The preparation of nanometer-sized structures of zinc oxide (ZnO) from zinc acetate and urea as raw materials was performed using conventional water bath heating and a microwave hydrothermal (MH) method in an aqueous solution. The oxide formation is controlled by decomposition of the added urea in the sealed autoclave. The influence of urea and the synthesis method on the final product formation are discussed. Broadband photoluminescence (PL) behavior in visible-range spectra was observed with a maximum peak centered in the green region which was attributed to different defects and the structural changes involved with ZnO crystals which were produced during the nucleation process.

Zn 1−x Mn x O nanostructures were synthesized via the microwave-assisted hydrothermal method, which rapidly produces particles of controlled size and morphology. Samples were analyzed considering the effects of manganese ion concentration. XRD revealed that all samples had wurtzite-type structure with Mn 2+ ions incorporated in the oxide lattice. UV−vis spectra showed absorption bands from the d−d transitions of Mn 2+ ions. As the doping concentration increased, the value of the energy gap decreased, indicating intermediary energy levels within the band gap in the Mn-doped ZnO samples. All samples produced broadband photoluminescence (PL) emissions in the yellow−orange− red range. Additionally, the PL intensity decreased with Mn 2+ ion incorporation into the ZnO lattice due to the creation of new recombination centers. Microscopy images showed that manganese in the ZnO matrix produced homogeneously distributed nanostructures. EPR results indicated two locations of Mn 2+ ions in the ZnO lattice, lower concentrations in the core of the lattice and higher concentrations at the surface.

Reduced graphene oxide-zinc oxide (rGO-ZnO) nanocomposites were successfully synthesized using a facile microwave-hydrothermal method under mild conditions, and their electrocatalytic properties towards O 2 evolution were investigated. The microwave radiation played an important role in obtainment of well dispersed ZnO nanoparticles directly on reduced graphene oxide sheets without any additional reducing reagents or passivation agent. X-ray diffraction (XRD), Raman and infrared spectroscopies indicated the reduction of GO as well as the successful synthesis of rGO-ZnO nanocomposites. The chemical states of the samples were shown by XPS analyses. Due to the synergic effect, the resulting nanocomposites exhibited high electronic interaction between ZnO and rGO sheets, which improved the electrocatalytic oxidation of water with low onset potential of 0.48 V (vs. Ag/AgCl) in neutral pH and long-term stability, with high current density during electrolysis. The overpotential for water oxidation decreased in alkaline pH, suggesting useful insight on the catalytic mechanism for O 2 evolution.

Rapid synthesis of CO, NI CO-doped ZnO nanoparticles: Optical and electrochemical properties, Journal of Solid State Chemistry, http://dx. AbstractWe report for the first time a rapid preparation of Zn 1-2x Co x Ni x O nanoparticles via a versatile and environmentally friendly route, microwave-assisted hydrothermal (MAH) method. The Co, Ni co-doped ZnO nanoparticles present an effect on photoluminescence and electrochemical properties, exhibiting excellent electrocatalytic performance compared to undoped ZnO sample. Photoluminescence spectroscopy measurements indicated the reduction of the green-orange-red visible emission region after adding Co and Ni ions, revealing the formation of alternative pathways for the generated recombination. The presence of these metallic ions into ZnO creates different defects, contributing to a local structural disorder, as revealed by Raman spectra.Electrochemical experiments revealed that the electrocatalytic oxidation of dopamine on ZnO attached to multi-walled carbon nanotubes improved significantly in the Co, Ni codoped ZnO samples when compared to pure ZnO.

A B S T R A C TRegular sized nanostructures of indium oxide (In 2 O 3 ) were homogeneously grown using a facile route, i.e. a microwave-hydrothermal method combined with rapid thermal treatment in a microwave oven. The presence of Er 3+ doping plays an important role in controlling the formation of cubic (bcc) and rhombohedral (rh) In 2 O 3 phases. The samples presented broad photoluminescent emission bands in the green-orange region, which were attributed to the recombination of electrons at oxygen vacancies. The photocatalytic activities of pure bcc-In 2 O 3 and a bcc-rh-In 2 O 3 mixture towards the UVA degradation of methylene blue (MB) were also evaluated. The results showed that Er +3 doped In 2 O 3 exhibited the highest photocatalytic activity with a photonic efficiency three times higher than the pure oxide. The improved performance was attributed to the higher surface area, the greater concentration of electron traps due the presence of the dopant and the possible formation of heterojunctions between the cubic and rhombohedral phases.

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rGO–TiO2 nanocomposites exhibited greater electrocatalytic activity for H2O oxidation in neutral and alkaline medium as compared with pure TiO2.

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