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Application of state-multipole Heisenberg equations to Raman excitation dynamics

B. Shore, Robert N. Sacks, Shrikrishna N. Joshi

Published Sep 10, 1987• 0 citations
OpenAlex

Abstract

Description of detailed temporal excitation dyanmics for coherent excitation, such as is produced by idealized laser radiation, contrasts with evaluation of rate coefficients by means of generalized Golden Rule procedures; it requires an appropriate time-dependent Schroedinger equation. When the atom undergoing excitation is also affected by incoherent processes, such as collisions, this equation no longer suffices. The Heisenberg equations, or equivalent density-matrix equations, permit treatment in which coherence and incoherence play comparable roles in the excitation dynamics. Unlike rate equations, such equations must incorporate complexities that originate in the orientation degeneracy expressed by magnetic quantum numbers. In simple cases of coherent excitation, both for single-photon and multiphoton excitation, the sublevels merely require an average of 2J+1 independent Schroedinger equations. Relaxation couples the independent equations. It has been known for some time that appropriate state-multipole operators can simplify the description of many phenomena connected with optical pumping. This memo discusses application of these multipole operators to the description of Raman (or more general multiphoton) coherent excitation. In some simple limiting cases the equations simplify, but in general one has a hierarchy of coupled multipole polarizations and coherences in place of the populations and coherences that occur as variables in nondegenerate systems. 28 refs., 4 figs.

