The rational combination of plasmonic and all-dielectric concepts within hybrid nanomaterials provides a promising route toward devices with ultimate performance and extended modalities. Spectral matching of plasmonic and Mie-type resonances for such nanostructures can only be achieved for their dissimilar characteristic sizes, thus making the resulting hybrid nanostructure geometry complex for practical realization and large-scale replication. Here, we produced amorphous TiO2 nanospheres decorated and doped with Au nanoclusters via single-step nanosecond-laser irradiation of commercially available TiO2 nanopowders dispersed in aqueous HAuCl4. Fabricated hybrids demonstrate remarkable light-absorbing properties (averaged value ≈96%) in the visible and near-IR spectral range mediated by bandgap reduction of the laser-processed amorphous TiO2 as well as plasmon resonances of the decorating Au nanoclusters. The findings are supported by optical spectroscopy, electron energy loss spectroscopy, transmission electron microscopy, and electromagnetic modeling. Light-absorbing and plasmonic properties of the produced hybrids were implemented to demonstrate catalytically passive SERS biosensor for identification of analytes at trace concentrations and solar steam generator that permitted to increase water evaporation rate by 2.5 times compared with that of pure water under identical 1 sun irradiation conditions.

Recent progress in hybrid optical nanomaterials composed of dissimilar constituents permitted an improvement in the performance and functionality of novel devices developed for optoelectronics, catalysis, medical diagnostics, and sensing. However, the rational combination of contrasting materials such as noble metals and semiconductors within individual hybrid nanostructures via a ready-to-use and lithography-free fabrication approach is still a challenge. Here, we report on a two-step synthesis of hybrid Au-Si microspheres generated by laser ablation of silicon in isopropanol followed by laser irradiation of the produced Si nanoparticles in the presence of HAuCl 4 . Thermal reduction of [AuCl 4 ] − species to a metallic gold phase, along with its subsequent mixing with silicon under laser irradiation, creates a nanostructured material with a unique composition and morphology, as revealed by electron microscopy, tomography, and elemental analysis. A combination of basic plasmonic and nanophotonic materials such as gold and silicon within a single microsphere allows for efficient light-to-heat conversion, as well as single-particle SERS sensing with temperature-feedback modality and expanded functionality. Moreover, the characteristic Raman signal and hot-electron-induced nonlinear photoluminescence coexisting within the novel Au-Si hybrids, as well as the commonly criticized randomness of the nanomaterials prepared by laser ablation in liquid, were proved to be useful for the realization of anticounterfeiting labels based on a physically unclonable function approach.

Fighting against falsification of valuable items remains crucial social-threatening challenge stimulating never-ending search for novel anti-counterfeiting strategies. The demanding security labels must simultaneously address multiple requirements (high density of the...

Using direct femtosecond laser patterning of metal-insulator-metal (MIM) sandwich designed to support Fabry-Perot mode in the visible spectral range we demonstrate new practically relevant strategy for high-resolution color printing. Irradiation of the MIM sandwich by tightly focused laser pulses allows to produce unique 3D surface nanostructures – hollow nanobumps and nanojets - locally modulating surface reflectivity. Laser processing parameters control the 3D shape of such nanostructures allowing to gradually tune the reflected color from reddish brown to pure green. Up-scalable ablation-free laser fabrication method paves the way towards various applications ranging from large-scale structural color printing to optical sensors and security labeling at a lateral resolution of 25,000 dots per inch.