Abstract
For over two decades, most high-performance organic photovoltaics (OPVs) have been made with donor:acceptor bulk heterojunctions with domain sizes limited by exciton diffusion, where charge separation mostly takes place through the dissociation of the interfacial charge-transfer (xCT) excitons. Recently, nonfullerene acceptor (NFA)-based OPVs have shown excellent compatibility to device structures with large domains in active layers. However, it remains elusive how the excitations that are distant from the interfaces are converted into free charges. Here, we report the identification of a new charge separation channel in model copolymer/NFA blends mediated by intra-moiety delocalized excitations in both planar heterojunctions and donor-enriched bulk heterojunctions. The delocalized excitations induced by interchromophore electronic interactions in copolymer donors mediate the long-range charge separation and dissociate into free charges without forming the bound xCT states first, releasing the constraints associated with the short exciton diffusion length in organic materials. The long-range charge separation mechanism uncovered in this work, in cooperation with the short-range xCT-mediated pathway, holds the potential to further optimize OPVs with diverse device structures.
Published Version
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