Resistance to Overdoping Allows Over 2000 S cm <sup>−1</sup> Conductivity in P(g <sub>3</sub> BTTT) With Anion‐Exchange Doping

B Basil Hunger (Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland) M Maximilian M. Horn (Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland) E Eva Röck (Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland) D Diego Rosas Villalva (Materials Science and Engineering Physical Science and Engineering (PSE) Division King Abdullah University of Science and Technology (KAUST) Thuwal Saudi Arabia) L Lize Bynens (Hasselt University, Institute for Materials Research (imo-imomec), Design & Synthesis of Organic Semiconductors (DSOS), Martelarenlaan 42, B-3500 Hasselt, Belgium) J Jochen Vanderspikken (Hasselt University, Institute for Materials Research (imo-imomec), Design & Synthesis of Organic Semiconductors (DSOS), Martelarenlaan 42, B-3500 Hasselt, Belgium) C Christina Kousseff (Department of Chemistry Chemistry Research Laboratory University of Oxford Oxford UK) S Silène Gobeil (Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland) O Olivier Bardagot (Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland) N Nesibe Akmanşen‐Kalayci (Department of Chemistry and Biochemistry University of California Los Angeles California USA) S Sarah H. Tolbert (Department of Chemistry and Biochemistry University of California Los Angeles California USA) I Iain McCulloch (Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, U.K.) W Wouter Maes (Hasselt University, Institute for Materials Research (imo-imomec), Design & Synthesis of Organic Semiconductors (DSOS), Martelarenlaan 42, B-3500 Hasselt, Belgium) D Demetra Tsokkou (FemtoMat Research Group, Department Für Chemie Biochemie und Pharmazie, University of Bern Bern Switzerland) N Natalie Banerji (FemtoMat Research Group, Department Für Chemie Biochemie und Pharmazie, University of Bern Bern Switzerland)

Abstract

ABSTRACT Chemical doping of conjugated polymers significantly enhances their conductivity, making them attractive for a large range of applications. Recently, anion‐exchange doping, where the dopant counterion is replaced by inorganic anions by exposure of a p‐doped film to an electrolyte, has been demonstrated as an effective way to overcome the limitations of molecular dopants in terms of bulkiness, stability and energetics. Here, we demonstrate anion‐exchange doping for polymers bearing oligoether side chains and report over 2000 S cm −1 electrical conductivity for the P(g 3 BTTT) polymer. We investigate several thiophene and thienothiophene‐based polymers in the high‐doping regime to understand this high conductivity. We show that transport involves delocalized charges, that all generated charges participate to the transport, and that the mobility is resilient over nanometer to micrometer length scales. However, the high‐doping regime also shows a trade‐off between high charge density and high mobility, limiting the conductivity at excess concentrations of doubly charged species. Surprisingly, P(g 3 BTTT) is resistant to this ‘overdoping’ effect and sustains particularly high levels of doubly charged species without drop in mobility. The exceptional conductivity of doped P(g 3 BTTT) can thus be related to the high doping level that is achieved thanks to the oligoether side chains, without significant trade‐off on the concomitantly high mobility.

Article Details

Volume / Issue Vol. 1, Issue 1
Published April 04, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (15)

B

Basil Hunger

Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland

M

Maximilian M. Horn

Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland

E

Eva Röck

Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland

D

Diego Rosas Villalva

Materials Science and Engineering Physical Science and Engineering (PSE) Division King Abdullah University of Science and Technology (KAUST) Thuwal Saudi Arabia

L

Lize Bynens

Hasselt University, Institute for Materials Research (imo-imomec), Design & Synthesis of Organic Semiconductors (DSOS), Martelarenlaan 42, B-3500 Hasselt, Belgium

J

Jochen Vanderspikken

Hasselt University, Institute for Materials Research (imo-imomec), Design & Synthesis of Organic Semiconductors (DSOS), Martelarenlaan 42, B-3500 Hasselt, Belgium

C

Christina Kousseff

Department of Chemistry Chemistry Research Laboratory University of Oxford Oxford UK

S

Silène Gobeil

Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland

O

Olivier Bardagot

Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland

N

Nesibe Akmanşen‐Kalayci

Department of Chemistry and Biochemistry University of California Los Angeles California USA

S

Sarah H. Tolbert

Department of Chemistry and Biochemistry University of California Los Angeles California USA

I

Iain McCulloch

Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, U.K.

W

Wouter Maes

Hasselt University, Institute for Materials Research (imo-imomec), Design & Synthesis of Organic Semiconductors (DSOS), Martelarenlaan 42, B-3500 Hasselt, Belgium

D

Demetra Tsokkou

FemtoMat Research Group, Department Für Chemie Biochemie und Pharmazie, University of Bern Bern Switzerland

N

Natalie Banerji

FemtoMat Research Group, Department Für Chemie Biochemie und Pharmazie, University of Bern Bern Switzerland