ABSTRACT The difficulty in the powder reuse favors the study of materials in the form of thin films. ZnO based films have high photocatalytic potential. In this work, ZnO:xSm3+ (x = 0, 1, 2 and 4 %mol) thin films were prepared by spin coating method. The resins obtained to manufacture the thin films were prepared by complex polymerization method. The samples were characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), field emission scanning electron microscopy (FE-SEM) and spectroscopy UV-Vis. XRD patterns indicate that doping with 4%Sm forms Sm2O3 as the secondary phase. FE-SEM images of the cross section of thin films indicated a uniform thickness ranging from 354 to 367 nm between samples. The incorporation of Sm3+ ions in the ZnO lattice increases the Egap of the films. The photocatalytic performance of the films was tested with the photodegradation of methylene blue dye. Pure ZnO and ZnO:1%Sm3+ exhibited the best activity in the photodegradation. Thin films of pure ZnO exhibit the best photocatalytic results for the first cycle, but considerably reduce their efficiency with reuse. Sm3+ incorporation, without secondary phase formation, was efficient for the maintenance of the photocatalytic property after 3 cycles.

Crystalline europium-doped indium hydroxide (In(OH)3:Eu) nanostructures were prepared by rapid and efficient Microwave-Assisted Hydrothermal (MAH) method. Nanostructures were obtained at low temperature. FE-SEM images confirm that these samples are composed of 3D nanostructures. XRD, optical diffuse reflectance and photoluminescence (PL) measurements were used to characterize the products. Emission spectra of europium-doped indium hydroxide (IH:xEu) samples under excitation (350.7 nm) presented broad band emission regarding the indium hydroxide (IH) matrix and 5D0 → 7F0, 5D0 → 7F1, 5D0 → 7F2, 5D0 → 7F3 and 5D0 → 7F4 europium transitions at 582, 596, 618, 653 and 701 nm, respectively. Relative intensities of Eu3+ emissions increased as the concentration of this ion increased from 0, 1, 2, 4 and 8 mol %, of Eu3+, but the luminescence is drastically quenched for the IH matrix.

Rechargeable solid-state batteries have long been considered an attractive power source for a wide variety of applications, and in particular, lithium-ion batteries are emerging as the technology of choice for portable electronics. One of the main challenges in the design of these batteries is to ensure that the electrodes maintain their integrity over many discharge-recharge cycles. Fe3O4 deserves great attention as one of the most important electrode active materials due to its high theoretical capacity (926 mAhg- 1), low cost, being environmental-friendly and naturally abundance in worldwide. A simple strategy to synthesize magnetite nanoparticles (Fe3O4) by microwave-assisted hydrothermal method in a short processing time without further treatment is reported. The material obtained was tested as anode active material for lithium ions batteries. Impedance spectroscopy revealed that small differences in cell performance on cycling observed between samples cannot be strictly correlated to cell resistance. A high reversible capacity of 768.5 mAhg- 1 at 1C over 50 cycles was demonstrated, suggesting its prospective use as anode material for high power lithium ion batteries.