Molecular Design and Synthetic Approaches for the Realization of Multichannel Radiative Decay Pathways in Gold(III) Complexes and Their Applications in Organic Light-Emitting Devices

Ming-Yi Leung, Man-Chung Tang, Shun-Cheung Cheng, Ziyong Chen, Shiu-Lun Lai, Wai Kit Tang, Mei-Yee Chan, Chi-Chiu Ko*, Vivian Wing-Wah Yam*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

16 Citations (Scopus)

Abstract

A unique class of tridentate diaryltriazine ligand-containing gold(III) complexes with thermally activated delayed fluorescence (TADF) and/or thermally stimulated delayed phosphorescence (TSDP) properties has been designed and synthesized. With a simple structural modification on the coordination of carbazole moiety in the monodentate ligand, a large spectral shift of ∼160 nm (ca. 4900 cm-1) spanning from sky blue to red emissions has been demonstrated in solid-state thin films. Three-state or four-state models have been employed in fitting the emission lifetimes of the gold(III) complexes at various temperatures. The findings clearly indicate the presence of three emitting states, S1, T1, and T1′, suggesting the coexistence of TADF, phosphorescence, and TSDP. Notably, a minor structural change in the donor moiety between phenylcarbazolyl and diphenylaminoaryl has been demonstrated to turn on/off the TSDP, resulting in TADF-TSDP-phosphorescence or TADF-phosphorescence emitters. The TADF and/or TSDP properties have also been supported by temperature-dependent ultrafast transient absorption studies, with the direct observation of reverse intersystem crossing (RISC) and reverse internal conversion (RIC) and the determination of the activation parameters and excited state dynamics. Solution-processed and vacuum-deposited organic light-emitting devices (OLEDs) have been prepared, in which sky blue emitting devices based on 5 exhibit an operational lifetime LT70 ∼ 5 times longer than the previously reported sky blue emitting analogue that shows only TSDP property. These results have provided valuable insights into the manipulation of the excited states via rational molecular design toward the realization of gold(III)-based TSDP and/or TADF materials with multiple radiative decay pathways that show enhanced radiative decay rate constants (kr) for practical OLED applications. © 2024 American Chemical Society.
Original languageEnglish
Pages (from-to)30901–30912
JournalJournal of the American Chemical Society
Volume146
Issue number45
Online published30 Oct 2024
DOIs
Publication statusPublished - 13 Nov 2024

Funding

V.W.-W.Y. acknowledges support from The University of Hong Kong (HKU). The work described in this paper was supported by a grant from Hong Kong Quantum AI Lab Ltd under the AIR@InnoHK administered by the Innovation and Technology Commission (ITC), a grant from the Innovation and Technology Support Programme (ITSP) Mainland-Hong Kong Joint Funding Scheme (MHKJFS) of the Innovation and Technology Fund (ITF) (MHP/199/23), and the Collaborative Research Fund (CRF) (C7075-21GF) from the Research Grant Council of the Hong Kong Special Administrative Region, P. R. China. The computations were performed using the HKU ITS research computing facilities. Dr. Kam-Hung Low is acknowledged for his assistance in X-ray crystal structure data collection and discussion on structure determination. Dr. Maggie Ng is acknowledged for her initial discussion on the computation studies. Dr. Wing-Kei Kwok is acknowledged for her assistance in finalizing the manuscript.

RGC Funding Information

  • RGC-funded

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