Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Chemische Physik und Polymerphysik Montag<br />
Fachsitzungen<br />
– Haupt-, Kurzvorträge und Posterbeiträge –<br />
CPP 1 Polymer Surfaces I<br />
Zeit: Montag 09:30–10:45 Raum: H 37<br />
Hauptvortrag CPP 1.1 Mo 09:30 H 37<br />
Thin, nanostructured block copolymer films — •Christine M.<br />
Papadakis — Fakultät für Physik und Geowissenschaften, Universität<br />
Leipzig, now at Physik Department, Technische Universität München<br />
Block copolymer films can be used for patterning surfaces on a submicrometer<br />
length scale. In order to understand the surface structures<br />
observed as well as their stability and their response to outer stimuli, it<br />
is important to gain knowledge both on the surface structures as well<br />
as on the inner film structure. The combination of direct visualization<br />
of the surface texture by atomic force microscopy with scattering methods<br />
elucidating the inner film structure has proven to give a wealth of<br />
information. By means of grazing-incidence small-angle X-ray scattering<br />
(GISAXS), structures normal to the substrate as well as lateral structures<br />
can be detected simultaneously. In addition, time-resolved GISAXS<br />
measurements can be used to study the structural changes of the films<br />
upon outer stimuli in-situ. In my talk, I will present results on thin films<br />
of a series of polystyrene-polybutadiene diblock copolymers, where we<br />
have found a previously unknown molar-mass dependence of the lamellar<br />
orientation. The structural changes of he films when subjected to a<br />
vapor atmosphere were monitored in-situ.<br />
CPP 1.2 Mo 10:00 H 37<br />
Volume Phase Transition of PNIPAM-Microgel Paricles Studied<br />
with Laser-AFM — •Lothar Zitzler 1 , Frieder Mugele 1 ,<br />
and Stephan Herminghaus 1,2 — 1 Angewandte Physik, Universität<br />
Ulm, Albert-Einstein-Allee 11, 89081 Ulm — 2 Max-Planck-Institut für<br />
Strömungsforschung, Bunsenstraße 10, 37073 Göttingen<br />
Poly(N-isopropylacrylamide) (PNIPAM) is a polymer with a lower critical<br />
solution temperature (LCST) of TLCST ≈ 32˚C. It shows a conformational<br />
change from a coil to a globule state upon increasing the temperature<br />
above TLCST. Here we present AFM-studies (in aqueous environment)<br />
of PNIPAM-co-poly(vinyl acetic acid) microgel particles adsorbed<br />
on glass substrates. Like in solutions the adsorbed particles also show<br />
a pronounced change in volume of approximately 200% with respect to<br />
the globular state. The different elastic properties of the particles in the<br />
coil and globular states could be distinguished clearly in amplitude- and<br />
phase-distance curves, obtained by AFM in Tapping Mode.<br />
To study the dynamics of this coil to globule transition we combined the<br />
AFM with an intense cw-laser (5W at 532nm). We generated laser pulses<br />
of variable width (10ns-100µs) with an acousto-optical modulator. The<br />
laser pulses were used to trigger the volume phase transition by heating<br />
the particles above TLCST. By synchronizing the laser pulses with<br />
CPP 2 Polymer Surfaces II<br />
the cantilever oscillation and by varying the relative time delay one can<br />
obtain information on the dynamics of the phase transition.<br />
CPP 1.3 Mo 10:15 H 37<br />
Influence of the chain microstructure in the surface properties<br />
of polyketone terpolymers — •Sabine Hild 1 , Othmar Marti 1 ,<br />
Frank Hollmann 2 , David Perez Foullerat 2 , and Bernhard<br />
Rieger 2 — 1 Experimental Physics, University of Ulm, Albert-Einstein-<br />
Allee 11, 89081 Ulm — 2 Inorganic Chemistry II, University of Ulm,<br />
Albert-Einstein-Allee 11, 89081 Ulm<br />
Terpolymers of carbonmonoxide (CO), ethene and propene combine<br />
unique physical properties with intrinsic hydrophilic properties. Tailoring<br />
the chain microstructure of such polyketones lead to polymeric materials<br />
