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Journal of Physics B Atomic Molecular and Optical Physics

Finite size cavity effect on nS rubidium Rydberg state lifetimes

B. F. Magnani, Cristian Mojica-Casique, Luís Gustavo Marcassa

Published Jan 10, 2020• 5 citations
Publisher

Abstract

Abstract In this work, we present lifetime measurements of nS states of Rb as a function of the principal quantum number (40 ≤ n ≤ 70) using a sample of cold atoms held in a magneto-optical trap, which is performed in a finite size metal vacuum chamber. The Rydberg states are excited through a two-photon transition, and detected by pulsed field ionization. Our measurements are larger than the predictions by well established theoretical model (1984 Phys. Rev. A 30 2881 and 2009 Phys. Rev. A 79 052504). We have implemented a theoretical model, which considers the vacuum chamber as a lossy Fabry–Perot cavity with a discrete spectrum, and compared with experimental results. Such comparison indicates that the blackbody radiation contribution on Rydberg state lifetime can be decreased by using a small size metal cavity, without the need of cryogenic environment. This effect may have application in experiments where longer Rydberg lifetimes are required.

DOI
10.1088/1361-6455/ab6a34

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Abstract In this work, we present lifetime measurements of nS states of Rb as a function of the principal quantum number (40 ≤ n ≤ 70) using a sample of cold atoms held in a magneto-optical trap, which is performed in a finite size metal vacuum chamber. The Rydberg states are excited through a two-photon transition, and detected by pulsed field ionization. Our measurements are larger than the predictions by well established theoretical model (1984 Phys. Rev. A 30 2881 and 2009 Phys. Rev. A 79 052504). We have implemented a theoretical model, which considers the vacuum chamber as a lossy Fabry–Perot cavity with a discrete spectrum, and compared with experimental results. Such comparison indicates that the blackbody radiation contribution on Rydberg state lifetime can be decreased by using a small size metal cavity, without the need of cryogenic environment. This effect may have application in experiments where longer Rydberg lifetimes are required.
We have measured the radiative lifetimes of ns, np and nd Rydberg states of rubidium in the range 28 < n < 45. To enable long-lived states to be measured, our experiment uses slow-moving Rb atoms in a magneto-optical trap (MOT). Two experimental techniques have been adopted to reduce random and systematic errors. First, a narrow-bandwidth pulsed laser is used to excite the target Rydberg state, resulting in minimal shot-to-shot variation in the initial state population. Second, we monitor the target state population as a function of time delay from the laser pulse using a short-duration, millimetre-wave pulse that is resonant with a one- or two-photon transition. We then selectively field ionize the monitor state, and detect the resulting electrons with a micro-channel plate. This signal is an accurate mirror of the target state population, and is uncontaminated by contributions from other states which are populated by black body radiation. Our results are generally consistent with other recent experimental results obtained using a less sensitive method, and are also in excellent agreement with theory.
In this paper, I review some recent high-precision Rydberg state lifetime measurements using a cold-trapped sample of neutral atoms held in a magneto-optical trap. The measurements were performed in rubidium for the S, P and D states varying the principal quantum number from n =26 to 45 using the field ionization technique. The experimental results were compared with quantum mechanical calculations and good agreement was observed. This is an important demonstration of how cold atomic samples can be used to perform high-precision spectroscopy in the time domain.
We have studied the decay of Rydberg excitations in a cold Rb gas. A 10 ns, pulsed-dye-amplified diode laser excites Rb atoms at $70\phantom{\rule{0.28em}{0ex}}\ensuremath{\mu}\mathrm{K}$ in a magneto-optical trap to nsnsns or npnpnp Rydberg states with principal quantum numbers $26\ensuremath{\le}n\ensuremath{\le}40$. Time-delayed state-selective field ionization is used to directly monitor the population in the initial and neighboring Rydberg levels. The measured time dependence of the Rydberg population is well described by numerical simulations which consider only spontaneous emission and population transfer by blackbody radiation. No evidence for collective decay is found at atom densities up to $3\ifmmode\times\else\texttimes\fi{}{10}^{9}\phantom{\rule{0.16em}{0ex}}{\mathrm{cm}}^{\ensuremath{-}3}$. This result is in contrast to a previous study [Wang et al., Phys. Rev. A 75, 033802 (2007)], in which superradiant decay was theoretically predicted and experimentally inferred for atom density and laser focal volume conditions very similar to those considered here. Suppression of collective emission is likely due to variations in transition energies within the atom sample, dominated by inhomogeneities in dipole-dipole exchange interactions for initial sss states, or by a combination of dipole-dipole and electric field inhomogeneities for the initial ppp states.
We report experimental measurements of the rates of blackbody-radiation-induced transitions between high-lying (n>60n>60n>60) SSS, P,P,P, and DDD Rydberg levels of rubidium atoms in a magneto-optical trap using a hybrid field ionization and state-selective depumping technique [Archimi et al., Phys. Rev. A 100, 030501(R) (2019); Simonelli et al., Phys. Rev. A 96, 043411 (2017)]. Our results reveal significant deviations of the measured transition rates from theory for well-defined ranges of the principal quantum number. We assume that the most likely cause for those deviations is a modified blackbody spectrum inside the glass cell in which the magneto-optical trap is formed, and we test this assumption by installing electrodes to create an additional microwave cavity around the cell. From the results, we conclude that it should be possible to use such external cavities to control and suppress the blackbody-radiation-induced transitions.
This paper reports on the results of experiments with cold rubidium Rydberg atoms in a magneto-optical trap. The specific feature of the experiments is the excitation of Rydberg atoms in a small volume within a cloud of cold atoms and the sorting of measured signals and spectra according to the number of detected Rydberg atoms. The effective lifetime of the 37 P Rydberg state and its polarizability in a weak electric field are measured. The results obtained are in good agreement with theoretical calculations. It is demonstrated that the localization of the excitation volume in the vicinity of the zero-magnetic-field point makes it possible to improve the spectral resolution and to obtain narrow microwave resonances in Rydberg atoms without switching off the quadrupole magnetic field of the trap. The dependence of the amplitude of dipole-dipole interaction resonances in Rydberg atoms on the number of atoms is measured. This dependence exhibits a linear behavior and agrees with the theory for a weak dipole-dipole interaction.
The lifetimes of nS1/2 and nD5/2 (n = 60–83) cesium Rydberg states are measured accurately in a magneto-optical trap using the field ionization technique and analyzed with the existing theoretical model. The room temperature blackbody radiation (BBR) and interaction between Rydberg atoms can enhance the decay rate and reduce the spontaneous lifetime of the given Rydberg atom. The measured lifetime shows a good agreement with the calculation accounting a room temperature BBR at low enough Rydberg atomic density. The dependence of measured lifetime on atomic density shows that the collision and interaction between Rydberg atoms have a large effect on the lifetime at higher Rydberg atomic density. The scaling laws of n2.55±0.02 for nD5/2 state and n2.30±0.01 for nS1/2 state within n = 60–83 range are obtained and agreement with the model calculation with a relative deviation less than 3%.