Composition dependence of the multifunctional properties of Nd-doped Bi4Ti3O12 ceramics

被引:33
作者
Ivanov, Sergey A. [1 ,2 ]
Sarkar, Tapati [1 ]
Fortalnova, Elena A. [3 ]
Politova, Ekaterina D. [2 ]
Stefanovich, Sergey Yu. [2 ]
Safronenko, Marina G. [3 ]
Nordblad, Per [1 ]
Mathieu, Roland [1 ]
机构
[1] Uppsala Univ, Dept Engn Sci, Box 534, S-75121 Uppsala, Sweden
[2] Karpov Inst Phys Chem, Ul Vorontsovo Pole,10, Moscow 105064, Russia
[3] RUDN Univ, Ul Miklukho Maklaya 6, Moscow 117198, Russia
基金
瑞典研究理事会; 俄罗斯基础研究基金会;
关键词
BISMUTH TITANATE; CATION DISORDER; FERROELECTRIC PROPERTIES; DIELECTRIC-PROPERTIES; NEUTRON-DIFFRACTION; AURIVILLIUS PHASES; CRYSTAL-STRUCTURE; POLARIZATION; LA; SUBSTITUTION;
D O I
10.1007/s10854-017-6463-z
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Sample preparation, evolution of the crystal structure with Nd content at room temperature, as well as dielectric and magnetic properties of polycrystalline Bi4-xNdxTi3O12 solid solutions (x = 0.0, 0.5, 1.0, 1.5, and 2.0) are reported. These solid solutions were structurally characterized by X-ray powder diffraction using Rietveld refinements. For x <= 1.0, the samples crystallize in an orthorhombic symmetry. The structural data could be refined using the polar orthorhombic space group B2cb. The orthorhombicity decreases with increasing Nd3+ concentration, and a paraelectric tetragonal structure (space group I4/mmm) is stabilized for x > 1. The ferroelectric Curie temperature was found to monotonously decrease with increasing Nd concentration. A polar-to-nonpolar phase transition takes place near x = 1, reflecting the existence of a morphotropic phase boundary between 1.0 < x < 1.5 at room temperature. All samples were found to be paramagnetic down to 5 K, however, the presence of significant antiferromagnetic interaction is inferred from Curie-Weiss analyses of the temperature dependence of the magnetic susceptibility of the doped samples. The effect of Nd3+ substitution on structure-property relationship is discussed and compared to that of other lanthanide cations.
引用
收藏
页码:7692 / 7707
页数:16
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