de Souza J Pedro, Pivnic Karina, Bazant Martin Z, Urbakh Michael, Kornyshev Alexei A
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
School of Chemistry, The Sackler Center for Computational Molecular and Materials Science, Tel Aviv University, Tel Aviv, 6997801, Israel.
J Phys Chem B. 2022 Feb 17;126(6):1242-1253. doi: 10.1021/acs.jpcb.1c09441. Epub 2022 Feb 8.
Ionic liquids (ILs) are charged fluids composed of anions and cations of different size and shape. The ordering of charge and density in ILs confined between charged interfaces underlies numerous applications of IL electrolytes. Here, we analyze the screening behavior and the resulting structural forces of a representative IL confined between two charge-varied plates. Using both molecular dynamics simulations and a continuum theory, we contrast the screening features of a more-realistic asymmetric system and a less-realistic symmetric one. The ionic size asymmetry plays a nontrivial role in charge screening, affecting both the ionic density profiles and the disjoining pressure distance dependence. Ionic systems with size asymmetry are stronger coupled systems, and this manifests itself both in their response to the electrode polarization and spontaneous structure formation at the interface. Analytical expressions for decay lengths of the disjoining pressure are obtained in agreement with the pressure profiles computed from molecular dynamics simulations.
离子液体(ILs)是由不同大小和形状的阴离子和阳离子组成的带电流体。限制在带电界面之间的离子液体中的电荷和密度排序是离子液体电解质众多应用的基础。在这里,我们分析了限制在两个电荷变化平板之间的代表性离子液体的屏蔽行为和由此产生的结构力。使用分子动力学模拟和连续介质理论,我们对比了一个更现实的不对称系统和一个不太现实的对称系统的屏蔽特征。离子大小不对称在电荷屏蔽中起着重要作用,影响离子密度分布和分离压力与距离的依赖关系。具有大小不对称的离子系统是更强的耦合系统,这在它们对电极极化的响应和界面处的自发结构形成中都有体现。得到了分离压力衰减长度的解析表达式,与分子动力学模拟计算得到的压力分布一致。