Engineering flexible dopamine biosensors: blended EGylated conjugated and radical polymers in organic electrochemical transistors
Abstract We demonstrate an enhancement in the figure of merit (μC*) of a flexible organic electrochemical transistor (OECT) and its dopamine (DA) biosensor by blending various open-shell, non-conjugated radical polymers featuring nitroxide radical active sites as pendant groups with closed-shell, et...
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| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-05-01
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| Series: | npj Flexible Electronics |
| Online Access: | https://doi.org/10.1038/s41528-025-00412-9 |
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| Summary: | Abstract We demonstrate an enhancement in the figure of merit (μC*) of a flexible organic electrochemical transistor (OECT) and its dopamine (DA) biosensor by blending various open-shell, non-conjugated radical polymers featuring nitroxide radical active sites as pendant groups with closed-shell, ethylene glycol (EG)-functionalized conjugated polymers as a macromolecular active layer system. The precisely controlled ionic transport of the OECT by the radical polymer modulated the doping level of the EGylated polymer, ensuring well-regulated redox activity and resulting in μC* values exceeding 192 F V-¹ cm-¹ s-¹, along with an on/off ratio of 104. Additionally, we achieved an ultrasensitive detection limit for DA at the clinically relevant level of 1 pM, along with exceptional specificity, effectively distinguishing DA even in the presence of a substantial excess of interfering substances. These findings underscore the potential of a systematic design approach for developing an advanced, flexible OECT-based biosensor platform through the strategic selection and processing of open- and closed-shell macromolecules. |
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| ISSN: | 2397-4621 |