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Plenarvorträge - DPG-Tagungen

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Oberflächenphysik Montag<br />

UHV conditions lowers the density of thiole molecules at the Au(111)<br />

surface which results in an alignment of the thiole molecules parallel to<br />

the Au surface. The focus is on the properties of the line-structure phase<br />

with the lowest surface density [1][2]. Al clusters are evaporated on the<br />

regions of the thiol line-structure in order to investigate where the Al<br />

atoms adsorb. With the STM we find that the Al clusters preferably<br />

adsorb onto the sulphur head of the thiol. Additionally, we investigate<br />

in AFM measurements with Al functionalized tips the forces acting on<br />

different parts of the thiol chain.<br />

[1] Poirer G.E. Langmuir 1999, 15, 1167-1175<br />

[2] Staub R., Toerker M., Fritz T., Schmitz-Hübsch T., Sellam F., Leo<br />

K. Langmuir 1998, 14, 6693-6698<br />

O 14.75 Mo 18:00 Bereich C<br />

Nanoscale Conductivity Spectroscopy on Solid Electrolytes using<br />

an Atomic Force Microscope — •Ahmet Taskiran, Andre<br />

Schirmeisen, Harald Fuchs, Frank Natrup, and Harmut<br />

Bracht — Physikalisches Institut and CeNTech, University of Muenster,<br />

Wilhelm-Klemm-Str.10, 48149 Muenster, Germany<br />

Ion conducting solid materials play an important role as electrolytes<br />

in energy conversion systems, such as batteries and fuel cells, and also in<br />

electrochemical sensors. An important prerequisite for further progress<br />

in this field is a better understanding of the ion transport mechanisms<br />

on microscopic and nanoscopic length scales.<br />

We are using atomic force microscopy (AFM) to measure the ionic<br />

conductivity in nanoscale volumes of dielectric glasses. The AFM is operated<br />

in the non-contact mode in vacuum. After a sudden change of the<br />

tip voltage, the relaxation of the electrostatic force between tip and sample<br />

is measured as a function of time. We measure these relaxation curves<br />

as a function of sample temperatures ranging from 100K to 675K. The<br />

observed relaxation curves are fitted well with a stretched exponential<br />

function and we can determine the activation energy of the conduction<br />

processes of the ions. First results indicate a good agreement of the activation<br />

energies for several prototype ionic glas conductors with values<br />

from macroscopic measurements. This method allows us to study fundamental<br />

processes of ionic transport and is in particular interesting for the<br />

investigation of nanostructured solid electrolytes.<br />

O 14.76 Mo 18:00 Bereich C<br />

Optical phase effects and resonance shift in scattering-type<br />

near-field infrared microscopy — •Thomas Taubner 1 , Fritz<br />

Keilmann 1 , and Rainer Hillenbrand 2 — 1 Max-Planck-Institut für<br />

Biochemie, Am Klopferspitz 18a, 82152 Martinsried — 2 Nano-Photonics<br />

Group, Max-Planck-Institut für Biochemie, Am Klopferspitz 18a, 82152<br />

Martinsried<br />

A scattering-type near-field optical microscope (s-SNOM) detects light<br />

scattered at the sharp tip of a probing needle and allows imaging with<br />

subwavelength resolution, independent of the wavelength used for illumination[1].<br />

We now study amplitude and phase of light scattered from a s-<br />

SNOM’s tip probing a flat SiC sample, at mid-infrared frequencies where<br />

surface phonon polaritons resonantly enhance the tip-sample near-field<br />

interaction [2]. A nanometer-scale variation of the gap width between tip<br />

and sample causes the optical phase to change dramatically and the resonance<br />

to shift. Both effects can be explained by theory that treats the<br />

system as a point dipole (tip) interacting with its image dipole (sample),<br />

in electrostatic approximation. The phase effects and resonance shifts are<br />

not restricted to phonon polariton excitation in polar dielectrics like SiC,<br />

