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Plenarvorträge - DPG-Tagungen

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Oberflächenphysik Dienstag<br />

structural distortion. It can be affected by thermal fluctuations and other<br />

metallic states in the system.<br />

Recent progress in photoelectron spectroscopy and synchrotron radi-<br />

ation instrumentation allow to study these effects directly and k-space<br />

resolved. Various examples on surfaces, in quasi-one dimensional crystals,<br />

and in magnetic materials will be shown.<br />

O 17 Elektronische Struktur (Experiment und Theorie) II<br />

Zeit: Dienstag 11:15–13:15 Raum: H36<br />

O 17.1 Di 11:15 H36<br />

Stark Effect for Shockley Surface States of Au(111) and Cu(111)<br />

— •J. Kröger 1 , L. Limot 1 , R. Berndt 1 , and P. Johansson 2<br />

— 1 Christian-Albrechts-Universität zu Kiel, D-24098 Kiel, Germany —<br />

2 University of Örebro, S-70182 Örebro, Sweden<br />

We present scanning tunneling spectroscopy data of Au(111) and<br />

Cu(111) acquired at 9 K. Increasing the electric field between tip and<br />

sample surface leads to a gradual downward shift of the surface state<br />

binding energies for both surfaces. The observed shift is attributed to<br />

the Stark effect as was previously observed for Ag(111) by Limot et al.<br />

[1]. Experimental data are compared with calculations performed within<br />

a one-dimensional model. In the limit of infinitely large tip-surface<br />

distances the photoemission binding energy values are obtained.<br />

[1] L. Limot, T. Maroutian, R. Berndt, and P. Johansson, Phys. Rev.<br />

Lett. 91, 196801 (2003).<br />

O 17.2 Di 11:30 H36<br />

Temperaturabhängige Untersuchung des Cr(001)-Oberflächenzustands<br />

mittels SP-STM/STS — •Torben Hänke, Stefan<br />

Krause, Robert Ravlić, Matthias Bode und Roland Wiesendanger<br />

— Institut für Angewandte Physik, Universität Hamburg,<br />

Jungiusstraße 11, 20355 Hamburg<br />

Die magnetische Struktur der Cr(001)-Oberfläche läßt sich durch<br />

den topologischen Antiferromagnetismus beschreiben, d.h. Terrassen,<br />

die durch monoatomare Stufen getrennt sind, weisen eine alternierende<br />

Magnetisierung auf. Typisch für eine solche bcc(001)-Oberfläche<br />

ist ein spinpolarisierter d z 2-artiger Oberflächenzustand nahe der<br />

Fermi-Kante [1]. Bei Raumtemperatur zeigt spinpolarisierte Rastertunnelspektroskopie<br />

