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Real-space observation of spin-split molecularorbitals of adsorbed single-molecule magnets

机译:吸附单分子磁体的自旋分裂分子轨道的真实空间观察

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摘要

A key challenge in the field of molecular spintronics, and for the design of single-moleculemagnet-based devices in particular, is the understanding and control of the molecular couplingat the electrode interfaces. It was demonstrated for the field of molecular electronics thatthe characterization of the molecule-metal-interface requires the precise knowledge of theatomic environment as well as the molecular orbitals being involved in electron transport.To extend the field of molecular electronics towards molecular spintronics, it is of utmostimportance to resolve the spin character of molecular orbitals interacting with ferromagneticleads. Here we present first direct real-space images of spin-split molecular orbitals of asingle-molecule magnet adsorbed on a ferromagnetic nanostructure. moreover, we are able todetermine quantitatively the magnitude of the spin-splitting as well as the charge state of theadsorbed molecule.
机译:在分子自旋电子学领域,特别是对于基于单分子磁体的设备的设计,一个关键的挑战是对电极界面上的分子偶联的理解和控制。在分子电子学领域已经证明,分子-金属-界面的表征需要对原子环境的精确了解以及与电子传输有关的分子轨道。为了将分子电子学领域扩展到分子自旋电子学,最重要的是解决与铁磁引线相互作用的分子轨道的自旋特性。在这里,我们提出了吸附在铁磁纳米结构上的单分子磁体的自旋分裂分子轨道的第一个直接的真实空间图像。此外,我们能够定量确定自旋分裂的大小以及吸附分子的电荷状态。

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