Controlling Light Propagation: Surface plasmons are light-induced collective electronic excitations in a metal that offer the possibility of manufacturing optoelectronic devices at nanometer scale. Before such shrinking can be achieved, the propagation direction and lifetime of the plasmonic excitations have to be controlled (see the Perspective by Miroshnichenko and Kivshar ). Rodríguez-Fortuño et al. (p. 328 ) show how this is done using polarized light. Alternatively, using an array of metallic nanoantennae (in this case, slits) patterned into a thin gold film, Lin et al. (p. 331 ) present a further improvement on current plasmonic coupling schemes that has the potential to encode information contained in both the intensity and polarization of light.

Optical nanoantennas have shown a great capacity for efficient extraction of photons from the near to the far field, enabling directional emission from nanoscale single-photon sources. However, their potential for the generation and extraction of multi-photon quantum states remains unexplored. Here we experimentally demonstrate the nanoscale generation of two-photon quantum states at telecommunication wavelengths based on spontaneous parametric down-conversion in an optical nanoantenna. The antenna is a crystalline AlGaAs nanocylinder, possessing Mie-type resonances at both the pump and the bi-photon wavelengths, and when excited by a pump beam it generates photon pairs with a rate of 35 Hz. Normalized to the pump energy stored by the nanoantenna, this rate corresponds to 1.4 GHz/Wm, being 1 order of magnitude higher than conventional on-chip or bulk photon-pair sources. Our experiments open the way for multiplexing several antennas for coherent generation of multi-photon quantum states with complex spatial-mode entanglement and applications in free-space quantum communications and sensing.

We review recent achievements in the field of nanoscale nonlinear AlGaAs photonics based on all-dielectric optical antennas. After discussing the motivation and main technological challenges for the development of an AlGaAs monolithic platform for χ ⁽²⁾ nonlinear nanophotonics, we present numerical and experimental investigations of the second-order nonlinear response and physical reasons for high efficiency of second-order nonlinear interactions in the AlGaAs nano-antennas. In particular, we emphasize the role of the dipolar resonances at the fundamental frequency and the multipolar resonances at the second harmonic wavelength. We also discuss second-harmonic generation directionality and show possible strategies to engineer the radiation pattern of nonlinear antennas.

Dielectric nanocavities are emerging as a versatile and powerful tool for the linear and nonlinear manipulation of light at the nanoscale. In this work, we exploit the effective coupling of electric and toroidal modes in AlGaAs nanodimers to locally enhance both electric and magnetic fields while minimizing the optical scattering, thereby optimizing their second-harmonic generation efficiency with respect to the case of a single isolated nanodisk. We also demonstrate that proper near-field coupling can provide further degrees of freedom to control the polarization state and the radiation diagram of the second-harmonic field.