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arXiv:1208.0680 · Physical Review A

Detrimental adsorbate fields in experiments with cold Rydberg gases near surfaces

H. Hattermann, Markus Mack, Florian Karlewski, Florian Jessen, Daniel Cano, József Fortágh

Published Aug 17, 2012• 67 citations
arXivHTMLPDF

Abstract

We observe the shift of Rydberg levels of rubidium close to a copper surface when atomic clouds are repeatedly deposited on it. We measure transition frequencies of rubidium to $S$ and $D$ Rydberg states with principal quantum numbers $n$ between 31 and 48 using the technique of electromagnetically induced transparency. The spectroscopic measurement shows a strong increase of electric fields towards the surface that evolves with the deposition of atoms. Starting with a clean surface, we measure the evolution of electrostatic fields in the range between 30 and 300 $\ensuremath{\mu}$$\mathrm{m}$ from the surface. We find that after the deposition of a few hundred atomic clouds, each containing $\ensuremath{\sim}$${10}^{6}$ atoms, the field of adsorbates reaches 1 V/cm for a distance of 30 $\ensuremath{\mu}$m from the surface. This evolution of the electrostatic field sets serious limitations on cavity QED experiments proposed for Rydberg atoms on atom chips.

DOI
10.1103/physreva.86.022511

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On one side, atom-chip experiments have demonstrated to be a versatile tool to study quantum physics in cold atoms systems. On the other side, Rydberg atoms have exaggerated properties that makes them good candidates to study quantum information and quantum simulations protocols. In this thesis both system are put together with the aim to study Rydberg physics (in particular atom-atom interaction) in an atom-chip experiment. Due to the exaggerated properties of Rydberg atoms they are very sensitive to electric fields. Thus, the combination of Rydberg atoms with surfaces can be challenging. Therefore a detailed characterization of the mentioned stray electric fields via the analysis of Stark-Zeeman maps is crucial. We employ two-photon Rydberg Stark spectroscopy of a micron-sized cloud of magnetically trapped ultracold rubidium atoms to characterize the electric fields near our atom-chip. Once we characterized the local electric fields we were able to study in more detail the effect of Rydberg excitation in the ultracold cloud of atoms. For instance we observed the formation of ultralong-range Rydberg molecules in our system. In these molecules a ground state atom is weakly bound to the Rydberg electron. We also attempted to observe the effect of Rydberg blockade in the system by looking at the characteristics of Rydberg spectra. Finally we studied the possibility of inducing rf transitions within a Rydberg state manifold in order to enhance our detection method and populate states that are not accessible directly with a two-photon laser transition.

