电场
水溶液
化学物理
偶极子
化学
领域(数学)
分析化学(期刊)
材料科学
物理化学
色谱法
有机化学
物理
数学
量子力学
纯数学
作者
Hanqing Xiong,Jae Kyoo Lee,Richard N. Zare,Wei Min
标识
DOI:10.1021/acs.jpclett.0c02061
摘要
Chemical reactions in aqueous microdroplets often exhibit unusual kinetic and thermodynamic properties not observed in bulk solution. While an electric field has been implicated at the water interface, there has been no direct measurement in aqueous microdroplets, largely due to the lack of proper measurement tools. Herein, we employ newly developed stimulated Raman excited fluorescence microscopy to measure the electric field at the water-oil interface of microdroplets. As determined by the vibrational Stark effect of a nitrile-bearing fluorescent probe, the strength of the electric field is found to be on the order of 107 V/cm. This strong electric field aligns probe dipoles with respect to the interface. The formation of the electric field likely arises from charge separation caused by the adsorption of negative ions at the water-oil interface of microdroplets. We suggest that this strong electric field might account in part for the unique properties of chemical reactions reported in microdroplets.
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