4.8 Article

Triplet Excitons and Associated Efficiency-Limiting Pathways in Organic Solar Cell Blends Based on (Non-) Halogenated PBDB-T and Y-Series

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 33, Issue 12, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202212640

Keywords

halogenation; non-fullerene acceptors; organic photovoltaics; spin physics; triplet excitons

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The development of non-fullerene acceptors (NFAs) in organic photovoltaics (OPV) has led to a significant progress in power conversion efficiencies, reaching nearly 20%. However, triplet states have been found to negatively affect device performance, leading to non-radiative losses and device degradation. A study using various spin-sensitive methods and quantum-chemical calculations identified the presence of triplet excitons in OPV blends, providing insights into the pathways for triplet formation and suggesting potential for improved charge generation to enhance OPV efficiencies.
The great progress in organic photovoltaics (OPV) over the past few years has been largely achieved by the development of non-fullerene acceptors (NFAs), with power conversion efficiencies now approaching 20%. To further improve device performance, loss mechanisms must be identified and minimized. Triplet states are known to adversely affect device performance, since they can form energetically trapped excitons on low-lying states that are responsible for non-radiative losses or even device degradation. Halogenation of OPV materials has long been employed to tailor energy levels and to enhance open circuit voltage. Yet, the influence on recombination to triplet excitons has been largely unexplored. Using the complementary spin-sensitive methods of photoluminescence detected magnetic resonance and transient electron paramagnetic resonance corroborated by transient absorption and quantum-chemical calculations, exciton pathways in OPV blends are unravelled employing the polymer donors PBDB-T, PM6, and PM7 together with NFAs Y6 and Y7. All blends reveal triplet excitons on the NFA populated via non-geminate hole back transfer and, in blends with halogenated donors, also by spin-orbit coupling driven intersystem crossing. Identifying these triplet formation pathways in all tested solar cell absorber films highlights the untapped potential for improved charge generation to further increase plateauing OPV efficiencies.

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