Poly(Alkoxythiophene) Rod‐Coil Block Copolymers for Organic Electrochemical Transistors
8 affiliations
- 1Chemistry Research Laboratory University of Oxford Oxford UK
- 2Organic Bioelectronics Laboratory Biomedical Sciences Division King Abdullah University of Science and Technology (KAUST) Thuwal Thuwal Saudi Arabia
- 3School of Chemistry University of Birmingham Edgbaston Birmingham UK
- 4Department of Materials Science and Engineering Stanford University Stanford California USA
- 5Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA
- 6Andlinger Center For Energy and the Environment and Department of Electrical and Computer Engineering Princeton University Princeton NJ USA
- 7Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA
- 8School of Physics and Astronomy University of Birmingham Edgbaston Birmingham UK
Abstract
Conjugated rod‐coil block copolymers provide a promising route to decouple the optimisation of ionic and electronic transport in organic electrochemical transistors (OECTs). Poly(3‐alkoxythiophene) (P3AOT)‐based rod‐coil block copolymers with precisely tuned polyethylene glycol (PEG), and poly(L‐lactide) (PLLA) coil blocks are synthesised through a modular approach combining Kumada coupling transfer polymerisation (KCTP) and Knoevenagel condensation. An evaluation of the thin film morphology and subsequent OECT performance of a range of rod‐coil copolymers reveals that device performance can be enhanced compared to the corresponding homopolymer, establishing rod‐coil block copolymers as a versatile material platform and providing fundamental insight for the use of block copolymer in OECTs.
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BibTeX
@article{tian2026polyalkoxythiophene,
title = {{Poly(Alkoxythiophene) Rod‐Coil Block Copolymers for Organic Electrochemical Transistors}},
author = {Junfu Tian and Wentao Shan and Rachael Found and Paola Mantegazza and Francesco Leoni and Andreas W. Erhardt and Yuyun Yao and Matus Stredansky and Arianna Magni and Adam Marks and Elena Chulanova and Zeinab Hamid and Yueying Huang and Wanpeng Lu and Xian'e Li and Baopu Zhang and Qingpei Wan and Christina Kousseff and Matilde Concilio and Ruth Theresia Arwani and Caroline A. Ross and Sahika Inal and Giovanni Costantini and Iain McCulloch},
journal = {Advanced Materials (Deerfield Beach, Fla.)},
year = {2026},
month = sep,
doi = {10.1002/adma.74978},
url = {https://doi.org/10.1002/adma.74978},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Poly(Alkoxythiophene) Rod‐Coil Block Copolymers for Organic Electrochemical Transistors
AU - Junfu Tian
AU - Wentao Shan
AU - Rachael Found
AU - Paola Mantegazza
AU - Francesco Leoni
AU - Andreas W. Erhardt
AU - Yuyun Yao
AU - Matus Stredansky
AU - Arianna Magni
AU - Adam Marks
AU - Elena Chulanova
AU - Zeinab Hamid
AU - Yueying Huang
AU - Wanpeng Lu
AU - Xian'e Li
AU - Baopu Zhang
AU - Qingpei Wan
AU - Christina Kousseff
AU - Matilde Concilio
AU - Ruth Theresia Arwani
AU - Caroline A. Ross
AU - Sahika Inal
AU - Giovanni Costantini
AU - Iain McCulloch
PY - 2026
DA - 2026/09/13
JO - Advanced Materials (Deerfield Beach, Fla.)
DO - 10.1002/adma.74978
UR - https://doi.org/10.1002/adma.74978
AB - Conjugated rod‐coil block copolymers provide a promising route to decouple the optimisation of ionic and electronic transport in organic electrochemical transistors (OECTs). Poly(3‐alkoxythiophene) (P3AOT)‐based rod‐coil block copolymers with precisely tuned polyethylene glycol (PEG), and poly(L‐lactide) (PLLA) coil blocks are synthesised through a modular approach combining Kumada coupling transfer polymerisation (KCTP) and Knoevenagel condensation. An evaluation of the thin film morphology and subsequent OECT performance of a range of rod‐coil copolymers reveals that device performance can be enhanced compared to the corresponding homopolymer, establishing rod‐coil block copolymers as a versatile material platform and providing fundamental insight for the use of block copolymer in OECTs.
SN - 0935-9648
SN - 1521-4095
ER -