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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 2912-2918 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The success of the "cluster variation method" (CVM) in reproducing quite accurately the free energies of Monte Carlo (MC) calculations on Ising models is explained in terms of identifying a cancellation of errors: We show that the CVM produces correlation functions that are too close to zero, which leads to an overestimation of the exact energy, E, and at the same time, to an underestimation of −TS, so the free energy F=E−TS is more accurate than either of its parts. This insight explains a problem with "hybrid methods" using MC correlation functions in the CVM entropy expression: They give exact energies E and do not give significantly improved −TS relative to CVM, so they do not benefit from the above noted cancellation of errors. Additionally, hybrid methods suffer from the difficulty of adequately accounting for both ordered and disordered phases in a consistent way. A different technique, the "entropic Monte Carlo" (EMC), is shown here to provide a means for critically evaluating the CVM entropy. Inspired by EMC results, we find a universal and simple correlation to the CVM entropy which produces individual components of the free energy with MC accuracy, but is computationally much less expensive than either MC thermodynamic integration or EMC. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 60 (1996), S. 821-824 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We present a technique to generate Cartesian Gaussian bases for electronic configuration and cross-section calculations on molecules. The technique is specially useful for pseudopotential work, when the bases cannot be tabulated because they depend on the specific choice of the pseudopotential. © 1996 John Wiley & Sons, Inc.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 16 (1979), S. 1021-1031 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We consider the effects of a non-muffin-tin charge density in the multiple-scattering method. The study is carried out by means of a parametrized electronic density, which is used in a variational expression for the energy of the molecular system. We show that, at least in two situations, the parametrized density reproduces the true density very well. In a numerical study of the electronic configuration of the CH4 molecule, we show that the non-muffin-tin density may shift the one-electron energies by as much as 1 eV and the total energy by as much as 1 Ry.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 30 (1986), S. 313-323 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have developed a new version of the variational cellular method for the calculation of the electronic structure of polyatomic systems. It is a very attractive method for large systems, such as solids and large molecules, and capable of giving calculated results with a degree of precision at least as good as those obtained by Hartree-Fock calculations. We are now improving the method by the introduction of crystalline boundary conditions with the intention to apply it to the study of impurities in semiconductors. The results for the ZnS clusters simulating the pure crystal show that the method leads to a fairly consistent description of the bulk electronic structure.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This is the third paper on the cellular method for polyatomic systems. We show how to deal with nonspherical Coulomb potentials. We also show how to modify the variational expression for the energy eigenvalues so as to obtain a faster convergence in the angular momentum series for the wavefunctions. We apply both techniques to the self-consistent calculation of SF6. Contrary to what we obtained in CH4 and SiH4, the cellular method cannot yield the correct equilibrium interatomic distance in the present case. The calculated ionization potentials are in the correct order but are all shifted by 2-3 eV. This shift is attributed to the wrong expression for exchange correlation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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