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Register a new userRing gap resonant modes on disk/film coupling system caused by strong interaction
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Peculiar ring gap modes on the surface of disk close to the metallic thin film are excited in the visible light regime. We apply plasmon hybridization method to illustrate the ring gap modes arising from the interaction between localized disk plasmons and continuum surface plasmons, which cannot be easily excited by the plane wave with polarization parallel to the film interface. In the coupled system, the hybrid modes energy and the surface charge distribution of nanoparticle are investigated both in simulation and hybridization method, showing consistence with each other. The excitation of ring gap modes provides further insight into strong coupling of the plasmon and the design of novel nanostructures.
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By using the stripline Microwave Vector Network Analyzer Ferromagnetic Resonance and Pulsed Inductive Microwave Magnetometry spectroscopy techniques, we study a strong coupling regime of magnons to microwave photons in the planar geometry of a lithographically formed split-ring resonator (SRR) loaded by a single-crystal epitaxial yttrium-iron garnet (YIG) film. Strong anti-crossing of the photon modes of SRR and of the magnon modes of the YIG film is observed in the applied-magnetic-field resolved measurements. The coupling strength extracted from the experimental data reaches 9 percent at 3 GHz. Theoretically, we propose an equivalent circuit model of an SRR loaded by a magnetic film. This model follows from the results of our numerical simulations of the microwave field structure of the SRR and of the magnetization dynamics in the YIG film driven by the microwave currents in the SRR. The equivalent circuit model is in good agreement with the experiment. It provides a simple physical explanation of the process of mode anti-crossing. Our findings are important for future applications in microwave quantum photonic devices as well as in magnetically tunable metamaterials exploiting the strong coupling of magnons to microwave photons.
Circular dichroism (CD) caused by the response of a chiral object to circularly polarized light has been well established, and the strong CD of plasmonic meta-molecules has also become of interest in recent years; however, their response if the light also has orbital angular momentum is unclear. In this paper, the dichroism of a plasmonic cuboid-protuberance chiral structure under the illumination of a light beam with both orbital and spin angular momentums is numerically investigated. Distinguished spectra are observed under the different momentums. The circular dichroism under the combination of vortex beam and light spin is enhanced. This phenomenon is attributed to the partial spatial excitation of the nanoparticle, and the strong dichroism is simultaneously caused because of the interaction of the induced electric and magnetic modes and other higher-order modes caused by the partial excitation of the vortex beam. This research provides further insight into chiral light-matter interactions and the dichroism of light with orbital angular momentum.
Strong coupling of two-dimensional semiconductor excitons with plasmonic resonators enables control of light-matter interaction at the subwavelength scale. Here we develop strong coupling in plasmonic nano-gap resonators that allow modification of exciton number contributing to the coupling. Using this system, we not only demonstrate a large vacuum Rabi splitting up to 163 meV and splitting features in photoluminescence spectra, but also reveal that the exciton number can be reduced down to single-digit level (N<10), which is an order lower than that of traditional systems, close to single-exciton based strong coupling. In addition, we prove that the strong coupling process is not affected by the large exciton coherence size that was previously believed to be detrimental to the formation of plasmon-exciton interaction. Our work provides a deeper understanding of storng coupling in two-dimensional semiconductors, paving the way for room temperature quantum optics applications.
We demonstrate that a ionising transition can be strongly coupled to a photonic resonance. The strong coupling manifests itself with the appearance of a narrow optically active resonance below the ionisation threshold. Such a resonance is due to electrons transitioning into a novel bound state created by the collective coupling of the electron gas with the vacuum field of the photonic resonator. Applying our theory to the case of bound-to-continuum transitions in microcavity-embedded doped quantum wells, we show how those strong-coupling features can be exploited as a novel knob to tune both optical and electronic properties of semiconductor heterostructures.
We consider the one-dimensional Schroedinger equation on a ring, with the cubic term, of either self-attractive or repulsive sign, confined to a narrow segment. This setting can be realized in optics and Bose-Einstein condensates. For the nonlinearity coefficient represented by the delta-function, all stationary states are obtained in an exact analytical form. The states with positive chemical potentials are found in alternating bands for the cases of the self-repulsion and attraction, while solutions with negative chemical potentials exist only in the latter case. These results provide a possibility to obtain exact solutions for bandgap states in the nonlinear system. Approximating the delta-function by a narrow Gaussian, stability of the stationary modes is addressed through numerical computation of eigenvalues for small perturbations, and verified by simulations of the perturbed evolution. For positive chemical potentials, the stability is investigated in three lowest bands. In the case of the self-attraction, each band contains a stable subband, the transition to instability occurring with the increase of the total norm. As a result, multi-peak states may be stable in higher bands. In the case of the self-repulsion, a single-peak ground state is stable in the first band, while the two higher ones are populated by weakly unstable two- and four-peak excited states. In the case of the self-attraction and negative chemical potentials, single-peak modes feature instability which transforms them into persistently oscillating states.
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