We present experimental observations of atom-light interactions within tens of nanometers (down to 11 nm) of a sapphire surface. Using photon counting we detect the fluorescence from of order one thousand Rb or Cs atoms, confined in a vapor with thickness much less than the optical excitation wavelength. The asymmetry in the spectral line shape provides a direct readout of the atom-surface potential. A numerical fit indicates a power law -C(α)/r(α) with α = 3.02 ± 0.06 confirming that the van der Waals interaction dominates over other effects. The extreme sensitivity of our photon-counting technique may allow the search for atom-surface bound states.

We measure the resonance line shape of atomic vapor layers with nanoscale thickness confined between two sapphire windows. The measurement is performed by scanning a probe laser through resonance and collecting the scattered light. The line shape is dominated by the effects of Dicke narrowing, self-broadening, and atom-surface interactions. By fitting the measured line shape to a simple model we discuss the possibility to extract information about the atom-surface interaction. arXiv:1505.07004v1 [physics.atom-ph]

Atom-light interactions in micro-and nanoscale systems hold great promise for alternative technologies based on integrated emitters and optical modes. We present the design architecture, construction method, and characterization of an all-glass alkali-metal vapor cell with nanometer-scale internal structure. Our cell has a glue-free design that allows versatile optical access, in particular with high numerical aperture optics, and incorporates a compact integrated heating system in the form of an external deposited indium tin oxide layer. By performing spectroscopy in different illumination and detection schemes, we investigate atomic densities and velocity distributions in various nanoscopic landscapes. We apply a two-photon excitation scheme to atoms confined in one dimension within our cells, achieving resonance line widths more than an order of magnitude smaller than the Doppler width. We also demonstrate sub-Doppler line widths for atoms confined in two dimensions to micron-sized channels. Furthermore, we illustrate control over vapor density within our cells through nanoscale confinement alone, which could offer a scalable route towards room-temperature devices with single atoms within an interaction volume. Our design offers a robust platform for miniaturized devices that could easily be combined with integrated photonic circuits.

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Publisher's copyright statement:Reprinted with permission from the American Physical Society: Whittaker, K. A. and Keveaney, J. and Hughes, I. G. and Adams, C. S. (2015) 'Hilbert transform : applications to atomic spectra.', Physical review A., 91 (3). 032513 c 2015 by the American Physical Society. Readers may view, browse, and/or download material for temporary copying purposes only, provided these uses are for noncommercial personal purposes. Except as provided by law, this material may not be further reproduced, distributed, transmitted, modi ed, adapted, performed, displayed, published, or sold in whole or part, without prior written permission from the American Physical Society. Use policyThe full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-pro t purposes provided that:• a full bibliographic reference is made to the original source • a link is made to the metadata record in DRO • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders.Please consult the full DRO policy for further details. In many areas of physics, the Kramers-Kronig relations are used to extract information about the real part of the optical response of a medium from its imaginary counterpart. In this paper we discuss an alternative but mathematically equivalent approach based on the Hilbert transform. We apply the Hilbert transform to transmission spectra to find the group and refractive indices of a Cs vapor and thereby demonstrate how the Hilbert transform allows indirect measurement of the refractive index, group index, and group delay while avoiding the use of complicated experimental setups.