Alkylated indacenodithieno[3,2-b]thiophene-based all donor ladder-type conjugated polymers for organic thin film transistors
Anthopoulos, Thomas D.
KAUST DepartmentKAUST Solar Center (KSC)
Material Science and Engineering Program
Physical Science and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/627046
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AbstractWe report the synthesis of a series of indacenodithieno[3,2-b]thiophene (IDTT) based conjugated polymers by copolymerization with three different electron rich co-monomers [thiophene (T), thieno[3,2-b]thiophene (TT) and dithieno[3,2-b:2',3'-d]thiophene (DTT)] under Stille coupling conditions. The resulting all-donor polymers show very good solubility in common solvents and exhibit similar optical, thermal and electronic properties. However, the performance of these semiconductors in thin film transistor devices varied and was highly dependent on the nature of the co-monomer. All polymers exhibited unipolar p-type charge transport behaviour, with the mobility values following the trend of IDTT-TT>IDTT-DTT>IDTT-T. The peak saturation mobility value of IDTT-TT was extracted to be 1.1 cm2V-1s-1, amongst the highest mobility for all-donor conjugated polymers reported to date.
CitationLu R, Han Y, Zhang W, Zhu X, Fei Z, et al. (2018) Alkylated indacenodithieno[3,2-b]thiophene-based all donor ladder-type conjugated polymers for organic thin film transistors. Journal of Materials Chemistry C. Available: http://dx.doi.org/10.1039/c7tc05162j.
SponsorsThis work was supported by the National Natural Science Foundation of China (21464003), the Natural Science Foundation of Guangxi (2014GXNSFAA118054), the Guangxi Key Laboratory of Chemistry and Engineering of Forest Products (2013B03), the Program of Innovation Team of Guangxi Universities (GJR201147-12) and EPSRC (EP/L016702/1). The data that supports the findings of this study are available in figshare at dx.doi.org/10.6084/m9.figshare.5803140
PublisherRoyal Society of Chemistry (RSC)
JournalJournal of Materials Chemistry C