Two-point Functions and Quantum Fields in de Sitter Universe

We present a theory of general two-point functions and of generalized free fields in d-dimensional de Sitter space-time which closely parallels the corresponding minkowskian theory. The usual spectral condition is now replaced by a certain geodesic spectral condition, equivalent to a precise thermal characterization of the corresponding ``vacuum''states. Our method is based on the geometry of the complex de Sitter space-time and on the introduction of a class of holomorphic functions on this manifold, called perikernels, which reproduce mutatis mutandis the structural properties of the two-point correlation functions of the minkowskian quantum field theory. The theory contains as basic elementary case the linear massive field models in their ``preferred'' representation. The latter are described by the introduction of de Sitter plane waves in their tube domains which lead to a new integral representation of the two-point functions and to a Fourier-Laplace type transformation on the hyperboloid. The Hilbert space structure of these theories is then analysed by using this transformation. In particular we show the Reeh-Schlieder property. For general two-point functions, a substitute to the Wick rotation is defined both in complex space-time and in the complex mass variable, and substantial results concerning the derivation of Kallen-Lehmann type representation are obtained.Comment: 51 p, uuencoded, LaTex, epsf, 2 figures include

Dispersive response of atoms trapped near the surface of an optical nanofiber with applications to quantum nondemolition measurement and spin squeezing

We study the strong coupling between photons and atoms that can be achieved in an optical nanofiber geometry when the interaction is dispersive. While the Purcell enhancement factor for spontaneous emission into the guided mode does not reach the strong-coupling regime for individual atoms, one can obtain high cooperativity for ensembles of a few thousand atoms due to the tight confinement of the guided modes and constructive interference over the entire chain of trapped atoms. We calculate the dyadic Green's function, which determines the scattering of light by atoms in the presence of the fiber, and thus the phase shift and polarization rotation induced on the guided light by the trapped atoms. The Green's function is related to a full Heisenberg-Langevin treatment of the dispersive response of the quantized field to tensor polarizable atoms. We apply our formalism to quantum nondemolition (QND) measurement of the atoms via polarimetry. We study shot-noise-limited detection of atom number for atoms in a completely mixed spin state and the squeezing of projection noise for atoms in clock states. Compared with squeezing of atomic ensembles in free space, we capitalize on unique features that arise in the nanofiber geometry including anisotropy of both the intensity and polarization of the guided modes. We use a first principles stochastic master equation to model the squeezing as function of time in the presence of decoherence due to optical pumping. We find a peak metrological squeezing of ~5 dB is achievable with current technology for ~2500 atoms trapped 180 nm from the surface of a nanofiber with radius a=225 nm.Comment: To be appeared on PR