Soluble acetylenic molecular glasses based on dithienyldiketopyrrolopyrrole for organic solar cells. (March 2016)
- Record Type:
- Journal Article
- Title:
- Soluble acetylenic molecular glasses based on dithienyldiketopyrrolopyrrole for organic solar cells. (March 2016)
- Main Title:
- Soluble acetylenic molecular glasses based on dithienyldiketopyrrolopyrrole for organic solar cells
- Authors:
- Xia, Yan
Tan, Wan-Yi
Wang, Li-Ping
Zhang, Chun-Hui
Peng, Ling
Zhu, Xu-Hui
Peng, Junbiao
Cao, Yong - Abstract:
- Abstract: We present the synthesis and photovoltaic response of soluble glass-forming molecules containing a dithienyldiketopyrrolopyrrole core and difluorenylarylamine endgroups, linked through an acetylene bond. Introducing the 2, 6-naphthylene moiety vs. 1, 4-phenylene leads to an increased glass transition temperature ( T g ) and hole mobility. Thus, T g = 107.7 °C, μ h = 7.95 × 10 −5 cm 2 V −1 s −1 for the 1, 4- phenylene compound, while T g = 119.4 °C, μ h = 9.17 × 10 −5 cm 2 V −1 s −1 for the 2, 6-naphthylene compound. Thermal annealing the as-cast films of both compounds below T g resulted in little change in optical absorption. The preliminary characterization of the bulk hetero-junction solar cells showed that the 2, 6-naphthylene compound generally provides a higher power conversion efficiency than the 1, 4-phenylene compound, due probably to its enhanced hole transport. The photoluminescence experiments show a weak exciplex emission around 880 nm for the blends containing the new dyes and PC61 BM. The present work may be useful for further efforts toward high-performance cost-effective acetylenic organic semiconductors for organic solar cells with thermally stable morphology. Graphical abstract: Introducing the 2, 6-naphthyl moiety vs. 1, 4-phenyl increases T g and hole mobility, thus contributing to enhancing the power conversion efficiency. Highlights: Soluble acetylenic molecular glasses based onDT-DPP for OSCs have been reported. The opticalAbstract: We present the synthesis and photovoltaic response of soluble glass-forming molecules containing a dithienyldiketopyrrolopyrrole core and difluorenylarylamine endgroups, linked through an acetylene bond. Introducing the 2, 6-naphthylene moiety vs. 1, 4-phenylene leads to an increased glass transition temperature ( T g ) and hole mobility. Thus, T g = 107.7 °C, μ h = 7.95 × 10 −5 cm 2 V −1 s −1 for the 1, 4- phenylene compound, while T g = 119.4 °C, μ h = 9.17 × 10 −5 cm 2 V −1 s −1 for the 2, 6-naphthylene compound. Thermal annealing the as-cast films of both compounds below T g resulted in little change in optical absorption. The preliminary characterization of the bulk hetero-junction solar cells showed that the 2, 6-naphthylene compound generally provides a higher power conversion efficiency than the 1, 4-phenylene compound, due probably to its enhanced hole transport. The photoluminescence experiments show a weak exciplex emission around 880 nm for the blends containing the new dyes and PC61 BM. The present work may be useful for further efforts toward high-performance cost-effective acetylenic organic semiconductors for organic solar cells with thermally stable morphology. Graphical abstract: Introducing the 2, 6-naphthyl moiety vs. 1, 4-phenyl increases T g and hole mobility, thus contributing to enhancing the power conversion efficiency. Highlights: Soluble acetylenic molecular glasses based onDT-DPP for OSCs have been reported. The optical absorption of the dye films was little affected by thermal annealing below T g . The difluorenyl(2-naphthyl)amine endgroup contributes to increasing μ hole and PCE. … (more)
- Is Part Of:
- Dyes and pigments. Volume 126(2016)
- Journal:
- Dyes and pigments
- Issue:
- Volume 126(2016)
- Issue Display:
- Volume 126, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 126
- Issue:
- 2016
- Issue Sort Value:
- 2016-0126-2016-0000
- Page Start:
- 96
- Page End:
- 103
- Publication Date:
- 2016-03
- Subjects:
- Acetylene -- Amorphous -- Arylamine -- Dithienyldiketopyrrolopyrrole -- Organic solar cells -- Small molecules
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2015.11.018 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 281.xml