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  • 1
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 124, No. 7 ( 2006-02-21)
    Kurzfassung: We simulate the effects of two types of dephasing processes, a nonlocal dephasing of system eigenstates and a dephasing of semilocal eigenstates, on the rate and mechanism of electron transfer (eT) through a series of donor-bridge-acceptor systems, D-BN-A, where N is the number of identical bridge units. Our analytical and numerical results show that pure dephasing, defined as the perturbation of system eigenstates through the system-bath interaction, does not disrupt coherent eT because it induces no localization; electron transfer may proceed through superexchange in a system undergoing only pure dephasing. A more physically reasonable description may be obtained via a system-bath interaction that reflects the perturbation of more local electronic structure by local nuclear distortions and dipole interactions. The degree of locality of this interaction is guided by the structure of the system Hamiltonian and by the nature of the measurement performed on the system (i.e., the nature of the environment). We compare our result from this “semilocal” model with an even more local phenomenological dephasing model. We calculate electron transfer rate by obtaining nonequilibrium steady-state solutions for the elements of a reduced density matrix; a semigroup formalism is used to write down the dissipative part of the equation of motion.
    Materialart: Online-Ressource
    ISSN: 0021-9606 , 1089-7690
    Sprache: Englisch
    Verlag: AIP Publishing
    Publikationsdatum: 2006
    ZDB Id: 3113-6
    ZDB Id: 1473050-9
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  • 2
    Online-Ressource
    Online-Ressource
    IOP Publishing ; 2010
    In:  New Journal of Physics Vol. 12, No. 1 ( 2010-01-19), p. 015003-
    In: New Journal of Physics, IOP Publishing, Vol. 12, No. 1 ( 2010-01-19), p. 015003-
    Materialart: Online-Ressource
    ISSN: 1367-2630
    Sprache: Unbekannt
    Verlag: IOP Publishing
    Publikationsdatum: 2010
    ZDB Id: 1464444-7
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  • 3
    Online-Ressource
    Online-Ressource
    American Chemical Society (ACS) ; 2014
    In:  The Journal of Physical Chemistry C Vol. 118, No. 38 ( 2014-09-25), p. 21798-21805
    In: The Journal of Physical Chemistry C, American Chemical Society (ACS), Vol. 118, No. 38 ( 2014-09-25), p. 21798-21805
    Materialart: Online-Ressource
    ISSN: 1932-7447 , 1932-7455
    RVK:
    Sprache: Englisch
    Verlag: American Chemical Society (ACS)
    Publikationsdatum: 2014
    ZDB Id: 2256522-X
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  • 4
    Online-Ressource
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    American Chemical Society (ACS) ; 1998
    In:  The Journal of Physical Chemistry A Vol. 102, No. 47 ( 1998-11-01), p. 9360-9366
    In: The Journal of Physical Chemistry A, American Chemical Society (ACS), Vol. 102, No. 47 ( 1998-11-01), p. 9360-9366
    Materialart: Online-Ressource
    ISSN: 1089-5639 , 1520-5215
    RVK:
    Sprache: Englisch
    Verlag: American Chemical Society (ACS)
    Publikationsdatum: 1998
    ZDB Id: 2006031-2
    ZDB Id: 1357795-5
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  • 5
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    American Chemical Society (ACS) ; 2002
    In:  The Journal of Physical Chemistry B Vol. 106, No. 33 ( 2002-08-01), p. 8479-8483
    In: The Journal of Physical Chemistry B, American Chemical Society (ACS), Vol. 106, No. 33 ( 2002-08-01), p. 8479-8483
    Materialart: Online-Ressource
    ISSN: 1520-6106 , 1520-5207
    RVK:
    Sprache: Englisch
    Verlag: American Chemical Society (ACS)
    Publikationsdatum: 2002
    ZDB Id: 1357799-2
    ZDB Id: 2006039-7
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  • 6
    Online-Ressource
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    AIP Publishing ; 1982
    In:  The Journal of Chemical Physics Vol. 77, No. 6 ( 1982-09-15), p. 2841-2846
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 77, No. 6 ( 1982-09-15), p. 2841-2846
    Kurzfassung: The vibrational line shapes expected for a case of ’’excitation mixed valency’’ (defined, in analogy, to ordinary electronic mixed valency, as one exciton moving between two equivalent electronic sites) is studied using a semigroup formalism to include relaxation effects. We include the quadratic electron-vibration coupling, corresponding to frequency changes. The results demonstrate the line narrowing expected in the rapid exchange limit, but also show that similar behavior may be caused by rapid electronic excitation. The simple model is readily extended to include transfer rates and ordinary (electronic) mixed valency. The relaxation process introduced a new time scale into the problem; when this becomes of the order of other relevant time scales (transfer, vibration, barrier residence) interesting line shape phenomena may be observed.
    Materialart: Online-Ressource
    ISSN: 0021-9606 , 1089-7690
    Sprache: Englisch
    Verlag: AIP Publishing
    Publikationsdatum: 1982
    ZDB Id: 3113-6
    ZDB Id: 1473050-9
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  • 7
    Online-Ressource
    Online-Ressource
    Wiley ; 2004
    In:  Israel Journal of Chemistry Vol. 44, No. 1-3 ( 2004-10), p. 53-64
    In: Israel Journal of Chemistry, Wiley, Vol. 44, No. 1-3 ( 2004-10), p. 53-64
    Kurzfassung: Conical intersections occur on potential energy surfaces of many medium‐sized and larger molecules. Their investigation, which has been ongoing for more than six decades, shows that vibronic coupling and relaxation behaviors at conical intersections can become quite complex and show large quantum effects. We present calculations of dynamical behavior in very simple (two‐dimensional, degenerate, non‐displaced) conical intersection models. The focus is placed on the effects of bath interactions on conical behavior—that is, the extent to which electronic dephasing, nuclear relaxation, and electronic relaxation affect the initially excited wave packet evolving on conical intersection surface. The calculations are carried through using a density matrix picture, with a Lindblad semi‐group formalism to characterize relaxation. We observe large quantum effects that act particularly on true conical structures (anti‐symmetric with respect to the mixing coordinate), as opposed to comparable‐strength interactions without this symmetry. Significant changes in excited‐state population decay, and even larger and more striking changes in the (observable) bleach recovery signal, are found.
