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Register a new userTrap-induced resonances in controlled collisions of cesium atoms
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We consider the feasibility of observing a trap-induced resonance [Stock et al., Phys. Rev. Lett. 91, 183201 (2003)] for the case of two 133Cs atoms, trapped in separated wells of a polarization-gradient optical lattice, and interacting through a multichannel scattering process. Due to the anomalously large scattering length of cesium dimers, a strong coupling can occur between vibrational states of the trap and a weakly bound molecular state that is made resonant by the ac-Stark shift of the lattice. We calculate the energy spectrum of the two-atom system as a function of the distance between two potential wells by connecting the solutions of the Schroedinger equation for the short-range molecular potential to that of the long-range trap in a self-consistent manner. The short-range potential is treated through a multichannel pseudopotential, parametrized by the K matrix, calculated numerically for atoms in free space in a close-coupling approximation. This captures both the bound molecular spectrum as well as the energy-dependent scattering for all partial waves. We establish realistic operating conditions under which the trap-induced resonance could be observed and show that this strong and coherent interaction could be used as a basis for high-fidelity two-qubit quantum logic operations.
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We report the measurement of collision rate coefficient for collisions between ultracold Cs atoms and low energy Cs+ ions. The experiments are performed in a hybrid trap consisting of a magneto-optical trap (MOT) for Cs atoms and a Paul trap for Cs+ ions. The ion-atom collisions impart kinetic energy to the ultracold Cs atoms resulting in their escape from the shallow MOT and, therefore, in a reduction in the number of Cs atoms in the MOT. By monitoring, using fluorescence measurements, the Cs atom number and the MOT loading dynamics and then fitting the data to a rate equation model, the ion-atom collision rate is derived. The Cs-Cs+ collision rate coefficient $9.3(pm0.4)(pm1.2)(pm3.5) times 10^{-14}$ m$^{3}$s$^{-1}$, measured for an ion distribution with most probable collision energy of 95 meV ($approx k_{B}.1100$ K), is in fair agreement with theoretical calculations. As an intermediate step, we also determine the photoionization cross section of Cs $6P_{3/2}$ atoms at 473 nm wavelength to be $2.28 (pm 0.33) times 10^{-21}$ m$^{2}$.
We report on cooling of an atomic cesium gas closely above an evanescent-wave. Our first evaporation experiments show a temperature reduction from 10muK down to 300nK along with a gain in phase-space density of almost two orders of magnitude. In a series of measurements of heating and spin depolarization an incoherent background of resonant photons in the evanescent-wave diode laser light was found to be the limiting factor at this stage.
We report on cooling of an atomic cesium gas closely above an evanescent-wave atom mirror. At high densitities, optical cooling based on inelastic reflections is found to be limited by a density-dependent excess temperature and trap loss due to ultracold collisions involving repulsive molecular states. Nevertheless, very good starting conditions for subsequent evaporative cooling are obtained. Our first evaporation experiments show a temperature reduction from 10muK down to 300nK along with a gain in phase-space density of almost two orders of magnitude.
We describe an easily implementable method for non-destructive measurements of ultracold atomic clouds based on dark field imaging of spatially resolved Faraday rotation. The signal-to-noise ratio is analyzed theoretically and, in the absence of experimental imperfections, the sensitivity limit is found to be identical to other conventional dispersive imaging techniques. The dependence on laser detuning, atomic density and temperature is characterized in a detailed comparison with theory. Due to low destructiveness, spatially resolved images of the same cloud can be acquired up to 2000 times. The technique is applied to avoid the effect of shot-to-shot fluctuations in atom number calibration, to demonstrate single-run vector magnetic field imaging and single-run spatial imaging of the systems dynamic behavior. This demonstrates that the method is a useful tool for the characterization of static and dynamically changing properties of ultracold atomic clouds.
The control of the ultracold collisions between neutral atoms is an extensive and successful field of study. The tools developed allow for ultracold chemical reactions to be managed using magnetic fields, light fields and spin-state manipulation of the colliding particles among other methods. The control of chemical reactions in ultracold atom-ion collisions is a young and growing field of research. Recently, the collision energy and the ion electronic state were used to control atom-ion interactions. Here, we demonstrate spin-controlled atom-ion inelastic processes. In our experiment, both spin-exchange and charge-exchange reactions are controlled in an ultracold Rb-Sr$^+$ mixture by the atomic spin state. We prepare a cloud of atoms in a single hyperfine spin-state. Spin-exchange collisions between atoms and ion subsequently polarize the ion spin. Electron transfer is only allowed for (RbSr)$^+$ colliding in the singlet manifold. Initializing the atoms in various spin states affects the overlap of the collision wavefunction with the singlet molecular manifold and therefore also the reaction rate. We experimentally show that by preparing the atoms in different spin states one can vary the charge-exchange rate in agreement with theoretical predictions.
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