Counterion Dependent Side-Chain Relaxation Stiffens a Chemically Doped Thienothiophene Copolymer
Meghna Jha a, Mariavittoria Craighero a, Veronica Flores Vela a, Joost Kimpel a, Andreas Schaefer a, Jiali Guo b, Jesika Asatryan c, Alberto Peinador Veiga c, Shuichi Haraguchi a, Per-Anders Carlsson a, Jaime Martín c, Mariano Campoy-Quiles b, Christian Müller a
a Chalmers University of Technology, Sweden, Fysikgränd, 3, Gothenburg, Sweden
b Materials Science Institute of Barcelona (ICMAB-CSIC), Barcelona, Spain
c Universidade da Coruña, As Carballeiras, s/n. Campus de Elviña, A Coruña, Spain
Proceedings of MATSUS Spring 2026 Conference (MATSUSSpring26)
B3 Chemical and Electrochemical Doping of Organic Semiconductors
Barcelona, Spain, 2026 March 23rd - 27th
Organizers: Mariano Campoy Quiles and Christian Müller
Oral, Meghna Jha, presentation 064
Publication date: 15th December 2025

The electrical conductivity and elastic modulus of doped conjugated polymers tend to increase in
tandem, which complicates the design of soft conductors. This work investigates how different dopant
counterions influence the electrical and mechanical properties of a thienothiophene copolymer with
triethylene glycol side chains. Sequential doping and proton-coupled electron-transfer were used to
prepare samples with a comparable oxidation level neutralized with different counterions. Highly
oxidized films featured a comparable electrical conductivity of about 100 S cm-1 irrespective of the
counterion size. Dynamic mechanical analysis revealed that the choice of counterion strongly impacts
the sub-glass transition temperature, which varied from -44 to -3 ºC. As a result, the elastic modulus
at room temperature ranged from 0.05 to 0.7 GPa for materials with a comparable oxidation level.
Evidently, it is possible to decouple the electrical and mechanical properties of doped polymers,
which are governed by charge transport along the backbone and side-chain relaxation, respectively.
This insight opens up new opportunities for the design of soft conductors and more sustainable
bioelectronic and wearable devices whose various soft and rigid components could be created with the
same polymer.

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