Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Oberflächenphysik Montag<br />
O 12 Magnetismus in reduzierten Dimensionen<br />
Zeit: Montag 15:45–17:00 Raum: H45<br />
O 12.1 Mo 15:45 H45<br />
Magnetische Röntgenstreuung an lateral strukturierten<br />
Co/CoO Filmen — •Arndt Remhof, Johannes Grabis,<br />
Alexei Nefedov und Hartmut Zabel — Experimentalphysik/Festkörperphysik,<br />
Ruhr-Universität Bochum<br />
Nano- und Mikrostrukturierung von dünnen magnetischen Systemen<br />
ermöglicht das Ummagnetisierungsverhalten, d. h. die Hystereseschleife,<br />
gezielt zu verändern. Wir haben ein quadratisches Muster aus Co/CoO<br />
Inseln mittels Elektronenstrahl-Lithographie hergestellt. Die Inseln haben<br />
einen Durchmesser von 1µm und eine Periode von 3µm. Die magnetische<br />
Hysterese wurde mit Bragg-MOKE und mit resonanter magnetischer<br />
Röntgenstreuung (XRMS) an der Co L2,3 bei verschiedener Ordnung der<br />
Interferenz bestimmt. Bragg-MOKE liefert eine Fourieranalyse des Magnetisierungsprofils<br />
während des Ummagnetisierungs-prozesses. Analog<br />
dazu liefern auch Hysteresen, die mit XRMS an verschiedenen Ordnungen<br />
von Bragg-Reflexen gemessen werden, eine Fourieranalyse der Ummagnetisierung.<br />
Im Vergleich zu Bragg-MOKE zeichnet sich XRMS durch<br />
Elementspezifität und durch höhere Eindringtiefen aus. Wir präsentieren<br />
erste Ergebnisse, die mit Bragg-MOKE und XRMS an strukturierten<br />
Co/CoO Proben gewonnen wurden, und vergleichen die Ergebnisse.<br />
Gefördert durch SFB 491.<br />
O 12.2 Mo 16:00 H45<br />
Spin effects in Coulomb blockade of Fe/MgO/Fe — •Wulf<br />
Wulfhekel 1 , F. Zavaliche 1,2 , M. Klaua 1 , C.C. Kuo 1,3 , M.T.<br />
Lin 1,3 , and J. Kirschner 1 — 1 MPI für Mikrostrukturphysik, Weinberg<br />
2, 06120 Halle — 2 Departement de physique, Universite de Montreal,<br />
Quebec H3C 3J7, Canada — 3 Department of Physics, National Taiwan<br />
University, Taipei 106, Taiwan<br />
The Coulomb blockade (CB) of nanometer sized Fe islands grown on<br />
single crystalline MgO films on Fe(001) was studied using scanning tunneling<br />
microscopy (STM) at 25 K in ultra high vacuum. After deposition<br />
of 3-4 monolayers (ML) MgO, a sub-ML amount of Fe was deposited<br />
leading to the formation of Fe islands on the MgO films as observed by<br />
STM. Scanning tunneling spectroscopy was then used to locally measure<br />
the tunneling characteristics for tunneling from the tip via the island<br />
into the Fe substrate. The I(V) curves showed the characteristic steps of<br />
CB. The position of the steps in the I(V) characteristics of periodicity<br />
UC are proportional to the Coulomb charging energy e/C, where e is<br />
the electron charge and C the islands capacitance. A plot of UC versus<br />
e/C for the Fe islands, where C was estimated from the island size as<br />
observed with STM, reveals a linear dependence in agreement with CB.<br />
We, however, observe a constant and positive offset in UC by 1 eV, which<br />
cannot be explained by spin independent tunneling. We propose a model<br />
for spin-dependent CB, that relates the offset to the exchange the additional<br />
electron feels in the Fe islands. No systematic offset in UC has<br />
been found for identical experiments with Pd islands indicating that the<br />
observed offset is related to the island material.<br />
O 12.3 Mo 16:15 H45<br />
Valence band electronic structure and chemical reactivity in<br />
MgO/Fe(100) and MgO/Co/Fe(100) oxide-metal interfaces<br />
grown on GaAs(100) — •Liu-Niu Tong 1 , Frank Matthes 1 ,<br />
and C.M. Schneider 2 — 1 Leibniz Institut für Festkörper- und<br />
Werkstoffforschung — 2 Institut für Elektronische Eigenschaften,<br />
Forschungszentrum<br />
O 13 Methodisches (Experiment und Theorie)<br />
The interface electronic structure of MgO/Fe(100) and MgO/Co/<br />
Fe(100) films epitaxially grown on GaAs(100) was studied by employing<br />
spin-polarized photoemission spectroscopy (SPPES) and magnetic circular<br />
dichroism (MCD) techniques. With increasing excitation energy from<br />
30 eV to 60 eV, we observe an enhanced spectral intensity in the SPPES<br />
data of pure Fe for transitions from bulk ∆ 1 and ∆ 5 initial states near<br />
the Fermi energy that is accompanied with an increase in the detected<br />
spin polarization. After covering the Fe(100) surface by 0.5 ML MgO,<br />
