TY - JOUR
T1 - The effect of imprint on remanent piezoelectric properties and ferroelectric aging of PbZr0.52Ti0.48O3 thin films
AU - Akkopru-Akgun, Betul
AU - Zhu, Wanlin
AU - Lanagan, Michael T.
AU - Trolier-McKinstry, Susan
N1 - Publisher Copyright:
© 2019 The American Ceramic Society
PY - 2019/9
Y1 - 2019/9
N2 - Ferroelectric films suffer from both aging and degradation under high ac-field drive conditions due to loss of polarization with time. In this study, the roles of defect chemistry and internal electric fields on the long-term stability of the properties of piezoelectric films were explored. For this purpose, lead zirconate titanate (PZT) films with a Zr/Ti ratio of 52/48 doped with Mn- (PMZT) or Nb- (PNZT) were deposited on Pt coated Si substrates by the sol-gel method. It was demonstrated that the magnitude of the internal field is much higher in PMZT films compared to PNZT films after poling in the temperature range of 25-200°C under an electric field of −240 kV/cm. The development of the internal field is thermally activated, with activation energies from 0.5 ± 0.06 to 0.8 ± 0.1 eV in Mn doped films and from 0.8 ± 0.1 to 1.2 ± 0.2 eV in Nb doped films. The different activation energies for imprint suggests that the physical mechanism underlying the evolution of the internal field in PMZT and PNZT films differs; the enhanced internal field upon poling is attributed to (a) alignment of oxygen vacancy—acceptor ion defect dipoles ((Formula presented.), (Formula presented.)) in PMZT films, and (b) thermionic injection of electron charges and charge trapping in PNZT films. In either case, the internal field reduces back switching, enhances the remanent piezoelectric properties, and dramatically improves the aging behavior. PMZT films exhibited the greatest enhancement, with reduced high temperature (180°C) aging rates of 2%-3%/decade due to improved stability of the poled state. In contrast, PNZT films showed significantly larger high temperature aging rates (15.5%/decade) in the piezoelectric coefficient, demonstrating that the fully poled state was not retained with time.
AB - Ferroelectric films suffer from both aging and degradation under high ac-field drive conditions due to loss of polarization with time. In this study, the roles of defect chemistry and internal electric fields on the long-term stability of the properties of piezoelectric films were explored. For this purpose, lead zirconate titanate (PZT) films with a Zr/Ti ratio of 52/48 doped with Mn- (PMZT) or Nb- (PNZT) were deposited on Pt coated Si substrates by the sol-gel method. It was demonstrated that the magnitude of the internal field is much higher in PMZT films compared to PNZT films after poling in the temperature range of 25-200°C under an electric field of −240 kV/cm. The development of the internal field is thermally activated, with activation energies from 0.5 ± 0.06 to 0.8 ± 0.1 eV in Mn doped films and from 0.8 ± 0.1 to 1.2 ± 0.2 eV in Nb doped films. The different activation energies for imprint suggests that the physical mechanism underlying the evolution of the internal field in PMZT and PNZT films differs; the enhanced internal field upon poling is attributed to (a) alignment of oxygen vacancy—acceptor ion defect dipoles ((Formula presented.), (Formula presented.)) in PMZT films, and (b) thermionic injection of electron charges and charge trapping in PNZT films. In either case, the internal field reduces back switching, enhances the remanent piezoelectric properties, and dramatically improves the aging behavior. PMZT films exhibited the greatest enhancement, with reduced high temperature (180°C) aging rates of 2%-3%/decade due to improved stability of the poled state. In contrast, PNZT films showed significantly larger high temperature aging rates (15.5%/decade) in the piezoelectric coefficient, demonstrating that the fully poled state was not retained with time.
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U2 - 10.1111/jace.16367
DO - 10.1111/jace.16367
M3 - Article
AN - SCOPUS:85063031721
SN - 0002-7820
VL - 102
SP - 5328
EP - 5341
JO - Journal of the American Ceramic Society
JF - Journal of the American Ceramic Society
IS - 9
ER -