Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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