High Efficiency of Ternary Blend Organic Solar Cells with a BTP-4F/BTP-4H Derivative
Source abstract
Abstract
Organic solar cells (OSCs) are renowned for their flexibility, cost-efficiency, and creative design options, yet persistent challenges drive ongoing research for improvement. One approach involves the replacement of fullerene acceptors with nonfullerene acceptors (NFAs) to address issues related to narrow absorption bands and low oxidation stability stemming from structural limitations. Another strategy tackles the limited absorption range and energy losses associated with bulk heterojunction (BHJ) OSCs by introducing ternary blend. In our study, we harnessed NFAs and ternary blend to address these OSC shortcomings. We engineered a novel NFA, Y5-BT, by modifying the side chain and extending the conjugation in the end group of Y5. This tailored NFAs demonstrated promise in improving energy level charge transport when incorporated into the ternary OSC PM6/Y6/Y5-BT, acting like an alloy-like model. In our optimized PM6/Y6/Y5-BT device, we achieved an open-circuit voltage ( V OC ) = 0.873 V, a short-circuit current density ( J SC ) = 27.2 mA cm –2, a fill factor (FF) = 73.5%, and a power conversion efficiency (PCE) = 17.6%.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Engineering and Convergence Technology, Gyeongsang National University, Jinju 52828, Republic of Korea
Department of Chemistry and RIGET, Gyeongsang National University, Jinju 660-701, Republic of Korea
Department of Chemistry, Inha University, Incheon 22212, Republic of Korea
Funding
National Research Foundation of Korea
References (36)
Show source-provided references
1. 10.1126/science.270.5243.178910.1126/science.270.5243.1789 ↗
2. 10.1039/b812502n10.1039/b812502n ↗
3. 10.1038/nphoton.2012.1110.1038/nphoton.2012.11 ↗
4. 10.1038/nature0249810.1038/nature02498 ↗
5. 10.1063/1.11579710.1063/1.115797 ↗
6. 10.1002/anie.20070250610.1002/anie.200702506 ↗
7. 10.1063/1.182507010.1063/1.1825070 ↗
8. 10.1039/c3ee43080d10.1039/c3ee43080d ↗
9. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
10. 10.1038/natrevmats.2018.310.1038/natrevmats.2018.3 ↗
11. 10.1002/adma.20150057710.1002/adma.201500577 ↗
12. 10.1021/acs.accounts.5b0019910.1021/acs.accounts.5b00199 ↗
13. 10.1021/acs.accounts.5b0019910.1021/acs.accounts.5b00199 ↗
14. 10.1016/j.mattod.2013.04.00510.1016/j.mattod.2013.04.005 ↗
15. 10.1039/C5TA10759H10.1039/C5TA10759H ↗
16. 10.1039/D0EE00862A10.1039/D0EE00862A ↗
17. 10.1002/aenm.20200357010.1002/aenm.202003570 ↗
18. 10.1002/eem2.1238110.1002/eem2.12381 ↗
19. 10.1021/acsenergylett.0c0053710.1021/acsenergylett.0c00537 ↗
20. 10.1002/aenm.20160200010.1002/aenm.201602000 ↗
21. 10.1021/cr400353v10.1021/cr400353v ↗
22. 10.1038/nature0194910.1038/nature01949 ↗
23. 10.1021/accountsmr.0c0003310.1021/accountsmr.0c00033 ↗
24. 10.1039/C9TA06929A10.1039/C9TA06929A ↗
25. 10.1002/aenm.20190172810.1002/aenm.201901728 ↗
26. 10.1002/adma.20200234410.1002/adma.202002344 ↗
27. 10.1021/jacs.7b1305410.1021/jacs.7b13054 ↗
28. 10.1038/nphoton.2015.12810.1038/nphoton.2015.128 ↗
29. 10.1002/adma.20210083010.1002/adma.202100830 ↗
30. 10.1016/j.orgel.2021.10606310.1016/j.orgel.2021.106063 ↗
31. 10.1038/s41560-021-00820-x10.1038/s41560-021-00820-x ↗
32. 10.1021/acsami.9b0846210.1021/acsami.9b08462 ↗
33. 10.1039/C9TA01111K10.1039/C9TA01111K ↗
34. 10.1039/C9EE03710A10.1039/C9EE03710A ↗
35. 10.1021/acsami.2c0788310.1021/acsami.2c07883 ↗
36. 10.1016/j.joule.2021.04.00710.1016/j.joule.2021.04.007 ↗