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Register a new userQuantum plasmonic excitation in graphene and robust-to-loss propagation
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We investigate the excitation of quantum plasmonic states of light in graphene using end-fire and prism coupling. In order to model the excitation process quantum mechanically we quantize the transverse-electric and transverse-magnetic surface plasmon polariton (SPP) modes in graphene. A selection of regimes are then studied that enable the excitation of SPPs by photons and we show that efficient coupling of photons to graphene SPPs is possible at the quantum level. Futhermore, we study the excitation of quantum states and their propagation under the effects of loss induced from the electronic degrees of freedom in the graphene. Here, we investigate whether it is possible to protect quantum information using quantum error correction techniques. We find that these techniques provide a robust-to-loss method for transferring quantum states of light in graphene over large distances.
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We describe a powerful and intuitive technique for modeling light-matter interactions in classical and quantum nanoplasmonics. Our approach uses a quasinormal mode expansion of the Green function within a metal nanoresonator of arbitrary shape, together with a Dyson equation, to derive an expression for the spontaneous decay rate and far field propagator from dipole oscillators outside resonators. For a single quasinormal mode, at field positions outside the quasi-static coupling regime, we give a closed form solution for the Purcell factor and generalized effective mode volume. We augment this with an analytic expression for the divergent LDOS very near the metal surface, which allows us to derive a simple and highly accurate expression for the electric field outside the metal resonator at distances from a few nanometers to infinity. This intuitive formalism provides an enormous simplification over full numerical calculations and fixes several pending problems in quasinormal mode theory.
We report direct evidence of the bosonic nature of surface plasmon polaritons (SPPs) in a scattering-based beamsplitter. A parametric down-conversion source is used to produce two indistinguishable photons, each of which is converted into a SPP on a metal-stripe waveguide and then made to interact through a semi-transparent Bragg mirror. In this plasmonic analog of the Hong-Ou-Mandel experiment, we measure a coincidence dip with a visibility of 72%, a key signature that SPPs are bosons and that quantum interference is clearly involved.
Localized-surface plasmon resonance is of importance in both fundamental and applied physics for the subwavelength confinement of optical field, but realization of quantum coherent processes is confronted with challenges due to strong dissipation. Here we propose to engineer the electromagnetic environment of metallic nanoparticles (MNPs) using optical microcavities. An analytical quantum model is built to describe the MNP-microcavity interaction, revealing the significantly enhanced dipolar radiation and consequentially reduced Ohmic dissipation of the plasmonic modes. As a result, when interacting with a quantum emitter, the microcavity-engineered MNP enhances the quantum yield over 40 folds and the radiative power over one order of magnitude. Moreover, the system can enter the strong coupling regime of cavity quantum electrodynamics, providing a promising platform for the study of plasmonic quantum electrodynamics, quantum information processing, precise sensing and spectroscopy.
In this letter, we present a detailed, all optical study of the influence of different excitation schemes on the indistinguishability of single photons from a single InAs quantum dot. For this study, we measure the Hong-Ou-Mandel interference of consecutive photons from the spontaneous emission of an InAs quantum dot state under various excitation schemes and different excitation conditions and give a comparison.
The extraordinary sensitivity of plasmonic sensors is well known in the optics and photonics community. These sensors exploit simultaneously the enhancement and the localization of electromagnetic fields close to the interface between a metal and a dielectric. This enables, for example, the design of integrated biochemical sensors at scales far below the diffraction limit. Despite their practical realization and successful commercialization, the sensitivity and associated precision of plasmonic sensors are starting to reach their fundamental classical limit given by quantum fluctuations of light -- known as the shot-noise limit. To improve the sensing performance of these sensors beyond the classical limit, quantum resources are increasingly being employed. This area of research has become known as `quantum plasmonic sensing and it has experienced substantial activity in recent years for applications in chemical and biological sensing. This review aims to cover both plasmonic and quantum techniques for sensing, and shows how they have been merged to enhance the performance of plasmonic sensors beyond traditional methods. We discuss the general framework developed for quantum plasmonic sensing in recent years, covering the basic theory behind the advancements made, and describe the important works that made these advancements. We also describe several key works in detail, highlighting their motivation, the working principles behind them, and their future impact. The intention of the review is to set a foundation for a burgeoning field of research that is currently being explored out of intellectual curiosity and for a wide range of practical applications in biochemistry, medicine, and pharmaceutical research.
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