TY - JOUR
T1 - Structure, phase transition behaviors and electrical properties of Nd substituted aurivillius polycrystallines Na0.5NdxBi 2.5-xNb2O9 (x = 0.1, 0.2, 0.3, and 0.5)
AU - Long, Changbai
AU - Fan, Huiqing
AU - Ren, Pengrong
PY - 2013/5/6
Y1 - 2013/5/6
N2 - New high temperature Aurivillius piezoelectrics Na0.5Nd xBi2.5-xNb2O9 (NDBNx, x = 0.1, 0.2, 0.3, and 0.5) with Nd substitution for Bi at the A site were synthesized using a solid state reaction process. Crystal structures of NDBN0.2 and NDBN0.5 were refined with the Rietveld method with powder X-ray diffraction, and they crystallized in the orthorhombic space group A21am [a = 5.48558(8) Å, b = 5.46326(9) Å, c = 24.8940(4) Å, and Z = 4 for NDBN0.2 and a = 5.46872(5) Å, b = 5.46730(5) Å, c = 24.80723(25) Å, and Z = 4 for NDBN0.5], at room temperature. The refinement results and Raman spectroscopy of NDBNx verified that Nd occupied both the A site in the perovskite layers and the cation site in the (Bi2O2) 2+ layers. The Nd substitution induced an enhancement in cation disordering between the A site and the (Bi2O2) 2+ layer and an increase in the degree of the relaxation behavior for NDBNx. The ferroelectric to paraelectric phase transition temperature (T c) of NDBNx ranged from 735 to 764 C. Furthermore, the isovalent substitution of Nd for Bi had a great influence on microstructure (grain size and shape), defect concentration (mainly oxygen vacancies), preferred grain orientation (texture), and distortion of the octahedron. The coaction between these effects determined the structure characteristics, phase transition behaviors, and electrical properties of NDBNx.
AB - New high temperature Aurivillius piezoelectrics Na0.5Nd xBi2.5-xNb2O9 (NDBNx, x = 0.1, 0.2, 0.3, and 0.5) with Nd substitution for Bi at the A site were synthesized using a solid state reaction process. Crystal structures of NDBN0.2 and NDBN0.5 were refined with the Rietveld method with powder X-ray diffraction, and they crystallized in the orthorhombic space group A21am [a = 5.48558(8) Å, b = 5.46326(9) Å, c = 24.8940(4) Å, and Z = 4 for NDBN0.2 and a = 5.46872(5) Å, b = 5.46730(5) Å, c = 24.80723(25) Å, and Z = 4 for NDBN0.5], at room temperature. The refinement results and Raman spectroscopy of NDBNx verified that Nd occupied both the A site in the perovskite layers and the cation site in the (Bi2O2) 2+ layers. The Nd substitution induced an enhancement in cation disordering between the A site and the (Bi2O2) 2+ layer and an increase in the degree of the relaxation behavior for NDBNx. The ferroelectric to paraelectric phase transition temperature (T c) of NDBNx ranged from 735 to 764 C. Furthermore, the isovalent substitution of Nd for Bi had a great influence on microstructure (grain size and shape), defect concentration (mainly oxygen vacancies), preferred grain orientation (texture), and distortion of the octahedron. The coaction between these effects determined the structure characteristics, phase transition behaviors, and electrical properties of NDBNx.
UR - http://www.scopus.com/inward/record.url?scp=84877246861&partnerID=8YFLogxK
U2 - 10.1021/ic302769h
DO - 10.1021/ic302769h
M3 - 文章
AN - SCOPUS:84877246861
SN - 0020-1669
VL - 52
SP - 5045
EP - 5054
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 9
ER -