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Inducing glassy magnetism in Co-ferrite nanoparticles through crystalline nanostructure

机译:通过晶体纳米结构在钴铁氧体纳米颗粒中诱导玻璃态磁性

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This work reports on the study of three samples of 8 nm Co-ferrite particles prepared by standard methods based on the thermal decomposition of metal-organic precursors. Although all samples are single phase according to conventional techniques of structural and chemical characterization, they show strongly sample-dependent magnetic properties ranging from bulk-like ferrimagnetism to glassy magnetic behaviour. We show that the presence of crystallite domains associated with crystallographic defects throughout the particles leads to highly-frustrated ferrimagnetic cores that are responsible for the glassy phenomenology, while only samples almost free of structural imperfections show bulk-like magnetic properties. These results suggest the key role of the crystal quality in the large variability of magnetic properties previously reported for Co-ferrite nanoparticles. Besides, achieving control of the amount of structural defects in monodisperse, stoichiometric Co-ferrite nanoparticles can be an additional nano-structuring procedure to tailor their final magnetic properties.
机译:这项工作报告了基于金属有机前体的热分解,通过标准方法制备的三个8 nm铁氧体颗粒样品的研究。尽管根据常规的结构和化学表征技术,所有样品均为单相,但它们显示出与样品密切相关的磁性能,范围从块状亚铁磁性到玻璃态磁行为。我们表明,与整个颗粒中的晶体学缺陷相关的微晶域的存在会导致高度沮丧的亚铁磁芯,这是玻璃态现象的原因,而只有几乎没有结构缺陷的样品才显示出大块状的磁性能。这些结果表明晶体质量在先前报道的钴铁氧体纳米粒子的磁性能大变化中起着关键作用。此外,要实现对单分散,化学计量的Co-ferrite纳米粒子中结构缺陷数量的控制,可以作为一种额外的纳米结构化方法来调整其最终的磁性。

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