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Journal of the Optical Society of America B

Close coupled scattering calculations on the collisional redistribution of light

Paul S. Julienne, Frederick H. Mies, Linda L. Vahala

Published Feb 1, 1987• 0 citations
OpenAlex

Abstract

The close coupled theory of collisions in a radiation field provides a natural tool for studying the interaction of light with colliding atoms. Since the radiative and collisional interactions are treated equivalently in the set of coupled equations, the theory allows us to calculate the distribution of excited atomic product states which result from the nonadiabatic dynamics following photon absorption during an atomic collision.

Related papers

Nonadiabatic theory of atomic line broadening: Final-state distributions and the polarization of redistributed radiation

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The close-coupled theory of atomic collisions in the presence of a radiation field may be used to calculate the distribution of final atomic states which results from absorption of polarized light during a collision. The theory applies equally well to optical collisions (line broadening) and to radiative collisions (laser-induced collisional energy transfer). For an optical collision the detuning $\ensuremath{\omega}\ensuremath{-}{\ensuremath{\omega}}_{\ensuremath{\infty}}$ is restricted to be larger than either the Rabi frequency or the widths due to natural, Doppler, or pressure broadening. The radiation field is assumed to be weak enough that the transition probabilities are linear in field intensity. The molecular picture is emphasized in which the wave function is expanded in a basis of field-free molecular states and the Hamiltonian is blocked in accordance with molecular quantum numbers. The quantities needed to predict experimental observables are reduced radiative scattering $S$-matrix elements ${s}_{\ensuremath{\omega}}$ in the asymptotic Hund's case-(e) representation. The theory of product orientation and alignment is equivalent to that which has been developed for molecular photodissociation. It requires coherent sums of ${s}_{\ensuremath{\omega}}$ matrix elements from different transition branches, that is, for $P$-, $Q$-, and $R$-type transitions corresponding to changes of -1, 0, and +1 in total molecular angular momentum. On the other hand, the total absorption coefficient and the branching ratio to different final fine-structure states irrespective of orientation or alignment depend on incoherent sums of the same matrix elements.

