RESUMEN
The evanescent field surrounding nanoscale optical waveguides offers an efficient interface between light and mesoscopic ensembles of neutral atoms. However, the thermal motion of trapped atoms, combined with the strong radial gradients of the guided light, leads to a time-modulated coupling between atoms and the light mode, thus giving rise to additional noise and motional dephasing of collective states. Here, we present a dipole force free scheme for coupling of the radial motional states, utilizing the strong intensity gradient of the guided mode and demonstrate all-optical coupling of the cesium hyperfine ground states and motional sideband transitions. We utilize this to prolong the trap lifetime of an atomic ensemble by Raman sideband cooling of the radial motion which, to the best of our knowledge, has not been demonstrated in nano-optical structures previously. This Letter points towards full and independent control of internal and external atomic degrees of freedom using guided light modes only.
RESUMEN
We produce a 600-ns pulse of 1.86-dB squeezed vacuum at 795 nm in an optical parametric amplifier and store it in a rubidium vapor cell for 1 mus using electromagnetically induced transparency. The recovered pulse, analyzed using time-domain homodyne tomography, exhibits up to 0.21+/-0.04 dB of squeezing. We identify the factors leading to the degradation of squeezing and investigate the phase evolution of the atomic coherence during the storage interval.
RESUMEN
We experimentally demonstrate a communication protocol that enables frequency conversion and routing of quantum information in an adiabatic and thus robust way. The protocol is based on electromagnetically induced transparency (EIT) in systems with multiple excited levels: transfer and/or distribution of optical states between different signal modes is implemented by adiabatically changing the control fields. The proof-of-principle experiment is performed using the hyperfine levels of the rubidium D1 line.