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Quantum Electronics

Stimulated IR emission in an optically pumped cesium vapour

M. G. Sitnikov, Nikolay V Znamenskiy, Eduard A. Manykin, Evgenii A Petrenko, Grigorii G Grigoryan

Published Mar 31, 2000• 2 citations
Publisher

Abstract

It is demonstrated that the optical pumping of a Cs vapour with light pulses of a dye laser tunable within the range of 15390–17920 cm -1 gives rise to high-power stimulated IR emission on several atomic transitions. Analysis of threshold, energy, and spectral characteristics of this emission allowed the mechanism underlying this effect to be explained.

DOI
10.1070/qe2000v030n03abeh001691

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Stimulated electronic Raman scattering, SERS, is a simple method of efficiently generating widely tunable infrared radiation. This work describes techniques by which the tuning capability of this process may be extended. To this end several schemes in Caesium and Barium vapours have been investigated. In Barium vapour two Raman transitions were studied using fixed frequency lasers. Poor performance of one of these transitions led to the application of biharmonic pumping or 'coherent Raman mixing' to enable generation of infrared light, and was the first observation of this process in an atomic vapour. This technique was subsequently used to generate infrared light from tunable dye laser light, which gave continuous tuning from 1.16µm to 1.5µm. The process was found to be limited by atomic saturation. The effect which saturation has on the generation efficiency is considered theoretically, and predicts quite accurately the observed tuning behaviour. Two methods aimed at reducing molecular absorption effects in SERS in alkali vapours were investigated. The techniques employed either laser excitation and dissociation of the molecules or a reduction in their ground state concentration by superheating of the vapour. Some degree of success was achieved in improving the available tuning from the 6s-7s transition in Caesium. However, the inclusion of the effect of collision broadening of atomic transitions into a calculation of the Raman threshold suggests that little further improvement can be obtained on this transition. A direct measurement of the Raman threshold power on the 6s-5d5/2 transition in Caesium gave excellent agreement with theoretical predictions based on collision broadening of this Raman transition. In addition, this work gave an insight into the role photoionization plays in increasing the threshold under certain circumstances. The analysis suggests that laser pulse duration and vapour column length are important in determining whether Raman threshold can be exceeded.

•Jan 1, 1982•0 citations
It is demonstrated that the optical pumping of a Cs vapour with light pulses of a dye laser tunable within the range of 15390–17920 cm -1 gives rise to high-power stimulated IR emission on several atomic transitions. Analysis of threshold, energy, and spectral characteristics of this emission allowed the mechanism underlying this effect to be explained.
The conversion of a visible dye laser output into tunable infrared (IR) laser radiation via stimulated Raman scattering in Cs vapor was investigated. Small-signal gain, threshold intensity, and conversion efficiency measurements were obtained versus pump laser detuning. Fixed-frequency IR outputs at other wavelengths were also observed. One of these, the7P_{3/2}-5D_{5/2}transition, had a strong lasing component polarized perpendicular to the pump laser polarization. Lasing near the 8523-Å resonance line was attributed to a four-wave parametric interaction as a plausible generation mechanism.
Stimulated emission on the ultraviolet and blue transitions in Cs has been achieved by pumping via two-photon absorption and four-wave mixing for the pump transition 62S12→82D32,52. The emission performance of the optically pumped cesium vapor laser operating in ultraviolet and blue has been extended to 650 nJ/pulse for 387 nm, 1 to 3 μJ/pulse for 388 nm, 200 nJ/pulse for 455 nm, and 500 nJ/pulse for 459 nm. Emission performance improves dramatically as the cesium vapor density is increased, and no scaling limitations associated with energy pooling or ionization kinetics have been observed.
Stimulated electronic Raman scattering, SERS, is a simple method of efficiently generating widely tunable infrared radiation. This work describes techniques by which the tuning capability of this process may be extended. To this end several schemes in Caesium and Barium vapours have been investigated. In Barium vapour two Raman transitions were studied using fixed frequency lasers. Poor performance of one of these transitions led to the application of biharmonic pumping or 'coherent Raman mixing' to enable generation of infrared light, and was the first observation of this process in an atomic vapour. This technique was subsequently used to generate infrared light from tunable dye laser light, which gave continuous tuning from 1.16µm to 1.5µm. The process was found to be limited by atomic saturation. The effect which saturation has on the generation efficiency is considered theoretically, and predicts quite accurately the observed tuning behaviour. Two methods aimed at reducing molecular absorption effects in SERS in alkali vapours were investigated. The techniques employed either laser excitation and dissociation of the molecules or a reduction in their ground state concentration by superheating of the vapour. Some degree of success was achieved in improving the available tuning from the 6s-7s transition in Caesium. However, the inclusion of the effect of collision broadening of atomic transitions into a calculation of the Raman threshold suggests that little further improvement can be obtained on this transition. A direct measurement of the Raman threshold power on the 6s-5d5/2 transition in Caesium gave excellent agreement with theoretical predictions based on collision broadening of this Raman transition. In addition, this work gave an insight into the role photoionization plays in increasing the threshold under certain circumstances. The analysis suggests that laser pulse duration and vapour column length are important in determining whether Raman threshold can be exceeded.