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Register a new userCoherent optical transfer of Feshbach molecules to a lower vibrational state
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Added by
Johannes Hecker Denschlag
Publication date
2006
fields
Physics
and research's language is
English
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Using the technique of stimulated Raman adiabatic passage (STIRAP) we have coherently transferred ultracold 87Rb2 Feshbach molecules into a more deeply bound vibrational quantum level. Our measurements indicate a high transfer efficiency of up to 87%. As the molecules are held in an optical lattice with not more than a single molecule per lattice site, inelastic collisions between the molecules are suppressed and we observe long molecular lifetimes of about 1 s. Using STIRAP we have created quantum superpositions of the two molecular states and tested their coherence interferometrically. These results represent an important step towards Bose-Einstein condensation (BEC) of molecules in the vibrational ground state.
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We explore the rich internal structure of Cs_2 Feshbach molecules. Pure ultracold molecular samples are prepared in a CO_2-laser trap, and a multitude of weakly bound states is populated by elaborate magnetic-field ramping techniques. Our methods use different Feshbach resonances as input ports and various internal level crossings for controlled state transfer. We populate higher partial-wave states of up to eight units of rotational angular momentum (l-wave states). We investigate the molecular structure by measurements of the magnetic moments for various states. Avoided level crossings between different molecular states are characterized through the changes in magnetic moment and by a Landau-Zener tunneling method. Based on microwave spectroscopy, we present a precise measurement of the magnetic-field dependent binding energy of the weakly bound s-wave state that is responsible for the large background scattering length of Cs. This state is of particular interest because of its quantum-halo character.
We study the spontaneous dissociation of diatomic molecules produced in cold atomic gases via magnetically tunable Feshbach resonances. We provide a universal formula for the lifetime of these molecules that relates their decay to the scattering length and the loss rate constant for inelastic spin relaxation. Our universal treatment as well as our exact coupled channels calculations for $^{85}$Rb dimers predict a suppression of the decay over several orders of magnitude when the scattering length is increased. Our predictions are in good agreement with recent measurements of the lifetime of $^{85}$Rb$_2$.
We present measurements of the binding energies of $^6$Li p-wave Feshbach molecules formed in combinations of the (F = 1/2, m_F = +1/2), (1), and (F = 1/2, m_F = -1/2), (2), states. The binding energies scale linearly with magnetic field detuning for all three resonances. The relative molecular magnetic moments are found to be $113 pm 7 mu$K/G, $111 pm 6 mu$K/G and $118 pm 8 mu$K/G for the (1)-(1), (1)-(2) and (2)-(2) resonances, respectively, in good agreement with theoretical predictions. Closed channel amplitudes and the size of the p-wave molecules are obtained theoretically from full closed-coupled calculations.
We experimentally demonstrate Cs2 Feshbach molecules well above the dissociation threshold, which are stable against spontaneous decay on the timescale of one second. An optically trapped sample of ultracold dimers is prepared in an l-wave state and magnetically tuned into a region with negative binding energy. The metastable character of these molecules arises from the large centrifugal barrier in combination with negligible coupling to states with low rotational angular momentum. A sharp onset of dissociation with increasing magnetic field is mediated by a crossing with a g-wave dimer state and facilitates dissociation on demand with a well defined energy.
We use laser light near resonant with an optical bound-to-bound transition to shift the magnetic field at which a Feshbach resonance occurs. We operate in a regime of large detuning and large laser intensity. This reduces the light-induced atom-loss rate by one order of magnitude compared to our previous experiments [D.M. Bauer et al. Nature Phys. 5, 339 (2009)]. The experiments are performed in an optical lattice and include high-resolution spectroscopy of excited molecular states, reported here. In addition, we give a detailed account of a theoretical model that describes our experimental data.
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