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Physical Review A

Stimulated radiative corrections in hydrogen in the presence of a strong laser field

Edmond Arnous, J. Bastian, A. Maquet

Published Feb 1, 1983• 21 citations
Publisher

Abstract

The stimulated radiative corrections (or ac-Stark shift, or light shift...) of the energy levels of a hydrogenic atom irradiated by an intense, nonresonant, monomode laser field, are evaluated within the framework of the time-dependent perturbation theory, up to and including fourth order. The calculation is performed by using a Sturmian representation of the Coulomb Green's function. Whenever it is possible, comparison is made with other results, and several limiting cases are considered. If the laser frequency $\ensuremath{\omega}\ensuremath{\rightarrow}0$, one recovers the results of the dc-Stark effect. If $2\ensuremath{\omega}$ becomes larger than the ionization energy of the atomic state considered, the fourth-order level shift acquires an imaginary part which may be connected, via an extension of the optical theorem, to the two-photon ionization cross section. We point out also the difficulties encountered, when trying to get sensible estimates from partial summation of the infinite sums entering the perturbative expression of the fourth-order amplitudes. Finally, the order of magnitude of these various corrections is discussed.

DOI
10.1103/physreva.27.977

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•Oct 17, 2005•16 citations
The stimulated radiative corrections (or ac-Stark shift, or light shift...) of the energy levels of a hydrogenic atom irradiated by an intense, nonresonant, monomode laser field, are evaluated within the framework of the time-dependent perturbation theory, up to and including fourth order. The calculation is performed by using a Sturmian representation of the Coulomb Green's function. Whenever it is possible, comparison is made with other results, and several limiting cases are considered. If the laser frequency \ensuremathω\ensuremath→0\ensuremath{\omega}\ensuremath{\rightarrow}0\ensuremathω\ensuremath→0, one recovers the results of the dc-Stark effect. If 2\ensuremathω2\ensuremath{\omega}2\ensuremathω becomes larger than the ionization energy of the atomic state considered, the fourth-order level shift acquires an imaginary part which may be connected, via an extension of the optical theorem, to the two-photon ionization cross section. We point out also the difficulties encountered, when trying to get sensible estimates from partial summation of the infinite sums entering the perturbative expression of the fourth-order amplitudes. Finally, the order of magnitude of these various corrections is discussed.
Second-order and fourth-order intensity-dependent corrections to the energy levels of the hydrogen atom are calculated. By comparing the results obtained for these two orders and for various values of the principal quantum number, it is seen that, at a given intensity, the second-order correction becomes more and more questionable as one approaches the ionization limit. It is shown how the divergences, which appear in calculating the matrix elements of the shift operator in a discrete basis of continuum functions, can be avoided by performing the computation in the velocity gauge. The relevant second-order numerical results indicate serious modifications of the continuum spectrum. Intrinsic limitations of the second-order calculations are discussed.
The resonant multiphoton resonances shifts and widths and ionization cross-sections for multielectron atoms in a intense laser radiation field are studied. It is carried out a new consistent approach to atom in a strong realistic laser field, based on the relativistic energy formalism (S-matrix adiabatic formalism), relativistic Dirac equation Green function method and relativistic many-body perturbation theory with the Dirac-Kohn-Sham zeroth approximation. In relativistic theory, the Gell-Mann and Low adiabatic formula for energy shift is connected with electrodynamical scattering matrice, which includes interaction with as a laser field as a photon vacuum field (radiative decay). The optimized basis of the relativistic orbitals is generated with using a minimization procedure for the gauge-non-invariant contribution (the fourth-order of the QED perturbation theory) to the radiation width of atomic state. An approach to treating the multiphoton atomic processes is outlined on example of H, Cs, Kr,Mg etc. Analysis shows that the shift and width of the multi-photon resonance line for the interaction “atom- multimode laser pulse” is greater than the corresponding shift and width for a case of the “atom- single-mode pulse” (the Lorenz pulse model) interaction. From the physical point of view it is naturally provided by action of the photon-correlation effects and influence of the laser pulse multi-modity.
Analyses of the resonant multiphoton ionization of atoms require knowledge of ac Stark energy shifts and of multiphoton, bound-to-bound state, transition amplitudes. In this paper, we consider the three-photon photoionization of hydrogen atoms at frequencies that are at and surrounding the two-photon 1s to 2s resonance. AC energy shift sums of both the 1s and 2s states are calculated as a function of the laser frequency along with two-photon 1s ? 2s resonant transition amplitude sums. These quantities are calculated using an extended version of a method, which has often been employed in a variety of ways, of calculating these sums by expressing them in terms of solutions to a variety of differential equations that are derived from the different sums being evaluated. We demonstrate how exact solutions are obtained to these differential equations, which lead to exact evaluations of the corresponding sums. A variety of different cases are analysed, some involving analytic continuation, some involving real number analysis and some involving complex number analysis. A dc Stark sum calculation of the 2s state is carried out to illustrate the case where analytic continuation, pole isolation and pole subtraction are required and where the calculation can be carried out analytically; the 2s state, ac Stark shift sum calculations involve a case where no analytic continuation is required, but where the solution to the differential equation produces complex numbers owing to the finite photoionization lifetime of the 2s state. Results from these calculations are then used to calculate three-photon ionization probabilities of relevance to an analysis of the multiphoton ionization data published by Kyrala and Nichols (1991 Phys. Rev. A 44, R1450).
We compare the derivation of the dynamic Stark shift of hydrogenic energy levels in a classical framework with an adiabatically damped laser-atom interaction, which is equivalent to the Gell-Mann-Low-Sucher formula, and a treatment based on time-independent perturbation theory, with a second-quantized laser-atom dipole interaction Hamiltonian. Our analysis applies to a laser that excites a two-photon transition in atomic hydrogen or in a hydrogenlike ion with low nuclear charge number. Our comparisons serve to demonstrate why the dynamic Stark shift may be interpreted as a stimulated radiative correction and illustrates connections between the two derivations. The simplest of the derivations is the fully quantized approach. The classical and the second-quantized treatment are shown to be equivalent in the limit of large photon numbers.
We compare the derivation of the dynamic Stark shift of hydrogenic energy levels in a classical framework with an adiabatically damped laser-atom interaction, which is equivalent to the Gell-Mann-Low-Sucher formula, and a treatment based on time-independent perturbation theory, with a second-quantized laser-atom dipole interaction Hamiltonian. Our analysis applies to a laser that excites a two-photon transition in atomic hydrogen or in a hydrogenlike ion with low nuclear charge number. Our comparisons serve to demonstrate why the dynamic Stark shift may be interpreted as a stimulated radiative correction and illustrates connections between the two derivations. The simplest of the derivations is the fully quantized approach. The classical and the second-quantized treatment are shown to be equivalent in the limit of large photon numbers.