二甲基硫醚
硫黄
云凝聚核
气溶胶
粒子(生态学)
甲硫醇
化学
接口(物质)
辐射传输
冷凝
二甲基磺酰丙酸盐
二甲基二硫化物
羰基硫醚
环境化学
硫化物
光化学
大气化学
硫循环
化学工程
大气(单位)
沉积(地质)
自然(考古学)
二氧化硫
粒径
硫化氢
无机化学
自然发生
烟灰
焊剂(冶金)
对流层
作者
He Tang,Xihe Yang,Fengjian Chu,Shiwen Zhou,Wangyu Li,Yongqi Li,Haiyan Zhang,Zechen Yu,Hongru Feng,Yuanjiang Pan
标识
DOI:10.1021/acsenvironau.5c00168
摘要
Dimethyl sulfide (CH3SCH3), methanethiol (CH3SH), and dimethyl disulfide (CH3SSCH3) are the most predominant marine organic sulfur compounds that drive cloud formation by acting as a critical precursor of cloud condensation nuclei. However, discrepancies of natural aerosol radiative effects and climatic impacts between climate model simulations and satellite observations highlight an incomplete understanding of organic sulfur oxidation pathways. Here, we demonstrate a previously unrecognized rapid oxidation mechanism at the air-water interface of microdroplets, where volatile sulfides convert to particle precursors within milliseconds. Combining DFT calculation, QM/MM simulation, and sequential oxidation of possible intermediates, we proposed a new pathway of atmospheric particle precursor formation at the air-water interface of microdroplets, which is different from the traditional gas-phase oxidation pathway, offering a mechanistic solution to re-evaluate the model simulation gaps in natural aerosol radiative effects and climatic impacts.
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