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Translating local binding energy to a device effective one

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One of the puzzles in the field of organic photovoltaic cells (OPVs) is the high exciton dissociation (charge generation) efficiency even though simple Coulomb based arguments would predict a binding energy of 150–500 meV that would suppress such dissociation. Not knowing which mechanism drives such high dissociation efficiency prevents researchers from establishing clear design rules. The common approach to solve this puzzle is to assume that the binding energy must be lower due to delocalization, disorder or entropy considerations. However, using these theories to quantitatively reproduce the dissociation is challenging. Here, considering entropy and disorder, a new approach is suggested using exciton dissociation efficiency as the parameter to weigh the effect of the energetic disorder. The effective entropy–disorder (EED) model predicts the device-equivalent charge generation efficiency, and provides a consistent new definition for the effective binding energy (Eb,eff). For the first time, it is possible to directly compare a model with experimental results of a non-fullerene acceptor organic solar cell. Such comparison reveals that high dissociation efficiency does not require Eb,eff lower than 100 meV and that high dissociation efficiency is driven by a combined effect of the energy landscape and a mobility that is significantly higher than the steady state one.

Graphical abstract: Translating local binding energy to a device effective one

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The article was received on 13 Nov 2019, accepted on 15 Nov 2019 and first published on 15 Nov 2019

Article type: Paper
DOI: 10.1039/C9SE01095E
Sustainable Energy Fuels, 2020, Advance Article

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    Translating local binding energy to a device effective one

    D. Liraz, P. Cheng, Y. Yang and N. Tessler, Sustainable Energy Fuels, 2020, Advance Article , DOI: 10.1039/C9SE01095E

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