“…However, redox synergy between atomic hydrogen (H*) and •OH has been found to achieve highly efficient degradation of persistent refractory chlorinated organics. ,, Herein, considering that p -chloroaniline (4-CN) as the chemical raw material has been widely used for synthesizing pesticides, dyes, plastics, preservatives, and medicines, − the presence of this organochlorine and its intermediate metabolites in the aqueous environment certainly will pose a risk to the ecological system . In addition to the limited removal rate, the generation of a high concentration of degradation intermediates was the other restriction toward 4-CN removal by •OH alone dominated oxidation reactions. , In contrast, the redox synergy could effectively reduce the reaction energy barriers of 4-CN removal, which was mainly attributed to the H*-initiating nucleophilic hydrodechlorination and •OH-initiating electrophilic oxidization of critical intermediates (Figure S1). ,, The resulting intermediates produced were unstable and could be further converted to H 2 O, CO 2 , and other harmless products, leading to their effective removal.…”