We study the hybridized plasmonic-photonic modes supported by two-dimensional arrays of metallic nanoparticles coupled to light-emitting optical waveguides. Localized surface plasmon polaritons in the metallic nanoparticles can couple to guided modes in the underlying waveguide, forming quasi-guided hybrid modes, or to diffracted orders in the plane of the array, forming surface lattice resonances. We consider three kinds of samples: one sustains quasi-guided modes only, another sustains surface lattice resonances only, and a third sample sustains both modes. This third sample constitutes the first demonstration of simultaneous coupling of localized surface plasmons to guided modes and diffracted orders. The dispersive properties of the modes in the samples are investigated through light extinction and emission spectroscopy. We elucidate the conditions that lead to the coexistence of surface lattice resonances and quasi-guided hybrid modes, and assess their potential for enhancing the luminescence of emitters embedded in the coupled waveguide. We find the largest increase in emission intensity for the surface lattice resonances, reaching up to a factor of 20.

An enhanced emission of high quantum yield molecules coupled to dielectric metasurfaces formed by periodic arrays of polycrystalline silicon nanoparticles is demonstrated. Radiative coupling of the nanoparticles, mediated by in‐plane diffraction, leads to the formation of collective Mie scattering resonances or Mie surface lattice resonances (M‐SLRs), with remarkable narrow line widths. These narrow line widths and the intrinsic electric and magnetic dipole moments of the individual Si nanoparticles allow resolving electric and magnetic M‐SLRs. Incidence angle‐ and polarization‐dependent extinction measurements and high‐accuracy surface integral simulations show unambiguously that magnetic M‐SLRs arise from in‐ and out‐of‐plane magnetic dipoles, while electric M‐SLRs are due to in‐plane electric dipoles. Pronounced changes in the emission spectrum of the molecules are observed, with almost a 20‐fold enhancement of the emission in defined directions of molecules coupled to electric M‐SLRs, and a fivefold enhancement of the emission of molecules coupled to magnetic M‐SLRs. These measurements demonstrate the potential of dielectric metasurfaces for emission control and enhancement, and open new opportunities to induce asymmetric scattering and emission using collective electric and magnetic resonances.

Exciton transport in most organic materials is based on an incoherent hopping process between neighboring molecules. This process is very slow, setting a limit to the performance of organic optoelectronic devices. In this Article, we overcome the incoherent exciton transport by strongly coupling localized singlet excitations in a tetracene crystal to confined light modes in an array of plasmonic nanoparticles. We image the transport of the resulting exciton-polaritons in Fourier space at various distances from the excitation to directly probe their propagation length as a function of the exciton to photon fraction. Exciton-polaritons with an exciton fraction of 50% show a propagation length of 4.4 μm, which is an increase by 2 orders of magnitude compared to the singlet exciton diffusion length. This remarkable increase has been qualitatively confirmed with both finite-difference time-domain simulations and atomistic multiscale molecular dynamics simulations. Furthermore, we observe that the propagation length is modified when the dipole moment of the exciton transition is either parallel or perpendicular to the cavity field, which opens a new avenue for controlling the anisotropy of the exciton flow in organic crystals. The enhanced exciton-polariton transport reported here may contribute to the development of organic devices with lower recombination losses and improved performance.

We demonstrate the generation of light in an optical waveguide strongly coupled to a periodic array of metallic nanoantennas. This coupling gives rise to hybrid waveguide-plasmon polaritons (WPPs), which undergo a transmutation from plasmon to waveguide mode and vice versa as the eigenfrequency detuning of the bare states transits through zero. Near zero detuning, the structure is nearly transparent in the far-field but sustains strong local field enhancements inside the waveguide. Consequently, light-emitting WPPs are strongly enhanced at energies and in-plane momenta for which WPPs minimize light extinction. We elucidate the unusual properties of these polaritons through a classical model of coupled harmonic oscillators.