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气溶胶颗粒表面极性与分子构型的光谱探测

Spectroscopic Probing of Polarity and Molecular Configuration at Aerosol Particle Surfaces.

作者信息

Qian Yuqin, Deng Gang-Hua, Rao Yi

机构信息

Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322, United States.

出版信息

J Phys Chem Lett. 2020 Aug 20;11(16):6763-6771. doi: 10.1021/acs.jpclett.0c02013. Epub 2020 Aug 6.

Abstract

The growth of aerosol particles in the atmosphere is related to chemical reactions in the gas and particle phases and at aerosol particle surfaces. While research regarding the gas and particle phases of aerosols is well-documented, physical properties and chemical reactivities at aerosol particle surfaces have not been studied extensively but have long been recognized. In particular, measurements of aerosol particle surfaces are just emerging. The main reason is a lack of suitable surface-specific analytical techniques for direct measurements of aerosol particles under ambient conditions. Here we develop surface-specific electronic sum frequency scattering (ESFS) to directly identify spectroscopic behaviors of molecules at aerosol particle surfaces. As an example, we applied an ESFS probe, malachite green (MG). We examined electronic spectra of MG at aerosol particle surfaces and found that the polarity of the surfaces is less polar than that in bulk. Our quantitative orientational analysis shows that MG is orientated with a polar angle of 25°-35° at the spherical particle surfaces of aerosols. The adsorption free energy of MG at the aerosol surfaces was found to be -20.75 ± 0.32 kJ/mol, which is much lower than that at the air/water interface. These results provide new insights into aerosol particle surfaces for further understanding the formation of secondary organic aerosols in the atmosphere.

摘要

大气中气溶胶颗粒的生长与气相、颗粒相以及气溶胶颗粒表面的化学反应有关。虽然关于气溶胶气相和颗粒相的研究已有充分记录,但气溶胶颗粒表面的物理性质和化学反应性尚未得到广泛研究,不过早已受到关注。特别是,气溶胶颗粒表面的测量才刚刚起步。主要原因是缺乏适用于在环境条件下直接测量气溶胶颗粒的表面特异性分析技术。在此,我们开发了表面特异性电子和频散射(ESFS)技术,以直接识别气溶胶颗粒表面分子的光谱行为。例如,我们应用了一种ESFS探针——孔雀石绿(MG)。我们研究了MG在气溶胶颗粒表面的电子光谱,发现表面的极性比本体中的极性小。我们的定量取向分析表明,MG在气溶胶球形颗粒表面的取向极角为25° - 35°。发现MG在气溶胶表面的吸附自由能为-20.75 ± 0.32 kJ/mol,这远低于其在空气/水界面的吸附自由能。这些结果为气溶胶颗粒表面提供了新的见解,有助于进一步理解大气中二次有机气溶胶的形成。

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