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水溶液界面附近离子吸附的电荷图像效应。

Image-charge effects on ion adsorption near aqueous interfaces.

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125.

Department of Chemistry, Pohang University of Science and Technology, Pohang 37673, South Korea.

出版信息

Proc Natl Acad Sci U S A. 2021 May 11;118(19). doi: 10.1073/pnas.2020615118.

Abstract

Electrostatic interactions near surfaces and interfaces are ubiquitous in many fields of science. Continuum electrostatics predicts that ions will be attracted to conducting electrodes but repelled by surfaces with lower dielectric constant than the solvent. However, several recent studies found that certain "chaotropic" ions have similar adsorption behavior at air/water and graphene/water interfaces. Here we systematically study the effect of polarization of the surface, the solvent, and solutes on the adsorption of ions onto the electrode surfaces using molecular dynamics simulation. An efficient method is developed to treat an electrolyte system between two parallel conducting surfaces by exploiting the mirror-expanded symmetry of the exact image-charge solution. With neutral surfaces, the image interactions induced by the solvent dipoles and ions largely cancel each other, resulting in no significant net differences in the ion adsorption profile regardless of the surface polarity. Under an external electric field, the adsorption of ions is strongly affected by the surface polarization, such that the charge separation across the electrolyte and the capacitance of the cell is greatly enhanced with a conducting surface over a low-dielectric-constant surface. While the extent of ion adsorption is highly dependent on the electrolyte model (the polarizability of solvent and solutes, as well as the van der Waals radii), we find the effect of surface polarization on ion adsorption is consistent throughout different electrolyte models.

摘要

静电相互作用在许多科学领域中都普遍存在。连续静电学预测,离子将被吸引到导电电极上,但会被介电常数低于溶剂的表面排斥。然而,最近的几项研究发现,某些“离液”离子在空气/水和石墨烯/水界面上具有相似的吸附行为。在这里,我们使用分子动力学模拟系统地研究了表面、溶剂和溶质的极化对离子在电极表面上吸附的影响。开发了一种有效的方法来处理两个平行导电表面之间的电解质系统,利用精确镜像电荷解的镜像扩展对称性。对于中性表面,溶剂偶极子和离子诱导的镜像相互作用在很大程度上相互抵消,因此无论表面极性如何,离子吸附轮廓都没有明显的净差异。在外电场作用下,离子的吸附强烈受到表面极化的影响,使得电解质的电荷分离和电池的电容大大增强,与低介电常数表面相比,导电表面的效果更为显著。虽然离子吸附的程度高度依赖于电解质模型(溶剂和溶质的极化率以及范德华半径),但我们发现表面极化对离子吸附的影响在不同的电解质模型中是一致的。

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