Brito Mariano E, Nägele Gerhard, Denton Alan R
Institute of Biological Information Processing, IBI-4, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.
Department of Physics, North Dakota State University, Fargo, North Dakota 58108-6050, USA.
J Chem Phys. 2023 Nov 28;159(20). doi: 10.1063/5.0180914.
Charge-stabilized colloidal suspensions display a rich variety of microstructural and thermodynamic properties, which are determined by electro-steric interactions between all ionic species. The large size asymmetry between molecular-scale microions and colloidal macroions allows the microion degrees of freedom to be integrated out, leading to an effective one-component model of microion-dressed colloidal quasi-particles. For highly charged colloids with strong macroion-microion correlations, nonlinear effects can be incorporated into effective interactions by means of charge renormalization methods. Here, we compare and partially extend several practical mean-field methods of calculating renormalized colloidal interaction parameters, including effective charges and screening constants, as functions of concentration and ionic strength. Within the one-component description, we compute structural and thermodynamic properties from the effective interactions and assess the accuracy of the different methods by comparing predictions with elaborate primitive-model simulations [P. Linse, J. Chem. Phys. 113, 4359 (2000)]. We also compare various prescriptions for the osmotic pressure of suspensions in Donnan equilibrium with a salt ion reservoir and analyze instances where the macroion effective charge becomes larger than the bare one. The methods assessed include single-center cell, jellium, and multi-center mean-field theories. The strengths and weaknesses of the various methods are critically assessed, with the aim of guiding optimal and accurate implementations.
电荷稳定的胶体悬浮液展现出丰富多样的微观结构和热力学性质,这些性质由所有离子物种之间的电空间相互作用决定。分子尺度的微离子与胶体大离子之间巨大的尺寸不对称性使得微离子的自由度能够被整合掉,从而产生一种微离子包裹的胶体准粒子的有效单组分模型。对于具有强的大离子 - 微离子相关性的高电荷胶体,非线性效应可以通过电荷重整化方法纳入有效相互作用中。在此,我们比较并部分扩展了几种计算重整化胶体相互作用参数(包括有效电荷和屏蔽常数)的实用平均场方法,这些参数是浓度和离子强度的函数。在单组分描述中,我们根据有效相互作用计算结构和热力学性质,并通过将预测结果与精细的原始模型模拟[P. 林斯,《化学物理杂志》113, 4359 (2000)]进行比较来评估不同方法的准确性。我们还比较了与盐离子库处于唐南平衡的悬浮液渗透压的各种规定,并分析了大离子有效电荷大于裸电荷的情况。所评估的方法包括单中心元胞、凝胶和多中心平均场理论。对各种方法的优缺点进行了严格评估,旨在指导最优且准确的实现。