A new diketopyrrolopyrrole-based 蟺-conjugated copolymer (PDPP5T) with high molecular weight has been synthesized by Stille coupling polymerization of 3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo-[3,4-c]pyrrole-1,4(2H,5H)-dione with 伪,伪鈥?bis(trimethylstannyl)-terthiophene. Its hole mobility without thermal annealing reaches 1.08 cm
2 V
鈥? s
鈥?, and a higher hole mobility of 3.46 cm
2 V
鈥? s
鈥? is obtained annealed at 200 掳C directly in an air atmosphere. This indicates that introducing a longer 尾-unsubstituted quinquethiophene (5T) unit into the main-chain of DPP-oligothiophene copolymer produces much pronounced p-type behavior and also reduces the steric hindrance of the bulk side-chain groups, which is favorable to enhance the molecular ordering capability at low temperatures and improve the organic thin-film transistors (OTFT) performances. This work demonstrates that PDPP5T is a promising material that can be applied to the cost-effective and large-scale production of OTFTs.
Keywords:
donor鈭抋cceptor copolymer; organic thin-film transistors; hole mobility