Terpolymer acceptors based on bithiophene imide for all-polymer solar cells. (February 2021)
- Record Type:
- Journal Article
- Title:
- Terpolymer acceptors based on bithiophene imide for all-polymer solar cells. (February 2021)
- Main Title:
- Terpolymer acceptors based on bithiophene imide for all-polymer solar cells
- Authors:
- Sun, Weipeng
Wang, Junwei
Shi, Yongqiang
Wu, Ziang
Tang, Yumin
Feng, Kui
Woo, Han Young
Guo, Xugang
Zhang, Fei-Bao - Abstract:
- Abstract: In order to improve light absorption and promote n-type performance, random copolymerization strategy was employed to afford a series of random terpolymer acceptors with acceptor1-acceptor2-acceptor3 (A1 -A2 -A3 ) type backbone. The polymers were synthesized from distannylated electron-deficient bithiophene imide monomer with various electron-deficient dibrominated co-monomers using the typical palladium-catalyzed Stille coupling condensation polymerization. Compared with their parent polymers, these A1 -A2 -A3 type terpolymer acceptors, particularly the dihexylthieno[3, 4- b ]pyrazine based terpolymer PBTP, can exhibit good miscibility, appropriate polymer crystallinity, and improved absorption in the long-wavelength region due to the incorporation of a third strong electron-withdrawing acceptor moiety thieno[3, 4- b ]pyrazine. Benefitting from the noncovalent S⋯N interactions, PBTP possessed a planar skeleton and achieved the highest power conversion efficiency (PCE) of 7.35% in the polymer series when serving as the acceptor material in all-polymer solar cells. These results indicate that the A1 -A2 -A3 type terpolymer acceptors should be promising candidates for developing high-performance all-polymer solar cells. Highlights: The New acceptor1-acceptor2-acceptor3 type backbone was designed to promote n-type performance. A random copolymerization strategy is an effective approach to tune organic semiconductor properties. All-polymer solar cells are prepared fromAbstract: In order to improve light absorption and promote n-type performance, random copolymerization strategy was employed to afford a series of random terpolymer acceptors with acceptor1-acceptor2-acceptor3 (A1 -A2 -A3 ) type backbone. The polymers were synthesized from distannylated electron-deficient bithiophene imide monomer with various electron-deficient dibrominated co-monomers using the typical palladium-catalyzed Stille coupling condensation polymerization. Compared with their parent polymers, these A1 -A2 -A3 type terpolymer acceptors, particularly the dihexylthieno[3, 4- b ]pyrazine based terpolymer PBTP, can exhibit good miscibility, appropriate polymer crystallinity, and improved absorption in the long-wavelength region due to the incorporation of a third strong electron-withdrawing acceptor moiety thieno[3, 4- b ]pyrazine. Benefitting from the noncovalent S⋯N interactions, PBTP possessed a planar skeleton and achieved the highest power conversion efficiency (PCE) of 7.35% in the polymer series when serving as the acceptor material in all-polymer solar cells. These results indicate that the A1 -A2 -A3 type terpolymer acceptors should be promising candidates for developing high-performance all-polymer solar cells. Highlights: The New acceptor1-acceptor2-acceptor3 type backbone was designed to promote n-type performance. A random copolymerization strategy is an effective approach to tune organic semiconductor properties. All-polymer solar cells are prepared from these non-fullerene acceptors. … (more)
- Is Part Of:
- Dyes and pigments. Volume 186(2021)
- Journal:
- Dyes and pigments
- Issue:
- Volume 186(2021)
- Issue Display:
- Volume 186, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 186
- Issue:
- 2021
- Issue Sort Value:
- 2021-0186-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-02
- Subjects:
- All-polymer solar cells -- Polymer acceptors -- Terpolymers -- Bithiophene imide -- Optical absorption
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.2020.109049 ↗
- 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:
- 15366.xml