Abstract
Fast, stable n-type organic mixed ionic-electronic conductors remain scarce. We report a donor glycolated, quinoidal design that facilitates efficient n-doping and spatially separates hydrophilic side chains from n-doping sites to preserve electronic pathways. The resulting polymer PQ-gT, synthesized from a glycolated bithiophene donor and a quinoidal bifuran-dione acceptor, exhibits high mixed conduction with a figure of merit of µC* = 10.9 F cm−1 V−1 s−1. In planar accumulation-mode organic electrochemical transistors (OECTs), it exhibits nearly symmetric sub-millisecond transients with switching on- and off-times of τon/τoff = 0.5/0.2 ms. These values represent the fastest operation for this type of device architecture. Partial donor replacement with dialkoxybithiazole tunes packing and suppresses swelling, raising µC* to 21.5 F cm−1 V−1 s−1 at 25% substitution, albeit with slower switching. In vertical OECTs, PQ-gT supports balanced ambipolar operation with ∼1 ms switching and enables a single-material complementary inverter (gain ≈ 40 V V−1 at VIN < 100 mV) that is stable over 10 000 cycles and functional up to 200 Hz. This donor-glycolated quinoidal strategy furnishes intrinsically fast, aqueous-stable n-type organic mixed ionic-electronic conductors for bioelectronic circuits.
| Original language | English |
|---|---|
| Journal | Angewandte Chemie - International Edition |
| DOIs | |
| State | Accepted/In press - 2026 |
| Externally published | Yes |
Keywords
- fast transient response
- figure of merit
- n-type organic mixed-ionic-electronic conductors
- organic electrochemical transistors
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