Synthesis and photophysical properties of N-alkyl dithieno[3, 2-b:2′, 3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application. Issue 28 (15th June 2022)
- Record Type:
- Journal Article
- Title:
- Synthesis and photophysical properties of N-alkyl dithieno[3, 2-b:2′, 3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application. Issue 28 (15th June 2022)
- Main Title:
- Synthesis and photophysical properties of N-alkyl dithieno[3, 2-b:2′, 3′-d]pyrrole based donor/acceptor-π-conjugated copolymers for solar-cell application
- Authors:
- Trinh, Cuc Kim
Nassar, Gamal M.
Abdo, Nabiha I.
Jung, Suhyun
Kim, Wonbin
Lee, Kwanghee
Lee, Jae-Suk - Abstract:
- Abstract : The relationships between the structure and the property of donor–acceptor copolymers based on dithieno[3, 2- b :2′, 3′- d ]pyrrole as a strong donor unit and isoindigo or thiazole as acceptor units are successfully studied. Abstract : Two kinds of donor–acceptor π-conjugated copolymer based on poly{[ N -hexyl-dithieno(3, 2- b :2′, 3′- d )pyrrole-2, 6-diyl] alt -[isoindigo]} (PDTP-IID) and poly{[ N -hexyl-dithieno(3, 2- b :2′, 3′- d )pyrrole-2, 6-diyl] alt -[thiazol-2, 5-diyl]} (PDTP-Thz) were investigated. These copolymers were synthesized via a Stille coupling reaction. The results showed the structure–property relationships of different donor–acceptor (D–A) combinations. The polymer structures and photophysical properties were characterized by 1 H NMR, TGA, DSC, UV-vis absorption spectroscopy, AFM, CV, and XRD measurement. Through UV-vis absorption and cyclic voltammetry (CV) measurements, it showed that the copolymers exhibit not only a low bandgap of 1.29 eV and 1.51 eV but also a deep highest occupied molecular orbital (HOMO) of −5.49 and −5.11 eV. Moreover, photovoltaic properties in combination with the fullerene derivatives were investigated. The device based on the copolymers with PC71 BM exhibited higher maximum power conversion efficiency and higher maximum short-circuit current density of 0.23% with 1.64 mA cm −2 of PDTP-IID:PC71 BM and 0.13% with 1.11 mA cm −2 of PDTP-Thz:PC71 BM than those of the copolymers with PC61 BM. Measurements performed for NAbstract : The relationships between the structure and the property of donor–acceptor copolymers based on dithieno[3, 2- b :2′, 3′- d ]pyrrole as a strong donor unit and isoindigo or thiazole as acceptor units are successfully studied. Abstract : Two kinds of donor–acceptor π-conjugated copolymer based on poly{[ N -hexyl-dithieno(3, 2- b :2′, 3′- d )pyrrole-2, 6-diyl] alt -[isoindigo]} (PDTP-IID) and poly{[ N -hexyl-dithieno(3, 2- b :2′, 3′- d )pyrrole-2, 6-diyl] alt -[thiazol-2, 5-diyl]} (PDTP-Thz) were investigated. These copolymers were synthesized via a Stille coupling reaction. The results showed the structure–property relationships of different donor–acceptor (D–A) combinations. The polymer structures and photophysical properties were characterized by 1 H NMR, TGA, DSC, UV-vis absorption spectroscopy, AFM, CV, and XRD measurement. Through UV-vis absorption and cyclic voltammetry (CV) measurements, it showed that the copolymers exhibit not only a low bandgap of 1.29 eV and 1.51 eV but also a deep highest occupied molecular orbital (HOMO) of −5.49 and −5.11 eV. Moreover, photovoltaic properties in combination with the fullerene derivatives were investigated. The device based on the copolymers with PC71 BM exhibited higher maximum power conversion efficiency and higher maximum short-circuit current density of 0.23% with 1.64 mA cm −2 of PDTP-IID:PC71 BM and 0.13% with 1.11 mA cm −2 of PDTP-Thz:PC71 BM than those of the copolymers with PC61 BM. Measurements performed for N -hexyl-dithieno(3, 2- b :2′, 3′- d )pyrrole-based copolymers proved the potential of these polymers to be applied in optoelectronic applications. … (more)
- Is Part Of:
- RSC advances. Volume 12:Issue 28(2022)
- Journal:
- RSC advances
- Issue:
- Volume 12:Issue 28(2022)
- Issue Display:
- Volume 12, Issue 28 (2022)
- Year:
- 2022
- Volume:
- 12
- Issue:
- 28
- Issue Sort Value:
- 2022-0012-0028-0000
- Page Start:
- 17682
- Page End:
- 17688
- Publication Date:
- 2022-06-15
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2ra02608b ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22276.xml