DOI: https://doi.org/10.29363/nanoge.aohm.2019.033
Publication date: 8th January 2019
Mixed-conductors are materials that conduct both electrons and ions, thereby allowing transduction between biological signals and electronics. Conjugated polymers (CP) have the potential to be high-performing mixed-conductors for bioelectronics due to their redox chemistry, flexibility, processability and biocompatibility.1 Previous work showed increased electrochemical oxidation in regio-regular poly(3-hexylthiophene) (P3HT) by OH-functionalization of the side chains, underlining the importance of hydrophilicity and ion mobility in mixed-conduction materials.2
This work demonstrates faster electrochemical doping in conjugated polymers by blending with hydrophilic components and their application in organic electrochemical transistors (OECTs). Poly(3-hydroxyhexylthiophene) (P3HHT) and random copolymer P3HT-co-P3HHT are blended with hydrophilic block copolymers (BCPs) of P3HT and polyethylene oxide (P3HT-b-PEO) where the PEO fraction is varied between 1 and 20 kg/mol. Electrochromic spectroscopy and electrochemical impedance spectroscopy are used to investigate the effect of blending the CP with BCPs on the doping kinetics and on the capacitance in thin films, respectively. Addition of hydrophilic BCPs induces higher doping rates and lowers the impedance with respect to neat CPs promoting ion penetration in the bulk of the thin film. Finally, the blends are implemented in OECTs to show the effect on mixed conduction properties. These results show how ion mobility in films of electroactive CP can be modulated by enhancing hydrophilicity through side-chain engineering and blending with hydrophilic components. Both strategies are viable and compatible to improve ionic conductivity in mixed-conductors for bioelectronics.
This research was supported by the Initiative d'excellence de l'Université de Bordeaux (IDEX Bordeaux). The authors would also like to thank Olivier Dautel for providing some of the polymers used in this study.