Abstract
AbstractImportant parameters for the design and performance of thermally activated delayed fluorescence (TADF) emitters are the forward and reverse intersystem crossing rates between singlet and triplet states. The magnitude of these rates is determined from the prompt and delayed transient photoluminescence decay. It is demonstrated that this photoluminescence decay strongly depends on the initial photoexcited population density due to exciton–exciton annihilation processes. By kinetic modeling of the power‐dependent time‐resolved photoluminescence of the TADF emitter 9,10‐bis(4‐(9H‐carbazol‐9‐yl)‐2,6‐dimethylphenyl)‐9,10‐diboraanthracene (CzDBA), singlet–triplet annihilation and triplet–triplet annihilation are identified as the main loss processes with rate constants in the order of 10−17 m3 s−1. Neglecting these quenching processes leads to erroneous estimates of the (reverse) intersystem crossing rates.
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