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arXiv:1609.02330 · Physical Review A

Charge-induced optical bistability in thermal Rydberg vapor

Daniel Weller, Alban Urvoy, Andy Rico, Robert Löw, Harald Kübler

Published Dec 8, 2016• 47 citations
arXivHTMLPDF

Abstract

We investigate the phenomenon of optical bistability in a driven ensemble of Rydberg atoms. By performing two experiments with thermal vapors of rubidium and cesium, we are able to shed light on the underlying interaction mechanisms causing such a nonlinear behavior. Due to the different properties of these two atomic species, we conclude that the large polarizability of Rydberg states in combination with electric fields of spontaneously ionized Rydberg atoms is the relevant interaction mechanism. In the case of rubidium, we directly measure the electric field in a bistable situation via two-species spectroscopy. In cesium, we make use of the different sign of the polarizability for different $l$ states and the possibility of applying electric fields. Both these experiments allow us to rule out dipole-dipole interactions and support our hypothesis of a charge-induced bistability.

DOI
10.1103/physreva.94.063820

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We investigate the phenomenon of optical bistability in a driven ensemble of Rydberg atoms. By performing two experiments with thermal vapors of rubidium and cesium, we are able to shed light on the underlying interaction mechanisms causing such a nonlinear behavior. Due to the different properties of these two atomic species, we conclude that the large polarizability of Rydberg states in combination with electric fields of spontaneously ionized Rydberg atoms is the relevant interaction mechanism. In the case of rubidium, we directly measure the electric field in a bistable situation via two-species spectroscopy. In cesium, we make use of the different sign of the polarizability for different lll states and the possibility of applying electric fields. Both these experiments allow us to rule out dipole-dipole interactions and support our hypothesis of a charge-induced bistability.
We investigate the phenomenon of bistability in a thermal gas of cesium atoms excited to Rydberg states. We present both measurements and a numerical model of the phenomena based on collisions. By directly measuring the plasma frequency, we show that the origin of the bistable behavior lies in the creation of a plasma formed by ionized Rydberg atoms. Recombination of ions and electrons manifests as fluorescence which allows us to characterize the plasma properties and study the transient dynamics of the hysteresis that occurs. We determine scaling parameters for the point of plasma formation, and verify our numerical model by comparing measured and simulated spectra. These measurements yield a detailed microscopic picture of ionization and avalanche processes occurring in thermal Rydberg gases. From this set of measurements, we conclude that plasma formation is a fundamental ingredient in the optical bistability taking place in thermal Rydberg gases and imposes a limit on usable Rydberg densities for many applications.
We present experimental results on nondegenerate four-wave mixing in a thermal vapor cell of rubidium atoms via highly excited Rydberg states. We observe sub-Doppler spectral features and a large sensitivity of the mixed light mode to small electric fields due to the large polarizabilities of the involved Rydberg state. We observe a saturation of the optical response due to the nonlinear four-level physics. The strong interaction between Rydberg atoms and the associated Rydberg blockade could potentially increase the nonlinearity dramatically.
We demonstrated stochastic switching in a bistable system implemented with the Rydberg atomic ensemble, which is realized by cascaded Rydberg excitation in a cesium vapor cell. Measurement of Rydberg state's population by means of the electromagnetically induced transparency allows us to investigate the nonlinear behavior in Rydberg atomic ensemble experimentally. The transition between the two states of the bistable system is driven by the intensity noise of the laser beams. Rydberg atomic ensemble accumulates energy in an equilibrium situation and brings the nonlinear system across the threshold, where stochastic switching occurs between the two states.
