AI Article Synopsis

  • Epitaxial graphene/ferromagnetic metal heterostructures are promising for spintronic devices due to their unique magnetic properties and stability.
  • The research focuses on understanding the spin-orbit coupling at the interface of graphene and cobalt on iridium, revealing that hybridization contributes to strong coupling effects.
  • Findings indicate that while thin cobalt layers exhibit significant spin-orbit effects, these vanish with thicker layers, highlighting the importance of graphene's electronic interactions for future spintronic applications.

Article Abstract

Epitaxial graphene/ferromagnetic metal (Gr/FM) heterostructures deposited onto heavy metals have been proposed for the realization of spintronic devices because of their perpendicular magnetic anisotropy and sizable Dzyaloshinskii-Moriya interaction (DMI), allowing for both enhanced thermal stability and stabilization of chiral spin textures. However, establishing routes toward this goal requires the fundamental understanding of the microscopic origin of their unusual properties. Here, we elucidate the nature of the induced spin-orbit coupling (SOC) at Gr/Co interfaces on Ir. Through spin- and angle-resolved photoemission spectroscopy along with density functional theory, we show that the interaction of the heavy metals with the Gr layer via hybridization with the FM is the source of strong SOC in the Gr layer. Furthermore, our studies on ultrathin Co films underneath Gr reveal an energy splitting of ∼100 meV for in-plane and negligible for out-of-plane spin polarized Gr π-bands, consistent with a Rashba-SOC at the Gr/Co interface, which is either the fingerprint or the origin of the DMI. This mechanism vanishes at large Co thicknesses, where neither in-plane nor out-of-plane spin-orbit splitting is observed, indicating that Gr π-states are electronically decoupled from the heavy metal. The present findings are important for future applications of Gr-based heterostructures in spintronic devices.

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http://dx.doi.org/10.1021/acsnano.4c02154DOI Listing

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