Bromination: An Alternative Strategy for Non‐Fullerene Small Molecule Acceptors. Issue 9 (28th February 2020)
- Record Type:
- Journal Article
- Title:
- Bromination: An Alternative Strategy for Non‐Fullerene Small Molecule Acceptors. Issue 9 (28th February 2020)
- Main Title:
- Bromination: An Alternative Strategy for Non‐Fullerene Small Molecule Acceptors
- Authors:
- Wang, Huan
Liu, Tao
Zhou, Jiadong
Mo, Daize
Han, Liang
Lai, Hanjian
Chen, Hui
Zheng, Nan
Zhu, Yulin
Xie, Zengqi
He, Feng - Abstract:
- Abstract: The concept of bromination for organic solar cells has received little attention. However, the electron withdrawing ability and noncovalent interactions of bromine are similar to those of fluorine and chlorine atoms. A tetra‐brominated non‐fullerene acceptor, designated as BTIC‐4Br, has been recently developed by introducing bromine atoms onto the end‐capping group of 2‐(3‐oxo‐2, 3‐dihydro‐1H‐inden‐1‐ylidene) malononitrile and displayed a high power conversion efficiency (PCE) of 12%. To further improve its photovoltaic performance, the acceptor is optimized either by introducing a longer alkyl chain to the core or by modulating the numbers of bromine substituents. After changing each end‐group to a single bromine, the BTIC‐2Br‐ m ‐based devices exhibit an outstanding PCE of 16.11% with an elevated open‐circuit voltage of V oc = 0.88 V, one of the highest PCEs reported among brominated non‐fullerene acceptors. This significant improvement can be attributed to the higher light harvesting efficiency, optimized morphology, and higher exciton quenching efficiencies of the di‐brominated acceptor. These results demonstrate that the substitution of bromine onto the terminal group of non‐fullerene acceptors results in high‐efficiency organic semiconductors, and promotes the use of the halogen‐substituted strategy for polymer solar cell applications. Abstract : The bromination of non‐fullerene acceptors provides a promising alternative approach for the creation ofAbstract: The concept of bromination for organic solar cells has received little attention. However, the electron withdrawing ability and noncovalent interactions of bromine are similar to those of fluorine and chlorine atoms. A tetra‐brominated non‐fullerene acceptor, designated as BTIC‐4Br, has been recently developed by introducing bromine atoms onto the end‐capping group of 2‐(3‐oxo‐2, 3‐dihydro‐1H‐inden‐1‐ylidene) malononitrile and displayed a high power conversion efficiency (PCE) of 12%. To further improve its photovoltaic performance, the acceptor is optimized either by introducing a longer alkyl chain to the core or by modulating the numbers of bromine substituents. After changing each end‐group to a single bromine, the BTIC‐2Br‐ m ‐based devices exhibit an outstanding PCE of 16.11% with an elevated open‐circuit voltage of V oc = 0.88 V, one of the highest PCEs reported among brominated non‐fullerene acceptors. This significant improvement can be attributed to the higher light harvesting efficiency, optimized morphology, and higher exciton quenching efficiencies of the di‐brominated acceptor. These results demonstrate that the substitution of bromine onto the terminal group of non‐fullerene acceptors results in high‐efficiency organic semiconductors, and promotes the use of the halogen‐substituted strategy for polymer solar cell applications. Abstract : The bromination of non‐fullerene acceptors provides a promising alternative approach for the creation of high‐performance organic solar cells. BTIC‐2Br‐ m ‐based devices exhibit an outstanding power conversion efficiency of 16.11% with an elevated open circuit voltage of 0.88 V, representing one of the highest efficiencies in brominated non‐fullerene acceptors. … (more)
- Is Part Of:
- Advanced science. Volume 7:Issue 9(2020)
- Journal:
- Advanced science
- Issue:
- Volume 7:Issue 9(2020)
- Issue Display:
- Volume 7, Issue 9 (2020)
- Year:
- 2020
- Volume:
- 7
- Issue:
- 9
- Issue Sort Value:
- 2020-0007-0009-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-02-28
- Subjects:
- bromination -- intermolecular interactions -- non‐fullerene acceptors -- open‐circuit voltage -- polymer solar cells
Science -- Periodicals
505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2198-3844 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/advs.201903784 ↗
- Languages:
- English
- ISSNs:
- 2198-3844
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
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