Abstract
Two perylenediimide derivatives (3T-PDI2 and 6T-PDI4) based on dendritic terthiophene (3T) and sexithiophene (6T) cores were designed and synthesized. The rigid and dendritic oligothiophene core ensures a non-planar structure of these two compounds, which was confirmed by theoretical molecular structure simulation. The optical and electrochemical investigation results showed that both compounds have similar LUMO energy level of −4.1 eV, demonstrating that the LUMO orbital is mainly localized on the PDI moiety. Polymer solar cells using 3T-PDI2 and 6T-PDI4 as the electron acceptor, and PTB7-Th as the donor were fabricated and tested. A power conversion efficiency (PCE) of 4.12% was obtained for the 6T-PDI4 based device, which is higher than that of 3T-PDI2 based device (3.41%). Higher charge carrier mobility and less Shockley-Read-Hall recombination were also measured for the 6T-PDI4 based device. The current work demonstrates that dendritic PDI derivatives could serve as non-fullerene acceptor for use in polymer solar cells.
Original language | English |
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Pages (from-to) | 498-508 |
Number of pages | 11 |
Journal | Dyes and Pigments |
Volume | 139 |
DOIs | |
Publication status | Published - 1 Apr 2017 |
Keywords
- Dendritic molecular structure
- Non-fulerene acceptors
- Oligothiophene
- Organic solar cells
- Perylenediimide