Tuning of the Stretchability and Charge Transport of Bis‐Diketopyrrolopyrrole and Carbazole‐Based Thermoplastic Soft Semiconductors by Modulating Soft Segment Contents

Abstract Polymer semiconductors are promising materials for stretchable, wearable, and implantable devices due to their intrinsic flexibility, facile functionalization, and solution processability at low temperatures. However, the crystalline domain of the conjugated structure for high charge carrier mobility in semiconducting polymers exhibits lower stretchability than that of the semi‐crystalline or amorphous domains. Herein, a set of thermoplastic soft semiconductors is synthesized with different ratios of diketopyrrolopyrrole–carbazole–diketopyrrolopyrrole (DPP‐Cz‐DPP)‐based hard segments and thiophene‐based aliphatic soft segments, having the similar structure of thermoplastic elastomers. The polymers exhibit decreased glassy temperatures with the increased content of the soft segments. The polymers show high crystallinity after copolymerization with a large‐sized DPP‐Cz‐DPP core and non‐conjugated segments due to an aggregation property of the conjugated core, still possessing a semi‐crystalline domain after annealing. The polymer films exhibit stretchability under strains of up to 60%. Organic field‐effect transistors fabricated using stretchable polymers show a mobility range of 0.125–0.005 cm 2 V −1 s −1 with different proportions of the soft segment. The stretchability is improved significantly and the mobilities are decreased less when the content of the soft segment is increased. Therefore, this study presents a design principle for the development of a high‐performance stretchable semiconducting polymer.