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On the interplay between CT and singlet exciton emission in organic solar cells with small driving force and its impact on voltage loss

  • The interplay between free charge carriers, charge transfer (CT) states and singlet excitons (S-1) determines the recombination pathway and the resulting open circuit voltage (V-OC) 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 (E-CT) is varied by 130 meV while leaving the S-1 energy of the polymer (ES1\[{E_{{{\rm{S}}_1}}}\]) unaffected. It is found that the polymer exciton dominates the radiative properties of the blend when ECT\[{E_{{\rm{CT}}}}\] approaches ES1\[{E_{{{\rm{S}}_1}}}\], while the V-OC 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 V-OC limit (V-OC,V-rad), but not because it is more emissive. The analysis further suggests that electronic coupling between the CT state and the S-1 will not improveThe interplay between free charge carriers, charge transfer (CT) states and singlet excitons (S-1) determines the recombination pathway and the resulting open circuit voltage (V-OC) 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 (E-CT) is varied by 130 meV while leaving the S-1 energy of the polymer (ES1\[{E_{{{\rm{S}}_1}}}\]) unaffected. It is found that the polymer exciton dominates the radiative properties of the blend when ECT\[{E_{{\rm{CT}}}}\] approaches ES1\[{E_{{{\rm{S}}_1}}}\], while the V-OC 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 V-OC limit (V-OC,V-rad), but not because it is more emissive. The analysis further suggests that electronic coupling between the CT state and the S-1 will not improve the V-OC, but rather reduce the V-OC,V-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.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Tobias FritschORCiD, Jona KurpiersORCiDGND, Steffen RolandORCiDGND, Nurlan TokmoldinORCiDGND, Safa ShoaeeORCiDGND, Thomas FerronORCiD, Brian A. CollinsORCiD, Silvia JanietzORCiDGND, Koen VandewalORCiDGND, Dieter NeherORCiDGND
DOI:https://doi.org/10.1002/aenm.202200641
ISSN:1614-6832
ISSN:1614-6840
Titel des übergeordneten Werks (Englisch):Advanced energy materials
Verlag:Wiley-VCH
Verlagsort:Weinheim
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:28.06.2022
Erscheinungsjahr:2022
Datum der Freischaltung:24.05.2024
Freies Schlagwort / Tag:external quantum efficiency; organic photovoltaics; ternary blends; voltage losses
Band:12
Ausgabe:31
Aufsatznummer:2200641
Seitenanzahl:11
Fördernde Institution:(German Science Foundation DFG) [256605806, 460766640]; US National; Science Foundation [1905790]; DOE Office of Science User Facility; [DE-AC02-05CH11231]; Projekt DEAL
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Physik und Astronomie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 53 Physik / 530 Physik
Peer Review:Referiert
Publikationsweg:Open Access / Hybrid Open-Access
Lizenz (Deutsch):License LogoCC-BY - Namensnennung 4.0 International
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