自旋电子学
自旋极化
抗磁性
凝聚态物理
磁强计
自旋(空气动力学)
分子电子学
自旋等离子体光子学
磁各向异性
磁场
单分子磁体
材料科学
磁化
物理
分子
零场分裂
铁磁性
量子力学
热力学
电子
作者
T. Pei,James Oscar Thomas,Simen Sopp,Ming-Yee Tsang,Nicola Dotti,Jonathan Baugh,Nicholas F. Chilton,Salvador Cardona‐Serra,Alejandro Gaita‐Ariño,Harry L. Anderson,Lapo Bogani
标识
DOI:10.1038/s41467-022-31909-w
摘要
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.
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