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Electron-Rich Anthracene Semiconductors Containing Triarylamine for Solution-Processed Small-Molecule Organic Solar Cells

Authors
Choi, HyejuKo, Haye MinCho, NaraSong, KihyungLee, Jae KwanKo, Jaejung
Issue Date
2012
Publisher
WILEY-V C H VERLAG GMBH
Keywords
anthracenes; bulk heterojunctions; charge transfer; semiconductor; solar cells
Citation
CHEMSUSCHEM, v.5, no.10, pp.2045 - 2052
Indexed
SCIE
SCOPUS
Journal Title
CHEMSUSCHEM
Volume
5
Number
10
Start Page
2045
End Page
2052
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/109353
DOI
10.1002/cssc.201200242
ISSN
1864-5631
Abstract
New electron-rich anthracene derivatives containing triarylamine hole stabilizers, 2,6-bis[5,5'-bis(N,N'-diphenylaniline)-2,2'-bithiophen-5-yl]-9,10-bis-[(triisopropylsilyl)ethynyl]anthracene (TIPSAntBTTPA) and 2,6-bis(5,5'-bis{4-[bis(9,9-dimethyl-9H-fluoren-2-yl)amino]phenyl}-2,2'-bithiophen-5-yl)-9,10-bis-[(triisopropylsilyl)ethynyl]anthracene (TIPSAntBTbisDMFA), linked with p-conjugated bithiophene bridges, were synthesized and their photovoltaic characteristics were investigated in solution-processed small-molecule organic solar cells (SMOSCs). These new materials exhibited superior intramolecular charge transfer from triarylamine to anthracene, leading to a more electron-rich anthracene core that facilitated electron transfer into phenyl-C61-butyric acid methyl ester. Compared with TIPSAntBT and triarylamine, these materials show a threefold improvement in hole-transporting properties and better photovoltaic performance in solution-processed SMOSCs, with the best power conversion efficiency being 2.96?% at a high open-circuit voltage of 0.85 V.
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