Tunable Stability and Performance of Fused Thienothiophene Based Polymers for Organic Electrochemical Transistors and Artificial Synapse Based on A Side Chain Reorganization Strategy

H Hailiang Liao (Division of Physical Science and Engineering, Chemistry Program King Abdullah University of Science and Technology (KAUST) Thuwal Saudi Arabia) L Linqu Luo Y Yazhou Wang (School of Medicine, Chongqing University) W Wentao Shan Y Yu‐Ying Yang (Division of Physical Science and Engineering, Chemistry Program King Abdullah University of Science and Technology (KAUST) Thuwal Saudi Arabia) J Joel Luke A Adam V. Marsh (Department of Physical Science and Engineering King Abdullah University of Science & Technology (KAUST) Thuwal 23955–6900 Kingdom of Saudi Arabia) T Tania Cecilia Hidalgo Castillo A Adel Hama H Hendrik Faber X Xabier Rodríguez‐Martínez (Centro de Investigación en Tecnoloxías Navais e Industriais (CITENI) Universidade Da Coruña Campus de Esteiro s/n Ferrol Spain) J Jaime Martín (POLYMAT, University of the Basque Country UPV/EHU, Av. de Tolosa 72, San Sebastián 20018, Spain) A Achilleas Savva (Department of Microelectronics, Faculty of Electrical Engineering, Mathematics and Computer Science, Delft University of Technology, Mekelweg 4, Delft 2628 CD, The Netherlands) T Thomas D. Anthopoulos S Sahika Inal (Organic Bioelectronics Laboratory, Biological and Environmental Sciences and Engineering Division) M Martin Heeney (Division of Physical Sciences & Engineering, Chemistry Program)

Abstract

ABSTRACT We report a series of novel polymeric mixed ionic‐electronic conductors based upon the incorporation of fused thieno[3,2‐ b ]thiophene and bithiophene with isomeric sidechains. The enhanced rigidity in the polymer backbone facilitated the formation of stabilized bipolarons, while the reorganized ethylene glycol side chains not only maintained the polymer's hydrophilicity but also unexpectedly enhanced the crystallinity of the polymer film. This design strategy led to the development of 4gTT‐2gT, a high‐performance and stable organic mixed ionic‐electronic conductor. The polymer exhibited a maximum µC * of 729 F V −1 cm −1 s −1 , one of the highest values among low‐threshold voltage polythiophene derivatives, while demonstrating excellent operational stability, retaining 99% of its maximum current after 1‐h device switching cycles and 94% after 9‐h at lower bias. We implemented the material in OECT‐based artificial synapses, which maintained functionality under a large temperature range (23–373 K). These combined properties establish 4gTT‐2gT as a prime candidate for next‐generation mixed conductor devices.

Article Details

Volume / Issue Vol. 1, Issue 1
Published December 26, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (16)

H

Hailiang Liao

Division of Physical Science and Engineering, Chemistry Program King Abdullah University of Science and Technology (KAUST) Thuwal Saudi Arabia

L

Linqu Luo

Y

Yazhou Wang

School of Medicine, Chongqing University

W

Wentao Shan

Y

Yu‐Ying Yang

Division of Physical Science and Engineering, Chemistry Program King Abdullah University of Science and Technology (KAUST) Thuwal Saudi Arabia

J

Joel Luke

A

Adam V. Marsh

Department of Physical Science and Engineering King Abdullah University of Science & Technology (KAUST) Thuwal 23955–6900 Kingdom of Saudi Arabia

T

Tania Cecilia Hidalgo Castillo

A

Adel Hama

H

Hendrik Faber

X

Xabier Rodríguez‐Martínez

Centro de Investigación en Tecnoloxías Navais e Industriais (CITENI) Universidade Da Coruña Campus de Esteiro s/n Ferrol Spain

J

Jaime Martín

POLYMAT, University of the Basque Country UPV/EHU, Av. de Tolosa 72, San Sebastián 20018, Spain

A

Achilleas Savva

Department of Microelectronics, Faculty of Electrical Engineering, Mathematics and Computer Science, Delft University of Technology, Mekelweg 4, Delft 2628 CD, The Netherlands

T

Thomas D. Anthopoulos

S

Sahika Inal

Organic Bioelectronics Laboratory, Biological and Environmental Sciences and Engineering Division

M

Martin Heeney

Division of Physical Sciences & Engineering, Chemistry Program