Exciton bimolecular annihilation dynamics in supramolecular nanostructures of conjugated oligomers

We present femtosecond transient absorption measurements on π-conjugated supramolecular assemblies in a high-pump-fluence regime. $Oligo(p{-}phenylenevinylene)$ monofunctionalized with $ureido{-}s{-}triazine$ (MOPV) self-assembles into chiral stacks in dodecane solution below $75^∘{}C$ at a concentration of $4×{}{10}^{{-}4}M.$ We observe exciton bimolecular annihilation in MOPV stacks at high excitation fluence, indicated by the fluence-dependent decay of ${1}¹{B}ᵤ{-}exciton$ spectral signatures and by the sublinear fluence dependence of time- and wavelength-integrated photoluminescence (PL) intensity. These two characteristics are much less pronounced in MOPV solution where the phase equilibrium is shifted significantly away from supramolecular assembly, slightly below the transition temperature. A mesoscopic rate-equation model is applied to extract the bimolecular annihilation rate constant from the excitation fluence dependence of transient absorption and PL signals. The results demonstrate that the bimolecular annihilation rate is very high with a square-root dependence in time. The exciton annihilation results from a combination of fast exciton diffusion and resonance energy transfer. The supramolecular nanostructures studied here have electronic properties that are intermediate between molecular aggregates and polymeric semiconductors.