On the Interplay between CT and Singlet Exciton Emission in Organic Solar Cells with Small Driving Force and Its Impact on Voltage Loss
Source abstract
Abstract
Abstract The interplay between free charge carriers, charge transfer (CT) states and singlet excitons (S1) determines the recombination pathway and the resulting open circuit voltage (VOC) of organic solar cells. By combining a well‐aggregated low bandgap polymer with different blend ratios of the fullerenes PCBM and ICBA, the energy of the CT state (ECT) is varied by 130 meV while leaving the S1 energy of the polymer () unaffected. It is found that the polymer exciton dominates the radiative properties of the blend when approaches , while the VOC remains limited by the non‐radiative decay of the CT state. It is concluded that an increasing strength of the exciton in the optical spectra of organic solar cells will generally decrease the non‐radiative voltage loss because it lowers the radiative VOC limit (VOC,rad), but not because it is more emissive. The analysis further suggests that electronic coupling between the CT state and the S1 will not improve the VOC, but rather reduce the VOC,rad. It is anticipated that only at very low CT state absorption combined with a fairly high CT radiative efficiency the solar cell benefit from the radiative properties of the singlet excitons.
Source: crossref · 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
Institute of Physics and Astronomy University of Potsdam 14476 Potsdam Germany
Department 8.5 Micro‐NDT Federal Institute of Materials Research and Testing Unter den Eichen 87 12205 Berlin Germany
Department of Physics and Astronomy Washington State University 100 Dairy Road Pullman WA 99164 USA
Polymers and Electronics Fraunhofer Institute for Applied Polymer Research Geiselbergstr. 69 14476 Potsdam Germany
Institute for Materials Research (IMO‐IMOMEC) Hasselt University Wetenschapspark 1 Diepenbeek BE – 3590 Belgium
References (47)
Show source-provided references
1. 10.1063/1.134583410.1063/1.1345834 ↗
2. Cui Y. · Adv. Mater. · 2021 · 33 · 41
3. 10.1016/j.joule.2021.12.01710.1016/j.joule.2021.12.017 ↗
4. 10.1002/aenm.20200357010.1002/aenm.202003570 ↗
5. 10.1038/nenergy.2017.5310.1038/nenergy.2017.53 ↗
6. 10.1038/s41563-019-0324-510.1038/s41563-019-0324-5 ↗
7. 10.1021/jacs.9b0146510.1021/jacs.9b01465 ↗
8. 10.1038/s41563-018-0128-z10.1038/s41563-018-0128-z ↗
9. 10.1038/s41560-020-00684-710.1038/s41560-020-00684-7 ↗
10. 10.1021/acsenergylett.0c0257210.1021/acsenergylett.0c02572 ↗
11. 10.1021/acs.jpcc.1c0365610.1021/acs.jpcc.1c03656 ↗
12. Chen X.‐K. · Nat. Energy · 2021 · 6 · 8
13. Dong Y. · J. Am. Chem. Soc. · 2021 · 143 · 20
14. 10.1021/ja311214310.1021/ja3112143 ↗
15. 10.1117/1.JPE.5.05720310.1117/1.JPE.5.057203 ↗
16. 10.1002/ijch.20218010110.1002/ijch.202180101 ↗
17. Zhang Y. · Macromolecules · 2012 · 45 · 13
18. Albrecht S. · J. Am. Chem. Soc. · 2012 · 134 · 36
19. 10.1038/s41467-018-04386-310.1038/s41467-018-04386-3 ↗
20. 10.1038/s41563-017-0005-110.1038/s41563-017-0005-1 ↗
21. 10.1038/nmat192810.1038/nmat1928 ↗
22. Lee J. K. · J. Am. Chem. Soc. · 2008 · 130 · 11
23. 10.1039/C1SC00674F10.1039/C1SC00674F ↗
24. 10.1021/ja104272610.1021/ja1042726 ↗
25. 10.1021/acs.jpcc.7b0228810.1021/acs.jpcc.7b02288 ↗
26. 10.1103/PhysRevB.76.08530310.1103/PhysRevB.76.085303 ↗
27. 10.1002/aenm.20200182810.1002/aenm.202001828 ↗
28. 10.1038/s41467-018-05987-810.1038/s41467-018-05987-8 ↗
29. 10.1002/aenm.20150133510.1002/aenm.201501335 ↗
30. 10.1039/C5EE03095A10.1039/C5EE03095A ↗
31. 10.1002/adfm.20120314810.1002/adfm.201203148 ↗
32. 10.1039/C8MH00564H10.1039/C8MH00564H ↗
33. 10.1103/PhysRevApplied.15.06400910.1103/PhysRevApplied.15.064009 ↗
34. 10.1002/aenm.20150012310.1002/aenm.201500123 ↗
35. 10.1002/adma.20210178410.1002/adma.202101784 ↗
36. 10.1038/s41467-020-19029-910.1038/s41467-020-19029-9 ↗
37. 10.1103/PhysRevB.86.03521210.1103/PhysRevB.86.035212 ↗
38. 10.1038/s41467-018-07707-810.1038/s41467-018-07707-8 ↗
39. Azzouzi M. · Phys. Rev. X · 2018 · 8 · 3
40. Wang T. · Chem. Mater. · 2019 · 31 · 16
41. Graham K. R. · J. Am. Chem. Soc. · 2014 · 136 · 27
42. 10.1021/jacs.6b1285710.1021/jacs.6b12857 ↗
43. Chen X.‐K. · Adv. Energy Mater. · 2016 · 6 · 24
44. 10.1038/s41467-017-00107-410.1038/s41467-017-00107-4 ↗
45. Zheng Z. · Adv. Energy Mater. · 2019 · 9 · 14
46. 10.1016/j.joule.2019.09.01010.1016/j.joule.2019.09.010 ↗
47. 10.1038/s41563-020-00835-x10.1038/s41563-020-00835-x ↗