130 research outputs found

    Measurement of the Angular Dependence of the Dipole-Dipole Interaction Between Two Individual Rydberg Atoms at a F\"orster Resonance

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    We measure the angular dependence of the resonant dipole-dipole interaction between two individual Rydberg atoms with controlled relative positions. By applying a combination of static electric and magnetic fields on the atoms, we demonstrate the possibility to isolate a single interaction channel at a F\"orster resonance, that shows a well-defined angular dependence. We first identify spectroscopically the F\"orster resonance of choice and we then perform a direct measurement of the interaction strength between the two atoms as a function of the angle between the internuclear axis and the quantization axis. Our results show good agreement with the expected angular dependence (13cos2θ)\propto(1-3\cos^2\theta), and represent an important step towards quantum state engineering in two-dimensional arrays of individual Rydberg atoms.Comment: 5 pages, 4 figure

    Engineering Gaussian states of light from a planar microcavity

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    Quantum fluids of light in a nonlinear planar microcavity can exhibit antibunched photon statistics at short distances due to repulsive polariton interactions. We show that, despite the weakness of the nonlinearity, the antibunching signal can be amplified orders of magnitude with an appropriate free-space optics scheme to select and interfere output modes. Our results are understood from the unconventional photon blockade perspective by analyzing the approximate Gaussian output state of the microcavity. In a second part, we illustrate how the temporal and spatial profile of the density-density correlation function of a fluid of light can be reconstructed with free-space optics. Also here the nontrivial (anti)bunching signal can be amplified significantly by shaping the light emitted by the microcavity

    Coherent dipole-dipole coupling between two single atoms at a F\"orster resonance

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    Resonant energy transfers, i.e. the non-radiative redistribution of an electronic excitation between two particles coupled by the dipole-dipole interaction, lie at the heart of a variety of chemical and biological phenomena, most notably photosynthesis. In 1948, F\"orster established the theoretical basis of fluorescence resonant energy transfer (FRET), paving the ground towards the widespread use of FRET as a "spectroscopic ruler" for the determination of nanometer-scale distances in biomolecules. The underlying mechanism is a coherent dipole-dipole coupling between particles, as already recognized in the early days of quantum mechanics, but this coherence was not directly observed so far. Here, we study, both spectroscopically and in the time domain, the coherent, dipolar-induced exchange of electronic excitations between two single Rydberg atoms separated by a controlled distance as large as 15 microns, and brought into resonance by applying a small electric field. The coherent oscillation of the system between two degenerate pair states occurs at a frequency that scales as the inverse third power of the distance, the hallmark of dipole-dipole interactions. Our results not only demonstrate, at the most fundamental level of two atoms, the basic mechanism underlying FRET, but also open exciting prospects for active tuning of strong, coherent interactions in quantum many-body systems.Comment: 4 pages, 3 figure

    Nonlinear optics in the fractional quantum Hall regime

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    Engineering strong interactions between optical photons is a great challenge for quantum science. Envisioned applications range from the realization of photonic gates for quantum information processing to synthesis of photonic quantum materials for investigation of strongly-correlated driven-dissipative systems. Polaritonics, based on the strong coupling of photons to atomic or electronic excitations in an optical resonator, has emerged as a promising approach to implement those tasks. Recent experiments demonstrated the onset of quantum correlations in the exciton-polariton system, showing that strong polariton blockade could be achieved if interactions were an order of magnitude stronger. Here, we report time resolved four-wave mixing experiments on a two-dimensional electron system embedded in an optical cavity, demonstrating that polariton-polariton interactions are strongly enhanced when the electrons are initially in a fractional quantum Hall state. Our experiments indicate that in addition to strong correlations in the electronic ground state, exciton-electron interactions leading to the formation of polaron polaritons play a key role in enhancing the nonlinear optical response. Besides potential applications in realization of strongly interacting photonic systems, our findings suggest that nonlinear optical measurements could provide information about fractional quantum Hall states that is not accessible in linear optical response

