溶剂化
卤素
溴
卤键
化学
硝酸盐
环境化学
光化学
有机化学
分子
烷基
作者
Ye‐Guang Fang,Chang Yuan,Shun Wang,Chongqin Zhu,Wei‐Hai Fang
标识
DOI:10.1021/acs.jpclett.5c00497
摘要
The reactive uptake of bromine nitrate (BrONO2) into aqueous aerosols is a pivotal process in atmospheric bromine chemistry. BrONO2 forms halogen bonds with adjacent water molecules, disrupting hydrogen-bond networks and potentially triggering unique chemical behaviors. However, the role of halogen bonds in interfacial reactions remains an open question. Herein, we employ a comprehensive approach combining quantum chemistry calculations, classical molecular dynamics, ab initio molecular dynamics (AIMD) simulations, and advanced enhanced sampling methods to investigate the solvation and hydrolysis of bromine nitrate (BrONO2) at the air-water interface. Our simulations reveal that BrONO2 can stably exist at the interface, providing favorable conditions for its hydrolysis. The interplay between halogen bonding and solvation facilitates the spontaneous formation of H2OBrONO2 at the interface, which subsequently reacts to produce HOBr and HNO3. Free energy calculations indicate that this reaction is both kinetically and thermodynamically favorable at the air-water interface with an energy barrier of approximately 3.0 kcal/mol at 300 K. The insights from this simulation study will help guide future experiments to explore how water clouds affect halogen chemistry.
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