Abstract
Purely organic light-emitting materials, which can harvest both singlet and triplet excited states to offer high electron-to-photon conversion efficiencies, are essential for the realization of high-performance organic light-emitting diodes (OLEDs) without using precious metal elements. Donor-acceptor architectures with an intramolecular charge-transfer excited state have been proved to be a promising system for achieving these requirements through a mechanism of thermally activated delayed fluorescence (TADF). Here, luminescent wedge-shaped molecules, which comprise a central phthalonitrile or 2,3-dicyanopyrazine acceptor core coupled with various donor units, are reported as TADF emitters. This set of materials allows systematic fine-tuning of the band gap and exhibits TADF emissions that cover the entire visible range from blue to red. Full-color TADF-OLEDs with high maximum external electroluminescence quantum efficiencies of up to 18.9% have been demonstrated by using these phthalonitrile and 2,3-dicyanopyrazine-based TADF emitters.
| Original language | English |
|---|---|
| Pages (from-to) | 1813-1821 |
| Number of pages | 9 |
| Journal | Advanced Functional Materials |
| Volume | 26 |
| Issue number | 11 |
| DOIs | |
| State | Published - 15 Mar 2016 |
Keywords
- delayed fluorescence
- donor-acceptor
- full color
- organic light-emitting diodes
- organic semiconductors
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