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  • Articles  (280)
  • Articles: DFG German National Licenses  (280)
  • 1995-1999  (159)
  • 1980-1984  (121)
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  • Articles  (280)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 20 (1984), S. 83-87 
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-8892
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 10485-10491 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We consider the electronic spectroscopy of dilute CH3I in supercritical Ar fluid. Absorption line shapes for the B←X transition of CH3I have been measured previously in low-density argon, which yielded results for the CH3I/Ar pair potentials. Using these potentials, Kalbfleisch et al. [J. Chem. Phys. 105, 7034 (1996)] have performed molecular dynamics simulations to calculate the absorption line shapes at higher densities, and also the solvation correlation function. We compare the results of several analytic theories to the simulated line shapes and solvation correlation functions. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 9312-9318 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We consider the problem of calculating the electronic absorption spectrum of a chromophore with intramolecular degrees of freedom coupled to a condensed phase environment. We approach this calculation in the framework of the imaginary-time path integral Monte Carlo techniques, and focus on the problem of the analytic continuation of the imaginary-time data to the real-time axis. Two alternative analytic continuation methods are considered: the maximum entropy method and the singular value decomposition method. An exactly solvable model is introduced to test the accuracy of these methods. Exact numerical results for the absorption spectra are compared to the spectra reconstructed by the analytic continuation methods; it is found that the singular value decomposition method gives systematically higher resolution than the maximum entropy method and is capable of reproducing the fine vibronic structure of the absorption spectrum. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 77 (1995), S. 6239-6243 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The diffusion of platinum in thin copper films has been studied by Rutherford backscattering spectrometry (RBS) under the kinetic conditions B (within the temperature range of 200–290 °C) and C (room temperature). The RBS spectra were modified to concentration curves for both bulk and grain boundary (GB) diffusion. Under the kinetic regime B the triple products KδDb (Db is the GB diffusion coefficient, δ is the GB width, K is the enrichment ratio) were obtained using Whipple's model. Under the kinetic regime C the absolute value of the GB diffusion coefficient of Pt in Cu films was obtained. A comparison between the data on GB diffusion for the kinetics B extrapolated to room temperature and the data on GB diffusion for the kinetics C enables one to derive the product Kδ and to separate the contribution of segregation into the GB diffusion of Pt in Cu films. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 7745-7755 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A major problem still confronting molecular simulations is how to determine time-correlation functions of many-body quantum systems. In this paper the results of the maximum entropy (ME) and singular value decomposition (SVD) analytic continuation methods for calculating real time quantum dynamics from path integral Monte Carlo calculations of imaginary time time-correlation functions are compared with analytical results for quantum mechanical vibrational relaxation processes. This system studied is an exactly solvable system: a harmonic oscillator bilinearly coupled to a harmonic bath. The ME and SVD methods are applied to exact imaginary-time correlation functions with various level of added random noise, and also to imaginary-time data from path integral Monte Carlo (PIMC) simulations. The information gathered in the present benchmark study is valuable for the application of the analytic continuation of PIMC data to complex systems. © 1998 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 1407-1422 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We consider the problem of calculating the vibronic absorption spectrum of a diatomic molecule coupled to a condensed phase environment, where all nuclear degrees of freedom are taken in the quadratic approximation, and where the two electronic states couple differently to the solvent. This simple model is used to examine several commonly used semiclassical approximations. The method of Kubo–Toyozawa is adapted to enable exact calculation of the real-time dipole autocorrelation function for the quantum mechanical treatment. Alternatively, we derive an expression for this correlation function in terms of a path-integral influence functional, which is not limited to a finite number of bath modes and could be applied to treat anharmonic solutes in condensed matter. We then obtain an analytical solution for the classical treatment of nuclear dynamics, and develop a mixed quantum-classical approach, where the dynamics of the diatomic vibrational mode is treated quantum mechanically and the bath is treated classically. It is shown that the mixed quantum-classical treatment provides better agreement with the exact quantum treatment than the other approximations for a wide range of parameters. Exact analytical results similar to the pure dephasing theory of Skinner and Hsu are obtained for the asymptotic long time behavior of the dipole autocorrelation functions. © 1998 American Institute of Physics.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 5238-5248 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We consider the problem of calculating the nonradiative multiphonon transition rate between two electronic states of an impurity embedded in a condensed-phase environment, where all the nuclear degrees of freedom of the bath are taken in the harmonic approximation, and the two electronic states are coupled to the bath diagonally and off-diagonally. The diagonal coupling term includes displacements of the equilibrium positions of the bath modes, the frequency shifts, and Duschinsky rotations of the bath modes between the two electronic states. We consider two forms of the off-diagonal coupling term—the first assumes that this term is independent of the nuclear degrees of freedom, and thus the coupling between the two diabatic electronic states is taken to be a constant; the second is based on the Born–Oppenheimer method in which the off-diagonal coupling term between the two adiabatic electronic states is taken to be a function of the bath momenta operators. This general model is used to examine the accuracy of several commonly used mixed quantum-classical approximations where the two electronic states are treated quantum mechanically while the bath modes are treated classically. We use the lowest-order perturbation theory to calculate the transition rate between the two electronic states, which is given in terms of the Fourier transform of the off-diagonal coupling-element time correlation function. Following the methodology of Kubo and Toyozawa, we obtain an analytic solution for the fully quantum mechanical time correlation function, and extend our method [S. A. Egorov, E. Rabani and B. J. Berne, J. Chem. Phys. 108, 1407 (1998)] to obtain its mixed quantum–classical counterpart. It is shown that the nonradiative transition rate between the two electronic states calculated using the mixed quantum-classical treatment can deviate by several orders of magnitude from the exact quantum mechanical result. However, the agreement is improved when the classical time propagation of the bath modes is performed with the arithmetic average of the ground- and excited-state nuclear Hamiltonians, and thermal averaging over the initial classical distribution is replaced with the averaging over the corresponding Wigner distribution. © 1999 American Institute of Physics.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 109 (1998), S. 6376-6381 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have extended our study of the vibronic absorption spectrum in condensed matter [S. A. Egorov, E. Rabani, and B. J. Berne, J. Chem. Phys. 108, 1407 (1998)] to the case when the electronic dephasing rate is slow compared to the vibrational relaxation rate in both electronic states. We find that under such circumstances, unlike the case of fast electronic dephasing, treating all nuclear degrees of freedom classically provides better agreement with the exact quantum treatment than the mixed quantum-classical approximation. These results are consistent with the conclusions reached by Bader and Berne in their study of mixed quantum-classical treatments of vibrational relaxation processes. © 1998 American Institute of Physics.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 110 (1999), S. 3196-3199 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new approach is proposed for numerical calculations of optical line shapes for disordered molecular aggregates using the excitonic Hamiltonian. The method proposed previously for Gaussian disorder is generalized. A fluctuating origin of the energy scale is introduced as a new independent variable. The integration over this variable eliminates the energy delta function from the integrand, which drastically simplifies the Monte Carlo procedure. The new approach is suitable for calculations using both the diagonalization of the Hamiltonian and the resolvent of the Hamiltonian. As an example, optical line shapes have been calculated for aggregates with bi-Gaussian disorder. © 1999 American Institute of Physics.
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