    Materialart: Online-Ressource
    ISSN: 0021-2148 , 1869-5868
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2004
    ZDB Id: 2066481-3
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  • 8
    Online-Ressource
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    AIP Publishing ; 2005
    In:  The Journal of Chemical Physics Vol. 123, No. 13 ( 2005-10-01)
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 123, No. 13 ( 2005-10-01)
    Kurzfassung: The dynamics of a system incorporating a conical intersection, in the presence of a dissipative environment, is studied with the purpose of identifying observable ultrafast spectroscopic signatures. A model system consisting of two vibronically coupled electronic states with two nuclear degrees of freedom is constructed. Dissipation is treated by two different methods, Lindblad semigroup formalism and the surrogate Hamiltonian approach. Pump-probe experimental expectation values such as transient emission and transient absorption are calculated and compared to the adiabatic and diabatic population transfer. The ultrafast population transfer reflecting the conical intersection is not mirrored in transient absorption measurements such as the recovery of the bleach. Emission from the excited state can be suppressed on the ultrafast time scale, but the existence of a conical intersection is only one of the possible mechanisms that can provide ultrafast damping of emission.
    Materialart: Online-Ressource
    ISSN: 0021-9606 , 1089-7690
    Sprache: Englisch
    Verlag: AIP Publishing
    Publikationsdatum: 2005
    ZDB Id: 3113-6
    ZDB Id: 1473050-9
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  • 9
    Online-Ressource
    Online-Ressource
    AIP Publishing ; 1984
    In:  The Journal of Chemical Physics Vol. 80, No. 6 ( 1984-03-15), p. 2352-2362
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 80, No. 6 ( 1984-03-15), p. 2352-2362
    Kurzfassung: Absorption spectra are calculated for four model systems using two different methods for the calculation: The first is the standard linear response technique, while the second involves direct calculation of the energy dissipated in the sample interacting with the applied field, thus corresponding exactly to what is in fact measured experimentally. This latter technique, which we call the direct method, agrees with a linear response (as it must) for weakly applied fields for which the first-order perturbation analysis underlying linear response is in fact valid. For cases in which the system/field interaction is stronger, the linear approximation becomes poor, and the direct method, which includes the field-induced dynamics and in itself contains no approximations, is far better. The four systems considered consist of either single or coupled pairs of harmonic oscillators or two-level systems (spins) each in a thermal bath and coupled to the field by a displacement coupling. For both linear-response and direct calculations the system/field dynamics is solved exactly and the system/bath dynamics treated using a semigroup technique. For the harmonic oscillators, for which the population in any single excited state can never become large, the nonlinear effects (those present in the direct but not in the linear response) are quite minor. For the two-level/spin/systems, however, substantial corrections to the linear-response result are found in the direct calculation. These include power (or saturation) broadening and the appearance, when the two spins are coupled strongly to each other and one is coupled strongly to the field, of a new line at the averaged frequency of the two spins. For even stronger coupling, the line shape becomes very complex (corresponding to the full 15D algebra of the two spins plus the field), exhibiting several peaks and Fano antiresonances. The direct method, which is based on work of Lebowitz, seems to offer substantial advantages for the analysis of systems in which the applied field interactions are strong: This situation, common in microwave and magnetic resonance spectroscopy, is also relevant to high-energy laser studies.
    Materialart: Online-Ressource
    ISSN: 0021-9606 , 1089-7690
    Sprache: Englisch
    Verlag: AIP Publishing
    Publikationsdatum: 1984
    ZDB Id: 3113-6
    ZDB Id: 1473050-9
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  • 10
    Online-Ressource
    Online-Ressource
    Wiley ; 1990
    In:  Israel Journal of Chemistry Vol. 30, No. 1-2 ( 1990-01), p. 45-58
    In: Israel Journal of Chemistry, Wiley, Vol. 30, No. 1-2 ( 1990-01), p. 45-58
    Kurzfassung: The effects of electronic structure on bridge‐assisted electron transfer are considered. Using static perturbation theory, time‐dependent perturbation theory, and direct time‐dependent dynamics within generalized tight binding models, we examine the role of energy gaps, relative energetics of donor and acceptor orbitals with hole‐type and electron‐type superexchange sites, damping and dephasing, and overall energetics in electron transfer. We find that a generalization of the simple McConnell relationship to nonresonant transfer can in fact be made, but that no simple formula describes all limits; this is important in applications to a number of systems, including photosynthetic reaction centers, in which such superexchange occurs. The dynamical studies indicate some important and unexpected phenomena: these include quantum interferences between different pathways, recurrences and oscillations, and competitive effects of hole‐type and electron‐type superexchange. We suggest that direct dynamical study, as has begun to appear from several laboratories, provides an excellent way to visualize the intermediate state contributions to intramolecular electron transfer processes.
    Materialart: Online-Ressource
    ISSN: 0021-2148 , 1869-5868
    URL: Issue
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 1990
    ZDB Id: 2066481-3
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