摘要
Reactive chlorine species significantly influence atmospheric chemistry, yet their sources remain inadequately defined. We have discovered a spontaneous formation pathway for substantial molecular chlorine (Cl 2 ) from the oxidation of chloride (Cl – ) through interfacial oxidation by O 2 on acidic microdroplets. This efficient interfacial reaction is facilitated by protons (H + ), which enrich Cl – at the gas–liquid interface and mediate the electron-transfer process, concurrently releasing gaseous Cl 2 and hydroxyl radicals (OH). Given the prevalence of acidic, chloride-containing droplets in marine and polluted urban environments, this formation mechanism constitutes a substantial and previously unaccounted tropospheric chlorine source. Unlike established mechanisms, this pathway generates active halogens without consuming gaseous oxidants like O 3 or OH, instead producing particulate reactive oxygen species (ROS). Consequently, current atmospheric models likely underestimate the contribution of reactive halogens to atmospheric oxidation capacity.
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