4.2 Article

Simple Double Hetero[5]helicenes Realize Highly Efficient and Narrowband Circularly Polarized Organic Light-Emitting Diodes

Journal

CCS CHEMISTRY
Volume 4, Issue 11, Pages 3463-3471

Publisher

CHINESE CHEMICAL SOC
DOI: 10.31635/ccschem.022.202101661

Keywords

helical chirality; multiple-resonance; thermally activated delayed fluorescence; circularly polarized organic light-emitting diodes; double hetero[5]helicene

Funding

  1. National Natural Science Foundation of China [52130308, 51903160, 52022071]
  2. Shenzhen Science and Technology Program [KQTD20170330110107046]
  3. Shenzhen Technology and Innovation Commission [JCYJ20180507182244027]

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In this study, a new type of helicene-based enantiomers with inherent circularly polarized luminescence and narrow thermally activated delayed fluorescence characteristics were developed. By optimizing their thermal/photophysical/chiroptical properties, high-efficiency circularly polarized organic light-emitting diodes were achieved.
Helicene-based emitters with unique inherent circularly polarized luminescence (CPL) are promising yet remain a formidable challenge for highly efficient circularly polarized organic light-emitting diodes (CP-OLEDs), ascribed to their tough synthesis, low emission efficiency, and easy racemization in the thermal deposition process. Herein, a pair of helicene-based enantiomers, namely (P)-helicene-BN and (M)-helicene-BN, were developed, which merge helical chirality and the B/N/S inserted polycyclic aromatic framework to concurrently feature CPL and narrow thermally activated delayed fluorescence (TADF) characteristics. Benefiting from the excellent thermal/photophysical/chiroptical properties, the narrowband green CP-OLEDs based on enantiomers achieved maximum external quantum efficiencies (EQE(max)) of up to 31.5%, and dissymmetry factor (|g(EL)|) of 2.2 x 10(-3). This work reveals the great potential of helicene-based emitters in CP-OLEDs.

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