A scaled-ionic-charge simulation model that reproduces enhanced and suppressed water diffusion in aqueous salt solutions

被引:125
|
作者
Kann, Z. R.
Skinner, J. L. [1 ]
机构
[1] Univ Wisconsin, Inst Theoret Chem, Madison, WI 53706 USA
关键词
MOLECULAR-DYNAMICS SIMULATIONS; ELECTROLYTE-SOLUTIONS; DIELECTRIC FRICTION; LIQUID WATER; SELF-DIFFUSION; FREE-ENERGY; HOFMEISTER SERIES; FORCE-FIELDS; MOVING ION; TEMPERATURE;
D O I
10.1063/1.4894500
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
Non-polarizable models for ions and water quantitatively and qualitatively misrepresent the salt concentration dependence of water diffusion in electrolyte solutions. In particular, experiment shows that the water diffusion coefficient increases in the presence of salts of low charge density (e.g., CsI), whereas the results of simulations with non-polarizable models show a decrease of the water diffusion coefficient in all alkali halide solutions. We present a simple charge-scaling method based on the ratio of the solvent dielectric constants from simulation and experiment. Using an ion model that was developed independently of a solvent, i.e., in the crystalline solid, this method improves the water diffusion trends across a range of water models. When used with a good-quality water model, e. g., TIP4P/2005 or E3B, this method recovers the qualitative behaviour of the water diffusion trends. The model and method used were also shown to give good results for other structural and dynamic properties including solution density, radial distribution functions, and ion diffusion coefficients. (c) 2014 AIP Publishing LLC.
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页数:7
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