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Plenarvorträge - DPG-Tagungen

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Oberflächenphysik Dienstag<br />

able to demonstrate an optical resolution of 30 nm.<br />

[1] A. Naber et al., Phys. Rev. Lett. 89, 210801 (2002).<br />

O 23.2 Di 16:00 H36<br />

Energy dissipation in non-contact AFM — •Domenique Weiner,<br />

Andre Schirmeisen, and Harald Fuchs — Physikalisches Institut<br />

and CeNTech, University of Muenster, Wilhelm-Klemm-Str. 10, 48149<br />

Muenster, Germany<br />

The atomic force microscope (AFM) driven in the non-contact mode<br />

offers the possibility to measure long-range and short-range forces. Furthermore,<br />

energy dissipation mechanisms can be studied which are up<br />

to now not well-understood and are subject of current research [1]. One<br />

important step towards a better understanding of the energy dissipation<br />

is to study the temperature dependence of the effect [2].<br />

We measure the damping signal on a Au (111) surface which is prepared<br />

under ultra-high vacuum (UHV) conditions by sputtering and annealing.<br />

The commercial silicon cantilevers are covered with a PtIr-layer<br />

of about 30 nm thickness to ensure the measurement of a true metal contact.<br />

We use an UHV-VT-AFM (Omicron) which is integrated in a two<br />

chamber-apparatus. We investigate the frequency shift and the damping<br />

simultaneously as a function of tip-sample separation for different sample<br />

temperatures. Therefore we are able to gain quantitative values of<br />

the dissipation which are compared to current dissipation models like<br />

van der Waals friction [1], electrical dissipation [3] or dissipation induced<br />

by inhomogeneous tip-sample electric fields [2].<br />

[1] Volokitin, Persson, Phys. Rev. Lett. 91, 06101, 2003<br />

[2] B. C. Stipe, H. J. Mamin, T. D. Stowe, T. W. Kenny, D. Rugar,<br />

Phys. Rev. Lett. 87, 096801, 2001.<br />

[3] W. Denk, D. W. Pohl, Appl. Phys. Lett., Vol. 59, No. 17, 1991<br />

O 23.3 Di 16:15 H36<br />

Local interfacial dipoles of alkali chloride thin films on Au(111)<br />

investigated with Kelvin probe force microscopy — •Ulrich<br />

Zerweck, Christian Loppacher, Stefan Grafström, and<br />

Lukas M. Eng — Institute of Applied Photophysics, University of<br />

Technology, D-01062 Dresden<br />

Interface dipole formation of alkali chloride thin films on Au(111) is<br />

investigated under ultrahigh vacuum conditions at room temperature by<br />

noncontact atomic force microscopy in combination with Kelvin-probe<br />

force microscopy (KPFM). Sample preparation is carried out in-situ and<br />

optimized in order to achieve a sub-monolayer coverage on Au(111) with<br />

extended alkali chloride islands.<br />

The local surface potential for LiCl, NaCl, KCl, and RbCl thin films<br />

on Au(111) was determined by KPFM, with the bare Au(111) substrate<br />

serving as a reference. We thus directly probe the local and absolute<br />

change in the work function ∆Φ which is found to vary linearly as a<br />

function of the radius of the alkali ion. Furthermore, good agreement<br />

was obtained when checking our KPFM measurements with ultraviolet<br />

photoemission spectroscopy on a larger scale.<br />

O 23.4 Di 16:30 H36<br />

Scattering-type near-field microscopy for optical nanoanalytics<br />

— •Rainer Hillenbrand — Nano-Photonics Group, Max-Planck Institut<br />

für Biochemie, 82152 Martinsried<br />

We present a scattering-type scanning near-field optical microscope<br />

(s-SNOM) that allows optical imaging at 10nm spatial resolution [1] independent<br />

of the wavelength. In our s-SNOMs the tip apex of an atomic<br />

force microscope (AFM) is illuminated either by a HeNe laser at 633nm<br />

or a CO2 laser at about 10um wavelength. Interferometric detection [2]<br />

of the scattered light allows us to visualize the optical eigenfield patterns<br />

of 91 diameter, plasmon resonant nanoparticles at 633nm wavelength<br />

[3]. When operating the microscope at mid-infrared frequencies we find<br />

a strongly resonant near-field coupling between tip and a SiC sample<br />

due to local excitation of phonon polaritons in SiC [4]. Such phononenhanced<br />

