TY - JOUR
T1 - Original Reaction Sequence of Pb(Yb1/2Nb1/2)O3-PbTiO3
T2 - Consequences on dielectric properties and chemical order
AU - Cochard, Charlotte
AU - Karolak, Fabienne
AU - Bogicevic, Christine
AU - Guedes, Orland
AU - Janolin, Pierre-Eymeric
PY - 2015/12/31
Y1 - 2015/12/31
N2 - The solid solution [Pb(Yb1/2Nb1/2)O3]1-x-[PbTiO3]x was synthesized with x ≤ 60 %, using several high-temperature techniques as well as room-temperature mechanosynthesis. The high-temperature synthesis reveals a reaction path involving the synthesis first of the end-members before the solid solution. The density and dielectric constant measured on the ceramics prepared from these powders indicate the crucial role of the synthesis technique in the subsequent properties. Mechanosynthesis results in ceramics with higher density and dielectric constant. Identical optimized sintering conditions were then applied to all investigated compositions and the resulting dielectric properties and chemical orders were compared. All polar orders (antiferroelectricity, ferroelectricity, and relaxor behavior) were evidenced. The 1: 1 chemical order on the B-site of Pb(Yb1/2Nb1/2)O3 results in the formation of a double perovskite Pb2YbNbO6, and the superstructures in the X-ray diagrams signing the existence of this order persist up to 30% PbTiO3. The underlying mechanism for substitution of Yb or Nb by Ti is presented.
AB - The solid solution [Pb(Yb1/2Nb1/2)O3]1-x-[PbTiO3]x was synthesized with x ≤ 60 %, using several high-temperature techniques as well as room-temperature mechanosynthesis. The high-temperature synthesis reveals a reaction path involving the synthesis first of the end-members before the solid solution. The density and dielectric constant measured on the ceramics prepared from these powders indicate the crucial role of the synthesis technique in the subsequent properties. Mechanosynthesis results in ceramics with higher density and dielectric constant. Identical optimized sintering conditions were then applied to all investigated compositions and the resulting dielectric properties and chemical orders were compared. All polar orders (antiferroelectricity, ferroelectricity, and relaxor behavior) were evidenced. The 1: 1 chemical order on the B-site of Pb(Yb1/2Nb1/2)O3 results in the formation of a double perovskite Pb2YbNbO6, and the superstructures in the X-ray diagrams signing the existence of this order persist up to 30% PbTiO3. The underlying mechanism for substitution of Yb or Nb by Ti is presented.
UR - http://www.scopus.com/inward/record.url?scp=84956946903&partnerID=8YFLogxK
U2 - 10.1155/2015/408101
DO - 10.1155/2015/408101
M3 - Article
AN - SCOPUS:84956946903
SN - 1687-8434
VL - 2015
JO - Advances in Materials Science and Engineering
JF - Advances in Materials Science and Engineering
M1 - 408101
ER -