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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Hofmann, Anna

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Chalmers University of Technology

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2023Advanced structural brain aging in preclinical autosomal dominant Alzheimer disease4citations
  • 2019Thermally Activated in Situ Doping Enables Solid-State Processing of Conducting Polymers.18citations
  • 2019Solar Energy Storage by Molecular Norbornadiene–Quadricyclane Photoswitches: Polymer Film Devices65citations
  • 2018Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide47citations
  • 2018Enhanced n-Doping Efficiency of a Naphthalenediimide-Based Copolymer through Polar Side Chains for Organic Thermoelectrics249citations

Places of action

Chart of shared publication
Lund, Anja
1 / 10 shared
Müller, Christian
3 / 43 shared
Kroon, Renee
2 / 28 shared
Mansø, Mads
1 / 1 shared
Moth-Poulsen, Kasper
1 / 8 shared
Wang, Zhihang
1 / 3 shared
Sumby, Christopher
1 / 1 shared
Jevric, Martyn
1 / 4 shared
Petersen, Anne
1 / 1 shared
Fillols, Méritxell
1 / 1 shared
Muller, Christian
1 / 7 shared
Biskup, Till
1 / 6 shared
Olsson, Eva
1 / 12 shared
Koster, Lja
1 / 32 shared
Sun, Hengda
1 / 8 shared
Kiefer, David
1 / 4 shared
Koopmans, Marten
1 / 8 shared
Rivnay, Jonathan
1 / 10 shared
Giovannitti, Alexander
1 / 11 shared
Cendra, Camila
1 / 3 shared
Mcculloch, Iain
1 / 44 shared
Weber, Stefan
1 / 7 shared
Fabiano, Simone
1 / 34 shared
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2023
2019
2018

Co-Authors (by relevance)

  • Lund, Anja
  • Müller, Christian
  • Kroon, Renee
  • Mansø, Mads
  • Moth-Poulsen, Kasper
  • Wang, Zhihang
  • Sumby, Christopher
  • Jevric, Martyn
  • Petersen, Anne
  • Fillols, Méritxell
  • Muller, Christian
  • Biskup, Till
  • Olsson, Eva
  • Koster, Lja
  • Sun, Hengda
  • Kiefer, David
  • Koopmans, Marten
  • Rivnay, Jonathan
  • Giovannitti, Alexander
  • Cendra, Camila
  • Mcculloch, Iain
  • Weber, Stefan
  • Fabiano, Simone
OrganizationsLocationPeople

article

Highly stable doping of a polar polythiophene through co-processing with sulfonic acids and bistriflimide

  • Hofmann, Anna
  • Müller, Christian
  • Kroon, Renee
Abstract

Doping of organic semiconductors is currently an intensely studied field, since it is a powerful tool to optimize the performance of various organic electronic devices, ranging from organic solar cells, to thermoelectric modules, and bio-medical sensors. Despite recent advances, there is still a need for the development of highly conducting polymer:dopant systems with excellent long term stability and a high resistance to elevated temperatures. In this work we study the doping of the polar polythiophene derivative p(g42T-T) by various sulfonic acids and bistriflimide via different processing techniques. We demonstrate that simple co-processing of p(g42T-T) with an acid dopant yields conductivities of up to 120 S cm−1, which remain stable for more than six months under ambient conditions. Notably, a high conductivity is only achieved if the doping is carried out in air, which can be explained with a doping process that involves an acid mediated oxidation of the polymer through O2. P(g42T-T) doped with the non-toxic and inexpensive 1,3-propanedisulfonic acid was found to retain its electrical conductivity for at least 20 hours upon annealing at 120 °C, which allowed the bulk processing of the doped polymer into conducting, free-standing and flexible films and renders the di-acid a promising alternative to commonly used redox dopants.

Topics
  • impedance spectroscopy
  • polymer
  • semiconductor
  • annealing
  • electrical conductivity