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Recent trends to employ high-index dielectric particles in nanophotonics are motivated by their reduced dissipative losses and large resonant enhancement of nonlinear effects at the nanoscale. Because silicon is a centrosymmetric material, the studies of nonlinear optical properties of silicon nanoparticles have been targeting primarily the third-harmonic generation effects. Here we demonstrate, both experimentally and theoretically, that resonantly excited nanocrystalline silicon nanoparticles fabricated by an optimized laser printing technique can exhibit strong second-harmonic generation (SHG) effects. We attribute an unexpectedly high yield of the nonlinear conversion to a nanocrystalline structure of nanoparticles supporting the Mie resonances. The demonstrated efficient SHG at green light from a single silicon nanoparticle is 2 orders of magnitude higher than that from unstructured silicon films. This efficiency is significantly higher than that of many plasmonic nanostructures and small silicon nanoparticles in the visible range, and it can be useful for a design of nonlinear nanoantennas and silicon-based integrated light sources. [ABSTRACT FROM AUTHOR]

We propose a novel photothermal approach based on resonant dielectric nanoparticles, which possess imaginary part of permittivity significantly smaller as compared to metal ones. We show both experimentally and theoretically that a spherical silicon nanoparticle with a magnetic quadrupolar Mie resonance converts light to heat up to 4 times more effectively than similar spherical gold nanoparticle at the same heating conditions. We observe photoinduced temperature raise up to 900 K with the silicon nanoparticle on a glass substrate at moderate intensities (<2 mW/μm²) and typical laser wavelength (633 nm). The advantage of using crystalline silicon is the simplicity of local temperature control by means of Raman spectroscopy working in a broad range of temperatures, that is, up to the melting point of silicon (1690 K) with submicrometer spatial resolution. Our CMOS-compatible heater-thermometer nanoplatform paves the way to novel nonplasmonic photothermal applications, extending the temperature range and simplifying the thermoimaging procedure. [ABSTRACT FROM AUTHOR]

We studied the nonlinear response of a dimer composed of two identical Mie-resonant dielectric nanoparticles illuminated normally by a circularly polarized light. We developed a general theory describing hybridization of multipolar modes of the coupled nanoparticles and reveal nonvanishing nonlinear circular dichroism (CD) in the second-harmonic generation (SHG) signal enhanced by the multipolar resonances in the dimer, provided its axis is oriented under an angle to the crystalline lattice of the dielectric material. We supported our multipolar hybridization theory by experimental results obtained for the AlGaAs dimers placed on an engineered substrate.