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Springer series in chemical physics

Doppler-Free Raman Spectroscopy and Suppression of Molecular Doppler-Broadened Transitions Induced by Laser Field

A. K. Popov, L. N. Talashkevich

Published Jan 1, 1979• 0 citations
Publisher
DOI
10.1007/978-3-642-67254-5_43

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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.
We report here the first experimental demonstration of Doppler-free three-photon spectroscopy. The Doppler broadening is eliminated by insuring that the sum of the momenta of the three photons simultaneously exchanged between the atom and the laser beams is equal to 0. This is accomplished by making a proper choice of the angles between the three exciting beams. The observation has been made on the sodium $3{S}_{\frac{1}{2}}\ensuremath{-}3{P}_{\frac{1}{2}}$ transition with absorption of two photons and induced emission of one.