反键分子轨道
催化作用
化学
化学物理
工作(物理)
机制(生物学)
原子轨道
材料科学
无定形固体
纳米技术
反应机理
硫黄
氧气
终端(电信)
结晶学
氧化磷酸化
计算化学
反应条件
氧原子
碳纤维
不稳定性
四面体
作者
Peigen Liu,J. X. Song,Shaokang Yang,Zixiang Huang,Yu Bai,Qichen Liu,Rongao Zhang,Hongliang Li,Xun Hong,DingSheng WANG,Xusheng Zheng
标识
DOI:10.1002/anie.202519413
摘要
Abstract High‐valent Co(IV)═O species have garnered significant attention as a promising non‐radical reactive species. However, their selective generation encounters substantial challenges due to the oxo wall rule that emphasizes intrinsic instability of the terminal metal–oxygen (M─O) bond. Here, we propose an amorphization strategy for TiO 2 support to circumvent the limitation of oxo wall, favoring the formation of high‐valent Co(IV)═O species. The advantages of Co(IV)═O species in terms of oxidative activity, durability, and environmental tolerance were investigated by Fenton‐like catalysis. Mechanistic studies revealed that amorphous TiO 2 endowed Co single atoms with a Co‐O 4 tetrahedral structure and a high‐spin state of 3 d electron, leading to strong Co 3 d ‐O 2 p interactions that promote peroxymonosulfate (PMS) activation. Notably, the produced Co(IV)═O species adopted a trigonal‐bipyramidal‐like configuration, which mitigated the electron occupation in the antibonding orbitals of terminal M─O bond, thus bypassing the oxo wall. This work enhances the understanding of the mechanism underlying heterogeneous Co(IV)═O formation and broadens strategies for preparing efficient catalysts for critical oxidation reactions.
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