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Physical Review A

Atomic motion in a two-mode laser field

Leonard Rosenberg

Published Oct 10, 2000• 2 citations
Publisher

Abstract

A modified perturbation theory is developed for the calculation of the time-dependent wave function describing the propagation of an atom in a two-mode laser field. With the mode frequencies nearly equal, a first approximation is obtained that reproduces and extends known results, for both resonant and nonresonant transitions. This lowest-order solution sums terms that describe the absorption of a photon from one mode and emission into the other, leaving the total number of photons unchanged and shifting the momentum of the atom accordingly. Corrections are generated by expansion of a resolvent from which the nearly degenerate states have been projected out. These approximate solutions are used to construct asymptotic states in a formulation of atom-atom scattering in the two-mode field. In close analogy with the soft-photon approximation, a ``soft-pair'' approximation is developed based on the dominance of those asymptotic interactions in which the transfer of energy from the field to the atom is small, allowing one to relate the scattering amplitude in the presence of the field to the field-free amplitude. When the atomic ground state and an excited state are closely coupled by the field, the asymptotic wave function can have mixed parity allowing for long-range contributions to the effective potential. In addition to an enhancement of forward-scattering probabilities, this leads to a threshold anomaly that is analyzed here, in the resonant case, with the aid of a modified effective-range theory.

DOI
10.1103/physreva.62.053401

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A modified perturbation theory is developed for the calculation of the time-dependent wave function describing the propagation of an atom in a two-mode laser field. With the mode frequencies nearly equal, a first approximation is obtained that reproduces and extends known results, for both resonant and nonresonant transitions. This lowest-order solution sums terms that describe the absorption of a photon from one mode and emission into the other, leaving the total number of photons unchanged and shifting the momentum of the atom accordingly. Corrections are generated by expansion of a resolvent from which the nearly degenerate states have been projected out. These approximate solutions are used to construct asymptotic states in a formulation of atom-atom scattering in the two-mode field. In close analogy with the soft-photon approximation, a ``soft-pair'' approximation is developed based on the dominance of those asymptotic interactions in which the transfer of energy from the field to the atom is small, allowing one to relate the scattering amplitude in the presence of the field to the field-free amplitude. When the atomic ground state and an excited state are closely coupled by the field, the asymptotic wave function can have mixed parity allowing for long-range contributions to the effective potential. In addition to an enhancement of forward-scattering probabilities, this leads to a threshold anomaly that is analyzed here, in the resonant case, with the aid of a modified effective-range theory.
Dressed states of an atom in a classical laser field of frequency close to an atomic transition frequency are obtained, which are a considerable improvement over the usual two-level rotating-wave approximation. These wave functions are used in a calculation of the cross section for elastic electron-atom scattering in a laser field. Numerical calculations for electron-hydrogen scattering demonstrate that scattering involving absorption or emission of photons can be strongly influenced by coupling to the nonresonant states, regardless of the field strength. Inclusion of the counter-rotating terms in the calculation is shown to be essential for extending the applicability of the theory to scattering in nonresonant fields, where a first-order perturbation-theoretic treatment of the atom-field interaction would be expected to be quite justified.
The motion of a two-level atom in a standing-wave laser field is studied using an approximation to the resolvent operator in the form of a truncated eigenfunction expansion, with the field treated in the occupation-number representation. The formalism provides expressions for the time-dependent S -matrix for transitions into both ground and excited atomic states. The effective Hamiltonian for purely elastic scattering is constructed, allowing for the direct study of scattering in the Bragg regime. Contact with standard treatments of Bragg scattering in terms of Mathieu functions is obtained by imposition of additional approximations. Comparison of numerical results obtained with and without imposition of these approximations provides an indication of their range of validity. The dependence of excitation probabilities on field strength and detuning is studied. These numerical illustrations provide evidence that in cases of physical interest excitation probabilities can be significant and can be reliably estimated for a broad range of field parameters using the present formalism.
A successive-approximation procedure for calculating multiphoton-transition amplitudes is presented. The theory, designed for use in the strong-field domain where ordinary perturbative methods are unsuitable, provides an extension of previous work along these lines by inclusion of the effects of free-free transitions, i.e., interactions with the field which take the atomic system from one continuum state to another. This approach is based on the introduction of an effective Hamiltonian which operates only in the subspace of states, degenerate or nearly degenerate, among which real transitions can take place. Contributions from virtual intermediate states are included in the structure of the effective potential. This approach provides the framework for the construction of models, defined by the approximations made for the effective potential, which build in the constraints of unitarity and which properly account for the effects of intermediate-state resonances. The present work is focussed on those new features of the problem which arise from the fact that both the electron and the residual atom to which it was originally bound can interact with the field in asymptotic states. To avoid complications associated with long-ranged Coulomb effects, the residual atom is assumed to be neutral. (The initial state is a negative ion.) An approximation procedure is described for calculating the field-modified asymptotic states appropriate for such a system. By way of an illustrative example a low-frequency approximation is given which leads to considerable simplification of the calculational procedure.
A wave function for laser dressed atom is derived as a perturbative solution of the time-dependent Schrodinger equation in the velocity gauge. With the use of the average excitation energy approximation and the closure approximation, the solution is reduced to a time-dependent operator acting on the ”bare” atomic state. In soft-photon approximation, the average excitation energy only appears in the first and second order terms of field frequency. Such a simplified dressed wave function is useful in the calculation of laser-assisted scattering, especially in the laser-assisted rearrangement collisions.
We develop a time-dependent perturbation theory (PT) beyond the dipole approximation to analyze the two-photon ionization dynamics of atoms exposed to short laser pulses with an arbitrary polarization. In a wide range of laser parameters, the good performance of the PT method is validated by comparing the results of a number of physical quantities with those calculated by numerically solving the time-dependent Schr\"odinger equation beyond the dipole approximation. Subsequent applications of the PT method in the nonresonant regime allow us to unveil the important role of the interferences between the dipole and nondipole transition pathways to the photoelectron momentum shift along the laser-propagation direction. In particular, we find that the ratio of the probability of each dipole transition channel to the total ionization probability oscillates with the increase of the photon energy. The interferences among different pathways and the oscillatory behavior of the ratios jointly lead to a series of minima in the linear momentum transfer for the case of the linear polarization.
Resonant two-photon absorption is discussed for the case in which the exciting field may be intense enough and near enough to resonance to cause appreciable saturation. A single pair of levels in an otherwise quite general atom is assumed to satisfy the appropriate resonance condition, and equations are derived governing the time evolution of the associated 2 \ifmmode\times\else\texttimes\fi{} 2 submatrix of the full atomic density matrix. Atomic relaxation is treated explicitly. The analysis, which treats both inversion-symmetric and inversion-nonsymmetric cases within the same general formalism, is developed systematically, the necessary approximations receiving careful discussion. The results are analogous to those for the corresponding one-photon process, but with a shift in the resonance frequency proportional to the intensity of the exciting field. This frequency shift is not identical to the one calculated by time-independent (second-order) perturbation theory, and becomes large when the energy of an intermediate state of the atom approaches the mean of the energies of the active states.