气溶胶
水溶液
化学
化学工程
化学物理
粒子(生态学)
单层
电场
肺表面活性物质
拉曼光谱
材料科学
荧光
烟灰
光谱学
超临界流体
环境化学
硫酸铵
氢氧化物
荧光光谱法
硫酸盐
污染物
分析化学(期刊)
氢
离散偶极子近似
化学反应
金属
燃烧
荧光光谱法
微型反应器
作者
Yangyang Liu,Sonali Srivastava,Delicia Gonsalves,Peter J. Vikesland
标识
DOI:10.1073/pnas.2604717123
摘要
Aerosol acidity (pH) is a fundamental property governing atmospheric multiphase chemistry, as it influences pollutant partitioning, secondary organic aerosol formation, and trace metal solubility. Thermodynamic models typically assume the internal homogeneity of submicron particles; however, fresh aerosols produced via biomass burning often possess complex core–shell morphologies wherein an aqueous core is coated by organic surfactants. Here, we report that a size-dependent “alkaline shell” exists for aqueous ammonium sulfate microdroplets coated with stearic acid, a ubiquitous constituent of biomass burning. Using single-droplet surface-enhanced Raman spectroscopy and confocal fluorescence imaging, we identify a critical size regime (50 to 150 µm) where alignment of the surfactant monolayer generates strong interfacial electric fields (~10 8 V/m). This field drives local partitioning of protons and hydroxide ions, sustaining a hyperalkaline surface shell (pH ~9 to 11). We attribute this phenomenon to a feedback loop, distinct from bulk equilibria, involving surfactant dipole alignment, hydrophobic confinement of hydroxide, and interfacial charge transfer. These findings add critical nuance to bulk thermodynamic predictions, demonstrating that while the aerosol core remains acidic, the interface of organic-coated aerosols can act as a unique, high-pH microreactor in the atmosphere, potentially accelerating base-catalyzed reactions and altering the environmental fate of biomass emissions.
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