We explore a situation where the van der Waals long-range atom-surface interaction is repulsive. This repulsion originates in a resonant coupling between a virtual emission at 12.15 mm of a Cs ‫ء‬ ͑6D 3͞2 ͒ atom and a virtual excitation of a surface polariton in sapphire. The experimental evidence is based upon the analysis of the spectroscopic response of Cs* in the near-infrared range with a technique that probes a distance range ϳ100 nm away from the sapphire surface. We also demonstrate the critical dependence of atom-surface forces on the sapphire crystal orientation. PACS numbers: 34.50.Dy, 12.20.Fv, 71.36. + c The van der Waals (vW) force between neutral polarizable systems [1,2] represents a universal interaction of paramount importance in numerous fields of physics, chemistry, and biology. Its attractive character is essential for the cohesion of many chemical or biological systems. vW attraction between atomic systems and metallic or dielectric bodies is also a fundamental property in cavity quantum electrodynamics (QED) [3], and its main characteristics have been experimentally studied by means of mechanical approaches (atomic beam deflection produced by surfaces [4,5], energy threshold in atomic mirrors [6]), or, in our group, spectroscopic approaches (spectral monitoring of surface-induced atomic level shifts [7-10]).In the nonretarded regime, the vW interaction between an atom and a surface originates in the quantum fluctuations of the atomic dipole: The fluctuating dipole polarizes the surface, and induces a dipole image instantaneously correlated with the atomic dipole. This near-field image is responsible for the attractive character of the vW interaction, which scales in 1͞z 3 (z is the atom-surface distance) [1].Is it possible to turn this near-field attraction into a repulsion? The answer is yes, if a resonant coupling between the fluctuating atomic dipole and a surface excitation can occur [11][12][13]. For a dispersive dielectric medium with a complex permittivity´͑v͒, the well-known electrostatic image coefficient S ͑´2 1͒͑͞´1 1͒ (with 0 # S # 1) has to be generalized to a complex frequency-dependent surface response [13]:whose resonances ("surface polaritons" [14]) are determined by the poles of S͑v͒.Consider an excited atom for which one of the dipoleallowed deexcitation channels (at frequency v a ) is near resonant with a surface polariton. Because of nonradiative, virtual coupling between the atom and surface (atomic decay followed by surface excitation), the surface response at frequency v a is magnified, implying a dielectric image coefficient, 2Re͓S͑v a ͔͒, possibly larger than one-the value obtained for an ideal reflector. Because of the resonant enhancement, S is complex and the image dipole is dephased as well. When this image is phase reversed, the near-field vW attraction is turned into a near-field vW repulsion, also scaling in 1͞z 3 . This is one among the rare situations of a long-range, state-selective repulsion exerted by a cavity wall on an atom, at distances spanning f...

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We have studied relative-intensity fluctuations for a variable set of orthogonal elliptic polarization components of a linearly polarized laser beam traversing a resonant 87 Rb vapor cell. Significant polarization squeezing at the threshold level (-3dB) required for the implementation of several continuous variables quantum protocols was observed. The extreme simplicity of the setup, based on standard polarization components, makes it particularly convenient for quantum information applications.PACS numbers: 42.50. Lc,42.50.Ct,32.80.Qk In recent years, large attention has been given to the use of continuous variables for quantum information processing. A foreseen goal is the distribution of entanglement between distant nodes. For this, quantum correlated light beams are to interact with separate atomic systems in order to build quantum mechanical correlations between them [1,2].A particular kind of quantum correlation between two light beams occurs when the intensity difference between them has fluctuations smaller than the standard quantum limit (SQL), that is smaller than the fluctuations of the intensity difference of two coherent states of the same intensity. The two beams are said to present relative-intensity squeezing (RIS). RIS has been generated through different nonlinear optics techniques. One of the most successful is parametric down conversion in a nonlinear χ (2) crystal. Up to 9.7 dB RIS has been obtained with this method [3]. Such experiments require a relatively elaborate and expensive setup. The resulting light beams are spectrally broad and usually far detuned from convenient alkali atoms D transitions. An alternative approach has considered the use of four-wave mixing in atomic samples [4][5][6][7].Reduced relative-intensity fluctuations have been observed between light beams of different frequency. However, RIS can also occur between orthogonal polarization components of a single light beam. In such case, the field is said to be polarization squeezed [8,9] and the noise reduction is described in terms of squeezing of the fluctuations of one of the Stokes operators:Here a x , a y are the field destruction operators for the orthogonal linear polarizations x and y. Polarization squeezing has been produced via propagation in optical fibers [10,11], through the combination on a polarizing beam splitter of two quadrature squeezed light beams [12] and through the interaction of linearly polarized light with cold atoms inside an optical cavity [9,13].It has been recently demonstrated that the single passage of a linearly polarized pump beam through a few-cmlong atomic vapor cell results in squeezing of the polarization orthogonal to that of the pump (vacuum squeezing) [14][15][16][17] as a consequence of the nonlinear optics mechanism known as polarization self-rotation (PSR) [18][19][20]. Vacuum squeezing via PSR has been observed for the D1 [15][16][17] and D2 [14] transitions using 87 Rb vapor. As noted in [9], the existence of polarization squeezing can be inferred from these results.In this ...

Nonlinear magneto-optical (NMO) resonances occurring for near-zero magnetic field are studied in Rb vapor using light-noise spectroscopy. With a balanced detection polarimeter, we observe high contrast variations of the noise power (at fixed analysis frequency) carried by diode laser light resonant with the 5S 1/2 (F = 2) → 5P 1/2 (F = 1) transition of 87 Rb and transmitted through a rubidium vapor cell, as a function of magnetic field B. A symmetric resonance doublet of anticorrelated noise is observed for orthogonal polarizations around B = 0 as a manifestation of ground state coherence. We also observe sideband noise resonances when the magnetic field produces an atomic Larmor precession at a frequency corresponding to one half of the analysis frequency. The resonances on the light fluctuations are the consequence of phase to amplitude noise conversion owing to nonlinear coherence effects in the response of the atomic medium to the fluctuating field. A theoretical model (derived from linearized Bloch equations) is presented that reproduces the main qualitative features of the experimental signals under simple assumptions.