auf benachbarten Terrassen gemäß dieser Interpretation<br />

eine alternierende Peak-Höhe dieses Zustands [2]. Demgegenüber steht<br />

eine STS-Untersuchung bei 4,2 K [3], in der eine scharfe Resonanz<br />

26meV oberhalb der Fermi-Kante beobachtet wird. Diese Resonanz des<br />

Spektrums wird als orbitale Kondo-Resonanz (TK = 180K), hervorgerufen<br />

durch die Bildung eines orbitalen Singlet-Zustandes, erklärt.<br />

Dieser Zustand entsteht aus dem virtuellen Übergang zwischen dxy und<br />

dyz Oberflächenzuständen über Hybridisierung mit dem sp-Band. In<br />

diesem Beitrag wurde der Oberflächenzustand mittels SP-STM/STS bei<br />

Temperaturen von 20-300 K untersucht, und die Ergebnisse werden im<br />

Hinblick auf die verschiedenen Interpretationen diskutiert.<br />

[1] J. A. Stroscio et al., Phys. Rev. Lett. 75 2960 (1995).<br />

[2] M. Kleiber et al., Phys. Rev. Lett. 85 4606 (2000).<br />

[3] O. Yu. Kolesnychenko et al., Nature 415 507 (2002).<br />

O 17.3 Di 11:45 H36<br />

STM-Thermovoltage measurements of surface electronic states<br />

on Ag/Au(111) — •Winfried Langenkamp, Bastian Weyers,<br />

and Rolf Möller — Universität Duisburg-Essen, Institut für Experimentelle<br />

Physik, Universitätsstr. 3-5, 45141 Essen<br />

Submonolayer films of silver on Gold(111) have been examined with<br />

a thermovoltage-STM to determine the shift in the fermi wavelength of<br />

surface state electrons.<br />

If tip and sample of an STM are at different temperatures, a thermovoltage<br />

arises which is correlated to the derivative of the sample’s density<br />

of electronic states at the fermi level.<br />

This voltage is measured by a feedback loop for a bias voltage tuning<br />

the average current to zero. Simultaneously the tip-sample separation is<br />

adjusted by the current resulting from a small alternating bias voltage.<br />

The thermovoltage can be used to analyze atoms of different chemical<br />

nature and standing waves of surface state electrons. [1]<br />

In the experiments discussed the equivalent of less then a monolayer<br />

of Ag was evaporated on Au(111) leading to the formation of silver islands<br />

of monoatomic height. The thermovoltage provides information to<br />

distinguish gold and silver areas below the tip as well as on the standing<br />

waves of surface states on Au(111) and on 1 ML Ag/Au(111).<br />

[1] D. Hoffmann et al., Thermovoltage in scanning tunnelling microscopy,<br />

J. Electron Spectroscopy, 109 (2000) 117<br />

O 17.4 Di 12:00 H36<br />

Shockley surface states at close-packed surfaces — •Frederik<br />

Schiller 1,2 , Vito Servedio 3 , and Clemens Laubschat 1 —<br />

1 Institut für Festkörperphysik, TU Dresden, D-01062 Dresden, Germany<br />

— 2 Donostia International Physics Center, E-20018 Donostia/San<br />

Sebastian, Spain — 3 Sezione INFM and Dip. di Fisica, Università “La<br />

Sapienza”, P. le A. Moro 2, I-00185 Roma, Italy<br />

Valence-band photoemission spectra of close-packed surfaces of the divalent<br />

alkali-earth metals Be and Mg reveal huge peaks due to Shockley<br />

surface states with a free-electron like dispersion parallel to the surface.<br />

Similar states have been observed for close-packed surfaces of the noble<br />

metals Cu, Ag, Au, and the trivalent metal Al. Surprisingly, for the divalent<br />

metals Ca, Sr, Eu, and Yb as well as for all trivalent rare-earth<br />

metals such Shockley states are missing. Instead, rare-earth metals exhibit<br />

a d-like Tamm state that reveals almost no dispersion. On the basis<br />

of band-structure calculations, we show that this different behavior is<br />

caused by the d bands that convert the Shockley-inverted energy gaps at<br />

the close-packed surfaces of Be, Mg, Cu, Ag, Au, and Al into conventional<br />

gaps in the latter group of metals.<br />

Supported by DFG, project La 655/7-2 and SFB 463, TP B4.<br />

O 17.5 Di 12:15 H36<br />

Quantum-well states in thin films of Yb/W(110) studied by<br />

scanning tunnelling spectroscopy — •Daniel Wegner, Andreas<br />

Bauer, and Günter Kaindl — Freie Universität Berlin, Institut für<br />

Experimentalphysik, Arnimallee 14, 14195 Berlin-Dahlem<br />

We have studied the electronic structure of thin films of Yb/W(110)<br />

by low-temperature scanning tunnelling spectroscopy at 10 Kelvin.<br />

Quantum-well states around the Fermi energy, with small dispersion<br />

parallel to the film plane, result in a series of sharp, well resolved peaks<br />

in the tunnelling spectra. Due to the high lateral resolution of STS, the<br />

quantum-well states and their film-thickness dependence can be nicely<br />

observed on films with variations of the local thickness over a range<br />

of 10 monolayers. Close to the Fermi level, the electronic structure is<br />

complex.<br />

This work was supported by the DFG, Sfb-290.<br />

O 17.6 Di 12:30 H36<br />

Confinement and quantization of the Ag(111) surface state in<br />

hexagonal vacancy islands — •Henning Jensen, Jörg Kröger,<br />

and Richard Berndt — Institut für Experimentelle und Angewandte<br />

Physik, Universität Kiel, D-24098 Kiel, Germany<br />

The Shockley surface state of the noble metal (111) faces provides an<br />

experimentally accessible model system for a two-dimensional free electron<br />

gas. We report on the scattering and confinement of the Ag(111) surface<br />

state by hexagonal sputtering-induced surface defects of monatomic<br />

depth. Low-temperature STS measurements of the local density of states<br />

inside these defects reveal a series of resonance peaks, which are compared<br />

with potential well calculations and related experimental results.<br />

Examination of the line width vs. binding energy relation provides an<br />

estimate of surface state electron life time.<br />

O 17.7 Di 12:45 H36<br />

Electronic properties of a 2D-Superlattice of Ce Adatoms on<br />

Ag(111) — •M. Ternes 1 , C. Weber 2 , M. Pivetta 1 , F. Patthey 1 ,<br />

J. Pelz 3 , T. Giamarchi 4 , F. Mila 2 , and W.-D. Schneider 1 —<br />

1 Institut de Physique des Nanostructures, EPFL, CH-1015 Lausanne<br />

— 2 Institut de Physique Théorique, EPFL, CH-1015 Lausanne —<br />

3 Departement of Physics, The Ohio State University, Columbus, Ohio<br />

43210, USA — 4 DPMC, Université de Genève, CH-1211 Genève<br />

Recently we have shown that Ce adatoms on a clean Ag(111) surface<br />

form a hexagonal superlattice at liquid He temperatures [1]. This<br />

superlattice is created by long-range Ag(111) surface state mediated interactions<br />

between the Ce adatoms. We present here local STS measure-

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