Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2016Azido-Functionalized Thiophene as a Versatile Building Block to Cross-Link Low-Bandgap Polymers30citations

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Gann, Eliot
1 / 22 shared
Thelakkat, Mukundan
1 / 14 shared
Mueller, Christian J.
1 / 2 shared
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2016

Co-Authors (by relevance)

  • Gann, Eliot
  • Thelakkat, Mukundan
  • Mueller, Christian J.
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article

Azido-Functionalized Thiophene as a Versatile Building Block to Cross-Link Low-Bandgap Polymers

  • Klein, Tobias
  • Gann, Eliot
  • Thelakkat, Mukundan
  • Mueller, Christian J.
Abstract

<p>We unveil a concept for the design of cross-linkable semiconducting polymers that is based on a modular tercopolymerization which stands out by its low synthetic effort, easy accessibility, and its broad range of applications. 3-(6-Azidohexyl)thiophene was used as a comonomer in the synthesis of a variety of low-bandgap copolymers using different polymerization techniques such as Suzuki-Miyaura cross-coupling and Stille cross-coupling. We show that when only a small amount (5-10 mol %) of azide groups is introduced into the polymers, the impact on absorption and electrochemical properties (HOMO/LUMO values) is negligible. The small amount of azide functionality is however enough to obtain polymers that can easily be cross-linked by UV illumination. Thermal stability of the solid state packing and alignment is studied in neat polymer thin films as well as in blends with [6,6]-phenyl-C<sub>71</sub>-butyric acid methyl ester (PC<sub>70</sub>BM) as a relevant model blend system. Solvent resistivity of these polymer films is investigated by absorption and photoluminescence measurements. It is finally shown in organic field effect transistors that the introduction of 10% azide-functionalized monomer does not considerably influence hole transport mobility (0.20-0.45 cm<sup>2</sup> V<sup>-1</sup> s<sup>-1</sup>).</p>

Topics
  • impedance spectroscopy
  • photoluminescence
  • resistivity
  • mobility
  • thin film
  • copolymer
  • ester