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Optics and Spectroscopy

Quantum beats in stimulated electronic raman scattering of ultrashort laser pulses

Anahit L. Gogyan, Yu. P. Malakyan

Published Nov 1, 2006• 6 citations
Publisher

Abstract

A theory of quantum beats in a Stokes signal observed in pump-probe experiments upon excitation of four-level atoms with two close upper lying levels by femtosecond laser pulses is developed. Quantum beats arise in the intensity of the Stokes field due to the interference of two atomic wave packets generated by ultrashort pump and probe pulses. An analytical solution of the non-steady-state Maxwell-Bloch equations is obtained, and the dependence of the Stokes radiation intensity on the delay time between two laser pulses is investigated. The theoretical results describe qualitatively well the observed features of quantum beats.

DOI
10.1134/s0030400x06110154

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Physical Review A•Jul 1, 1973•76 citations
A theory of quantum beats in a Stokes signal observed in pump-probe experiments upon excitation of four-level atoms with two close upper lying levels by femtosecond laser pulses is developed. Quantum beats arise in the intensity of the Stokes field due to the interference of two atomic wave packets generated by ultrashort pump and probe pulses. An analytical solution of the non-steady-state Maxwell-Bloch equations is obtained, and the dependence of the Stokes radiation intensity on the delay time between two laser pulses is investigated. The theoretical results describe qualitatively well the observed features of quantum beats.
A quantum theory of stimulated Raman scattering is presented that takes into account three-dimensional propagation and collisional dephasing, allowing the study of the spatial and temporal coherence properties of the generated Stokes light. Maxwell-Bloch equations for the Stokes field operator and the collective atomic operators are solved analytically under low-signal-gain conditions, where the laser field and the atomic ground states remain undepleted. The intensity and the space-time autocorrelation function of the Stokes field are calculated. The Stokes field is expanded into a set of statistically independent ``coherence modes,'' which are determined explicitly for the case of a cylindrically shaped pumped volume. The Stokes pulse energy W is found to fluctuate from pulse to pulse. The probability distribution function for pulse energies P(W) is calculated for a range of Fresnel numbers of the excited volume and collisional dephasing rates. For small values of Fresnel number and dephasing rate, P(W) is a negative exponential distribution. For large values of either, P(W) narrows and approaches a Gaussian-shaped distribution. This occurs because many independent modes contribute to the Stokes emission, making it spatially and/or temporally incoherent.
A quantum theory of stimulated Raman scattering is established that takes into account the time-dependence of pump laser pulse, two-photon detuning and atomic populations, allowing the general transient and spatial propagation study of Raman memory. Heisenberg–Langevin and Maxwell equations for the collective atomic operators are solved analytically under adiabatic condition , where the electric field envelopes and the collective atomic operators vary slowly. The analytical solution of Stokes/anti-Stokes signal electric field operator is obtained. The spatial–temporal intensity of quantum signal field is studied numerically and analytically for different two-photon detunings and initial populations.
A three-dimensional quantum theory of stimulated Raman scattering is presented which takes into account a general transverse shape of the pump laser. The transverse spatial autocorrelation function and the intensity of the Stokes pulse are derived analytically, by use of the Maxwell-Bloch equations in low-signal-gain conditions and introduction of a many-spatial-modes approximation. We find that the spatial and temporal coherence are coupled. The transverse coherence depends on the pump-laser shape, and the coherence area increases with increasing gain. Time scales for the buildup of stimulated intensity and correlations for the various transverse parts of the Stokes pulse are obtained.
A theory of stepwise pulsed-laser excitation of cascade Zeeman quantum beats has been developed for a four-level system. The laser pulses are treated in the broad-line approximation and the full optical-pumping equations for the atomic-density matrix of each level have been obtained. These can be used to describe saturation and light shift effects. The weak-pumping theory solutions to the optical pumping equations have been used to obtain expressions for the cascade quantum-beat intensity versus time curves. Larmor precession, spontaneous-emission decay and the populating of the final cascade level during the excitation pulse are all allowed for. A Wiener-Levy phase diffusion model with slowly varying amplitudes is used for the laser pulses, and the final theoretical expressions for the quantum beats depend on the time-dependent intensities of the laser pulses as well as on their polarisations. Hyperfine effects have been ignored. The theory applies to both coincident pulses and to pulses with a time delay between them. An illustrative application to the case of two very short but coincident pulses (during which Larmor precession, spontaneous emission etc. can be ignored) is given. In an accompanying paper the theoretical expressions are further evaluated and successfully applied to the interpretation of cascade Zeeman quantum beat experiments in Fe I.
Recent femtosecond transmission-correlation measurements1 of large organic dye molecules revealed surprising details concerning the ultrafast relaxation dynamics of such dyes. Superposed on simple exponential decays, the observation of damped sinusoidal oscillations with a period of ~ 150 fs has been puzzling. We theoretically and numerically demonstrate that such oscillatory behavior could be due to quantum beats of closely spaced two levels, whose coherent superposition state is optically prepared and monitored by a pair of femtosecond pulses. Although studies of quantum beats have been developed in both fluorescence-type2 and nonfluorescence-type measurements, such as those based on photon echoes3 or polarization spectroscopy,4 this simple method gives a new approach to femtosecond time domain spectroscopy. The generalized perturbation theory5 of optical coherent transients is extended to the case of optical transmission-correlation or pump-probe-type experiments. The model used is a three-level system which has split levels in either the ground or optically excited states. Especially, if the ground state has sublevels, the system becomes quite similar to the case of coherent Raman beats. Both cases are shown to give quantum beats when the excitation pulses are short compared with the inverse sublevel splitting. The period and decay time of the damped sinusoid represent the separation energy and the dephasing time between the sublevels, respectively. Using third-order perturbation theory, the transmission-correlation signal STC(τ) as a function of the first-to-second pulse delay time Is derived for arbitrary-shaped excitation pulses and is given in the form of fourfold integrals with many terms.
The phenomenon of coherent Raman beats observed recently by Shoemaker and Brewer is analyzed through solutions of the coupled Maxwell-Schr\"odinger equations. The effect arises in coherently prepared molecular samples where the level degeneracy is suddenly removed by Stark-pulse switching. The problem divides into two parts: (a) a steady-state preparative regime whereby the initially degenerate quantum levels are placed in superposition by a resonant laser field, and (b) a transient regime in which coherent forward Raman scattering decays in the presence of the same laser field during a nonresonant condition. The laser and Raman light thus propagate together and produce at a detector a coherent beat with a frequency that corresponds to the level splitting between initial and final states. The beat signal possesses the remarkable property of being entirely independent of longitudinal molecular velocity in the case of a plane-wave laser beam and of being almost so for milliradian divergence. It follows that relaxation involving velocity-changing collisions and that Doppler dephasing effects are absent in coherent Raman beats, in agreement with experimental measurements of the decay rate. The effect of off-resonance excitation on the dephasing time and on the period of the beat signal is also discussed, and the possibility of a small rotation of the plane of polarization of the scattered light is included. The subject presents a new aspect of Raman scattering which can now yield precise radio-frequency splittings directly and offers a selective way of examining relaxation phenomena.