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首页> 外文期刊>Journal of Applied Physics >Structural and magnetic properties of chemically synthesized Sn_(1-x)Mn_xO_2 nanocrystalline powders
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Structural and magnetic properties of chemically synthesized Sn_(1-x)Mn_xO_2 nanocrystalline powders

机译:化学合成Sn_(1-x)Mn_xO_2纳米晶粉末的结构和磁性

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Sn_(1-x)Mn_xO_2 nanocrystalline powders were synthesized by a wet chemical method (x ≤ 0.08). X-ray diffraction reveals that single-phase rutile Sn_(1-x)Mn_xO_2 was obtained for x up to about 0.06. Evolution of cell parameters, x-ray photoelectron spectroscopy measurements, thermogravimetric analysis, and quantitative evaluation of the magnetization data all indicate that Mn element acts as Mn~(4+) for x=0.01 and as Mn~(3+) for x=0.02 and 0.04 at room temperature, but as Mn~(3+) for all the samples at 5 K. Magnetization data show that the average magnetic moment per Mn site decreases with increasing x at 5 K, while the effective fraction of the Mn ions contributing to the magnetization decreases. The magnetic properties of the Sn_(1-x)Mn_xO_2 are discussed based on the competition between the free carrier mediated Ruderman-Kittel-Kasuya-Yosida interaction and antiferromagnetic superexchange interaction in the system.
机译:通过湿化学法(x≤0.08)合成了Sn_(1-x)Mn_xO_2纳米晶体粉末。 X射线衍射表明,对于x直至约0.06,获得了单相金红石型Sn_(1-x)Mn_xO_2。电池参数的演变,x射线光电子能谱测量,热重分析和磁化数据的定量评估都表明,对于x = 0.01,Mn元素充当Mn〜(4+),对于x = Mn充当Mn〜(3+)。室温下为0.02和0.04,但在5 K时所有样品的Mn〜(3+)。磁化数据显示,在5 K时,每个Mn位置的平均磁矩随x的增加而减小,而Mn离子的有效分数有助于磁化的减少。基于系统中自由载体介导的Ruderman-Kittel-Kasuya-Yosida相互作用与反铁磁超交换相互作用之间的竞争,讨论了Sn_(1-x)Mn_xO_2的磁性。

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