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The Journal of Chemical Physics

Quasicontinuum effects in molecular excitation

Erkki Kyrola, Joseph H. Eberly

Published Feb 15, 1985• 46 citations
Publisher

Abstract

We study a model where two discrete levels are coupled to a band of closely spaced levels forming a quasicontinuum (QC). This model describes how the initial-stage coherence in multiphoton excitation of polyatomic molecules interferes with the recurrent time dynamics due to the QC coupling. The time evolution of the system is solved exactly assuming the QC to be infinite, flat, and uniform; and a detailed investigation of different special cases is carried out. Weak QC excitation is found to exhibit features which are connected to few level dynamics rather than to an irreversible decay, and we study how this modifies the absorption cross section and the Rabi oscillations. The conditions for coherent trapping are discussed.

DOI
10.1063/1.448368

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The Journal of Chemical Physics•Feb 1, 1980•40 citations
We study a model where two discrete levels are coupled to a band of closely spaced levels forming a quasicontinuum (QC). This model describes how the initial-stage coherence in multiphoton excitation of polyatomic molecules interferes with the recurrent time dynamics due to the QC coupling. The time evolution of the system is solved exactly assuming the QC to be infinite, flat, and uniform; and a detailed investigation of different special cases is carried out. Weak QC excitation is found to exhibit features which are connected to few level dynamics rather than to an irreversible decay, and we study how this modifies the absorption cross section and the Rabi oscillations. The conditions for coherent trapping are discussed.
The photoexcitation of a quasicontinuum of atomic or molecular levels by a laser pulse with a fast rise-time is considered. We first generalize non-perturbative treatments of quasicontinuum excitation. A second general theoretical method is developed in which resonant states are considered non-perturbatively whereas background non-resonant states are included through a perturbative approximation. As a simple example we show how our method describes the photoexcitation of a quasicontinuum of equally spaced levels, exhibiting Rabi oscillations periodically perturbed by background states. We then examine the case of a Rydberg series of highly excited states coherently excited from a low-lying initial state. The time evolution of the coherent superposition of Rydberg levels is shown to be a perturbed Rabi oscillation, but without the periodic disruption of the equally spaced quasicontinuum. Finally, we include the effect of further excitation to a second continuum.
We study the coupling of an initially occupied single level to an N-level quasi-continuum (QC) using perturbation theory. The single-level amplitude is expressed as a sum of harmonically oscillating factors whose dephasings and rephasings give rise to decay and recurrences, respectively. In particular, we study the most common model of this coupling in which the QC is infinite, uniform, and flat. We derive simple approximate formulas for resonant and nonresonant excitation that display absorption-rate reversal and enhancement effects and periodic time evolution. We show how these properties can be connected to few-level dynamics. The limits of applicability of few-level approximations are investigated.
We use a semlclassical, effective-state approach to laser pulse propagation in a gas of polyatomic molecules. Our numerical model of multiple-photon excitation includes quasicontinuum transitions to calculate the effects of coherent propagation on multiple- photon absorption. The molecular model consists of a single ground state and several bands of discrete states, which are successively connected by means of electric-dipole transitions.1 This model correctly simulates some of the major characteristics of multiple- photon absorption, such as power threshold, fluence-dependent absorption, and complete population inversion at large fluences. As the pulse propagates, the Rabi oscillations induced in the lower-level states are encoded onto the pulse and create a series of peaks and troughs similar to those found in pulse propagation in two-level systems.2 Another coherent propagation effect that can change the excitation process is coherent sideband generation. Temporal distortions and the generation of new frequencies result in changes in the population distribution among the states, as well as changes in the total population transferred to the quasicontinuum. The effective increase in total population transfer by propagation effects is offset by the decrease in fluence. The resulting transfer of energy from the pulse to the molecule depends strongly on the initial characteristics of the pulse.
Using a semiclassical, effective-state approach to laser pulse propagation in a dilute gas of polyatomic molecules, a numerical model of multiphoton excitation which includes quasi- continuum transitions is used to calculate the effects of coherent propagation on multi-photon absorption. The initial laser field is assumed to be a quasimonochromatic Gaussian envelope which is nearly resonant with a portion of the lower vibrational states of the molecule. The molecular model consists of a single ground state and several bands of discrete states which are successively connected via electric dipole transitions. This model correctly mimics some of the major characteristics of multiphoton absorption, such as power threshold, fluence dependent absorption, and complete population inversion at high fluences. The model also allows for the calculation of the polarization induced in the medium by the electric field, and the subsequent influence that the polarization has on the field. As the pulse propagates, the Rabi oscillations induced in the lower level states become encoded onto the pulse, creating a series of peaks and troughs similar to the behavior of pulse propagation in two-level systems. Another coherent propagation effect which can change the excitation process is coherent sideband generation. The temporal distortions and the generation of new frequencies results in changes in the population distribution among the states, as well as changes in the total population transferred to the quasi-continuum. The pulse reshaping occurs while the total fluence of the pulse is decreasing due to energy loss to the quasi-continuum. The effective increase in total population transfer due to propagation effects is offset by the decrease in fluence. The resulting transfer of energy from the pulse to the molecule depends strongly on the initial characteristic of the pulse. These processes play an important role in any system where the efficient transfer of laser energy to the medium is required, such as laser-induced chemistry and laser isotope separation.
In this paper we present a quantum mechanical theory of multiphoton photodissociation of large, collision-free, molecules, which rests on the notion that the radiative coupling terms between adjacent sets of congested bound molecular states in the quasicontinuum exhibit a wide variation both in terms of magnitude and of sign. Invoking the rotating-wave approximation, neglecting spontaneous infrared decay, and assuming that near-resonant radiative coupling prevails, the equations of motion were solved within the framework of the random radiative coupling model for the radiative interactions in the quasicontinuum. In the low energy range (range I) the equations of motion for the amplitudes are determined by the effective Hamiltonian formalism, while in the quasicontinuum (range II) the populations are governed by kinetic equations for sequential reversible decay. All the features of coherent excitation are preserved for range I, while in range II intramolecular erosion of phase coherence effects prevails. This model provides a set of reasonable predictions.
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.