Abstract
A nonfullerene acceptor, IDTT-OB, employing indacenodithieno[3,2-b]thiophene (IDTT) decorated with asymmetric substituents as the core, is designedly prepared. In comparison with the analogue IDT-OB, extending the five-heterocyclic indacenodithiophene (IDT) core to seven-heterocyclic fused ring endows IDTT-OB with more broad absorption and elevated highest occupied molecular orbital energy level. In addition, IDTT-OB shows a more intense molecular packing and a higher crystalline behavior with a strong face-on orientation in the neat film and the PBDB-T:IDTT-OB blend film. Furthermore, an ideal nanomorphology with a domain size of 19 nm can be obtained, which is in favor of exciton diffusion and charge separation. Accordingly, PBDB-T:IDTT-OB-based polymer solar cells demonstrate a maximum power conversion efficiency (PCE max ) of 11.19% with an impressive fill factor of 0.74, comparable to the state-of-the-art acceptors with similar molecular backbones. More importantly, IDTT-OB-based devices show good tolerance to the film thickness, which maintain a high PCE of 10.20% with a 250 nm thick active layer, demonstrating that the asymmetric acceptor is profound for fabricating high-efficiency thick-film nonfullerene solar cells.
| Original language | English |
|---|---|
| Pages (from-to) | 3098-3106 |
| Number of pages | 9 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 11 |
| Issue number | 3 |
| DOIs | |
| State | Published - 23 Jan 2019 |
Keywords
- asymmetric side chains
- face-on orientation
- non-fullerene acceptor
- solar cells
- thick film
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