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Design and Synthesis of Boron-embedded Multi-Resonant Thermally Activated Delayed Fluorescent (MR-TADF) Materials using Phenazine Donor for Fabricating Red Organic Light-emitting Diodes

Implementing Organization

Principal Investigator
Dr. Calvin Samuel.P
Indian Institute Of Science
calvin_cal95@ymail.com

Project Overview

In the last decade, thermally activated delayed fluorescent (TADF) materials have emerged as a forerunner for the next generation Organic light-emitting diodes (OLEDs) due to their internal quantum efficiency (IQE) of 100% via the triplet to singlet reverse intersystem crossing channel (RISC).¹ Efficient RISC is attained by minimizing the energy gap (ΔEST) between the lowest excited singlet (S₁) and triplet (T₁) states. This is typically achieved by designing molecules with a twisted donor (D)-acceptor (A) configuration. Though conventional TADF materials still suffer from low photoluminescence quantum yield (PLQY) due to greater separation of highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO), and show broad emission, which means less colour purity. To overcome these shortcomings, Hatakeyama et al. introduced multiple-resonance (MR) induced TADF wherein the molecules were designed to take advantage of the complementary resonance effect which enables atomically separated HOMO and LUMO orbitals.² MR-TADF emitters have sufficiently small ΔEST while showing narrowband emission (FWHM ≤ 40 nm) and PLQY near unity. In recent years, many research groups have developed blue and green colour-based MR-TADF emitters, while examples of orange or red MR-TADF emitters are a bit scarce, as they require even lower ΔEST to obtain emission bands in the range of 600-690 nm.³ Some strategies employed to achieve red-emitting MR-TADF include constructing para-boron (B-π-B) in the molecule and increasing the electron-donation ability of the donors.⁴ This proposal aims to fabricate red-emitting OLED by developing MR-TADF materials using phenazine as donor. Phenazine, which has been utilized in conventional TADF and is more powerful than donors like carbazole, phenoxazine, etc.,⁵ has not been employed in MR-TADF. Employment of phenazine in the para-boron framework will increase the electron-donating ability and will potentially lead to a stronger D-A association, leading to a robust system. The purpose of this proposal is to synthesize di- and tetra-boron-embedded molecules that can act as red MR-TADF by using phenazine as a donor and fabricating OLEDs using these emitters. Reference: 1. Nagata, M.; Min, H.; Watanabe, E.; Fukumoto, H.; Mizuhata, Y.; Tokitoh, N.; Agou, T.; Yasuda, T. Angew. Chem. Int. Ed. 2021, 60, 20280-20285 2. Kondo, Y.; Yoshiura, K.; Kitera, S.; Nishi, H.; Oda, S.; Gotoh, H.; Sasada, Y.; Yanai, M.; Hatakeyama, T. Nat. Photonics 2019, 13, 678. 3. Keerthika, P.; Konidena, R. K. Adv. Optical Mater. 2023, 11, 2301732. 4. Hua, T.; Li, N.; Huang, Z.; Zhang, Y.; Wang, L.; Chen, Z.; Miao, J.; Cao, X.; Wang, X.; Yang, C. Angew. Chem. Int. Ed. 2024, 63, e202318433. 5. a) Im, Y.; Kim, M.; Cho, Y. J.; Seo, J.; Yook, K. S.; Lee, J. Y. Chem. Mater. 2017, 29, 1946; b) Tonge, C. M.; Paisley, N. R.; Polgar, A.; Lix, K.; Algar, W. R.; Hudson, Z. M. ACS Appl. Mater. Interfaces 2020, 12, 6525.
Funding Organization
Quick Information
Area of Research
Chemical Sciences
Focus Area
Inorganic Chemistry, Catalysis, Supramolecular Chemistry
Start Date
25 Nov 2025
End Date
24 Nov 2027
Status
ongoing
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
00
Publications
00
No. of Patents
Filed : 00
Grant : 00
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