Ion pairing in model electrolytes:: A study via three-particle correlation functions

被引:13
作者
Jiménez-Angeles, F
Messina, R
Holm, C
Lozada-Cassou, M
机构
[1] Inst Mexicano Petr, Programa Ingn Mol, Inst Mexicano Petr, Mexico City 07730, DF, Mexico
[2] Univ Autonoma Metropolitana Iztapalapa, Dept Fis, Mexico City 09340, DF, Mexico
[3] Univ Dusseldorf, Inst Theoret Phys 2, D-40225 Dusseldorf, Germany
[4] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
D O I
10.1063/1.1596912
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
A novel integral equations approach is applied for studying ion pairing in the restricted primitive model electrolyte, i.e., the three-point extension (TPE) to the Ornstein-Zernike integral equations. In the TPE approach, the three-particle correlation functions g([3])(r(1),r(2),r(3)) are obtained. The TPE results are compared to molecular dynamics (MD) simulations and other theories. Good agreement between TPE and MD is observed for a wide range of parameters, particularly where standard integral equations theories fail, i.e., low salt concentration and high ionic valence. Our results support the formation of ion pairs and aligned ion complexes. (C) 2003 American Institute of Physics.
引用
收藏
页码:4842 / 4856
页数:15
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