4.8 Article

Efficient Orange-Red Thermally Activated Delayed Fluorescence Emitters Feasible for Both Thermal Evaporation and Solution Process

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 32, Pages 29086-29093

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b08729

Keywords

thermally activated delayed fluorescence; orange-red OLED; solution process; thermal evaporation; rigid segment

Funding

  1. National Key Research & Development Program of China [2016YFB0401002]
  2. National Natural Science Foundation of China [51533005, 51821002, 51773029]
  3. China Postdoctoral Science Foundation [2018M640517, 2018M642307]
  4. Collaborative Innovation Center of Suzhou Nano Science Technology
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  6. 111 Project
  7. Joint International Research Laboratory of Carbon-Based Functional Materials and Devices

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Development of red thermally activated delayed fluorescence (TADF) emitters has been lagging behind when compared with those of blue and green fluorophores, especially for solution-processable ones. In this work, two novel orange-red TADF emitters 3,6-di(10H-phenoxazin-10-yl)dibenzo[a,c]phenazine (DBPZ-DPXZ) and 10,10'-(11,12-bis(3,5-di-tert-butylphenyl)dibenzo[a,c]phenazine-3,6-diyObis(10H-phenoxazine) (tDBBPZ-DPXZ) are developed. A high-performance orange-red TADF emitter, DBPZ-DPXZ, is first prepared by connecting a rigid acceptor and two rigid donor segments. While this design strategy endows DBPZ-DPXZ with an excellent TADF performance leading to a vacuum-processed organic light-emitting diode (OLED) with a high external quantum efficiency (EQE) of 17.8%, the rigid segments limit its solubility and applications in solution-processed devices. Based on this prototype, tDBBPZ-DPXZ is designed with the addition of 3,5-di-tert-butylphenyl groups to boost its solubility with barely an influence on the photophysical properties. In particular, tDBBPZ-DPXZ maintains nearly an identical photoluminescence quantum yield of 83% and singlet triplet energy splitting of 0.03 eV with EQE of 17.0% in a vacuum-processed orange-red OLED. Furthermore, it can be applied on the orange-red solution-processed OLED realizing an EQE as high as 10.1%, representing one of the state-of-the-art results of the reported orange-red solution-processed TADF-OLEDs. This work provides an effective strategy to address the conflicting requirements between high efficiency and good solubility and develop efficient soluble orange-red TADF emitters.

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