ZnO nanorods decorated with gold nanoparticles of ~20 nm average size were fabricated by microwave-assisted chemical synthesis. For the surface-attached growth of metal nanoparticles, the ZnO nanostructures were first functionalized by sodium citrate and then the metal ions were reduced under microwave heating. While the incorporation of gold nanoparticles at the surface seen to quench both the band edge and visible emissions of the ZnO nanostructures, it enhances the degradation rate of Rhodamine 6G up to 3 folds under UV emission. The mechanisms of citrate functionalization, growth of Au nanoparticles on the surface of the oxide nanostructures, luminescence emission quenching, and enhanced photocatalytic activity of the composite nanostructures have been discussed.

Effects of Ag doping on the crystallinity and optical properties of zinc oxide (ZnO) nanoparticles have been studied by x-ray diffraction, diffuse reflectance spectroscopy, micro-Raman, and photoluminescence spectroscopy. It has been observed that while Ag-doping at low concentration improves the optoelectronic properties of ZnO nanostructures, Ag-doping at high concentrations drastically modify the emission behavior and lattice vibrational characteristics of the nanostructures. High Ag content in ZnO nanostructures causes lattice deformation, induces silent vibrational modes in Raman spectra, and reduces excitonic UV emission due to concentration quenching.

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Well crystalline, near-stoichiometric zinc oxide nanostructures of different morphologies are fabricated in large scale, utilizing a simple, cost effective mechanochemical synthesis in absence of solvent. Effects of ionic and nonionic surfactants along with the concentration of hydrolyzing agent on the evolution of nanostructure morphology have been studied. It has been observed that while a cationic surfactant such as Cetyltrimethylammonium Bromide (CTAB) favors the nanostructures to growth along their polar c-axis, a nonionic surfactant such as Polyvinylpyrrolidone (PVP) reduces their preferred c-axis growth. Increase of hydrolyzing agent in the reaction mixture enhances the growth rate of the nanostructures. The nanostructures have been tested for photodegradation of anionic dye molecules such as Methylene Blue (MB). All the nanostructures manifest high photocatalytic performance. Apart from morphology, the specific surface area, crystal plane orientation and the concentration of basic sites at surface are seen to contribute significantly to the photocatalytic performance of the zinc oxide nanostructures.

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