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We observe the shift of Rydberg levels of rubidium close to a copper surface when atomic clouds are repeatedly deposited on it. We measure transition frequencies of rubidium to SSS and DDD Rydberg states with principal quantum numbers nnn between 31 and 48 using the technique of electromagnetically induced transparency. The spectroscopic measurement shows a strong increase of electric fields towards the surface that evolves with the deposition of atoms. Starting with a clean surface, we measure the evolution of electrostatic fields in the range between 30 and 300 \ensuremath{\mu}$$\mathrm{m} from the surface. We find that after the deposition of a few hundred atomic clouds, each containing \ensuremath{\sim}$${10}^{6} atoms, the field of adsorbates reaches 1 V/cm for a distance of 30 \ensuremathμ\ensuremath{\mu}\ensuremathμm from the surface. This evolution of the electrostatic field sets serious limitations on cavity QED experiments proposed for Rydberg atoms on atom chips.
We demonstrate spatially resolved, coherent excitation of Rydberg atoms on an atom chip. Electromagnetically induced transparency (EIT) is used to investigate the properties of the Rydberg atoms near the gold-coated chip surface. We measure distance-dependent shifts ( ~ 101010 MHz) of the Rydberg energy levels caused by a spatially inhomogeneous electric field. The measured field strength and distance dependence is in agreement with a simple model for the electric field produced by a localized patch of Rb adsorbates deposited on the chip surface during experiments. The EIT resonances remain narrow (<4<4<4 MHz) and the observed widths are independent of atom-surface distance down to  ~ 202020 $\ensuremath{\mu}$m, indicating relatively long lifetime of the Rydberg states. Our results open the way to studies of dipolar physics, collective excitations, quantum metrology, and quantum information processing involving interacting Rydberg excited atoms on atom chips.
We investigate the behavior of electric fields originating from adsorbates deposited on a cryogenic atom chip as it is cooled from room temperature to cryogenic temperature. Using Rydberg electromagnetically induced transparency, we measure the field strength versus distance from a 1 mm square of yttrium barium copper oxide (YBCO) patterned onto a yttria stabilized zirconia chip substrate. We find a localized and stable dipole field at room temperature and attribute it to a saturated layer of chemically adsorbed rubidium atoms on the YBCO. As the chip is cooled towards 83 K we observe a change in sign of the electric field as well as a transition from a localized to a delocalized dipole density. We relate these changes to the onset of physisorption on the chip surface when the van der Waals attraction overcomes the thermal desorption mechanisms. Our findings suggest that through careful selection of substrate materials, it may be possible to reduce the electric fields caused by atomic adsorption on chips, opening up experiments to controlled Rydberg-surface coupling schemes.
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).
Abstract We theoretically propose that electromagnetically induced transparency (EIT) with cold Rydberg atoms in the proximity to a metallic chip surface can be applied to detect and investigate the Casimir–Polder effect. The absorption spectrum of the probe laser is numerically computed by the Monte Carlo method, taking into account atom-surface interactions (Casimir–Polder effect). The results show that the Casimir–Polder effect shifts the energy level of the Rydberg state and leads to a shift in the EIT transparency window. The shift of resonant frequency depends on the principal quantum number, atom-surface distance and atomic density. The atom-surface interactions have observable impacts on the nonlinear optic response of the ‘Rydberg EIT medium’ near atom chips.
Experiments handling Rydberg atoms near surfaces must necessarily deal with the high sensitivity of Rydberg atoms to (stray) electric fields that typically emanate from adsorbates on the surface. We demonstrate a method to modify and reduce the stray electric field by changing the adsorbate distribution. We use one of the Rydberg excitation lasers to locally affect the adsorbed dipole distribution. By adjusting the averaged exposure time we change the strength (with the minimal value less than 0.2V/cm0.2\phantom{\rule{0.28em}{0ex}}\mathrm{V}/\mathrm{cm}0.2V/cm at $78\phantom{\rule{0.28em}{0ex}}\ensuremath{\mu}\mathrm{m}$ from the chip) and even the sign of the perpendicular field component. This technique is a useful tool for experiments handling Rydberg atoms near surfaces, including atom chips.
On one side, atom-chip experiments have demonstrated to be a versatile tool to study quantum physics in cold atoms systems. On the other side, Rydberg atoms have exaggerated properties that makes them good candidates to study quantum information and quantum simulations protocols. In this thesis both system are put together with the aim to study Rydberg physics (in particular atom-atom interaction) in an atom-chip experiment. Due to the exaggerated properties of Rydberg atoms they are very sensitive to electric fields. Thus, the combination of Rydberg atoms with surfaces can be challenging. Therefore a detailed characterization of the mentioned stray electric fields via the analysis of Stark-Zeeman maps is crucial. We employ two-photon Rydberg Stark spectroscopy of a micron-sized cloud of magnetically trapped ultracold rubidium atoms to characterize the electric fields near our atom-chip. Once we characterized the local electric fields we were able to study in more detail the effect of Rydberg excitation in the ultracold cloud of atoms. For instance we observed the formation of ultralong-range Rydberg molecules in our system. In these molecules a ground state atom is weakly bound to the Rydberg electron. We also attempted to observe the effect of Rydberg blockade in the system by looking at the characteristics of Rydberg spectra. Finally we studied the possibility of inducing rf transitions within a Rydberg state manifold in order to enhance our detection method and populate states that are not accessible directly with a two-photon laser transition.