47 research outputs found

    La-doped and La/Mn-co-doped Barium Titanate Ceramics

    Get PDF
    Barium titanate ceramics doped with 0.3 mol.% lanthanum and co-doped with 0.3 mol.% lanthanum and 0.05 mol.% manganese were investigated. The powders were prepared by a modified polymeric precursor method based on the Pechini process. The ceramics were obtained by sintering at 1300 degrees C for 8 h. The influence of dopants on structural changes and grain size reduction was analyzed. The presence of dopants influenced the tetragonality of the barium titanate crystal structure. Reduction of polygonal grain size with dopant addition was noticed. In the doped ceramics, characteristic phase transitions were shifted to lower temperatures in comparison with pure barium titanate. The dielectric permittivity value showed the tendency of a slight increase with lanthanum addition and further increase with adding of manganese. La as a single dopant increased the diffuseness of phase transitions indicating the formation of a diffuse ferroelectric material but in the co-doped ceramics the phase transition diffuseness decreased. The resistivity of the co-doped ceramics was higher than for lanthanum doped ceramics, indicating possible segregation of manganese at grain boundaries that influenced the total resistivity of the material

    PZT-NZF/CF ferrite flexible thick films: Structural, dielectric, ferroelectric, and magnetic characterization

    Get PDF
    The preparation and properties of thick flexible three-phase composite films based on lead zirconium titanate (PZT) and various ferrites (nickel zinc ferrite (NZF) and cobalt ferrite (CF)) were reported in this study. Properties of three-phase composite films were compared with pure polyvinylidene fluoride (PVDF) and PZT-PVDF films. X-ray diffraction data indicated the formation of well crystallized structure of PZT and NZF/CF phases, without the presence of undesirable phases. Scanning electron micrographs showed that the ceramic particles were dispersed homogeneously in the PVDF matrix and atomic force microscopy confirmed that the size of the particles is around 30 nm. Non-saturated hysteresis loops were evident in all samples due to the presence of highly conductive ferrite phases. Under magnetic field of 10 kOe, composite films exhibited a typical ferromagnetic response. Dielectric properties were investigated in the temperature range from -128 to 250 degrees C and frequency range of 400 Hz-1 MHz. The results showed that the value of dielectric constant of the PVDF/PZT/ferrite composites increased about 25% above the one obtained for pure PVDF

    Temperature-Induced Structural Transformations in Undoped and Eu3+-Doped Ruddlesden–Popper Phases Sr2SnO4 and Sr3Sn2O7: Relation to the Impedance and Luminescence Behaviors

    Get PDF
    We report that luminescence of Eu3+ ion incorporated into Ruddlesden–Popper phases allows monitoring phase transition in powders (instead of single crystals), in a time-efficient manner (compared to neutron diffraction), and importantly, with greater sensitivity than previous methods. Crystal structure and dielectric response of undoped and 0.5%Eu3+-doped Sr3Sn2O7 ceramics were studied as a function of temperature over the temperature range of 300–800 K. The luminescence studies of 0.5%Eu3+-doped Sr2SnO4 and Sr3Sn2O7 samples were performed in the temperature range of 80–500 K. These results were compared with the respective dependences for the undoped compounds. The structural transformations in 0.5%Eu3+-doped Sr3Sn2O7 were found at 390 and 740 K. The former is associated with the isostructural atomic rearrangement that resulted in a negative thermal expansion along two of three orthorhombic crystallographic axes, while the latter corresponds to the structural transition from the orthorhombic Amam phase to the tetragonal I4/mmm one. A similar temperature behavior with the structural transformations in the same temperature ranges was observed in undoped Sr3Sn2O7, although the values of lattice parameters of the Eu3+-doped and undoped compounds were found to be slightly different indicating an incorporation of europium in the crystal lattice. A dielectric anomaly associated with a structural phase transition was observed in Sr3Sn2O7 at 390 K. Optical measurements performed over a wide temperature range demonstrated a clear correlation between structural transformations in Eu3+-doped Sr2SnO4 and Sr3Sn2O7 and the temperature anomalies of their luminescence spectra, suggesting the efficacy of this method for the determination of subtle phase transformations

    Suppression of phase transitions and glass phase signatures in mixed cation halide perovskites

    Get PDF
    Cation engineering provides a route to control the structure and properties of hybrid halide perovskites, which has resulted in the highest performance solar cells based on mixtures of Cs, methylammonium, and formamidinium. Here, we present a multi-technique experimental and theoretical study of structural phase transitions, structural phases and dipolar dynamics in the mixed methylammonium/dimethylammonium MA1-xDMAxPbBr3 hybrid perovskites (0 ≤ x ≤ 1). Our results demonstrate a significant suppression of the structural phase transitions, enhanced disorder and stabilization of the cubic phase even for a small amount of dimethylammonium cations. As the dimethylammonium concentration approaches the solubility limit in MAPbBr3, we observe the disappearance of the structural phase transitions and indications of a glassy dipolar phase. We also reveal a significant tunability of the dielectric permittivity upon mixing of the molecular cations that arises from frustrated electric dipoles

    LOCAL PIEZOELECTRICITY IN SrTiO3-BiTiO3 CERAMICS

    Get PDF
    Local piezoelectric properties of Bi-doped SrTiO3 ceramics have been investigated by piezoresponse force microscopy. The appearance of both out-of-plane and in-plane polarization components confirmed the piezoelectric nature of the obtained signal. The absence of labyrinth-like structures in observed piezoelectric contrast is not consistent with the expected existence of a relaxor ferroelectric state in this material. The close similarity of local piezoelectric properties in Bi-doped SrTiO3 with pure SrTiO3 suggests that the origin of obtained piezoresponse can be attributed to the flexoelectric phenomenon. Bi-doping leads to occurrence of oxygen vacancies and negative charge on the surface of the sample

    Metastable perovskite Bi1-xLaxFe0.5Sc0.5O3 phases in the range of the compositional crossover

    Get PDF
    Perovskite ceramics of the Bi1- xLaxFe0.5Sc0.5O3 composition (0.30 ≤ x ≤ 0.35) that cannot be sintered in bulk form as a single phase using the conventional ceramic route were successfully prepared using the high-pressure/high-temperature technique. It has been shown that the room-temperature compositional crossover from the antipolar phase whose incommensurate modulation of displacements of Bi/La and oxygen is described by the Imma(00γ)s00 superspace group to the non-polar Pnma phase occurs in the narrow range between x = 0.33 and x = 0.34 with no phase coexistence. The features of this compositional crossover are discussed in comparison with that observed in the Bi1- xLaxFeO3 system.publishe

    Distribution of relaxation times in PMN single crystal

    No full text
    The dielectric permittivity of PMN single crystal was measured in the frequency range from 20 Hz to 3 GHz. Dielectric dispersion was observed in all investigated frequency range. From the frequency dependence of the real and imaginary parts of dielectric permittvity, the distribution of relaxation times was calculated. The low frequency limit of the distribution of the relaxation times diverge according to the Vogel – Fulcher law with the freezing temperature T0_{0} = 228 K, which is in good agreement with mean relaxation time temperature dependence obtained from Cole – Cole equation. Broadening of the relaxation time distribution function at low temperatures indicates the existence of two different components making contribution to the total dielectric spectrum of PMN
    corecore