Pei Tian, Thomas James O, Sopp Simen, Tsang Ming-Yee, Dotti Nicola, Baugh Jonathan, Chilton Nicholas F, Cardona-Serra Salvador, Gaita-Ariño Alejandro, Anderson Harry L, Bogani Lapo
Department of Materials, University of Oxford, 16 Parks Road, Oxford, OX1 3PH, UK.
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Oxford, OX1 3TA, UK.
Nat Commun. 2022 Aug 3;13(1):4506. doi: 10.1038/s41467-022-31909-w.
Many spintronic devices rely on the presence of spin-polarized currents at zero magnetic field. This is often obtained by spin exchange-bias, where an element with long-range magnetic order creates magnetized states and displaces the hysteresis loop. Here we demonstrate that exchange-split spin states are observable and usable in the smallest conceivable unit: a single magnetic molecule. We use a redox-active porphyrin as a transport channel, coordinating a dysprosium-based single-molecule-magnet inside a graphene nano-gap. Single-molecule transport in magnetic field reveals the existence of exchange-split channels with different spin-polarizations that depend strongly on the field orientation, and comparison with the diamagnetic isostructural compound and milikelvin torque magnetometry unravels the role of the single-molecule anisotropy and the molecular orientation. These results open a path to using spin-exchange in molecular electronics, and offer a method to quantify the internal spin structure of single molecules in multiple oxidation states.
许多自旋电子器件依赖于零磁场下自旋极化电流的存在。这通常通过自旋交换偏置来实现,其中具有长程磁序的元素会产生磁化状态并使磁滞回线发生位移。在此,我们证明了交换分裂自旋态在最小可想象单元——单个磁性分子中是可观测且可用的。我们使用一种氧化还原活性卟啉作为传输通道,在石墨烯纳米间隙内配位一个基于镝的单分子磁体。在磁场中的单分子输运揭示了具有不同自旋极化的交换分裂通道的存在,这些通道强烈依赖于磁场方向,并且与抗磁性同构化合物以及毫开尔文扭矩磁强计的比较揭示了单分子各向异性和分子取向的作用。这些结果为在分子电子学中利用自旋交换开辟了一条道路,并提供了一种量化处于多种氧化态的单分子内部自旋结构的方法。