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铁磁-有机化学键在Fe3O4/有机分子纳米颗粒体系中对自旋注入的影响

Effects of ferromagnet-molecule chemical bonding on spin injection in Fe3O4-molecule granular system

中文摘要英文摘要

在 Fe3O4 纳米颗粒体系中, 揭示了Fe3O4 和有机分子之间化学成键(ChemNPs)和物理吸附(PhysNPs)两种不同的接触方式对Fe3O4 /有机分子界面处自旋注入的影响。PhysNPs颗粒体系的电阻比在ChemNPs体系中的电阻大两个量级。这表明PhysNPs体系的电阻主要由Fe3O4-有机分子间的界面势垒决定。ChemNPs的颗粒的磁电阻在室温下就达到了-12 %,与PhysNPs体系中0的磁电阻形成鲜明的对比。这反映出化学成键对于自旋注入有极其重要的作用。我们把这种实验现象归结为,在自旋相关的隧穿过程中,由于近邻效应使得有机分子磁化。另外,在化学成键体系中得到的高的自旋极化率,显示了界面处电子的杂化和Fe3O4表面的氧的含量的提高。

Spin injection at the interface of Fe3O4/stearic acid molecule has been investigated in a comparative study of Fe3O4 nanoparticles chemically-bonded with molecules (ChemNPs) and Fe3O4 nanoparticles physically-absorbed with molecules (PhysNPs). The resistance of PhysNPs is two orders of magnitude larger than that of ChemNPs, indicating that the resistance of PhysNPs is dominated by the energy barrier at the Fe3O4-molecule interface. A magnetoresistance of -12% under a field of 5.8 kOe at room temperature is observed in ChemNPs, in sharp contrast to the zero magnetoresistance in PhysNPs, reflecting that the chemical bonding is crucial for spin injection. We attribute this result to the induced magnetic moment in molecules by proximity effect, which is likely the origin of the spin-dependent tunneling through molecules. In addition, the estimated relative large spin polarization of ChemNPs suggests that electronic hybridization at interface and improved oxygen stoichiometry of Fe3O4 surface.

丁海峰、王申、岳风娟、吴镝、林立

物理学半导体技术电子元件、电子组件

磁电阻纳米颗粒有机分子

magnetoresistancenanoparticlesmolecules

丁海峰,王申,岳风娟,吴镝,林立.铁磁-有机化学键在Fe3O4/有机分子纳米颗粒体系中对自旋注入的影响[EB/OL].(2012-02-15)[2025-08-02].http://www.paper.edu.cn/releasepaper/content/201202-468.点此复制

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