Direct measurement of the domain switching contribution to the dynamic piezoelectric response in ferroelectric ceramics

2006 ◽  
Vol 89 (9) ◽  
pp. 092901 ◽  
Author(s):  
Jacob L. Jones ◽  
Mark Hoffman ◽  
John E. Daniels ◽  
Andrew J. Studer
2002 ◽  
Vol 17 (6) ◽  
pp. 1376-1384 ◽  
Author(s):  
Marlyse Demartin Maeder ◽  
Dragan Damjanovic ◽  
Cyril Voisard ◽  
Nava Setter

The dynamic piezoelectric response of SrBi4Ti4O15 ceramics with Aurivillius structure was investigated at high alternating stress, low frequencies (0.01 to 100 Hz), and temperatures from 20 to 200 °C. The piezoelectric nonlinearity, observed only at high pressures (>10 MPa) and elevated temperatures (>150 °C), is interpreted in terms of contributions from non-180° domain walls. At weak fields, the frequency dependence of the longitudinal piezoelectric coefficient was explained in terms of Maxwell–Wagner piezoelectric relaxation. The Maxwell–Wagner units are identified as colonies that consist of highly anisotropic grains which sinter together, and whose distribution in the ceramic is strongly dependent on sintering conditions.


2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Yoshihiro Kuroiwa ◽  
Sangwook Kim ◽  
Ichiro Fujii ◽  
Shintaro Ueno ◽  
Yuki Nakahira ◽  
...  

Abstract A large piezoelectric response in ferroelectric ceramics is typically associated with extrinsic contributions from ferroelectric domain structures. However, such domain structures cannot be expected in systems with pseudo-cubic symmetry. In this study, we determine the mechanism of significant piezoelectricity and ferroelectricity in 0.3BaTiO3–0.1Bi(Mg1/2Ti1/2)O3–0.6BiFeO3 ceramic with a perovskite-type pseudo-cubic symmetry. Synchrotron radiation X-ray diffraction reveals that the Bi ions in this ceramic essentially prefer to be off-centered at six sites by approximately 0.4 Å, in the cubic <100> directions. A phase transition occurs at TC ~725 K. However, the crystal seems to present a cubic symmetry even at room temperature. The large piezoelectric response is caused by the combinational partial ordering of the off-centered Bi ions, adapted to any direction of the applied electric field to the ceramic grains. The proposed mechanism for the emergence of a high polarization in the above system will enable designing novel Pb-free ceramics by controlling the fluctuated and off-centered ions under an applied electric field.


2016 ◽  
Vol 84 (2) ◽  
Author(s):  
Charles S. Wojnar ◽  
Dennis M. Kochmann

Microstructural mechanisms such as domain switching in ferroelectric ceramics dissipate energy, the nature, and extent of which are of significant interest for two reasons. First, dissipative internal processes lead to hysteretic behavior at the macroscale (e.g., the hysteresis of polarization versus electric field in ferroelectrics). Second, mechanisms of internal friction determine the viscoelastic behavior of the material under small-amplitude vibrations. Although experimental techniques and constitutive models exist for both phenomena, there is a strong disconnect and, in particular, no advantageous strategy to link both for improved physics-based kinetic models for multifunctional rheological materials. Here, we present a theoretical approach that relates inelastic constitutive models to frequency-dependent viscoelastic parameters by linearizing the kinetic relations for the internal variables. This enables us to gain qualitative and quantitative experimental validation of the kinetics of internal processes for both quasistatic microstructure evolution and high-frequency damping. We first present the simple example of the generalized Maxwell model and then proceed to the case of ferroelectric ceramics for which we predict the viscoelastic response during domain switching and compare to experimental data. This strategy identifies the relations between microstructural kinetics and viscoelastic properties. The approach is general in that it can be applied to other rheological materials with microstructure evolution.


1999 ◽  
Vol 14 (7) ◽  
pp. 2940-2944 ◽  
Author(s):  
Fei Fang ◽  
Wei Yang ◽  
Ting Zhu

Lanthanum-modified lead zirconate titanate ferroelectric ceramics (Pb0.96La0.04)(Zr0.40Ti0.60)0.99O3 were synthesized by the conventional powder processing technique. X-ray diffraction experiments revealed that the samples belong to the tetragonal phase with a = b = 0.4055 nm, c = 0.4109 nm, and c/a = 1.013. After being poled, the samples were indented with a 5-kg Vickers indenter, and lateral electric fields of 0.4 Ec, 0.5 Ec, and 0.6 Ec (Ec = 1100 V/mm) were applied, respectively. Field-emission scanning electron microscopy showed that 90° domain switching appeared near the tip of the indentation crack under a lateral electric field of 0.6 Ec. A mechanism of 90° domain switching near the crack tip under an electric field is discussed.


Sign in / Sign up

Export Citation Format

Share Document