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Eur. Phys. J. Appl. Phys. 37, 93-99 (2007)
DOI: 10.1051/epjap:2006156
Ferroelectric and piezoelectric properties of Ag modified PMN-PZT solid solutions
R. Koduri and M. LopezDepartmento de Ingeneria de Materials, (DIMAT), Facultad de Ingenieria, Universidad de Concepcion, Edmundo Larenas 270, Casilla 160 C, Concepcion, Chile
ramamk@udec.cl
(Received: 5 June 2006 / Received in final form: 18 September 2006 / Accepted: 4 October 2006 / Published online: 13 December 2006 )
Abstract
The ferroelectric and piezoelectric properties of Ag
doped xPb(Mg1/3Nb2/3)O3-(1-x) Pb(Zr0.532Ti0.468)O3
ceramics, for Ag = 0.5, 1 and 1.5 mole%, synthesized by the columbite
precursor method were investigated. The experimental results indicate that
stoichiometry plays a significant role in the solubility of Ag and it
affects the physical properties. The factors influencing microstructural
development of Ag doped PMN-PZT are the Ag and PMN concentrations and Ag
diffusion during the sintering process as can be observed from the scanning
electron micrograph. Grain growth is considerably enhanced up to 4.05
m in 1 mole% Ag doped 0.7PMN-0.3PZT, while the apparent density continuously increased up to 7.89 gm/cm3 in 1 mole% Ag doped 0.8PMN-0.2PZT, respectively. It was observed that 1 mole% Ag doped
0.7PMN-0.3PZT attained maximum values for the dielectric permittivity
(
) at room temperature and the dielectric
permittivity at the Curie temperature (
),
respectively. The ferroelectric properties exhibited optimum values of
Pr = 36.82
C/cm2 and
Ps = 45.29
C/cm2 in 1 mole% Ag doped 0.7PMN-0.3PZT, respectively while the Ec showed a decreasing trend throughout the series. The piezoelectric properties (
d33 = 297 pC/N and
kp = 0.377) were enhanced in 1 mole% Ag
doped 0.4PMN-0.6PZT and 0.7PMN-0.3PZT, respectively.
77.84.-s - Dielectric, piezoelectric, ferroelectric, and antiferroelectric materials.
77.84.Dy - Niobates, titanates, tantalates, PZT ceramics, etc..
77.80.Dj - Domain structure; hysteresis.
77.22.-d - Dielectric properties of solids and liquids.
© EDP Sciences 2006
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