Synthesis, structure, and dielectric properties of a novel perovskite-based nanopowders via sol–gel method: (1–x)BaTiO3–xDyScO3
A sol–gel method was adopted to synthesize novel perovskite-based nanopowders: (1– x )BaTiO 3 – x DyScO 3 (0 ≤ x ≤ 0.06), which exhibited a relatively pure pseudo-cubic perovskite structure when xerogel was calcined at 750 °C. Through the employment of PEG 400 as dispersant, narrow size distribute...
Gespeichert in:
Veröffentlicht in: | Journal of materials science 2013-06, Vol.48 (11), p.3958-3966 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | A sol–gel method was adopted to synthesize novel perovskite-based nanopowders: (1–
x
)BaTiO
3
–
x
DyScO
3
(0 ≤
x
≤ 0.06), which exhibited a relatively pure pseudo-cubic perovskite structure when xerogel was calcined at 750 °C. Through the employment of PEG 400 as dispersant, narrow size distributed particles of ~15–20 nm were achieved. Pellets pressed from the nanopowders can be densified at a lower sintering temperature of 1150 °C, compared with 1475 °C by solid-state reaction method. The phase formation, microstructure, dielectric properties, and relaxor behavior of (1–
x
)BaTiO
3
–
x
DyScO
3
were investigated systematically. With an increasing DyScO
3
doping concentration in BaTiO
3
, a tetragonal to pseudo-cubic phase transition appeared at
x
= 0.03, and two different doping behaviors (donor or acceptor-type) of Dy
3+
in (1–
x
)BaTiO
3
–
x
DyScO
3
were discussed. The grain growth of BaTiO
3
ceramics was inhibited, and the grain size was decreased to 200 nm for
x
= 0.06. The dielectric peak was broadened and the curie temperature dropped gradually, accompanied by an increased room-temperature permittivity. Furthermore, a typical relaxor behavior was observed at
x
= 0.05 and 0.06, according to the modified Curie–Weiss law. |
---|---|
ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-013-7203-2 |