near-field interaction is not only sensitive to the local chemical<br />

composition but also to the local crystal structure of the surface and<br />

thus allows besides chemical imaging also mapping of crystal quality at<br />

nanoscale resolution. Altogether, we envisage optical nanospectroscopy<br />

and imaging of physical, chemical and biological nanocomposites.<br />

[1] R. Hillenbrand, F. Keilmann, Appl. Phys. Lett. 80, 25 (2002)<br />

[2] R. Hillenbrand, F. Keilmann, Phys. Rev. Lett. 85, 3029 (2000)<br />

[3] R. Hillenbrand et.al., Appl. Phys. Lett. 83, 368 (2003)<br />

[4] R. Hillenbrand, T. Taubner, F. Keilmann, Nature 418, 159 (2002)<br />

O 23.5 Di 16:45 H36<br />

NanoSAM: Instrument characterisation at ultimate SAM resolution<br />

— •Jörg Westermann, Ulrich Roll, and Georg Schäfer<br />

— OMICRON NanoTechnology GmbH, 65232 Taunusstein<br />

During the last few years, we have developed a new electron source<br />

as an excitation source for UHV applications such as low voltage SEM,<br />

SAM / small spot Auger, cathodoluminescense and others (BMBF FKZ<br />

13N7486/7). Finally, we now report about the first results in small spot<br />

Auger and Scanning Auger Microscopy utilising this source. We present<br />

images and spectra demonstrating the ultimate lateral resolution and<br />

energy resolution of the setup on various samples. These include gold<br />

nanoparticles on HOPG, silver islands on silicon, and semiconductor heterostructures.<br />

Furthermore, we compare the achieved results with theoretical<br />

calculations and Monte Carlo simulations at different beam energies.<br />

O 23.6 Di 17:00 H36<br />

An Ultra High Vacuum Scanning Tunneling Microscope system<br />

operating at 300 mK and 14 T — •Focko Meier 1 , Jens<br />

Wiebe 1 , Andre Wachowiak 2 , Daniel Haude 1 , Markus Morgenstern<br />

1 , and Roland Wiesendanger 1 — 1 Institute of Applied<br />

Physics, Hamburg University, Jungiusstr. 11, D-20355 Hamburg, Germany<br />

— 2 University of California at Berkeley, Department of Physics,<br />

366 Le Conte Hall, 7300 Berkeley, CA 94720-7300, USA<br />

For scanning tunneling spectroscopy (STS) on low dimensional electron<br />

systems, an ultra high vacuum (UHV) scanning tunneling microscope<br />

(STM) operating at T=300 mK and in magnetic fields up to B=14<br />

T has been built up.<br />

The STM sitting in a bakeable UHV-insert within the 3 He-cryostat<br />

can be operated continuously for about 30 hours witout any refill of the<br />

cryogenic liquid. It achieves a z-noise level below 5 pm. Using superconducting<br />

tips and samples first experimental STS results show that the<br />

energy resolution reached is close to the predicted theoretical limit of 75<br />

µ V. For exchanging tips and samples the insert with STM can be moved<br />

to a UHV chamber. Further connected UHV chambers contain different<br />

equipment for tip and sample preparation and characterisation, i.e.<br />

a RT-STM , a LEED/Auger system, several evaporators and a variable<br />

temperature system to detect the magnetooptical Kerr-effect (MOKE).<br />

O 23.7 Di 17:15 H36<br />

SPM goes video rate and beyond — •M.J. Rost, T.H. Oosterkamp,<br />

J.W.M. Frenken, and et al. — Kamerlingh Onnes Laboratory,<br />

Leiden University, P.O. Box 9504, 2300 RA Leiden<br />

The low imaging rates of conventional scanning probe microscopes<br />

(SPMs) makes these instruments impractical for many applications. We<br />

have developed a novel, flexible SPM control system that can be easily<br />

connected to any SPM, which allows up to 50 Hz imaging rates with 256<br />

x 256 pixels per image. Since fast scanning is impossible without fast<br />

feedback electronics, we have also developed a low-noise STM-feedback<br />

system with a total bandwidth of 600 kHz (including the preamp). We<br />

present high-speed STM movies (images) with 25 Hz frame rate and tip<br />

speeds up to 0.3 mm/s while keeping atomic step resolution on Cu(001),<br />

obtained with a conventional STM. With a new, compact scanner we<br />

have even reached 200 Hz frame rate on graphite while still obtaining<br />

atomic resolution.<br />

O 23.8 Di 17:30 H36<br />

Apertureless SNOM with vibrating AFM probes — •Ralf Vogelgesang,<br />

Ruben Esteban, Alpan Bek, and Klaus Kern — MPI<br />

für Festkörperforschung, 70569 Stuttgart<br />

In the so called apertureless Scanning Near Field Optical Microscopy<br />

(a-SNOM), strongly localized enhancement of the near fields at the apex<br />

of a conical tip probe excited by external radiation is used to achieve<br />

spatial resolution of optical surface properties in the range ∼ 10 nm at<br />

infrared or visible frequencies.<br />

We use Multiple Multipole (MMP) simulations to quantitatively understand<br />

the interaction between the tip and substrate. We study the<br />

variations due to changing tip sample distance in the near field and consequently<br />

in the scattered far field, i.e., the measurable physical magnitude.<br />

For a better understanding of the level of sophistication necessary,<br />

different models are considered, ranging from a point dipole in the static<br />

case to spheres or a conical tip with spherical apex including retardation.<br />

In general two different regions are observed, slowly varying field<br />

strengths for distances of several hundred nm or more and rapid increases<br />

in field strengths for less than 10 nm. This strongly nonlinear dependence

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