The Experts below are selected from a list of 222 Experts worldwide ranked by ideXlab platform

Artit Hutem - One of the best experts on this subject based on the ideXlab platform.

Vladislav Belous - One of the best experts on this subject based on the ideXlab platform.

  • Reference potential approach to the Energy Eigenvalue problem of a rotating diatomic molecule
    Chemical Physics Letters, 2008
    Co-Authors: M. Selg, Vladislav Belous
    Abstract:

    Abstract A two-stage analytical–numerical method is described, which enables to accurately solve the Energy Eigenvalue problem of a rotating oscillator. First, using a simple analytic algorithm, one constructs reliable Morse approximants to all rotational–vibrational states of the given effective potential. Thereafter, the Schrodinger equation is transformed into an equivalent pair of coupled first-order differential equations (Gordon equations), which are solved numerically. Integration step h = 0.05  A is sufficient to ensure at least 6-digit accuracy for all Energy levels of the examined model potential for H2 molecule.

R. W. Robinett - One of the best experts on this subject based on the ideXlab platform.

  • Wave packet revivals and the Energy Eigenvalue spectrum of the quantum pendulum
    Annals of Physics, 2003
    Co-Authors: Michael A. Doncheski, R. W. Robinett
    Abstract:

    Abstract The rigid pendulum, both as a classical and as a quantum problem, is an interesting system as it has the exactly soluble harmonic oscillator and the rigid rotor systems as limiting cases in the low- and high-Energy limits, respectively. The Energy variation of the classical periodicity ( τ ) is also dramatic, having the special limiting case of τ →∞ at the ‘top’ of the classical motion (i.e., the separatrix.) We study the time-dependence of the quantum pendulum problem, focusing on the behavior of both the (approximate) classical periodicity and especially the quantum revival and superrevival times, as encoded in the Energy Eigenvalue spectrum of the system. We provide approximate expressions for the Energy Eigenvalues in both the small and large quantum number limits, up to fourth order in perturbation theory, comparing these to existing handbook expansions for the characteristic values of the related Mathieu equation, obtained by other methods. We then use these approximations to probe the classical periodicity, as well as to extract information on the quantum revival and superrevival times. We find that while both the classical and quantum periodicities increase monotonically as one approaches the ‘top’ in Energy, from either above or below, the revival times decrease from their low- and high-Energy values until very near the separatrix where they increase to a large, but finite value.

  • Periodic orbit theory analysis of the circular disk or annular billiard: Nonclassical effects and the distribution of Energy Eigenvalues
    American Journal of Physics, 1999
    Co-Authors: R. W. Robinett
    Abstract:

    Periodic orbit (PO) theory can be used to make connections between the quantum Energy Eigenvalue spectrum and the closed orbits of the corresponding classical system. The two-dimensional annular billiard or circular disk system (namely, a particle in the plane confined between inner and outer infinite circular walls at fR≡Rin

M. Selg - One of the best experts on this subject based on the ideXlab platform.

  • Reference potential approach to the Energy Eigenvalue problem of a rotating diatomic molecule
    Chemical Physics Letters, 2008
    Co-Authors: M. Selg, Vladislav Belous
    Abstract:

    Abstract A two-stage analytical–numerical method is described, which enables to accurately solve the Energy Eigenvalue problem of a rotating oscillator. First, using a simple analytic algorithm, one constructs reliable Morse approximants to all rotational–vibrational states of the given effective potential. Thereafter, the Schrodinger equation is transformed into an equivalent pair of coupled first-order differential equations (Gordon equations), which are solved numerically. Integration step h = 0.05  A is sufficient to ensure at least 6-digit accuracy for all Energy levels of the examined model potential for H2 molecule.

Chanun Sricheewin - One of the best experts on this subject based on the ideXlab platform.