Nature of the singlet and triplet excitations mediating thermally activated delayed fluorescence

Y. Olivier, B. Yurash, L. Muccioli, G. D'Avino, O. Mikhnenko, J. C. Sancho-García, C. Adachi, T. Q. Nguyen, D. Beljonne

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Abstract

Despite significant efforts, a complete mechanistic understanding of thermally activated delayed fluorescence (TADF) materials has not yet been fully uncovered. Part of the complexity arises from the apparent dichotomy between the need for close energy resonance and for a significant spin-orbit coupling between alike charge-transfer singlet and triplet excitations. Here we show, in the case of reference carbazole derivatives, that this dichotomy can be resolved in a fully atomistic model accounting for thermal fluctuations of the molecular conformations and microscopic electronic polarization effects in amorphous films. These effects yield electronic excitations with a dynamically mixed charge-transfer and localized character, resulting in thermally averaged singlet-triplet energy differences and interconversion rates in excellent agreement with careful spectroscopic studies.

Original languageEnglish
Article number075602
JournalPhysical Review Materials
Volume1
Issue number7
DOIs
Publication statusPublished - 27 Dec 2017
Externally publishedYes

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    Olivier, Y., Yurash, B., Muccioli, L., D'Avino, G., Mikhnenko, O., Sancho-García, J. C., Adachi, C., Nguyen, T. Q., & Beljonne, D. (2017). Nature of the singlet and triplet excitations mediating thermally activated delayed fluorescence. Physical Review Materials, 1(7), [075602]. https://doi.org/10.1103/PhysRevMaterials.1.075602