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- W2912193353 abstract "We describe herein the comprehensive theoretical and experimental studies on the transistor mobility of organic semiconductors by correlating a two-dimensional (2D) intermolecular interaction with thin-film morphology and the electronic coupling structure. We developed a novel bis-lactam-based small molecule, 1,5-dioctyl-3,7-di(thiophen-2-yl)-1,5-naphthyridine-2,6-dione (C8-NTDT), with a 2D-type C–H···O═C intermolecular interaction along the in-plane directions of the crystal packing structure, which is characteristically different from the one-dimensional-type intermolecular interaction shown in the typical bis-lactam molecule of 2,5-dioctyl-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4-dione (C8-DPPT). Experimentally and theoretically, C8-NTDT exhibited more favorable thin-film morphology and an electronic coupling structure for charge transport because of its unique 2D intermolecular interactions compared with C8-DPPT. In fact, C8-NTDT exhibited a hole mobility of up to 1.29 cm2 V–1 s–1 and an on/off ratio of 107 in a vacuum-processed device. Moreover, the high solubility with the 2D electronic coupling structure of C8-NTDT enables versatile solution processing for device fabrication without performance degradation compared to the vacuum-processed device. As an example, we could demonstrate a hole mobility of up to 1.10 cm2 V–1 s–1 for the spin-coated devices, which is one of the best performances among the solution-processed organic field-effect transistors based on bis-lactam-containing small molecules." @default.
- W2912193353 created "2019-02-21" @default.
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- W2912193353 date "2019-01-30" @default.
- W2912193353 modified "2023-10-15" @default.
- W2912193353 title "Structural and Electronic Origin of Bis-Lactam-Based High-Performance Organic Thin-Film Transistors" @default.
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- W2912193353 doi "https://doi.org/10.1021/acsami.8b20168" @default.
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