Abstract
Nonfullerene acceptors (NFAs) have played an important role in the development of organic solar cells. However, the optical absorption of most NFAs is limited within 600-900 nm, prohibiting further improvement of short-circuit current density (Jsc). To alleviate this problem, a fused-ring I-core BzS was designed by combining weakly electron-withdrawing benzotriazole (Bz) and strongly electron-donating selenophene together. Besides, the length of N-alkyl chain on the Bz moiety was engineered to tune the morphology, affording two NFAs mBzS-4F and EHBzS-4F. Both NFAs possess an absorption edge approaching 1000 nm, as resulted from the enhanced intramolecular charge transfer in conjunction with efficient intra- A nd intermolecular interactions. Binary photovoltaic devices based on PM6:mBzS-4F showed a power conversion efficiency of 17.02% with a very high Jsc of 27.72 mA/cm2 and a low energy loss of 0.446 eV. This work provides a strategy for future design of efficient NIR-responsive materials.
| Original language | English |
|---|---|
| Pages (from-to) | 9-15 |
| Number of pages | 7 |
| Journal | ACS Energy Letters |
| Volume | 6 |
| Issue number | 1 |
| Early online date | 20 Nov 2020 |
| DOIs | |
| Publication status | Published - 8 Jan 2021 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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