Improving the stability and color purity of a BT.2020 blue multiresonance emitter by alleviating hydrogen repulsion.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37172084.
- Also identified by DOI 10.1126/sciadv.adh1434 and PMC identifier 10181185.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Stable deep blue multiresonance emitters with small full width at half maximum (FWHM) are attractive for wide color-gamut organic light-emitting diodes (OLEDs). However, the steric repulsion from the spatially close hydrogens would twist the multiresonance skeletons, causing spectral broadening and molecular instability issues. Here, we strategically introduce a mesitylboron locking unit into a carbazole-embedded multiresonance model emitter, alleviating the hydrogen repulsions and also strengthening the para-positioned weak carbon-nitrogen bond in anionic states. An emission peaking at 452 nm with an FWHM of merely 14 nm and nearly BT.2020 blue chromaticity coordinates are obtained in toluene, affording a high maximum external quantum efficiency of 33.9% in a sensitizing device. Moreover, an impressive LT97 (time to decay to 97% of the initial luminance) of 178 hours at a constant current density of 12 mA/cm<sup>2</sup> was achieved in a stable device with a small <i>y</i> coordinate of 0.057, nearly 20 times longer than the model emitter with even a substantially red-shifted emission.