期刊
CHEMPHOTOCHEM
卷 -, 期 -, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cptc.202300064
关键词
triplet-triplet annihilation; rate equations; delayed fluorescence; time-resolved luminescence; TTA efficiency
This study examines the molecular processes of triplet-triplet annihilation (TTA) in solvents at room temperature, with special focus on nonlinear kinetic reactions. Time- and spectrally resolved spectroscopy is used to simulate, measure, and fit the kinetic parameters of TET and TTA rate reactions without approximations. The study reveals that viscosity/diffusion and the excited triplet lifetime of the annihilator are crucial parameters for high TTA induced delayed fluorescence.
The molecular processes taking place during triplet-triplet annihilation (TTA) in solvents at room temperature are examined in detail. Special attention is paid to modelling of the nonlinear kinetic reactions. Using time- and spectrally resolved spectroscopy of DPA and Pt/Pd-OEP based sensitizer and annihilators, it is shown how the kinetic of parameters, such as the triplet energy transfer (TET) and TTA of the rate-reactions, can be simulated, measured and fitted, without approximations, using a numerical scheme. Studies of DPA in the solvents DMSO, THF and toluene at room temperature revealed that viscosity/diffusion together with the excited triplet lifetime of the annihilator are the most crucial parameters for high TTA induced delayed fluorescence. From an analysis of the experimentally determined rates an efficiency of 16-40 % was determined for the combined TET and TTA processes using THF, DMSO and toluene as solvents. (DPA=9,10-diphenylanthracene, OEP=2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphyrin)
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