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Journal of Physics B Atomic and Molecular Physics

Effect of adiabatic and near-adiabatic field turn-on on the resonance fluorescence spectrum of a two-level atom

M Edwards

Published Mar 14, 1983• 8 citations
Publisher

Abstract

The author has studied the effect of an adiabatically and near-adiabatically increasing field intensity on the resonance fluorescence spectrum of the two-level atom. There is an asymmetry in the spectrum for off-resonance excitation and that this is due to the fact that the field turn-on repopulates the dressed state which has been depopulated by spontaneous emission. Also found are the conditions under which the temporal shape of the field turn-on may be found in a simple way. Corrections to this shape due to atomic recoil are discussed, and found to be small under typical experimental conditions.

DOI
10.1088/0022-3700/16/5/011

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The author has studied the effect of an adiabatically and near-adiabatically increasing field intensity on the resonance fluorescence spectrum of the two-level atom. There is an asymmetry in the spectrum for off-resonance excitation and that this is due to the fact that the field turn-on repopulates the dressed state which has been depopulated by spontaneous emission. Also found are the conditions under which the temporal shape of the field turn-on may be found in a simple way. Corrections to this shape due to atomic recoil are discussed, and found to be small under typical experimental conditions.
We experimentally study the resonance fluorescence from an excited two-level atom when the atomic upper level is coupled by a nonresonant field to a higher-lying state in a rubidium atomic beam. The heights, widths and positions of the fluorescence peaks can be controlled by modifying the detuning of the auxiliary field. We explain the observed spectrum with the transition properties of the dressed states generated by the coupling of the two laser fields. We also attribute the line narrowing to the effects of Spontaneously Generated Coherence between the close-lying levels in the dressed state picture generated by the auxiliary field. And the corresponding spectrum can be viewed as the evidence of Spontaneously Generated Coherence. The experimental results agree well with calculations based on the density-matrix equations.
We study the transient fluorescence spectra of two-level atoms driven by a strong optical field when the atoms are initially prepared in pure dressed states of the atom-field Hamiltonian. Spectra obtained here differ qualitatively from those observed in the steady state. In the case of steady-state resonant excitation, a three-peaked spectrum symmetric about the laser frequency is obtained; with pure-dressed-state preparation, the symmetry of the spectrum about the driving field is broken---one side peak is initially enhanced and the other is initially suppressed. Furthermore, the temporal oscillations of fluorescence intensity observed in previous calculations of transient fluorescence spectra appropriate to atoms prepared in a superposition of dressed states [J. H. Eberly et al., J. Phys. B 13, 217 (1980)] are suppressed when pure-dressed-state preparation is considered.
The effects of different laser line shapes on the intensity and spectrum of resonance fluorescence from a two-level atom are investigated. The laser model considered is that of an ideal single-mode laser operating high above threshold, with constant amplitude and undergoing phase-frequency fluctuations analogous to Brownian motion. As the correlation time of the frequency fluctuations increases from zero to infinity, the laser line shape changes from Lorentzian to Gaussian in a continuous way. It is shown that for intermediate and strong fields, the average intensity of fluorescence in the case of a resonant broadband Lorentzian line shape is higher than that in the case of a Gaussian line shape with the same bandwidth and total power. This is in contrast to the weak-field case where the higher peak power of the Gaussian line shape makes it more effective than the Lorentzian line shape. It is also shown that in the case of a nonzero frequency correlation time (non-Lorentzian line shape) the intensity of fluorescence undergoes non-Markovian fluctuations. In relation to the spectrum of resonance fluorescence, it is shown that as the line shape is varied from Lorentzian to Gaussian the following changes take place: In the case of off-resonance excitation, the asymmetry of the spectrum decreases. In the case of resonant excitation, the center-peak to side-peak height ratio for the triplet structure increases. Moreover, the recently predicted center-line dip, which develops in the spectrum in the case of broadband excitation when the Rabi frequency and the bandwidth are nearly equal, becomes increasingly deeper.
The resonance fluorescence spectrum of one and two two-level atoms in an ideal cavity with one resonant mode is investigated as a function of the initial excitation of the system. The analysis is carried out in the Stark representation with respect to the cavity's field and in first-order perturbation theory with respect to the fluorescence field. In the absence of the field of the cavity (n c = 0) and under an initial excitation of one atom only, the spectrum consists of two lines which are symmetrical with respect to ωa. In all other cases the spectrum has a central line at ωa and other lines at ωa ± 2 Ω. The intensity of the higher (ωa ± 4 Ω) harmonics is small and decreases as 1/ 2 c c with increasing n>c. The nonlinearity of the interaction hamiltonian results in the parametric (with respect to the field of the cavity) amplification of the ωa + 2 Ω harmonic and the attenuation of the ωa − 2 Ω harmonic. The stimulated emission of the ωa ± 2 Ω harmonics, vanishing in a strong (n c » 1) field, is shown to exist for two atoms.
The resonance fluorescence of a two-level atom interacting with a laser pulse is studied, following the short-pulse approximation. The authors demonstrate that an explicit expression of the energy spectrum in terms of atomic-state amplitudes holds also for an off-resonance excitation. Some analytically solvable cases are studied in detail, showing that the main spectral properties of the fluorescence emitted under adiabatic and non-adiabatic pulsed excitation can be easily described. For the first time the continuous dependence of the fluorescence spectrum on laser detuning is reported for a smooth pulse.