Chiral Octahydro-Binaphthol Compound-Based Thermally Activated Delayed Fluorescence Materials for Circularly Polarized Electroluminescence with Superior EQE of 32.6% and Extremely Low Efficiency Roll-Off.
basic_science · Level V
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- Record sourced from PubMed, PMID 31106503.
- Also identified by DOI 10.1002/adma.201900524.
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Abstract
Circularly polarized organic light-emitting diodes (CP-OLEDs) are particularly favorable for the direct generation of CP light, and they demonstrate a promising application in 3D display. However, up to now, such CP devices have suffered from low brightness, insufficient efficiency, and serious efficiency roll-off. In this study, a pair of octahydro-binaphthol (OBN)-based chiral emitting enantiomers, (R/S)-OBN-Cz, are developed by ingeniously merging a chiral source and a luminophore skeleton. These chirality-acceptor-donor (C-A-D)-type and rod-like compounds concurrently generate thermally activated delayed fluorescence with a small ΔE<sub>ST</sub> of 0.037 eV, as well as a high photoluminescence quantum yield of 92% and intense circularly polarized photoluminescence with dissymmetry factors (|g<sub>PL</sub> |) of ≈2.0 × 10<sup>-3</sup> in thin films. The CP-OLEDs based on (R/S)-OBN-Cz enantiomers not only display obvious circularly polarized electroluminescence signals with a |g<sub>EL</sub> | of ≈2.0 × 10<sup>-3</sup> , but also exhibit superior efficiencies with maximum external quantum efficiency (EQE<sub>max</sub> ) up to 32.6% and extremely low efficiency roll-off with an EQE of 30.6% at 5000 cd m<sup>-2</sup> , which are the best performances among the reported CP devices to date.