A new generation of polythiophene-based polyelectrolytes is reported to address fundamental issues in organic electrochemical transistors (OECTs). In such devices, the semiconductor must be able to transport and store ions and possess simultaneously a very high electronic mobility. For this, the ion-conducting 6-(thiophen-3-yl) hexane-1-sulfonate tetramethylammonium monomer (THS – TMA + ) is copolymerized with the hole-conducting 3-hexylthiophene (3HT) to obtain copolymers, PTHS – TMA + - co -P3HT 1 – 3 with a gradient architecture. The copolymers having up to 50 mol % 3HT content are easily oxidizable and are crystalline. Consequently, for the copolymers, a higher stability in water is achieved, thus reducing the amount of cross-linker needed to stabilize the film. Furthermore, OECTs using copolymers with 75 and 50 mol % of PTHS – TMA + content exhibit 2–3 orders of magnitude higher ON/OFF ratio and an extremely lower threshold voltage (−0.15 V) compared to PTHS – TMA + . Additionally, high volumetric capacitance ( C * > 100 F/cm 3 ) is achieved, indicating that the ion transport is not hampered by the hydrophobic 3HT up to 50 mol %, for which a very high OECT hole mobility of 0.017 cm 2 /(V s) is also achieved. Thus, the concept of copolymerization to combine both ionic and electronic charge transport in an organic mixed conductor offers an elegant approach to obtain high-performance OECT materials.
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Schmode et al. (2019) studied this question.
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