Energy-Scaled Debye-Huckel Theory for the Electrostatic Solvation Free Energy in Size-Asymmetric Electrolyte Solutions

被引:1
|
作者
Xiao, Tiejun [1 ]
Zhou, Yun [1 ]
Li, Bo [1 ]
机构
[1] Guizhou Educ Univ, Guizhou Synerget Innovat Ctr Sci Big Data Adv Mfg, Guizhou Prov Key Lab Computat Nanomat Sci, Guiyang 550018, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2024年 / 128卷 / 04期
基金
中国国家自然科学基金;
关键词
CONTINUUM SOLVENT MODEL; ION-ION INTERACTIONS; EFFECTIVE CHARGES; SIMULATIONS; DYNAMICS; LIQUIDS; PROTEIN; FORCES; WATER; SATURATION;
D O I
10.1021/acs.jpcb.3c07233
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this report, an energy-scaled Debye-Hu''ckel theory is developed for fast and accurate evaluation of the electrostatic solvation free energy in size-asymmetric electrolyte solutions. A size-asymmetric electrolyte solution is mapped to a dielectric continuum medium with Debye-Hu''ckel-like response. Based on the scaling relation of the electrostatic energy of a spherical ion in the small and large size limits, a Pade polynomial is used to interpolate the electrostatic energy at finite size. The Pade polynomial is further interpreted as the electrostatic energy of an effective Debye-Hu''ckel mean field model, depicted by a modified Debye parameter and a surface charge density due to the size asymmetry of the solvent ions. This theory can distinguish the electrostatic energies and the electrostatic solvation free energies of solutes with the same size but opposite charges. Application to charged hard and charged soft spheres demonstrates the accuracy of our approach.
引用
收藏
页码:1029 / 1039
页数:11
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