| Home > Publications database > Revealing noncollinear magnetic ordering at the atomic scale via XMCD > print |
| 001 | 454942 | ||
| 005 | 20250716150828.0 | ||
| 024 | 7 | _ | |a 10.1038/s41598-021-82518-4 |2 doi |
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| 100 | 1 | _ | |a Kielgast, Fridtjof |0 P:(DE-H253)PIP1024937 |b 0 |e Corresponding author |
| 245 | _ | _ | |a Revealing noncollinear magnetic ordering at the atomic scale via XMCD |
| 260 | _ | _ | |a [London] |c 2021 |b Macmillan Publishers Limited, part of Springer Nature |
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| 520 | _ | _ | |a 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. |
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| 773 | _ | _ | |a 10.1038/s41598-021-82518-4 |g Vol. 11, no. 1, p. 2996 |0 PERI:(DE-600)2615211-3 |n 1 |p 2996 |t Scientific reports |v 11 |y 2021 |x 2045-2322 |
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