but should be observable also for resonances related to plasmons and<br />

excitons.<br />

[1] T. Taubner, R. Hillenbrand and F. Keilmann, Journal of Microscopy<br />

210, 311 (2003)<br />

[2] R. Hillenbrand, T. Taubner and F. Keilmann, Nature 418, 159<br />

(2002)<br />

O 14.77 Mo 18:00 Bereich C<br />

Investigations on nanocrystals in silicondioxide by atomic force<br />

microscopy — •E. Beyreuther 1 , R. Beyer 1 , K. Walzer 1 , S.<br />

Behrendt 1 , V. Beyer 2 , J. von Borany 2 , J. Weber 1 , and L. Eng 1<br />

— 1 Technische Universität Dresden, Institut für Angewandte Physik, D-<br />

01062 Dresden — 2 Forschungszentrum Rossendorf, Institut für Ionenstrahlphysik<br />

und Materialforschung, PF 510119, D-01314 Dresden<br />

Nanocrystals in SiO2 are promising structures for future optoelectronic<br />

and memory devices. Optimization of the synthesis process needs detailed<br />

information about structure and morphology.<br />

Within the present work SiO2 layers of 100 nm thickness were ther-<br />

mally grown on Si(100). Subsequently Si or Ge nanocrystals were fabricated<br />

within those oxide films by ion implantation and rapid thermal<br />

annealing. Etching in buffered HF-solution with a low rate of 12nm/min<br />

removed the top oxide layer and uncovered the nanocrystals to a certain<br />

depth. The surfaces of several samples, which had undergone varied<br />

implantation and annealing conditions as well as different etching times<br />

were imaged by tapping-mode AFM down to scan sizes of 200x200 µm 2 .<br />

The apparent nanocrystal size and density were found to be dependent<br />

on the synthesis parameters and the position within the oxide layer.<br />

In comparison to TEM investigations of the same structures we discuss<br />

critically the determination of the cluster size.<br />

O 14.78 Mo 18:00 Bereich C<br />

Detection of dopant profiles in silicon by scanning capacitance<br />

microscopy and related techniques: the role of the passivation<br />

layer — •Reinhard Beyer 1 , Elke Beyreuther 1 , Bernd<br />

Schmidt 2 , Stefan Polzin 3 , and Jörg Weber 1 — 1 Technische Universität<br />

Dresden, Institut für Angewandte Physik, D-01062 Dresden —<br />

2 Forschungszentrum Rossendorf, Institut für Ionenstrahlphysik und Materialforschung,<br />

PF 510119, D-01314 Dresden — 3 Fraunhofer-Institut für<br />

Photonische Mikrosysteme, Grenzstrasse 28, D-01109 Dresden<br />

Scanning capacitance microscopy (SCM) was employed for the study<br />

of dopant profiles in silicon test structures. The samples were fabricated<br />

by implantation of boron and phosphorous into n-type silicon. The oxide<br />

mask for the implantation was shaped by photolithography. Hence,<br />

stripe patterns with a size of 2 µm of the implanted region and different<br />

widths of the interregion were obtained. The implantation dose was<br />

5 × 10 12 , 5 × 10 13 and 5 × 10 14 cm −2 for both implanted ions. Samples<br />

with native oxide coverage and with a 7 nm thick silicondioxide layer<br />

were compared in this study. SCM measurements were performed in the<br />

contact-mode. We show, that the contrast of the SCM signal between<br />

differently doped regions depends not only on the dc bias applied during<br />

the scan, but also on charge instabilities and trapping effects. The latter<br />

appeared mostly for samples with native oxide and resulted in hysteresis<br />

effects which could be observed with local dC/dV vs. V spectroscopy.<br />

The charge instabilities are discussed in a MOS-model. The results are<br />

compared with scanning spreading resistance measurements and with<br />

non-contact SCM.<br />

O 14.79 Mo 18:00 Bereich C<br />

Study of particle-substrate interaction by nanomanipulation experiments<br />

with dynamic scanning force microscopy — •Claudia<br />

Ritter 1 , Markus Heyde 2 , and Klaus Rademann 1 — 1 Humboldt-<br />

Universität zu Berlin, Institute of Chemistry, Brook-Taylor-Str. 2, D-<br />

12489 Berlin, Germany — 2 Fritz-Haber-Institute of the Max-Planck-<br />

Society, Faradayweg 4-6, D-14195 Berlin, Germany<br />

We utilise an advanced homebuilt SFM in the dynamic mode, in<br />

conjunction with a special homebuilt software, to perform precise<br />

nanomanipulation experiments. The corresponding experimental technique<br />

should be denoted as Dynamic Surface Modification (DSM), comprising<br />

both the dynamic technique of the SFM, as well as the manipulation<br />

(translation, in-plane rotation, cutting) of structurally unchanged<br />

particles on a given substrate surface. It is easily possible to switch between<br />

imaging mode and DSM mode, enabling the direct manipulation<br />

of nanoparticles under ambient conditions with high precision and simultaneously<br />

studying particle-substrate interaction to give evidence about<br />

motion and tribological values of the sample system. We have successfully<br />

manipulated miscellaneous nanoparticles on surfaces, e.g. antimony<br />

islands, gold islands, tin islands, nanotubes, small latex spheres as well<br />

as cells.<br />

O 14.80 Mo 18:00 Bereich C<br />

In-situ SPM usage at MOVPE-conditions — •Markus<br />

Breusing, Bert Rähmer, Raimund Kremzow, and Wolfgang<br />

Richter — TU-Berlin, Institut für Festkörperphysik, Hardenbergstr.<br />

36, 10623 Berlin<br />

In-situ scanning probe techniques which are applicable in an MOVPE<br />

growth environment to directly give quantitative information about the<br />

nano-scale topography of the sample do not exist up to now.<br />

Developing a SPM for in-situ MOVPE measurements requires a completely<br />

new setup. In comparison to the commercially available SPMsolutions,<br />

a number of additional problems have to be solved. The limited<br />

space in the MOVPE reactors and the high temperature caused by the<br />

thermal conductivity of the carrier gas during growth near the suszeptor<br />

requires a special design of the components of the SPM. On the other

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