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Producing cold and ultracold Cs2 and CsH molecules through photoassociation and reactions

Marin Pichler

Published Jan 1, 2001• 0 citations
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Abstract

Several different experiments involving the making of cold and ultracold molecules are performed and proposed. Ultracold cesium molecules are produced in a magneto-optical trap (MOT) by photoassociation near the 6P j, 7Pj, 9S 1/2, 6D3/2, 7D3/2 and doubly excited asymptotes. Perturbation effects related to resonant channel coupling were observed in photoassociation spectra below the 6 P1/2 asymptote. Such effects are used to illustrate a ground state ultracold molecule formation mechanism, which can also be formed in one step photoassociation to the double minimum 31S+m state. In addition, a new technique of making cold molecules of cesium hydride is proposed, using a cold hydrogen beam source and a cesium MOT. Due to reaction energetics, the formed CsH molecules should be in their lowest rovibrational states. ^

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arXiv:1111.3503•Laser Physics•Sep 3, 2012•23 citations
Several different experiments involving the making of cold and ultracold molecules are performed and proposed. Ultracold cesium molecules are produced in a magneto-optical trap (MOT) by photoassociation near the 6P j, 7Pj, 9S 1/2, 6D3/2, 7D3/2 and doubly excited asymptotes. Perturbation effects related to resonant channel coupling were observed in photoassociation spectra below the 6 P1/2 asymptote. Such effects are used to illustrate a ground state ultracold molecule formation mechanism, which can also be formed in one step photoassociation to the double minimum 31S+m state. In addition, a new technique of making cold molecules of cesium hydride is proposed, using a cold hydrogen beam source and a cesium MOT. Due to reaction energetics, the formed CsH molecules should be in their lowest rovibrational states. ^
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 ultracold ground electric-state cesium molecules produced directly in a magneto—optical trap with a good signal-to-noise ratio. These molecules arise from the photoassociation of magneto—optical trap lasers and they are detected by resonantly enhanced multiphoton ionization technology. The production rate of ultracold cesium molecules is up to 4×10 4 s −1 . We measure the characteristic time of the ground electric-state cesium molecules generated in the experiment and investigate the Cs 2 + molecular ion intensity as a function of the trapping laser intensity and the ionization pulse laser energy. We conclude that the production of cold cesium molecules may be enhanced by using appropriate experimental parameters, which is useful for future experiments involving the production and trapping of ultracold ground electric-state molecules.
In recent years several groups of researchers have succeeded in making samples of cold molecules, at temperatures below 1 K, and of ultracold molecules, at temperatures below 1 mK. We concentrate on the formation of Cs2 dimers. Starting with laser-cooled atoms, photoassociation forms molecules in an excited electronic state. Various mechanisms are presented for stabilizing these molecules by spontaneous emission into a bound level of the ground electronic state. The design of new formation schemes requires precise knowledge of molecular potential curves that is well beyond the accuracy of ab initio calculations. We show that analytical long-range potentials can be fitted on photoassociation spectra and yield, through the determination of the C3 long-range coefficient, a value of the radiative lifetime of the 6P3/2 cesium level with an unprecedented accuracy. For short-range potentials it is possible to avoid explicit calculations by using asymptotic methods that generalize to long-range molecules the quantum-defect concepts developed for Rydberg atoms. Considering two coupled channels, we show how generalized Lu–Fano plots can extract precise information from experimental spectra.
A new approach for production of very cold molecules is described. This includes an experimental system for producing and observing Csast+H2rightarrowCSCs^{\\ast}+H_{2}\\rightarrow CSCsast+H2​rightarrowCS chemical reactions below 10 K. The ground state Cs atoms are trapped and cooled down to few hundred microKelvin in a standard magneto-optical trap (MOT), and then excited to the 7P1/27 P_{1/2}7P1/2​ or 7P3/27 P_{3/2}7P3/2​ state. A cold para H2H_{2}H2​ beam (up to 10 K) collides with Cs+Cs^{+}Cs+ atoms. Due to the reaction energetics, the CsH molecules produced by the 7P1/27 P_{1/2}7P1/2​ reaction must be in the lowest rovibrational state. Detection techniques to be employed include LIF and REMPI.
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.
The formation of ultracold metastable RbCs molecules is observed in a double species magneto-optical trap through photoassociation below the 85 Rb(5S 1/2 ) + 133 Cs(6P 3/2 ) dissociation limit followed by spontaneous emission. The molecules are detected by resonance enhanced two-photon ionization. Using accurate quantum chemistry calculations of the potential energy curves and transition dipole moment, we interpret the observed photoassociation process as occurring at short internuclear distance, in contrast with most previous cold atom photoassociation studies. The vibrational levels excited by photoassociation belong to the 5th 0 + or the 4th 0 − electronic states correlated to the Rb(5P 1/2, 3/2 ) + Cs(6S 1/2 ) dissociation limit. The computed vibrational distribution of the produced molecules shows that they are stabilized in deeply bound vibrational states of the lowest triplet state. We also predict that a noticeable fraction of molecules is produced in the lowest level of the electronic ground state.