Corrigendum to “Role of electron withdrawing moieties in phenoxazine–oxadiazole-based donor–acceptor compounds towards enriching TADF emission” [J. Photochem. Photobiol. A Chem. 457 (2024) 115925] (Journal of Photochemistry & Photobiology, A: Chemistry (2024) 457, (S1010603024004696), (10.1016/j.jphotochem.2024.115925))

Sivaraman Somasundaram, P. Justin Jesuraj, Paramasivam Mahalingavelar, Chang Min Lee, Insung Ha, Seung Yoon Ryu, Sanghyuk Park

Research output: Contribution to journalComment/debate

Abstract

The authors apologize for the errors occurred in the published version of the article. There are some typo errors in the abstract and author affiliation parts. We fully agree and accept our negligence while preparing the final version of the manuscript and deeply regret for the same. The corrected abstract and the author affiliation parts are given above. Abstract: Herein, we reported the effect of electron withdrawing units, such as trifluoromethyl (CF3) and cyanide (CN), substitution on a thermally activated delayed fluorescent (TADF) molecule (10-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenyl)-10H-phenoxazine (PXZ-OXD)). The addition of electron withdrawing units has increased the acceptor strength and reduced the interaction between PXZ and OXD, thus reducing the gap between the singlet and triplet states (ΔEST) of excitons. To understand the variation in the acceptor strength of PXZ-OXD as a function of its molecular structure and density of states, density functional theory (DFT) and time-dependent DFT (TDDFT) were conducted. Transition density matrix investigations revealed that the addition of CF3 and CN to PXZ-OXD triggers CT excitons, while inducing lower ΔEST values. Particularly, the lowest ΔEST (0.05 eV) with a notable red shift in the emission spectrum was observed with 4′-CF3PXZOXD. The delayed component lifetime of PXZOXD is found to be reduced after the substitution ofCN and CF3. Despite the weak charge transfer transitions, the substitution of conjugative CN group is found to be beneficial in improving the HOMO-LUMO overlap with a moderate decrease in reverse intersystem crossing (KRISC), which attained enhancement in the photoluminescent quantum yield. Additionally, the substitution of the above electron withdrawing units on PXZ-OXD yielded a red shift in the electroluminescence spectrum. Furthermore, the external quantum efficiency (at 100 cd/m2, i.e., EQE100) of the 4′-CNPXZOXD-based organic light-emitting diode is found to improve by 21.13 % against the PXZOXD (16.9 %). Furthermore, a small error in the corresponding author details in the supporting file. For reference, we have updated the first page of the supporting file as below.

Original languageEnglish
Article number116031
JournalJournal of Photochemistry and Photobiology A: Chemistry
Volume459
DOIs
StatePublished - 1 Feb 2025

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