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Plenarvorträge - DPG-Tagungen

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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

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