Large Magnetic Anisotropy of a Single Atomic Spin Embedded in a Surface Molecular Network

TLDR

Magnetic anisotropy allows magnets to maintain their direction of magnetization over time. Using a scanning tunneling microscope to observe spin excitations, we determined the orientation and strength of the anisotropies of individual iron and manganese atoms on a thin layer of copper nitride. The inelastic tunneling intensities match dipolar interactions, first‑principles calculations show the magnetic atoms integrate into a polar covalent copper‑nitride surface network, and these atomically accessible structures could enable engineered anisotropies sufficient to stabilize single‑atom magnetization at low temperatures.

Abstract

Magnetic anisotropy allows magnets to maintain their direction of magnetization over time. Using a scanning tunneling microscope to observe spin excitations, we determined the orientation and strength of the anisotropies of individual iron and manganese atoms on a thin layer of copper nitride. The relative intensities of the inelastic tunneling processes are consistent with dipolar interactions, as seen for inelastic neutron scattering. First-principles calculations indicate that the magnetic atoms become incorporated into a polar covalent surface molecular network in the copper nitride. These structures, which provide atom-by-atom accessibility via local probes, have the potential for engineering anisotropies large enough to produce stable magnetization at low temperatures for a single atomic spin.