Light sources based on reliable and energy-efficient light-emitting diodes (LEDs) are instrumental in the development of solid-state lighting (SSL). Most research efforts in SSL have focused on improving both the intrinsic quantum efficiency (QE) and the stability of light emitters. For this reason, it is broadly accepted that with the advent of highly efficient (QE close to 1) and stable emitters, the fundamental research phase of SSL is coming to an end. In this study, we demonstrate a very large improvement in SSL emission (above 70-fold directional enhancement for p-polarized emission and 60-fold enhancement for unpolarized emission) using nanophotonic structures. This is attained by coupling emitters with very high QE to collective plasmonic resonances in periodic arrays of aluminum nanoantennas. Our results open a new path for fundamental and applied research in SSL in which plasmonic nanostructures are able to mold the spectral and angular distribution of the emission with unprecedented precision.

Metallic nanostructures provide a toolkit for the generation of coherent light below the diffraction limit. Plasmonicbased lasing relies on the population inversion of emitters (such as organic fluorophores) along with feedback provided by plasmonic resonances. In this regime, known as weak light-matter coupling, the radiative characteristics of the system can be described by the Purcell effect. Strong light-matter coupling between the molecular excitons and electromagnetic field generated by the plasmonic structures leads to the formation of hybrid quasi-particles known as plasmon-exciton-polaritons (PEPs). Due to the bosonic character of these quasi-particles, exciton-polariton condensation can lead to laser-like emission at much lower threshold powers than in conventional photon lasers. Here, we observe PEP lasing through a dark plasmonic mode in an array of metallic nanoparticles with a low threshold in an optically pumped organic system. Interestingly, the threshold power of the lasing is reduced by increasing the degree of light-matter coupling in spite of the degradation of the quantum efficiency of the active material, highlighting the ultrafast dynamic responsible for the lasing, i.e., stimulated scattering. These results demonstrate a unique roomtemperature platform for exploring the physics of exciton-polaritons in an open-cavity architecture and pave the road toward the integration of this on-chip lasing device with the current photonics and active metamaterial planar technologies.

We demonstrate an improvement by more than 1 order of magnitude of the figure of merit (FoM) of plasmonic nanoparticle sensors by means of the diffractive coupling of localized surface plasmon resonances. The coupling in arrays of nanoparticles leads to Fano resonances with narrow line widths known as surface lattice resonances, which are very suitable for the sensitive detection of small changes in the refractive index of the surroundings. We focus on the sensitivity to the bulk refractive index and find that the sensor FoM scales solely with the frequency difference between the surface lattice resonance and the diffracted order grazing to the surface of the array. This result, which can be extended to other systems with coupled resonances, enables the design of plasmonic sensors with a high FoM over broad spectral ranges with unprecedented accuracy.