Affiliation:
1. Department of Environmental Science and Engineering School of Resource and Environmental Sciences Wuhan University Wuhan 430079 China
2. Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resource Recycle Nanchang Hangkong University Nanchang 330063 China
Abstract
AbstractGenerating FeIV=O on single‐atom catalysts by Fenton‐like reaction has been established for water treatment; however, the FeIV=O generation pathway and oxidation behavior remain obscure. Employing an Fe−N−C catalyst with a typical Fe−N4moiety to activate peroxymonosulfate (PMS), we demonstrate that generating FeIV=O is mediated by an Fe−N−C−PMS* complex—a well‐recognized nonradical species for induction of electron‐transfer oxidation—and we determined that adjacent Fe sites with a specific Fe1−Fe1distance are required. After the Fe atoms with an Fe1‐Fe1distance <4 Å are PMS‐saturated, Fe−N−C−PMS* formed on Fe sites with an Fe1‐Fe1distance of 4–5 Å can coordinate with the adjacent FeII−N4, forming an inter‐complex with enhanced charge transfer to produce FeIV=O. FeIV=O enables the Fenton‐like system to efficiently oxidize various pollutants in a substrate‐specific, pH‐tolerant, and sustainable manner, where its prominent contribution manifests for pollutants with higher one‐electron oxidation potential.
Funder
National Natural Science Foundation of China
Cited by
7 articles.
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