chen,Shengnan Sun,Samuel Jun Hoong Ong,Shibo Xi,Caozheng Diao,Yonghua Du,Jiaou Wang,Mark B. H. Breese,Shuzhou Li,Hua Zhang,Zhichuan J. Xu
出处
期刊:Nature Catalysis [Nature Portfolio]
卷期号:3 (7): 554-563 被引量:581
标识
DOI:10.1038/s41929-020-0465-6
摘要

Spinel oxides have attracted growing interest over the years for catalysing the oxygen evolution reaction (OER) due to their efficiency and cost-effectiveness, but fundamental understanding of their structure–property relationships remains elusive. Here we demonstrate that the OER activity on spinel oxides is intrinsically dominated by the covalency competition between tetrahedral and octahedral sites. The competition fabricates an asymmetric MT−O−MO backbone where the bond with weaker metal–oxygen covalency determines the exposure of cation sites and therefore the activity. Driven by this finding, a dataset with more than 300 spinel oxides is computed and used to train a machine-learning model for screening the covalency competition in spinel oxides, with a mean absolute error of 0.05 eV. [Mn]T[Al0.5Mn1.5]OO4 is predicted to be a highly active OER catalyst and subsequent experimental results confirm its superior activity. This work sets mechanistic principles of spinel oxides for water oxidation, which may be extendable to other applications. Spinel oxides have attracted interest as water oxidation catalysts due to their efficiency and cost-effectiveness. Now, the covalency competition between tetrahedral and octahedral sites is shown to dominate the OER activity on spinel oxides, and the design principle is used to predict and confirm the superior activity of [Mn]T[Al0.5Mn1.5]OO4.
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