Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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.