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Physical Review A

Time profile of harmonics generated by a single atom in a strong electromagnetic field

Philippe Antoine, Bernard Piraux, A. Maquet

Published Mar 1, 1995• 357 citations
Publisher

Abstract

We show that the time profile of the harmonics emitted by a single atom exposed to a strong electromagnetic field may be obtained through a wavelet or a Gabor analysis of the acceleration of the atomic dipole. This analysis is extremely sensitive to the details of the dynamics and sheds some light on the competition between the atomic excitation or ionization processes and photon emission. For illustration we study the interaction of atomic hydrogen with an intense laser pulse.

DOI
10.1103/physreva.51.r1750

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We show that the time profile of the harmonics emitted by a single atom exposed to a strong electromagnetic field may be obtained through a wavelet or a Gabor analysis of the acceleration of the atomic dipole. This analysis is extremely sensitive to the details of the dynamics and sheds some light on the competition between the atomic excitation or ionization processes and photon emission. For illustration we study the interaction of atomic hydrogen with an intense laser pulse.
It is well established, both experimentally and theoretically, that atoms exposed to a strong laser pulse emit high order harmonics of the driving field. Although this process has been intensively studied theoretically, the main effort has been focused so far on the study of the harmonic spectrum while no attempt has been made to analyse systematically its time evolution. We show that the time profile of each harmonic may be obtained through a time-frequency analysis of the acceleration of the atomic dipole. We show also that such an analysis, which is very sensitive to the details of the dynamics, provides valuable information about the competition between photon emission and ionization processes.
The acceleration of the electron in a two-level atom driven by a short laser pulse of intermediate strength is calculated and therefore analysed through two wavelet transforms in order to obtain the temporal evolution of the spectrum of the emitted radiation. We show (i) the full spectrum at different instants and (ii) the time profile of some representative harmonics. The growth of the harmonics as well as the appearance and erratic behaviour of the hyper-Raman can be followed with the laser intensity.
We study harmonic generation by a single atom exposed to two short perpendicularly polarized laser pulses. The two perpendicular electric fields oscillate at two different frequencies ${\ensuremath{\omega}}_{1}$ and ${\ensuremath{\omega}}_{2}$. Hence, the resultant field has a polarization which depends on time. Since harmonics are emitted when the resultant oscillating field is linearly polarized, it is expected that a short pulse of harmonics may be emitted if the external field is linearly polarized during a short period of time. We show that, indeed, the atom may emit an ultrashort pulse of a given harmonic. This result has been obtained by time-frequency analyzing the acceleration of the induced dipole moment with a filter whose frequency bandwidth is smaller than twice the frequency of the external field. Our calculation of the dipole acceleration is based on the numerical solution of the time-dependent Schr\"odinger equation. We then address the question of how far it is possible to reduce the duration of the emitted pulse of one given harmonic by adjusting both ${\ensuremath{\omega}}_{1}$ and ${\ensuremath{\omega}}_{2}$ and keeping the amplitude of this pulse significant. In order to answer to this question, we used the quantum version of the two-step model [M. Lewenstein et al., Phys. Rev. A 49, 2117 (1994)].
Abstract A new approach for studying the spontaneous emission of an atomic system in the presence of a high-intensity laser field is used to study the process of harmonic generation. The analysis is based on consideration of quantum system interaction, with the quantized field modes being in the vacuum state, while the intense laser field is considered to be classically beyond perturbation theory. The numerical analysis of the emission from the single one-electron 1D atom irradiated by the femtosecond laser pulse of a Ti:Sa laser is discussed. It is demonstrated that not only odd, but also even harmonics can be emitted if the laser field is strong enough. The origin of the appearance of even harmonics is studied. The obtained results are compared with those found in the framework of the semiclassical approach that is widely used to study harmonic generation. It is found that the semiclassical approach is inapplicable in the strong-field limit.
Recent developments on intense laser sources is opening a new field of optical sciences. An intense coherent light beam strongly interacting with the matter causes a coherent motion of a particle, forming a strongly dressed excited particle. A photon emission from this dressed excited particle is a strong nonlinear process causing high-harmonic generation (HHG), where the perturbation analysis is broken down. In this work, we study a coherent photon emission from a strongly dressed excited atom in terms of complex spectral analysis in the extended Floquet-Hilbert-space. We have obtained the eigenstates of the total Hamiltonian with use of Feshbach-Brilloiun-Wigner projection method. In this extended space, the eigenstates of the total Hamiltonian consisting of the radiation field and the atom system have complex eigenvalues whose imaginary part represents the decay rate. Time evolution of the system is represented by the complex eigenvector expansion so that the correlation dynamics between the photon and the atom is fully taken into account. The HHG is interpreted as the irreversible spontaneous photon emission due to the resonance singularity in terms of the multiple Floquet states that are generated by periodic external field. We have found that the interference between the emitted photons over the different Floquet states causes spatial pulse emission correlated with the decay process of the excited atom.