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Article Abstract

Solution-processable organic light-emitting diodes (OLEDs) have attracted much attention from academia and industry because of their advantages such as low production cost and suitability for large-scale production. However, solution-processable deep-blue OLEDs that simultaneously have high efficiencies and satisfy the BT.2020 standard remain still a great challenge. To address this issue, here a tetraboron multiresonance thermally activated delayed fluorescence (MR-TADF) emitter, tBO-4B, embedded with two soluble 2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene groups is designed and synthesized with a linearly fully fused acceptor-donor-acceptor-type molecular structure. tBO-4B not only achieves an ultranarrow full width at half maximum of 12 nm but also has a negligibly small singlet-triplet energy gap and large spin‒orbit coupling, eventually leading to very fast reverse intersystem crossing rate (4.23 × 10 s). The sensitizer-free solution-processed OLED exploiting tBO-4B as the emitter achieves an ultrahigh maximum external quantum efficiency (EQE) of 30.3%, with Commission Internationale de l'Éclairage (CIE) coordinates of (0.147, 0.042) meeting the BT.2020 blue standard. In addition, the corresponding sensitizer-free vacuum-processed deep-blue devices also exhibit an impressive EQE of 39.6% and mild efficiency roll-off with CIE coordinates of (0.147, 0.043). This work will facilitate the development of high-efficiency ultrapure deep-blue MR-TADF materials for solution- and vacuum-processed OLEDs.

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http://dx.doi.org/10.1002/adma.202500010DOI Listing

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