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纯 SnO2 和镍掺杂 SnO2 纳米颗粒的结构和磁性。

Structural and magnetic properties of pure and nickel doped SnO2 nanoparticles.

机构信息

Núcleo de Física Aplicada, Institute of Physics, Universidade de Brasília, Brasília, DF 70910-900, Brazil.

出版信息

J Phys Condens Matter. 2010 Dec 15;22(49):496003. doi: 10.1088/0953-8984/22/49/496003.

Abstract

Ni-doped SnO2 nanoparticles prepared by a polymer precursor method have been characterized structurally and magnetically. Ni doping (up to 10 mol%) does not significantly affect the crystalline structure of SnO2, but stabilizes smaller particles as the Ni content is increased. A notable solid solution regime up to ∼ 3 mol% of Ni, and a Ni surface enrichment for the higher Ni contents are found. The room temperature ferromagnetism with saturation magnetization (MS) ∼ 1.2 × 10 (- 3) emu g (- 1) and coercive field (HC) ∼ 40 Oe is determined for the undoped sample, which is associated with the exchange coupling of the spins of electrons trapped in oxygen vacancies, mainly located on the surface of the particles. This ferromagnetism is enhanced as the Ni content increases up to ∼ 3 mol%, where the Ni ions are distributed in a solid solution. Above this Ni content, the ferromagnetism rapidly decays and a paramagnetic behavior is observed. This finding is assigned to the increasing segregation of Ni ions (likely formed by interstitials Ni ions and nearby substitutional sites) on the particle surface, which modifies the magnetic behavior by reducing the available oxygen vacancies and/or the free electrons and favoring paramagnetic behavior.

摘要

采用聚合物前驱体法制备的 Ni 掺杂 SnO2 纳米粒子在结构和磁性方面进行了表征。Ni 掺杂(高达 10 mol%)不会显著影响 SnO2 的晶体结构,但随着 Ni 含量的增加,它会稳定更小的颗粒。发现了高达约 3 mol%的 Ni 的显著固溶区,以及更高 Ni 含量下的 Ni 表面富集。对于未掺杂的样品,确定了室温铁磁性,饱和磁化强度(MS)约为 1.2 × 10(-3)emu g(-1),矫顽力(HC)约为 40 Oe,这与电子在氧空位中被捕获的自旋的交换耦合有关,氧空位主要位于颗粒表面。随着 Ni 含量增加到约 3 mol%,这种铁磁性增强,其中 Ni 离子分布在固溶体中。在这个 Ni 含量以上,铁磁性迅速衰减并观察到顺磁性行为。这一发现归因于 Ni 离子(可能由间隙 Ni 离子和附近的替代位形成)在颗粒表面的逐渐分离,这通过减少可用的氧空位和/或自由电子来改变磁行为,并有利于顺磁性行为。

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