Department of Physical Chemistry, Adam Mickiewicz University, Umultowska 89b, 61-614 Poznań, Poland.
J Chem Phys. 2013 Aug 7;139(5):054703. doi: 10.1063/1.4817325.
The effect of anisotropic ion shapes on the structure and the differential capacitance of an electric double layer in the electrolyte solution regime is studied using the density functional theory and Monte Carlo simulations. The double layer is modelled by a uniformly charged, non-polarizable planar electrode next to an electrolyte where the cation is a dimer consisting of two tangentially touching rigid spheres one of which is positively charged while the other is neutral, the anion is a negatively charged rigid sphere, and the solvent is a dielectric continuum. Numerical results are reported for monovalent electrolytes at room temperature for a series of electrolyte concentrations and varying electrode surface charge densities. Asymmetry in ionic shape leads to more structure near the electrode when its charge is opposite to that of the non-spherical ions. Overall, the theoretically predicted density and mean electrostatic profiles reproduce the corresponding simulation results to a very good degree. The asymmetry of the ion shape also yields asymmetry in the differential capacitance curve plotted as a function of the electrode charge density. The differential capacity evolves from being distorted bactrian camel-shaped (a minimum flanked by a maximum on either side) at low electrolyte concentrations to being bell-like (a single broad maximum) at higher concentrations. The theoretical capacitance results again agree well with the simulations.
使用密度泛函理论和蒙特卡罗模拟研究各向异性离子形状对电解质溶液中双电层结构和微分电容的影响。双电层由带均匀电荷、不可极化的平面电极和电解质组成,阳离子是由两个相切的刚性球体组成的二聚体,其中一个带正电荷,另一个带中性电荷,阴离子是带负电荷的刚性球体,溶剂是介电连续体。在室温下,针对一系列电解质浓度和变化的电极表面电荷密度,报告了单价电解质的数值结果。当电极电荷与非球形离子的电荷相反时,离子形状的不对称会导致电极附近的结构更加不对称。总体而言,理论预测的密度和平均静电分布非常好地再现了相应的模拟结果。离子形状的不对称也导致微分电容曲线作为电极电荷密度的函数呈现出不对称性。微分电容从低电解质浓度下的变形双峰驼形状(两侧各有一个最小值)演变为高浓度下的钟形(单个宽最大值)。理论电容结果再次与模拟结果非常吻合。