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Plenarvorträge - DPG-Tagungen

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Chemische Physik und Polymerphysik Montag<br />

by AFM and by grazing incidence x-ray small angle scattering (GISAX).<br />

The LB-technique was found less effective than the gravity-sedimentation<br />

method. Using the latter we could prepare samples with a nearly monolayer<br />

covering (AFM).The GISAX measurement confirms that we produced<br />

an almost homogeneous covering over a large sample area (2 mm<br />

X 2 mm). Almost no agglomeration of colloidal spheres was observed.<br />

CPP 11.6 Mo 15:15 H 39<br />

Charged Interfaces of Colloidal Particles studied by Ellipsometric<br />

Scattering — •Andreas Erbe, Reinhard Sigel, and Klaus<br />

Tauer — Max Planck Institute of Colloids and Interfaces, D-14476<br />

Potsdam-Golm<br />

CPP 12 Colloids and Nanoparticles II<br />

A combination of conventional light scattering equipment with polarization<br />

optics can be used to obtain information about the interface<br />

between a colloidal particle and the solvent.<br />

Since charge-stabilized colloids are an important class of colloids, we<br />

investigate the influence of the salt (NaCl) concentration on the colloid’s<br />

interface. For this study, we use block copolymer particles with a<br />

water-insoluble core of Poly(methyl-methacrylate) and a water soluble,<br />

negatively charged layer consisting of Poly(styrenesulfonate).<br />

In addition, the behaviour of Poly(styrene) colloids stabilized by the<br />

surfactant perfluorooctancic acid (negatively charged under the chosen<br />

conditions) are investigated with low amounts of salt present.<br />

Zeit: Montag 15:45–17:15 Raum: H 39<br />

CPP 12.1 Mo 15:45 H 39<br />

SOLVENT-DEPENDENT CRYSTALLIZATION KINETICS<br />

OF COLLOIDAL PARTICLES — •Roy Goldberg, Patrick<br />

Wette und Thomas Palberg — Johannes Gutenberg-University<br />

Mainz, Institute of Physics, Staudingerweg 7, D-55099 Mainz<br />

For structural examinations of crystalline ordered particles and to avoid<br />

aging (Ostwald-ripening) and later coagulation it is advantageous that<br />

the crystals are kept in their original state. For this reason they will be<br />

imbedded in polymer matrices.<br />

By static light scattering we examined in which way the particleinteraction<br />

in a monomer-solution compared to aquatic dispersions with<br />

the same particle number density will change. Beside the investigation of<br />

structural parameters, the determination and comparison of crystallite<br />

sizes is possible and variations in the particle-interaction are thus directly<br />

observable . Additionally, changes in lattice features of colloidal crystals<br />

during imbedding in a polymer matrix and with further drying were investigated<br />

with microscopical methods as atomic-force-microscopy and<br />

electron-microscopy.<br />

CPP 12.2 Mo 16:00 H 39<br />

Wetting at the nanometric scale — •Hauke Schollmeyer 1 , Antonio<br />

Checco 2 , Jean Daillant 1,3 und Patrick Guenoun 1 —<br />

1 Service de Physique de l’Etat Condense, C.E.A. Saclay, F-91898 Orsay<br />

Cedex, France — 2 Department of Physics, Brookhaven National Laboratory,<br />

Upton, New York 11973 — 3 LURE, CNRS/CEA/MJENR, bat.<br />

209D, Centre Universitaire Paris-sud, F-91898 Orsay Cedex, France<br />

We have investigated the partial wetting of micrometric and nanometric<br />

alkane droplets on model substrates using true non-contact atomic<br />

force microscopy. The large droplet sizes accessible using this technique<br />

allowed us to determine the contact line curvature dependence of contact<br />

angle with unprecedented accuracy. Whereas previous studies aimed at<br />

explaining such a dependence by a line tension effect, our results and<br />

calculations on a model system exclude such an effect. Our results point<br />

to an extreme sensitivity to weak substrate heterogeneities confirmed by<br />

numerical simulations. Our goal is to prove this result for model substrates<br />

without heterogeneities. For this we use self assembled monolayer<br />

of long chained alkanes on silicon substrate. At room temperature these<br />

form a smooth and solid surface.<br />

CPP 12.3 Mo 16:15 H 39<br />

Electrophoretic investigations of surface-modified silica nanoparticles<br />

— •Holger Reiber and Thomas Palberg — Johannes<br />

Gutenberg-Universität, Institut für Physik, Staudingerweg 7, D-55099<br />

Mainz<br />

Because of strong coulombic interactions, dispersions of electrostatically<br />

stabilised colloidal silica particles show a characteristic behaviour<br />

in the case of very low salt conditions. The strength of the interactions<br />

between the single particles is a function of the surface charge, and therefore,<br />

