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arXiv:1709.07419 · Physical Review A

Long-lived complexes and signatures of chaos in ultracold K2 +Rb collisions

James F. E. Croft, N. Balakrishnan, Brian K. Kendrick

Published Dec 18, 2017• 40 citations
arXivHTMLPDF

Abstract

Lifetimes of complexes formed during ultracold collisions are of current experimental interest as a possible cause of trap loss in ultracold gases of alkali-metal dimers. Microsecond lifetimes for complexes formed during ultracold elastic collisions of ${\mathrm{K}}_{2}$ with Rb are reported, from numerically exact quantum-scattering calculations. Thermally averaged lifetimes are compared with those calculated using a simple density-of-states approach, which are shown to be reasonable. This validates the density-of-states approach and suggests that the formation of long-lived complexes is indeed the cause of observed experimental trap loss in ultracold alkali-metal-dimer systems. Long-lived complexes correspond to narrow scattering resonances which we examine for the statistical signatures of quantum chaos, finding that the positions and widths of the resonances are in good agreement with the Wigner-Dyson and Porter-Thomas distributions, respectively.

DOI
10.1103/physreva.96.062707

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Lifetimes of complexes formed during ultracold collisions are of current experimental interest as a possible cause of trap loss in ultracold gases of alkali-metal dimers. Microsecond lifetimes for complexes formed during ultracold elastic collisions of K2{\mathrm{K}}_{2}K2​ with Rb are reported, from numerically exact quantum-scattering calculations. Thermally averaged lifetimes are compared with those calculated using a simple density-of-states approach, which are shown to be reasonable. This validates the density-of-states approach and suggests that the formation of long-lived complexes is indeed the cause of observed experimental trap loss in ultracold alkali-metal-dimer systems. Long-lived complexes correspond to narrow scattering resonances which we examine for the statistical signatures of quantum chaos, finding that the positions and widths of the resonances are in good agreement with the Wigner-Dyson and Porter-Thomas distributions, respectively.
Compared to purely atomic collisions, ultracold molecular collisions potentially support a much larger number of Fano-Feshbach resonances due to the enormous number of ro-vibrational states available. In fact, for alkali-metal dimers we find that the resulting density of resonances cannot be resolved at all, even on the sub-μμμK temperature scale of ultracold experiments. As a result, all observables become averaged over many resonances and can effectively be described by simpler, non-resonant scattering calculations. Two particular examples are discussed: non-chemically reactive RbCs and chemically reactive KRb. In the former case, the formation of a long-lived collision complex may lead to the ejection of molecules from a trap. In the latter case, chemical reactions broaden the resonances so much that they become unobservable.
Compared to purely atomic collisions, ultracold molecular collisions potentially support a much larger number of Fano-Feshbach resonances due to the enormous number of rovibrational states available. In fact, for alkali-metal dimers we find that the resulting density of resonances cannot be resolved at all, even on the sub-$\ensuremath{\mu}$K temperature scale of ultracold experiments. As a result, all observables become averaged over many resonances and can effectively be described by simpler, nonresonant scattering calculations. Two particular examples are discussed: nonchemically reactive RbCs and chemically reactive KRb. In the former case, the formation of a long-lived collision complex may lead to the ejection of molecules from a trap. In the latter case, chemical reactions broaden the resonances so much that they become unobservable.
A thorough understanding of molecular scattering in the ultralow temperature regime is crucial for realizing long coherence times and enabling tunable interactions in molecular gases, systems which offer many opportunities in quantum simulation, quantum information, and precision measurement.Of particular importance is the nature of the long-lived intermediate complexes which may be formed in ultracold molecular collisions, as such complexes can dramatically affect the stability of molecular gases, even when exothermic reaction channels are not present.Here, we investigate collisional loss in an ultracold mixture of 40 K 87 Rb molecules and 87 Rb atoms, where chemical reactions between the two species are energetically forbidden.Through direct detection of the KRb 2 Ã intermediate complexes formed from atom-molecule collisions, we show that a 1064 nm laser source used for optical trapping of the sample can efficiently deplete the complex population via photoexcitation, an effect which can explain the strong twobody loss observed in the mixture.By monitoring the time evolution of the KRb 2 Ã population after a sudden reduction in the 1064 nm laser intensity, we measure the lifetime of the complex [0.39(6) ms], as well as the photoexcitation rate for 1064 nm light [0.50ð3Þμs -1 ðkW=cm 2 Þ -1 ].The observed lifetime, which is ∼10 5 times longer than recent estimates based on the Rice-Ramsperger-Kassel-Marcus statistical theory, calls for new theoretical insight to explain its origin.
Abstract we report on signatures of classical chaos in ultracold collisions between a trapped ion and a free atom. Using numerical simulations, we show that the scattering dynamics can be highly sensitive to initial conditions for various mass ratios and trapping frequencies, indicating the onset of chaos. We quantify this chaotic dynamics by calculating its fractal dimension. We show that for a trapped 88 Sr + ion and a free 87 Rb atom chaotic dynamic appears under experimentally relevant conditions, and find its characteristic energy scale. The observation of classical chaos in atom-trapped-ion collisions suggests that signatures of quantum chaos might appear, for example, through a Wigner–Dyson distribution of collisional resonances.
Estimates for the lifetime of collision complexes formed during ultracold molecular collisions based on density-of-states arguments are shown to be consistent with similar estimates based on classical trajectory calculations. In the classical version, these collisions are shown to exhibit chaos and their fractal dimension is calculated versus collision energy. From these results, a picture emerges that ultracold collisions are likely classically ergodic, justifying the density-of-states estimates for lifetimes. These results point the way toward using the techniques of classical and quantum chaos to interpret molecular collisions in the ultracold regime.
This review describes recent experimental and theoretical advances in forming molecules in ultracold gases of trapped alkali metal atoms, both by magnetic tuning through Feshbach resonances and by photoassociation. Molecular Bose-Einstein condensation of long-range states of both boson dimers and fermion dimers was achieved in 2002-3. Condensates of boson dimers were found to be short-lived, but long-lived condensates of fermion dimers have been produced. Signatures of triatomic and tetraatomic molecules have recently been observed. Both homonuclear and heteronuclear molecules have been formed by photoassociation, mostly in very high vibrational levels. Recent attempts to produce ultracold molecules in short-range states (low vibrational levels) are described. Experimental and theoretical work on collisions of ultracold molecules is discussed.