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首页> 外文期刊>Solid state sciences >Preparation, crystal structure and magnetic properties of Ruddlesden-Popper phases La1.2Sr1.8Mn2-xRuxO7 (X=0, 0.05, 0.1, 0.2, 0.5)
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Preparation, crystal structure and magnetic properties of Ruddlesden-Popper phases La1.2Sr1.8Mn2-xRuxO7 (X=0, 0.05, 0.1, 0.2, 0.5)

机译:Ruddlesden-Popper相La1.2Sr1.8Mn2-xRuxO7的制备,晶体结构和磁性能(X = 0,0.05,0.1,0.2,0.5)

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Single phase products of La1.2Sr1.8Mn2 - xRuxO7 (0 less than or equal to x less than or equal to 0.5) were prepared by solid state reaction of La2O3, SrCO3, Mn2O3 and RuO2 in several heating cycles. The samples have been studied by X-ray powder diffraction techniques and the crystal structures were refined using the Rietveld method. The compounds La1.2Sr1.8Mn2 (-) xRuxO7 belong to the Ruddlesden-Popper phases A(n+1)B(n)O(3n+1) with n = 2, which crystallize in the tetragonal space group I4/mmm (No. 139). In the crystal structure two crystallographic sites are occupied by La and Sr: the perovskite site shows a higher occupation with La, while the rocksalt site refines to a higher occupation with Sr. The lattice parameters a and c as well as the unit cell volume V increase monotonically with increasing ruthenium content. Probably because of the larger cation radius of ruthenium ions in comparison to manganese ions the average distance between transition metal and oxygen atoms was found to increase. Magnetization and AC susceptibility measurements show an enhancement of the ferromagnetic Curie temperature with increasing Ru substitution from 121 to 160 K, which gives evidence for the unique role of Ru when substituted in manganates. A sequence of magnetic transitions observed above T-C is probably related to effects of quasi-two-dimensional magnetic ordering (in stacking faults or of intrinsic nature). Metallic conduction is maintained up to x = 0.1 in La1.2Sr1.8Mn2 - xRuxO7. Possible magnetic exchange interactions of Ru and Mn in the compounds are discussed. (C) 2004 Elsevier SAS. All rights reserved.
机译:La1.2Sr1.8Mn2-xRuxO7(0小于或等于x小于或等于0.5)的单相产物是通过在多个加热循环中进行La2O3,SrCO3,Mn2O3和RuO2的固相反应制得的。通过X射线粉末衍射技术研究了样品,并使用Rietveld方法精制了晶体结构。化合物La1.2Sr1.8Mn2(-)xRuxO7属于Ruddlesden-Popper相A(n + 1)B(n)O(3n + 1),n = 2,在四方空间群I4 / mmm(第139号)。在晶体结构中,La和Sr占据两个晶体学位点:钙钛矿位点对La的占有率更高,而岩盐位点对Sr的占有率提高到更高的占有率;晶格参数a和c以及晶胞体积V随着钌含量的增加单调增加。可能是由于钌离子的阳离子半径比锰离子的阳离子半径大,因此发现过渡金属和氧原子之间的平均距离增加了。磁化和交流磁化率测量表明,随着Ru取代度从121 K增加到160 K,铁磁性居里温度升高,这证明了Ru在锰酸盐中取代时的独特作用。在T-C上方观察到的一系列磁跃迁可能与准二维磁序效应有关(在叠层断层或本征性质中)。在La1.2Sr1.8Mn2-xRuxO7中,金属导电性维持在x = 0.1。讨论了化合物中Ru和Mn可能的磁交换相互作用。 (C)2004 Elsevier SAS。版权所有。

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