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Indolo[3,2-b]indole-Containing Donor-Acceptor Copolymers for High-Efficiency Organic Solar Cells
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- Title
- Indolo[3,2-b]indole-Containing Donor-Acceptor Copolymers for High-Efficiency Organic Solar Cells
- DGIST Authors
- Hwang, Jae Young ; Park, Jeong Hun ; Kim, Yu Jin ; Ha, Yeon Hee ; Park, Chan Eon ; Chung, Dae Sung ; Kwon, Soon Ki ; Kim, Yun Hi
- Issued Date
- 2017-03
- Citation
- Hwang, Jae Young. (2017-03). Indolo[3,2-b]indole-Containing Donor-Acceptor Copolymers for High-Efficiency Organic Solar Cells. doi: 10.1021/acs.chemmater.6b04745
- Type
- Article
- Article Type
- Article
- Keywords
- FIELD-EFFECT TRANSISTORS ; CONJUGATED POLYMERS ; CHARGE-TRANSPORT ; PHOTOVOLTAICS
- ISSN
- 0897-4756
- Abstract
-
The organic solar cell (OSC) performance of a series of new donor-acceptor copolymers containing indolo[3,2-b]indole as a key donor block and benzothiadiazole (BT) units with various degrees of fluorination as acceptors is reported. Compared with the simple carbazole unit, the strategically developed indolo[3,2-b]indole unit is found to significantly extend π-conjugation and thus increase the intermolecular interactions of the resulting copolymer, as probed by density functional theory calculations, photophysical studies, and structural/morphological analyses. In addition, fluorination of BT can facilitate nanostructuring of the copolymers, mainly due to further planarization of the backbone, which leads to apparently higher hole/electron charge carrier mobilities. The OSC properties of this series of new copolymers blended with fullerene show a strong dependence on the fine and continuous fibrous nanostructure of the blend film. The indolo[3,2-b]indole-based copolymer with singly fluorinated BT units possesses optimal intermolecular interactions and achieves the highest power conversion efficiency of 8.84% under AM 1.5G illumination. This result shows the potential of π-extended carbazole moieties for achieving high-performance OSCs with many of the favorable properties induced by large heteroacene blocks. © 2017 American Chemical Society.
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- Publisher
- American Chemical Society
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