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Journal of the Optical Society of America B

Dressed-state perturbation theory for multiphoton ionization of atoms

Liwen Pan, Bala Sundaram, Lloyd Armstrong

Published May 1, 1987• 23 citations
Publisher

Abstract

We introduce a perturbation theory using dressed bound states to include higher-order transition processes in the calculation of atomic multiphoton ionization. We calculate the ionization probability of hydrogen atoms using this theory and compare the results with the lowest-order perturbation result. We also calculate the shift of the hydrogen atom’s ground state that is due to the external field.

DOI
10.1364/josab.4.000754

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We introduce a perturbation theory using dressed bound states to include higher-order transition processes in the calculation of atomic multiphoton ionization. We calculate the ionization probability of hydrogen atoms using this theory and compare the results with the lowest-order perturbation result. We also calculate the shift of the hydrogen atom’s ground state that is due to the external field.
We have discussed the problems of non linear interaction between electromagnetic radiations with atoms from semi-classical point of view. Time dependent Schrödinger equation for single electron system is solved by using perturbative technique to obtain transition probability. Higher order perturbation is also discussed which is used in multiple processes, in which two or more quanta are emitted instead of a single photon. The theory is based on assumption that the perturbation is small. From this transition probability ionization rate and absorption cross-section of hydrogen atom is calculated. Its variation with photon energy and field strength is analyzed which agrees very well with experimental observations.The Himalayan PhysicsVol. 3, No. 32012Page : 40-43
The strong-field multiphoton ionization of atoms is considered and a theoretical approach dealing nonperturbatively with the radiation field formulated. The general computational scheme is the conventional perturbation theory, but the intermediate states are dressed by the field. We present in detail a method to dress the continuum states and to study the dipole transitions within the continuum. In the high-frequency domain, the proposed procedure rapidly converges over a wide range of field intensity and offers an interesting framework for calculating ionization rates for arbitrary numbers of absorbed (above-threshold) photons and field polarization.
Within the framework of time-dependent perturbation theory, general expressions are derived for the cross section of multiphoton processes induced by radiation acting on a hydrogen atom. Bound-bound transitions involving emission of a single quantum and bound-free transitions are calculated for a wide range of photon energies. In the case of resonance, the transition probability is also discussed. The procedure used to evaluate the sums over intermediate states is described. The numerical computation allows one to compare the results obtained for various competing processes.
The general theory of multiphoton ionization of hydrogen atoms by simultaneous absorption of several photons is discussed. In the nonrelativistic dipole approximation, the calculations lead to a recursion relationship concerning angular functions and involve radial matrix elements containing many summations over intermediate states. A general method for exactly evaluating several sums is described in detail and applied to the photo-ionization of atomic hydrogen in the ground state. Numerical results are presented as dispersion curves of the transition rate $\frac{{\ensuremath{\sigma}}_{n}}{{I}^{N\ensuremath{-}1}}$ for a range of wavelengths from 1000 up to 7200 \AA{}.
The multiphoton transitions in the hydrogen atom are investigated by taking into account the higher-order terms arising from the SSS-operator expansion. These higher-order effects originate induced shifts and induced breadths on the virtual-atomic-energy levels. It is shown that these perturbations play an important role for resonant multiphoton processes. In this case, the theory predicts a particular flux dependence of the transition rates. Furthermore, the well-known dispersion curves are strongly modified in the neighborhood of any resonance. Thus the transition rates can exhibit several peaks. Numerical results are given for a three-photon bound-free transition from the 2S2S2S state of hydrogen.