| Home > Publications database > Revealing noncollinear magnetic ordering at the atomic scale via XMCD |
| Journal Article | PUBDB-2021-00849 |
; ; ; ;
2021
Macmillan Publishers Limited, part of Springer Nature
[London]
This record in other databases:
Please use a persistent id in citations: doi:10.1038/s41598-021-82518-4 doi:10.3204/PUBDB-2021-00849
Abstract: Mass-selected V and Fe monomers, as well as the heterodimer Fe1V1, were deposited on a Cu(001) surface. Their electronic and magnetic properties were investigated via X-ray absorption (XAS) and X-ray magnetic circular dichroism (XMCD) spectroscopy. Anisotropies in the magnetic moments of the deposited species could be examined by means of angle resolving XMCD, i.e. changing the X-ray angle of incidence. A weak adatom-substrate-coupling was found for both elements and, using group theoretical arguments, the ground state symmetries of the adatoms were determined. For the dimer, a switching from antiparallel to parallel orientation of the respective magnetic moments was observed. We show that this is due to the existence of a noncollinear spin-flop phase in the deposited dimers, which could be observed for the first time in such a small system. Making use of the two magnetic sublattices model, we were able to find the relative orientations for the dimer magnetic moments for different incidence angles.
|
The record appears in these collections: |