Abstract
In contrast to classical bulk heterojunction (BHJ) in organic solar cells (OSCs), the quasi-homojunction (QHJ) with extremely low donor content (≤10 wt.%) is unusual and generally yields much lower device efficiency. Here, representative polymer donors and nonfullerene acceptors are selected to fabricate QHJ OSCs, and a complete picture for the operation mechanisms of high-efficiency QHJ devices is illustrated. PTB7-Th:Y6 QHJ devices at donor:acceptor (D:A) ratios of 1:8 or 1:20 can achieve 95% or 64% of the efficiency obtained from its BHJ counterpart at the optimal D:A ratio of 1:1.2, respectively, whereas QHJ devices with other donors or acceptors suffer from rapid roll-off of efficiency when the donors are diluted. Through device physics and photophysics analyses, it is observed that a large portion of free charges can be intrinsically generated in the neat Y6 domains rather than at the D/A interface. Y6 also serves as an ambipolar transport channel, so that hole transport as also mainly through Y6 phase. The key role of PTB7-Th is primarily to reduce charge recombination, likely assisted by enhancing quadrupolar fields within Y6 itself, rather than the previously thought principal roles of light absorption, exciton splitting, and hole transport.
| Original language | English |
|---|---|
| Article number | 2206717 |
| Journal | Advanced Materials |
| Volume | 34 |
| Issue number | 50 |
| Early online date | 3 Oct 2022 |
| DOIs | |
| Publication status | Published - 15 Dec 2022 |
Bibliographical note
Publisher Copyright:© 2022 Wiley-VCH GmbH.
Research Groups and Themes
- Physical & Theoretical
Keywords
- fused-ring electron acceptor
- nonfullerene
- organic solar cell
- quasi-homojunction
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