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Journal of Physics B Atomic and Molecular Physics

The physical spectra of a two-level atom driven by an exponentially-decaying pulse

S Kryszewski

Published Jul 14, 1985• 9 citations
Publisher

Abstract

Resonance fluorescence from the two-level atom in the field of a resonant, exponentially-decaying pulse is considered when the spontaneous linewidth may be neglected. The analytical expressions for the physical spectra are given and discussed for any field strength and any pulse decay time. The approximation schemes for large and small pulse areas are presented and illustrated by numerical results. In the latter case line narrowing is obtained, while the former corresponds to the near-adiabatic case.

DOI
10.1088/0022-3700/18/13/015

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Resonance fluorescence from the two-level atom in the field of a resonant, exponentially-decaying pulse is considered when the spontaneous linewidth may be neglected. The analytical expressions for the physical spectra are given and discussed for any field strength and any pulse decay time. The approximation schemes for large and small pulse areas are presented and illustrated by numerical results. In the latter case line narrowing is obtained, while the former corresponds to the near-adiabatic case.
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We have considered the induced processes that occur in a driven two-level atom, where a laser photon is absorbed and emitted by the ground and by the excited states of the atom, respectively. In the low-intensity limit of the laser field, the induced spectra arising when a laser photon is absorbed by the ground state of the atom consist of two peaks describing induced-absorption and stimulated-emission processes, respectively, where the former prevails over the latter. Asymmetry of the spectral lines occurs at off-resonance and its extent depends on the detuning of the laser field. The physical, process where a laser photon is emitted by the excited state is the reverse of that arising from the absorption of a laser photon by the ground state of the atom. The former differs from the latter in that the emission of a laser photon by the excited state occurs in the low-frequency regime and that the stimulated-emission process prevails over that of the induced absorption. In this case, amplification of ultrashort pulses is likely to occur without the need of population inversion between the optical transitions. The computed spectra are graphically presented and discussed.
We investigate the steady-state spontaneous emission spectrum of a three-level atom driven by two coherent fields and the absorption spectrum of a weak probe passing through a collection of such driven atoms. We find that the fluorescence spectrum is strongly affected by the decay rates of all the levels involved in the atomic evolution and not just by the decay parameters of the specific transition whose emission spectrum is being monitored. In particular, the spectral components can acquire very different widths and peak heights relative to the case of the standard resonance fluorescence in which a two-level system is driven by a single near-resonant field. An external probe signal passing through the gas of three-level atoms may be absorbed or amplified, as in the standard two-level case, but under specific operating conditions, amplification (or absorption) occurs over the entire range where the atomic response is appreciable. In this case the existence of amplification or absorption is controlled solely by the population difference between two dressed states of the system. We provide numerical results in support of our arguments for arbitrary values of the atomic and field parameters and also develop an analytic description in the limit of strong driving fields that leads to explicit line-shape and linewidth formulas.
A study is presented for the time-dependent resonance-fluorescence spectrum of two-level atoms irradiated by hyperbolic-secant pulsed lasers, allowing for an arbitrary spontaneous-emission rate from the excited level to the ground level. Novel features of the temporally transient spectrum have been observed. The spectrum is dominated by a central peak which oscillates in time and is accompanied by multiple side peaks. Asymptotically (i.e., after the pulse has passed) the side peaks disappear, leaving a tail at the line center which displays a Lorentzian shape of width equal to the sum of the spontaneous-emission rate and the width of the spectrometer considered and of magnitude proportional to the instantaneous intensity of the pulse. The exact behavior of the spectrum is dictated by the area of the engaged pulse and by how the atom is prepared initially. In particular, it is found that the spectrum can be asymmetric even when the laser is tuned to exact resonance if the atoms are initially prepared in a certain class of proper coherent states, irrespective of how the field amplitude may vary in time. An analysis of the spectral symmetry without resorting to any explicit evaluation of the spectrum itself is also presented. Furthermore, the associated optical Bloch equations are solved analytically in terms of hypergeometric functions in a similar manner to that done previously for the undamped two-level Schr\"odinger equation. Specific numerical results are presented for pulses of area equal to \ensuremath{\pi}, 2\ensuremath{\pi}, 3\ensuremath{\pi}, 4\ensuremath{\pi}, and 5\ensuremath{\pi} for both symmetric and asymmetric cases.