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Register a new userProduction of cold molecules via magnetically tunable Feshbach resonances
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Magnetically tunable Feshbach resonances were employed to associate cold diatomic molecules in a series of experiments involving both atomic Bose as well as two spin component Fermi gases. This review illustrates theoretical concepts of both the particular nature of the highly excited Feshbach molecules produced and the techniques for their association from unbound atom pairs. Coupled channels theory provides the rigorous formulation of the microscopic physics of Feshbach resonances in cold gases. Concepts of dressed versus bare energy states, universal properties of Feshbach molecules, as well as the classification in terms of entrance- and closed-channel dominated resonances are introduced on the basis of practical two-channel approaches. Their significance is illustrated for several experimental observations, such as binding energies and lifetimes with respect to collisional relaxation. Molecular association and dissociation are discussed in the context of techniques involving linear magnetic field sweeps in cold Bose and Fermi gases as well as pulse sequences leading to Ramsey-type interference fringes. Their descriptions in terms of Landau-Zener, two-level mean field as well as beyond mean field approaches are reviewed in detail, including the associated ranges of validity.
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Pairs of trapped atoms can be associated to make a diatomic molecule using a time dependent magnetic field to ramp the energy of a scattering resonance state from above to below the scattering threshold. A relatively simple model, parameterized in terms of the background scattering length and resonance width and magnetic moment, can be used to predict conversion probabilities from atoms to molecules. The model and its Landau-Zener interpretation are described and illustrated by specific calculations for $^{23}$Na, $^{87}$Rb, and $^{133}$Cs resonances. The model can be readily adapted to Bose-Einstein condensates. Comparison with full many-body calculations for the condensate case show that the model is very useful for making simple estimates of molecule conversion efficiencies.
We observe magnetically tuned collision resonances for ultracold Cs2 molecules stored in a CO2-laser trap. By magnetically levitating the molecules against gravity, we precisely measure their magnetic moment. We find an avoided level crossing which allows us to transfer the molecules into another state. In the new state, two Feshbach-like collision resonances show up as strong inelastic loss features. We interpret these resonances as being induced by Cs4 bound states near the molecular scattering continuum. The tunability of the interactions between molecules opens up novel applications such as controlled chemical reactions and synthesis of ultracold complex molecules.
We report on the observation of ultracold heteronuclear Feshbach molecules. Starting with a $^{87}$Rb BEC and a cold atomic gas of $^{85}$Rb, we utilize previously unobserved interspecies Feshbach resonances to create up to 25,000 molecules. Even though the $^{85}$Rb gas is non-degenerate we observe a large molecular conversion efficiency due to the presence of a quantum degenerate $^{87}$Rb gas; this represents a key feature of our system. We compare the molecule creation at two different Feshbach resonances with different magnetic-field widths. The two Feshbach resonances are located at $265.44pm0.15$ G and $372.4pm1.3$ G. We also directly measure the small binding energy of the molecules through resonant magnetic-field association.
Ultracold molecules have experienced increasing attention in recent years. Compared to ultracold atoms, they possess several unique properties that make them perfect candidates for the implementation of new quantum-technological applications in several fields, from quantum simulation to quantum sensing and metrology. In particular, ultracold molecules of two-electron atoms (such as strontium or ytterbium) also inherit the peculiar properties of these atomic species, above all the possibility to access metastable electronic states via direct excitation on optical clock transitions with ultimate sensitivity and accuracy. In this paper we report on the production and coherent manipulation of molecular bound states of two fermionic $^{173}$Yb atoms in different electronic (orbital) states $^1$S$_0$ and $^3$P$_0$ in proximity of a scattering resonance involving atoms in different spin and electronic states, called orbital Feshbach resonance. We demonstrate that orbital molecules can be coherently photoassociated starting from a gas of ground-state atoms in a three-dimensional optical lattices by observing several photoassociation and photodissociation cycles. We also show the possibility to coherently control the molecular internal state by using Raman-assisted transfer to swap the nuclear spin of one of the atoms forming the molecule, thus demonstrating a powerful manipulation and detection tool of these molecular bound states. Finally, by exploiting this peculiar detection technique we provide first information on the lifetime of the molecular states in a many-body setting, paving the way towards future investigations of strongly interacting Fermi gases in a still unexplored regime.
We measure the binding energies of weakly bound Feshbach molecules formed between Na and Rb atoms in their lowest hyperfine Zeeman levels. We form molecules at the Feshbach resonance near 347.64 G and dissociate them by magnetic field modulation. We use the binding energies to refine the singlet and triplet potential energy curves, using coupled-channel bound-state calculations. We then use coupled-channel scattering calculations on the resulting potentials to produce a high-precision mapping between magnetic field and scattering length. We also observe 10 additional $s$-wave Feshbach resonances for Na and Rb in different combinations of Zeeman sublevels of the $F = 1$ hyperfine states. Some of the resonances show 2-body inelastic decay due to spin exchange. We compare the resonance properties with coupled-channel scattering calculations that full take account of inelastic properties.
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