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Plenarvorträge - DPG-Tagungen

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Symposium Organic and Hybrid Systems for Future Electronics Donnerstag<br />

or bionic devices require a high degree of functionality as well as a good<br />

stability of surfaces against degradation. In this context, the nanopatterning<br />

of organically modified surfaces has attracted great attention<br />

because such functionalized surfaces offer an excellent passivation and<br />

at the same time the possibility to attach different biological species<br />

(including DNA, proteins and complex systems). In the present work,<br />

strategies for the nanopatterning of chemically modified silicon surfaces<br />

using different lithographic approaches will be presented. It will be shown<br />

that organic monolayers can be used as a new class of organic-based resists<br />

for direct electron-beam writing as well as atomic force microscope<br />

nanoscratching. The use of organic monolayers as positive or negative<br />

resists will be highlighted by exploiting the contrast in reactivity via<br />

chemical deposition (electroless technique) and plating of metals. The<br />

high resolution achieved through the use of such organic-based resists<br />

will be discussed.The processes presented here open new perspectives for<br />

selective deposition and direct patterning of Si surfaces and can be used<br />

not only for chemical and electrochemical nanogrowth but also for the<br />

nanopatterning of chemical and relevant biological species on semiconductor<br />

surfaces.<br />

SYOH 5.10 Do 18:00 B<br />

Blinking and Emission Quenching of CdSe Nanocrystals in Organic<br />

Environments — •Thomas Blaudeck 1 , Abey Issac 2 , Frank<br />

Cichos 1 , Edward Zenkevich 3 , Alexander Shulga 3 , and Christian<br />

von Borczyskowski 2 — 1 Institut für Physik 123705, TU Chemnitz,<br />

09107 Chemnitz — 2 Institut für Physik 121501, TU Chemnitz,<br />

09107 Chemnitz — 3 Institute of Molecular and Atomic Physics and<br />

B.I. Stepanov Institute of Physics National Academy of Sciences, 70 F.<br />

Skaryna Avenue, 220072 Minsk, Belarus<br />

The interaction of ZnS capped CdSe nanocrystals with their environment<br />

is studied on an ensemble and single nanocrystal (NC) level. Individual<br />

CdSe NC’s show an emission intermittency (blinking), which<br />

is commonly related to an NC photo-ionization by electron tunneling.<br />

The statistics of this blinking is found to be independent of the studied<br />

NC even though NCs may differ in size and local structure of the<br />

surrounding polymer matrix. We analyze the obtained blinking statistics<br />

in terms of charge diffusion through trap states in the NCs vicinity and<br />

further compare this to current blinking model. Despite the insensitivity<br />

of the blinking process to the surrounding polymer matrix a strong interaction<br />

between CdSe NCs and pyridyl containing porphyrin molecules<br />

is found. The porphyrin molecules self-organize on the NC surface by<br />

ligation effects. The interaction of porphyrin and NC introduces a fast<br />

non-radiative decay of the NC emission, which is ascribed to an electron<br />

transfer process by electron tunneling. The dependence of this tunneling<br />

process on the NC size is discussed.<br />

SYOH 5.11 Do 18:00 B<br />

Temperature-Dependent Growth of Porphyrin and Phthalocyanine<br />

Thin Films on Modified Silicon Surfaces — •Christian<br />

Kelting 1 , Ossamah Abdallah 2 , Marinus Kunst 2 , Natalia<br />

Bazyakina 3 , Dieter Wöhrle 3 , and Derck Schlettwein 1 —<br />

1 Physical Chemistry 1, University of Oldenburg, Germany — 2 Hahn-<br />

Meitner- Institute, Berlin, Germany — 3 Institute of Organic and<br />

Macromolecular Chemistry, University of Bremen, Germany<br />

Films of phthalocyaninatozinc (PcZn) and Tetraphenylporphyrinatozinc<br />

(TPPZn) were evaporated on thin films of microcrystalline Si and<br />

on hydrogen-terminated Si-wafers (111) as a model surface for microcrystalline<br />

Si under conditions of its preparation. The goal is to embed<br />

molecular sensitizers into microcrystalline Si as a new concept for thin<br />

film solar cells. The maximum substrate temperature for a successful deposition<br />

of PcZn and TPPZn was determined to 523 K for PcZn and 423<br />

K for TPPZn on H-Si (111). UV-Vis differential reflection spectroscopy<br />

was measured in situ. At 300 K, a 50 nm PcZn film survived for 5h, but<br />

slowly evaporated during this time. The morphology of the deposited<br />

films was investigated by atomic force microscopy. Larger particles with<br />

well- defined shape indicating crystallinity of the films were detected at<br />

these higher substrate temperatures. Changes in the crystal structure<br />

of PcZn were also observed on the silicon substrates. The alpha- modification<br />

