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Japanese Journal of Applied Physics

Optical Free Induction Decay in Cold85Rb Atoms

Unyob Shim, S. B. Cahn, Anantharaman Kumarakrishnan, Tycho Sleator, Jin‐Tae Kim

Published Jun 15, 2002• 9 citations
Publisher

Abstract

We have observed optical free induction decay (FID) in cold 85 Rb atoms. The shortening of the FID lifetime with increasing optical depth of the trap has been found. This shortening is explained by an anomalous absorption for FID propagating in a homogeneous and resonant sample. Theoretical calculations are consistent with experimental results. The Rabi oscillations of FID amplitude have been observed by increasing the pulse area.

DOI
10.1143/jjap.41.3688

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We have observed optical free induction decay (FID) in cold 85 Rb atoms. The shortening of the FID lifetime with increasing optical depth of the trap has been found. This shortening is explained by an anomalous absorption for FID propagating in a homogeneous and resonant sample. Theoretical calculations are consistent with experimental results. The Rabi oscillations of FID amplitude have been observed by increasing the pulse area.
We report theoretical and experimental studies of the propagation of a square-modulated laser pulse through a laser-cooled atomic ensemble of two-level absorbers, as well as through a three-level system with electromagnetically induced transparency. We find that the transmission characteristics over a wide range of optical depth can be fully accounted for as optical coherent transients excited by the wide spectral content of the square-modulated optical pulse. We show that both time-domain atom-field coupled equations and frequency-domain linear dispersion theory give precisely the same description of the optical transients at a weak power limit. At low optical depth with moderate absorption, resonant excitation dominates and free-induction decay (FID) contributes mostly to the transient field. At high optical depth when absorption and propagation effects become significant, lossless optical precursors start to dominate the transient response. By varying the optical depth from 0 to 45, we observe that optical transients evolve gradually from FID to optical precursors. We thus show that FID and optical precursors, which have been considered as two different optical transients for many decades, can be unified within a single theoretical frame and they are the manifestations of the same physical process in two different regimes.
Optical free-induction decay (FID) of laser-cooled 85{}^{85}85Rb has been observed. Considerably good agreements are obtained between experiments and theoretical calculations in the condition of no inhomogeneous broadening. The possibility to apply optical FID measurements to the studies of phase relaxation in a dense atom trap is discussed.
We report the observation of coherent two-photon free-induction decay (FID) in a three-level Lambda system excited by a low-intensity square-modulated laser pulse. Using electromagnetically induced transparency in an Rb85 cold atomic cloud, for what we believe to be the first time, we observe FID signals with coherence time exceeding the relevant atomic excited-state natural lifetime. Because of the on-resonance enhancement, the two-photon FID signal can be observed at the falling edge without using heterodyne means.
The after-saturation free-induction-decay (FID) rate of an electron spin transition has been measured in a dilute ruby sample, and a marked departure from the Bloch-like behavior has been found. The similarity with the results obtained recently by Szabo and Muramoto [Phys. Rev. A 39, 3992 (1989)] in the same system but for optical FID points out the close link between the non-Bloch behavior of the FID emission observed in optics and in magnetic-resonance systems. Our results are compared with the theoretical predictions of a statistical theory of the FID emission, but poor agreement is found.
Large-amplitude oscillations are predicted in the free-induction decay (FID) of atomic or spin two-level quantum systems that are coherently prepared by a resonant electromagnetic field in the form of a square amplitude pulse of duration TTT. The effect should be detectable in nuclear magnetic resonance (NMR) or in optical resonance experiments when the transition line shape is inhomogeneously broadened (${T}_{2}^{*}\ensuremath{\ll}{T}_{2}$) and the applied field is intense enough that the pulse area $\ensuremath{\chi}T\ensuremath{\ge}2\ensuremath{\pi}$, where $\ensuremath{\chi}$ is the Rabi frequency. Physically, the effect is due to Rabi oscillations which are generated in the preparative stage and are then reproduced because of atomic memory in the radiative period which follows. The atomic polarization derived from the Bloch equations assumes the form of an integral over the inhomogeneous line shape, and can be evaluated numerically for arbitrary linewidth $\ensuremath{\sigma}$ or analytically when $\ensuremath{\sigma}\ensuremath{\rightarrow}\ensuremath{\infty}$. The characteristics of the oscillation are unusual since the oscillation frequency, which is of order $\ensuremath{\chi}$, increases with time while the oscillation envelope vanishes identically for times $t\ensuremath{\ge}2T$. Coherent emission is therefore confined to one pulse width TTT immediately following the pulse. Previous NMR and infrared FID experiments with small-area pulses ($\ensuremath{\chi}T\ensuremath{\le}4\ensuremath{\pi}$), interpreted erroneously in terms of an edge echo effect, support the oscillatory FID behavior described here. For the case $\ensuremath{\chi}T>4\ensuremath{\pi}$, an experimental test would be even more decisive, as the oscillations are more pronounced.
A new feature of optical free induction decay (FID) is observed in a coherently prepared sample of 13CH^{13}\mathrm{CH}13CH3F_{3}\mathrm{F}3​F by the method of Stark switching. The preparative phase is due to the resonant steady-state excitation by a cw laser beam, and is followed by FID upon sudden application of a dc Stark field that switches the molecular sample out of resonance. The emission is not observed as a simple decay but instead appears as a train of sharp pulses regularly spaced in time as a result of a repetitive interference. This situation arises because an entire set of infrared transitions within the Stark split manifold are initially prepared, in contrast to our previous study of a nondegenerate transition. The emission, which beats with the laser, produces a heterodyne beat spectrum, consisting of a set of regularly spaced frequencies, that is the Fourier transform of the slowly decaying pulse progression observed. We thus demonstrate what is the optical analog of the well-known NMR method of high-resolution pulse Fourier spectroscopy. The detailed behavior of the pulse train agrees well with an FID theory that assumes the transitions to be uncoupled. The subtle behavior of FID near the time origin is explored also by approximate analytic expressions that reveal either a near zero amplitude or sizable amplitude depending on the degree of saturation in the preparative stage. The experimental technique discussed offers an attractive way for obtaining high-resolution optical spectra without Doppler broadening, and for generating an optical pulse train whose time scale can be compressed by simply increasing the Stark field.