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Physical Review A

Ultracold dimer association induced by a far-off-resonance optical lattice

Eric L. Bolda, Eite Tiesinga, Paul S. Julienne

Published Mar 9, 2005• 17 citations
Publisher

Abstract

We investigate a process by which an optical lattice potential can transfer two unbound ultracold atoms in a lattice site to an untrapped dimer. The transition is mediated by the anharmonic terms in the lattice potential, which couple the relative and center-of-mass coordinates of the two atoms. We calculate the rate of decay from the ground state in a lattice cell to the last bound dimer state as a function of the -wave scattering length and optical lattice depth. The decay rate has a maximum value of , where is the atomic recoil energy. Consequently typical molecular production rates are much smaller than . Explicit results are given for atoms tuned near a Feshbach resonance.

DOI
10.1103/physreva.71.033404

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•Jan 1, 2009•0 citations
We investigate a process by which an optical lattice potential can transfer two unbound ultracold atoms in a lattice site to an untrapped dimer. The transition is mediated by the anharmonic terms in the lattice potential, which couple the relative and center-of-mass coordinates of the two atoms. We calculate the rate of decay from the ground state in a lattice cell to the last bound dimer state as a function of the -wave scattering length and optical lattice depth. The decay rate has a maximum value of , where is the atomic recoil energy. Consequently typical molecular production rates are much smaller than . Explicit results are given for atoms tuned near a Feshbach resonance.
A theoretical approach was developed for an exact numerical description of a pair of ultracold atoms interacting via a central potential, which is trapped in a three-dimensional optical lattice. The coupling of center-of-mass and relative-motion coordinates is explicitly considered using a configuration-interaction (exact-diagonalization) technique. Deviations from the harmonic approximation are discussed for several heteronuclear alkali-metal atom pairs trapped in a single site of an optical lattice. The consequences are discussed for the analysis of a recent experiment [C. Ospelkaus et al., Phys. Rev. Lett. 97, 120402 (2006)] in which radio-frequency association was used to create diatomic molecules from a fermionic and a bosonic atom and to measure their binding energies close to a magnetic Feshbach resonance.
When two atoms interact in the presence of an anharmonic potential, such as an optical lattice, the center of mass motion cannot be separated from the relative motion. In addition to generating a confinement-induced resonance (or shifting the position of an existing Feshbach resonance), the external potential changes the resonance picture qualitatively by introducing new resonances where molecular excited center of mass states cross the scattering threshold. We demonstrate the existence of these resonances, give their quantitative characterization in an optical superlattice and propose an experimental scheme to detect them through controlled sweeping of the magnetic field.
A detailed study of the anharmonicity-induced resonances caused by the coupling of center-of-mass and relative motion is presented for a system of two ultracold atoms in single-well potentials. As has been confirmed experimentally, these inelastic confinement-induced resonances are of interest since they can lead to coherent molecule formation, losses, and heating in ultracold atomic gases. A perturbative model is introduced to describe the resonance positions and the coupling strengths. The validity of the model and the behavior of the resonances for different confinement geometries are analyzed in comparison with exact numerical ab initio calculations. While such resonances have so far only been detected for large positive values of the s-waves\text{-wave}s-wave scattering length, it is found that they are present also for negative s-waves\text{-wave}s-wave scattering lengths, i.e., for attractive interactions. The possibility to coherently tune the resonances by a variation of the external confinement geometry might pave the way for coherent molecule association where magnetic Feshbach resonances are inaccessible.
We study the molecular behavior of two atoms interacting near a Feshbach resonance in the presence of a 1D periodic potential. The critical value of the scattering length needed to produce a molecule and the binding energy at resonance are calculated as a function of the intensity of the periodic potential. Because of the non-separability of the center of mass and relative motion, the binding energy depends on the quasimomentum of the molecule. This has dramatic consequences on the molecular tunneling properties, which become strongly dependent on the scattering length.
We model two bosons in an optical lattice near a Feshbach or photoassociation resonance, focusing on the Bose-Hubbard model in one dimension. Whereas the usual atoms-only theory with a tunable scattering length yields one bound state for a molecular dimer for either an attractive or repulsive atom-atom interaction, for a sufficiently small direct background interaction between the atoms a two-channel atom-molecule theory may give two bound states that represent attractively and repulsively bound dimers occurring simultaneously. Such unusual molecular physics may be observable for an atom-molecule coupling strength comparable to the width of the dissociation continuum of the lattice dimer, which is the case, for instance, with narrow Feshbach resonances in Na, 87Rb^{87}\mathrm{Rb}87Rb, and 133Cs^{133}\mathrm{Cs}133Cs or low-intensity photoassociation in 174Yb^{174}\mathrm{Yb}174Yb.
In this dissertation, we develop simple single-band effective Hamiltonians for a fermionic gas across a Feshbach resonance in both a quasi-low-dimensional optical trap and a three-dimensional optical lattice. The proper theoretical description of these systems is nontrivial due to the multiband nature of the dimers which form in the ground state of the strongly interacting gas. For the quasi-low-dimensional case, we show that the ground state of the gas has a significant population in the excited levels of the transverse trap. Hence, the effective low-dimensional (single-band) Hamiltonian must include the effects of this real population frozen in many transverse modes. We accomplish this through the definition of a "dressed molecule" state which incorporates the excited fraction. For the three-dimensional case, a valid single-band lattice model at first seems impossible for strong interactions. However, we find effective single-band lattice models that remain valid by subtly accounting for the nontrivial structure of the on-site dimer. We perform explicit numerical calculations for two fermions in a double-well to demonstrate the range of validity of the models and their parameter values. In the process of investigation leading to these models we find other interesting results such as a ground state level crossing for three fermions in a single well and a set of Feshbach resonances induced by anharmonicity of the optical potential. The ultracold neutral atom experiments related to the work presented within provide a flexible and well-controlled tool to observe aspects of quantum physics not easily accessible or controllable in other systems. The combination of optical lattice trapping techniques with the ability to manipulate the interactions via a Feshbach resonance allows for the study of novel strongly correlated physics. This work addresses an important and fundamentally interesting issue for these systems and serves as a proper starting point for further theoretical studies in conjunction with experiment.