TY - JOUR
T1 - Semiclassical molecular dynamics simulations of low-temperature clusters
T2 - Applications to (Ar)13; (Ne)13; (H2O)n, n = 2,3,5
AU - Fredj, E.
AU - Gerber, R. B.
AU - Ratner, M. A.
PY - 1996/7/15
Y1 - 1996/7/15
N2 - Semiclassical molecular dynamics simulations are developed as a tool for studying anharmonic clusters and solids at energies near the zero point. The method employs the time-dependent self-consistent-field approximation, that describes each mode as moving in the mean dynamical field of all other modes. The method further describes each mode by a semiclassical Gaussian wave packet. The scheme is carried out in normal modes. The method is restricted to systems of moderate anharmonicity at low temperatures. It is, however, computationally efficient and practically applicable to large systems. It can be used for the dynamics of nonstationary states as well as for stationary ones. Structural, dynamical and a variety of spectroscopic properties can easily be evaluated. The method is tested for thermal equilibrium states of (Ne)13, (Ar)13 against "numerically exact" quantum Feynman path integral simulations. Excellent quantitative agreement is found for the atom-atom pair distribution functions. The method is also applied to (H2O)n clusters. Good agreement is found with experimentally available fundamental stretch-mode frequencies.
AB - Semiclassical molecular dynamics simulations are developed as a tool for studying anharmonic clusters and solids at energies near the zero point. The method employs the time-dependent self-consistent-field approximation, that describes each mode as moving in the mean dynamical field of all other modes. The method further describes each mode by a semiclassical Gaussian wave packet. The scheme is carried out in normal modes. The method is restricted to systems of moderate anharmonicity at low temperatures. It is, however, computationally efficient and practically applicable to large systems. It can be used for the dynamics of nonstationary states as well as for stationary ones. Structural, dynamical and a variety of spectroscopic properties can easily be evaluated. The method is tested for thermal equilibrium states of (Ne)13, (Ar)13 against "numerically exact" quantum Feynman path integral simulations. Excellent quantitative agreement is found for the atom-atom pair distribution functions. The method is also applied to (H2O)n clusters. Good agreement is found with experimentally available fundamental stretch-mode frequencies.
UR - http://www.scopus.com/inward/record.url?scp=0000420279&partnerID=8YFLogxK
U2 - 10.1063/1.471956
DO - 10.1063/1.471956
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AN - SCOPUS:0000420279
SN - 0021-9606
VL - 105
SP - 1121
EP - 1130
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 3
ER -