Temperature dependence of the phosphorescence and of the thermally activated delayed fluorescence of 12C70 and 13C70 in amorphous polymer matrices. Is a second triplet involved?

Abstract

The phosphorescence and thermally activated delayed fluorescence (TADF) lifetimes of 12C70 and 13C70 in two different glassy hydrocarbon polymers, one aliphatic (cyclic polyolefin) and one aromatic (polystyrene), were measured between −200 and 100 ºC. The temperature dependence of the lifetimes is equally well described by a three-state mechanism (ground state, S0, and two excited states in thermal equilibrium, T1 and S1, the lifetime of T1 being temperature dependent) and by a four-state mechanism (ground state, S0, and three excited states in thermal equilibrium, T1, T2 and S1, all with temperature-independent lifetimes). The estimated S1–T1 and T2–T1 energy gaps (four-state mechanism) are in good agreement with spectroscopic measurements. These and the determined quantum yield of triplet formation, 0.997 ± 0.001, are found to be essentially independent of the polymer matrix and of the isotopic composition of the fullerene. On the other hand, the lifetimes of both T1 and T2 (four-state mechanism) are weakly dependent on the polymer matrix but strongly vary with the fullerene isotopic composition, nearly doubling when going from 12C70 to 13C70. A parameter useful for the characterization of TADF, the on-set temperature T0, is also introduced.