Low-energy, ultrafast spin reorientation at competing hybrid interfaces with tunable operating temperature
Servet Ozdemir, Matthew Rogers, Jaka Strohsack, Hari Babu Vasili, Manuel Valvidares, Thahabh Haddadi, Parvathy Harikumar, David ORegan, Gilberto Teobaldi, Timothy Moorsom, Mannan Ali, Gavin Burnell, B J Hickey, Tomaz Mertelj, Oscar Cespedes

TL;DR
This study demonstrates a tunable, low-energy, ultrafast spin reorientation transition at hybrid organic-metal interfaces, with potential applications in heat-assisted magnetic storage technologies.
Contribution
It reveals a controllable spin reorientation in molecular interfaces of ferromagnetic films driven by competing anisotropies, tunable near room temperature by material parameters.
Findings
Spin reorientation transition observed in molecular interfaces.
Switching of magnetization easy axis with low energy input.
Transition tunable by film thickness and molecular overlayer.
Abstract
Information can be stored in magnetic materials by encoding with the direction of the magnetic moment of elements. A figure of merit for these systems is the energy needed to change the information rewrite the storage by changing the magnetic moment. Organic molecules offer a playground to manipulate spin order, with metallo molecular interfaces being a promising direction for sustainable devices. Here, we demonstrate a spin reorientation transition in molecular interfaces of high magnetisation 3d ferromagnetic films due to a competition between a perpendicular magnetic anisotropy (PMA) induced by a heavy metal that dominates at high temperatures, and an in-plane anisotropy generated by molecular coupling at low temperatures. The transition can be tuned around room temperature by varying the ferromagnet thickness (1.4 to 1.9 nm) or the choice of molecular overlayer, with the organic…
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