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Effect of isovalent B-site doping on structural and electrical properties of Bismuth-Sodium-Titanate

机译:异戊二型B-位掺杂对钛酸铋结构和电性能的影响

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Samples exhibiting substitution of Titanium in Bismuth-Sodium-Titanate (BNT) by isovalent Zirconium, Tin and Germanium (Bi_(0.5)Na_(0.5)Ti(1-x)D_xO3 with D = Zr, Ge and Sn and x = 0.0025; 0.0050; 0.01; 0.02; 0.04; 0.08) were investigated with respect to microstructure, relative permittivity, loss factor and polarization. The substituents differ in mass, ionic radius and d-electron configuration. The shift of transitions observed in plots of permittivity and loss factor vs. temperature indicate the influence of the ionic radius. The occurrence of a pinched hysteresis loop at ambient temperature in the Sn-doped samples and the absence of any pinching in the hysteresis loops of Zr- and Ge-doped samples give rise to the assumption that this feature of polarization is connected to the ionic radius combined with the d~(10) electron configuration of Sn~(4+).
机译:通过具有异戊锆,锡和锗(Bi_(0.5)Na_(0.5)Ti(1-X)D_XO3,用D = Zr,Ge和Sn和x = 0.0025,在铋 - 钠 - 钛酸盐(Bnt)中替代钛酸钠(bnt)取代钛钛(Bnt)取代钛(Bi_(0.5)Na_(0.5),x = 0.0025;研究相对于微观结构,相对介电常数,损耗因子和极化研究0.0050; 0.02; 0.04; 0.08)。取代基不同于质量,离子半径和D-电子构造。在介电常数和损耗因子与温度的曲线图中观察到的转变表明离子半径的影响。在Sn掺杂样品中的环境温度下发生夹持滞后回路的发生,并且在Zr-和Ge-掺杂样品的滞后环中没有任何夹持的任何夹持的假设是偏振的这种特征与离子半径相连的假设结合SN〜(4+)的D〜(10)电子构型。

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