Y6 Homojunction Organic Solar Cells with Over 5% Power Conversion Efficiency by Controlling the Active Layer Morphology
Source abstract
Abstract
ABSTRACT Solution‐processable single chromophore homojunction organic solar cells (OSCs) offer a simpler pathway toward device manufacturing and performance reproducibility. However, using a molecule composed of a single chromophore that absorbs light and generates and transports charge efficiently is a challenge. Herein, we report how manipulating the phases in a film can improve the efficiency of homojunction OSCs. Specifically, it is shown that the addition of small amounts of 1,8‐diiodooctane or 1‐chloronaphthalene to a chloroform solution of Y6 can be used to produce a film with different phases. When 1,8‐diiodooctane is used as the additive, the different phases formed provided the energy offset to generate free charge carriers with a maximum internal quantum efficiency of 60%. The optimized Y6 film morphology has electron and hole mobilities of 15.5 ± 1.3 ×10 −5 cm 2 V −1 s −1 and 30.7 ± 3.4 × 10 −5 cm 2 V −1 s −1 , respectively. The best small OSC (0.08 cm 2 ) has a power conversion efficiency of 5.4%, with the efficiency of a 1.3 cm 2 OSC being a creditable 3.1%. These results show that the latest generation of non‐fullerene acceptors also opens new avenues for the development of simplified large‐scale homojunction OSCs that move beyond the bulk heterojunction approach.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · TiO2 Photocatalysis and Solar Cells · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Centre For Organic Photonics & Electronics School of Chemistry and Molecular Biosciences The University of Queensland Brisbane QLD Australia
References (54)
Show source-provided references
1. 10.1002/adma.20230158310.1002/adma.202301583 ↗
2. 10.1038/s41563-020-00836-w10.1038/s41563-020-00836-w ↗
3. 10.1002/smtd.20210154810.1002/smtd.202101548 ↗
4. 10.1002/adfm.20240932310.1002/adfm.202409323 ↗
5. 10.1038/s41467-022-30127-810.1038/s41467-022-30127-8 ↗
6. 10.1002/ange.20210515610.1002/ange.202105156 ↗
7. 10.1038/s41467‐020‐19029‐910.1038/s41467‐020‐19029‐9 ↗
8. 10.1021/acs.chemrev.7b0053510.1021/acs.chemrev.7b00535 ↗
9. 10.1038/s41570‐022‐00409‐210.1038/s41570‐022‐00409‐2 ↗
10. 10.1038/s42254-024-00719-y10.1038/s42254-024-00719-y ↗
11. 10.1002/aenm.20210298710.1002/aenm.202102987 ↗
12. 10.1038/s41467‐020‐18439‐z10.1038/s41467‐020‐18439‐z ↗
13. 10.1038/nmat211910.1038/nmat2119 ↗
14. 10.1002/solr.20230034210.1002/solr.202300342 ↗
15. 10.1002/smll.20240948510.1002/smll.202409485 ↗
16. 10.1038/s41467-023-37234-010.1038/s41467-023-37234-0 ↗
17. 10.1039/D1TA05268C10.1039/D1TA05268C ↗
18. 10.1002/adma.20170711410.1002/adma.201707114 ↗
19. 10.1016/j.enchem.2024.10012910.1016/j.enchem.2024.100129 ↗
20. 10.1016/j.cclet.2023.10937810.1016/j.cclet.2023.109378 ↗
21. 10.1021/ja710079w10.1021/ja710079w ↗
22. 10.1002/adfm.20130009910.1002/adfm.201300099 ↗
23. 10.1021/cm501048310.1021/cm5010483 ↗
24. 10.1021/cm503198710.1021/cm5031987 ↗
25. 10.1016/j.orgel.2020.10569010.1016/j.orgel.2020.105690 ↗
26. 10.1021/acsami.0c0284310.1021/acsami.0c02843 ↗
27. 10.1039/D2MH01411D10.1039/D2MH01411D ↗
28. 10.1016/j.orgel.2016.04.01410.1016/j.orgel.2016.04.014 ↗
29. 10.1063/1.289815310.1063/1.2898153 ↗
30. 10.1039/C5TA00833F10.1039/C5TA00833F ↗
31. 10.1039/C7TC02088K10.1039/C7TC02088K ↗
32. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
33. 10.1039/D3TA05177C10.1039/D3TA05177C ↗
34. 10.1002/solr.20200049810.1002/solr.202000498 ↗
35. 10.1021/acs.jpclett.4c0311910.1021/acs.jpclett.4c03119 ↗
36. 10.1021/jacsau.4c0004610.1021/jacsau.4c00046 ↗
37. 10.1039/D4TA05438E10.1039/D4TA05438E ↗
38. 10.1016/j.xcrp.2022.10089510.1016/j.xcrp.2022.100895 ↗
39. 10.1002/solr.20190018410.1002/solr.201900184 ↗
40. 10.1021/acs.jpclett.9b0117510.1021/acs.jpclett.9b01175 ↗
41. 10.1039/C6TA00126B10.1039/C6TA00126B ↗
42. 10.1002/solr.20250042110.1002/solr.202500421 ↗
43. 10.1021/acsami.5c0113410.1021/acsami.5c01134 ↗
44. 10.1016/j.joule.2019.01.00410.1016/j.joule.2019.01.004 ↗
45. 10.1021/acsami.4c0286410.1021/acsami.4c02864 ↗
46. 10.1039/D0TC00587H10.1039/D0TC00587H ↗
47. 10.1002/aenm.20130095410.1002/aenm.201300954 ↗
48. 10.1002/adma.20100088310.1002/adma.201000883 ↗
49. 10.3390/molecules2518411810.3390/molecules25184118 ↗
50. 10.1016/j.mattod.2024.09.00910.1016/j.mattod.2024.09.009 ↗
51. 10.1021/jacs.0c0489010.1021/jacs.0c04890 ↗
52. 10.1021/acs.jpcc.1c0644810.1021/acs.jpcc.1c06448 ↗
53. 10.1016/0009‐2614(95)00584‐Q10.1016/0009‐2614(95)00584‐Q ↗
54. 10.1039/D3TC02740F10.1039/D3TC02740F ↗