12,429 research outputs found

    Functional advantages offered by many-body coherences in biochemical systems

    Full text link
    Quantum coherence phenomena driven by electronic-vibrational (vibronic) interactions, are being reported in many pulse (e.g. laser) driven chemical and biophysical systems. But what systems-level advantage(s) do such many-body coherences offer to future technologies? We address this question for pulsed systems of general size N, akin to the LHCII aggregates found in green plants. We show that external pulses generate vibronic states containing particular multipartite entanglements, and that such collective vibronic states increase the excitonic transfer efficiency. The strength of these many-body coherences and their robustness to decoherence, increase with aggregate size N and do not require strong electronic-vibrational coupling. The implications for energy and information transport are discussed.Comment: arXiv admin note: text overlap with arXiv:1706.0776

    Pulsed Generation of Quantum Coherences and Non-classicality in Light-Matter Systems

    Get PDF
    We show that a pulsed stimulus can be used to generate many-body quantum coherences in light-matter systems of general size. Specifically, we calculate the exact real-time evolution of a driven, generic out-of-equilibrium system comprising an arbitrary number N qubits coupled to a global boson field. A novel form of dynamically-driven quantum coherence emerges for general N and without having to access the empirically challenging strong-coupling regime. Its properties depend on the speed of the changes in the stimulus. Non-classicalities arise within each subsystem that have eluded previous analyses. Our findings show robustness to losses and noise, and have potential functional implications at the systems level for a variety of nanosystems, including collections of N atoms, molecules, spins, or superconducting qubits in cavities -- and possibly even vibration-enhanced light harvesting processes in macromolecules.Comment: 9 pages, 4 figure

    Thermalization and Cooling of Plasmon-Exciton Polaritons: Towards Quantum Condensation

    Get PDF
    We present indications of thermalization and cooling of quasi-particles, a precursor for quantum condensation, in a plasmonic nanoparticle array. We investigate a periodic array of metallic nanorods covered by a polymer layer doped with an organic dye at room temperature. Surface lattice resonances of the array---hybridized plasmonic/photonic modes---couple strongly to excitons in the dye, and bosonic quasi-particles which we call plasmon-exciton-polaritons (PEPs) are formed. By increasing the PEP density through optical pumping, we observe thermalization and cooling of the strongly coupled PEP band in the light emission dispersion diagram. For increased pumping, we observe saturation of the strong coupling and emission in a new weakly coupled band, which again shows signatures of thermalization and cooling.Comment: 8 pages, 5 figures including supplemental material. The newest version includes new measurements and corrections to the interpretation of the result

    From weak to strong coupling of localized surface plasmons to guided modes in a luminescent slab

    Get PDF
    We investigate a periodic array of aluminum nanoantennas embedded in a light-emitting slab waveguide. By varying the waveguide thickness we demonstrate the transition from weak to strong coupling between localized surface plasmons in the nanoantennas and refractive index guided modes in the waveguide. We experimentally observe a non-trivial relationship between extinction and emission dispersion diagrams across the weak to strong coupling transition. These results have implications for a broad class of photonic structures where sources are embedded within coupled resonators. For nanoantenna arrays, strong vs. weak coupling leads to drastic modifications of radiation patterns without modifying the nanoantennas themselves, thereby representing an unprecedented design strategy for nanoscale light sources
    corecore