with adjustable mechanical properties. The aim of this study is<br />
to investigated if also surface properties, resp. the surface energy, can be<br />
influenced by varying the block structure of the copolymers. For this purpose<br />
ethylene-CO-propylene-CO-(ECO-PCO) and ethylene-CO-hexene-<br />
CO-(ECO-HCO) terpolymers with similar amount of ECO but different<br />
block length have been synthesized. This results in copolymers featuring<br />
either a triblock or multiblock structure. The surface morphology of this<br />
terpolymers is investigated by Scanning Force Microscopy. The surface<br />
tension has been estimated by from surface tension measurement. It has<br />
been found, that if the ECO content is higher than 50 percent the surface<br />
properties are determined by the microstructure of the ECO phase.<br />
CPP 1.4 Mo 10:30 H 37<br />
AFM-studies of layered Au/hexaphenyl nanofiber systems —<br />
•Laxman Kankate 1 , Frank Balzer 1 , Horst Niehus 1 , and Horst-<br />
Günter Rubahn 2 — 1 Humboldt-Universität zu Berlin, Institut für<br />
Physik / ASP — 2 SDU Odense, Fysisk Institut, Denmark<br />
In this paper we study in detail the growth of parahexaphenyl<br />
nanofibers on ultrathin Au layers on mica. We use fluorescence microscopy<br />
and atomic force microscopy to obtain the size distribution and<br />
the alignment of the nanofibers. As a function of the thickness of the<br />
Au layer in the range between 1 and 5 nm it is observed that the alignment<br />
of the fibers decreases, whereas for thicker Au films no alignment<br />
at all with the mica electric surface dipoles has been found. The mean<br />
length of the fibers decreases from several ten µm to 1 µm, but their<br />
mean height increases from 50 nm to 300 nm. Such sandwich systems of<br />
organic and metallic constituents are important model systems for future<br />
nanoelectronic applications.<br />
Zeit: Montag 11:00–12:30 Raum: H 37<br />
CPP 2.1 Mo 11:00 H 37<br />
Scanning thermal microscopy for investigation of mechanical<br />
properties of thin polymer films — •Martin Hinz 1 , Andreas<br />
Kleiner 1 , Sabine Hild 1 , Othmar Marti 1 , Urs Dürig 2 , Bernd<br />
Gotsmann 2 , Ute Drechsler 2 , Peter Vettiger 2 , and Tom R. Albrecht<br />
2 for the IBM Research Division, Zurich Research Laboratory,<br />
Switzerland collaboration — 1 Department of Experimental Physics, University<br />
of Ulm, D-89069 Ulm — 2 IBM Research Division, Zurich Research<br />
Laboratory, CH-8803 Rüschklikon<br />
Mechanical properties of bulk polymers have been investigated by different<br />
methods over decades, but in recent times the mechanics of thin<br />
polymer films became of large interest. Scanning Force Microscopy (SFM)<br />
provides a possibility to probe mechanical properties on nanometer scale.<br />
In this study Scanning thermal microscopy (SThM) is applied to investigate<br />
the temperature dependent indentation process of a pulse heated<br />
SFM-tip (heating pulse less than 100 Mikroseconds) with tip temperatures<br />
between 300 and 500 ◦ C on Polymethylmethacrylate films of 35<br />
nm thickness which were produced by spin-coating on Silicon substrates.<br />
Additional application of an electro-static force acting between tip and<br />
sample enhances the indentation process. Additionally these experiments<br />
are carried out on samples heated on a heating device. The remanent topography<br />
is analysed as function of tip and sample temperature, heating<br />
pulse duration and electrostatic force.<br />
CPP 2.2 Mo 11:15 H 37<br />
Homo- and heteropolymer adsorption onto homogeneous<br />
and chemically structured surfaces: the role of correlations<br />
— •Alexey Polotsky, Andreas Degenhard, and Friederike<br />
Schmid — Universität Bielefeld, Fakultät für Physik, Universitätsstraße<br />
25, 33615 Bielefeld<br />
Using a variational approach, an analytical theory of adsorption was