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Optics Communications

Laser ionization and time-resolved ion collection in cesium vapor

E. Arimondo, F. Giammanco, Antonio Sasso, M. I. Schisano

Published Oct 1, 1985• 14 citations
Publisher
DOI
10.1016/0030-4018(85)90180-4

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The use of in situ ion detection in alkali vapors coupled with multiphoton ionization provides a technique of highest sensitivity for the investigation of the spectroscopy of excimer states involving alkali atoms. This technique has been applied in this work to the molecular components of the spectrum of the $6S\ensuremath{-}7P$ absorption doublet of cesium. The dispersion curve was obtained with a tunable dye laser for the two-photon ionization of cesium over the 4500-4600-\AA{} wavelength range as a function of vapor pressure and source intensity. Strongly developed satellite bands were observed to be associated with the atomic lines $6^{2}S_{\frac{1}{2}}\ensuremath{\rightarrow}7^{2}P_{\frac{1}{2}}$ and $6^{2}S_{\frac{1}{2}}\ensuremath{\rightarrow}7^{2}P_{\frac{3}{2}}$, and were found to have well-defined band heads at 29.4 and 31.4 ${\mathrm{cm}}^{\ensuremath{-}1}$ to longer wavelengths, respectively. Sensitivity was observed to be an order of magnitude in excess of that obtained from classical absorption techniques, and the observation of a quadratic dependence of the molecular components confirmed the multiphoton nature of the detection sequence.
In the interaction of a QQQ-switched Nd-glass laser radiation with cesium vapor, the molecular cesium component seems to play an important role in the multiphoton ionization process at low laser intensity.