Photophysical modeling identifies an excitation power threshold for efficient upconversion in multicomponent organic systems, enabling theoretical efficiency predictions from molecular parameters.
We have analyzed the dynamics of the upconversion-induced delayed fluorescence for a model multicomponent organic system, in which high concentrations of triplet states can be sustained in steady-state conditions. At different excitation powers, two regimes have been identified depending on the main deactivation channel for the triplets, namely, the spontaneous decay and the bimolecular annihilation. The excitation power density at which triplet bimolecular annihilation becomes dominant is the threshold (Iₜₕ) to have efficient upconversion generation. The simple equation obtained for Iₜₕ allows us to predict the theoretical efficiency of a generic system on the basis of few parameters of the constituent molecules.
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Monguzzi et al. (2008) studied this question.
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