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Orbital Redistribution Enhanced Perpendicular Magnetic Anisotropy of CoFe3N Nitrides by Adsorbing Organic Molecules

机译:轨道再分配通过吸附有机分子来增强COFE3N氮化物的垂直磁各向异性

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Organic/ferromagnetic spinterface plays a significant role in organic spintronics and the manipulation of spinterface will help to optimize the performance of molecular devices. Here, we systematically investigate how the magnetic anisotropy can be tailed by adsorbing different organic molecules on CoFe3N surface. It is found that the adsorption of C6H6, C6F6, and SC4H4 molecules on the FeCo-hollow site enhances the perpendicular magnetic anisotropy (PMA) of CoFe3N. The redistribution of Fe/Co d-orbitals near the Fermi level has an important effect on the modulation of PMA. Asymmetric SC4H4 adsorbed system has a larger PMA than symmetric C6H6 and its halide due to the hybridization between S pZ and Fe/Co d-orbitals instead of C atom. Our results indicate that appropriate organic molecule adsorption can improve the magnetic properties of ferromagnets, which benefits organic spintronic devices.
机译:有机/铁磁性纺织件在有机闪光灯中发挥着重要作用,并且纺锤面的操纵将有助于优化分子装置的性能。 这里,我们系统地研究如何通过吸附在COFE3N表面上的不同有机分子来挖掘磁各向异性。 发现C6H6,C6F6和SC4H4分子对FeCo-中空部位的吸附增强了CoFe3N的垂直磁各向异性(PMA)。 费米水平附近的Fe / Co D轨道的再分配对PMA的调节具有重要影响。 由于S PZ和Fe / Co D-轨道代替C原子而不是C原子,不对称SC4H4吸附系统具有比对称C6H6的PMA更大的PMA及其卤化物。 我们的结果表明,适当的有机分子吸附可以改善铁圆形磁性的磁性,这有利于有机旋转式装置。

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