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arXiv:1606.01705 · Physical Review A

Enhanced high-order-harmonic generation and wave mixing via two-color multiphoton excitation of atoms and molecules

H. K. Avetissian, B. R. Avchyan, G. F. Mkrtchian

Published Jul 29, 2016• 6 citations
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Abstract

We consider harmonics generation and wave mixing by two-color multiphoton resonant excitation of three-level atoms and molecules in strong laser fields. The coherent part of the spectra corresponding to multicolor harmonics generation is investigated. The obtained analytical results on the basis of a generalized rotating wave approximation are in a good agreement with numerical calculations. The results applied to the hydrogen atoms and homonuclear diatomic molecular ions show that one can achieve efficient generation of moderately high multicolor harmonics via multiphoton resonant excitation by appropriate laser pulses.

DOI
10.1103/physreva.94.013856

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We consider harmonics generation and wave mixing by two-color multiphoton resonant excitation of three-level atoms and molecules in strong laser fields. The coherent part of the spectra corresponding to multicolor harmonics generation is investigated. The obtained analytical results on the basis of a generalized rotating wave approximation are in a good agreement with numerical calculations. The results applied to the hydrogen atoms and homonuclear diatomic molecular ions show that one can achieve efficient generation of moderately high multicolor harmonics via multiphoton resonant excitation by appropriate laser pulses.
The coherent scattering spectrum of a three-level atom driven by an intense laser field with multiphoton resonant excitation is considered. The spectrum corresponding to harmonic generation is investigated both analytically and numerically for different initial atomic states. The analytical calculations are based on the generalized rotating wave approximation, which allows one to explain obtained spectra containing in general both even and odd harmonics. The results applied to the hydrogen atom show that one can achieve efficient generation of moderately high harmonics using multiphoton resonant excitation by appropriate laser pulses.
An analytic study is presented of the efficient multiphoton excitation and strong harmonic generation in three-level systems specified by a pair of nearly degenerate, strongly dipole-coupled excited states. Such systems are physically formed by the three lowest states in, e.g., the hydrogen atom or evenly charged homonuclear diatomic molecular ions under reasonably chosen laser intensities. As a detailed analytic result, we found that the laser pulse of photon energy 2.05eV2.05\text{eV}2.05eV, duration 0.23ps0.23\text{ps}0.23ps, and intensity $5\ifmmode\times\else\texttimes\fi{}{10}^{13}\frac{\mathrm{W}}{{\mathrm{cm}}^{2}}$ is able to produce complete inversion of the initial population in the hydrogen atom through the five-photon excitation. At the same photon energy, the pulse of duration 0.41ps0.41\text{ps}0.41ps and intensity $3.44\ifmmode\times\else\texttimes\fi{}{10}^{14}\frac{\mathrm{W}}{{\mathrm{cm}}^{2}}$ was found to produce the same effect in the molecular ion but through the nine-photon excitation. We show that the accompanying scattering of light has very rich spectrum differing substantially from that of the two-level system.
We present a theoretical study of the main characteristics of two-color photoionization spectra obtained when atoms are subjected to an intense radiation pulse containing the fundamental of an infrared laser and one of its higher harmonics. The frequency of the latter is chosen to be high enough that the atom can be ionized by a single photon. The calculation is performed by numerical integration of the time-dependent Schrödinger equation for a (three-dimensional) hydrogen atom. We present the general properties of the spectra and angular distributions as well as the possible occurrence of interferences between the laser-assisted process and above-threshold ionization. Our results indicate that such interference effects, which can lead to partial coherent control of the photoionization process, can be observed at moderate laser intensities within the reach of currently operated laser and harmonic sources.