TY  - JOUR
AU  - Pohlmann, Tobias
AU  - Kuschel, Timo
AU  - Rodewald, Jari
AU  - Thien, Jannis
AU  - Ruwisch, Kevin
AU  - Bertram, Florian
AU  - Weschke, Eugen
AU  - Shafer, Padraic
AU  - Wollschlaeger, Joachim
AU  - Kuepper, Karsten
TI  - Cation- and lattice-site-selective magnetic depth profiles of ultrathin Fe<sub>3</sub>O<sub>4</sub> (001) films
JO  - Physical review / B
VL  - 102
IS  - 22
SN  - 2469-9969
CY  - Woodbury, NY
PB  - Inst.
M1  - PUBDB-2021-01433
SP  - 220411
PY  - 2020
AB  - A detailed understanding of ultrathin film surface properties is crucial for the proper interpretation of spectroscopic, catalytic, and spin-transport data. We present x-ray magnetic circular dichroism (XMCD) and x-ray resonant magnetic reflectivity (XRMR) measurements on ultrathin Fe<sub>3</sub>O<sub>4</sub> films to obtain magnetic depth profiles for the three resonant energies corresponding to the different cation species Fe<sup>2+</sup><sub>oct</sub>, Fe<sup>3+</sup><sub>tet</sub>, and Fe<sup>3+</sup><sub>oct</sub> located on octahedral and tetrahedral sites of the inverse spinel structure of Fe<sub>3</sub>O<sub>4</sub>. By analyzing the XMCD spectrum of Fe<sub>3</sub>O<sub>4</sub> using multiplet calculations, the resonance energy of each cation species can be isolated. Performing XRMR on these three resonant energies yields magnetic depth profiles that each correspond to one specific cation species. The depth profiles of both kinds of Fe<sup>3+</sup> cations reveal a (3.9±1.0)−Å-thick surface layer of enhanced magnetization, which is likely due to an excess of these ions at the expense of the Fe<sup>2+</sup><sub>oct</sub> species in the surface region. The magnetically enhanced Fe<sup>3+</sup><sub>tet</sub> layer is additionally shifted about 2.9±0.4Å farther from the surface than the Fe<sup>3+</sup><sub>oct</sub> layer.  
LB  - PUB:(DE-HGF)16
UR  - <Go to ISI:>//WOS:000602252200002
DO  - DOI:10.1103/PhysRevB.102.220411
UR  - https://bib-pubdb1.desy.de/record/456282
ER  -