Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userProbing Fermionic Condensates by Fast-Sweep Projection onto Feshbach Molecules
92
0
0.0
(
0
)
Added by
Marzena Hanna Szymanska
Publication date
2008
fields
Physics
and research's language is
English
Ask ChatGPT about the research
No Arabic abstract
Fast sweep projection onto Feshbach molecules has been widely used as a probe of fermionic condensates. By determining the exact dynamics of a pair of atoms in time varying magnetic fields, we calculate the number of condensed and noncondensed molecules created after fast magnetic field sweeps from the BCS to the BEC side of the resonances in $^{40}$K and $^{6}$Li, for different sweep rates and a range of initial and final fields. We discuss the relation between the initial fermionic condensate fraction and the molecular condensate fraction measured after the sweep.
rate research
Read More
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 predict the resonance enhanced magnetic field dependence of atom-dimer relaxation and three-body recombination rates in a $^{87}$Rb Bose-Einstein condensate (BEC) close to 1007 G. Our exact treatments of three-particle scattering explicitly include the dependence of the interactions on the atomic Zeeman levels. The Feshbach resonance distorts the entire diatomic energy spectrum causing interferences in both loss phenomena. Our two independent experiments confirm the predicted recombination loss over a range of rate constants that spans four orders of magnitude.
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 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$_2$.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
