9, 9′‐Bifluorenylidene‐Core Perylene Diimide Acceptors for As‐Cast Non‐Fullerene Organic Solar Cells: The Isomeric Effect on Optoelectronic Properties. Issue 16 (19th February 2018)
- Record Type:
- Journal Article
- Title:
- 9, 9′‐Bifluorenylidene‐Core Perylene Diimide Acceptors for As‐Cast Non‐Fullerene Organic Solar Cells: The Isomeric Effect on Optoelectronic Properties. Issue 16 (19th February 2018)
- Main Title:
- 9, 9′‐Bifluorenylidene‐Core Perylene Diimide Acceptors for As‐Cast Non‐Fullerene Organic Solar Cells: The Isomeric Effect on Optoelectronic Properties
- Authors:
- Zhao, Yuan
Wang, Huan
Xia, Shengpeng
Zhou, Feng
Luo, Zhenghui
Luo, Jiajia
He, Feng
Yang, Chuluo - Abstract:
- Abstract: Two different non‐fullerene small‐molecule acceptors, m ‐PIB and p ‐PIB, based on 9, 9′‐bifluorenylidene (BF) and perylene diimide (PDI) were designed and synthesized. Four β‐substituted PDIs were linked to BF in different positions. Based on DFT analysis, derivative p ‐PIB exhibited reduced intramolecular twisting between the PDI moieties, more delocalized wave function, and sufficiently wider π‐electron delocalization than that of m ‐PIB . The absorption ability of p ‐PIB was enhanced due to increased intermolecular interactions. By blending p ‐PIB with poly{4, 8‐bis[5‐(2ethylhexyl)thiophen‐2‐yl]benzo[1, 2‐ b :4, 5‐ b′ ]dithiophene‐ co ‐3‐fluorothieno[3, 4‐ b ]‐thiophene‐2‐carboxylate} (PTB7‐Th), organic solar cells (OSCs) based on p ‐PIB obtained a maximum power conversion efficiency of 5.95 % without any treatments. Due to the improved and balanced hole and electron mobilities, the short‐circuit current and fill factor of OSCs based on PTB7‐Th and p ‐PIB were significantly increased. The AFM and TEM results revealed that the PTB7‐Th: p ‐PIB film had favorable nanoscale phase separation and formed a bicontinuous interpenetrating network. Abstract : Core configuration : Isomeric effect on the optoelectronic properties of two small‐molecule non‐fullerene acceptors based on bifluorenylidene and perylene diimide were investigated. Organic solar cells based on these materials achieved the highest power conversion efficiency of 5.95 % without any treatments (seeAbstract: Two different non‐fullerene small‐molecule acceptors, m ‐PIB and p ‐PIB, based on 9, 9′‐bifluorenylidene (BF) and perylene diimide (PDI) were designed and synthesized. Four β‐substituted PDIs were linked to BF in different positions. Based on DFT analysis, derivative p ‐PIB exhibited reduced intramolecular twisting between the PDI moieties, more delocalized wave function, and sufficiently wider π‐electron delocalization than that of m ‐PIB . The absorption ability of p ‐PIB was enhanced due to increased intermolecular interactions. By blending p ‐PIB with poly{4, 8‐bis[5‐(2ethylhexyl)thiophen‐2‐yl]benzo[1, 2‐ b :4, 5‐ b′ ]dithiophene‐ co ‐3‐fluorothieno[3, 4‐ b ]‐thiophene‐2‐carboxylate} (PTB7‐Th), organic solar cells (OSCs) based on p ‐PIB obtained a maximum power conversion efficiency of 5.95 % without any treatments. Due to the improved and balanced hole and electron mobilities, the short‐circuit current and fill factor of OSCs based on PTB7‐Th and p ‐PIB were significantly increased. The AFM and TEM results revealed that the PTB7‐Th: p ‐PIB film had favorable nanoscale phase separation and formed a bicontinuous interpenetrating network. Abstract : Core configuration : Isomeric effect on the optoelectronic properties of two small‐molecule non‐fullerene acceptors based on bifluorenylidene and perylene diimide were investigated. Organic solar cells based on these materials achieved the highest power conversion efficiency of 5.95 % without any treatments (see figure). … (more)
- Is Part Of:
- Chemistry. Volume 24:Issue 16(2018)
- Journal:
- Chemistry
- Issue:
- Volume 24:Issue 16(2018)
- Issue Display:
- Volume 24, Issue 16 (2018)
- Year:
- 2018
- Volume:
- 24
- Issue:
- 16
- Issue Sort Value:
- 2018-0024-0016-0000
- Page Start:
- 4149
- Page End:
- 4156
- Publication Date:
- 2018-02-19
- Subjects:
- donor–acceptor systems -- organic solar cells -- perylene diimides -- photochemistry -- steric hindrance
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201705480 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6175.xml