Nour Beydoun

Surface plasmon resonance devices typically rely on the use of gold-coated surfaces, but the use of more abundant metals is desirable for the long-term development of plasmonic biochips. As a substitute for gold, thin copper films have been deposited on glass coverslips by thermal evaporation. As expected, these films immersed in a water solution initially exhibit an intense plasmonic resonance comparable to gold. However, without protection, an angle-resolved optical analysis shows a rapid degradation of the copper, characterized by a continuous angular shift of the plasmonic resonance curve. We show that copper films protected with a thin layer of aluminum oxide of a few nanometers can limit the oxidation rate for a sufficient time to perform some standard measurements. As the process is simple and compatible with the current biochip production technique, such an approach could pave the way for the production of alternative and more sustainable biochips.

In this study, we fabricated a hybrid plasmonic/semiconductor material by combining the chemical bath deposition of zinc oxide nanowires (ZnONWs) with the physical vapor deposition of aluminum nanostructures (AlNSs) under controlled temperature and atmosphere. The morphological and the optical properties of the ZnONWs/AlNSs hybrid material fabricated at different temperatures (250, 350, and 450 °C) and thicknesses (5, 7, and 9 nm) of Al layers were investigated. By adjusting the deposition and annealing parameters, it was possible to tune the size distribution of the AlNSs. The resonant coupling between the plasmonic AlNSs and ZnONWs leads to an enhanced photoluminescence response. The photocatalytic activity was studied through photodegradation under UV-light irradiation of methylene blue (MB) adsorbed at the surface of ZnO. The MB photodegradation experiment reveals that the ZnONWs covered with 7 nm aluminum film and annealed at 450 °C exhibit the highest degradation efficiency. The comparison between ZnONws and ZnONws/AlNSs shows a photoluminescence enhancement factor of 1.7 and an increase in the kinetics constant of photodegradation with a factor of 4.

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.