Unraveling abnormal collective effects via the non-monotonic number dependence of electron transfer in confined electromagnetic fields.

Strong light-matter coupling within an optical cavity leverages the collective interactions of molecules and confined electromagnetic fields, giving rise to the possibilities of modifying chemical reactivity and molecular properties. While collective optical responses, such as enhanced Rabi splitting, are often observed, the overall effect of the cavity on molecular systems remains ambiguous for a large number of molecules. In this paper, we investigate the non-adiabatic electron transfer process in electron donor-acceptor pairs influenced by collective excitation and local molecular dynamics.