46 research outputs found

    Phase transitions and local polarity above TC in a PbZr0.87Ti0.13O3 single crystal

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    Solid solutions of PbZr1_xTixO3 (PZT) are one of the most widely used piezoelectric materials with perovskite structure. Despite the decades of research, the phase diagram of PZT reported in 1971 has not been resolved yet. Recently, it turned out that single crystals of good quality of these solid solutions can be grown. By means of top-seeded solution growth (TSSG) technique, we succeeded to grow a single PbZr0.87Ti0.13O3 crystal. Hence, a partial verification of the diagram could be performed through investigations of the optical, dielectric, pyroelectric and elastic properties of this crystal, in a wide temperature range. The obtained results confirmed that the PbZr0.87Ti0.13O3 crystal undergoes a sequence of phase transitions, such as those observed in ceramics of similar chemical composition. However, additional anomalies of investigated physical properties were observed and discussed. Moreover, the influence of electric field on optical properties has been investigated for the first time and has proven the existence of local polar character of the phase above TC in a limited temperature range

    Strong piezoelectric properties and electric-field-driven changes in domain structures in a PbZr0.87Ti0.13O3 single crystal

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    PbZr 1-x Tix O3 perovskite materials, known as PZT, are highly applicable, mainly due to their extraordinary piezoelectric properties. Recently, a technology of PZT crystals growth has been elaborated and opened new investigation possibilities for these compounds. In this paper, we demonstrate a highly piezoelectric response in PbZr 0.87 Ti 0.13 O3 single crystal. Under the action of an electric field, the piezoelectric coefficient d 33 turns out to be over 2500 pm V -1. The optical studies performed have proved a significant influence of the domain dynamics on such high-efficiency piezoelectric response. Monoclinic M and rhombohedral R phases have been observed in the lead zirconate-titanate crystals with a low Ti content. This coex- istence of phases with different symmetries and dense domain walls are the primary sources of high piezoelectric response. We have observed that strong electric fields may act on randomly oriented po- larization vectors so that the total piezoelectric activity disappears, and the unusual isotropization point near 250 °C appears

    The noise of many needles: Jerky domain wall propagation in PbZrO3 and LaAlO3

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    Measurements of the sample length of PbZrO3 and LaAlO3 under slowly increasing force (3-30 mN/min) yield a superposition of a continuous decrease interrupted by discontinuous drops. This strain intermittency is induced by the jerky movement of ferroelastic domain walls through avalanches near the depinning threshold. At temperatures close to the domain freezing regime, the distributions of the calculated squared drop velocity maxima N(υm2) follow a power law behaviour with exponents ε=1.6±0.2. This is in good agreement with the energy exponent ε=1.8±0.2 recently found for the movement of a single needle tip in LaAlO3 [R. J. Harrison and E. K. H. Salje, Appl. Phys. Lett. 97, 021907 (2010)]. With increasing temperature, N(υm2) changes from a power law at low temperatures to an exponential law at elevated temperatures, indicating that thermal fluctuations increasingly enable domain wall segments to unpin even when the driving force is smaller than the corresponding barrier

    Monoclinic domain populations and enhancement of piezoelectric properties in a PZT single crystal at the morphotropic phase boundary

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    The origin of the strong piezoelectric phenomenon in PbZr1−xTixO3 (PZT) perovskites still suffers from a lack of complete understanding. It concerns the distinction between the intrinsic and extrinsic mechanisms that govern PZT's piezo activity. These two mechanisms have been investigated in single crystal PbZr0.54Ti0.46O3 at the morphotropic phase boundary. After poling in a DC electric field, the piezoelectric properties were examined on the same crystal by observing piezoelectric resonances to determine the piezoelectric coefficient d31 and measuring quasistatic deformation to determine the coefficient d33. The domain populations were investigated during and after poling in a DC electric field. These populations were also investigated as a function of DC fields for strengths similar to those used to measure quasistatic piezoelectric properties for a poled crystal. The experiments indicate that the intrinsic origin of the enhancement of the piezoelectric properties is connected with a change in the population of domains with monoclinic symmetry, in which there is an easy polarization rotation under the action of the electric field

    Ultrahigh Piezoelectric Strains in PbZr1−xTixO3 single crystals with controlled Ti content close to the tricritical point

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    Intensive investigations of PbZr Ti O (PZT) materials with the ABO perovskite structure are connected with their extraordinary piezoelectric properties. Especially well known are PZT ceramics at the Morphotropic Phase Boundary (MPB), with x~0.48, whose applications are the most numerous among ferroelectrics. These piezoelectric properties are often obtained by doping with various ions at the B sites. Interestingly, we have found similar properties for undoped PZT single crystals with low Ti content, for which we have confirmed the existence of the tricritical point near x~0.06. For a PbZr Ti O crystal, we describe the ultrahigh strain, dielectric, optical and piezoelectric properties. We interpret the ultrahigh strain observed in the region of the antiferroelectric-ferroelectric transition as an inverse piezoelectric effect generated by the coexistence of domains of different symmetries. The complex domain coexistence was confirmed by determining optical indicatrix orientations in domains. The piezoelectric coefficient in this region reached an extremely high value of 5000 pm/V. We also verified that the properties of the PZT single crystals from the region near the tricritical point are incredibly susceptible to a slight deviation in the Ti content

    A neutron diffuse scattering study of PbZrO<sub>3</sub> and Zr-rich PbZr<sub>1-x</sub>Ti<sub>x</sub>O<sub>3</sub>

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    A combined neutron diffuse scattering study and model analysis of the antiferroelectric crystal PbZrO3is described. Following on from earlier X-ray diffuse scattering studies, supporting evidence for disordering of oxygen octahedral tilts and Pb displacements is shown in the high-temperature cubic phase. Excess diffuse scattering intensity is found at theMandRpoints in the Brillouin zone. A shell-model molecular dynamics simulation closely reproduces the neutron diffuse scattering pattern. Both in-phase and antiphase tilts are found in the structural model, with in-phase tilts predominating. The transition between disordered and ordered structure is discussed and compared with that seen in Zr-rich PbZr1−xTixO3.</jats:p

    Supplemental Material of the article Weak low-temperature polarity in a PbZrO3 single crystal

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    Supplement Material 1 describes in detail the experimental techniques used. -- Supplement Material 2 presents a film showing changes in indicatrix orientations during the low-temperature transition in PbZrO3 single crystals.Weak low-temperature_supplementary_material_1.pdfPeer reviewe

    Weak low-temperature polarity in a PbZr O3 single crystal

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    We report the existence of a low-temperature polar phase in PbZrO3 below 270 K. The temperature dependence of resultant polarization was assigned from pyroelectric current changes measured after poling the single crystal or ceramic in a DC electric field. This was observed in single crystals and ceramics and may have a connection with the presence of polar (ferrielectric) antiphase boundaries inside the antiferroelectric phase. The transition point is demonstrated by changes in domain structure and anomalies in dielectric permittivity and losses in as-grown single crystals and ceramic samples.This research was funded by the National Science Centre, Poland, with Grant No. 2020/37/B/ST3/02015.Peer reviewe
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