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What controls the orientation of TADF emitters?

Research output: Contribution to journalArticle

Author(s)

Bilal Naqvi, Markus Schmid, Ettore Crovini, Prakhar Sahay, Tassilo Naujoks, Francesco Rodella, Zhen Zhang, Peter Strohriegl, Stefan Bräse, Eli Zysman-Colman, Wolfgang Bruetting

School/Research organisations

Abstract

Thermally-activated delayed fluorescence (TADF) emitters—just like phosphorescent ones—can in principle allow for 100% internal quantum efficiency of organic light-emitting diodes (OLEDs), because the initially formed electron-hole pairs in the non-emissive triplet state can be efficiently converted into emissive singlets by reverse intersystem crossing. However, as compared to phosphorescent emitter complexes with their bulky—often close to spherical—molecular structures, TADF emitters offer the advantage to align them such that their optical transition dipole moments (TDMs) lie preferentially in the film plane. In this report, we address the question which factors control the orientation of TADF emitters. Specifically, we discuss how guest-host interactions may be used to influence this parameter and propose an interplay of different factors being responsible. We infer that emitter orientation is mainly governed by the molecular shape of the TADF molecule itself and by the physical properties of the host—foremost, its glass transition temperature Tg and its tendency for alignment being expressed, e.g., as birefringence or the formation of a giant surface potential of the host. Electrostatic dipole-dipole interactions between host and emitter are not found to play an important role.
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Details

Original languageEnglish
Article number750
Number of pages11
JournalFrontiers in Chemistry
Volume8
DOIs
Publication statusPublished - 4 Sep 2020

    Research areas

  • OLEDs, TADF, emitter orientation, Molecular orientation, Emitter-Host Interaction

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