Goel Teena, Patra Chandra N
Theoretical Chemistry Section, Chemistry Group, Bhabha Atomic Research Centre, Mumbai 400085, India.
J Chem Phys. 2007 Jul 21;127(3):034502. doi: 10.1063/1.2750335.
A density functional theory is presented for the structure of spherical electric double layers within the restricted primitive model, where the macroion is considered as a hard sphere having uniform surface charge density, the small ions as charged hard spheres, and the solvent is taken as a dielectric continuum. The theory is partially perturbative as the hard-sphere contribution to the one-particle correlation function is evaluated using suitably averaged weighted density and the ionic part is obtained through a second-order functional Taylor expansion around the uniform fluid. The theory is in quantitative agreement with Monte Carlo simulation for the density profiles and the zeta potentials over a wide range of macroion sizes and electrolyte concentrations. The theory is able to provide interesting insights about the layering and the charge inversion phenomena occurring at the interface.
本文提出了一种密度泛函理论,用于研究受限原始模型中球形电双层的结构。其中,大离子被视为具有均匀表面电荷密度的硬球,小离子为带电硬球,溶剂被当作介电连续体。该理论部分采用微扰法,即硬球对单粒子关联函数的贡献通过适当平均的加权密度来评估,而离子部分则通过围绕均匀流体的二阶泛函泰勒展开获得。在大离子尺寸和电解质浓度的广泛范围内,该理论在密度分布和zeta电位方面与蒙特卡罗模拟结果在定量上一致。该理论能够为界面处发生的分层和电荷反转现象提供有趣的见解。