Valence variations in titanium-leased perovskite oxides by high-pressure and high-temperature method

被引:2
作者
Li, LP
Li, GS [1 ]
Miao, JP
Su, WH
Inomata, H
机构
[1] Jilin Univ, Dept Phys, Changchun 130023, Peoples R China
[2] Tohoku Univ, Res Ctr Supercrit Fluid Technol, Dept Chem Engn, Sendai, Miyagi 9808579, Japan
基金
中国国家自然科学基金;
关键词
D O I
10.1557/JMR.2001.0063
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Typical titanium-based perovskite oxides Eu1-xBaxTiO3 (x = 0.6-0.8), Eu1-xKxTiO3 (x = 0.2,0,32), and La-0.7(Na,K)(0.3)TiO3 were synthesized by high pressure and temperature using RE2O3 (RE = La,Eu), TiO2, alkaline, or alkaline earth carbonates as the starting materials. X-ray diffraction data analysis showed that there was a structural transformation in Eu1-xBaxTiO3 by varying Ba content [i.e., from cubic (x = 0.6,0.7) to tetragonal (x = 0,8)], and that samples Eu1-xKxTiO3 and La-0.7(Na,K)(0.3)TiO3 crystallized in the cubic perovskite structure. Eu-151 Mossbauer spectroscopy and electron paramagnetic resonance measurements revealed mixed valence of Eu2+/Eu3+ in samples Eu1-xBaxTiO3 and Eu1-xKxTiO3, while Ti ions were present in pure Ti4+ state. Cubic Eu1-xKxTiO3 was metastable, which decomposed into a mixture of perovskite and pyrochlore phases at high temperatures as accompanied by an oxidation process from Eu2+ to Eu3+ For samples La-0.7(Na,K)(0.3)TiO3, Ti3+ signals were clearly observed. The reduction mechanisms for Eu ions at A site and Ti ions at B site in the perovskite oxides are discussed in terms of the chemical nature of the framework ions and substitution ions under high pressure and temperature.
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页码:417 / 424
页数:8
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