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Experimental study of the structural, microscopy and magnetic properties of Ni-doped SnO2 nanoparticles

机译:掺Ni的SnO2纳米粒子的结构,显微和磁性的实验研究

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摘要

A polymer precursor method has been used to synthesize Ni-doped SnO 2 nanoparticles. X-ray diffraction (XRD) data analyses indicate the exclusive formation of nanosized particles with rutile-type phase (tetragonal SnO2) for Ni contents below 10 mol%. In this concentration range, the particle sizes decrease with increasing Ni content and a bulk solid solution limit was determined at ~ 1 mol%. Ni surface enrichment is present at concentrations higher than the solution limit. Only above 10 mol% Ni, the formation of a second NiO-related phase has been determined. Magnetization measurements suggest the occurrence of ferromagnetism for samples in the solid solution regime (below ~ 1 mol%). This ferromagnetism is associated with the exchange interaction between electron spins trapped on oxygen vacancies, and is enhanced as the amount of Ni2+ substituting at Sn4+ sites increases. Above the solid solution limit, ferromagnetism is destroyed by the Ni surface enrichment and the system behaves as a paramagnet.
机译:已经使用聚合物前体方法来合成掺Ni的SnO 2纳米颗粒。 X射线衍射(XRD)数据分析表明,当Ni含量低于10 mol%时,会形成金红石型相(四方SnO2)纳米颗粒。在此浓度范围内,粒度随Ni含量的增加而减小,并且确定固相固溶极限为〜1 mol%。 Ni表面富集的浓度高于溶液极限。仅确定高于10mol%的Ni,已经确定了第二NiO相关相的形成。磁化测量表明,在固溶体状态(低于1 mol%)下,样品会发生铁磁性。这种铁磁性与捕获在氧空位上的电子自旋之间的交换相互作用有关,并且随着取代在Sn4 +位上的Ni2 +的数量增加而增强。在固溶极限以上,铁磁性会被镍表面富集所破坏,并且系统会表现为顺磁性。

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