Abstract
A strategy that employs the central-core regiochemistry to develop two isomeric perylene diimide (PDI)-based small molecular acceptors (SMAs), BPT-Se and BPT-Se1, is introduced, and the effect of the central-core regiochemistry on the optical, electronic, charge-transport, photovoltaic, and morphological properties of the molecules and their devices is investigated. The PDBT-T1:BPT-Se1-based device delivers a power conversion efficiency (PCE) of 9.54% with an excellent fill factor (FF) of 73.2%, while the BPT-Se-based device yields a PCE of 7.78%. The large improvement of PCE upon isomerization of BPT-Se should be ascribed to the concurrent enhancement of FF, short circuit current (J SC ), and open circuit voltage (V OC ) of the PDBT-T1:BPT-Se1 devices. The higher FF of the organic solar cells (OSCs) based on PDBT-T1:BPT-Se1 can be attributed to the higher charge dissociation and charge collection efficiency, less bimolecular combination, more balanced µ h /µ e , better molecular packing and a more favorable morphology. It is worth mentioning that the FF of 73.2% is the highest value for PDI-based SMAs OSCs to date. The result shows that regiochemistry of the central core in PDI-based SMAs greatly affects the physicochemical properties and photovoltaic performance. The success of the isomerization strategy offers exciting prospects for the molecular design of PDI-based SMAs.
| Original language | English |
|---|---|
| Article number | 1802065 |
| Journal | Advanced Science |
| Volume | 6 |
| Issue number | 6 |
| DOIs | |
| State | Published - 20 Mar 2019 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 7 Affordable and Clean Energy
Keywords
- fill factor
- isomerization
- organic solar cells
- perylene diimide
- small molecular acceptors
Fingerprint
Dive into the research topics of 'Isomerization of Perylene Diimide Based Acceptors Enabling High-Performance Nonfullerene Organic Solar Cells with Excellent Fill Factor'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver