Ben Q. Baragiola

N-photon wave packets interacting with an arbitrary quantum system

We present a theoretical framework that describes a wave packet of light prepared in a state of definite photon number interacting with an arbitrary quantum system (e.g., a quantum harmonic oscillator or a multilevel atom). Within this framework we derive master equations for the system as well as for output field quantities such as quadratures and photon flux. These results are then generalized to wave packets with arbitrary spectral distribution functions. Finally, we obtain master equations and output field quantities for systems interacting with wave packets in multiple spatial and/or polarization modes.

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 Greens 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 Greens 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.

Quantum trajectories for propagating Fock states

We derive quantum trajectories (also known as stochastic master equations) that describe an arbitrary quantum system probed by a propagating wave packet of light prepared in a continuous-mode Fock state. We consider three detection schemes of the output light: photon counting, homodyne detection, and heterodyne detection. We generalize to input field states in superpositions and mixtures of Fock states and illustrate our formalism with several examples.

Room-temperature spontaneous superradiance from single diamond nanocrystals.

Superradiance (SR) is a cooperative phenomenon which occurs when an ensemble of quantum emitters couples collectively to a mode of the electromagnetic field as a single, massive dipole that radiates photons at an enhanced rate. Previous studies on solid-state systems either reported SR from sizeable crystals with at least one spatial dimension much larger than the wavelength of the light and/or only close to liquid-helium temperatures. Here, we report the observation of room-temperature superradiance from single, highly luminescent diamond nanocrystals with spatial dimensions much smaller than the wavelength of light, and each containing a large number (~ 103) of embedded nitrogen-vacancy (NV) centres. The results pave the way towards a systematic study of SR in a well-controlled, solid-state quantum system at room temperature.Previously, superradiance was observed from sizeable crystals or close to liquid-helium temperatures. Here, Bradec et al. report the observation of room-temperature superradiance from single, highly luminescent diamond nanocrystals with spatial dimensions much smaller than the wavelength of light.

Three-dimensional light-matter interface for collective spin squeezing in atomic ensembles

We study the three-dimensional nature of the quantum interface between an ensemble of cold, trapped atomic spins and a paraxial laser beam, coupled through a dispersive interaction. To achieve strong entanglement between the collective atomic spin and the photons, one must match the spatial mode of the collective radiation of the ensemble with the mode of the laser beam while minimizing the effects of decoherence due to optical pumping. For ensembles coupling to a probe field that varies over the extent of the cloud, the set of atoms that indistinguishably radiates into a desired mode of the field defines an inhomogeneous spin wave. Strong coupling of a spin wave to the probe mode is not characterized by a single parameter, the optical density, but by a collection of different effective atom numbers that characterize the coherence and decoherence of the system. To model the dynamics of the system, we develop a full stochastic master equation, including coherent collective scattering into paraxial modes, decoherence by local inhomogeneous diffuse scattering, and backaction due to continuous measurement of the light entangled with the spin waves. This formalism is used to study the squeezing of a spin wave via continuous quantum nondemolition measurement. We find that the greatest squeezing occurs in parameter regimes where spatial inhomogeneities are significant, far from the limit in which the interface is well approximated by a one-dimensional, homogeneous model.

Collective uncertainty in partially polarized and partially decohered spin-(1/2) systems

It has become common practice to model large spin ensembles as an effective pseudospin with total angular momentum

Encoding qubits into oscillators with atomic ensembles and squeezed light

J=\mathit{Nj}

Cooperatively-enhanced atomic dipole forces in optically trapped nanodiamonds containing NV centres, in liquid

, where

Continuous-variable topological quantum codes enable anonymous broadcasting of classical information

j

Magnetometry via a double-pass continuous quantum measurement of atomic spin

is the spin per particle. Such approaches (at least implicitly) restrict the quantum state of the ensemble to the so-called symmetric Hilbert space. Here, we argue that symmetric states are not generally well preserved under the type of decoherence typical of experiments involving large clouds of atoms or ions. In particular, symmetric states are rapidly degraded under models of decoherence that act identically but locally on the different members of the ensemble. Using an approach [Phys. Rev. A 78, 052101 (2008)] that is not limited to the symmetric Hilbert space, we explore potential pitfalls in the design and interpretation of experiments on spin-squeezing and collective atomic phenomena when the properties of the symmetric states are extended to systems where they do not apply.