SFTS has been endemic to Japan, and SFTSV has been circulating naturally within the country.

Developing organic luminophores with unique capability of strong narrowband emission is both crucial and challenging for the further advancement of organic light‐emitting diodes (OLEDs). Herein, a nanographitic fused‐nonacyclic π‐system (BSBS‐N1), which was strategically embedded with multiple boron, nitrogen, and sulfur atoms, was developed as a new multi‐resonance thermally activated delayed fluorescence (MR‐TADF) emitter. Narrowband sky‐blue emission with a peak at 478 nm, full width at half maximum of 24 nm, and photoluminescence quantum yield of 89 % was obtained with BSBS‐N1. Additionally, the spin‐orbit coupling was enhanced by incorporating two sulfur atoms, thereby facilitating the spin‐flipping process between the excited triplet and singlet states. OLEDs based on BSBS‐N1 as a sky‐blue MR‐TADF emitter achieved a high maximum external electroluminescence quantum efficiency of 21.0 %, with improved efficiency roll‐off.

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As one of the three primary colors, blue is significant for display and lighting applications and the development of blueemitting molecules with high quantum efficiency, and color purity for organic light-emitting diodes (OLEDs) remains a key challenge. Herein, a new series of blue thermally activated delayed fluorescence (TADF) materials featuring π-extended ladderoxaborin and thiaborin acceptors has been developed. Steadystate and time-resolved photophysical measurements revealed the advantages of the ladder-oxaborin emitter, including a tiny singlet− triplet energy splitting of 10 meV, an ideal photoluminescence quantum yield of 100%, and an ultrashort TADF lifetime of 780 ns. The TADF-OLEDs incorporating the ladder-oxaborin (deep-blue) and thiaborin (sky-blue) emitters achieved significantly high external electroluminescence quantum efficiencies of up to 20.1% and 25.9%, respectively, accompanied by suppressed efficiency roll-offs.