it also influences electrophoretic properties as for example the particle<br />

mobility. For this reason, we investigate silica nano-particles which we<br />

synthesised using a variation of the Stöber-syntheses by means of laser<br />

Doppler velocimetry. The particles differ from each other only with respect<br />

to number and/or type of the ionic surface groups, but not with<br />

respect to typical properties such as diameter, density or polydispersity.<br />

For this reason, our measurements can show the influence of a variable<br />

surface charge on system properties of nano-particles such as the mobility.<br />

CPP 12.4 Mo 16:30 H 39<br />

Surface modification of carbon nanotubes: by deposition of<br />

nanosized — •Miguel Correa-Duarte and Michael Giersig —<br />

Caesar Research Center, Dept. Nanotechnology, Ludwig-Erhard Allee 2,<br />

53175 Bonn<br />

In this presentation we will discuss the covering of multi-walled carbon<br />

nanotubes (MWCNTs) with nanosized metallic and semiconductor<br />

nanoparticles. In the first step MWCNTs have been positively or<br />

negatively charged (depending on the nanoparticles charge) by covering<br />

with cationic poly(diallyldimethylammonium) chloride (PDDA) or<br />

anionic poly(sodium 4-styrenesulfonate) (PSS) polyelectrolyte. The following<br />

step was the deposition of nanosized metallic (Au, SiO2@Au) and<br />

semiconductor (CdSe, CdTe) particles. The successive covering process<br />

was optically registered and was correlated with the structural characterization<br />

by high resolution transmission and scanning electron microscopy.<br />

CPP 12.5 Mo 16:45 H 39<br />

ION DISTRIBUTION AT CHARGED INTERFACES —<br />

•Patrick Koelsch and Hubert Motschmann — Max-Planck-<br />

Institute of Colloids and Interfaces, Am Muehlenberg, 14476 Potsdam<br />

The distribution of ions close to a charged wall is a classical problem<br />

in colloid and interface science. The traditional approach consists in a<br />

mean field analysis of the counterion distribution leading to the Poisson-<br />

Boltzmann theory. Recently this field has attracted renewed attention<br />

with several theoretical papers addressing effects beyond the mean field<br />

level such as fluctuations, discreteness of charges or 2D-correlations.<br />

These papers reveal certain new features which are not captured in the<br />

mean field picture. We already demonstrated, that the combination of<br />

nonlinear (suface Second Harmonic Generation SHG) and linear optical<br />

technics (Ellipsometry) allows a direct determination of the prevailing<br />

ion distribution. A simple analytical expression was derived which can<br />

be used to retrieve the number of condensed counterions within the compact<br />

or so called Stern-layer. In this contribution we apply this formalism<br />

on experimental data gained on aqueous cationic surfactants by varying<br />

the counterions in order to quantify specific ion effects at the interface<br />

following the Hofmeister series. The derived formalism relates the ellipsometric<br />

signal to the surface charge and promises great potential in order<br />

to discard or proof recently published theoretical approaches.<br />

CPP 12.6 Mo 17:00 H 39<br />

High-resolution photoemission study of CdS nanoparticles with<br />

narrow size distribution: preparation, different sulfur components,<br />

and beam damage effects — •Sanjeev Joshi 1 , L. Weinhardt<br />

1 , C. Kumpf 1 , S. K. Kulkarni 2 , R. Fink 3 , C. Heske 1 , and<br />

E. Umbach 1 — 1 Exp. Phys. II, Univ. Würzburg, 97074 Würzburg —<br />

2 Dept. Physics, Univ. Pune, Pune 411 007, India — 3 Phys. Chem. II,<br />

Univ. Erlangen, 91058 Erlangen<br />

We report on high resolution X-ray photoemission data of very small<br />

CdS nanoparticles of two different sizes, 1.4 nm and 2.7 nm diameter,<br />

respectively. A detailed analysis is performed to identify the sizes and<br />

their distribution and the various signal constituents. The signal is composed<br />

of five S components, which can be assigned to the S atoms of<br />

the particle in different environments. The peak assignment is done by<br />

comparing the experimental data with intensity estimates, considering<br />

the intensity attenuation and contributions of the various S atoms using<br />

three structural models. Furthermore, it is discussed how beam damage

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