the shape of the Fe ∆ 5 minority-spin peak becomes significantly broadened,<br />
while the shape of the Fe ∆ 1 majority-spin peak is only weakly<br />
affected. Additionally, we observed that 1 ML MgO on top of Fe(100)<br />
suppresses almost all contribution from the Fe ∆ 5 minority transition in<br />
the measured spin polarization data. This observed effect is especially<br />
strong for an excitation energy of 40 eV. Furthermore, our MCD data<br />
show that the O 2p peak is shifting towards the Fermi level as a function<br />
of time after preparation, indicating a slow change in the film chemistry.<br />
This chemical reaction can also be seen for MgO/Fe samples that were<br />
immediately covered after preparation with an additional Fe film on top.<br />
O 12.4 Mo 16:30 H45<br />
X-ray magnetic circular dichroism sum rule correction for the<br />
light transition metals — •Eberhard Goering — Max-Planck-<br />
Insitut für Metallforschung, 70569 Stuttgart<br />
Quantum mechanical mixing of the L2 and L3 edge excitations strongly<br />
increases with reduced 2p spin-orbit-splitting. For a large number of<br />
2p→3d absorption spectra the shape has been fitted nearly perfectly by a<br />
model, which takes into account lifetime and jj-mixing effects. X-ray magnetic<br />
circular dichroism (XMCD) sum rule correction factors have been<br />
determined for V and Cr, which are consistent to complementary investigations.<br />
This fitting procedure and the estimated correction factors are<br />
the basis for a future light element XMCD effective spin renormalization<br />
technique.<br />
O 12.5 Mo 16:45 H45<br />
Spin-resolved inverse photoemission with improved energy resolution<br />
— •Michael Budke, Volker Renken, Helmut Liebl,<br />
Georgi Rangelov, and Markus Donath — Physikalisches Institut,<br />
Universität Münster, Wilhelm-Klemm-Str. 10, 48149 Münster<br />
Spin-resolved inverse photoemission (IPE) is a powerful tool that measures<br />
the spin-dependend electronic structure above the Fermi level of<br />
magnetic surfaces and thin films. We have developed a source for spinpolarized<br />
electrons with variable energy resolution from 150 meV to 400<br />
meV (FWHM) at currents between 0.5 µA and 5 µA on the sample. The<br />
photon detector consists of a conventional Geiger tube filled with either<br />
acetone or iodine [1,2]. MgF2 is used as entrance window, followed by a<br />
SrF2- or CaF2-window. The transmission cutoff was shifted by varying<br />
the temperature of the windows. With this arrangement the energy resolution<br />
of the counters is continuously variable between 150 meV and 400<br />
meV (FWHM). Depending on the experimental requirements the total<br />
energy resolution of our IPE system can therefore be varied between 500<br />
meV and nearly 200 meV. The latter value is an improvement of the<br />
energy resolution by a factor of two compared to previous spin-resolved<br />
IPE systems [3]. [1] Dose V., Appl. Phys. 14, 117 (1977) [2] Funnemann<br />
D., Merz H., J. Phys. E: Sci. Instrum. 19, 554 (1986) [3] Dose V., Fauster<br />
T., Schneider R., Appl. Phys. A 40, 203 (1986)<br />
Zeit: Montag 17:00–17:30 Raum: H45<br />
O 13.1 Mo 17:00 H45<br />
Experimente mit kinematischen stehenden Röntgenwellen an<br />
CaF2/Si(111) — •Martin Tolkiehn 1 , Dmitri V. Novikov 1 und<br />
Cunrang Wang 2 — 1 HASYLAB am DESY, Notkestraße 85, D-22603<br />
Hamburg — 2 Institut für Halbleiterbauelemente und Werkstoffe, Universität<br />
Hannover, Appelstraße 11A, D-30167 Hannover<br />
Die Methode der stehenden Röntgenwellen (XSW) ist sehr gut geeignet<br />
zur Bestimmung der Position von Adsorbatatomen an Oberflächen<br />
und Dotieratomen in perfekten Kristallen [1,2]. Sie beruht auf der Ver-<br />
änderung der Phase des stehenden Wellenfelds in der Nähe eines Bragg–<br />
Reflexes, die mit Hilfe der dynamischen Theorie der Röntgenbeugung<br />
berechnet wird. Die Anwendung dieser Theorie auf nicht perfekte Kristalle<br />
ist ohne weiteres nicht möglich. Das stehende Wellenfeld ist jedoch<br />
auch noch bei größeren Abweichungen vom Braggwinkel vorhanden, bei<br />
denen die kinematische Näherung gilt.<br />
Wir zeigen theoretisch und experimentell am Beispiel CaF2/Si(111)<br />
[3], daß sich der Bereich fern vom Bragg–Winkel zur Bestimmung der<br />
Adsorbatposition nutzen läßt und dasselbe Ergebnis liefert wie die kon-