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Thin film nanocomposites with mixed connectivity, composed by CoFe2O4 grains, deposited by electrophoresis on Si|Pt substrates, and subsequently covered by a laser ablation deposited BaTiO3 layer were prepared with different cobalt ferrite concentrations. Their structure presented a combination of BaTiO3, with its tetragonal and the orthorhombic phases coexisting at room temperature, and CoFe2O4 with the cubic spinel structure. The cobalt ferrite nanograins were under in-plane tensile stress, while the BaTiO3 phase was under in-plane compressive stress. The dielectric measurements showed that as the barium titanate grain size decreased, its ferroelectric Curie temperature shifted to lower temperatures relative to the bulk. This grain size dependent TC shift was associated and modeled by a core-shell structure of BaTiO3 grains in the films, with a tetragonal core and cubic shell. Additionally, a diffuse tetragonal-orthorhombic phase transition was observed and, in agreement with Raman spectroscopy results, associated to the coexistence of barium titanate orthorhombic and tetragonal phases in the room temperature region. This led to the formation of polar nanoclusters with random polarization orientations, which induced a frustrated phase transition between the tetragonal and orthorhombic phases of barium titanate in the films.

The ferroelectric polymorph of lead metaniobate (PbNb2O6) presents an orthorhombic structure that is metastable at room temperature. This phase is obtained by quenching from high temperature. The fabrication of lead niobate thin films with this orthorhombic form has been reported to be difficult due to the presence of phases with the rhombohedric form or other nonstoichiometric phases. In this work, lead niobate thin films have been prepared by laser ablation, at different oxygen pressures and with different substrate temperatures. Their structure was studied by X-ray diffraction and their surface was examined by scanning electron microscopy (SEM). The results show that for low deposition temperatures the films presented a rhombohedric-PbNb2O6 structural phase. As Tdep increases the films started to develop an orthorhombic- PbNb2O6 structure that appeared at 400°C and remains up to 600°C. For lower oxygen pressure during deposition, a mixture of this phase and other orthorhombic lead deficient phases are present in the films. On the other hand, by increasing the oxygen pressure the lead deficient phases are strongly reduced and the films present only the orthorhombic- PbNb2O6 structure.

Premature degradation of ordinary Portland cement (OPC) concrete infrastructures is a current and serious problem with overwhelming costs amounting to several trillion dollars. The use of concrete surface treatments with waterproofing materials to prevent the access of aggressive substances is an important way of enhancing concrete durability. The most common surface treatments use polymeric resins based on epoxy, silicone (siloxane), acrylics, polyurethanes or polymethacrylate. However, epoxy resins have low resistance to ultraviolet radiation while polyurethanes are sensitive to high alkalinity environments. Geopolymers constitute a group of materials with high resistance to chemical attack that could also be used for coating of concrete infrastructures exposed to harsh chemical environments.This article presents results of an experimental investigation on the resistance to chemical attack (by sulfuric and nitric acid) of several materials: OPC concrete, high performance concrete (HPC), epoxy resin, acrylic painting and a fly ash based geopolymeric mortar. Two types of acids, each with high concentrations of 10%, 20% and 30%, were used to simulate long term degradation by chemical attack. The results show that the epoxy resin had the best resistance to chemical attack, irrespective of the acid type and acid concentration.

Detailed structural, microstructural and magnetic measurements were performed on (PbNb2O6)1-x-(CoFe2O4)x nanocomposite thin films deposited by laser ablation on Si(001)\Pt substrates, with different ferrite concentrations. The tuning of the lead concentration, due to the lead volatility, was found to be particularly important in order to obtain the orthorhombic (ferroelectric) lead niobate phase. The lattice parameter of CoFe2O4 was below the bulk value, indicating the presence of compressive strains on this phase. A magnetic anisotropy was observed, which favored the orientation of the magnetization in the direction perpendicular to the plane of the films, for cobalt ferrite concentrations 40-50%. The shape, stress and magnetocrystalline anisotropy fields on the composites were calculated and compared. It was found that the perpendicular magnetic anisotropy was induced by the presence of strain on the ferrite phase in the films.