Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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Symposium X-RAY Magneto-Optics Dienstag<br />
Fachsitzungen<br />
– Hauptvorträge –<br />
SYXM 1 X-Ray Magneto-Optics<br />
Zeit: Dienstag 14:30–18:00 Raum: H1<br />
Hauptvortrag SYXM 1.1 Di 14:30 H1<br />
Magneto-optical polarisation spectroscopy with soft x-rays<br />
— •Hans-Christoph Mertins 1 , Sergio Valencia 2 , Andreas<br />
Gaupp 2 , Wolfgang Gudat 2 , and Peter Oppeneer 3 — 1 University<br />
of Applied Sciences, Münster, Stegerwaldstr. 39, 48565 Steinfurt —<br />
2 BESSY, Berlin, Germany — 3 IFW-Dresden, Germany<br />
Among the x-ray magneto-optical spectroscopy techniques, the polarisation<br />
analysis of light after its interaction with the material gaines<br />
increasing importance since it reveals both, the intensity and the phase.<br />
Thus it directly gives the complete magneto-optical constants, something<br />
that is not possible with a single intensity measurement.<br />
Polarisation effects appear when linearly polarized light interacts with<br />
a sample that has a magnetization component parallel to the light propagation<br />
direction k. Behind the sample the light polarisation plane is<br />
rotated and the polarisation has changed to elliptical. This effect has been<br />
observed in transmission (Faraday effect [1]) and recently in reflection (L-<br />
MOKE [2]). Both effects are even in the magnetization M allowing for<br />
investigations of ferromagnetic materials. Antiferromagnetic ordering can<br />
be probed by second order effects by applying a perpendicular orientation<br />
between k and M (Voigt effect [3]).<br />
The applicability of these effects for the characterization of magnetic<br />
materials and devices is demonstrated with x-ray rotation and ellipticity<br />
spectra across the 3p and 2p edges of Mn, Fe, Co and Ni.<br />
[1] J. Kunes et al., Phys. Rev. B 64, 174417 (2001)<br />
[2] H.-Ch. Mertins et al., Phys. Rev. B, in press (2003)<br />
[3] H.-Ch. Mertins et al., Phys. Rev. Lett. 87, 047401 (2001).<br />
Hauptvortrag SYXM 1.2 Di 15:00 H1<br />
Magnetization profiling by resonant magnetic x-ray reflectometry<br />
— •G. Schütz, J. Geissler, and E. Goering — Max-Planck<br />
Institut für Metallforschung, Stuttgart<br />
The asymmetry ratio of resonant magnetic x-ray reflection shows a<br />
strong variation with the angle of incidence. The maximum value of the<br />
complex magnetic reflection profile is in the order of the corresponding<br />
XMCD signal, from which the main magnetic contribution of the<br />
absorptive scattering amplitude can be deduced while the dispersive<br />
part is calculated via Kramers Kronig relations. If the correlation of<br />
the XMCD effect to the atomic magnetic moment is known, the magnetization<br />
depth profile can be deduced by an artificial slicing method<br />
utilizing the Parratt algorithm [1]. For hard x-rays (e.g. L2,3 edges for 4f<br />
or 5d elements) with scattering vector of less than one degree cross and<br />
scalar products can be simplified. The application of this theoretical<br />
model is much more complicated for soft x-rays and related to large<br />
scattering angles. However, this energy range covers the L2,3 edges of 3d<br />
transition elements, which exhibit large asymmetry ratios amounting to<br />
50 % [2]. The potential of this method especially for technical relevant<br />
GMR/TMR systems, whose magneto-electric properties can strongly<br />
depend on the interphase morphogy, is demonstrated for a Pt/Co/Cu<br />
trilayer. For this composition it was possible to determine the variation<br />
of the magnetic interface depth profile for each layer reaching an<br />
accuracy of about 10 % for Pt and Co with a depth resolution up to 0.1<br />
nm. Even for the Cu component an estimation of the induced magnetic<br />
moment at the Co-Cu interface is possible [3].<br />
[1] J. Geissler et al., Phys. Rev. B 65, 020405 (2001)<br />
[2] J. Geissler et al., Z. Metallkd. 93, 946 (2002)<br />
[3] E. Goering et al., in preparation<br />
Hauptvortrag SYXM 1.3 Di 15:30 H1<br />
X-ray magneto-optics of lanthanide materials: principles and<br />
