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Physical Review A

Observation of flux enhancement in collisions between ultracold atoms

V. Sánchez-Villicaña, S. D. Gensemer, P. L. Gould

Published Nov 1, 1996• 24 citations
Publisher

Abstract

We have observed a significant cooperative effect in ultracold trap loss collisions induced by two separate lasers. One laser, tuned close to the atomic resonance, excites the atom pair to an attractive potential at long range. The resulting acceleration and deflection give rise to an enhancement in the collisional flux of ground-state atoms reaching short range, as probed by a second laser. Enhancements up to a factor of \ensuremath{\sim}3 have been observed. This indicates that the atomic pair-distribution function can be significantly distorted in a typical laser trap environment.

DOI
10.1103/physreva.54.r3730

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Physical Review Letters•Jul 27, 1998•9 citations
We have observed a significant cooperative effect in ultracold trap loss collisions induced by two separate lasers. One laser, tuned close to the atomic resonance, excites the atom pair to an attractive potential at long range. The resulting acceleration and deflection give rise to an enhancement in the collisional flux of ground-state atoms reaching short range, as probed by a second laser. Enhancements up to a factor of \ensuremath{\sim}3 have been observed. This indicates that the atomic pair-distribution function can be significantly distorted in a typical laser trap environment.
In laser-induced collisions between ultracold atoms, the combination of low velocities and long-range interactions results in collision times which can exceed the excited-state lifetime. We use a cooperative effect between two lasers to explicitly observe this time dependence. The first laser, tuned near resonance, excites the atom pair at long range and enhances the collisional flux available for short-range excitation by a second, far-detuned laser. Using pulsed excitation, we find this collisional process to take place on a ${10}^{\ensuremath{-}6}\mathrm{s}$ time scale, in reasonable agreement with trajectory simulations.
Measurements of the temperature dependence of trap loss collisions of laser-cooled rubidium atoms are presented. A significant suppression of the rate of collisions between ground- and excited-state atoms is observed for temperatures below $\\sim$70 mu\\mumuK. In such inelastic collisions, the atomic excitation takes place at long range and must survive against spontaneous decay to short range. Our results are consistent with recent predictions for the low temperature suppression of these collisions due to reduced survival of atomic excitation at low collision velocities.^ We report on measurements of trap loss collisions between ultracold Rb atoms which are confined in a magneto-optical trap. Both isotopes sp85\\sp{85}sp85Rb and sp87\\sp{87}sp87Rb have been studied over wide range of trap laser intensities and detunings. The trap loss collision rates exhibit variations over 3 orders of magnitude. We observe significant differences between the isotopes. At large detunings the ability of the trap to recapture products of the hyperfine-changing collisions is significantly diminished. This finding is supported by our numerical simulations of the recapture process. The trap loss rates due to collisions with room temperature background gas have also been measured.^ Using laser light tuned to a repulsive molecular potential, we have been able to suppress inelastic ground-state hyperfine changing collisions between ultracold sp87\\sp{87}sp87Rb atoms. Adiabatic excitation to the repulsive curve alters the atomic trajectories and prevents the atoms from approaching close enough for the hyperfine change to occur. Experimental results show suppressions up to $\\sim$50% and are in reasonable agreement with a simple Landau-Zener model.^ Finally, we have observed a significant cooperative effect in ultracold trap loss collisions induced by two separate lasers. One laser, tuned close to the atomic resonance, excites the atom pair to an attractive potential at long range. The resulting acceleration and deflection give rise to an enhancement in the collisional flux of ground-state atoms reaching short range, as probed by a second laser. Enhancements up to a factor of $\\sim$3 have been observed. ^
We report on the dynamics of ultracold collisions induced by near-resonant frequency-chirped light. A series of identical chirped pulses, separated by a variable delay, is applied to an ultracold sample of 85Rb^{85}\mathrm{Rb}85Rb, and the rate of inelastic trap-loss collisions is measured. For small detunings of the chirped light below the atomic resonance, we observe that the rate of collisions induced by a given pulse can be increased by the presence of an earlier pulse. We attribute this to the enhancement of short-range collisional flux by the long-range excitation of atom pairs to an attractive molecular potential. For larger detunings and short delays, we find that a leading pulse can suppress the rate of collisions caused by a following pulse. This is due to a depletion of short-range atom pairs by the earlier pulse. Comparison of our data to classical Monte Carlo simulations of the collisions yields reasonable agreement.
Understanding collisions between ultracold molecules is crucial for making stable molecular quantum gases and harnessing their rich internal degrees of freedom for quantum engineering. Transient complexes can strongly influence collisional physics, but in the ultracold regime, key aspects of their behavior have remained unknown. To explain experimentally observed loss of ground-state molecules from optical dipole traps, it was recently proposed that molecular complexes can be lost due to photoexcitation. By trapping molecules in a repulsive box potential using laser light near a narrow molecular transition, we are able to test this hypothesis with light intensities three orders of magnitude lower than what is typical in red-detuned dipole traps. This allows us to investigate light-induced collisional loss in a gas of nonreactive fermionic 23Na40K^{23}\mathrm{Na}^{40}\mathrm{K}23Na40K molecules. Even for the lowest intensities available in our experiment, our results are consistent with universal loss, meaning unit loss probability inside the short-range interaction potential. Our findings disagree by at least two orders of magnitude with latest theoretical predictions, showing that crucial aspects of molecular collisions are not yet understood and provide a benchmark for the development of new theories.
Two recent developments in ultracold atomic collision physics are discussed. The first is the “optical shielding” of ultracold atomic collisions by optical radiation that is tuned to the blue of an atomic resonance. This radiation couples a pair of colliding atoms to repulsive excited states and prevents their close approach. This effect may substantially suppress inelastic collision rates, and is an interesting example of the control of a cold collision process by a weak perturbing field. The second topic is ultracold atom photoassociation spectroscopy. In this work, high resolution free‐bound absorption spectra are obtained which provide detailed information on the long‐range states of the two interacting atoms. The physics of these states has an appealing simplicity, and in addition is of importance for a complete understanding of the effects of atomic interactions in cold atom experiments. The photoassociation spectra also provide a unique probe of cold collisions.
We have observed violet photon emission resulting from energy-pooling collisions between ultracold Rb atoms illuminated by two colors of near-resonant infrared laser light. We have used this emission as a probe of doubly excited state ultracold collision dynamics. We have observed the lowest saturation intensity for light-induced ultracold collisions seen to date which we identify as due to depletion of incoming ground state flux. We have also varied the detuning of the lasers which allows us to clearly identify the effect of spontaneous emission and optical shielding.