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Molecular Packing of Non-Fullerene Acceptors for Organic Solar Cells: Distinctive Local Morphology in Y6 Versus ITIC Derivatives

preprint
submitted on 08.04.2021, 19:19 and posted on 09.04.2021, 10:53 by Grit Kupgan, XianKai Chen, Jean-Luc Bredas
Since a couple of years ago, Y6 has emerged as one of the main non-fullerene acceptors for organic solar cells as its use leads to superior power conversion efficiencies. It is thus of major interest to investigate the multi-scale phenomena that are responsible for Y6’s efficacy. Here, we modeled neat films of Y6 and earlier non-fullerene acceptors, IT-4F and ITIC, using a combination of density functional theory calculations and molecular dynamics simulations, to investigate the various factors that control their charge and exciton transport rates. We find that the molecular packing in Y6 is drastically different from that in IT-4F and ITIC. At the nano-scale, the local morphology of Y6 consists of a large number of directional face-on stackings and well-connected transport networks. Y6 also consistently shows higher electronic couplings for LUMOs, HOMOs, and local excitations than ITIC-type acceptors, which results in fast transport rates for electron, holes, and excitons. Importantly, when considering dimers, their configurations in Y6 are more diverse than in ITIC-type acceptors, with many of those similar to the configurations observed in the Y6 crystal structure reported recently. Most Y6 dimer configurations exhibit strong binding interactions, large electronic couplings, and high transport rates, which when taken together rationalize the better performance of OSCs based on Y6.

Funding

Department of the Navy, Office of Naval Research (Award No. N00014-20-1-2110)

History

Email Address of Submitting Author

gkupgan@arizona.edu

Institution

The University of Arizona

Country

USA

ORCID For Submitting Author

0000-0001-8163-9786

Declaration of Conflict of Interest

No conflict of interest

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