applications — •José Emilio Prieto, Franziskus Heigl, Oleg<br />
Krupin, Kristian Döbrich, Günter Kaindl, and Kai Starke —<br />
Institut für Experimentalphysik, Freie Universität Berlin, Germany<br />
Lanthanides are frequently employed in technical magnetic systems<br />
to achieve high anisotropies. In contrast to transition metals, magnetic<br />
moments are carried mainly by the localized 4f electrons, and their correlation<br />
energies give rise to rich multiplet structures in optical excitation<br />
spectra whenever the 4f shell is involved. This results in strong magnetic<br />
dichroism in x-ray absorption and, due to the connection between real<br />
and imaginary parts of the refractive index, also in large magneto-optical<br />
effects in resonant reflectivity [1].<br />
Soft x-ray magneto-optics is well suited to study magnetization<br />
reversal processes in external magnetic fields. Yet in order to obtain<br />
quantitative information on the magnetization from reflectivity data,<br />
comparison with model calculations is required. Here we report on<br />
recent progress in determining the soft x-ray magneto-optical constants<br />
of lanthanides [2,3] and show examples of applying specular resonant<br />
reflectivity to analyse the magnetization reversal of thin films and<br />
exchange-coupled trilayer systems in an element specific way.<br />
[1] K. Starke, F. Heigl, A. Vollmer, M. Weiss, G. Reichardt, and<br />
G. Kaindl, Phys. Rev. Lett. 86, 3415 (2001)<br />
[2] J. E. Prieto, F. Heigl, O. Krupin, G. Kaindl, and K. Starke, Phys.<br />
Rev. B 66, 172408 (2002)<br />
[3] J. E. Prieto, F. Heigl, O. Krupin, G. Kaindl, and K. Starke, Phys.<br />
Rev. B 68, 134453 (2003)<br />
Hauptvortrag SYXM 1.4 Di 16:00 H1<br />
Resonant soft x-ray diffuse scattering from magnetic multilayers<br />
— •Maurizio Sacchi 1 , Carlo Spezzani 1 , Renaud Delaunay 2 ,<br />
and Coryn F. Hague 1,2 — 1 LURE, Centre Universitaire Paris Sud, Orsay,<br />
France — 2 LCP–MR, Université P. et M. Curie, Paris, France<br />
We have applied resonant diffuse scattering of polarized soft x-rays<br />
to the investigation of the field dependent magnetic structure in Co/Cu<br />
multilayers. At remanence, and for weak applied fields, Co layers break<br />
up into magnetic domains with a high degree of AF coupling normal<br />
to the stacked layers. We estimate the degree of AF coupling and the<br />
average size of the AF domains as a function of the applied field.<br />
The analysis of the domain size distribution, and of its correlation with<br />
magnetoresistance, after a demagnetization process gives further evidence<br />
that the remanent magnetic structure is influenced by the magnetic history<br />
of the multilayer.<br />
We have compared the field dependence of the sample resistance and of<br />
the scattered intensity at various off-specular angles. Our results suggest<br />
that at high fields non-negligible variations in the resistance may be due<br />
to the persistence of small magnetically hard domains.<br />
Hauptvortrag SYXM 1.5 Di 16:30 H1<br />
Ab-initio calculations for adatoms and clusters on surfaces<br />
— •Peter H. Dederichs — Institut für Festkörperforschung,<br />
Forschungszentrum Jülich, D-52425 Juelich<br />
Adatoms and small clusters on surfaces have a considerably lower coordination<br />
number than in a bulk environment. Therefore one expects<br />
that these nanostructures exhibit considerably larger spin and orbital<br />
moments than in the bulk. Here we review a series of ab-initio results for<br />
adatoms and small clusters on surfaces of the noble metals (Cu, Ag, Au,<br />
Pt) and the ferromagnets Fe and Ni. The calculations were performed<br />
within the density-functional formalism by using the KKR-Green’s function<br />
method. On the noble metal surfaces, we find strongly enhanced<br />
spin moments, and even small clusters of 4d atoms are magnetic. A much<br />
stronger enhancement is found for the orbital moments and anisotropy<br />
energies. Compared to this, the enhancement of the moments on the<br />
surfaces of Fe and Ni are rather moderate, being a result of the much<br />
stronger hybridisation of the adatoms with the substrate d states.