戒毒(替代医学)
光激发
化学
电子转移
生态毒性
光化学
催化作用
水处理
苯
羟基自由基
环境毒理学
过程(计算)
纳米技术
静电
饮用水净化
环境化学
Boosting(机器学习)
作者
Yue Xie,Chao Zhang,Luming Wei,Shibo Zhu,Shuna Fu,Wenjie Mai,Yiyun Xie,Xinzhi Wang,Wanbing Zheng,Zihan Shen,Junxing Liu,Harald Horn,Mingzhi Huang,Han-Qing Yu
标识
DOI:10.1021/acs.est.5c13091
摘要
N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) forms the highly toxic quinone analogue 6PPD-Q during the Fenton processes, posing risks to aquatic organisms and humans. To bridge this gap, we optimally designed Ag–Pt dual-atom catalysts (DACs) that harness visible-light-induced interfacial charge transfer to enhance atomic H* generation, thereby directing 6PPD detoxification through direct hydrogenation of benzene rings (to terminate 6PPD-Q formation) and selective enhancement of hydroxyl radical (•OH) activation in a Fenton-like process. Multiple lines of evidence demonstrated that photoexcitation enables directional electron transfer from Ag to Pt, boosting the generation of atomic H*, a single-electron donor that spontaneously activates a Fenton-like process without secondary pollution, selectively facilitating •OH generation for further 6PPD detoxification. Intermediate identification and ecotoxicity assessment reconfirmed 6PPD detoxification without 6PPD-Q accumulation. This study offers mechanistic insights into DAC-enhanced atomic H* generation under visible light and achieves complete detoxification of 6PPD within the Fenton-like process.
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