Excitonic splittings in molecular dimers: why static ab initio calculations cannot match them

Abstract

After decades of research on molecular excitons, only few molecular dimers are available on which exciton and vibronic coupling theories can be rigorously tested. In centrosymmetric H-bonded dimers consisting of identical (hetero)aromatic chromophores, the monomer electronic transition dipole moment vectors subtract or add, yielding S₀ → S₁ and S₀ → S₂ transitions that are symmetry-forbidden or -allowed, respectively. Symmetry breaking by ¹²C/¹³C or H/D isotopic substitution renders the forbidden transition weakly allowed. The excitonic coupling (Davydov splitting) can then be measured between the S₀ → S₁ and S₀ → S₂ vibrationless bands. We discuss the mass-specific excitonic spectra of five H-bonded dimers that are supersonically cooled to a few K and investigated using two-color resonant two-photon ionization spectroscopy. The excitonic splittings Δ_calc predicted by ab initio methods are 5–25 times larger than the experimental excitonic splittings Δ_exp. The purely electronic ab initio splittings need to be reduced (“quenched”), reflecting the coupling of the electronic transition to the optically active vibrations of the monomers. The so-called quenching factors Γ < 1 can be determined from experiment (Γ_exp) and/or calculation (Γ_calc). The vibronically quenched splittings Γ·Δ_calc are found to nicely reproduce the experimental exciton splittings.