Polarizable molecular interactions in condensed phase and their equivalent nonpolarizable models

被引:81
作者
Leontyev, Igor V. [1 ]
Stuchebrukhov, Alexei A. [1 ]
机构
[1] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
关键词
CLASSICAL DRUDE OSCILLATOR; EMPIRICAL FORCE-FIELD; EFFECTIVE PAIR POTENTIALS; DYNAMICS SIMULATIONS; LIQUID WATER; DIELECTRIC-CONSTANT; IONIC LIQUIDS; ELECTRONIC POLARIZATION; AQUEOUS-SOLUTION; 1ST PRINCIPLES;
D O I
10.1063/1.4884276
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
Earlier, using phenomenological approach, we showed that in some cases polarizable models of condensed phase systems can be reduced to nonpolarizable equivalent models with scaled charges. Examples of such systems include ionic liquids, TIPnP-type models of water, protein force fields, and others, where interactions and dynamics of inherently polarizable species can be accurately described by nonpolarizable models. To describe electrostatic interactions, the effective charges of simple ionic liquids are obtained by scaling the actual charges of ions by a factor of 1/root epsilon el, which is due to electronic polarization screening effect; the scaling factor of neutral species is more complicated. Here, using several theoretical models, we examine how exactly the scaling factors appear in theory, and how, and under what conditions, polarizable Hamiltonians are reduced to nonpolarizable ones. These models allow one to trace the origin of the scaling factors, determine their values, and obtain important insights on the nature of polarizable interactions in condensed matter systems. (C) 2014 AIP Publishing LLC.
引用
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页数:12
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