4.8 Article

Spiral Donor Design Strategy for Blue Thermally Activated Delayed Fluorescence Emitters

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 4, Pages 5302-5311

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c19302

Keywords

organic light-emitting diodes; organic electronics; spiral donor; nonadiabatic vibronic coupling; thermally activated delayed fluorescence

Funding

  1. National Natural Science Foundation of China [51625301, 91833304, 51861145301, U1601651, 52003088]
  2. Basic and Applied Basic Research Foundation of Guangdong Province [2019B1515120023]
  3. Guangdong Provincial Department of Science and Technology [2016B090906003, 2016TX03C175, 2019A1515012059]
  4. Science and Technology Program of Guangzhou [201806010149]
  5. Dongguan Innovative Research Team Program [2018607201002]
  6. China Postdoctoral Science Foundation [2019M662903]
  7. Fundamental Research Funds for the Central Universities [2020ZYGXZR023]

Ask authors/readers for more resources

This study investigates the importance of energy level relationships between spiral donors and luminophores on the photoluminescent quantum yields of materials, and proposes the use of quantum chemistry simulations to accurately predict these relationships. The optimized molecular structure and energy alignment play a key role in enhancing the performance of TADF emitters. Ultimately, the TADF emitter DspiroS-TRZ achieved remarkable results with 99.9% PLQY and 38.4% EQE, the highest reported among all blue TADF emitters to date.
Thermally activated delayed fluorescence (TADF) emitters with a spiral donor show tremendous potential toward high-level efficient blue organic light-emitting diodes (OLEDs). However, the underlying design strategy of the spiral donor used for blue TADF emitters remains unclear. As a consequence, researchers often do try and error work in the development of new functional spiral donor fragments, making it slow and inefficient. Herein, we demonstrate that the energy level relationships between the spiral donor and the luminophore lead to a significant effect on the photoluminescent quantum yields (PLQYs) of the target materials. In addition, a method involving quantum chemistry simulations that can accurately predict the aforementioned energy level relationships by simulating the spin density distributions of the triplet excited states of the spiral donor and corresponding TADF emitters and the triplet excited natural transition orbitals of the TADF emitters is established. Moreover, it also revealed that the steric hindrance in this series of molecules can form a nearly unchanged singlet (S-1) state geometry, leading to a reduced nonradiative decay and high PLQY, while a moderated donor-acceptor (D-A) torsion in the triplet (T-1) state can induce a strong vibronic coupling between the charge-transfer triplet ((CT)-C-3) state and the local triplet ((LE)-L-3) state, achieving an effective reverse intersystem crossing (RISC) process. Furthermore, an electric-magnetic coupling is formed between the high-lying (LE)-L-3 state and the charge-transfer singlet ((CT)-C-1) state, which may open another RISC channel. Remarkably, in company with the optimized molecular structure and energy alignment, the pivotal TADF emitter DspiroS-TRZ achieved 99.9% PLQY, an external quantum efficiency (EQE) of 38.4%, which is the highest among all blue TADF emitters reported to date.

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