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arXiv:physics/0504022 · Physical Review Letters

Back and Forth Transfer and Coherent Coupling in a Cold Rydberg Dipole Gas

Marcel Carto Constantin Mudrich, Nassim Zahzam, Thibault Vogt, D. Comparat, P. Pillet

Published Nov 29, 2005• 39 citations
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Abstract

Coupling by the resonant dipole-dipole energy transfer between cold cesium Rydberg atoms is investigated using time-resolved narrow-band deexcitation spectroscopy. This technique combines the advantage of efficient Rydberg excitation with high-resolution spectroscopy at variable interaction times. Dipole-dipole interaction is observed spectroscopically as avoided level crossing. The coherent character of the process is linked to back and forth transfer in the np + np <--> ns + (n + 1)s reaction. Decoherence in the ensemble has two different origins: the atom motion induced by dipole-dipole interaction and the migration of the s-Rydberg excitation in the environment of p-Rydberg atoms.

DOI
10.1103/physrevlett.95.233002

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Coupling by the resonant dipole-dipole energy transfer between cold cesium Rydberg atoms is investigated using time-resolved narrow-band deexcitation spectroscopy. This technique combines the advantage of efficient Rydberg excitation with high-resolution spectroscopy at variable interaction times. Dipole-dipole interaction is observed spectroscopically as avoided level crossing. The coherent character of the process is linked to back and forth transfer in the np + np <--> ns + (n + 1)s reaction. Decoherence in the ensemble has two different origins: the atom motion induced by dipole-dipole interaction and the migration of the s-Rydberg excitation in the environment of p-Rydberg atoms.
Coupling by the resonant dipole-dipole energy transfer between cold cesium Rydberg atoms is investigated using time-resolved narrow-band de-excitation spectroscopy. This technique combines the advantage of efficient Rydberg excitation with high-resolution spectroscopy at variable interaction times. The coherent character of the process is studied by back and forth transfer in the np+np <--> ns+(n+1)s reaction. The evolution of coherence is mostly due to the motion between the atoms induced by the dipole-dipole interaction. Dipole-dipole interaction is observed spectroscopically as avoided level crossing.
High resolution laser excitation of np Rydberg states of cesium atoms shows a dipole blockade at Förster resonances corresponding to the resonant dipole-dipole energy transfer of the np+np --> ns+(n+1)s reaction. The dipole-dipole interaction can be tuned on and off by the Stark effect, and such a process, observed for relatively low n(25-41), is promising for quantum gate devices. Both Penning ionization and saturation in the laser excitation can limit the range of observation of the dipole blockade.
The dipole-dipole interaction strongly couples ultracold highly excited atoms, known as Rydberg atoms, and is the dominant mechanism for energy exchange among such atoms on microsecond time scales. I present the results of experiments that investigate this interaction using rubidium atoms excited to Rydberg states with an all-diode laser system. In the first of these, high resolution dipole-dipole interaction spectra for different magnetic sublevels of the 32d5/2 state are collected and analyzed. In the second experiment, ultracold rubidium atoms are implusively excited to coherent superpositions of three closely spaced |mj|sublevels of the 32d5/2 state in a weak electric field. The magnitude of the field sets the energy level spacing between these states, and hence the frequency of the phase dependent oscillations resulting from interference in resonant energy exchange processes. In the third experiment, the dipole-dipole interaction induced resonant energy exchange between columns of ultracold rubidium Rydberg atoms is imaged using a new technique involving selective field ionization with a spatially sensitive ion detector.
High resolution laser excitation of np Rydberg states of cesium atoms shows a dipole blockade at Förster resonances corresponding to the resonant dipole-dipole energy transfer of the np + np → ns + (n + 1)s reaction. The dipole-dipole interaction can be tuned on and off by the Stark effect, and such a process observed for relatively low n (25 − 41) is promising for quantum gate devices. Both Penning ionization and saturation in the laser excitation can limit the range of observation of the dipole blockade
We demonstrate a novel time-domain method to probe electronic coherence in ensembles of cold Rydberg atoms coupled via nearly resonant dipole-dipole interactions. Short laser pulses create coherent superpositions of few-electron eigenstates which evolve under the influence of pulsed electric fields. The pulses steer the dynamics, enhancing the probability for finding atoms in np, rather than initially excited ns states. The enhancement reflects the underlying electronic coherence which persists for >10 μs, 2 orders of magnitude longer than previously measured dephasing times in the same system. Simulations suggest that atom motion is responsible for the eventual decoherence.
We have observed resonant energy transfer between cold Rydberg atoms in spatially separated cylinders. Resonant dipole-dipole coupling excites the 49s atoms in one cylinder to the 49p state while the 41d atoms in the second cylinder are transferred down to the 42p state. We have measured the production of the 49p state as a function of separation of the cylinders (0-80 microm) and the interaction time (0-25 micros). In addition, we measured the width of the electric field resonances. A full many-body quantum calculation reproduces the main features of the experiments.