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Bulletin of the American Physical Society

"Uber-Resonant Scattering of Ultracold Molecules

Michael Mayle, Brandon Ruzic, John L. Bohn

Published Jun 7, 2012• 0 citations
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Abstract

Abstract Compared to purely atomic collisions, ultracold molecular collisions potentially support a muchlarger number of Fano-Feshbach resonances due to the enormous number of ro-vibrational statesavailable. In fact, for alkali-metal dimers we nd that the resulting density of resonances cannotbe resolved at all, even on the sub-K temperature scale of ultracold experiments. As a result, allobservables become averaged over many resonances and can e ectively be described by simpler, non-resonant scattering calculations. Two particular examples are discussed: non-chemically reactiveRbCs and chemically reactive KRb. In the former case, the formation of a long-lived collisioncomplex may lead to the ejection of molecules from a trap. In the latter case, chemical reactionsbroaden the resonances so much that they become unobservable. PACS numbers: 34.50.-s, 34.50.Cx 1 Present address: Laboratoire Aime Cotton, Universite Paris-Sud, CNRS, B^at. 505, 91405, Orsay, France 1 arXiv:1210.4955v1 [physics.atom-ph] 17 Oct 2012

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Abstract Compared to purely atomic collisions, ultracold molecular collisions potentially support a muchlarger number of Fano-Feshbach resonances due to the enormous number of ro-vibrational statesavailable. In fact, for alkali-metal dimers we nd that the resulting density of resonances cannotbe resolved at all, even on the sub-K temperature scale of ultracold experiments. As a result, allobservables become averaged over many resonances and can e ectively be described by simpler, non-resonant scattering calculations. Two particular examples are discussed: non-chemically reactiveRbCs and chemically reactive KRb. In the former case, the formation of a long-lived collisioncomplex may lead to the ejection of molecules from a trap. In the latter case, chemical reactionsbroaden the resonances so much that they become unobservable. PACS numbers: 34.50.-s, 34.50.Cx 1 Present address: Laboratoire Aime Cotton, Universite Paris-Sud, CNRS, B^at. 505, 91405, Orsay, France 1 arXiv:1210.4955v1 [physics.atom-ph] 17 Oct 2012
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.
II. Inelastic atom -molecule collisions 2 A. Vibrational and rotational relaxation 2 1. Collisions at cold and ultracold temperatures 2 2. Shape resonances in molecular collisions 6 3. Feshbach resonances in molecular collisions 6 B. Quasi-resonant transitions 7 C. Atom -molecular ion collisions 8 III.Chemical Reactions at ultracold temperatures 9 A. Tunneling dominated reactions 9 1.Reactions at zero temperature 10 2. Feshbach resonances in reactive scattering 12 B. Barrierless reactions 14 1.Collision systems of three alkali metal atoms 14 2. Role of PES in determining ultracold reactions 16 3.Relaxation of vibrationally excited alkali metal dimers 18 4. Reactions of heteronuclear and isotopically substituted alkali-metal dimer systems 19 IV.Inelastic molecule -molecule collisions 20 A. Molecules in the ground vibrational state 20 B. Vibrationally inelastic transitions 22 V. Summary and outlook 24 References 24 I. A. Vibrational and rotational relaxation 1. Collisions at cold and ultracold temperatures
Compared to purely atomic collisions, ultracold collisions involving molecules have the potential to support a much larger number of Fano-Feshbach resonances due to the huge amount of ro-vibrational states available. In order to handle such ultracold atom-molecule collisions, we formulate a theory that incorporates the ro-vibrational Fano-Feshbach resonances in a statistical manner while treating the physics of the long-range scattering, which is sensitive to such things as hyperfine states, collision energy, and any applied electromagnetic fields, exactly within multichannel quantum defect theory. Uniting these two techniques, we can assess the influence of highly resonant scattering in the threshold regime, and in particular its dependence on the hyperfine state selected for the collision. This allows us to explore the onset of Ericson fluctuations in the regime of overlapping resonances, which are well known in nuclear physics but completely unexplored in the ultracold domain.
We investigate the presence of Feshbach resonances in ultracold alkali-dialkali reactive collisions. A potential-energy surface of Na3{\text{Na}}_{3}Na3​ in the lowest quartet state is constructed and used in quantum scattering calculations. An analysis of scattering features is performed through a systematic variation in the nonadditive three-body interaction potential. Our results should provide useful information for interpreting future atom-molecule collision experiments.
It has recently become possible to form molecules in ultracold gases of trapped alkali metal atoms. Once formed, the molecules may undergo elastic, inelastic and reactive collisions. Inelastic and reactive collisions are particularly important because they release kinetic energy and eject atoms and molecules from the trap. The theory needed to handle such collisions is presented and recent quantum dynamics calculations on ultracold atom–diatom collisions of spin-polarized Li + Li2, Na + Na2 and K + K2 are described. All these systems have potential energy surfaces on which barrierless atom exchange reactions can occur, and both inelastic and reactive rates are very fast (typically k inel > 10-10 cm3 s−1 in the Wigner regime).