Impact of 2-Ethylhexyl Stereoisomers on the Electrical Performance of Single-Crystal Field-Effect Transistors

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 30(2018), 44 vom: 15. Nov., Seite e1804032
1. Verfasser: He, Tao (VerfasserIn)
Weitere Verfasser: Leowanawat, Pawaret, Burschka, Christian, Stepanenko, Vladimir, Stolte, Matthias, Würthner, Frank
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article chirality diketopyrrolopyrroles organic electronics single-crystal field-effect transistors
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520 |a Many organic semiconductors (OSCs) inherit chiral alkyl chains, which ensure the desirable high solubility for solution-processing but may also lead to disorder, inhomogeneous film-formation, as well as interfacial defects due to the presence of mixtures of stereoisomers or diastereomers, which impair their peak performance. Here, single-crystal field-effect transistors (SCFETs) of a diketopyrrolopyrrole-based organic semiconductor with chiral 2-ethylhexyl substituents by sublimation in air and organic ribbon mask method are fabricated. Devices of the mesomer (R/S), both enantiomers (R/R, S/S), as well as mixtures of these three stereoisomers measured under ambient conditions exhibit all appreciable p-channel charge carrier mobilities of > 0.1 cm2 V-1 s-1 despite different packing arrangement in the R/S, R/R (or S/S), and racemate crystal structures. These results suggest a surprising tolerance for isomeric impurities. The highest literature-reported p-channel mobility so far for a diketopyrrolopyrrole-based OSC of 3.4 cm2 V-1 s-1 (Ion /Ioff of 1 × 106 ) is, however, only obtained for the pure R/S mesomer, illustrating the inherent potential of stereochemical purity. These results on SCFETs are further substantiated by studies on organic thin-film transistors (OTFTs) of pure and mixed thin films of the different stereoisomers 
650 4 |a Journal Article 
650 4 |a chirality 
650 4 |a diketopyrrolopyrroles 
650 4 |a organic electronics 
650 4 |a single-crystal field-effect transistors 
700 1 |a Leowanawat, Pawaret  |e verfasserin  |4 aut 
700 1 |a Burschka, Christian  |e verfasserin  |4 aut 
700 1 |a Stepanenko, Vladimir  |e verfasserin  |4 aut 
700 1 |a Stolte, Matthias  |e verfasserin  |4 aut 
700 1 |a Würthner, Frank  |e verfasserin  |4 aut 
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773 1 8 |g volume:30  |g year:2018  |g number:44  |g day:15  |g month:11  |g pages:e1804032 
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