arXiv subjects

Philipp V. Demekhin

Publications and source records attributed to Philipp V. Demekhin.

23 records · Page 2Linked to original sources

arXiv2017

Impact of two-electron dynamics and correlations on high-order harmonic generation in He

The interaction of a helium atom with intense short 800 nm laser pulse is studied theoretically beyond the single-active-electron approximation. For this purpose, the time-dependent Schrödinger equation for the two-electron wave packet driven by a linearly-polarized infrared pulse is solved by the time-dependent restricted-active-space configuration-interaction method (TD-RASCI) in the dipole velocity gauge. By systematically extending the space of active configurations, we investigate the role of the collective two-electron dynamics in the strong field ionization and high-order harmonic generation (HHG) processes. Our numerical results demonstrate that allowing both electrons in He to be dynamically active results in a considerable extension of the computed HHG spectrum.

physics.atm-clus↗

arXiv2013

Photoionization of hydrogen atom by coherent intense high-frequency short laser pulses: Direct propagation of electron wave packets on large spatial grids

The time-dependent Schrödinger equation for the hydrogen atom and its interaction with coherent intense high-frequency short laser pulses is solved numerically exactly by propagating the single-electron wave packets. Thereby, the wavefunction is followed in space and time for times longer than the pulse duration. Results are explicitly shown for 3 and 10 fs pulses. Particular attention is paid to identifying the effect of dynamic interference of photoelectrons emitted with the same kinetic energy at different times during the rising and falling sides of the pulse predicted in [\emph{Ph.V. Demekhin and L.S. Cederbaum}, Phys. Rev. Lett. \textbf{108}, 253001 (2012)]. In order to be able to see the dynamic interference pattern in the computed electron spectra, the photoelectron wave packet has to be propagated over long distances. Clearly, complex absorption potentials often employed to compute spectra of emitted particles cannot be used to detect dynamic interference. For the considered high-frequency pulses of 3 and 10 fs durations, this requires enormously large spatial grids. The presently computed photoionization and above-threshold ionization spectra are found to exhibit pronounced dynamic interference patterns. Where available, the patterns are in very good agreement with previously published results on the photoionization spectra which have been computed using a completely different method, thus supporting the previously made assumption that the above-threshold ionization processes are very weak for the considered pulse intensities and high carrier frequency. The quiver motion in space and time of a free electron in strong laser pulses is also investigated numerically. Finally, a discussion is presented of how fast the atom is ionized by an intense pulse.

physics.atom-ph↗

arXiv2012

Coherent intense resonant laser pulses lead to interference in the time domain observable in the spectrum of the emitted particles

The dynamics of atomic levels resonantly coupled by a coherent and intense short high-frequency laser pulse is discussed and it is advocated that this dynamics is sensitively probed by measuring the spectra of the particles emitted. It is demonstrated that the time-envelope of this laser pulse gives rise to two waves emitted with a time delay with respect to each other at the rising and falling sides of the pulse, which interfere in the time domain. By computing numerically and analyzing explicitly analytically a show-case example of sequential two-photon ionization of an atom by resonant laser pulses, we argue that this dynamic interference should be a general phenomenon in the spectroscopy of strong laser fields. The emitted particles do not have to be photoelectrons. Our results allow also to interpret the already studied resonant Auger effect of an atom by intense free electron laser pulses, and also to envisage experiments in which photons are emitted.

physics.atm-clus↗

arXiv2011

Exploring Interatomic Coulombic Decay by Free Electron Lasers

To exploit the high intensity of laser radiation, we propose to select frequencies at which single-photon absorption is of too low energy and two or more photons are needed to produce states of an atom that can undergo interatomic Coulombic decay (ICD) with its neighbors. For Ne dimer it is explicitly demonstrated that the proposed scheme to investigate interatomic processes by multiphoton absorption is much more efficient than with single-photon absorption of sufficiently large frequency as used until now. Extensive calculations on Ne dimer including all the involved nuclear dynamics and the losses by ionization of the participating states show how the low-energy ICD electrons and Ne$^+$ pairs are produced for different laser intensities and pulse durations. At higher intensities the production of Ne$^+$ pairs by successive ionization of the two atoms becomes competitive and the respective emitted electrons interfere coherently with the ICD electrons. It is also demonstrated that a measurement after a time delay can be used to determine the contribution of ICD even at high laser intensity.

physics.atm-clus↗

arXiv2011

Resonant Auger decay of the core-excited C$^\ast$O molecule in intense X-ray laser fields

The dynamics of the resonant Auger (RA) process of the core-excited C$^\ast$O(1s$^{-1}π^\ast,v_r=0$) molecule in an intense X-ray laser field is studied theoretically. The theoretical approach includes the analogue of the conical intersections of the complex potential energy surfaces of the ground and `dressed' resonant states due to intense X-ray pulses, taking into account the decay of the resonance and the direct photoionization of the ground state, both populating the same final ionic states coherently, as well as the direct photoionization of the resonance state itself. The light-induced non-adiabatic effect of the analogue of the conical intersections of the resulting complex potential energy surfaces gives rise to strong coupling between the electronic, vibrational and rotational degrees of freedom of the diatomic CO molecule. The interplay of the direct photoionization of the ground state and of the decay of the resonance increases dramatically with the field intensity. The coherent population of a final ionic state via both the direct photoionization and the resonant Auger decay channels induces strong interference effects with distinct patterns in the RA electron spectra. The individual impact of these physical processes on the total electron yield and on the CO$^+(A^2Π)$ electron spectrum are demonstrated.

physics.atm-clus↗