Abstract
Single-material organic solar cells have recently attracted research attention due to their simplicity, morphological robustness and high yield of exciton dissociation. Using α-sexithiophene as a model system, we show that the single-event probability of the exciton dissociation at the boundaries of polycrystalline domains with different molecular orientation is extremely low (∼0.5%), while a high efficiency of charge generation is gained via hundred-fold crossings of the domain boundaries due to the long exciton diffusion length (∼45 nm). This journal is
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CITATION STYLE
Hoang, N. V., Nikolis, V. C., Baisinger, L., Vandewal, K., & Pshenichnikov, M. S. (2021). Diffusion-enhanced exciton dissociation in single-material organic solar cells. Physical Chemistry Chemical Physics, 23(37), 20848–20853. https://doi.org/10.1039/d1cp03328j
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