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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/10117
Title: 
Dielectric response features and oxygen migration on rare earth modified lead titanate ferroelectric ceramics
Author(s): 
Institution: 
  • Univ La Habana
  • Universidade Estadual Paulista (UNESP)
  • Univ Autonoma Madrid
  • ICIMAF
  • Universidade Federal de São Carlos (UFSCar)
ISSN: 
0022-2461
Sponsorship: 
  • Third World Academy of Sciences
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
  • ICTP
  • Latin-American Network of Ferroelectric Materials
Sponsorship Process Number: 
  • TWAS: RG/PHYS/LA No. 99-050
  • TWAS: 02-225
  • TWASciences: 05-043
  • FAPESP: 06/60013-5
Abstract: 
Rare earth (RE) and manganese-modified lead titanate ceramics were studied concerning the presence of two peaks in the temperature dependence of the dielectric permittivity. An eventual incorporation of the RE into A-site and/or B-site in the perovskite structure and the oxygen migration were considered as causes of the observed phenomenon. The structural analysis showed that at least a small amount of Ti(4+) could be substituted by the RE ions. It was considered from the pyroelectric and electrical conductivity results that, even when an eventual incorporation of the RE into the A-site and/or B-site of the structure could be possible, both peaks could not be associated with paraelectric-ferroelectric (PE-FE) phase transitions. The observed peak at lower temperatures has been associated with the PE-FE phase transitions, whereas the hopping of oxygen vacancies has been considered as the cause for the dielectric anomaly observed at higher temperatures.
Issue Date: 
1-Jan-2009
Citation: 
Journal of Materials Science. New York: Springer, v. 44, n. 1, p. 204-211, 2009.
Time Duration: 
204-211
Publisher: 
Springer
Source: 
http://dx.doi.org/10.1007/s10853-008-3100-5
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/10117
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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