journal article·2023-11-10Open access

Green Additive Limits Runaway Crystallinity in PM6:Y6 Organic Solar Cells but Causes Field-Independent Geminate Recombination

Obaid Alqahtani, Awwad Alotaibi, Michael Burnes, Brian A. Collins

ACS Energy Letters· Volume 8· Issue 11

Abstract

Solvent additives are well-established for improving device performance of organic solar cells by enhancing nanodomain phase separation and crystallization. However, optimum additive concentrations are typically at trace amounts with slight fluctuations causing runaway crystallinity that short the device and limit scale-up potential. Here we show that a nonhalogenated solvent additive 1-phenylnaphthalene (PN) can be used to optimize high-performance PM6:Y6 devices, but without runaway crystallinity even at concentrations 10× above the optimum. Our holistic analysis of device losses shows that PN increases photoabsorption while decreasing bimolecular recombination. However, above the optimum, charge generation is reduced due to field-independent geminate recombination of charge transfer states that overcomes the other benefits. Rotated Y6 crystallite orientation is a likely culprit, where the device electric field is ineffective at separating the charges. Despite this, device performance remains higher than that of traditional additives, indicating a route to avoiding the high sensitivity of performance to processing conditions.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Physics and Astronomy, Washington State University, Pullman, Washington 99164, United States

Department of Physics, Prince Sattam bin Abdulaziz University, Alkharj 11942, KSA

Funding

Basic Energy Sciences · National Science Foundation

References (26)

Show source-provided references
1. 10.1002/adma.20221076010.1002/adma.202210760 ↗
2. 10.1038/s41560-021-00820-x10.1038/s41560-021-00820-x ↗
3. 10.1039/D1EE01220G10.1039/D1EE01220G ↗
4. 10.1016/j.dyepig.2021.10996310.1016/j.dyepig.2021.109963 ↗
5. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
6. 10.1039/D0EE04012F10.1039/D0EE04012F ↗
7. 10.1039/D1QM00060H10.1039/D1QM00060H ↗
8. 10.1002/smll.20220241110.1002/smll.202202411 ↗
9. 10.1016/j.joule.2022.06.00810.1016/j.joule.2022.06.008 ↗
10. 10.1016/j.nanoen.2020.10531010.1016/j.nanoen.2020.105310 ↗
11. 10.1007/s40843-017-9080-x10.1007/s40843-017-9080-x ↗
12. 10.1038/nenergy.2015.2710.1038/nenergy.2015.27 ↗
13. 10.1002/adma.20190676310.1002/adma.201906763 ↗
14. 10.1039/C8TA12336E10.1039/C8TA12336E ↗
15. 10.1021/acs.jpclett.0c0386310.1021/acs.jpclett.0c03863 ↗
16. 10.1002/adma.20100088310.1002/adma.201000883 ↗
17. 10.1021/acsenergylett.0c0257210.1021/acsenergylett.0c02572 ↗
18. 10.1038/nmat380710.1038/nmat3807 ↗
19. 10.1002/aenm.20140092210.1002/aenm.201400922 ↗
20. 10.1002/pol.2021041410.1002/pol.20210414 ↗
21. 10.1021/jacs.8b1298210.1021/jacs.8b12982 ↗
22. 10.1038/nphoton.2014.5510.1038/nphoton.2014.55 ↗
23. 10.1002/adfm.20130421610.1002/adfm.201304216 ↗
24. 10.1002/aenm.20200344110.1002/aenm.202003441 ↗
25. 10.1038/s41467-020-17867-110.1038/s41467-020-17867-1 ↗
26. 10.1021/acs.jpclett.6b0217810.1021/acs.jpclett.6b02178 ↗