Two-atom systems in small traps are of fundamental interest for understanding the role of interactions in degenerate cold gases and for the creation of quantum gates in quantum information processing with single-atom traps. One of the key quantities is the inelastic relaxation (decay) time when one of the atoms or both are in a higher hyperfine state. Here we measure this quantity in a heteronuclear system of (87)Rb and (85)Rb in a micro optical trap and demonstrate experimentally and theoretically the presence of both fast and slow relaxation processes, depending on the choice of the initial hyperfine states. This experimental method allows us to single out a particular relaxation process thus provides an extremely clean platform for collisional physics studies. Our results have also implications for engineering of quantum states via controlled collisions and creation of two-qubit quantum gates.
Two-atom systems in small traps are of fundamental interest for understanding the role of interactions in degenerate cold gases and for the creation of quantum gates in quantum information processing with single-atom traps. One of the key quantities is the inelastic relaxation (decay) time when one of the atoms or both are in a higher hyperfine state. Here we measure this quantity in a heteronuclear system of (87)Rb and (85)Rb in a micro optical trap and demonstrate experimentally and theoretically the presence of both fast and slow relaxation processes, depending on the choice of the initial hyperfine states. This experimental method allows us to single out a particular relaxation process thus provides an extremely clean platform for collisional physics studies. Our results have also implications for engineering of quantum states via controlled collisions and creation of two-qubit quantum gates.
Measurements of the temperature dependence of trap loss collisions of laser-cooled rubidium atoms are presented. A significant suppression of the rate of collisions between ground- and excited-state atoms is observed for temperatures below $\\sim$70 muK. In such inelastic collisions, the atomic excitation takes place at long range and must survive against spontaneous decay to short range. Our results are consistent with recent predictions for the low temperature suppression of these collisions due to reduced survival of atomic excitation at low collision velocities.^ We report on measurements of trap loss collisions between ultracold Rb atoms which are confined in a magneto-optical trap. Both isotopes sp85Rb and sp87Rb have been studied over wide range of trap laser intensities and detunings. The trap loss collision rates exhibit variations over 3 orders of magnitude. We observe significant differences between the isotopes. At large detunings the ability of the trap to recapture products of the hyperfine-changing collisions is significantly diminished. This finding is supported by our numerical simulations of the recapture process. The trap loss rates due to collisions with room temperature background gas have also been measured.^ Using laser light tuned to a repulsive molecular potential, we have been able to suppress inelastic ground-state hyperfine changing collisions between ultracold sp87Rb atoms. Adiabatic excitation to the repulsive curve alters the atomic trajectories and prevents the atoms from approaching close enough for the hyperfine change to occur. Experimental results show suppressions up to $\\sim$50% and are in reasonable agreement with a simple Landau-Zener model.^ Finally, we have observed a significant cooperative effect in ultracold trap loss collisions induced by two separate lasers. One laser, tuned close to the atomic resonance, excites the atom pair to an attractive potential at long range. The resulting acceleration and deflection give rise to an enhancement in the collisional flux of ground-state atoms reaching short range, as probed by a second laser. Enhancements up to a factor of $\\sim$3 have been observed. ^
We investigate quantum-mechanical interactions between ultracold rubidium and cesium in an optical trap at temperatures of a few microkelvin. Our results provide, on the one hand, an experimental key to understand the collisional properties and, on the other hand, a tool to control the interspecies interactions. By performing loss measurements we locate several Feshbach resonances, which provide insight into the energy structure of weakly bound RbCs molecules near the dissociation threshold and allow for the production of such heteronuclear Feshbach molecules. In the future we will transfer these loosely-bound molecules into the absolute internal ground state. The availability of ultracold heteronuclear ground state molecules will open the door to investigate phenomena associated with ultracold polar quantum gases. In our new experimental set-up we are able to trap and cool rubidium and cesium atoms in their lowest internal states. First we load both species into a two-color magneto-optical trap, having full control over the single-species atom number. We extend the technique of degenerate Raman-sideband cooling to a two-color version, which is able to simultaneously cool and polarize both rubidium and cesium. Thereafter we load the atoms into a levitated crossed optical dipole trap. Because of the presence of the gradient magnetic field the trap is highly state selective and consequently provides perfect spin-polarization of the sample. Furthermore, a coincidence of the magnetic-moment-to-mass ratios of the two species allows for simultaneous levitation of both, which assures an almost perfect spatial overlap between the species. We perform Feshbach spectroscopy in two different spin channels of the mixture within a magnetic field ranging from 20 to 300G. In the lowest spin combination of the species we locate 23 interspecies Feshbach resonances, while in a higher spin mixture we find 2 resonances. The high number of resonances found within this range of magnetic field is unusual for alkali mixtures. The presence of many resonances points to scattering properties of the mixture, which include higher-order coupling mechanisms. The obtained data on the Feshbach spectroscopy provide, on one hand, fundamental experimental input to characterize the Rb-Cs scattering properties and, on the other hand, identification of possible starting points for the association of ultracold heteronuclear RbCs molecules. In addition we show preliminary results on spectroscopy of the binding energy of RbCs dimers, based on a modulation of the magnetic field. The recently obtained Bose-Einstein condensate of Cs atoms, which represents a benchmark for the performance of the present apparatus, will be discussed as well as the potential pathways towards a double-degenerate mixture. We follow two main goals, first the production of a double Bose-Einstein condensate and, second, the transfer of shallow bound Feshbach molecules to the absolute internal ground state. The production of heteronuclear ground state molecules allows to enter the world of ultracold polar quantum systems.
