Simulation of Ab Initio Optical Absorption Spectrum of β‑Carotene with Fully Resolved S₀ and S₂ Vibrational Normal Modes

The electronic absorption spectrum of β-carotene (β-Car) is studied using quantum chemistry and quantum dynamics simulations. Vibrational normal modes were computed in optimized geometries of the electronic ground state S₀ and the optically bright excited S₂ state using the time-dependent density functional theory. By expressing the S₂-state normal modes in terms of the ground-state modes, we find that no one-to-one correspondence between the ground- and excited-state vibrational modes exists. Using the ab initio results, we simulated the β-Car absorption spectrum with all 282 vibrational modes in a model solvent at 300 K using the time-dependent Dirac–Frenkel variational principle and are able to qualitatively reproduce the full absorption line shape. By comparing the 282-mode model with the prominent 2-mode model, widely used to interpret carotenoid experiments, we find that the full 282-mode model better describes the high-frequency progression of carotenoid absorption spectra; hence, vibrational modes become highly mixed during the S₀ → S₂ optical excitation. The obtained results suggest that electronic energy dissipation is mediated by numerous vibrational modes.