The curious case of the water hexamer: Cage vs. Prism

被引:42
作者
Babin, Volodymyr [1 ]
Paesani, Francesco [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
POTENTIAL-ENERGY SURFACE; AB-INITIO; DENSITY FUNCTIONALS; 1ST PRINCIPLES; LIQUID WATER; MOLECULAR-DYNAMICS; RELATIVE ENERGIES; SMALL CLUSTERS; DIPOLE-MOMENT; MODEL;
D O I
10.1016/j.cplett.2013.06.041
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
Small water clusters, such as the hexamer, provide a unique opportunity to advance the molecular-level understanding of water in all its phases. In particular, the water hexamer is the smallest cluster that possesses several nearly iso-energetic non-planar isomeric forms whose relative stability at low temperatures can be probed experimentally and investigated theoretically. Here, we report on the equilibrium populations of the isomers in the temperature range from 30K to 150 K for both H2O and D2O as predicted by four different water potentials. The simulations, performed using path-integral molecular dynamics combined with the replica exchange method, highlight some deficiencies of empirical water models while providing support for the accuracy of more recent ab initio-based potentials. The theoretical predictions for the cage/prism isomeric equilibrium upon isotopic substitution suggest that rotational spectra measured for the deuterated cluster could deliver further insights on the ground-state properties of the water hexamer. (C) 2013 Elsevier B.V. All rights reserved.
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页码:1 / 8
页数:8
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