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DDC: 530 × Subject: Time dependent ×

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Now showing 1 - 6 of 6
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    Atomic and molecular suite of R-matrix codes for ultrafast dynamics in strong laser fields and electron/positron scattering
    (Bristol : IOP Publ., 2020) Wragg, J.; Benda, J.; Mašín, Z.; Armstrong, G.S.J.; Clarke, D.D.A.; Brown, A.C.; Ballance, C.; Harvey, A.G.; Houfek, K.; Sunderland, A.; Plummer, M.; Gorfinkiel, J.D.; Van Der Hart, H.
    We describe and illustrate a number of recent developments of the atomic and molecular ab initio R-matrix suites for both time-dependent calculations of ultrafast laser-induced dynamics and time-independentcalculations of photoionization and electron scattering. © 2019 Published under licence by IOP Publishing Ltd.
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    General Time-Dependent Configuration-Interaction Singles II: The Atomic Case
    (Woodbury, NY : Inst., 2022-10-10) Carlström, Stefanos; Bertolino, Mattias; Dahlström, Jan Marcus; Patchkovskii, Serguei
    We present a specialization of the grid-based implementation of the time-dependent configuration-interaction singles described in the preceding paper [S. Carlström et al., preceding paper, Phys. Rev. A 106, 043104 (2022)]. to the case of spherical symmetry. We describe the intricate time propagator in detail and conclude with a few example calculations. Among these, of note are high-resolution photoelectron spectra in the vicinity of the Fano resonances in photoionization of neon and spin-polarized photoelectrons from xenon, in agreement with recent experiments.
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    General Time-Dependent Configuration-Interaction Singles I: The Molecular Case
    (Woodbury, NY : Inst., 2022-10-10) Carlström, Stefanos; Spanner, Michael; Patchkovskii, Serguei
    We present a grid-based implementation of the time-dependent configuration-interaction singles method suitable for computing the strong-field ionization of small gas-phase molecules. After outlining the general equations of motion used in our treatment of this method, we present example calculations of strong-field ionization of He, LiH, H2O, and C2H4 that demonstrate the utility of our implementation. The following paper [S. Carlström et al., following paper, Phys. Rev. A 106, 042806 (2022)] specializes to the case of spherical symmetry, which is applied to various atoms.
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    Some remarks on a model for rate-independent damage in thermo-visco-elastodynamics
    (Bristol : IOP Publ., 2016) Lazzaroni, Giuliano; Rossi, Riccarda; Thomas, Marita; Toader, Rodica
    This note deals with the analysis of a model for partial damage, where the rate- independent, unidirectional flow rule for the damage variable is coupled with the rate-dependent heat equation, and with the momentum balance featuring inertia and viscosity according to Kelvin-Voigt rheology. The results presented here combine the approach from Roubicek [1, 2] with the methods from Lazzaroni/Rossi/Thomas/Toader [3]. The present analysis encompasses, differently from [2], the monotonicity in time of damage and the dependence of the viscous tensor on damage and temperature, and, unlike [3], a nonconstant heat capacity and a time-dependent Dirichlet loading.
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    Attosecond time delays in C60 valence photoemissions at the giant plasmon
    (Bristol : IOP Publ., 2015) Barillot, T.; Magrakvelidze, M.; Loriot, V.; Bordas, C.; Hervieux, P.-A.; Gisselbrecht, M.; Johnsson, P.; Laksman, J.; Mansson, E.P.; Sorensen, S.; Canton, S.E.; Dahlström, J.M.; Dixit, G.; Madjet, M.E.; Lépine, F.; Chakraborty, H.S.
    We perform time-dependent local density functional calculations of the time delay in C60 HOMO and HOMO-1 photoionization at giant plasmon energies. A semiclassical model is used to develop further insights.
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    Non-instantaneous third-order optical response of gases in low-frequency fields
    (Washington, DC : Soc., 2022) Morales, Felipe; Richter, Maria; Ivanov, Misha; Husakou, Anton
    It is commonly assumed that for low-intensity short optical pulses far from resonance, the third-order optical nonlinear response is instantaneous. We solve the three-dimensional time-dependent Schrödinger equation for the hydrogen atom and show that this is not the case: the polarization is not simply proportional to the cube of the electric field even at low intensities. We analyze the fundamental-frequency and third-harmonic nonlinear susceptibilities of hydrogen, investigate their dependence on intensity, and find that the delays in the Kerr response rapidly approach the femtosecond time-scale at higher intensities, while the delays in the third harmonic generation remain much lower. We also propose an experimental scheme to detect and characterize the above effects.