TY - JOUR
T1 - Spontaneous Chlorine Generation via Interfacial Oxidation of Chloride by O2 on Acidic Microdroplets
AU - Li, Shuying
AU - Wang, Zhuo
AU - Cao, Yiqun
AU - Ma, Wei
AU - Li, Hao
AU - Chen, Tianzeng
AU - Wang, Yonghong
AU - Zhang, Peng
AU - Liu, Pengfei
AU - Chu, Biwu
AU - Liu, Chang
AU - Liu, Yongchun
AU - Mu, Yujing
AU - Zhang, Xiuhui
AU - Wang, Tao
AU - Ma, Qingxin
AU - Francisco, Joseph S.
AU - He, Hong
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/8/26
Y1 - 2026/8/26
N2 - Reactive chlorine species significantly influence atmospheric chemistry, yet their sources remain inadequately defined. We have discovered a spontaneous formation pathway for substantial molecular chlorine (Cl2) from the oxidation of chloride (Cl–) through interfacial oxidation by O2 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 Cl2 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 O3 or OH, instead producing particulate reactive oxygen species (ROS). Consequently, current atmospheric models likely underestimate the contribution of reactive halogens to atmospheric oxidation capacity.
AB - Reactive chlorine species significantly influence atmospheric chemistry, yet their sources remain inadequately defined. We have discovered a spontaneous formation pathway for substantial molecular chlorine (Cl2) from the oxidation of chloride (Cl–) through interfacial oxidation by O2 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 Cl2 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 O3 or OH, instead producing particulate reactive oxygen species (ROS). Consequently, current atmospheric models likely underestimate the contribution of reactive halogens to atmospheric oxidation capacity.
UR - https://www.scopus.com/pages/publications/105048892874
U2 - 10.1021/jacs.6c10175
DO - 10.1021/jacs.6c10175
M3 - Article
C2 - 42677537
AN - SCOPUS:105048892874
SN - 0002-7863
VL - 148
SP - 36053
EP - 36061
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 33
ER -