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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 2895-2900 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 2277-2279 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 126-135 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Renormalization effects of the bath-induced vibronic population transfer on resonant light scattering (RLS) from molecules in condensed phases are theoretically studied based on the Markoffian master equation approach. By using the double space diagram technique, the self-energy originated from the bath-induced vibronic population transfer is analytically solved, and the analytic expressions for the intensities both of the stationary and of the time-resolved RLS spectra are derived. The renormalization effect is analyzed in terms of dimensionless molecular parameters, and model calculations are also performed to confirm theoretical results.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 2910-2916 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The Fourier-expansion density matrix method is developed to describe the multiphoton processes of molecules interacting with the heat bath under the strong laser light. This method is applied to deriving expressions for the absorption spectra in the case in which a single-mode laser interacts with the molecular system of a three-level taking into account the dynamic Stark effect. Model calculations are performed to demonstrate the dynamic Stark effects on the absorption ability in the three-level system, and compared with the results of the weak laser light case. The calculated band shapes of the two-photon absorption are analyzed in terms of the simultaneous and sequential mechanisms. The sequential mechanism is characterized by bath-induced intramolecular transitions. As the laser intensity is increased the simultaneous mechanism makes a dominant contribution with increased dynamic Stark effects.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 5960-5973 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The resonance secondary emission (RSE) in femtosecond laser excitation is discussed in reference to the motion of the created wave packet moving on the excited state potential surface. The density matrix of emitted light for the multi-intermediate-level system is outlined, from which the emission correlation function is derived. The correlation function is put into the theoretical expression of the time-dependent "physical spectrum'' for the Fabry–Perot interferometer (which is used in order to consider temporal and energetic resolution inherent in detection). The compact and practical expressions obtained connect the time- and frequency-resolved spectrum with the time evolution of the wave packet. Numerical results for a displaced harmonic oscillator model indicate that the time- and frequency-resolved spectrum can reveal how the wave packet created by a fs laser pulse travels on the excited potential surface if the response time 1/Γd of the photodetector satisfies the relation that Ω〈Γd 〈∼ the Stokes shift (where Ω is the vibrational frequency). It is shown that the excited state wave function can be split into two terms, the one that adiabatically follows the temporal change in incident light (the adiabatic term) and the one that represents the effect of spectral broadening of light (the Fourier broadening term). It is only the Fourier broadening term that survives after the termination of incident light and reflects the motion of the created wave packet on the excited potential surface. In off-resonance excitation, the adiabatic term produces Raman-like emission and the Fourier broadening one produces fluorescence-like emission. In resonance excitation, these two terms are indistinguishable from each other with respect to emission frequency: for the duration of incident light, the adiabatic term offsets the Fourier broadening one, leading to a slow buildup of intensity in the time- and frequency-resolved spectrum (which is slower than the initial rise of the incident pulse profile).
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 34-41 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Effects of the coherence transfer induced by the molecule–heat bath interactions on the ultrashort time-resolved coherent anti-Stokes Raman scattering (CARS) from molecules in liquids are theoretically studied. Based on the perturbative density matrix formalism an expression for the CARS intensity is derived taking into account the coherence transfer between the Raman active vibrational transitions of two molecules in liquids. The coherence transfer constants and dephasing constants are properly incorporated with the aid of Liouville space Feynman diagrams. The structure of the coherence transfer matrix element which expresses the time evolution of the coherence between the relevant transitions is clarified by solving the Master equation with the coherence transfer and dephasing constants in the Markoff approximation. Frequency shifts of the quantum beats appear in the time-resolved CARS as a result of the coherence transfer. A multispherical layer model is adopted in evaluating the coherence transfer effects in liquids in femtosecond time domains. Model calculations of time-resolved CARS spectra have been carried out to demonstrate the coherence transfer effects in both short and long range coherence transfer cases. It is predicted that the quantum beats are amplified in the time-resolved CARS spectra of molecules in liquids in a long range coherence transfer case when there exist differences in the coherence transfer constants between each spherical layer.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 3012-3032 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A theory of the emission spectrum from a multilevel molecular system pumped by strong resonant radiation fields based on the double space theory of the density matrix is developed. We are especially concerned with a three-level, one-laser system, and a three-level, two-laser system. It is shown that the band structure cannot always be estimated by the energy level structure of the dressed states. In fact, in both model systems, triplet structures of the emission spectra can be observed in the case where the magnitude of the molecule-field interaction is larger than that of the detuning. The characteristic features of the band structure are interpreted in terms of the dressed state picture based on analytically solvable models. Several numerical calculations are performed to show how the multiplet band structure in the emission spectrum is influenced by the detuning and the power of the pump field(s).
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 3903-3915 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Effects of vibronic coherence transfer induced by the heat bath on ultrafast time-resolved resonant light scattering (RLS) spectra are theoretically investigated within the master equation approach. The vibronic coherence initially created by a coherent optical excitation transfers to other vibronic coherent states due to inelastic interactions between the vibronic system concerned (the relevant system) and the heat bath. The vibronic coherence transfer results in the quantum beats in the time-resolved RLS spectra. The bath-induced vibronic transition operator is derived in the double space representation of the density matrix theory. Model calculations of the femtosecond (fs) time-resolved RLS spectra are performed to demonstrate the effects of the bath-induced vibronic coherence transfer.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 60 (1986), S. 4191-4196 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: In order to obtain semiconductivity, rutile crystals have been doped with Nb by means of diffusion. The resulting Nb-doped rutile crystals have an electrical resistivity (approximately-equal-to)80 Ω cm at room temperature. Impedance analysis of a Nb-doped TiO2-Au diode suggests that the measurement frequency must be lower than 10 kHz to detect the capacitance and conductance of the depletion layer. Thus, an admittance spectroscopic method is used to study traps in the diode of the Nb-doped TiO2-Au. Two trap levels, located at 0.24 and 0.37 eV below the bottom of the conduction band, have been detected by this method. The state densities and capture cross sections of these trap levels are also determined.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 8321-8331 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Bath-induced coherence transfer effects on a time- and frequency-resolved resonant light scattering spectrum is theoretically investigated using the Markoff master equation. According to Eberly and Wódkiewicz, a general expression for an experimentally observable spectrum in terms of a molecular response function is derived within the density matrix formalism. To generalize our previous results of the bath-induced coherence transfer which were derived based on a displaced harmonic oscillator model [Y. Ohtsuki and Y. Fujimura, J. Chem. Phys. 91, 3903 (1989)], an eigenstate basis is used to represent a relevant system for investigating characteristics of the transfer. By the present model, we clarify the dependence of the bath-induced coherence transfer on the energy-level structure of the intermediate states associated with the transfer, i.e., energy mismatch effects. It is shown that if the energy mismatch of these states is smaller than dephasing rates, the bath-induced coherence transfer occurs resonantly. In the other cases, the energy mismatch brings about a modulation in the time evolution of the superposition state created by the bath-induced coherence transfer, which strongly diminishes the efficiency of the transfer. The resonance condition is derived analytically and is confirmed by numerical calculations of quantum beats induced by the bath-induced coherence transfer. The possibility of very rapid dephasing of a quantum beat signal which cannot be explained in terms of dephasing rates is also shown, when the transition moments have such values that give π-phase-shifted quantum beats in bath-induced fluorescence. © 1996 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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