4.8 Article

The role of charge recombination to triplet excitons in organic solar cells

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NATURE
卷 597, 期 7878, 页码 666-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03840-5

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  1. National Research Foundation of Korea [4199990414701] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The majority of charge recombination in organic solar cells that use NFAs occurs through non-emissive NFA triplet excitons under open-circuit conditions, reducing the open-circuit voltage. Engineering substantial hybridization between NFA triplet excitons and spin-triplet charge-transfer excitons can suppress this non-radiative recombination pathway, potentially leading to organic solar cells with power conversion efficiencies of 20% or more.
The use of non-fullerene acceptors (NFAs) in organic solar cells has led to power conversion efficiencies as high as 18%(1). However, organic solar cells are still less efficient than inorganic solar cells, which typically have power conversion efficiencies of more than 20%(2). A key reason for this difference is that organic solar cells have low open-circuit voltages relative to their optical bandgaps(3), owing to non-radiative recombination(4). For organic solar cells to compete with inorganic solar cells in terms of efficiency, non-radiative loss pathways must be identified and suppressed. Here we show that in most organic solar cells that use NFAs, the majority of charge recombination under open-circuit conditions proceeds via the formation of non-emissive NFA triplet excitons; in the benchmark PM6:Y6 blend(5), this fraction reaches 90%, reducing the open-circuit voltage by 60 mV. We prevent recombination via this non-radiative channel by engineering substantial hybridization between the NFA triplet excitons and the spin-triplet charge-transfer excitons. Modelling suggests that the rate of back charge transfer from spin-triplet charge-transfer excitons to molecular triplet excitons may be reduced by an order of magnitude, enabling re-dissociation of the spin-triplet charge-transfer exciton. We demonstrate NFA systems in which the formation of triplet excitons is suppressed. This work thus provides a design pathway for organic solar cells with power conversion efficiencies of 20% or more. A substantial pathway for energy loss in organic solar cells may be suppressed by engineering hybridization between non-fullerene acceptor triplet excitons and spin-triplet charge transfer excitons.

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