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      Role of Exciton Diffusion and Lifetime in Organic Solar Cells with a Low Energy Offset

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          Abstract

          Despite general agreement that the generation of free charges in organic solar cells is driven by an energetic offset, power conversion efficiencies have been improved using low-offset blends. In this work, we explore the interconnected roles that exciton diffusion and lifetime play in the charge generation process under various energetic offsets. A detailed balance approach is used to develop an analytic framework for exciton dissociation and free-charge generation accounting for exciton diffusion to and dissociation at the donor–acceptor interface. For low-offset systems, we find the exciton lifetime to be a pivotal component in the charge generation process, as it influences both the exciton and CT state dissociation. These findings suggest that any novel low-offset material combination must have long diffusion lengths with long exciton lifetimes to achieve optimum charge generation yields.

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          18% Efficiency organic solar cells

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            Charge photogeneration in organic solar cells.

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              Single‐Junction Organic Photovoltaic Cell with 19% Efficiency

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                Author and article information

                Journal
                J Phys Chem Lett
                J Phys Chem Lett
                jz
                jpclcd
                The Journal of Physical Chemistry Letters
                American Chemical Society
                1948-7185
                12 May 2022
                26 May 2022
                : 13
                : 20
                : 4402-4409
                Affiliations
                [1]Sustainable Advanced Materials Programme (Sêr SAM), Department of Physics, Swansea University , Singleton Park, Swansea SA2 8PP, United Kingdom
                Author notes
                Author information
                https://orcid.org/0000-0001-6688-0694
                https://orcid.org/0000-0002-6129-5354
                https://orcid.org/0000-0003-3778-8746
                Article
                10.1021/acs.jpclett.2c00791
                9150110
                35549280
                4f85f528-2457-4daf-a16c-a58b7ae91b7c
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 17 March 2022
                : 03 May 2022
                Funding
                Funded by: UK Research and Innovation, doi 10.13039/100014013;
                Award ID: EP/T028511/1
                Funded by: Welsh European Funding Office, doi NA;
                Award ID: NA
                Funded by: European Regional Development Fund, doi 10.13039/501100008530;
                Award ID: NA
                Funded by: Swansea University, doi 10.13039/501100001317;
                Award ID: NA
                Funded by: Natural Sciences and Engineering Research Council of Canada, doi 10.13039/501100000038;
                Award ID: PGSD35456942020
                Categories
                Letter
                Custom metadata
                jz2c00791
                jz2c00791

                Physical chemistry
                Physical chemistry

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