Aksel, Elena ; Forrester, Jennifer S. ; Foronda, Humberto M. ; Dittmer, Robert ; Damjanovic, Dragan ; Jones, Jacob L. (2012):
Structure and properties of La-modified Na0.5Bi0.5TiO3 at ambient and elevated temperatures.
In: Journal of Applied Physics, 112 (5), pp. 054111(1-8). ISSN 00218979,
[Article]
Abstract
The crystal structure and property changes of sodium bismuth titanate (Na0.5Bi0.5TiO3, NBT) piezoelectric ceramics are reported as a function of La modification (0.5–2.0 at. %) and increasing temperature using high resolution x-ray diffraction, permittivity, depolarization, and polarization and strain hysteresis measurements. La substitution is found to decrease the depolarization temperature of NBT (e.g., 1.5 at. % La substitution lowers the depolarization temperature by 60 °C relative to the unmodified composition) with little impact on the room temperature polarization and strain hysteresis. The room temperature structures of the various NBT compositions were modeled using a mixture of the monoclinic Cc space group and the cubic Pmmathm phase, where the Pmmathm phase is used to model local regions in the material which do not obey the long range Cc space group. With increasing La substitution, the lattice parameter distortions associated with the Cc phase approached that of the prototypical cubic unit cell and the fraction of the Pmmathm phase increased. The relationship between these crystallographic changes and the depolarization behavior of La-modified NBT is discussed.
Item Type: | Article |
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Erschienen: | 2012 |
Creators: | Aksel, Elena ; Forrester, Jennifer S. ; Foronda, Humberto M. ; Dittmer, Robert ; Damjanovic, Dragan ; Jones, Jacob L. |
Title: | Structure and properties of La-modified Na0.5Bi0.5TiO3 at ambient and elevated temperatures |
Language: | English |
Abstract: | The crystal structure and property changes of sodium bismuth titanate (Na0.5Bi0.5TiO3, NBT) piezoelectric ceramics are reported as a function of La modification (0.5–2.0 at. %) and increasing temperature using high resolution x-ray diffraction, permittivity, depolarization, and polarization and strain hysteresis measurements. La substitution is found to decrease the depolarization temperature of NBT (e.g., 1.5 at. % La substitution lowers the depolarization temperature by 60 °C relative to the unmodified composition) with little impact on the room temperature polarization and strain hysteresis. The room temperature structures of the various NBT compositions were modeled using a mixture of the monoclinic Cc space group and the cubic Pmmathm phase, where the Pmmathm phase is used to model local regions in the material which do not obey the long range Cc space group. With increasing La substitution, the lattice parameter distortions associated with the Cc phase approached that of the prototypical cubic unit cell and the fraction of the Pmmathm phase increased. The relationship between these crystallographic changes and the depolarization behavior of La-modified NBT is discussed. |
Journal or Publication Title: | Journal of Applied Physics |
Volume of the journal: | 112 |
Issue Number: | 5 |
Divisions: | 11 Department of Materials and Earth Sciences > Material Science > Nonmetallic-Inorganic Materials DFG-Collaborative Research Centres (incl. Transregio) > Collaborative Research Centres > CRC 595: Electrical fatigue > A - Synthesis > Subproject A1: Manufacturing of ceramic, textured actuators with high strain 11 Department of Materials and Earth Sciences > Material Science DFG-Collaborative Research Centres (incl. Transregio) > Collaborative Research Centres > CRC 595: Electrical fatigue > A - Synthesis DFG-Collaborative Research Centres (incl. Transregio) > Collaborative Research Centres > CRC 595: Electrical fatigue 11 Department of Materials and Earth Sciences Zentrale Einrichtungen DFG-Collaborative Research Centres (incl. Transregio) > Collaborative Research Centres DFG-Collaborative Research Centres (incl. Transregio) |
Date Deposited: | 25 Sep 2012 12:28 |
URL / URN: | http://dx.doi.org/10.1063/1.4751357 |
Additional Information: | SFB 595 A1 |
Identification Number: | doi:10.1063/1.4751357 |
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