作者
Zetian Wang,Yongjun Song,Dajun Zhuang,Ting Li,Yanfang Li,Lei He
摘要
ABSTRACT Multiple resonance (MR) emitters demonstrate great potential for fabricating narrowband organic light‐emitting diodes (OLEDs), which, however, show low reverse intersystem crossing (RISC) rates ( k RISC ) and severe concentration‐quenching. Here, indolo[3,2,1‐ kl ]phenoxazine (IPXZ), indolo[3,2,1‐ kl ]phenothiazine (IPTZ), and indolo[3,2,1‐ kl ]phenoselenazine (IPSeZ) are developed as donors for a typical MR acceptor (DtBuCzB) in a through‐space charge transfer system, affording MR‐TADF materials ( BN1 , BN2, and BN3 , respectively) with high k RISC and largely suppressed concentration‐quenching. Close, cofacial donor/DtBuCzB alignments are formed within the emitters, which effectively accelerates the RISC and protects DtBuCzB from aggregation, especially for BN2 / BN3 with S / Se ‐containing donors. In the 2 wt.% doped films, the emitters exhibit narrowband blue‐green emission with high k RISC values up to 5.0 × 10 5 s −1 , which are markedly enhanced compared to that of DtBuCzB (1.0 × 10 4 s −1 ). In the 5–20 wt.% doped films, the emitters maintain narrowband emission and show high photoluminescence efficiencies, and the intermolecular donor/DtBuCzB interactions further enhance the k RISC values (up to 10 6 s −1 ). Non‐sensitized narrowband OLEDs using the emitters show maximum external quantum efficiencies (EQEs) up to 35.2% and EQEs at 1000 cd m −2 up to 26.1%. The maximum EQEs remain up to 27.1% at the 20 wt.% doping concentration.