论文标题
通过LA取代的单相BI4TI3O12-3BifeO3实心溶液的铁电和磁性特性操纵
Manipulation of ferroelectric and magnetic properties properties of single phase Bi4Ti3O12-3BiFeO3 solid solution through La substitution
论文作者
论文摘要
在这项工作中,通过精心研究相关的结构和物理特性,可以很好地探索了BI4TI3O12-3BifeO3作为单相和高温磁电材料作为单相和高温磁电材料的潜力。 Bi4TI3O12-3BI1-XlaxFeo3(x = 0,0.01,0.05,0.1,0.2)通过固态反应路线和X射线衍射数据合成,表明与la3+ contrimation contrimation nieR contrimation nieR nieR nieR in.contrirric nieR ry.contrricir nieR ry.contrriciring in.contrirric nieR nieR in。对应于父(X = 0)的铁电到副型过渡温度(TC)具有两个相变相位,803 K(宽)和983 K(更尖)(更尖锐),而相变是单一的单一偏移,随着LA替代的增加而逐渐变得更加敏捷。对于BI4TI3O12-3BifeO3,证明了铁电交换行为(极化(P)与电场(E)),而反映弱铁电序的LA取代组合物的残余极化显着降低。在详细的零场冷却和场冷却温度依赖性磁化测量测量中,Bi4TI3O12-3BifeO3在296 K左右显示TC。尽管LA替代组合物的磁化值的边际增加(X = 0.1和X = 0.2),但总体温度依赖磁力磁力曲线表示总体参数。结果更反映了关闭这些Aurivillius分层化合物中A位置稀土的远程铁磁秩序的可能性。
In this work, the potential to exploit Aurivillius higher order composition (n=6) given by Bi4Ti3O12-3BiFeO3 as single phase and high temperature magnetoelectric materials are well explored by elaborately studying the concerned structure and physical properties. Bi4Ti3O12-3Bi1-xLaxFeO3 (x=0, 0.01, 0.05, 0.1, 0.2) was synthesized via solid-state reaction route and X-ray diffraction data revealed that the lattice parameters associated with orthorhombic cell (space group P21am) decrease with increase in La3+ content confirming the incorporation of La. In the frequency dependent dielectric measurements, the ferroelectric to paraelectric transition temperature (Tc) corresponding to the parent (x=0) had two phase transitions vis., 803 K (broader) and 983 K (sharper) whereas phase transitions are single that progressively becomes sharper with increase in La substitution. Ferroelectric switching behavior (polarization (P) versus electric field (E)) was demonstrated for Bi4Ti3O12-3BiFeO3 and remnant polarization decreased significantly for La substituted compositions reflecting weaker ferroelectric ordering. In detailed Zero Field-cooled and Field cooled temperature dependent magnetization measurements, Bi4Ti3O12-3BiFeO3 exhibited Tc around 296 K. Though a marginal increase in the magnetization values for La substituted compositions (x=0.1 and x=0.2), the overall temperature dependent magnetization curves indicate overall paramagnetic nature. The results are more reflective of the switching off of the possibilities of long range ferromagnetic ordering with A-site rare earth doping in these Aurivillius layered compounds.