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Organic electrochemical transistors (OECTs) have garnered significant interest due to their ability to facilitate both ionic and electronic transport. A large proportion of research efforts thus far have focused on investigating high-performance materials that can serve as mixed ion doping and charge transport layers. However, relatively less attention has been given to the gate-electrode materials, which play a critical role in controlling operational voltage, redox processes, and stability, especially in the context of semiconductor-based OECTs working in accumulation mode. Moreover, the demand for planarity and flexibility in modern bioelectronic devices presents significant challenges for the commonly used Ag/AgCl electrodes in OECTs. Herein, we report the construction of high-performance accumulation-mode OECTs by utilizing a gate electrode made of three-dimensional (3D)-printed graphene oxide. The 3D-printed graphene oxide electrode incorporating one-dimensional (1D) carbon nanotubes, is directly printed using an aqueous-based ink and showcases exceptional mechanical flexibility and porosity properties, enabling high-throughput preparation for both top gates and integrated planar architecture, as well as fast ion/charge transport. OECTs with high performance comparable to that of Ag/AgCl-gated OECTs are thus achieved and present promising feasibility for electrocardiograph (ECG) signal recording. This provides a promising choice for the application of flexible bioelectronics in medical care and neurological recording.

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Publication history
Copyright
Acknowledgements

Publication history

Received: 30 May 2023
Revised: 26 July 2023
Accepted: 07 August 2023
Published: 12 September 2023
Issue date: November 2023

Copyright

© Tsinghua University Press 2023

Acknowledgements

Acknowledgements

The authors acknowledge financial support from the National Natural Science Foundation of China (Nos. 22222205, 52173176, 51773143, and 51821002) and the Suzhou Key Laboratory of Surface and Interface Intelligent Matter (No. SZS2022011). This work is also supported by the Collaborative Innovation Center of Suzhou Nano Science & Technology, the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), and the 111 Project.

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