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Room temperature ferromagnetism in SnO2 nanoparticles: an experimental and density functional study

机译:SnO2纳米粒子中的室温铁磁性:实验和密度泛函研究

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Room temperature ferromagnetism is observed in pristine SnO2 nanoparticles prepared via sol-gel method. Microstructural studies with XRD and Raman reveal the coexistence of SnO and SnO2 phases in vacuum annealed SnO2. Electron paramagnetic resonance (EPR) results confirm the presence of paramagnetic trapped hole in lattice oxygen atoms and superoxide radical species in air and vacuum annealed SnO2. It is observed that growth conditions have significant influence on the magnetism of the nanoparticle. Air and vacuum annealed SnO2 display clear ferromagnetic behavior at room temperature. However, the saturation magnetization decreases in vacuum annealed SnO2. We have compared the experimental results with ab initio density functional calculations and observed that the Sn vacancies are the main reason of magnetism in SnO2. The pattern of theoretical formation energy values shows that it is easier to form Sn vacancies in SnO2 under O rich limit (similar to air annealing). This is in conformity with the experimentally determined higher saturation magnetization values in air annealed SnO2. The spin polarization of lattice oxygen atoms by the presence of Sn vacancy gives rise to magnetism.
机译:在通过溶胶-凝胶法制备的原始SnO2纳米颗粒中观察到室温铁磁性。 XRD和Raman的微结构研究表明,真空退火的SnO2中SnO和SnO2相共存。电子顺磁共振(EPR)结果证实了在空气中和真空退火的SnO2中,晶格中的氧原子和超氧化物自由基物种中存在顺磁性陷阱。观察到生长条件对纳米颗粒的磁性具有显着影响。空气和真空退火的SnO2在室温下显示出清晰的铁磁行为。然而,在真空退火的SnO 2中,饱和磁化强度降低。我们将实验结果与从头算密度函数计算进行了比较,并观察到锡空位是SnO2中磁性的主要原因。理论形成能值的模式表明,在富氧极限下(类似于空气退火),在SnO2中更容易形成Sn空位。这与空气退火的SnO2中实验确定的较高的饱和磁化强度值一致。 Sn空位的存在导致晶格氧原子的自旋极化产生了磁性。

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