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arXiv 1710.01232cond-mat.mtrl-sci
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纳米多孔非晶氧化铝膜的d-零磁性

d-zero Magnetism in Nanoporous Amorphous Alumina Membranes

Amir Sajad Esmaeily, M. Venkatesan, S. Sen, J. M. D. Coey

摘要:

通过在草酸中在5 - 140 V的电位下进行轻度或硬质阳极化而制备的纳米多孔氧化铝膜具有高达膜面积200倍的可控孔表面积。他们表现出饱和的磁响应,是温度无关的,几乎无滞后低于室温。磁性不能用膜中存在的~1 ppm的过渡金属杂质来解释。的磁矩增加与开放的纳米孔的面积,达到0.6玻尔磁子每平方纳米的轻度阳极化和8 μ B/nm 2的硬阳极化的生长速度更快的值。膜的结晶或用水杨酸进行化学处理可使效果降低高达90%。因此,磁性与无定形Al 2 O3的开孔表面相关联,并且它与所施加的场相对于膜表面的取向无关。可能的解释与氧空位(F或F+中心)的电子方面进行了讨论,它的结论是,该效果是由于巨轨道顺磁性,而不是集体铁磁自旋顺序。

英文摘要:

Nanoporous alumina membranes produced by mild or hard anodisation in oxalic acid at potentials ranging from 5 - 140 V have a controllable pore surface area of up to 200 times the membrane area. They exhibit a saturating magnetic response that is temperature-independent and almost anhysteretic below room temperature. The magnetism cannot be explained by the ~1 ppm of transition-metal impurities present in the membranes. The magnetic moment increases with the area of the open nanopores, reaching values of 0.6 Bohr magnetons per square nanometer for mild anodisation and 8 muB/nm2 for hard anodisation where the growth rate is faster. Crystallization of the membrane or chemical treatment with salicylic acid reduces the effect by up to 90 %. The magnetism is therefore associated with the open pore surfaces of the amorphous Al2O3, and it is independent of the orientation of the applied field with respect to the membrane surface. Possible explanations in terms of electrons associated with oxygen vacancies (F or F+ centres) are discussed and it is concluded that the effect is due to giant orbital paramagnetism rather than collective ferromagnetic spin order.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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