B-site vacancy induced Raman scattering in BaTiO3-based ferroelectric ceramics

Defects, in particular vacancies, play a crucial role in substituted perovskite systems, influencing the structural features that underpin ferroelectricity. B-site vacancies introduce cation disorder in the perovskite lattice and are in fact one of the main driving forces for relaxor behaviour in barium titanate (BaTiO3, BT) based ferroelectrics. In this work, material systems are carefully selected to qualitatively study the change in B-site vacancy concentration for heterovalent substituted BT-based ferroelectric polycrystals. Raman spectroscopy was used to investigate those systems, and B-site vacancy specific Raman modes were identified unambiguously by comparison with charge-compensated BT, where B-site vacancies are absent. This study validates the hypothesis that vacancies induce Raman scattering because of symmetry breaking in the BT lattice, establishing this method as a vital tool to study substitutional defects in ceramic materials

Mechanosynthesis of the Whole Y_1−xBi_xMn_1−xFe_xO₃ Perovskite System: Structural Characterization and Study of Phase Transitions

Perovskite BiFeO3 and YMnO3 are both multiferroic materials with distinctive magnetoelectric coupling phenomena. Owing to this, the Y1−xBix Mn1−xFexO3 solid solution seems to be a promising system, though poorly studied. This is due to the metastable nature of the orthorhombic perovskite phase of YMnO3 at ambient pressure, and to the complexity of obtaining pure rhombohedral phases for BiFeO3-rich compositions. In this work, nanocrystalline powders across the whole perovskite system were prepared for the first time by mechanosynthesis in a high-energy planetary mill, avoiding high pressure and temperature routes. Thermal decomposition temperatures were determined, and structural characterization was carried out by X-ray powder diffraction and Raman spectroscopy on thermally treated samples of enhanced crystallinity. Two polymorphic phases with orthorhombic Pnma and rhombohedral R3c h symmetries, and their coexistence over a wide compositional range were found. A gradual evolution of the lattice parameters with the composition was revealed for both phases, which suggests the existence of two continuous solid solutions. Following bibliographic data for BiFeO3, first order ferroic phase transitions were located by differential thermal analysis in compositions with x ≥ 0.9. Furthermore, an orthorhombic-rhombohedral structural evolution across the ferroelectric transition was characterized with temperature-dependent X-ray diffraction

Thermal degradation of ceramic slurry-coated polyurethane foam used in making reticulated porous SiC ceramics

A 25-mu m-thick ceramic slurry-coated 12 ppi (pores per linear inch) polyurethane foam suitable for synthesis of oxide-bonded reticulated porous SiC ceramics was analysed by the thermal analysis techniques (thermogravimetry and differential thermal analysis) up to 700 A degrees C in air to investigate the polymer degradation reactions associated with the pyrolysis stage of the fabrication process. The kinetic parameters of the polymer degradation reactions were determined using the non-isothermal thermogravimetric data, and the degradation mechanism was evaluated. The effects of slurry coating on the foam degradation process were discussed, and slurry coating on foam was found to have insignificant effects on PUF degradation reactions

Raman spectra of fine-grained materials from first principles

Raman spectroscopy is an advantageous method for studying the local structure of materials, but the interpretation of measured spectra is complicated by the presence of oblique phonons in polycrystals of polar materials. Whilst group theory considerations and standard ab initio calculations are helpful, they are often valid only for single crystals. In this paper, we introduce a method for computing Raman spectra of polycrystalline materials from first principles. We start from the standard approach based on the (Placzek) rotation invariants of the Raman tensors and extend it to include the effect of the coupling between the lattice vibrations and the induced electric field, and the electro-optic contribution, relevant for polar materials like ferroelectrics. As exemplified by applying the method to rhombohedral BaTiO3, AlN, and LiNbO3, such an extension brings the simulated Raman spectrum to a much better correspondence with the experimental one. Additional advantages of the method are that it is general, permits automation, and thus can be used in high-throughput fashion

Ceramic processing and multiferroic properties of the perovskite YMnO3-BiFeO3 binary system

International audienceThe perovskite (1-x)YMnO3-xBiFeO(3) binary system is very promising because of its multiferroic end members. Nanocrystalline phases have been recently obtained by mechanosynthesis across the system, and the perovskite structural evolution has been described. Two continuous solid solutions with orthorhombic Pnma and rhombohedral R3c symmetries were found, which coexist within a broad compositional interval of 0.5 <= x <= 0.9. This might be a polar-nonpolar morphotropic phase boundary region, at which strong phase-change magnetoelectric responses can be expected. A major issue is phase decomposition at moderate temperatures that highly complicates ceramic processing. This is required for carrying out a sound electrical characterization and also for their use in devices. We present here the application of Spark Plasma Sintering to the ceramic processing of YMnO3-BiFeO3 phases. This advanced technique, when combined with nanocrystalline powders, allowed densifying phases at reduced processing temperatures and times, so that perovskite decomposition was avoided. Electrical measurements were accomplished, and the response was shown to be mostly dominated by conduction. Nonetheless, the intrinsic dielectric permittivity was obtained, and a distinctive enhancement in the phase coexistence region was revealed. Besides, Rayleigh-type behavior characteristic of ferroelectrics was also demonstrated for all rhombohedral phases. Magnetic characterization was performed in this region, and antiferromagnetism was shown

Atomic scale symmetry and polar nanoclusters in the paraelectric phase of ferroelectric materials

The nature of the “forbidden” local- and long-range polar order in nominally non-polar paraelectric phases of ferroelectric materials has been an open question since the discovery of ferroelectricity in oxide perovskites, ABO3. A currently considered model suggests locally correlated displacements of B-site atoms along a subset of cubic directions. Such off-site displacements have been confirmed experimentally; however, being essentially dynamic in nature they cannot account for the static nature of the symmetry-forbidden polarization implied by the macroscopic experiments. Here, in an atomically resolved study by aberration-corrected scanning transmission electron microscopy complemented by Raman spectroscopy, we reveal, directly visualize and quantitatively describe static, 2–4 nm large polar nanoclusters in the nominally non-polar cubic phases of (Ba,Sr)TiO3 and BaTiO3. These results have implications on understanding of the atomic-scale structure of disordered materials, the origin of precursor states in ferroelectrics, and may help answering ambiguities on the dynamic-versus-static nature of nano-sized clusters.ISSN:2041-172