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Physical Review A

Optical Free Induction Decay

Richard G. Brewer, R. L. Shoemaker

Published Dec 1, 1972• 312 citations
Publisher

Abstract

A simple application of the Stark-pulse technique, developed by Brewer and Shoemaker, demonstrates optical free induction decay-the optical analog of free induction decay in NMR. A molecular sample which is coherently prepared by a cw laser beam exhibits such a decay when it is suddenly switched out of resonance by a Stark field. Observations are presented for a nondegenerate Doppler-broadened infrared transition of N${\mathrm{H}}_{2}$D, where the sample is optically thin, and the decay behavior can be compared quantitatively with a solution of the Bloch equations. When the molecular sample is prepared under steady-state conditions, the solutions are analytic; for pulse excitation, a numerical solution is required. The treatment invokes a hard-collision relaxation model. Such characteristics as the abrupt termination of the decay and the related edge echo, which result from Doppler dephasing, can be examined for Stark pulses of finite extent.

DOI
10.1103/physreva.6.2001

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Interference pulses in optical free induction decay

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A new feature of optical free induction decay (FID) is observed in a coherently prepared sample of $^{13}\mathrm{CH}$$_{3}\mathrm{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.

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Oscillatory free-induction decay

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Laser saturation spectroscopy in the time-delayed mode. Theory of optical free induction decay in coupled Doppler-broadened systems

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Stark-induced optical transients in ruby

Arthur G. Szabo, Martin Kroll

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Optics Letters•Jan 1, 1978•38 citations
A simple application of the Stark-pulse technique, developed by Brewer and Shoemaker, demonstrates optical free induction decay-the optical analog of free induction decay in NMR. A molecular sample which is coherently prepared by a cw laser beam exhibits such a decay when it is suddenly switched out of resonance by a Stark field. Observations are presented for a nondegenerate Doppler-broadened infrared transition of NH2{\mathrm{H}}_{2}H2​D, where the sample is optically thin, and the decay behavior can be compared quantitatively with a solution of the Bloch equations. When the molecular sample is prepared under steady-state conditions, the solutions are analytic; for pulse excitation, a numerical solution is required. The treatment invokes a hard-collision relaxation model. Such characteristics as the abrupt termination of the decay and the related edge echo, which result from Doppler dephasing, can be examined for Stark pulses of finite extent.
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.
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.
This paper describes a new class of techniques, called time-delayed laser saturation spectroscopy, which combine frequency- and time-domain methods of laser spectroscopy to provide a way of studying a molecular system as it evolves from an initially prepared stationary state to a second, final state. The specific example analyzed here is three-level free induction decay, in which the time-dependent gain of a Doppler-broadened molecular transition is probed after the sudden termination of an intense field resonating with a coupled transition. The theoretical calculation is based on the coupled density-matrix equations of motion in the slowly-varying envelope approximation. The time-delayed line shapes, which may be studied in either transmission or side fluorescence, exhibit linewidth asymmetries, line-shape deformations, Ramsey-type fringes, power broadening and dephasing, and dynamic Stark splittings and oscillatory decays. The technique provides a unique way of distinguishing the influence of Raman-type processes from that of population saturation and a means to separately measure the associated decay rates. The relationship of the present work to other studies is also discussed.
The Stark-pulse technique of Brewer and Shoemaker allows one to observe phenomena such as optical free-induction decay, optical nutation, and two-photon superradiance. In this paper, we develop a theoretical treatment of these phenomena under the appropriate experimental conditions. The calculations of the free-induction decay and the corresponding optical nutation are shown to be in excellent agreement with experiment. We also discuss the two-photon superradiance phenomenon of Brewer and Shoemaker as a Raman effect appearing in first-order perturbation theory. The analysis illustrates the essential features of the experimental observation.
The optical analog of the nuclear magnetic resonance rotary saturation effect is demonstrated and analyzed. A 9.6-\ensuremath{\mu}m CO2{\mathrm{O}}_{2}O2​ laser resonance excitation of vibrational transitions in gaseous CH3{\mathrm{H}}_{3}H3​F creates an effective splitting in the interaction representation of the optical two-level system. A radio-frequency standing-wave Stark electric field is tuned in rotary saturation resonance with the splitting. The change in transmitted laser beam intensity, because of rotary resonance, is measured in terms of transient optical signals obtained by the Stark switching method of Brewer and Shoemaker. The measured single and multiphoton rotary saturation resonance signals are compared with perturbation and computer solutions of nonlinear Bloch-Maxwell macroscopic equations. Doppler-free rotary saturation spectra are obtained in the presence of inhomogeneous Doppler broadening by a special scheme of Fourier analysis. A discussion is presented of the coupling of energy between two traveling waves that are in double resonance with the optical two-level system. The concept of spin temperature is discussed in relation to a coherently excited optical level system with a long fluorescence lifetime. The possibility of a cross-relaxation double resonance experiment between an optical system and a spin system is outlined.