Local Structure of Amorphous EuO-TiO2 Thin Films Probed by X-Ray Absorption Fine Structure

被引:6
|
作者
Zong, Yanhua [1 ]
Fujita, Koji [1 ]
Akamatsu, Hirofumi [2 ]
Nakashima, Seisuke [3 ]
Murai, Shunsuke [1 ]
Tanaka, Katsuhisa [1 ]
机构
[1] Kyoto Univ, Dept Chem Mat, Grad Sch Engn, Nishikyo Ku, Kyoto 6158510, Japan
[2] Kyoto Univ, Dept Mat Sci & Engn, Grad Sch Engn, Sakyo Ku, Kyoto 6068501, Japan
[3] RIKEN, Adv Res Inst, Wako, Saitama 3510198, Japan
关键词
COORDINATION-NUMBER; MAGNETIC-PROPERTIES; EDGE XANES; GLASS; TI; SPECTROSCOPY; EUTIO3;
D O I
10.1111/j.1551-2916.2011.04849.x
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We have investigated the local structure of amorphous oxides in EuO-TiO2 system to understand the mechanism that gives rise to curious ferromagnetic properties recently observed in the system. X-ray absorption spectroscopy has been performed on amorphous EuTiO3 and Eu2TiO4 thin films prepared by the pulsed-laser-deposition method. The Ti K-edge X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) data analyses reveal that the coordination number of Ti4+ in the amorphous thin films is around 4, which is in sharp contrast to their crystalline counterparts, where Ti4+ ions are octahedrally coordinated by oxide ions. It is therefore inferred that Ti4+ acts as a network-forming cation in the random network structure of the amorphous oxides. From the Eu L-3-edge EXAFS data analyses, it is found that the coordination number of Eu2+ is much lower and the nearest Eu-O bond length is shorter in the amorphous thin films than in the crystalline counterparts. The amorphization-induced enhancement of ferromagnetic interactions observed in the EuO-TiO2 system is discussed in terms of the local environment around Eu2+ ions.
引用
收藏
页码:716 / 720
页数:5
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