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首页> 外文期刊>International Journal of Quantum Chemistry >Electron-doping through La-III-for-Sr-II substitution in (Sr1-xLax)(2)FeTaO6: Effects on the valences and ordering of the B-site cations, Fe and Ta
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Electron-doping through La-III-for-Sr-II substitution in (Sr1-xLax)(2)FeTaO6: Effects on the valences and ordering of the B-site cations, Fe and Ta

机译:通过(Sr1-xLax)(2)FeTaO6中的La-III-Sr-II取代进行电子掺杂:对B位阳离子,Fe和Ta的化合价和有序性的影响

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摘要

We have employed aliovalent A-site cation substitution, La-III-for-Sr-II, to dope the Sr(Fe0.5Ta0.5)03 perovskite oxide with electrons. Essentially single-phase samples of (Sr1-xLax)(Fe0.5Ta0.5)O-3 were successfully synthesized up to x approximate to 0.3 in a vacuum furnace at 1400 degrees C. The samples were found to crystallize (rather than with orthorhombic symmetry) in monoclinic space group P2(1) that accounts for the partial ordering of the B-site cations, Fe and Ta. With increasing La-substitution level, x. the degree of Fe/Ta order was found to increase such that the La-richest compositions are best described by the B-site ordered double-perovskite formula, (Sr,La)(2)FeTaO6. From Fe L-3 and Ta L-3 XANES spectra it was revealed that upon electron doping the two B-site cations, Fe-III and Ta-V. are both prone to reduction. Magnetic susceptibility measurements showed spin-glass type behaviour for all the samples with a transition temperature slightly increasing with increasing x. (c) 2005 Elsevier Inc. All rights reserved.
机译:我们已经采用了异价的A位阳离子取代,La-III-Sr-II,以电子掺杂Sr(Fe0.5Ta0.5)03钙钛矿氧化物。本质上(Sr1-xLax)(Fe0.5Ta0.5)O-3的单相样品已在1400摄氏度的真空炉中成功合成了高达x约0.3的样品。发现样品结晶了(而不是正交晶)单斜空间群P2(1)/ n中的对称性)解释了B位阳离子Fe和Ta的部分排序。随着La取代水平的提高,x。发现Fe / Ta有序度增加,从而使富含La的成分最好由B位有序双钙钛矿分子式(Sr,La)(2)FeTaO6来描述。从Fe L-3和Ta L-3 XANES光谱可以看出,在电子掺杂两个B位阳离子后,Fe-III和Ta-V。都容易减少。磁化率测量显示所有样品的自旋玻璃型行为,其转变温度随x的增加而略有增加。 (c)2005 Elsevier Inc.保留所有权利。

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