M. Dunce

PHASE TRANSITIONS IN Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 SOLID SOLUTIONS

ABSTRACT Studies of nature of polarization in ternary solid solutions of Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 were done, using measurements of dielectric properties and polarization hysteresis loops. Various stages of relaxor behavior depending on concentration of PbTiO3 were established and compared with other known ferroelectric relaxors.

Phase Transitions in Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 Solid Solutions

All sequential steps of transfer from relaxor to normal ferroelectric phase transition are found in Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 if concentration of PbTiO3 increases. The relaxor properties in Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 solid solutions are described by the power law and Vogel-Fulcher relationship. Concentration dependence of the relevant parameters is discussed. Stability of relaxor and ferroelectric phases is discussed by analyzing behaviour of critical electric fields.

Structure and Dielectric Properties of Na1/2Bi1/2TiO3-BaTiO3 Solid Solutions

Dielectric properties, polarization and x-ray diffraction are studied for (1-x)Na_1/2Bi_1/2TiO₃-xBaTiO₃ solid solutions in a concentration range above the morphotropic phase boundary. It is showed that all the studied compositions have tetragonal structure with maximal tetragonality slightly above the morphotropic phase boundary. Ferroelectric relaxor behavior is observed in a wide concentration range of BaTiO₃. Stability of the relaxor state decreases with increasing BaTiO₃ concentration, but only for compositions with low Na_1/2Bi_1/2TiO₃ content the normal ferroelectric-paraelectric phase transition, which is characteristic to pure BaTiO₃, occurs. Mechanisms, which influence the change of the phase transition character and promote the appearance of the relaxor state, are discussed. The phase diagram of (1-x)Na_1/2Bi_1/2TiO₃-xBaTiO₃ is revised.

SINTERING OF LEAD-FREE (K0.5Na0.5)NbO3 BASED SOLID SOLUTION

ABSTRACT In this study lead-free solid solution (K0.5Na0.5)NbO3 was prepared, structure, dielectric parameters of ceramics were investigated. The doping of sintering aids did not affect the crystallographic structure of the ceramics significantly; all ceramic samples had a single-phase perovskite structure. Added elements CdO, ZnO, MnO2, V2O5 effectively decreased the sintering temperature of KNN by 50°–80°C. All sintering aids influenced sinterability, microstructure and dielectric properties of ceramics. Dielectric constant for doped samples increased from 6000 up to 8000; Pr = 15 μC/cm2, Ec = 9 kV/cm, d33 = 110 pC/N, kp = 0.38 and Qm = 190 for MnO2 doped samples.

Structure and dielectric properties of Na0.5Bi0.5TiO3-CaTiO3 solid solutions

Despite wide studies of Na0.5Bi0.5TiO3, structure of this material and its connection with the observed physical properties still raise numerous questions due to mutually contradicting results obtained. Here, structure and dielectric properties of poled and unpoled Na0.5Bi0.5TiO3-CaTiO3 solid solutions are studied, projecting the obtained concentration dependence of structure and dielectric properties on pure Na0.5Bi0.5TiO3 as the end member of this material group. X-ray diffraction patterns for Na0.5Bi0.5TiO3-CaTiO3 solid solutions reveal dominating of an orthorhombic Pnma phase, even for the compositions approaching the end composition (Na0.5Bi0.5TiO3), whereas structure of pure Na0.5Bi0.5TiO3 can be considered, assuming coexistence of rhombohedral and orthorhombic phases. This allows one to avoid appearance of a large difference of rhombohedral distortions between the unpoled and poled Na0.5Bi0.5TiO3, if the rhombohedral distortion is calculated as for single R3c phase. Features of dielectric permittiv...

X-ray diffraction and Raman spectroscopy studies in Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 solid solutions

ABSTRACT The long and short range orders in 0.4Na1/2Bi1/2TiO3-(0.6-x)SrTiO3-xPbTiO3 solid solutions were studied by x-ray diffraction and Raman spectroscopy. X-ray diffraction patterns for these compositions in the relaxor state are different for bulk and powdered samples. It was found that, in spite of different tetragonality depending on PbTiO3 content, the Raman spectra suggest similarity of local structure for all studied compositions. Both methods indicate a disappearance of tetragonal phase upon increasing temperature.

Dynamics of Phase Transition in 0.4NBT-0.4ST-0.2PT Solid Solution

In this paper we present dielectric spectroscopy results of NBT-(0.6-x)ST-xPT with x = 0.2 solid solution. Dielectric investigations clearly showed a relaxor—normal ferroelectric phase transition at TPT = 419 K and low temperature and low frequency dispersion similar to coexistence of dipolar glass and ferroelectric phase. The mean relaxation time above the phase transition follows Vogel—Fulcher law with following parameters: E A = 0.179 eV, τ 0 = 3.39·10−14 s, T VF = 223 K.

Electrocaloric Effect in Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 Solid Solutions

Electrocaloric effect is studied in a group of triple solid solutions 0.4Na1/2Bi1/2TiO3-(0.6-y)SrTiO3-yPbTiO3. Contribution of electric field-induced phase transition in the total value of temperature change, caused by electric field, is evaluated. The highest value of electrocaloric effect is observed for composition 0.4Na1/2Bi1/2TiO3-0.4SrTiO3-0.2PbTiO3, in which the depolarization temperature, characteristic for relaxor ferroelectrics, merges with the temperature of maximum of dielectric permittivity. Applicability of thermodynamic description is discussed.

Description of Relaxor State in Na1/2Bi1/2TiO3-SrTiO3-PbTiO3 System of Solid Solutions

Vogel-Fulcher law, traditionally applied to describe dispersion of dielectric permittivity in relaxor ferroelectrics, requires introduction of two different relaxation mechanisms above and below freezing temperature correspondingly. Extending distribution function of relaxation times, previously known for low-temperature region, allows creating common description of relaxation in all range, where distribution function of relaxation times can be regarded as wide, without freezing at certain temperature.

Direct and indirect determination of electrocaloric effect in Na0.5Bi0.5TiO3

Direct and indirect studies of the electrocaloric effect were carried out in poled and depoled Na0.5Bi0.5TiO3. For this purpose, polarization and electrocaloric effect temperature change measurements were made at different electric field pulses as a function of temperature. The applicability of the widely used indirect electrocaloric effect determination method, using the Maxwell relation, was critically analyzed with respect to the reliable direct measurements. Quantitative differences were observed between the results obtained by both approaches in the case of the poled Na0.5Bi0.5TiO3 sample. These differences can be explained by the temperature-dependent concentration of domains oriented in the direction of the applied electric field. Whereas in depoled Na0.5Bi0.5TiO3, which is characterized by the electric field dependence of polar nanoregions embedded in a nonpolar matrix, the Maxwell relation is not applicable at all, as it is indicated by the obtained results. Possible mechanisms which could be res...