Rational design of dibenzo[a,c]phenazine-derived isomeric thermally activated delayed fluorescence luminophores for efficient orange-red organic light-emitting diodes

Ye, Hua; Yang, Jiaji; Stavrou, Kleitos; Li, Mengke; Liu, Fen; Li, Feiyun; Su, Shi-Jian; Monkman, Andrew P.

Abstract

It is an immense challenge to develop efficient long-wavelength (orange-to-red) thermally activated delayed fluorescence (TADF) materials due to the increasing nonradiative decay rates following the energy-gap law. Herein, two pairs of asymmetric isomers; DPyPzTPA and TPAPzDPy, and PyPzDTPA and DTPAPzPy based on electron-deficient moieties dibenzo[a,c]phenazine (Pz) and pyridine (Py) combined with electron-donor units of triphenylamine (TPA) were designed and synthesized. Their photophysical properties could be finely modulated by changing the position and number of Py groups as well as TPA fragments onto Pz cores. DPyPzTPA and DTPAPzPy possess much more rigidity and thus less geometry relaxation and non-radiative decay between ground states and excited states than those of PyPzDTPA and TPAPzDPy. Intriguingly, DPyPzTPA exhibits the highest relative photoluminescence quantum yield (ΦPL) and the fastest reverse intersystem crossing (rISC) rate among them owing to relatively stronger rigidity and spin-orbit coupling (SOC) interactions between the lowest singlet (S1) and energetically close-lying excited triplet state and therefore, the device showed the highest maximum external quantum efficiency (EQEmax) of 16.6% (60.9 lm/W, 53.3 cd/A) with Commission Internationale de I'Eclairage (CIE) coordinates of (0.43, 0.55), peak wavelength 556 nm. In stark contrast, due to its lower rigidity and extremely weak delayed fluorescence (DF) characteristic and thus the much lower ΦPL, TPAPzDPy-based devices are only half as efficient (30.8 lm/W, 27.5 cd/A, 8.3% EQE) despite the isomers possessing equal singlet-triplet energy gaps (ΔEST) of 0.43 eV. On the other hand, the device based on DTPAPzPy also demonstrated a strongly enhanced performance (59.1 lm/W, 52.7 cd/A, 16.1% EQE) than its isomer PyPzDTPA-based device (39.5 lm/W, 35.2 cd/A, 10.3% EQE). This work explicitly implicates that the asymmetric and isomeric molecular design is a potential strategy for promoting the development of highly efficient long-wavelength TADF materials.

Citation

Ye, H., Yang, J., Stavrou, K., Li, M., Liu, F., Li, F., …Monkman, A. P. (2023). Rational design of dibenzo[a,c]phenazine-derived isomeric thermally activated delayed fluorescence luminophores for efficient orange-red organic light-emitting diodes. Dyes and Pigments, 219, Article 111568. https://doi.org/10.1016/j.dyepig.2023.111568

• Journal Article Type: Article
• Acceptance Date: Jul 23, 2023
• Online Publication Date: Jul 24, 2023
• Publication Date: 2023-11
• Deposit Date: Feb 2, 2024
• Publicly Available Date: Feb 2, 2024
• Journal: Dyes and Pigments
• Print ISSN: 0143-7208
• Publisher: Elsevier
• Peer Reviewed: Peer Reviewed
• Volume: 219
• Article Number: 111568
• DOI: https://doi.org/10.1016/j.dyepig.2023.111568
• Public URL: https://durham-repository.worktribe.com/output/2189675