RESUMEN
We report the synthesis of vertically aligned silicon nanowire (VA-SiNW) oligomer arrays coated with Au nanoparticle (NP) monolayers via a combination of colloidal lithography, metal-assisted chemical etching, and directed NP assembly. Arrays of SiNW monomers (i.e., isolated NWs), dimers, and tetramers are synthesized, decorated with AuNPs, and tested for their performance in surface-enhanced Raman spectroscopy. The â¼20 nm AuNPs easily enter within the ca. 40 nm gaps of the SiNW oligomers, thus reaching the hot spot region. At 785 nm excitation, the AuNPs@SiNW dimer arrays provide the highest Raman signal, in agreement with electromagnetic simulations showing a high electric field enhancement at the Au/Si interface within the dimer gap region.
RESUMEN
Colloidal crystals are excellent model systems to study self-assembly and structural coloration because their periodicities coincide with the wavelength range of visible light. Different assembly methods inherently introduce characteristic defects and irregularities, even with nearly monodisperse colloidal particles. Here, we investigate how these imperfections influence the structural coloration by comparing two techniques to obtain colloidal crystals. 3D colloidal crystals produced by convective assembly are well-ordered and periodically arranged but show microscopic cracks. (2+1)D colloidal crystals fabricated by stacking individual monolayers show a decreased hexagonal order and limited crystal registration between single monolayers in the z-direction. We investigate the optical properties of both systems by comparing identical numbers of layers using correlative microspectroscopy. These measurements show that the less ordered (2+1)D colloidal crystals exhibit higher reflected light intensities. Macroscopic reflection integrating all angles shows that the reflected light intensity levels out with an increasing number of layers, whereas incoherent scattering increases. Although both types of colloidal crystal show similar angle-dependent color shifts in specular reflection, the less-ordered structure of the (2+1)D colloidal crystal scatters light within a larger angular range under diffusive illumination. Our results suggest that structural coloration is surprisingly robust toward local defects and irregularities.
RESUMEN
Colloidal crystals and glasses manipulate light propagation depending on their chemical composition, particle morphology, and mesoscopic structure. This light-matter interaction has been intensely investigated, but a knowledge gap remains for mesostructures comprising a continuous property gradient of the constituting particles. Here, a general synthetic approach to bottom-up fabrication of continuous size gradient colloidal ensembles is introduced. First, the technique synthesizes a dispersion with a specifically designed gradual particle size distribution. Second, self-assembly of this dispersion yields a photonic colloidal glass with a continuous size gradient from top to bottom. Local and bulk characterization methods are used to highlight the significant potential of this mesostructure, resulting in vivid structural colors along, and in superior light scattering across the gradient. The process describes a general pathway to mesoscopic gradients. It can expectedly be transferred to a variety of other particle-based systems where continuous gradients will provide novel physical insights and functionalities.