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arXiv:2101.01580 · Physical Review Letters

Collisions between Ultracold Molecules and Atoms in a Magnetic Trap

Sarunas Jurgilas, A. Chakraborty, C. J. H. Rich, Luke Caldwell, H. J. Williams, Noah J. Fitch, B. E. Sauer, Matthew D. Frye, Jeremy M. Hutson, Michael R. Tarbutt

Published Apr 13, 2021• 51 citations
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Abstract

We prepare mixtures of ultracold CaF molecules and Rb atoms in a magnetic trap and study their inelastic collisions. When the atoms are prepared in the spin-stretched state and the molecules in the spin-stretched component of the first rotationally excited state, they collide inelastically with a rate coefficient k_{2}=(6.6±1.5)×10^{-11} cm^{3}/s at temperatures near 100 μK. We attribute this to rotation-changing collisions. When the molecules are in the ground rotational state we see no inelastic loss and set an upper bound on the spin-relaxation rate coefficient of k_{2}<5.8×10^{-12} cm^{3}/s with 95% confidence. We compare these measurements to the results of a single-channel loss model based on quantum defect theory. The comparison suggests a short-range loss parameter close to unity for rotationally excited molecules, but below 0.04 for molecules in the rotational ground state.

DOI
10.1103/physrevlett.126.153401

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We prepare mixtures of ultracold CaF molecules and Rb atoms in a magnetic trap and study their inelastic collisions. When the atoms are prepared in the spin-stretched state and the molecules in the spin-stretched component of the first rotationally excited state, they collide inelastically with a rate coefficient k_{2}=(6.6±1.5)×10^{-11} cm^{3}/s at temperatures near 100 μK. We attribute this to rotation-changing collisions. When the molecules are in the ground rotational state we see no inelastic loss and set an upper bound on the spin-relaxation rate coefficient of k_{2}<5.8×10^{-12} cm^{3}/s with 95% confidence. We compare these measurements to the results of a single-channel loss model based on quantum defect theory. The comparison suggests a short-range loss parameter close to unity for rotationally excited molecules, but below 0.04 for molecules in the rotational ground state.
This thesis describes an experiment to produce the first laser cooled mixtures of atoms and polar molecules in magneto-optical and magnetic quadrupole traps. Inelastic collision processes between CaF molecules and Rb atoms are studied in both trapping arrangements. When molecules occupy the first rotationally excited state it is found that loss from either trap occurs at near the universal rate due to collisions with co-trapped atoms. When the molecular sample is transferred to the ground rotational state the loss rate is suppressed by at least an order of magnitude. The experimental results are compared to a quantum scattering model based on quantum defect theory and the results seem to be encouraging for observing a high ratio of elastic to inelastic collision rates in this system. In addition, improvements to the experimental apparatus are presented which led to the first measurements of the elastic cross-section for collisions between CaF and Rb. Although at the currently attainable number densities no thermalization is observed, an upper bound on the value of the cross section is placed.
Abstract We study inelastic collisions between CaF molecules and 87Rb atoms in a dual-species magneto-optical trap. The presence of atoms increases the loss rate of molecules from the trap. By measuring the loss rates and density distributions, we determine a collisional loss rate coefficient k 2 = (1.43 ± 0.29) × 10−10 cm3 s−1 at a temperature of 2.4 mK. We show that this is not substantially changed by light-induced collisions or by varying the populations of excited-state atoms and molecules. The observed loss rate is close to the universal rate expected in the presence of fast loss at short range, and can be explained by rotation-changing collisions in the ground electronic state.
Abstract Understanding ultracold collisions involving molecules is of fundamental importance for current experiments, where inelastic collisions typically limit the lifetime of molecular ensembles in optical traps. Here we present a broad study of optically trapped ultracold RbCs molecules in collisions with one another, in reactive collisions with Rb atoms, and in nonreactive collisions with Cs atoms. For experiments with RbCs alone, we show that by modulating the intensity of the optical trap, such that the molecules spend 75% of each modulation cycle in the dark, we partially suppress collisional loss of the molecules. This is evidence for optical excitation of molecule pairs mediated via sticky collisions. We find that the suppression is less effective for molecules not prepared in the spin-stretched hyperfine ground state. This may be due either to longer lifetimes for complexes in the dark or to laser-free decay pathways. For atom–molecule mixtures, RbCs + Rb and RbCs + Cs, we demonstrate that the rate of collisional loss of molecules scales linearly with the density of atoms. This indicates that, in both cases, the loss of molecules is rate-limited by two-body atom–molecule processes. For both mixtures, we measure loss rates that are below the thermally averaged universal limit.
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. ^
Abstract Ultracold atoms prepared in excited internal states can escape from the trap through inelastic collisions. A magnetic field can be used to suppress the s-wave loss rate coefficient near an s-wave Feshbach resonance. However, at the temperature of μK the p-wave loss rate coefficient becomes increasingly important as the temperature increases. The unsuppressed p-wave loss rate coefficient can far exceed the suppressed s-wave loss rate coefficient, and severely restricts the reduction of the total loss rate coefficient. We calculate the collision rate coefficients of ultracold 85Rb and 87Rb atoms prepared in excited hyperfine and Zeeman states using the coupled-channel method. We find that in R b 85 ( F 1 = 3 , m F 1 = 3 ) + R b 87 ( F 2 = 1 , m F 2 = − 1 ) and R b 85 ( F 1 = 2 , m F 1 = − 2 ) + R b 87 ( F 2 = 2 ,