Related Experiment Video
Updated: Jun 26, 2025

08:51
Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
9.6K
O-B(F)←N Functionalized Copolymers with Delayed Fluorescence and P-Type Semiconducting Characteristics
Xiaoling Wang1, Xueyan Tan1, Junyang Jian1
1College of Materials Science and Engineering, Huaqiao University, Xiamen, 361021, China.
Macromolecular Rapid Communications
|May 15, 2024
Summary
Researchers designed novel conjugated polymers integrating delayed fluorescence and photovoltaic properties. These materials, featuring a unique O-B(F)←N unit, show promise for efficient organic electronic devices.
Area of Science:
- Materials Science
- Organic Electronics
- Photophysics
Background:
- Conjugated polymers with both delayed fluorescence and photovoltaic properties are rare due to conflicting molecular design requirements.
- Achieving simultaneous delayed fluorescence and efficient charge generation in organic semiconductors remains a significant challenge.
Purpose of the Study:
- To design and synthesize novel conjugated polymers that exhibit both delayed fluorescence and photovoltaic responses.
- To investigate the structure-property relationships of these new polymers for potential applications in organic electronics.
Main Methods:
- Design of a novel O-B(F)←N functionalized fused unit (M) with specific photophysical properties.
- Copolymerization of the M unit with benzodithiophene (BDT) derivatives to create new polymer backbones.
- Characterization of the polymers' photophysical properties, including delayed fluorescence lifetime (τD) and singlet-triplet energy gap (ΔEST).
- Evaluation of the polymers' semiconductor characteristics, such as hole mobility.
- Fabrication and testing of organic photovoltaic (OPV) devices using the synthesized polymers as donors.
Main Results:
- A novel O-B(F)←N functionalized unit was designed, exhibiting delayed fluorescence (τD = 0.75 µs) and a small singlet-triplet energy gap (ΔEST = 0.23 eV).
- Copolymers incorporating this unit demonstrated sustained delayed fluorescence (τD = 0.4-0.5 µs) and p-type semiconductor behavior with hole mobilities of 10⁻⁶–10⁻⁵ cm²/Vs.
- Organic photovoltaic devices fabricated with these polymers achieved a preliminary power conversion efficiency of 5.05%.
Conclusions:
- The introduction of O-B(F)←N functional groups into conjugated polymer backbones is an effective strategy for integrating delayed fluorescence and photovoltaic properties.
- These novel polymers show significant potential for advanced organic electronic applications, particularly in energy conversion and light-emitting devices.
- This study provides a new molecular design approach for multifunctional conjugated polymers.
Keywords:
boron functionalized moleculesconjugated polymersmultiple resonanceorganic semiconductorsthermal activated delayed fluorescence
