Premium
A novel route to perovskite lead zirconate titanate from glycolate precursors via the sol–gel process
Author(s) -
Tangboriboon N.,
Jamieson A.,
Sirivat A.,
Wongkasemjit S.
Publication year - 2008
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.1357
Subject(s) - calcination , lead zirconate titanate , perovskite (structure) , tetragonal crystal system , chemistry , lead titanate , dielectric , zirconate , curie temperature , mineralogy , titanate , analytical chemistry (journal) , phase (matter) , ceramic , chemical engineering , inorganic chemistry , ferroelectricity , materials science , crystallography , organic chemistry , catalysis , physics , optoelectronics , quantum mechanics , ferromagnetism , engineering
A perovskite lead zirconate titanate was synthesized by the sol‐gel process, using lead glycolate, sodium tris(glycozirconate) and titanium glycolate as the starting precursors. For the mole ratio Pb:Zr:Ti of 1:0.5:0.5 [Pb(Zr 0.5 Ti 0.5 )O 3 ], TGA‐DSC thermal analysis indicated that the percentage of ceramic yield was 55.8, close to the calculated chemical composition value of 49.5. The exothermic peak occurred at 268 °C below the theoretical Curie temperature of 400 °C. The pyrolysis of Pb(Zr 0.5 Ti 0.5 )O 3 of the perovskite phase was investigated in terms of calcination temperature and time. The structure obtained was of the tetragonal form when calcined at temperatures below 400 °C; it transformed to the tetragonal and the cubic forms of the perovskite phase on calcination above the Curie temperature, as verified by X‐ray data. The lead zirconate titanate synthesized and calcined at 400 °C for 1 h had the highest dielectric constant, the highest electrical conductivity and the dielectric loss tangent of 10 190, 0.803 × 10 −3 (Ω.m) −1 and 1.513 at 1000 Hz, respectively. The lead zirconate titanate powder synthesized has potential applications as an electronic material. Copyright © 2008 John Wiley & Sons, Ltd.