4.8 Article

Polariton Decay in Donor-Acceptor Cavity Systems

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 12, Issue 40, Pages 9774-9782

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.1c02644

Keywords

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Funding

  1. Gordon and Betty Moore Foundation [GBMF7114]
  2. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering [DE-SC0012458]
  3. National Science Foundation [DGE-1656466]
  4. Princeton Center for Complex Materials (PCCM), a National Science Foundation (NSF)-MRSEC program [DMR-2011750]

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Enhanced delocalization is beneficial for absorbing molecules in organic solar cells, and polaritons offer exceptional delocalization that can improve the efficiency of bilayer organic photovoltaics by aiding in exciton delivery to the donor-acceptor interface. The decay of polaritons in bilayer cavities shows an additional pathway through charge transfer, indicating that the charge transfer from the polariton is fast enough to outcompete decay to the ground state.
Enhanced delocalization is beneficial for absorbing molecules in organic solar cells, and in particular bilayer devices, where excitons face small diffusion lengths as a barrier to reaching the charge-generating donor-acceptor interface. As hybrid light-matter states, polaritons offer exceptional delocalization which could be used to improve the efficiency of bilayer organic photovoltaics. Polariton delocalization can aid in delivering excitons to the donor-acceptor interface, but the subsequent charge transfer event must compete with the fast decay of the polariton. To evaluate the viability of polaritons as tools to improve bilayer organic solar cells, we studied the decay of the lower polariton in three cavity systems: a donor only, a donor-acceptor bilayer, and a donor-acceptor blend. Using several spectroscopic techniques, we identified an additional decay pathway through charge transfer for the polariton in the bilayer cavity, demonstrating charge transfer from the polariton is fast enough to outcompete the decay to the ground state.

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