BaTiO3-based ceramics are attractive as Pb-free relaxors with applications in microelectronics and wireless communications. Among the dopant ions, cerium is a special element with two oxidation states: Ce3+ and Ce4+, that can be incorporated at Ba-site (as Ce3+), while Ce4+ will be preferentially incorporated on Ti-sites. In the present paper, dense (98-99% relative density) and single phase BaCexTi1-x O3 (x = 0.02; 0.05; 0.10 and 0.20) ceramics were prepared by a conventional ceramic processing consisting of four fundamentals steps: preparation of the powder by solid state reaction, consolidation of the powder by isostatic pressing, sintering of the powder compact into a dense polycrystalline ceramic, cutting and polishing. They have been calcined at 1000 °C for 4h and sintered at 1450°C for 4h, resulting in dense single phase ceramics with homogeneous microstructures. The sample with 20% of Ce needed a sintering treatment at 1550? to become dense enough. X-ray diffraction on calcinated powders and sintered ceramics showed the formation of single phase BaTi1-xCexO3. The microstructural features (density, grain size and grain size distribution) of the dense ceramic were determinated from SEM images. Impedance spectroscopy in the temperature range of (20 to 180)oC shows a composition-induced ferroelectric-to-relaxor crossover with compositional-dependent shifts of the structural transition temperatures by comparison with ones of the pure BaTiO3. The dielectric characteristics indicate the possibility of either superposition of phases and/or the possible partial doping of Ce3+ on A positions. The nonlinear properties of samples were investigated at room temperature and the results were discussed in term of ferroelectric-relaxor crossover of the investigated ceramics.

Preparation and characterization of BaCexTi1-x O3 ceramics

G Canu;
2015

Abstract

BaTiO3-based ceramics are attractive as Pb-free relaxors with applications in microelectronics and wireless communications. Among the dopant ions, cerium is a special element with two oxidation states: Ce3+ and Ce4+, that can be incorporated at Ba-site (as Ce3+), while Ce4+ will be preferentially incorporated on Ti-sites. In the present paper, dense (98-99% relative density) and single phase BaCexTi1-x O3 (x = 0.02; 0.05; 0.10 and 0.20) ceramics were prepared by a conventional ceramic processing consisting of four fundamentals steps: preparation of the powder by solid state reaction, consolidation of the powder by isostatic pressing, sintering of the powder compact into a dense polycrystalline ceramic, cutting and polishing. They have been calcined at 1000 °C for 4h and sintered at 1450°C for 4h, resulting in dense single phase ceramics with homogeneous microstructures. The sample with 20% of Ce needed a sintering treatment at 1550? to become dense enough. X-ray diffraction on calcinated powders and sintered ceramics showed the formation of single phase BaTi1-xCexO3. The microstructural features (density, grain size and grain size distribution) of the dense ceramic were determinated from SEM images. Impedance spectroscopy in the temperature range of (20 to 180)oC shows a composition-induced ferroelectric-to-relaxor crossover with compositional-dependent shifts of the structural transition temperatures by comparison with ones of the pure BaTiO3. The dielectric characteristics indicate the possibility of either superposition of phases and/or the possible partial doping of Ce3+ on A positions. The nonlinear properties of samples were investigated at room temperature and the results were discussed in term of ferroelectric-relaxor crossover of the investigated ceramics.
2015
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
relaxor
barium titanate
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/291323
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact