Dual Role of Aerosols on Reactive Bromine Recycling in Extrapolar Marine and Continental Regions

Abstract Reactive bromine species play important roles in atmospheric chemistry and influence the abundance of climate‐ and air quality‐relevant trace gases. While extensive studies have focused on bromine chemistry in polar regions, the bromine species in extrapolar regions, particularly regarding pollution‐related bromine recycling, have received less attention. In this study, we examine the factors influencing the bromine recycling at a clean marine site of the North Atlantic (Cape Verde, CVAO), a semipolluted coastal site of the South China Sea (Hok Tsui, HT), and a polluted continental site of North China (Wangdu, WD), using an observation‐based model combined with updated halogen chemistry. Our results indicate that aerosol‐related multiphase processes significantly affect bromine recycling in these extrapolar sites. Nitrate photodissociation efficiently recycled bromide into the gas phase in regions characterized by strong aerosol acidity (HT) or high aerosol concentrations (WD). Concurrently, bromine species are lost from the gas phase toward aerosol surfaces, with this process being more effective at higher liquid water content (WD > HT > CVAO). In semipolluted and polluted sites, the aerosol‐related processes resulted in elevated bromine levels in the daytime compared to nighttime, leading to larger effects of bromine species on ozone than previously thought. Our study suggests the need for a better understanding of the complex effects of aerosols on reactive halogen chemistry.