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Related Experiment Video

Updated: Apr 24, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
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High efficiency in a solution-processed thermally activated delayed-fluorescence device using a delayed-fluorescence

Yong Joo Cho1, Kyoung Soo Yook, Jun Yeob Lee

  • 1Department of Polymer Science and Engineering, Dankook University, 126, Jukjeon-dong, Suji-gu, Yongin, Gyeonggi, 448-701, Korea.

Advanced Materials (Deerfield Beach, Fla.)
|September 3, 2014
PubMed
Summary

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Organic letters·2025

Researchers enhanced a common delayed fluorescence emitter with a tert-butyl substituent. This modification achieved over 18% quantum efficiency in a solution-processed device.

Area of Science:

  • Organic electronics
  • Photophysics
  • Materials science

Background:

  • Thermally activated delayed fluorescence (TADF) materials are crucial for efficient organic light-emitting diodes (OLEDs).
  • Solution-processing offers a cost-effective alternative to vacuum deposition for fabricating OLED devices.
  • Tuning molecular structure is key to optimizing the photophysical properties of TADF emitters.

Purpose of the Study:

  • To investigate the impact of tert-butyl substitution on the performance of a TADF emitter.
  • To achieve high quantum efficiency in a solution-processed TADF device.

Main Methods:

  • Synthesis of a modified TADF emitter incorporating a tert-butyl substituent.
  • Fabrication of OLED devices using the modified emitter via solution processing.
Keywords:
green devicesquantum efficiencysolution devicesthermally activated delayed-fluorescence

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  • Characterization of the photophysical properties and device performance, including quantum efficiency.
  • Main Results:

    • The modified TADF emitter exhibited excellent photophysical properties.
    • A high external quantum efficiency exceeding 18% was achieved in the solution-processed device.
    • The tert-butyl substituent effectively improved the performance of the TADF material.

    Conclusions:

    • Molecular modification of TADF emitters with tert-butyl groups is a viable strategy for enhancing device efficiency.
    • Solution-processed TADF devices can achieve high performance comparable to vacuum-processed counterparts.
    • This work contributes to the development of efficient and cost-effective organic electronic devices.