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Electronic and magnetic structure of C_(60)/Fe3O4(001): a hybrid interface for organic spintronics

机译:C_(60)/ Fe3O4(001)的电子和磁性结构:有机自旋电子学的混合界面

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We report on the electronic and magnetic characterization of the hybrid interface constituted of C_(60) molecules and an epitaxial Fe3O4(001) surface grown on GaAs(001). Using X-ray absorption spectroscopy (XAS) and X-ray magnetic circular dichroism (XMCD), we demonstrate that a stable C_(60) sub-monolayer (ML) can be retained on the Fe3O4(001) surface upon in situ annealing at 250 °C. A carbon K-edge dichroic signal of 1% with respect to the XAS C 1s→π* peak intensity has been observed, indicative of a weaker electronic interaction of C_(60) with Fe3O4(001) compared to the previously reported case of C_(60)/Fe(001). Remarkably, the Fe L-edge XMCD spectrum of Fe3O4(001) reveals a reduced Fe~(3+)/Fe~(2+) ratio upon C_(60) sub-ML adsorption. This observation has been ascribed to electron donation by the C_(60) molecules, as a consequence of the high work function of Fe3O4(001). Our present work underlines the significance of chemical interactions between inorganic magnetic surfaces and molecular adsorbates for tuning of the electronic and magnetic properties of the interfaces, which have a profound impact on spin-polarized charge transport in hybrid organic-inorganic spintronic devices.
机译:我们报告了由C_(60)分子和生长在GaAs(001)上的外延Fe3O4(001)表面组成的混合界面的电子和磁性表征。使用X射线吸收光谱(XAS)和X射线磁圆二向色性(XMCD),我们证明了在原位退火时,在Fe3O4(001)表面上可以保持稳定的C_(60)亚单层(ML) 250℃。已观察到相对于XAS C 1s→π*峰强度为1%的碳K边缘二向色性信号,表明与先前报道的C_情况相比,C_(60)与Fe3O4(001)的电子相互作用更弱(60)/铁(001)。值得注意的是,Fe3O4(001)的Fe L-edge XMCD光谱显示,经C_(60)sub-ML吸附,Fe〜(3 +)/ Fe〜(2+)的比例降低。由于Fe3O4(001)的高功函,这种观察归因于C_(60)分子给电子。我们目前的工作强调了无机磁性表面和分子吸附物之间化学相互作用对于调节界面的电子和磁性的重要性,这对混合有机-无机自旋电子器件中的自旋极化电荷传输具有深远的影响。

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