Highly excited (Rydberg) atoms have exaggerated properties making them extremely sensitive to external electromagnetic fields and interacting strongly with their environment. Atomic vapor cells represent an attractive platform for studying Rydberg atoms and fabricating quantum devices. For example, Rydberg atoms in vapor cells have been used as sensitive detectors of electric fields of frequencies ranging from DC up to the THz range but also as single photon sources for quantum technology applications exploiting collective phenomena due to the Rydberg blockade effect [1]. Rydberg atoms also find applications in fundamental physics, in particular for the measurement of dispersive interactions of the Casimir-Polder type (atom-surface interactions) [2]. One major advantage of Rydberg atoms is that they expose limitations in the traditional perturbative approach of Casimir-Polder (CP) theory [3, 4]. Indeed, in the extreme near-field, the dipole approximation breaks down and higher-order terms need to be considered. We report on extensive experimental measurements of the Rydberg-surface interaction using spectroscopy in cesium vapor nanocells of a thickness ranging roughly from 200-700nm, as well as selective reflection spectroscopy on a macroscopic cesium all-sapphire cell. Atoms are first excited to the Cs(6P) level with a 894nm pump laser and subsequently a green laser ≈ 510nm probes Rydberg nD or nS states, where the principal quantum number n ranges between 15-17. Our experiments evidence the dipole-dipole term of the Casimir-Polder interaction providing a measurement of the C3 coefficient for cesium Rydberg states. Furthermore, our experiment clearly evidences an additional interaction that induces shifts and broadens the linewidth of the probed transitions in the vicinity of the dielectric windows of our cells. We believe that this interaction is due to electric fields that are either generated by patch charges (trapped on the surface or induced by the excitation lasers), or by cesium adsorbants. We show that the different polarizability (of opposing sign) between S and D Rydberg states can be exploited to extract quantitative measurements of the strength and distance scaling (z-dependence) of such parasitic electrostatic interactions.Our experiments suggest that the sensitivity of Rydberg atoms to external electric fields could provide a unique tool for probing electrostatic interactions in the vicinity of surfaces. This could allow systematic error corrections in Casimir-Polder experiments with excited or even ground state atoms that aim at putting bounds on the existence of non-Newtonian gravity [5]. We are currently exploring the possibility of coating the internal window interfaces with conducting 2D material such as graphene to reduce the influence of parasitic charges. This could allow us to probe atoms closer to the surface, where quadrupole interactions could be experimentally attainable for the first time [4].References[1] H. Kubler, J. P. Shaffer, T. Baluktsian, R. Loew, T. Pfau, Nat. Photon., 4, 112–116 (2013).[2] V. Sandoghdar et al., Phys. Rev. Lett 68, 3432–3435 (1993).[3] J. A. Crosse et al., Phys. Rev. A 82, 3010901 (2010).[4] B. Dutta et al., Phys. Rev. Res. 6, L022035 (2024).[5] A. Laliotis, B-S. Lu, M. Ducloy, D. Wilkowski, AVS Quantum Sci. 3, 043501 (2021).
We experimentally studied the Rydberg level shift caused by the electric field, which is generated by Rydberg atom collision induced ionization in a cesium atomic ensemble. The density of charged particles caused by collisions between Rydberg atoms is changed by controlling the ground-state atomic density and optical excitation process. We measured the Rydberg level shift using Rydberg electromagnetically-induced-transparency (EIT) spectroscopy, and interpreted the physical origin using a semi-classical model. The experimental results are in good agreement with the numerical simulation. These energy shifts are important for the self-calibrated sensing of microwave field by the employing of Rydberg EIT. Moreover, in contrast to the resonant excitation case, narrow-linewidth spectroscopy with high signal-to-noise ratio would be useful for high-precision measurements.
We demonstrated a tuned dipole interaction between Rydberg atoms by employing a controllable electric field in a cold cesium ensemble. The | n P 3/2 ⟩ ( n = 38–40) Rydberg pairs are prepared with a three-photon scheme and detected via the state-selective field ionization technique. A weak DC electric field is used to tune the Rydberg pair interaction from the van der Waals interaction regime to the dipole–dipole interaction regime. The Förster resonant interaction and an adiabatic resonance energy transfer between the n P and n S Rydberg states are attained by precisely tuning the electric field. Rydberg excitation blockade with and without the electric field is investigated by changing the excitation pulse duration, which demonstrates that the dipole interaction–induced blockade effect is stronger than the van der Waals interaction–induced blockade effect. The precise control of the Rydberg interaction is of great significance to the coherent interaction in many-body systems and non-radiative collision processes.