We have realized a two-species mirror-magneto-optical trap containing a mixture of 87Rb(85Rb) and 133Cs atoms. Using this trap, we have measured the heteronuclear collisional loss rate ${\ensuremath{\beta}}_{\mathrm{Rb-Cs}}^{\ensuremath{'}}$ due to intraspecies cold collisions. We find a distinct difference in the magnitude and intensity dependence of ${\ensuremath{\beta}}_{\text{Rb-Cs}}^{\ensuremath{'}}$ for the two isotopes 87Rb and 85Rb which we attribute to the different ground-state hyperfine splitting energies of the two isotopes.
We study cold heteronuclear atom-ion collisions by immersing a trapped single ion into an ultracold atomic cloud. Using ultracold atoms as reaction targets, our measurement is sensitive to elastic collisions with extremely small energy transfer. The observed energy-dependent elastic atom-ion scattering rate deviates significantly from the prediction of Langevin but is in full agreement with the quantum mechanical cross section. Additionally, we characterize inelastic collisions leading to chemical reactions at the single particle level and measure the energy-dependent reaction rate constants. The reaction products are identified by in-trap mass spectrometry, revealing the branching ratio between radiative and nonradiative charge exchange processes.
The production and research of ultracold heteronuclear molecules have aroused the great interest recently. On the one hand, these molecules are extremely popular in experiments for exploring the collision dynamic behaviors in threshold, photoassociative spectrum and strong dipole-dipole interactions. On the other hand, ultracold polar molecules populated at deeply bound levels in the singlet ground state are the right candidates to investigate quantum memories for quantum simulation, and to study strongly interacting quantum degenerate gases. The precise knowledge of cold collision processes between two different types of alkali atoms is necessary for understanding and utilizing ultracold heteronuclear molecules, sympathetic cooling, and thus formation of two species BEC. The goal of the present investigation is to study the collisions between ultracold sodium atoms and cesium atoms. We systematically demonstrate simultaneously trapping ultracold sodium and cesium atoms in a dual-species magneto-optical trap (MOT). The sodium atom trap loss rate coefficient Na-Cs is measured as a function of Na trapping laser intensity. At low intensities, the trap loss is dominated by ground-state hyperfine-changing collisions, while at high intensities, collisions involving excited atoms are more important. A strong interspecies collision-induced loss for Na atoms in the MOT is observed. In order to obtain the trap loss coefficient Na-Cs, we proceed in two steps. First, the Cs repumping laser is blocked to avoid the formation of ultraold Cs atoms. The loading process of Na atoms is recorded when the Cs trapping laser is on. Second, the loading curves of the Na atoms are obtained as Cs atoms are present with the repumping laser beams. The total losses PNa and PNa' are acquired by fitting the two loading curves of trapped Na atoms. Thus, the trap loss coefficient Na-Cs can be derived from the difference between total losses PNa and PNa' divided by the density of the Cs atoms. The coefficient Na-Cs decreases in a range of 5-10mW/cm2, which originates from the hyperfine-state changing (HFC) collision. A Doppler model is used to calculate the Na atom trap depth, in that the atom trap depth and exoergic energy determine the behavior of the collisional trap loss rate coefficient. The three corresponding calculated critical intensities of Na trapping laser are 7.98, 14.82, 16.2 mW/cm2 respectively in the Na-Cs HFC collision process. The first calculated critical intensity value agrees well with the experimental result. Our work provides a valuable insight into HFC collision between Na and Cs atoms and also paves the way for the production of ultracold NaCs molecules using Photoassociation (PA) technology. Furthermore, the experimental results lay a great basis for the obtainments of high sensitive heteronuclear NaCs molecular PA spectrum and the creation of deeply bound ground state molecules.