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Register a new userSqueezing the angular momentum of an ensemble of complex multi-level atoms
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Squeezing of collective atomic spins has been shown to improve the sensitivity of atomic clocks and magnetometers to levels significantly below the standard quantum limit. In most cases the requisite atom-atom entanglement has been generated by dispersive interaction with a quantized probe field, or by state dependent collisions in a quantum gas. Such experiments typically use complex multilevel atoms like Rb or Cs, with the relevant interactions designed so atoms behave like pseudo-spin-$1/2$ particles. We demonstrate the viability of spin squeezing for collective spins composed of the physical angular momenta of $sim 10^6$ Cs atoms, each in an internal spin-4 hyperfine state. A peak metrological squeezing of $gtrsim -5$dB was generated by quantum backaction from a dispersive quantum nondemolition (QND) measurement, implemented using a two-color optical probe that minimizes tensor light shifts without sacrificing measurement strength. Other significant developments include the successful application of composite pulse techniques for accurate dynamical control of the collective spin, enabled by broadband suppression of background magnetic fields inside a state-of-the-art magnetic shield. The absence of classical noise has allowed us to compare the observed quantum projection noise and squeezing to a theoretical model that properly accounts for both the relevant atomic physics and the spatial mode of the collective spin, finding good quantitative agreement and thereby validating its use in other contexts. Thus, our work sets the stage for experiments on quantum feedback, deterministic squeezing, closed-loop magnetometry, and new types of quantum simulation based on continuous QND measurement and feedback.
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We report the experimental verification of nonclassical correlations for a four-wave-mixing process in an ensemble of cold two-level atoms, confirming theoretical predictions by Du et al. in 2007 for the violation of a Cauchy-Schwarz inequality in the system, and obtaining $R = (1.98pm0.03) leq 1$. Quantum correlations are observed in a nano-seconds timescale, in the interference between the central exciting frequency and sidebands dislocated by the detuning to the atomic resonance. They prevail without filters over the noise background coming from linear scattering from the same optical transition. These correlations are fragile with respect to processes that disturb the phase of the atomic excitation, but are robust to variations in number of atoms and to increasing light intensities.
Recently, atomic ensemble and single photons were successfully entangled by using collective enhancement [D. N. Matsukevich, textit{et al.}, Phys. Rev. Lett. textbf{95}, 040405(2005).], where atomic internal states and photonic polarization states were correlated in nonlocal manner. Here we experimentally clarified that in an ensemble of atoms and a photon system, there also exists an entanglement concerned with spatial degrees of freedom. Generation of higher-dimensional entanglement between remote atomic ensemble and an application to condensed matter physics are also discussed.
We generate entangled states of an ensemble of 5*10^4 rubidium-87 atoms by optical quantum nondemolition measurement. The resonator-enhanced measurement leaves the atomic ensemble, prepared in a superposition of hyperfine clock levels, in a squeezed spin state. By comparing the resulting reduction of quantum projection noise (up to 8.8(8) dB) with the concomitant reduction of coherence, we demonstrate a clock input state with spectroscopic sensitivity 3.0(8) dB beyond the standard quantum limit.
In recent years the interest in studying interactions of Rydberg atoms or ensembles thereof with optical and microwave frequency fields has steadily increased, both in the context of basic research and for potential applications in quantum information processing. We present measurements of the dispersive interaction between an ensemble of helium atoms in the 37s Rydberg state and a single resonator mode by extracting the amplitude and phase change of a weak microwave probe tone transmitted through the cavity. The results are in quantitative agreement with predictions made on the basis of the dispersive Tavis-Cummings Hamiltonian. We study this system with the goal of realizing a hybrid between superconducting circuits and Rydberg atoms. We measure maximal collective coupling strengths of 1 MHz, corresponding to 3*10^3 Rydberg atoms coupled to the cavity. As expected, the dispersive shift is found to be inversely proportional to the atom-cavity detuning and proportional to the number of Rydberg atoms. This possibility of measuring the number of Rydberg atoms in a nondestructive manner is relevant for quantitatively evaluating scattering cross sections in experiments with Rydberg atoms.
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.
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