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Physical Review A

Two-color above-threshold ionization of atoms

C. S. Han

Published Jun 1, 1996• 5 citations
Publisher

Abstract

A nonperturbative method is used to study the two-color multiphoton ionization of atoms by solving the Schr\"odinger equation in momentum space, which facilitates the extraction of the rapidly varying part of the wave function. Our method generalizes the problem for cases where an arbitrary number of ionization photons are absorbed, and also takes into account the threshold shifts due to both the high- and low-frequency fields. The photoelectron energy spectra of the hydrogen atoms are calculated and the dependence on the laser field strengths and frequencies is discussed. \textcopyright{} 1996 The American Physical Society.

DOI
10.1103/physreva.53.4268

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A nonperturbative method is used to study the two-color multiphoton ionization of atoms by solving the Schr"odinger equation in momentum space, which facilitates the extraction of the rapidly varying part of the wave function. Our method generalizes the problem for cases where an arbitrary number of ionization photons are absorbed, and also takes into account the threshold shifts due to both the high- and low-frequency fields. The photoelectron energy spectra of the hydrogen atoms are calculated and the dependence on the laser field strengths and frequencies is discussed. \textcopyright{} 1996 The American Physical Society.
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An approximate non-perturbative theory of multiphoton ionization of a hydrogen atom by two strong radiation fields is outlined. The special case is then considered for when one of the fields is of low intensity and high frequency and the other field is of high intensity and low frequency. A set of representative calculations has been performed for this case; that is, (a) angular distributions for given numbers of absorbed and emitted low-frequency photons and different geometries; (b) total cross-sections versus the strong-field intensity; (c) angular distributions summed over all the low-frequency photon exchanges, showing a fourfold symmetry in a geometry in which each ionization channel exhibits, instead, only a twofold symmetry; (d) the average energy gained by the ejected electrons. Calculations are performed for a strong low-frequency field of arbitrary polarization. In many respects, the present calculations are expected to complement those of single-field multiphoton ionization. It is hoped that the results of the calculations reported here may prompt systematic measurements also in this new class of processes, as the predictions are well within the state of the art of present multiphoton-ionization experiments.
To study the physical mechanism of atomic Rydberg state excitation (RSE) in two-color laser fields, we solve the time-dependent Schrödinger equation (TDSE) to calculate the ionization and excitation of hydrogen atoms. The relationship between the excited state population and the excitation rate of hydrogen atoms and the intensity of the fundamental frequency (FW) field can be observed by adjusting the laser intensity of the second harmonic (SH) field. The results demonstrate that multiphoton resonance absorption aligns with the physical mechanism of atomic resonant state excitation in two-color laser fields.
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.
Two-color two-photon photoionization of hydrogen and alkali atoms is presented. The method based on a perturbation expansion is valid for low to moderately intense radiation fields. Three processes are considered leading to the photoionization. For the first process both photons are below threshold, and for the second process one photon is above the threshold with an energy less than the final energy of the photoelectron. The last process is identical to the continuum Raman (Compton) scattering where the first photon is absorbed high in the continuum and the second low energy photon is scattered. Photoionization cross sections of hydrogen and the alkali atoms are given as functions of the first photon energy and the photoelectron energy.