Abstract
We report diketopyrrolopyrrole (DPP) based copolymers, poly (diketopyrrolopyrrole-cyclopentadithiophene) (PDPPTT-CPDT) and poly(diketopyrrolopyrrolebenzo[1,2-b:4,5-b’]dithiophene) (PDPPTT-BDT) to investigate donor unit structure effects on organic field-effect transistor (OFET) performance. The highest occupied molecular orbital (HOMO) level and copolymer band gap were tuned by introducing different donor units on the acceptor DPP backbone. PDPPTT-BDT OFETs show 10 fold higher hole field-effect mobility, up to 0.08 cm2 V−1 s−1, than PDPPTT-CPDT OFETs due to better crystallinity and higher HOMO energetic levels. PDPPTT-CPDT and PDPPTT-BDT were operationally stable with negligible threshold voltage shift after cycling.
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