of PcZn was found in depositions at 298 K whereas the betamodification<br />

was formed at 523 K.<br />

SYOH 5.12 Do 18:00 B<br />

The influence of carbon on the mono- and multilayer growth of<br />

p-quaterphenyl on Au(111) — •Adolf Winkler, Stefan Muellegger,<br />

Thomas Haber, and Roland Resel — Solid State Physics,<br />

Graz University of Technology<br />

The tailoring of the growth mode of ultra-thin organic films is of utmost<br />

importance for the application of electronic and optoelectronic devices.<br />

As a model system we have studied the monolayer adsorption and the<br />

multilayer growth of p-quaterphenyl on clean and carbon covered gold<br />

(111) surfaces. TDS, XPS, LEED and XRD-pole figure technique have<br />

been applied for these investigations. In TDS, the monolayer peaks are<br />

quite different for the Au(111) and Au(111)+C surface. Also LEED shows<br />

pronounced differences. The evaluation of the LEED patterns, in combination<br />

with quantitative TDS, suggests a monolayer structure with flat<br />

lying and side tilted 4P molecules on the clean, but with only side tilted<br />

molecules on the C-covered surface. These different monolayer structures<br />

lead to different multilayer film structures, as verified by XRD-pole figure<br />

technique and XPS. In the former case island growth is preferred,<br />

whereas in the latter case layer-like growth dominates.<br />

SYOH 5.13 Do 18:00 B<br />

Morpholoy and growth of organic semiconductor films on metal<br />

surfaces — •S. Söhnchen, S. Lukas, G. Beernink, K. Hänel, A.<br />

Birkner, G. Witte, and C. Wöll — Physikalische Chemie I, Ruhr-<br />

Universitaet Bochum<br />

Organic semiconducting materials have experienced a tremendous<br />

amount of attention because of the recent breakthrough in using such<br />

materials as active components in electronic or optoelectronic devices.<br />

Of particular interest for an optimization of such devices is a detailed<br />

understanding of the crystalline structure and growth properties of thin<br />

organic semiconductor films deposited on inorganic substrates.<br />

In this talk we compare the growth properties observed for pentacene<br />

and perylene films grown by OMBE on copper and gold<br />

single crystal surfaces as well as on a SAM modified gold surface.<br />

Although some of these films are well ordered and partly reveal even<br />

an epitaxial growth relation with respect to the substrate [1] they all<br />

have a large tendency for dewetting which causes the formation of islands.<br />

[1] Lukas et al. Chem. Phys. Chem (in press)<br />

SYOH 5.14 Do 18:00 B<br />

The Growth of Pentacene on Gold — •F.-J. Meyer zu Heringdorf<br />

1,2 , M.C. Reuter 1 , and R.M. Tromp 1 — 1 IBM T.J. Watson<br />

Research Center, Yorktown Heights, USA — 2 present address:Inst. für<br />

Laser- und Plasmaphysik, Universität Duisburg-Essen (Campus Essen)<br />

We used Low Energy Electron Microscopy and Atomic Force Microscopy<br />

to compare the growth of pentacene on Si(111) with the growth<br />

of pentacene on Au. In the LEEM Au films are prepared on Si(111)<br />

at elevated temperatures and their formation is monitored using quasisimultaneous<br />

imaging at different dark field conditions. At low coverages,<br />

Au forms a (5 × 2) reconstruction on the Si(111) substrate, and pentacene<br />

is observed to grow in the thin film phase, similar to growth on<br />

clean silicon. At coverages beyond 3/4 ML of Au, however, a ( √ 3 × √ 3)<br />

reconstruction is formed that causes the orientation of the pentacene<br />

film to rotate by almost 90 ◦ . The same result is found for pentacene on<br />

thick polycrystalline Au films. The adsorption of organic self-assembled<br />

monolayers (SAMs) prior to deposition of pentacene has been reported<br />

to improve the electrical contact between Au and pentacene. Here we<br />

show that thiol based SAMs on Au can restore the growth direction of<br />

pentacene to a crystal orientation as seen on Si. This demonstrates that<br />

carefully chosen organic substrate termination layers are likely to play a<br />

key role in the development of organic thin film semiconductor technology.<br />

SYOH 5.15 Do 18:00 B<br />

Dislocation Arrangements in Pentacene Films — •Bert Nickel<br />

— Ludwig-Maximilians-Universität München<br />

Organic molecules are currently at the focus of many research programms<br />

due to their applications in molecular electronics. Among the<br />

various materials under investigation, pentacene (C22H14), a long, flat,<br />

aromatic molecule is particularly promising, in part because pentacene<br />

easily forms layered crystals if deposited onto flat, inert surfaces, resulting<br />

in highly anisotropic transport properties. We have studied the<br />

growth of pentacene films (2-8 monolayers) on modified Si-wafer surfaces<br />

by means of synchrotron x-ray diffraction. A quantitative analysis of the

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