Test of the consistency of various linearized semiclassical initial value time correlation functions in application to inelastic neutron scattering from liquid para-hydrogen

被引:52
作者
Liu, Jian [1 ,2 ]
Miller, William H. [3 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, KS Pitzer Ctr Theoret Chem, Berkeley, CA 94720 USA
[3] Div Chem Sci, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
关键词
D O I
10.1063/1.2889945
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
The linearized approximation to the semiclassical initial value representation (LSC-IVR) is used to calculate time correlation functions relevant to the incoherent dynamic structure factor for inelastic neutron scattering from liquid para-hydrogen at 14 K. Various time correlations functions were used which, if evaluated exactly, would give identical results, but they do not because the LSC-IVR is approximate. Some of the correlation functions involve only linear operators, and others involve nonlinear operators. The consistency of the results obtained with the various time correlation functions thus provides a useful test of the accuracy of the LSC-IVR approximation and its ability to treat correlation functions involving both linear and nonlinear operators in realistic anharmonic systems. The good agreement of the results obtained from different correlation functions, their excellent behavior in the spectral moment tests based on the exact moment constraints, and their semiquantitative agreement with the inelastic neutron scattering experimental data all suggest that the LSC-IVR is indeed a good short-time approximation for quantum mechanical correlation functions. (C) 2008 American Institute of Physics.
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页数:15
相关论文
共 133 条
[1]   Semiclassical description of electronically nonadiabatic dynamics via the initial value representation [J].
Ananth, Nandini ;
Venkataraman, Charulatha ;
Miller, William H. .
JOURNAL OF CHEMICAL PHYSICS, 2007, 127 (08)
[2]   Momentum distribution and final-state effects in liquid He-4 [J].
Andersen, KH ;
Stirling, WG ;
Glyde, HR .
PHYSICAL REVIEW B, 1997, 56 (14) :8978-8987
[3]   COLLECTIVE EXCITATIONS IN LIQUID-HE-4 .1. EXPERIMENT AND PRESENTATION OF DATA [J].
ANDERSEN, KH ;
STIRLING, WG ;
SCHERM, R ;
STUNAULT, A ;
FAK, B ;
GODFRIN, H ;
DIANOUX, AJ .
JOURNAL OF PHYSICS-CONDENSED MATTER, 1994, 6 (04) :821-834
[4]   Microscopic collective dynamics in liquid para-H2 [J].
Bermejo, FJ ;
Fåk, B ;
Bennington, SM ;
Fernández-Perea, R ;
Cabrillo, C ;
Dawidowski, J ;
Fernández-Diaz, MT ;
Verkerk, P .
PHYSICAL REVIEW B, 1999, 60 (22) :15154-15162
[5]   Quantum effects on liquid dynamics as evidenced by the presence of well-defined collective excitations in liquid para-hydrogen [J].
Bermejo, FJ ;
Kinugawa, K ;
Cabrillo, C ;
Bennington, SM ;
Fåk, B ;
Fernández-Díaz, MT ;
Verkerk, P ;
Dawidowski, J ;
Fernández-Perea, R .
PHYSICAL REVIEW LETTERS, 2000, 84 (23) :5359-5362
[6]   COLLECTIVE EXCITATIONS IN LIQUID DEUTERIUM - NEUTRON-SCATTERING AND CORRELATED-DENSITY-MATRIX RESULTS [J].
BERMEJO, FJ ;
MOMPEAN, FJ ;
GARCIAHERNANDEZ, M ;
MARTINEZ, JL ;
MARTINMARERO, D ;
CHAHID, A ;
SENGER, G ;
RISTIG, ML .
PHYSICAL REVIEW B, 1993, 47 (22) :15097-15112
[7]  
Berne B. J., 1970, Advances in chemical physics vol. 18, P63, DOI 10.1002/9780470143636.ch3
[8]   MAXIMUM-ENTROPY ANALYSIS OF OVERSAMPLED DATA PROBLEMS [J].
BRYAN, RK .
EUROPEAN BIOPHYSICS JOURNAL, 1990, 18 (03) :165-174
[9]   Forward-backward semiclassical dynamics with information-guided noise reduction for a molecule in solution [J].
Bukhman, Edward ;
Makri, Nancy .
JOURNAL OF PHYSICAL CHEMISTRY A, 2007, 111 (44) :11320-11327
[10]   Semiclassical approximations to quantum dynamical time correlation functions [J].
Cao, JS ;
Voth, GA .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (01) :273-285