Eu doping in multiferroic BiFeO3 ceramics studied by Mossbauer and EXAFS spectroscopy

被引:53
|
作者
Kothari, Deepti [1 ]
Reddy, V. Raghavendra [1 ]
Gupta, Ajay [1 ]
Meneghini, Carlo [2 ]
Aquilanti, Giuliana [3 ]
机构
[1] UGC DAE Consortium Sci Res, Indore 452001, Madhya Pradesh, India
[2] Univ Roma Tre, Dipartimento Fis E Amaldi, I-00146 Rome, Italy
[3] Sincrotrone Trieste, I-34012 Trieste, Italy
关键词
HYPERFINE FIELD DISTRIBUTIONS; MAGNETIC-STRUCTURE; FERROMAGNETISM; SCATTERING; SPECTRA;
D O I
10.1088/0953-8984/22/35/356001
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Bismuth ferrite ceramics (BiFeO3) are multifunctional materials classified as multiferroics for their special magnetic and electric properties that can be modified by substitutional doping at the Bi and/or Fe sites. Understanding the relation between magnetoelectric response and structural/electronic modification upon doping is a relevant issue. In this work, the structure of Eu-doped multiferroic systems (Bi1-xEuxFeO3, x = 0, 0.5, 0.1, 0.15) as well as the valence state of Fe and Eu ions have been investigated combining Mossbauer and x-ray absorption fine structure (XAFS) spectroscopy techniques. The Eu3+ doping at the Bi site results in better magnetic properties. High temperature Fe-57 Mossbauer data and Fe K-edge XAFS results show that FeO6 octahedron distortions reduce with Eu3+ doping. It is conclusively shown that the observed magnetic properties in BiFeO3 with chemical substitution (Eu) are mainly due to the structural distortions and not due to Fe multiple valence. Eu-151 Mossbauer measurements show that the Eu3+(Bi3+) site is magnetically inactive in BiFeO3.
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页数:10
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