Hybrid quantum platforms based on highly excited Rydberg atoms coupled to nanophotonics devices offer a promising route toward scalable quantum networks and integrated quantum technologies. However, the close proximity of Rydberg atoms to dielectric nanostructures makes these systems particularly susceptible to uncontrolled surface electric fields that can lead to a degradation of the excitation process. Here, we experimentally investigate Rydberg excitation of laser-cooled $^{87}$Rb atoms via the evanescent field of an optical nanofiber in the presence of fiber-guided red- and blue-detuned light fields as used to trap ground state atoms in fiber-based dipole traps. We observe a time evolution of the Rydberg excitation spectrum when both the dipole trapping fields are on and the additional spectral features that appear can be suppressed by applying an external oscillating electric field to the system, strongly indicating that surface charge accumulation is responsible for the observed spectral feature. The experimental results are reproduced qualitatively by a model that incorporates DC energy level shifts arising from electric fields generated by charges deposited on the nanofiber surface. We identify Rydberg-ground state collisional ionization, which is enhanced by the dipole trapping fields, as the dominant mechanism for charge generation. These results provide new insight into charge dynamics at dielectric nanophotonic interfaces and establish practical guidelines for mitigating surface charge-induced electric fields in fiber-integrated Rydberg quantum systems.
Hybrid quantum platforms based on highly excited Rydberg atoms coupled to nanophotonics devices offer a promising route toward scalable quantum networks and integrated quantum technologies. However, the close proximity of Rydberg atoms to dielectric nanostructures makes these systems particularly susceptible to uncontrolled surface electric fields that can lead to a degradation of the excitation process. Here, we experimentally investigate Rydberg excitation of laser-cooled 87Rb atoms via the evanescent field of an optical nanofiber in the presence of fiber-guided red- and blue-detuned light fields as used to trap ground state atoms in fiber-based dipole traps. We observe a time evolution of the Rydberg excitation spectrum when both the dipole trapping fields are on and the additional spectral features that appear can be suppressed by applying an external oscillating electric field to the system, strongly indicating that surface charge accumulation is responsible for the observed spectral feature. The experimental results are reproduced qualitatively by a model that incorporates DC energy level shifts arising from electric fields generated by charges deposited on the nanofiber surface. We identify Rydberg-ground state collisional ionization, which is enhanced by the dipole trapping fields, as the dominant mechanism for charge generation. These results provide new insight into charge dynamics at dielectric nanophotonic interfaces and establish practical guidelines for mitigating surface charge-induced electric fields in fiber-integrated Rydberg quantum systems.
Abstract Cold Rydberg atoms, known for their long lifetimes and strong dipole-dipole interactions that lead to the Rydberg blockade phenomenon, are among the most promising platforms for quantum simulations, quantum computation and quantum networks. However, a major limitation to the performance of Rydberg atom-based platforms is dephasing, which can be caused by atomic motion within the trap. Here, we propose a trap for 87Rb cold atoms that confines both the electronic ground state and a Rydberg state, engineered to minimize the differential light shifts between the two states. This is achieved by combining a fictitious magnetic field induced by optical nanofiber (ONF) guided light and an external bias magnetic field. We calculate trap potentials for the cases of one- and two-guided modes with quasi-linear and quasi-circular polarizations, and calculate trap depths and trap frequencies for different values of laser power and bias fields. Moreover, we discuss the impact of the quadrupole polarisability of the Rydberg atoms on the trap potential and demonstrate how the size of a Rydberg atom influences the ponderomotive potential generated by the nanofiber-guided light field. This work expands on the idea of light-induced fictitious magnetic field traps and presents a practical approach for creating quantum networks using Rydberg atoms integrated with ONFs to generate 1D atom arrays.
Excitation of 87Rb Rydberg atoms to nS and nD states (n$\leq$68) via an optical nanofiber
Cold Rydberg atoms are a promising platform for quantum technologies and combining them with optical waveguides has the potential to create robust quantum information devices. Here, we experimentally observe the excitation of cold rubidium atoms to a large range of Rydberg S and D states through interaction with the evanescent field of an optical nanofiber. We develop a theoretical model to account for experimental phenomena present such as the AC Stark shifts and the Casimir-Polder interaction. This work strengthens the knowledge of Rydberg atom interactions with optical nanofibers and is a critical step toward the implementation of all-fiber quantum networks and waveguide QED systems using highly excited atoms.
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).
Cold Rydberg atoms are a promising platform for quantum technologies, and combining them with optical waveguides has the potential to create robust quantum information devices. Here, we experimentally observe the excitation of cold rubidium atoms to a large range of Rydberg S and D states through interaction with the evanescent field of an optical nanofiber. We develop a theoretical model to account for experimental phenomena present such as the AC Stark shifts and the Casimir–Polder interaction. This work strengthens the knowledge of Rydberg atom interactions with optical nanofibers and is a critical step toward the implementation of all-fiber quantum networks and waveguide quantum electrodynamics (QED) systems using highly excited atoms.
Photonics platforms combining laser-cooled atoms with optical nanofibres facilitate strong light–matter interactions across the classical and quantum regimes. The subwavelength confinement of the fibre-guided modes produces a large evanescent field, allowing efficient coupling of light to nearby atoms. We investigate atom-mediated processes in nanofibre-based platforms, with particular focus on Rydberg excitation of cold 87 Rb in close proximity to a dielectric. We identify key limitations to excitation efficiency and discuss alternative trapping strategies to overcome these effects.
We report on a controllable, hybrid quantum system consisting of cold Rydberg atoms and an optical nanofiber interface. Using a two-photon ladder-type excitation in 87Rb, we demonstrate both coherent and incoherent Rydberg excitation at submicron distances from the nanofiber surface. The 780-nm photon, near resonant to the 5S→5P transition, is mediated by the cooling laser, while the 482-nm light, near resonant to the 5P→29D transition, is mediated by the guided mode of the nanofiber. The population loss rate of the cold atom ensemble is used to measure the Rydberg population rate. A theoretical model is developed to interpret the results and link the population loss rate to the experimentally measured, effective Rabi frequency of the process. This work makes headway in the study of Rydberg atom-surface interactions at submicron distances and the use of cold Rydberg atoms for all-fibered quantum networks.