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New Journal of Physics

Generalization of the Kerr effect for high intensity, ultrashort laser pulses

Muhammad Nurhuda, Akira Suda, Katsumi Midorikawa

Published May 7, 2008• 45 citations
Publisher

Abstract

We have investigated the nonlinear susceptibility of atoms induced by high intensity, ultrashort laser pulses using a numerical solution of the time-dependent Schrödinger equation. We found that the instantaneous nonlinear susceptibility becomes saturated at high intensity. We also found that the saturation is closely linked to depletion of the ground state. Based on the numerical results, a simple model that generalizes the nonlinear susceptibility of atoms for high intensity, ultrashort laser pulses is proposed. We also investigated the ionization-induced dipole moment and found that the amplitude of the dipole moment induced by an ionized electron is, in general, smaller than that induced by a free-electron, and is attributable to a residual interaction between the ionized-electron and its parent ion.

DOI
10.1088/1367-2630/10/5/053006

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We have investigated the nonlinear susceptibility of atoms induced by high intensity, ultrashort laser pulses using a numerical solution of the time-dependent Schrödinger equation. We found that the instantaneous nonlinear susceptibility becomes saturated at high intensity. We also found that the saturation is closely linked to depletion of the ground state. Based on the numerical results, a simple model that generalizes the nonlinear susceptibility of atoms for high intensity, ultrashort laser pulses is proposed. We also investigated the ionization-induced dipole moment and found that the amplitude of the dipole moment induced by an ionized electron is, in general, smaller than that induced by a free-electron, and is attributable to a residual interaction between the ionized-electron and its parent ion.
Polarization response that appears in silver vapors in the field of a high-intensity femtosecond Ti:sapphire laser has been studied by the direct numerical integration of the time-dependent Schrödinger equation. The regions of applicability have been determined for perturbation theory and the power series expansion of the polarization in the field. The contribution of free electrons to the response at the frequency of the interacting field has been calculated, which is due to the photoionization process and limits the Kerr effect. An important contribution of laser-excited atomic states to nonlinear atomic responses of neutral atoms has been demonstrated.
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)].
We discuss the connection between strong-field ionization, saturation of the Kerr response and the formation of the Kramers–Henneberger (KH) atom and long-living excitations in intense infrared (IR) external fields. We present a generalized model for the intensity-dependent response of atoms in strong IR laser fields, describing deviations in the nonlinear response at the frequency of the driving field from the standard model. We show that shaping the driving laser pulse allows one to reveal signatures of the excited KH states in the Kerr response of an individual atom.
The influence of ultrashort low-frequency laser pulses of different intensities and pulse lengths on the dynamics of a resonantly driven atomic system is investigated theoretically. We demonstrate the periodical dependence of the total ionization rate on the appearance time of a strong few-cycle laser pulse. By depleting the excited state, the intense short pulse not only resets the Rabi oscillations, but also introduces a time shift that is proportional to the pulse length. This time shift can be employed to determine the ultrashort pulse length. In the case of ultrashort pulses with lower intensities, we observe side-bands in the two-photon ionization spectrum, whose intensities vary periodically with the appearance time of the pulse. This can be utilized to measure the period of Rabi oscillations. We have developed an S-matrix theory of two-colour ionization which can explain some of the observations of our numerical calculations. Furthermore, we have studied the high harmonic generation spectra as well as the attosecond pulses generated from the high harmonics. We show that the Rabi oscillation can be used to alter the ionization rate within laser sub-cycles and therefore select different quantum trajectories in the high harmonics generation.
Accurate modeling of optical nonlinearities is crucial to describe macroscopic laser propagation in a medium, including sum frequency generation, spectral broadening due to self-phase modulation, various ionization processes and soliton formation. For incident laser light the response of the medium is given by the induced polarization of the microscopic system. The polarization is usually expanded in a Taylor series for the electric field amplitude, which is truncated after the first non-linear term being of third order for isotropic media. A third-order nonlinearity leads to the well-known optical Kerr effect, where the refractive index of the medium becomes intensity dependent via n = n0+ n2I. This leads to an inherent problem when modeling laser propagation in two or more spatial dimensions, linked to the formal divergence (n2> 0) of the refractive index for increasing intensity.