Triplet Formation in Fullerene Multi‐Adduct Blends for Organic Solar Cells and Its Influence on Device Performance
Source abstract
Abstract
Abstract In organic solar cells, high open circuit voltages may be obtained by choosing materials with a high offset between the donor highest occupied molecular orbital (HOMO) and acceptor lowest unoccupied molecular orbital (LUMO). However, increasing this energy offset can also lead to photophysical processes that compete with charge separation. In this paper the formation of triplet states is addressed in blends of polyfluorene polymers with a series of PCBM multi‐adducts. Specifically, it is demonstrated that the formation of such triplets occurs when the offset energy between donor ionization potential and acceptor electron affinity is ∼1.6 eV or greater. Spectroscopic measurements support a mechanism of resonance energy transfer for triplet formation, influenced by the energy levels of the materials, but also demonstrate that the competition between processes at the donor–acceptor interface is strongly influenced by morphology.
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Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Photochemistry and Electron Transfer Studies
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References (33)
Show source-provided references
1. 10.1103/PhysRevLett.93.21660110.1103/PhysRevLett.93.216601 ↗
2. 10.1021/jp808671f10.1021/jp808671f ↗
3. 10.1039/b910675h10.1039/b910675h ↗
4. 10.1063/1.296929510.1063/1.2969295 ↗
5. 10.1002/adfm.20060109810.1002/adfm.200601098 ↗
6. 10.1016/j.cplett.2004.09.03010.1016/j.cplett.2004.09.030 ↗
7. 10.1021/ja801259810.1021/ja8012598 ↗
8. 10.1002/adfm.20090009010.1002/adfm.200900090 ↗
9. 10.1021/ja803054g10.1021/ja803054g ↗
10. 10.1016/j.cplett.2004.05.00610.1016/j.cplett.2004.05.006 ↗
11. 10.1103/PhysRevB.72.04521310.1103/PhysRevB.72.045213 ↗
12. 10.1021/jp902030710.1021/jp9020307 ↗
13. 10.1063/1.271047410.1063/1.2710474 ↗
14. 10.1016/j.cplett.2008.02.02110.1016/j.cplett.2008.02.021 ↗
15. 10.1002/adma.20050129710.1002/adma.200501297 ↗
16. 10.1063/1.312056610.1063/1.3120566 ↗
17. 10.1016/j.tsf.2005.12.03410.1016/j.tsf.2005.12.034 ↗
18. 10.1002/adma.20050171710.1002/adma.200501717 ↗
19. 10.1021/ar900139v10.1021/ar900139v ↗
20. 10.1126/science.114171110.1126/science.1141711 ↗
21. 10.1002/adfm.20060048410.1002/adfm.200600484 ↗
22. 10.1063/1.217149210.1063/1.2171492 ↗
23. 10.1002/(SICI)1521-3765(19980210)4:2<270::AID-CHEM270>3.0.CO;2-510.1002/(SICI)1521-3765(19980210)4:2<270::AID-CHEM270>3.0.CO;2-5 ↗
24. 10.1063/1.233852810.1063/1.2338528 ↗
25. 10.1038/nphoton.2009.6910.1038/nphoton.2009.69 ↗
26. 10.1002/adfm.20090045910.1002/adfm.200900459 ↗
27. 10.1002/adma.20070243810.1002/adma.200702438 ↗
28. J. M.Frost M.Faist J.Nelson unpublished.
29. 10.1088/0953-8984/20/47/47520310.1088/0953-8984/20/47/475203 ↗
30. 10.1021/jp805077410.1021/jp8050774 ↗
31. 10.1021/jp900708f10.1021/jp900708f ↗
32. 10.1063/1.203408310.1063/1.2034083 ↗
33. 10.1016/j.synthmet.2008.03.01610.1016/j.synthmet.2008.03.016 ↗