Cited 49 time in
Indolo[3,2-b]indole-Containing Donor-Acceptor Copolymers for High-Efficiency Organic Solar Cells
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hwang, Jaeyoung | - |
| dc.contributor.author | Park, Jeonghun | - |
| dc.contributor.author | Kim, Yu Jin | - |
| dc.contributor.author | Ha, Yeon Hee | - |
| dc.contributor.author | Park, Chan Eon | - |
| dc.contributor.author | Chung, Dae Sung | - |
| dc.contributor.author | Kwon, Soon-Ki | - |
| dc.contributor.author | Kim, Yun-Hi | - |
| dc.date.accessioned | 2022-12-26T18:48:48Z | - |
| dc.date.available | 2022-12-26T18:48:48Z | - |
| dc.date.issued | 2017-03 | - |
| dc.identifier.issn | 0897-4756 | - |
| dc.identifier.issn | 1520-5002 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/13819 | - |
| dc.description.abstract | The organic solar cell (OSC) performance of a series of new donor acceptor copolymers containing indolo[3,2b]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 pi-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 nano structuring 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 z-extended carbazole moieties for achieving high-performance OSCs with many of the favorable properties induced by large heteroacene blocks. | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | American Chemical Society | - |
| dc.title | Indolo[3,2-b]indole-Containing Donor-Acceptor Copolymers for High-Efficiency Organic Solar Cells | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acs.chemmater.6b04745 | - |
| dc.identifier.scopusid | 2-s2.0-85015619969 | - |
| dc.identifier.wosid | 000396639400025 | - |
| dc.identifier.bibliographicCitation | Chemistry of Materials, v.29, no.5, pp 2135 - 2140 | - |
| dc.citation.title | Chemistry of Materials | - |
| dc.citation.volume | 29 | - |
| dc.citation.number | 5 | - |
| dc.citation.startPage | 2135 | - |
| dc.citation.endPage | 2140 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | FIELD-EFFECT TRANSISTORS | - |
| dc.subject.keywordPlus | CONJUGATED POLYMERS | - |
| dc.subject.keywordPlus | CHARGE-TRANSPORT | - |
| dc.subject.keywordPlus | PHOTOVOLTAICS | - |
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