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Description of detailed temporal excitation dyanmics for coherent excitation, such as is produced by idealized laser radiation, contrasts with evaluation of rate coefficients by means of generalized Golden Rule procedures; it requires an appropriate time-dependent Schroedinger equation. When the atom undergoing excitation is also affected by incoherent processes, such as collisions, this equation no longer suffices. The Heisenberg equations, or equivalent density-matrix equations, permit treatment in which coherence and incoherence play comparable roles in the excitation dynamics. Unlike rate equations, such equations must incorporate complexities that originate in the orientation degeneracy expressed by magnetic quantum numbers. In simple cases of coherent excitation, both for single-photon and multiphoton excitation, the sublevels merely require an average of 2J+1 independent Schroedinger equations. Relaxation couples the independent equations. It has been known for some time that appropriate state-multipole operators can simplify the description of many phenomena connected with optical pumping. This memo discusses application of these multipole operators to the description of Raman (or more general multiphoton) coherent excitation. In some simple limiting cases the equations simplify, but in general one has a hierarchy of coupled multipole polarizations and coherences in place of the populations and coherences that occur as variables in nondegenerate systems. 28 refs., 4 figs.
Multiphoton excitation and dissociation of large molecules under collisionless conditions is discussed in terms of an intercontinuum random coupling model. The mathematical approach described in a previous paper is used to obtain the general solution for a system of consecutively coupled discrete states, quasicontinuous manifolds, and continuous (dissociative) manifolds of molecular levels (eigenstates of the total molecular Hamiltonian), where the radiative coupling matrix elements are assumed to be given as a linear combination of smoothly varying and randomly varying (over level indices in the molecular manifolds) components. In the range of discrete molecular levels the time evolution is coherent and described in terms of the optical Bloch equation. In the quasicontinuous and continuous ranges the time evolution may be described in terms of Markoffian kinetic equations for the number of photons absorbed by the molecule, provided that the intramolecular vibrational relaxation widths associated with the optically active molecular modes is much larger than the Rabi frequency associated with the excitation of these modes. The kinetic evolution itself consists of direct multiphoton excitation processes (simultaneous transitions from the upper discrete levels to all higher energy molecular manifolds) resulting from the smooth component in the radiative coupling, and a consecutive excitation process described by the Pauli master equation with rates given by the golden rule expression. The interaction which enters into the golden rule expression is the variance in the radiative coupling. The direct excitation component contributes a negligible part of the overall excitation even if the random and smooth radiative coupling components are comparable. The resulting incoherent time evolution of the multiphoton excitation process is consistent with available experimental results. Coherent effects in the time evolution are expected for higher radiation field intensities, where the Rabi frequency becomes comparable to the intramolecular vibrational relaxation rate.
Excitation dynamics for pulsed optical excitation are described with the density-matrix equations and the rate equations for a two-level system. A critical comparison of the two descriptions is made with complete and consistent formalisms that are amenable to the modeling of applied laser-diagnostic techniques. General solutions, resulting from numerical integration of the differential equations describing the excitation process, are compared for collisional conditions that range from the completely coherent limit to the steady-state limit, for which the two formalisms are identical. This analysis demonstrates the failure of the rate equations to correctly describe the transient details of the excitation process outside the steady-state limit. However, reasonable estimates of the resultant population are obtained for nonsaturating (linear) excitation. This comparison provides the laser diagnostician with the means to evaluate the appropriate model for excitation through a simple picture of the breakdown of the rate-equation validity.
The major portion of this monograph discusses how given pulses of laser radiation affect individual atoms. This chapter inverts that relationship, describing how the matter alters the fields. Those field changes provide quantitative measures of the quantum-state changes produced in the atoms. Their description therefore is an adjunct to Chap. 19. Basically the incident radiation produces excitation which, in turn, alters the various multipole moments of the atoms. When viewed as a macroscopic sample of matter, such changes alter the electric polarization field P and the magnetization field M of the matter through which the radiation must pass. The Maxwell equations, see App. C.1, provide the needed description of how the P and M fields alter the electric and magnetic fields E and B . The combination of the Maxwell equations for the fields and the Schrödinger, Bloch, or Liouville equations for the atoms provide the tools needed to construct a self-consistent description of radiation passing through matter – atoms responding to a pulsed field and traveling waves being modified by the resulting atomic changes [All87; Ale92; Muk99; Die06; Vit01a]. The present chapter, drawing on [Sho90, Chap. 12] and App. C, discusses this theory. Incoherent radiation passing through matter typically undergoes exponential attenuation in accord with eqn. (6.9). A measure of the incremental change of intensity in distance L by absorption coefficient κ is the optical depth κ L . This parameter appears in rateequation treatments of incoherent light attenuation.
The two-photon absorption process is discussed using a density matrix formalism. The electromagnetic field is described by means of coherent states, a technique that permits a simple evaluation of the effect of coherence on the transition probability. It is concluded that the latter is the same for a coherent and an incoherent pulse of radiation. In the case of a stationary field containing many modes, the transition probability is nearly the same in the coherent and incoherent cases, whereas for a single mode the transition probability is twice as high for the incoherent field. These conclusions are independent of the multipole expansion of the interaction Hamiltonian and are valid for electric dipole and higher multipole transitions.
The dynamical evolution of an excited-state population in a macroscopic volume of three-level molecules is considered where the population is driven optically between the initial ground state and the excited states by an externally applied (ccc-number) coherent pump. The intermediate and ground states are taken as nonradiatively coupled whereas the excited-to-intermediate-state transition is coupled to the radiation field which is treated quantum mechanically. It is found that stimulated Raman processes can significantly influence the dynamical evolution of population inversion and macroscopic polarization by producing coherence effects among the populations. We examine the evolution of collective relaxation between the excited and intermediate levels in the time regime of the pump pulse duration. It is shown, using the mean-field approximation, that for uniform pumping and conditions such that the pump Rabi rate ${\ensuremath{\omega}}_{R}$, the characteristic collective radiation time ${\ensuremath{\tau}}_{R}$, and the pump pulse duration ${\ensuremath{\tau}}_{P}$ satisfy the inequalities, ${\ensuremath{\omega}}_{R}>\frac{1}{{\ensuremath{\tau}}_{R}}>\ensuremath{\gamma}$ and ${\ensuremath{\tau}}_{P}\ensuremath{\gtrsim}{\ensuremath{\tau}}_{R}$ ($\ensuremath{\gamma}$ is a characteristic internal dephasing rate for the molecules), the system is left in a state with classical transverse polarization when the pump pulse terminates. The system can evolve collectively from such a state only as superradiant (classical) evolution. For superfluorescent evolution which requires a state of preparation of complete inversion (zero transverse polarization), it is shown that the pump pulse must be effectively of area $\ensuremath{\pi}$ and that ${\ensuremath{\tau}}_{P}<{\ensuremath{\tau}}_{R}$. Our results show that when the former conditions are satisfied the delay time ${\ensuremath{\tau}}_{D}$ for collective free pulse evolution is a function of both ${\ensuremath{\tau}}_{P}$ and ${\ensuremath{\tau}}_{R}$. It is shown further that the pump pulse shape as well as temporal duration significantly affect the final state of preparation. The results of this work are interpreted in connection with recent reported results of experiments in superfluorescence and superradiance.
The work is aimed at modeling coherence effects in a dissipative quantum system under the semi-classical density matrix formalism. A number of multiphoton coherence effects have been shown to be feasible by controlling the incoherent pumping mechanism in a generic four-level model. The specialty of the model is in finding inversionless gain without any restrictions being imposed on the decay rates of the driven transitions. Many of the coherence effects, such as absorption cancellation, inversionless gain at the line center, and sidebands of an absorptive line shape accompanied by dispersive switching, are explained using the same model under different parametric conditions. Further, it is shown that modulation in the coherence effects can effectively be controlled by the two- and three-photon excitation mechanisms with the proper choice of the rates of incoherent pumping under a stimulated Raman process. Different conditions of population inversion are found for both coherent and incoherent control of stimulated Raman resonance. In addition to Raman gain, gain without inversion in any standard state basis is found to be achieved in our present model. The proposed scheme can have potential application in controlling the properties of an optical field on propagation through rare earth ion-doped fiber material or other solid-state, as well as atomic, media.