Polymer nanocomposites containing noble metal nanoparticles are promising materials for plasmonic applications. In this paper, we report on a high-resolution negative-tone nanocomposite resist based on poly(vinyl alcohol) where silver nanoparticles and nanopatterns are simultaneously generated by electron-beam lithography. Our results indicate nanostructures with a relatively high concentration of nanoparticles and, consequently, an electromagnetic coupling among the nanoparticles. Therefore, the patternable nanocomposite described in this work may be a suitable material for future plasmonic circuitry.
In this work we demonstrate the use of nanocomposite thin films of poly(vinyl alcohol) with embedded silver NPs for chemosensing purposes. Silver NPs are in situ synthesized inside polyvinyl alcohol during the bake step of the formation of a nanocomposite thin film. The polymer in the nanocomposite provides an appropriate chemical and electromagnetic environment for metal NPs in order to interact with and hence detect the chemical species. A limit of detection below 20 nM is found when detecting 2-mercaptoethanol as the analyte, when measuring spectral changes (peak wavelength, linewidth and intensity) in the Localized Surface Plasmon Resonance. Potential qualitative and semi-quantitative sensors based on such nanocomposites would be easy-to-prepare, easy-to-use and low-cost, which are the basis of a fully disposable sensing platform technology.
SiO2 and TiO2 thin films with gold nanoparticles (NPs) are of particular interest as photovoltaic materials. A novel method for the preparation of spin‐coated SiO2–Au and TiO2–Au nanocomposites is presented. This fast and inexpensive method, which includes three separate stages, is based on the in situ synthesis of both the metal‐oxide matrix and the Au NPs during a baking process at relatively low temperature. It allows the formation of nanocomposite thin films with a higher concentration of Au NPs than other methods. High‐resolution transmission electron microscopy studies revealed a homogeneous distribution of NPs over the film volume along with their narrow size distribution. The optical manifestation of localized surface plasmon resonance was studied in more detail for TiO2‐based Au‐doped nanocomposite films deposited on glass (in absorption and transmittance) and silicon (in specular reflectance). Maxwell–Garnett effective‐medium theory applied to such metal‐doped nanocomposite films describes the peculiarities of the experimental spectra, including modification of the antireflective properties of bare TiO2 films deposited on silicon by varying the concentration of metal NPs. The antireflective capabilities of the film are increased after a wet etching process.
Here we report on the triggering of antibacterial activity by a new type of silver nanoparticle coated with porous silica, Ag@silica, irradiated at their surface plasmon resonant frequency. The nanoparticles are able to bind readily to the surface of bacterial cells, although this does not affect bacterial growth since the silica shell largely attenuates the intrinsic toxicity of silver. However, upon simultaneous exposure to light corresponding to the absorption band of the nanoparticles, bacterial death is enhanced selectively on the irradiated zone. Because of the low power density used for the treatments, we discard thermal effects as the cause of cell killing. Instead, we propose that the increase in toxicity is due to the enhanced electromagnetic field in the proximity of the nanoparticles, which indirectly, most likely through induced photochemical reactions, is able to cause cell death.
Here we report on the in situ synthesis of Ag and Au nanoparticles inside several polymer matrixes by solid-state chemical reduction of a metallic salt. Poly(ethyleneimine) (PEI), poly(hydroxyethyl methacrylate) (PHEMA), poly(vinylpyrrolidone) (PVP), novolak, poly(4-vinylphenol) (P4VP), poly(4-vinylphenol)-co-(methyl methacrylate) (P4VP-co-MMA) and poly(styrene-co-allyl alcohol) (PS-co-AA) were able to reduce Ag(I) and Au(III) to the corresponding nanoparticles during the baking process. The nanoparticle diameters of Ag and Au were found to range from 2 to 25 nm. TEM also indicated a uniform distribution of nanoparticles embedded in the thin film. This approach is suitable for controlling the size of the nanoparticles and its homogeneous distribution in the polymer matrix.
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