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Register a new userDemonstration of a state-insensitive, compensated nanofiber trap
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We report the experimental realization of an optical trap that localizes single Cs atoms ~215 nm from surface of a dielectric nanofiber. By operating at magic wavelengths for pairs of counter-propagating red- and blue-detuned trapping beams, differential scalar light shifts are eliminated, and vector shifts are suppressed by ~250. We thereby measure an absorption linewidth Gamma/2pi = 5.7 pm 0.1 MHz for the Cs 6S1/2,F=4 - 6P3/2,F=5 transition, where Gamma/2pi = 5.2 MHz in free space. Optical depth d~66 is observed, corresponding to an optical depth per atom d_1~0.08. These advances provide an important capability for the implementation of functional quantum optical networks and precision atomic spectroscopy near dielectric surfaces.
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We demonstrate optical transport of cold cesium atoms over millimeter-scale distances along an optical nanofiber. The atoms are trapped in a one-dimensional optical lattice formed by a two-color evanescent field surrounding the nanofiber, far red- and blue-detuned with respect to the atomic transition. The blue-detuned field is a propagating nanofiber-guided mode while the red-detuned field is a standing-wave mode which leads to the periodic axial confinement of the atoms. Here, this standing wave is used for transporting the atoms along the nanofiber by mutually detuning the two counter-propagating fields which form the standing wave. The performance and limitations of the nanofiber-based transport are evaluated and possible applications are discussed.
An accurate measurement of the bunching of photons in the fluorescent emission from an ultracold ensemble of thermal 87Rb atoms in a steady-state magneto-optical trap is presented. Time-delayed-intensity-interferometry (TDII) performed with a 5-nanosecond time resolution yielded a second-order intensity correlation function that has the ideal value of 2 at zero delay, and that shows coherent Rabi oscillations of upto 5 full periods - much longer than the spontaneous emission lifetime of the excited state of Rb. The oscillations are damped out by ~150ns, and thereafter, as expected from a thermal source, an exponential decay is observed, enabling the determination of the temperature of the atomic ensemble. Values so obtained compare well with those determined by standard techniques. TDII thus enables a quantitative study of the coherent and incoherent dynamics, even of a large thermal ensemble of atomic emitters.
State-insensitive dipole trapping of multilevel atoms can be achieved by an appropriate choice of the wavelength of the trapping laser, so that the interaction with the different transitions results in equal AC Stark shifts for the ground and excited states of interest. However this approach is severely limited by the availability of coherent sources at the required wavelength and of appropriate power. This work investigates state-insensitive trapping of caesium atoms for which the required wavelength of 935.6 nm is inconvenient in terms of experimental realization. Bichromatic state-insensitive trapping is proposed to overcome the lack of suitable laser sources. We first consider pairs of laser wavelengths in the ratio 1:2 and 1:3, as obtained via second- and third- harmonic generation. We found that the wavelength combinations 931.8-1863.6 nm and 927.5-2782.5 nm are suitable for state-insensitive trapping of caesium atoms. In addition, we examine bichromatic state-insensitive trapping produced by pairs of laser wavelengths corresponding to currently available high power lasers. These wavelength pairs were found to be in the range of 585-588 nm and 623-629 for one laser and 1064-1080 nm for the other.
Spin flips of a single proton were driven in a Penning trap with a homogeneous magnetic field. For the spin-state analysis the proton was transported into a second Penning trap with a superimposed magnetic bottle, and the continuous Stern-Gerlach effect was applied. This first demonstration of the double Penning trap technique with a single proton suggests that the antiproton magnetic moment measurement can potentially be improved by three orders of magnitude or more.
We report the operation of a dual Rb/Cs atomic fountain clock. 133Cs and 87Rb atoms are cooled, launched, and detected simultaneously in LNE-SYRTEs FO2 double fountain. The dual clock operation occurs with no degradation of either the stability or the accuracy. We describe the key features for achieving such a simultaneous operation. We also report on the results of the first Rb/Cs frequency measurement campaign performed with FO2 in this dual atom clock configuration, including a new determination of the absolute 87Rb hyperfine frequency.
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