TY - JOUR
T1 - Exchange-induced spin polarization in a single magnetic molecule junction
AU - Pei, Tian
AU - Thomas, James O.
AU - Sopp, Simen
AU - Tsang, Ming-Yee
AU - Dotti, Nicola
AU - Baugh, Jonathan
AU - Chilton, Nicholas F.
AU - Cardona-Serra, Salvador
AU - Gaita-Ariño, Alejandro
AU - Anderson, Harry L.
AU - Bogani, Lapo
PY - 2022/8/3
Y1 - 2022/8/3
N2 - 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.
AB - 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.
KW - Electronic devices
KW - Magnetic properties and materials
U2 - 10.1038/s41467-022-31909-w
DO - 10.1038/s41467-022-31909-w
M3 - Article
SN - 2041-1723
VL - 13
JO - Nature Communications
JF - Nature Communications
M1 - 4506
ER -