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Comparing XMCD and DFT with STM spin excitation spectroscopy for Fe and Co adatoms on Cu2N/Cu(100)

MPS-Authors
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Loth,  Sebastian
Dynamics of Nanoelectronic Systems, Independent Research Groups, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
Center for Free-Electron Laser Science, Luruper Chaussee 149, 22761 Hamburg, Germany;

Fulltext (public)

PhysRevB.92.184406.pdf
(Publisher version), 617KB

Supplementary Material (public)
There is no public supplementary material available
Citation

Etzkorn, M., Hirjibehedin, C. F., Lehnert, A., Ouazi, S., Rusponi, S., Stepanow, S., et al. (2015). Comparing XMCD and DFT with STM spin excitation spectroscopy for Fe and Co adatoms on Cu2N/Cu(100). Physical Review B, 92(18): 184406. doi:10.1103/PhysRevB.92.184406.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0029-22BD-9
Abstract
We report on the magnetic properties of Fe and Co adatoms on a Cu2N/Cu(100)−c(2×2) surface investigated by x-ray magnetic dichroism measurements and density functional theory (DFT) calculations including the local coulomb interaction. We compare these results with properties formerly deduced from STM spin excitation spectroscopy (SES) performed on the individual adatoms. In particular we focus on the values of the local magnetic moments determined by XMCD compared to the expectation values derived from the description of the SES data. The angular dependence of the projected magnetic moments along the magnetic field, as measured by XMCD, can be understood on the basis of the SES Hamiltonian. In agreement with DFT, the XMCD measurements show large orbital contributions to the total magnetic moment for both magnetic adatoms.