Significance of higher-order many-body interaction energy terms in water clusters and bulk water

被引:51
作者
Xantheas, SS
机构
[1] Theory, Modeling and Simulation, Environmental Molecular Sciences Laboratory, Pacific Northwest Laboratory, Richland, WA, 99352
来源
PHILOSOPHICAL MAGAZINE B-PHYSICS OF CONDENSED MATTER STATISTICAL MECHANICS ELECTRONIC OPTICAL AND MAGNETIC PROPERTIES | 1996年 / 73卷 / 01期
关键词
D O I
10.1080/13642819608239116
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The magnitudes of the two- and three-body energy terms and their contribution to the interaction energy are computed for different water trimer arrangements at the second- to the fourth-order many-body perturbation (MP2 and MP4) levels of theory. Configurations in which the water molecules act as proton donor-accepters, double accepters and double donors were considered. The energy separation between the 'cyclic' and 'open' water trimer minima was estimated at 42 kcal mol(-1). Its origin was quantitatively accounted for in terms of the difference between the two- and three-body energy terms for the two configurations. We have found that the three-body term is attractive and accounts for 18% of the binding energy of the 'cyclic' trimer but its contribution is less significant (6%) and repulsive for the 'open' trimer. It is also repulsive but smaller (4%) for an intermediate trimer configuration which has the arrangement double acceptor, double donor, donor-acceptor for the three water molecules. Many-body energy terms higher than two are, however, less significant for configurations resembling bulk water which have, on the average, two hydrogen bonds per water molecule. The MP4 results were found to differ only slightly (less than 2%) from the corresponding MP2 results.
引用
收藏
页码:107 / 115
页数:9
相关论文
共 23 条
[1]   CALCULATION OF SMALL MOLECULAR INTERACTIONS BY DIFFERENCES OF SEPARATE TOTAL ENERGIES - SOME PROCEDURES WITH REDUCED ERRORS [J].
BOYS, SF ;
BERNARDI, F .
MOLECULAR PHYSICS, 1970, 19 (04) :553-&
[2]   IMPLEMENTATION OF NONADDITIVE INTERMOLECULAR POTENTIALS BY USE OF MOLECULAR-DYNAMICS - DEVELOPMENT OF A WATER WATER POTENTIAL AND WATER ION CLUSTER INTERACTIONS [J].
CALDWELL, J ;
DANG, LX ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (25) :9144-9147
[3]   A NEW WATER POTENTIAL INCLUDING POLARIZATION - APPLICATION TO GAS-PHASE, LIQUID, AND CRYSTAL PROPERTIES OF WATER [J].
CIEPLAK, P ;
KOLLMAN, P ;
LYBRAND, T .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (11) :6755-6760
[4]  
CLEMENTI E, 1983, INT J QUANTUM CHEM S, V10, P31
[5]   ION SOLVATION IN POLARIZABLE WATER - MOLECULAR-DYNAMICS SIMULATIONS [J].
DANG, LX ;
RICE, JE ;
CALDWELL, J ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (07) :2481-2486
[6]   THE NONADDITIVE INTERMOLECULAR POTENTIAL FOR WATER REVISED [J].
DANG, LX .
JOURNAL OF CHEMICAL PHYSICS, 1992, 97 (04) :2659-2660
[7]   MONTE-CARLO LIQUID WATER SIMULATION WITH 4-BODY INTERACTIONS INCLUDED [J].
DETRICH, J ;
CORONGIU, G ;
CLEMENTI, E .
CHEMICAL PHYSICS LETTERS, 1984, 112 (05) :426-430
[9]  
Frisch M.J., 1992, GAUSSIAN 92 REVISION
[10]   WATER MOLECULE INTERACTIONS [J].
HANKINS, D ;
MOSKOWITZ, JW ;
STILLINGER, FH .
JOURNAL OF CHEMICAL PHYSICS, 1970, 53 (12) :4544-+