BODIPY bearing alkylthienyl side chains: a new building block to design conjugated polymers with near infrared absorption for organic photovoltaics. Issue 36 (14th August 2020)
- Record Type:
- Journal Article
- Title:
- BODIPY bearing alkylthienyl side chains: a new building block to design conjugated polymers with near infrared absorption for organic photovoltaics. Issue 36 (14th August 2020)
- Main Title:
- BODIPY bearing alkylthienyl side chains: a new building block to design conjugated polymers with near infrared absorption for organic photovoltaics
- Authors:
- Wang, Yinghui
Miao, Junhui
Dou, Chuandong
Liu, Jun
Wang, Lixiang - Abstract:
- Abstract : A new benzene-fused BODIPY unit for designing polymer donors with near-infrared absorption for organic photovoltaics. Abstract : To effectively harvest sunlight, polymer donors with near infrared (NIR) absorption properties are important for high-performance polymer solar cells (PSCs), especially semitransparent PSCs. However, building blocks to design this kind of polymer donor are rare. In this manuscript, we report 3, 11-dibromo-5, 9-bis(5-(2-decyltetradecyl)thiophen-2-yl)-7, 7-difluoro-7 H -6 λ 4, 7 λ 4 -[1, 3, 2]diazaborinino[4, 3- a :6, 1- a ′]diisoindole (BOPT) as a new building block to design polymer donors with NIR absorption. In BOPT, the 4-difluoro-4-bora-3a, 4a-diaza- s -indacene (BODIPY) core unit is fused with two benzene rings for a reduced bandgap and is attached with two alkylthienyl groups as conjugated side chains. We synthesized two polymers consisting of alternating BOPT units and thiophene or bithiophene units, respectively. The two polymers displayed near-infrared (NIR) light absorption with the maximum absorption peaks at wavelengths exceeding 800 nm and small bandgaps of ca. 1.3 eV. They showed high highest occupied molecular orbital (HOMO)/lowest unoccupied molecular orbital (LUMO) energy levels of about −5.0 eV/−3.5 eV and high hole mobilities of ca. 3 × 10 −3 cm 2 V −1 s −1 . PSC devices using the two polymers as electron donors exhibited power conversion efficiencies of 2.6%. These results indicate that BOPT is a promising buildingAbstract : A new benzene-fused BODIPY unit for designing polymer donors with near-infrared absorption for organic photovoltaics. Abstract : To effectively harvest sunlight, polymer donors with near infrared (NIR) absorption properties are important for high-performance polymer solar cells (PSCs), especially semitransparent PSCs. However, building blocks to design this kind of polymer donor are rare. In this manuscript, we report 3, 11-dibromo-5, 9-bis(5-(2-decyltetradecyl)thiophen-2-yl)-7, 7-difluoro-7 H -6 λ 4, 7 λ 4 -[1, 3, 2]diazaborinino[4, 3- a :6, 1- a ′]diisoindole (BOPT) as a new building block to design polymer donors with NIR absorption. In BOPT, the 4-difluoro-4-bora-3a, 4a-diaza- s -indacene (BODIPY) core unit is fused with two benzene rings for a reduced bandgap and is attached with two alkylthienyl groups as conjugated side chains. We synthesized two polymers consisting of alternating BOPT units and thiophene or bithiophene units, respectively. The two polymers displayed near-infrared (NIR) light absorption with the maximum absorption peaks at wavelengths exceeding 800 nm and small bandgaps of ca. 1.3 eV. They showed high highest occupied molecular orbital (HOMO)/lowest unoccupied molecular orbital (LUMO) energy levels of about −5.0 eV/−3.5 eV and high hole mobilities of ca. 3 × 10 −3 cm 2 V −1 s −1 . PSC devices using the two polymers as electron donors exhibited power conversion efficiencies of 2.6%. These results indicate that BOPT is a promising building block in designing polymer donors with near-infrared absorption for organic photovoltaics. … (more)
- Is Part Of:
- Polymer chemistry. Volume 11:Issue 36(2020)
- Journal:
- Polymer chemistry
- Issue:
- Volume 11:Issue 36(2020)
- Issue Display:
- Volume 11, Issue 36 (2020)
- Year:
- 2020
- Volume:
- 11
- Issue:
- 36
- Issue Sort Value:
- 2020-0011-0036-0000
- Page Start:
- 5750
- Page End:
- 5756
- Publication Date:
- 2020-08-14
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0py00868k ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14310.xml