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The close coupled theory of collisions in a radiation field provides a natural tool for studying the interaction of light with colliding atoms. Since the radiative and collisional interactions are treated equivalently in the set of coupled equations, the theory allows us to calculate the distribution of excited atomic product states which result from the nonadiabatic dynamics following photon absorption during an atomic collision.
The close-coupled theory of atomic collisions in the presence of a radiation field may be used to calculate the distribution of final atomic states which results from absorption of polarized light during a collision. The theory applies equally well to optical collisions (line broadening) and to radiative collisions (laser-induced collisional energy transfer). For an optical collision the detuning $\ensuremath{\omega}\ensuremath{-}{\ensuremath{\omega}}_{\ensuremath{\infty}}$ is restricted to be larger than either the Rabi frequency or the widths due to natural, Doppler, or pressure broadening. The radiation field is assumed to be weak enough that the transition probabilities are linear in field intensity. The molecular picture is emphasized in which the wave function is expanded in a basis of field-free molecular states and the Hamiltonian is blocked in accordance with molecular quantum numbers. The quantities needed to predict experimental observables are reduced radiative scattering SSS-matrix elements ${s}_{\ensuremath{\omega}}$ in the asymptotic Hund's case-(e) representation. The theory of product orientation and alignment is equivalent to that which has been developed for molecular photodissociation. It requires coherent sums of ${s}_{\ensuremath{\omega}}$ matrix elements from different transition branches, that is, for PPP-, QQQ-, and RRR-type transitions corresponding to changes of -1, 0, and +1 in total molecular angular momentum. On the other hand, the total absorption coefficient and the branching ratio to different final fine-structure states irrespective of orientation or alignment depend on incoherent sums of the same matrix elements.
We extend the theory of light scattering from an atom undergoing collisions to the case of strong laser fields, where the expansion in powers of $\ensuremath{\Omega}{\ensuremath{\tau}}_{c}$ that was used formerly in a series of papers by Burnett et al. breaks down. In particular we consider in detail the conditions necessary to relate the observable quantities to intense-field collisional rate constants in a dressed-state basis (such as those calculated by Light and Sz\"oke). We also show (following Rabin and Ben-Reuven) that by studying the spectrum emitted by the atoms in the presence of a strong field one may measure the collisional rates for transfer between the dressed states of atom plus radiation field.
Perturbation theory for the interaction of light with a binary system is applied to collisional redistribution of radiation in the weak-field limit. Within the very large domain of validity of the binary model applied to collisions between non-hydrogenic atoms and atomic perturbers at low densities, redistribution can be viewed as collisional-induced absorption followed by spontaneous decay during a second collision. The formalism can be applied from the quasimolecular domain at large detunings Delta omega 1 or Delta omega 2 up to the impact regime, but emphasis is placed here on the non-impact region, at small Delta omega 1 or Delta omega 2, where non-adiabatic effects are important in collision-induced radiative absorption or emission rates as well as in the redistribution. The impact limit of the redistribution function is easily rederived in this way.
We apply the analysis of paper I to degenerate atomic systems and calculate the effect of correlations between an atom (the absorber) and perturbers in the binary-collision approximation. The result of our calculation is a generalized absorption profile that specifies the final state of the atom an absorption event. This profile is then related to the total intensities of Rayleigh scattering and fluorescence (redistributed radiation) from the atom. The profile is expressed in terms of collision operators that depend on the index of the multipole of the atom that is created. Some of the operators represent correlations between radiative and collisional events and cannot, except in certain limits, be expressed in terms of the usual line-broadening operators. This, of course, implies that one needs extra dynamical information, on top of that obtainable from ordinary absorption experiments, to be able to describe redistribution. Conversely, redistribution offers a probe of collisional dynamics, not given by absorption experiments, via the polarization of fluorescent light. We give practical expressions for the calculation of these operators and discuss their implications.
We present a calculation of the scattering of monochromatic radiation by a degenerate atom in the binary-collision approximation. We limit ourselves to field strengths such that $\ensuremath{\Omega}{\ensuremath{\tau}}_{c}\ensuremath{\ll}1$, where $\ensuremath{\Omega}$ is the Rabi frequency for the atomic transition, and ${\ensuremath{\tau}}_{c}$ is the duration of a strong collision. Our calculation is not limited to the impact regime, $\ensuremath{\Delta}\ensuremath{\omega}\ensuremath{\ll}{\ensuremath{\tau}}_{c}^{\ensuremath{-}1}$, or to the region where thermal correlations may be neglected, i.e., $\ensuremath{\Delta}\ensuremath{\omega}\ensuremath{\ll}\frac{\mathrm{kT}}{\ensuremath{\hbar}}$. (Here $\ensuremath{\Delta}\ensuremath{\omega}$ is the difference between either the incoming or outgoing photon's frequency and the atom's natural frequency.) To do this we derive an equation of motion for the correlation function, valid outside the quantum-regression regime, whose solution for practical cases is straightforward. We present solutions for the weak-field (linear-response) regime in terms of generalized absorption and emission profiles that depend on the indices of the atomic multipoles created.
The close-coupled theory of collisions in a radiation field is used to calculate the absorption profile for the Sr $^{1}\ensuremath{\leftarrow}^{1}$S resonance line broadened by collisions with Ar. The calculations predict the polarization ratios of Sr 1P^{1}\mathrm{P}1P fluorescence following line wing excitation by either linear or circular polarized light. Ab initio calculations were used to obtain the ground and excited SrAr molecular-potential curves, which were adjusted to give improved agreement with experiment. The radiative-scattering theory gives a unified description of the absorption coefficient and polarization redistribution from the small detuning impact limit region to the far spectral wings. The cross sections for elastic and inelastic depolarizing collisions of Sr 1P1^{1}\mathrm{P}_{1}1P1​+Ar were also calculated. The calculated absorption coefficient, impact-broadening rate, linear- and circular-polarization ratios, and depolarization rate coefficients are for the most part in good agreement with experiment.