离子半径
结构精修
铋铁氧体
材料科学
结晶学
正交晶系
钙钛矿(结构)
晶体结构
相(物质)
离子
多铁性
化学
铁电性
电介质
光电子学
有机化学
作者
Maria Kireva,Ventsislav Tumbalev,Vladislav Kostov‐Kytin,Peter Tzvetkov,Daniela Kovacheva
出处
期刊:Minerals
[Multidisciplinary Digital Publishing Institute]
日期:2021-03-09
卷期号:11 (3): 278-278
被引量:10
摘要
BiFeO3 is an interesting material due to its multiferroic properties. It attracts attention due to its potential applications in spintronics and in microelectronics for data storage, among others. Single-phase bulk material from BiFeO3 is difficult to synthesize. The kinetics of perovskite phase formation most often leads to the presence of impurity phases. It has been shown that low levels of replacement of Bi with rare earth ions lead to stabilization of the perovskite phase. In the present work, Rietveld refinement of the crystal structure based on powder X-ray diffraction patterns was applied to study the influence of partial substitution of Bi by rare-earth (RE) elements with different ionic radii on structural and morphological properties of the ferrite phase. Substitution by large RE ions was found to preserve the rhombohedral symmetry of BiFeO3, whereas substitution by smaller RE ions led to the coexistence of two polymorphic perovskite phases with rhombohedral R3c and orthorhombic Pnma symmetries. The unit cell parameters as well as the interatomic distances and angles, not only around the A cation but also around the iron ions, were influenced by the substitution. The mean crystallite and particle size decreased with the decrease of ionic radius of substituting RE ion.
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