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Data · dataset · 2026

Delayed Cation Dynamics Enables Dual-Doped Organic Electrochemical Transistors with High Current Sensitivity

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Description

The coupling between ionic and electronic species and their dynamic interplay lay the foundation for organic electrochemical transistors (OECTs) to transduce and amplify bio(chemical) signals through ion-modulated conductivity. However, the operation of most reported OECTs is typically dominated by single ions, e.g. anions for p-type accumulation devices, mainly due to the challenge of regulating ion dynamics to enable both types of ions to play a role during the electrochemical doping process.

In this study, we propose that electrochemical doping of an OECT channel can occur via an anion-cation dual-doping mechanism, where cation expulsion and anion injection occur simultaneously. By designing a novel p-type organic mixed ionic-electronic conductor, Pu2gT, with strong side chain-cation interactions, we successfully decelerate the cation transport dynamics, allowing the dual-doping process to occur. As a result, Pu2gT OECT exhibits superior current sensitivity compared with the anion-dominated counterpart, showing potential in high-quality electrocardiogram signal acquisition and ion concentration discrimination.

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Furthermore, incorporating crown ether additives into Pu2gT enhances the dual-doping effect by further delaying cation dynamics, leading to even higher device performance. This novel dual-doping mechanism deepens the understanding of OECT working principles and opens new avenues for achieving state-of-the-art bioelectronic devices. 

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Inferred from text
Molecular and organic electronics 76%
Provenance · 1 source records, 11 field assertions
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ScienceDB10.57760/sciencedb.3178311 d agoJSON v1
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