    Reactivity effects of the proposed SNPO-C countermeasure explosive projectile destruct system

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    Single-atom trapping in holographic 2D arrays of microtraps with arbitrary geometries

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    We demonstrate single-atom trapping in two-dimensional arrays of microtraps with arbitrary geometries. We generate the arrays using a Spatial Light Modulator (SLM), with which we imprint an appropriate phase pattern on an optical dipole trap beam prior to focusing. We trap single 87Rb^{87}{\rm Rb} atoms in the sites of arrays containing up to 100\sim100 microtraps separated by distances as small as 3  μ3\;\mum, with complex structures such as triangular, honeycomb or kagome lattices. Using a closed-loop optimization of the uniformity of the trap depths ensures that all trapping sites are equivalent. This versatile system opens appealing applications in quantum information processing and quantum simulation, e.g. for simulating frustrated quantum magnetism using Rydberg atoms.Comment: 9 pages, 10 figure

    Single-Atom Addressing in Microtraps for Quantum-State Engineering using Rydberg Atoms

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    We report on the selective addressing of an individual atom in a pair of single-atom microtraps separated by 3  μ3\;\mum. Using a tunable light-shift, we render the selected atom off-resonant with a global Rydberg excitation laser which is resonant with the other atom, making it possible to selectively block this atom from being excited to the Rydberg state. Furthermore we demonstrate the controlled manipulation of a two-atom entangled state by using the addressing beam to induce a phase shift onto one component of the wave function of the system, transferring it to a dark state for the Rydberg excitation light. Our results are an important step towards implementing quantum information processing and quantum simulation with large arrays of Rydberg atoms.Comment: 4 pages, 3 figure

    Realizing quantum Ising models in tunable two-dimensional arrays of single Rydberg atoms

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    Spin models are the prime example of simplified manybody Hamiltonians used to model complex, real-world strongly correlated materials. However, despite their simplified character, their dynamics often cannot be simulated exactly on classical computers as soon as the number of particles exceeds a few tens. For this reason, the quantum simulation of spin Hamiltonians using the tools of atomic and molecular physics has become very active over the last years, using ultracold atoms or molecules in optical lattices, or trapped ions. All of these approaches have their own assets, but also limitations. Here, we report on a novel platform for the study of spin systems, using individual atoms trapped in two-dimensional arrays of optical microtraps with arbitrary geometries, where filling fractions range from 60 to 100% with exact knowledge of the initial configuration. When excited to Rydberg D-states, the atoms undergo strong interactions whose anisotropic character opens exciting prospects for simulating exotic matter. We illustrate the versatility of our system by studying the dynamics of an Ising-like spin-1/2 system in a transverse field with up to thirty spins, for a variety of geometries in one and two dimensions, and for a wide range of interaction strengths. For geometries where the anisotropy is expected to have small effects we find an excellent agreement with ab-initio simulations of the spin-1/2 system, while for strongly anisotropic situations the multilevel structure of the D-states has a measurable influence. Our findings establish arrays of single Rydberg atoms as a versatile platform for the study of quantum magnetism.Comment: This is the version of the manuscript as initially submitted to Natur

    A low-loss photonic silica nanofiber for higher-order modes

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    Optical nanofibers confine light to subwavelength scales, and are of interest for the design, integration, and interconnection of nanophotonic devices. Here we demonstrate high transmission (> 97%) of the first family of excited modes through a 350 nm radius fiber, by appropriate choice of the fiber and precise control of the taper geometry. We can design the nanofibers so that these modes propagate with most of their energy outside the waist region. We also present an optical setup for selectively launching these modes with less than 1% fundamental mode contamination. Our experimental results are in good agreement with simulations of the propagation. Multimode optical nanofibers expand the photonic toolbox, and may aid in the realization of a fully integrated nanoscale device for communication science, laser science or other sensing applications.Comment: 12 pages, 5 figures, movies available onlin
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