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X-ray diffraction and magnetization studies of BiFeO_3 multiferroic compounds substituted by Sm~(3+), Gd~(3+), Ca~(2+)

机译:Sm〜(3 +),Gd〜(3 +),Ca〜(2+)取代的BiFeO_3多铁化合物的X射线衍射和磁化研究

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摘要

The multiferroic compounds Bi_(0.9)Sm_(0.1)FeO_3, Bi_(0.9)Gd_(0.1)FeO_3, Bi_(0.9)Ca_(0.1)FeO_3, Bi_(0.9)Sm_(0.05)Ca_(0.05)FeO_3, and Bi_(0.9)Gd_(0.05)Ca_(0.05)FeO_3 were prepared by the conventional ceramic method and were characterized by X-ray diffraction, vibrating sample magnetometry, and differential scanning calorimetry. The compounds were found to have the rhombohedral perovskite-like structure, accompanied by a small residual Bi_2Fe4O_9 impurity phase. Magnetic hysteresis loops with enhanced remnant magnetization and coercive field were obtained for the Gd-containing compounds. The improvement of magnetic behavior of the Gd-containing compounds is thought to arise mainly from the partial suppression of the spiral spin structure and the stronger interaction between magnetic ions. The magnetic transition temperatures of the compounds were found to be in the range 300-310 °C.
机译:多铁化合物Bi_(0.9)Sm_(0.1)FeO_3,Bi_(0.9)Gd_(0.1)FeO_3,Bi_(0.9)Ca_(0.1)FeO_3,Bi_(0.9)Sm_(0.05)Ca_(0.05)FeO_3和Bi_(用常规陶瓷方法制备0.9)Gd_(0.05)Ca_(0.05)FeO_3,并通过X射线衍射,振动样品磁法和差示扫描量热法进行表征。发现这些化合物具有菱形钙钛矿状结构,并伴有少量残留的Bi_2Fe4O_9杂质相。对于含G的化合物,获得了具有增强的剩余磁化强度和矫顽场的磁滞回线。认为含Gd化合物的磁行为的改善主要是由于部分抑制了螺旋自旋结构以及磁离子之间的较强相互作用。发现化合物的磁转变温度为300-310℃。

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