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Register a new userOptimal geometry for efficient loading of an optical dipole trap
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Added by
Andrzej Szczepkowicz
Publication date
2008
fields
Physics
and research's language is
English
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One important factor which determines efficiency of loading cold atoms into an optical dipole trap from a magneto-optical trap is the distance between the trap centers. By studying this efficiency for various optical trap depths (2--110 mK) we find that for optimum dipole trap loading, longitudinal displacements up to 15 mm are necessary. An explanation for this observation is presented and compared with other work and a simple analytical formula is derived for the optimum distance between the trap centers.
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We demonstrate an efficient scheme for continuous trap loading based upon spatially selective optical pumping. We discuss the case of $^{1}$S$_{0}$ calcium atoms in an optical dipole trap (ODT), however, similar strategies should be applicable to a wide range of atomic species. Our starting point is a reservoir of moderately cold ($approx 300 mu$K) metastable $^{3}$P$_{2}$-atoms prepared by means of a magneto-optic trap (triplet-MOT). A focused 532 nm laser beam produces a strongly elongated optical potential for $^{1}$S$_{0}$-atoms with up to 350 $mu$K well depth. A weak focused laser beam at 430 nm, carefully superimposed upon the ODT beam, selectively pumps the $^{3}$P$_{2}$-atoms inside the capture volume to the singlet state, where they are confined by the ODT. The triplet-MOT perpetually refills the capture volume with $^{3}$P$_{2}$-atoms thus providing a continuous stream of cold atoms into the ODT at a rate of $10^7 $s$^{-1}$. Limited by evaporation loss, in 200 ms we typically load $5 times 10^5$ atoms with an initial radial temperature of 85 $mu$K. After terminating the loading we observe evaporation during 50 ms leaving us with $10^5$ atoms at radial temperatures close to 40 $mu$K and a peak phase space density of $6.8 times 10^{-5}$. We point out that a comparable scheme could be employed to load a dipole trap with $^{3}$P$_{0}$-atoms.
Examination of loading the isotopes $^{85}$Rb and $^{87}$Rb simultaneously into a shallow far-off-resonance trap (FORT) has revealed an unexpected decrease in maximum atom number loaded as compared to loading either isotope alone. The simultaneous loading of the FORT will be affected by additional homonuclear and heteronuclear light-assisted collisional losses. However, these losses are measured and found to be insufficient to explain the observed drop in total number of atoms loaded into the FORT. We find that our observations are consistent with a decrease in loading rate caused by inter-isotope disruptions of the efficient laser cooling required to load atoms into the optical trap.
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.
Recently, we have experimentally demonstrated a continuous loading mechanism for an optical dipole trap from a guided atomic beam [1]. The observed evolution of the number of atoms and temperature in the trap are consequences of the unusual trap geometry. In the present paper, we develop a model based on a set of rate equations to describe the loading dynamics of such a mechanism. We consider the collision statistics in the non-uniform trap potential that leads to twodimensional evaporation. The comparison between the resulting computations and experimental data allows to identify the dominant loss process and suggests ways to enhance the achievable steady-state atom number. Concerning subsequent evaporative cooling, we find that the possibility of controlling axial and radial confinement independently allows faster evaporation ramps compared to single beam optical dipole traps.
We present a novel optical cooling scheme that relies on hyperfine dark states to enhance loading and cooling atoms inside deep optical dipole traps. We demonstrate a seven-fold increase in the number of atoms loaded in the conservative potential with strongly shifted excited states. In addition, we use the energy selective dark-state to efficiently cool the atoms trapped inside the conservative potential rapidly and without losses. Our findings open the door to optically assisted cooling of trapped atoms and molecules which lack the closed cycling transitions normally needed to achieve low temperatures and the high initial densities required for evaporative cooling.
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