Evolution of the chemical bonding nature of ferroelectric bismuth titanate upon cation substitution

被引:33
作者
Hur, SG
Park, DH
Kim, TW
Hwang, SJ [1 ]
机构
[1] Konkuk Univ, Coll Nat Sci, Dept Appl Chem, Chungju 380701, Chungbuk, South Korea
[2] Konkuk Univ, Coll Nat Sci, Ctr Emerging Wireless Transmiss Technol, Chungju 380701, Chungbuk, South Korea
关键词
D O I
10.1063/1.1814818
中图分类号
O59 [应用物理学];
学科分类号
摘要
The effect of cation substitution on the crystal and electronic structures of ferroelectric bismuth titanate has been systematically investigated. According to the x-ray diffraction analyses on Bi(3.25)A(0.75)Ti(3)O(12) (A=Bi, La, Gd, and Y), it was found that the cation substitution gives rise to the contraction of the volume of the unit cell and to the decrease of the structural distortion of the bismuth titanate, as well. The present x-ray absorption spectroscopic results reveal that the local structural change upon chemical reduction is remarkably depressed by the cation substitution through the enhancement of (Ti-O) bonds. Such a stabilization of TiO6 octahedra can be understood by a competition between adjacent (Bi-O) and (Ti-O) bonds as well as the contraction of the unit cell. (C) 2004 American Institute of Physics.
引用
收藏
页码:4130 / 4132
页数:3
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