Atomic H* Production Amplified by Precisely Tailored Ag–Pt Dual-Atom Synergy: Crucial Roles in 6PPD Detoxification for Water Purification

<i>N</i>-(1,3-Dimethylbutyl)-<i>N'</i>-phenyl-<i>p</i>-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<b>*</b> 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<b>*</b> generation under visible light and achieves complete detoxification of 6PPD within the Fenton-like process.