论文标题

复杂电解质中的zwitterionic膜之间的相互作用

Interactions between Zwitterionic Membranes in Complex Electrolytes

论文作者

Buyukdagli, Sahin, Podgornik, Rudolf

论文摘要

我们研究了浸入由单一和多价离子组成的混合电解质中的zwitterionic膜的静电相互作用。我们表明,单价盐的存在是膜上存在有限的静电力的必要条件。结果,源自表面偶极子的平均场膜压力表现出非均匀的盐依赖性,其特征是增强稀盐条件和中间盐浓度下的降低。将多价阳离子添加到上层盐溶液中后,这些阳离子与表面偶极子的相反电荷的单独相互作用使膜间的压力在低膜分离距离处更加排斥,并且在中间距离处具有很强的吸引力,从而导致不连续的同样的递送转变,随后发生了膜结合过渡。通过扩展我们的形式主义以说明与较大盐浓度相关的相关校正,我们表明,即使没有多价阳离子,浸入摩尔盐溶液中的高表面偶极密度的膜也可能会发生膜结合过渡。因此,通过膜工程对表面极化力调整可以是调整浓盐溶液中偶极膜平衡构型的有效方法。

We investigate the electrostatic interactions of zwitterionic membranes immersed in mixed electrolytes composed of mono- and multivalent ions. We show that the presence of monovalent salt is a necessary condition for the existence of a finite electrostatic force on the membrane. As a result, the mean-field membrane pressure originating from the surface dipoles exhibits a non-uniform salt dependence, characterized by an enhancement for dilute salt conditions and a decrease at intermediate salt concentrations. Upon addition of multivalent cations to the submolar salt solution, the separate interactions of these cations with the opposite charges of the surface dipoles makes the intermembrane pressure more repulsive at low membrane separation distances and strongly attractive at intermediate distances, resulting in a discontinuous like-charge binding transition followed by the membrane binding transition. By extending our formalism to account for correlation corrections associated with large salt concentrations, we show that membranes of high surface dipole density immersed in molar salt solutions may undergo a membrane binding transition even without the multivalent cations. Hence, the tuning of the surface polarization forces by membrane engineering can be an efficient way to adjust the equilibrium configuration of dipolar membranes in concentrated salt solutions.

扫码加入交流群

加入微信交流群

微信交流群二维码

扫码加入学术交流群,获取更多资源