Exploring charge inversion in electrolyte mixtures of trivalent and monovalent ions

Li Xiang, Gutian Zhao, Di Zhang, Yunfei Chen
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Abstract

At room temperature ion-ion correlations and counterions volume effect play a crucial role in the description of the electrical double layer of colloidal particles. In fact, in many instances, the inclusion of the short range correlations between ions in the study of the ionic distribution and the consideration of the ion's size lead to quite different results with respect to the classical treatment (where ions are assumed to be points). In particular, these discrepancies become more noticeable for highly charged particles in the presence of moderate or highly multivalent counterion concentrations. Moreover, it can be shown that the existence of an electrolyte mixture consisting of multi- and monovalent counterions may cause that system to become overcharged, a feature that cannot be predicted from a classical point of view based on the Boltzmann distribution function. In order to explore the charge inversion in electrolyte mixtures of trivalent and monovalent ions, the interaction of mica surfaces in two different concentrations of LaCl3 before and after adding NaCl is investigated through the surface force apparatus(SFA) and these experimental results can demonstrate that the charge inversion is indeed enhanced by a monovalent salt.
探索三价和一价离子混合电解质中的电荷反转
在室温下,离子-离子相关和反离子体积效应在描述双电层胶体粒子中起着至关重要的作用。事实上,在许多情况下,在离子分布的研究中包括离子之间的短程相关性,并考虑离子的大小,导致与经典处理(假设离子是点)完全不同的结果。特别是,在存在中等或高度多价反离子浓度的高电荷粒子中,这些差异变得更加明显。此外,可以证明,由多价和单价反离子组成的电解质混合物的存在可能导致该系统变得过充电,这是基于玻尔兹曼分布函数的经典观点无法预测的特征。为了探索三价离子和一价离子混合电解质中的电荷反转,通过表面力仪(SFA)研究了两种不同浓度LaCl3中加入NaCl前后云母表面的相互作用,实验结果表明,一价盐确实增强了电荷反转。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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