电场
气溶胶
化学物理
大气(单位)
硫酸盐
化学
分子动力学
水溶液
化学反应
拉曼光谱
纳米技术
化学工程
材料科学
计算化学
气象学
物理
光学
物理化学
有机化学
量子力学
工程类
作者
Yangyang Liu,Qiuyue Ge,Tao Wang,Ruifeng Zhang,Kejian Li,Kedong Gong,Lifang Xie,Wei Wang,Longqian Wang,Wenbo You,Xuejun Ruan,Zhuocheng Shi,Jin Han,Runbo Wang,Hongbo Fu,Jianmin Chen,Chak K. Chan,Liwu Zhang
出处
期刊:Chem
[Elsevier]
日期:2023-10-26
卷期号:10 (1): 330-351
被引量:12
标识
DOI:10.1016/j.chempr.2023.09.019
摘要
Summary
How tiny aqueous aerosol droplets significantly accelerate the atmospheric multiphase reaction remains an open question. Here, we show both experimental and theoretical evidence that the strong electric field at the air/water interface of aerosol particles can be an important driving force contributing to the fast oxidation of SO2-forming sulfate. We mapped out the spatial surface enrichment of sulfate in nitrate microdroplets using 2D laser confocal Raman microscopy and molecular dynamics (MD) simulations. Strong electric fields up to ∼1 × 108 V cm−1 are determined for the aerosol air/water interface, thus highlighting an important role of electrostatic force in atmospherically relevant chemistry. The detailed SO2 oxidation reaction mechanism triggered by the electric field was further elucidated by density functional theory (DFT) calculations. Overall, this work provides a new perspective, we think, about chemical reactions in the atmosphere and may potentially change the framework of current knowledge concerning the atmospheric chemical process.
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