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Plenarvorträge - DPG-Tagungen

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Chemische Physik und Polymerphysik Dienstag<br />

sis) which would provide temporal as well as local information about the<br />

chemical environment if one labels the host (or guest) molecule with an<br />

atomic marker. To this end, we labelled Calixarenes with iodine markers<br />

and attached them to gold substrates with dialkyl-sulfide linkers. The<br />

film stechiometry, thickness and density were studied with XPS, AFM<br />

and imaging ellipsometry, respectively. The results support the expected<br />

elemental composition and a film thickness compatible with the molecular<br />

orientation perpendicular to the surface.<br />

CPP 16.20 Di 17:00 B<br />

Single Molecule Diffusion under Confinement and Shear —<br />

•Arne Schob und Frank Cichos — Institut für Physik 123705, TU<br />

Chemnitz, 09107 Chemnitz<br />

Liquids at solid surfaces may show a completely different structure<br />

compared to the bulk structure, since they may form a layering structure<br />

parallel to the surface. Such a structural difference immediately implies<br />

dynamical differences, which shows up in an anisotropic Brownian motion<br />

or even in a different shear viscosity. An understanding of this behavior is<br />

a key to understand lubrication and friction on a molecular scale. We employ<br />

fluorescent dye molecules to measure molecular mobility in ultrathin<br />

liquid films confined between two atomically flat surfaces. We use highly<br />

doped liquid films to measure the film thickness as a function of applied<br />

force. In this way we are able to calibrate our setup for single molecule<br />

experiments and to compare our results with other publications. Single<br />

molecules are tracked with a wide field fluorescence microscope coupled<br />

to a surface forces apparatus. The experiments show, that corresponding<br />

to measurements on free liquid films the diffusion of molecules is slowed<br />

down due to the interaction with the solid interface. We are further able<br />

to apply shear to the liquid film by moving one of the confining solid surfaces.<br />

By seperating their diffusive motion from the shear-driven motion,<br />

we have acces to the velocity within the sheared liquid on a molecular<br />

scale.<br />

CPP 16.21 Di 17:00 B<br />

Single Molecule Adsorption and Desorption on Solid Surfaces<br />

— •Jörg Schuster 1 , Frank Cichos 2 , and Christian von Borczyskowski<br />

1 — 1 Institut für Physik 121501, TU Chemnitz, 09107<br />

Chemnitz — 2 Institut für Physik 123705, TU Chemnitz, 09107 Chemnitz<br />

Adsorption and desorption are key elements in many processes in physical<br />

chemistry such as self assembly, self organization, surface chemical<br />

reactions or even chromatography. By means of single molecule tracking<br />

in wide field fluorescence microscopy we are able to follow directly the<br />

absorption and desorption of molecules on a solid surface. Experiments<br />

on ultrathin liquid films on solid surfaces show, that the re-adsorption<br />

process of single molecules on the surface is directly influenced by the<br />

reduced film thickness. While the re-adsorption time for a molecule at a<br />

liquid solid boundary is usually expected to follow a power law statistics,<br />

we observe an exponential statistics for liquid films of a few nanometer<br />

thickness. The exponential statistics is the result of the reflection of dye<br />

molecules on the liquid vapor interface. Therefore the mean re-adsorption<br />

time gets finite compared to an infinite time in the bulk and shows further<br />

an exponential tail. The decay time of the exponential tail is directly<br />

related to the film thickness and the diffusion constant perpendicular to<br />

the surface. The measurement of the film thickness and the re-adsorption<br />

statistics thus allows for the first time the determination of the diffusion<br />

