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.