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AIP conference proceedings

Formation of cold Cs[sub 2] molecules through photoassociation

A. Fioretti

Published Jan 1, 2000• 7 citations
Publisher

Abstract

We report on the formation of translationally cold Cs2 ground-state molecules through photoassociation of laser-cooled cesium atoms in a magneto-optical trap. The cold molecules are obtained after spontaneous decay of photoassociated molecules, and detected after pulsed-laser photoionization into Cs2+ ions. Photoassociation spectra of cesium attractive molecular states below the 6S1/2+6P3/2 dissociation limits are reported, obtained with both ion detection and trap-loss method. A temperature as low as 20−5+15 has been measured for the molecular cloud.

DOI
10.1063/1.1302653

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IEEE Journal of Quantum Electronics•Dec 1, 2000•66 citations
We report on the formation of translationally cold Cs2 ground-state molecules through photoassociation of laser-cooled cesium atoms in a magneto-optical trap. The cold molecules are obtained after spontaneous decay of photoassociated molecules, and detected after pulsed-laser photoionization into Cs2+ ions. Photoassociation spectra of cesium attractive molecular states below the 6S1/2+6P3/2 dissociation limits are reported, obtained with both ion detection and trap-loss method. A temperature as low as 20−5+15 has been measured for the molecular cloud.
We report on the observation of translationally cold Cs2 molecules at temperatures in the 300–70 μK range, produced by the photoassociation of cold Cs atoms in a vapor-cell magneto-optical trap. The detection method is based on pulsed-laser photoionization of Cs2 molecules into Cs2+ ions, selectively detected through a time-of-flight mass spectrometer. This technique, together with the usual trap-loss method, enables us to perform the spectroscopy of the long-range attractive molecular states below the 6s 2S1/2+6p 2P3/2 dissociation limit.
We have performed photoassociative spectroscopy of cold Cs atoms in a vapor-cell magneto-optical trap, within $10{\mathrm{cm}}^{\ensuremath{-}1}$ below the dissociation limit 6s2S1/2+6p2P3/26s^{2}S_{1/2}+6p^{2}P_{3/2}6s2S1/2​+6p2P3/2​. Our detection method is based on pulsed-laser photoionization of Cs2{\mathrm{Cs}}_{2}Cs2​ molecules, selectively detected through a time-of-flight mass spectrometer. Temporal and spatial analysis of Cs2+{\mathrm{Cs}}_{2}^{+}Cs2+​ ions show for the first time the formation of translationally cold Cs2{\mathrm{Cs}}_{2}Cs2​ triplet ground state molecules, at a temperature $T\ensuremath{\sim}300\ensuremath{\mu}\mathrm{K}$.
We have observed translationally cold electronic ground-state cesium dimers produced directly in a magneto-optical trap and also by photoassociation of cold atoms in this trap. These neutral molecules were detected using photoionization and time-of-flight spectroscopy. Initial experiments indicated a cold molecular formation rate of about $600{\mathrm{s}}^{\mathrm{\ensuremath{-}}1},$ with no photoassociation laser present. The measured translational temperature of the neutral cesium dimers was approximately 100 \ensuremath{\mu}K.
Summary form only given. In contrast to atoms, laser cooling of molecules is very difficult because of the lack of a closed two-level scheme for recycling the population. The molecular photoassociation of cold atoms opens a promising alternative for the formation of cold molecules. The photoassociative spectra are obtained by the usual trap-loss method as well as by pulsed laser photoionization of Cs/sub 2/ molecules into Cs/sub 2//sup +/ ions. Different schemes to obtain formation of cold molecules through photoassociation will be discussed.
In the molecular photoassociation process, two free cold atoms absorb one photon by a resonant way, to create an excited molecule in a well defined ro-vibrational state. The photoassociative spectroscopy of alkaline dimers yields accurate determinations for the long-range parts of molecular potential curves correlated to the first s + p asymptote. In contrast to atoms, laser cooling of molecules is very difficult because of the lack of a closed two-level scheme for recycling the population. The molecular photoassociation of cold atoms opens also a promising alternative for the formation of cold ground state molecules. Photoassociation of cold cesium atoms has permitted the first observation of translationally cold ground state molecules. The case of the cesium atom is very favorable because the 0 g - and 1 u purely long-range states below the dissociation limit 6s 1/2 +6p 3/2 present Condon points at intermediate distances. Such configurations offer rather efficient channels for the creation of singlet or triplet ground state Cs 2 molecules after spontaneous decay.
We report on the spectra of the long-range attractive molecular states of the Cs/sub 2/ dimer below the dissociation limits 6s+6p/sub 1/2/ and 6s+6p/sub 3/2/ which are accessible by molecular photoassociation of cold Cs atoms. For the states O/sub u//sup +/ and O/sub g//sup -/(6s+6p/sub 3/2/), we have performed trap-loss measurements, which are in good agreement with the theoretical calculations, performed in a perturbative approach. For the O/sub g//sup -/ and 1/sub u/(6s+6p/sub 3/2/) states, we observe, after spontaneous decay of the electronically excited molecules, the formation of translationally cold molecules. A rate of formation of cold molecules of the order of /spl sim/10/sup 6/ molecules per second is obtained in the case of the state O/sub g//sup $/.