constant perpendicular to the surface in a 4 nm film. The experiments<br />

show, that this diffusion is slowed down by 4 orders of magnitude compared<br />

to the in plane diffusion. Thus diffusion in liquid films close to solid<br />

surfaces can be extremely anisotropic.<br />

CPP 16.22 Di 17:00 B<br />

Roughness-Induced Acoustic Second Harmonic Generation<br />

(ASHG) During Electrochemical Metal Deposition on the<br />

Quartz Crystal Microbalance — •Katrin Wondraczek 1 ,<br />

Susanne Wehner 2 , Andreas Bund 2 , and Diethelm Johannsmann<br />

1 — 1 Institut fuer Physikalische Chemie, TU Clausthal,<br />

Arnold-Sommerfeld-Str. 4, D-38678 Clausthal-Zellerfeld — 2 Institut fuer<br />

Physikalische Chemie und Elektrochemie, TU Dresden, Mommsenstrasse<br />

13, D-01062 Dresden<br />

When operating a quartz crystal with a rough surface in liquids, there<br />

is an emission of shear and compressional waves at twice the frequency<br />

of the exciting wave (acoustic second harmonic generation, ASHG). We<br />

used electrochemically deposited copper layers whose roughnesses could<br />

be tuned via current density.<br />

Roughness is a source of ASHG if the liquid flow at the surface is<br />

not entirely laminar. The calculation of the Reynolds number shows that<br />

slight deviations from laminar flow can be reached at high amplitudes of<br />

shear oscillation. However, nonlinear effects in the operation of the QCM<br />

in liquids are small.<br />

Our experiments show that a rough surface is much more efficient<br />

in generating acoustic second harmonic waves than a smooth one. We<br />

present a model that relates ASHG to a roughness parameter independently<br />

obtained from resonance frequency and bandwidth. Such a parameter<br />

allows to distinguish the effects of trapped liquid and hydrodynamics<br />

on rough surfaces from the effects of deposited mass.<br />

CPP 16.23 Di 17:00 B<br />

Phtalocyanines at ZnO-Single Crystals — •Peter Kunze 1 , Malgorzata<br />

Boruszczak 2 , Christine Mattheus 1 , Derck Schlettwein<br />

1 , and Katharina Al-Shamery 1 — 1 Institute of Pure and Applied<br />

Chemistry, Faculty V, University of Oldenburg, Oldenburg, Germany<br />

— 2 Uniwersytet Lodz, Lodz, Poland<br />

The aim of this study is to build up solar cells made of zinc oxide<br />

and organic pigments, especially phthalocyanines and perylenes. This requires<br />

accurate knowledge about the structures and binding between the<br />

Zinc oxide and the organic component. In a UHV-chamber phthalocyanines,<br />

subphthalocyanine and MePTCDI have been deposited onto Zinc<br />

oxide of (0001)- and (10-10)-orientation. UV-VIS measurements reveal<br />

the formation of different film morphologies depending on the different<br />

surface orientations of zinc oxide. RHEED investigations showed no lateral<br />

ordering of the phthalocyanines either at the (0001) or the (10-10)<br />

surface. Additionally AFM measurements have been performed on these<br />

samples. They indicate Vollmer-Weber growth with Islands up to 15nm<br />

height and up to 100nm width at ZnO (0001). At ZnO (10-10) Stranski-<br />

Krastanov-growth is observed with the build up of closed monolayers on<br />

which islands of about 10nm height and up to 40nm width can be found.<br />

None of the phthalocyanines, but PcVO showed lateral ordering in the<br />

RHEED pictures. According to the AFM pictures PcVO showed elongated<br />

islands of about 100nm length and only 10nm width which appear<br />

to be ordered in small domains. Beside domains of different orientations<br />

unordered areas could be seen as well. This supports the results of the<br />

RHEED investigations.<br />

CPP 16.24 Di 17:00 B<br />

Debonding of pressure sensitive adhesives — •E. Maurer 1 , S.<br />

Loi 1 , E. Bauer 1 , T. Mehaddene 1 , S. Cunis 2 , and P. Müller-<br />

Buschbaum 1 — 1 TU München Physik Department LS E13, James-<br />

Franck-Str.1, 85747 Garching — 2 HASLYAB, Notkestr. 85, 22607 Hambung<br />

important class in adhesive technology. Typical examples in daily life<br />

are adhesive stickers, Scotch tape or stick-on notes. Symptomatic for this<br />

kind of adhesives is the dependence of adhesions quality on the bonding<br />

history. Important parameters are contact pressure and contact time. In<br />

most applications of PSA later a controlled debonding of the glued devices<br />

is desired. Despite high technological relevance, the physical mechanism<br />

of adhesion are still not fully understood. In addition the function of<br />

the fibrils appearing during debonding is not sufficiently clear. A macroscopic<br />

understanding of adhesion is provided by the so called tack test.<br />

A cylindrical punch is pressed under defined conditions (contact force,<br />

contact time) onto an adhesive film. While redrawing the punch with<br />

a constant velocity the force is measured. A microscopic investigation<br />

of the adhesion can be achieved by a scattering experiment during the<br />

tack test. We applied small angle x-ray scattering (SAXS). The combination<br />

of both, macroscopic mechanical data and microscopic information,<br />

is a promising attempt on the way to a detailed understanding of the<br />

mechanism underlying adhesion.<br />

CPP 16.25 Di 17:00 B<br />

Ultra-fast calorimetry using thin film sensor — •Sergey<br />

Adamovsky and Christoph Schick — Universitätsplatz,3, 18055,<br />

Rostock, Germany<br />

An application of an ultra-fast thin film calorimeter to polymer materials<br />

is described. A commercially available sensor, thermal conductivity<br />

gauge TCG-3880 (Xensor Integrations, NL) was utilized as a measuring<br />

cell for calorimetric measurements. The sensor consists of a 500-nm<br />

thin SiN membrane with a semiconducting heater and a semiconducting<br />

thermopile, which are produced using integrated-circuit (IC) technology.<br />

To allow fast scanning, sample size should be small too. Samples with<br />

masses of about 100 nanograms were measured.<br />

Heating as well as cooling with rates up to 10,000 K/s were realized.

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