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Two-dimensional extended pi-conjugated anthracene-based molecules bearing 4-ethynyl-7-(5-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazole at 2,6-and 9,10-substitution positions

Authors
Hur, Jung A.Kim, Sun JaeKim, Kyung HwanLee, Tae WanKim, KihyunShin, JicheolHwang, Kyung SeokChin, Byung DooChoi, Dong Hoon
Issue Date
Jan-2012
Publisher
ELSEVIER SCIENCE SA
Keywords
Conjugated molecules; Anthracene; Semiconductor; Mobility; Organic thin film transistor; Bulk heterojunction; Photovoltaic cell
Citation
SYNTHETIC METALS, v.161, no.23-24, pp.2776 - 2784
Indexed
SCIE
SCOPUS
Journal Title
SYNTHETIC METALS
Volume
161
Number
23-24
Start Page
2776
End Page
2784
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/106231
DOI
10.1016/j.synthmet.2011.10.019
ISSN
0379-6779
Abstract
New 4-ethynyl-7-(5-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazole-containing conjugated molecules were synthesized via the Sonogashira coupling reaction. The synthesized anthracene-based molecules showed good solubility in common organic solvents and had good self-film-forming properties. The semi-conducting properties of the two synthesized pi-conjugated molecules, 4 and 8, were evaluated by using the molecules in organic thin-film transistors (OTFTs). As-spun films of these molecules showed fairly high charge carrier mobilities, 0.010-0.10 cm(2) V-1 s(-1) (I-ON/I-OFF > 10(3)). The high charge carrier mobilities were attributed to the strong intermolecular interaction, which resulted in easy crystallization and dense coverage of the insulator surface. In addition, the two molecules were used to fabricate organic photovoltaic (OPV) cells with methanofullerene [6,6]-phenyl C-61-butyric acid methyl ester (PC61BM), without thermal annealing. The best preliminary results were obtained for the photovoltaic cell containing 8: the open-circuit voltage, short-circuit current density, and fill factor were 0.76V, 1.65 mA cm(-2), and 0.44, respectively, and the overall power conversion efficiency (PCE) was 0.55%. (C) 2011 Elsevier B.V. All rights reserved.
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