arXiv subjects
Publications and source records attributed to Felix Moumtsilis.
We report on the current development of a single photon source based on a long-range interacting room temperature rubidium vapor. We discuss the history of the project, the production of vapor cells, and the observation of Rabi-oscillations in the four-wave-mixing excitation scheme.
An ensemble of Rubidum atoms can be excited with lasers such that it evolves into an entangled state with just one collective excitation within the Rydberg blockade radius. The decay of this state leads to the emission of a single, antibunched photon. For a hot vapor of Rubidium atoms in a micro cell we numerically study the feasibility of such a single-photon source under different experimental conditions like the atomic density distribution and the choice of electronic states addressed by the lasers. For the excitation process with three rectangular lasers pulses, we simulate the coherent dynamics of the system in a truncated Hilbert space. We investigate the radiative behavior of the moving Rubidum atoms and optimize the laser pulse sequence accordingly. We find that the collective decay of the single-excitation leads to a fast and directed photon emission and further, that a pulse sequence similar to a spin echo increases the directionality of the photon. Finally, we analyze the residual double-excitations and find that they do not exhibit these collective decay properties and play only a minor deleterious role.
We exploit the effect of light-induced atomic desorption to produce high atomic densities ($n\gg k^3$) in a rubidium vapor cell. An intense off-resonant laser is pulsed for roughly one nanosecond on a micrometer-sized sapphire-coated cell, which results in the desorption of atomic clouds from both internal surfaces. We probe the transient atomic density evolution by time-resolved absorption spectroscopy.With a temporal resolution of $\approx1\,\mathrm{ns}$, we measure the broadening and line shift of the atomic resonances. Both broadening and line shift are attributed to dipole-dipole interactions. This fast switching of the atomic density and dipolar interactions could be the basis for future quantum devices based on the excitation blockade.