Effect of water on the local electric potential of simulated ionic micelles

被引:7
|
作者
Brodskaya, Elena N. [1 ]
Vanin, Alexander A. [1 ]
机构
[1] St Petersburg State Univ, Inst Chem, St Petersburg 198504, Russia
来源
JOURNAL OF CHEMICAL PHYSICS | 2015年 / 143卷 / 04期
基金
俄罗斯科学基金会;
关键词
MOLECULAR-DYNAMICS SIMULATION; DODECYL-SULFATE MICELLE; DOUBLE-LAYER; FORCE-FIELD; AQUEOUS-SOLUTIONS; SURFACE-TENSION; MODEL; HYDRATION; INTERFACE; PERMITTIVITY;
D O I
10.1063/1.4927089
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
Ionic micelles in an aqueous solution containing single-charged counter-ions have been simulated by molecular dynamics. For both cationic and anionic micelles, it has been demonstrated that explicit description of solvent has strong effect on the micelle's electric field. The sign of the local charge alters in the immediate vicinity of the micellar crown and the electric potential varies nonmonotonically. Two micelle models have been examined: the hybrid model with a rigid hydrocarbon core and the atomistic model. For three molecular models of water (Simple Point Charge model (SPC), Transferable Intermolecular Potential 5-Points (TIP5P) and two-centered S2), the results have been compared with those for the continuum solvent model. The orientational ordering of solvent molecules has strong effect on the local electric field surprisingly far from the micelle surface. (C) 2015 AIP Publishing LLC.
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页数:9
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