Abstract

AbstractOrganic electrochemical transistors (OECTs) have emerged as building blocks for low power circuits, biosensors, and neuromorphic computing. While p‐type polymer materials for OECTs are well developed, the choice of high‐performance n‐type polymers is limited, despite being essential for cation and metabolite biosensors, and crucial for constructing complementary circuits. N‐type conjugated polymers that have efficient ion‐to‐electron transduction are highly desired for electrochemical applications. In this contribution, three non‐fused, planar naphthalenediimide (NDI)‐dialkoxybithiazole (2Tz) copolymers, which systematically increase the amount of polar tri(ethylene glycol) (TEG) side chains: PNDI2OD‐2Tz (0 TEG), PNDIODTEG‐2Tz (1 TEG), PNDI2TEG‐2Tz (2 TEG), are reported. It is demonstrated that the OECT performance increases with the number of TEG side chains resulting from the progressively higher hydrophilicity and larger electron affinities. Benefiting from the high electron mobility, excellent ion conduction capability, efficient ion‐to‐electron transduction, and low‐lying lowest unoccupied molecular orbital energy level, the 2 TEG polymer achieves close to 105 on‐off ratio, fast switching, 1000 stable operation cycles in aqueous electrolyte, and has a long shelf life. Moreover, the higher number TEG chain substituted polymer exhibits good conductance state retention over two orders of magnitudes in electrochemical resistive random‐access memory devices, highlighting its potential for neuromorphic computing.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.