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Register a new userHeteronuclear molecules in an optical dipole trap
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We report on the creation and characterization of heteronuclear KRb Feshbach molecules in an optical dipole trap. Starting from an ultracold gas mixture of K-40 and Rb-87 atoms, we create as many as 25,000 molecules at 300 nK by rf association. Optimizing the association process, we achieve a conversion efficiency of 25%. We measure the temperature dependence of the rf association process and find good agreement with a phenomenological model that has previously been applied to Feshbach molecule creation by slow magnetic-field sweeps. We also present a measurement of the binding energy of the heteronuclear molecules in the vicinity of the Feshbach resonance and provide evidence for Feshbach molecules as deeply bound as 26 MHz.
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We report on the first creation of ultracold bosonic heteronuclear molecules of two fermionic species, 6Li and 40K, by a magnetic field sweep across an interspecies s-wave Feshbach resonance. This allows us to associate up to 4x10^4 molecules with high efficiencies of up to 50%. Using direct imaging of the molecules, we measure increased lifetimes of the molecules close to resonance of more than 100 ms in the molecule-atom mixture stored in a harmonic trap.
We present an evaporative cooling technique for atoms trapped in an optical dipole trap that benefits from narrow optical transitions. For an appropriate choice of wavelength and polarization, a single laser beam leads to opposite light-shifts in two internal states of the lowest energy manifold. Radio-frequency coupling between these two states results in evaporative cooling at a constant trap stiffness. The evaporation protocol is well adapted to several atomic species, in particular to the case of Lanthanides such as Er, Dy, and fermionic Yb, but also to alkali-earth metals such as fermionic Sr. We derive the dimensionless expressions that allow us to estimate the evaporation efficiency. As a concrete example, we consider the case of $^{162}$Dy and present a numerical analysis of the evaporation in a dipole trap near the $J=J$ optical transition at 832 nm. We show that this technique can lead to runaway evaporation in a minimalist experimental setup.
We report on the creation of ultracold heteronuclear molecules assembled from fermionic 40K and bosonic 87Rb atoms in a 3D optical lattice. Molecules are produced at a heteronuclear Feshbach resonance both on the attractive and the repulsive side of the resonance. We precisely determine the binding energy of the heteronuclear molecules from rf spectroscopy across the Feshbach resonance. We characterize the lifetime of the molecular sample as a function of magnetic field and measure between 20 and 120ms. The efficiency of molecule creation via rf association is measured and is found to decrease as expected for more deeply bound molecules.
In recent years, cold atoms could prove their scientific impact not only on ground but in microgravity environments such as the drop tower in Bremen, sounding rockets and parabolic flights. We investigate the preparation of cold atoms in an optical dipole trap, with an emphasis on evaporative cooling under microgravity. Up to $ 1times10^{6} $ rubidium-87 atoms were optically trapped from a temporarily dark magneto optical trap during free fall in the droptower in Bremen. The efficiency of evaporation is determined to be equal with and without the effect of gravity. This is confirmed using numerical simulations that prove the dimension of evaporation to be three-dimensional in both cases due to the anharmonicity of optical potentials. These findings pave the way towards various experiments on ultra-cold atoms under microgravity and support other existing experiments based on atom chips but with plans for additional optical dipole traps such as the upcoming follow-up missions to current and past spaceborne experiments.
We present studies of strong coupling in single-photon photoassociation of cesium dimers using an optical dipole trap. A thermodynamic model of the trap depletion dynamics is employed to extract absolute rate coefficents. From the dependence of the rate coefficient on the photoassociation laser intensity, we observe saturation of the photoassociation scattering probability at the unitarity limit in quantitative agreement with the theoretical model by Bohn and Julienne [Phys. Rev. A, 60, 414 (1999)]. Also the corresponding power broadening of the resonance width is measured. We could not observe an intensity dependent light shift in contrast to findings for lithium and rubidium, which is attributed to the absence of a p or d-wave shape resonance in cesium.
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