Here, we demonstrate for the first time a strategy to self-assemble ZnO nanoparticles (NP) on a large area by a facile one-step process. First, rough and random ZnO nanocrystals (NC), were produced by free-stabilizing aqueous synthesis. Therefore, a post thermal treatment at various temperatures ranging from 80 to 800 °C was necessary to obtain size-tunable and photoluminescent crystalline NP. The fabricated NP had both efficient UV photoluminescence and photocatalytic activity by photo-degradation of Methylene Blue (MB) dye. The annealed NP showed an absorption blue shift in the UV region with decreasing size. This shift was attributed to high quantum confinement effect since ZnO NP diameter reached values lower than the Bohr radius of ZnO (~2.7 nm). The photocatalytic activity displayed dependency on the particle’s size, number, and crystallinity. Subsequently, the NP were self-assembled inside poly(methyl methacrylate) (PMMA) nanoholes. Subsequently, large area substrate of homogenous properties ZnO NP was obtained. Moreover, the synthesis facility, photoemission and photocatalytic properties of ZnO NP could be a new insight into the realization of high performance and low cost UV laser devices.

This work describes a novel, one-shot strategy to fabricate ultrasensitive SERS sensors based on silver/poly(methyl methacrylate) (PMMA) nanocomposites. Upon spin coating of a dispersion of PMMA and silver precursor on N-doped silicon substrate, closely separated silver nanoparticles were self-assembled into uniform nanospheres. As a result, a thin hydrophobic PMMA layer embedded with Ag nanoparticles (AgNPs) was obtained on the whole silicon substrate. Consequently, a large-scale, reproducible SERS platform was produced through a rapid, simple, low-cost, and high-throughput technology. In addition, reproducible SERS features and high SERS enhancement factors were determined (SEF ~10¹⁵). This finding matches the highest SEF reported in literature to date (10¹⁴) for silver aggregates. The potential and novelty of this synthesis is that no reducing agent or copolymer was used, nor was any preliminary functionalization of the surface carried out. In addition, the AgNPs were fabricated directly on the substrate’s surface; consequently, there was no need for polymer etching. Then, the synthetic method was successfully applied to prepare opaque SERS platforms. Opaque surfaces are needed in photonic devices because of the absence of secondary back reflection, which makes optical analysis and applications easier.

We report an uncommon study of the insertion of distributions of both volume fraction and depolarization factors in the modeling of the plasmonic properties of implanted Ag nanoparticles (Ag-NPs) in a SiO₂ layer when using spectroscopic ellipsometry (SE) characterization. The Ag-NPs were embedded in the SiO₂ matrix by Ag⁺ ion implantation at various doses of 0.5 × 10¹⁶, 1 × 10¹⁶, 2 × 10¹⁶, and 5 × 10¹⁶ ions cm⁻². The formation of the Ag-NPs in a host matrix of SiO₂ was controlled by transmission electron microscopy (TEM). The Ag-NPs are self-organized in the layer, and their mean radius ranges between 2 and 20 nm. The optical properties of layers were extracted by modeling the SE parameters by taking into account the depth profile concentration of Ag-NPs. The mixture of SiO₂ and Ag-NP inclusions was modeled as an effective medium according to the shape distributed effective medium theory (SDEMT). In addition to the optical responses, it is shown that this model enables the explanation of the impact of NP shape distribution on the plasmon band and provides precious information about the NP shape characteristics. A good agreement was obtained between ellipsometry and TEM results. The distribution of the volume fraction in the film was found to lead to a gradient of effective dielectric function which was determined by the SDEMT model. The effective dielectric function reveals distinct Ag plasmon resonance varying as the Ag⁺ ions dose is varied. The real part of the dielectric function shows a significant variation around the plasmon resonance in accordance with the Kramers-Kronig equations. All determined optical parameters by SDEMT are provided and discussed. We highlight that SE combined with SDEMT calculations can be considered as a reliable tool for the determination of the NP shape and volume fraction distributions without the need of TEM.

In this paper, we explore the ability of extinction spectroscopy to characterize colloidal suspensions of gold nanoparticles (Au NPs). We demonstrate that the Au NPs’ size distribution can be deduced by analyzing their extinction spectra using Mie theory. Our procedure, based on the non-negative least square algorithm, takes advantage of the high sensitivity of the plasmon band to the Au NP size. In addition, this procedure does not require any a priori information on the Au NP size distribution. The Au NPs’ size distribution of monomodal or bimodal suspensions can be satisfactorily determined from their extinction spectra. Finally, we show that this characterization tool is compatible with in situ measurement and allows following the change in NPs’ radii during laser exposure.