Abstract
Four soluble dialkylated tetrathienoacene (TTAR)-based small molecular semiconductors featuring the combination of a TTAR central core, π-conjugated spacers comprising bithiophene (bT) or thiophene (T), and with/without cyanoacrylate (CA) end-capping moieties are synthesized and characterized. The molecule DbT-TTAR exhibits a promising hole mobility up to 0.36 cm2 V−1 s−1 due to the enhanced crystallinity of the microribbon-like films. Binary blends of the p-type DbT-TTAR and the n-type dicyanomethylene substituted dithienothiophene-quinoid (DTTQ-11) are investigated in terms of film morphology, microstructure, and organic field-effect transistor (OFET) performance. The data indicate that as the DbT-TTAR content in the blend film increases, the charge transport characteristics vary from unipolar (electron-only) to ambipolar and then back to unipolar (hole-only). With a 1:1 weight ratio of DbT-TTAR DTTQ-11 in the blend, well-defined pathways for both charge carriers are achieved and resulted in ambipolar transport with high hole and electron mobilities of 0.83 and 0.37 cm2 V−1 s−1, respectively. This study provides a viable way for tuning microstructure and charge carrier transport in small molecules and their blends to achieve high-performance solution-processable OFETs.
Original language | English |
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Article number | 1801025 |
Journal | Advanced Functional Materials |
Volume | 28 |
Issue number | 28 |
DOIs | |
State | Published - 11 Jul 2018 |
Keywords
- ambipolar charge transport
- blends
- organic field-effect transistors
- solution-shearing
- tetrathienoacene
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CCDC 1822413: Experimental Crystal Structure Determination
Vegiraju, S. (Contributor), Lin, C.-Y. (Contributor), Priyanka, P. (Contributor), Huang, D.-Y. (Contributor), Luo, X.-L. (Contributor), Tsai, H.-C. (Contributor), Hong, S.-H. (Contributor), Yeh, C.-J. (Contributor), Lien, W.-C. (Contributor), Wang, C.-L. (Contributor), Tung, S.-H. (Contributor), Liu, C.-L. (Contributor), Chen, M.-C. (Contributor) & Facchetti, A. (Contributor), The Cambridge Structural Database, 2020
DOI: 10.5517/ccdc.csd.cc1z5cj1, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc1z5cj1&sid=DataCite
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