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Physical Review Letters

Ultracold Collisions Observed in Real Time

S. D. Gensemer, P. L. Gould

Published Feb 2, 1998• 41 citations
Publisher

Abstract

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.

DOI
10.1103/physrevlett.80.936

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Physical Review Letters•Jul 27, 1998•9 citations
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−6s{10}^{\ensuremath{-}6}\mathrm{s}10\ensuremath−6s time scale, in reasonable agreement with trajectory simulations.
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.
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.
We present time-resolved spectroscopic measurements of Rydberg-Rydberg interactions between two Rydberg atoms in an ultracold gas, revealing the pair dynamics induced by long-range van der Waals interactions between the atoms. By detuning the excitation laser, a specific pair distribution is prepared. Penning ionization on a microsecond time scale serves as a probe for the pair dynamics under the influence of the attractive long-range forces. Comparison with a Monte Carlo model not only explains all spectroscopic features but also gives quantitative information about the interaction potentials. The results imply that the interaction-induced ionization rate can be influenced by the excitation laser. Surprisingly, interaction-induced ionization is also observed for Rydberg states with purely repulsive interactions.
Using 40 ns laser pulses, we probe the real-time dynamics of ultracold ionizing collisions in metastable xenon. We time resolve both shielding and enhancement effects, and observe the production of Xe2+{\mathrm{Xe}}_{2}^{+}Xe2+​ molecular ions through associative ionization. We estimate the rate of molecule formation in excited-state collisions, and directly measure the role of both flux enhancement and excited state survival in the collisional enhancement process. Conceptually simple theoretical models are used to predict the dynamics of the collisional shielding.
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.