Versatile asymmetric thiophene/benzothiophene flanked diketopyrrolopyrrole polymers with ambipolar properties for OFETs and OSCs. Issue 36 (23rd August 2017)
- Record Type:
- Journal Article
- Title:
- Versatile asymmetric thiophene/benzothiophene flanked diketopyrrolopyrrole polymers with ambipolar properties for OFETs and OSCs. Issue 36 (23rd August 2017)
- Main Title:
- Versatile asymmetric thiophene/benzothiophene flanked diketopyrrolopyrrole polymers with ambipolar properties for OFETs and OSCs
- Authors:
- Jiang, Zhaoyan
Ni, Zhenjie
Wang, Hanlin
Wang, Zhen
Zhang, Jianqi
Qiu, Gege
Fang, Jin
Zhang, Yajie
Dong, Huanli
Lu, Kun
Hu, Wenping
Wei, Zhixiang - Abstract:
- Abstract : Three novel asymmetric flanking diketopyrrolopyrrole based polymers with different π bridges were applied to organic solar cells as a donor or an acceptor, respectively. Abstract : Three novel asymmetric thiophene/benzothiophene-flanked diketopyrrolopyrrole (DPP)-based polymers with different π bridges, designated as PBTTDPP-BT, PBTTDPP-TT and PBTTDPP-2FBT, were designed, synthesized and employed in organic solar cells. Compared with the reported thiophene/pyridine-flanked DPP, these thiophene/benzothiophene-flanked DPP polymers exhibited narrower band gaps below 1.5 eV, leading to a broadened absorption that ranged from 500 nm to 850 nm. All polymers displayed promising ambipolar semiconducting properties. PBTTDPP-BT, PBTTDPP-TT and PBTTDPP-2FBT showed hole mobilities of 1.20, 1.68 and 1.50 cm 2 V −1 s −1, respectively. Their corresponding electron mobilities were 0.40, 0.14 and 0.35 cm 2 V −1 s −1 . Interestingly, PBTTDPP-TT and PBTTDPP-2FBT also showed ambipolar properties in organic solar cells. Photovoltaic device based on PBTTDPP-TT as a donor material reached a power conversion efficiency (PCE) of 6.96% with PC71 BM as an acceptor, while this device as the acceptor material achieved only 0.28% with poly(3-hexylthiophene) (P3HT) as the donor. In contrast, PCE of PBTTDPP-2FBT-based devices reached 5.62% with PC71 BM and 0.44% with P3HT. These results suggest that the adoption of asymmetric flankers in DPP polymers can effectively tune their ambipolarAbstract : Three novel asymmetric flanking diketopyrrolopyrrole based polymers with different π bridges were applied to organic solar cells as a donor or an acceptor, respectively. Abstract : Three novel asymmetric thiophene/benzothiophene-flanked diketopyrrolopyrrole (DPP)-based polymers with different π bridges, designated as PBTTDPP-BT, PBTTDPP-TT and PBTTDPP-2FBT, were designed, synthesized and employed in organic solar cells. Compared with the reported thiophene/pyridine-flanked DPP, these thiophene/benzothiophene-flanked DPP polymers exhibited narrower band gaps below 1.5 eV, leading to a broadened absorption that ranged from 500 nm to 850 nm. All polymers displayed promising ambipolar semiconducting properties. PBTTDPP-BT, PBTTDPP-TT and PBTTDPP-2FBT showed hole mobilities of 1.20, 1.68 and 1.50 cm 2 V −1 s −1, respectively. Their corresponding electron mobilities were 0.40, 0.14 and 0.35 cm 2 V −1 s −1 . Interestingly, PBTTDPP-TT and PBTTDPP-2FBT also showed ambipolar properties in organic solar cells. Photovoltaic device based on PBTTDPP-TT as a donor material reached a power conversion efficiency (PCE) of 6.96% with PC71 BM as an acceptor, while this device as the acceptor material achieved only 0.28% with poly(3-hexylthiophene) (P3HT) as the donor. In contrast, PCE of PBTTDPP-2FBT-based devices reached 5.62% with PC71 BM and 0.44% with P3HT. These results suggest that the adoption of asymmetric flankers in DPP polymers can effectively tune their ambipolar transporting properties for high-performance organic electronic devices. … (more)
- Is Part Of:
- Polymer chemistry. Volume 8:Issue 36(2017)
- Journal:
- Polymer chemistry
- Issue:
- Volume 8:Issue 36(2017)
- Issue Display:
- Volume 8, Issue 36 (2017)
- Year:
- 2017
- Volume:
- 8
- Issue:
- 36
- Issue Sort Value:
- 2017-0008-0036-0000
- Page Start:
- 5603
- Page End:
- 5610
- Publication Date:
- 2017-08-23
- 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/c7py00940b ↗
- 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:
- 4601.xml