Plasmonic antennas are well-known and extremely powerful platforms for optical spectroscopy, sensing, and manipulation of molecules and nanoparticles. However, resistive antenna losses, resulting in highly localized photothermal heat generation, may significantly compromise their applicability. Here we investigate how the interplay between plasmon-enhanced optical and thermal forces affects the dynamics of nanocolloids diffusing in close proximity to gold bowtie nanoantennas. The study is based on an anti-Stokes thermometry technique that can measure the internal antenna temperature with an accuracy of ∼5 K over an extended temperature range. We argue that Kapitza resistances have a significant impact on the local thermal landscape, causing an interface temperature discontinuity of up to ∼20% of the total photothermal temperature increase of the antenna studied. We then use the bowties as plasmonic optical tweezers and quantify how the antenna temperature influences the motion and distribution of nearby fluorescent colloids. We find that colloidal particle motion within the plasmonic trap is primarily dictated by a competition between enhanced optical forces and enhanced heating, resulting in a surprising insensitivity to the specific resonance properties of the antenna. Furthermore, we find that thermophoretic forces inhibit diffusion of particles toward the antenna and drive the formation of a thermal depletion shell that extends several microns. The study highlights the importance of thermal management at the nanoscale and points to both neglected problems and new opportunities associated with plasmonic photothermal effects in the context of nanoscale manipulation and analysis.

Enhancement of inelastic light emission processes through resonant excitation usually correlates with enhanced scattering of the excitation light, as is for example typically the case for surface-enhanced fluorescence and Raman scattering from plasmonic nanostructures. Here, we demonstrate an unusual case where a reverse correlation is instead observed, that is, we measure a multifold enhancement of Raman emission along with suppressed elastic scattering. The system enabling this peculiar effect is composed of silicon nanodisks excited in the so-called anapole state, for which electric and toroidal dipoles interfere destructively in the far-field, thereby preventing elastic scattering, while the optical fields in the core of the silicon particles are enhanced, thus, amplifying light–matter interaction and Raman scattering at the Stokes-shifted emission wavelength. Our results demonstrate an unusual relation between resonances in elastic and inelastic scattering from nanostructures and suggest a route toward background-free frequency conversion devices.

High-refractive-index silicon nanoresonators are promising low-loss alternatives to plasmonic particles in CMOS-compatible nanophotonics applications. However, complex 3D particle morphologies are challenging to realize in practice, thus limiting the range of achievable optical functionalities. Using 3D film structuring and a novel gradient mask transfer technique, the first intrinsically chiral dielectric metasurface is fabricated in the form of a monolayer of twisted silicon nanocrescents that can be easily detached and dissolved into colloidal suspension. The metasurfaces exhibit selective handedness and a circular dichroism as large as 160° µm due to pronounced differences in induced current loops for left-handed and right-handed polarization. The detailed morphology of the detached particles is analyzed using high-resolution transmission electron microscopy. Furthermore, it is shown that the particles can be manipulated in solution using optical tweezers. The fabrication and detachment method can be extended to different nanoparticle geometries and paves the way for a wide range of novel nanophotonic experiments and applications of high-index dielectrics.

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We demonstrate infrared femtosecond laser-induced inversion of ferroelectric domains. This process can be realised solely by using tightly focused laser pulses without application of any electric field prior to, in conjunction with, or subsequent to the laser irradiation. As most ferroelectric crystals like LiNbO3, LiTaO3, and KTiOPO4 are transparent in the infrared, this optical poling method allows one to form ferroelectric domain patterns much deeper inside a ferroelectric crystal than by using ultraviolet light and hence can be used to fabricate practical devices. We also propose in situ diagnostics of the ferroelectric domain inversion process by monitoring the Čerenkov second harmonic signal, which is sensitive to the appearance of ferroelectric domain walls.

In this paper, we present results of detailed studies on amplified spontaneous emission (ASE) and lasing achieved in a double-layer system consisted of a biopolymer based matrix loaded with 3-(1,1-dicyanoethenyl1)-1phenyl-4,5dihydro-1H-pyrazole organic nonlinear optical dye and photochromic polymer. The laser action was achieved via distributed feedback configuration with third order of Bragg scattering on surface relief grating generated in photochromic polymer. To excite the luminescence, we have used 6 ns pulses of Nd:YAG laser at 532 nm. The ASE and lasing thresholds were estimated to be 17 mJ/cm2 and 11 mJ/cm2, respectively.

We demonstrate an all-optical fabrication method of quasi-phase matching structures in lithium niobate (LiNbO₃) waveguides using a tightly focused femtosecond near-infrared laser beam (wavelength of 800 nm). In contrast to other all-optical schemes that utilize a periodic lowering of the nonlinear coefficient χ⁽²⁾ by material modification, here the illumination of femtosecond pulses directly reverses the sign of χ⁽²⁾ through the process of ferroelectric domain inversion. The resulting quasi-phase matching structures, therefore, lead to more efficient nonlinear interactions. As an experimental demonstration, we fabricate a structure with the period of 2.74 μm to frequency double 815 nm light. A maximum conversion efficiency of 17.45% is obtained for a 10 mm long waveguide.

This work presents a detailed analysis of the morphology of femtosecond laser-induced changes in bulk lithium niobate (LiNbO₃) - one of the most common host materials in photonics - using second-harmonic generation microscopy and scanning electron microscopy. It is shown that focused linearly polarized near-infrared pulses can produce two or three distinct axially separated regions of modified material, depending on whether the pulse propagation is along or perpendicular to the optical axis. When laser writing in LiNbO₃ is conducted in multi-shot irradiation mode and the focused light intensity is kept near the bulk damage threshold, periodic planar nanostructures aligned perpendicular to the laser polarization are produced inside the focal volume. These results provide a new perspective to laser writing in crystalline materials, including the fabrication of passive and active waveguides, photonic crystals, and optical data storage devices.