By incorporating ultrathin (80, low correlated color temperature of <3600 K, and high color stability at a wide voltage range of 5 V–9 V. These hybrid WOLEDs also reveal high forward‐viewing external quantum efficiencies (EQE) of 17.82%–19.34%, which are close to the theoretical value of 20%, indicating an almost complete exciton harvesting. In addition, the electroluminescence spectra of the hybrid WOLEDs can be easily improved by only changing the incorporating sequence of the ultrathin phosphorescence layers without device efficiency loss. For example, the hybrid WOLED with an incorporation sequence of ultrathin red/yellow/green phosphorescence layers exhibits an ultra‐high CRI of 96 and a high EQE of 19.34%. To the best of our knowledge, this is the first WOLED with good tradeoff among device efficiency, CRI, and color stability. The introduction of ultrathin (<0.1 nm) phosphorescence layers can also greatly reduce the consumption of phosphorescent emitters as well as simplify device structures and fabrication process, thus leading to low cost. Such a finding is very meaningful for the potential commercialization of hybrid WOLEDs.

First, oleophilic carbon dots (CDs) with a fluorescence quantum yield (QY) of 41% were synthesized by a one-pot microwave-assisted carbonization method. Then, CD-based electroluminescent light emitting diodes (CD-LEDs) were prepared. The impact of CD aggregation on the brightness of CD-LEDs was studied. The results show that, to some extent, with the decrease of the aggregation of the CD film, the luminescence quenching of the CD-LEDs gradually decreased, and the luminance of the CD-LEDs gradually increased. Hence, in order to improve the dispersion of CDs and reduce the aggregation of CDs and the luminescence quenching of the devices, host–guest doping was adopted to effectively improve the brightness of CD-LEDs. In this work, the yellow emission of the doped devices is mainly derived from the direct carrier trapping on CDs. Moreover, white and yellow CD-LEDs were obtained from the same oleophilic CDs by tuning the structure of the devices. The white CD-LEDs exhibit a high color rendering index (CRI) of 83 with a luminance of 455.2 cd m⁻². The yellow CD-LEDs show the maximum brightness of 339.5 cd m⁻² and excellent color stability. The results show that the luminescence quenching of CD-LEDs was resisted and the brightness of CD-LEDs was improved by using host–guest doping.

Long-wavelength materials are key for development of pure-color and white organic light-emitting devices (OLEDs). An organic molecule, combining hybridized local electron and charge-transfer (HLCT) states and aggregation-induced emission (AIE), not only breaks the 5% external quantum efficiency (EQE) limit but also overcomes emission quenching. Herein, we designed and synthesized four novel donor–acceptor compounds of TBAN, TBT, TBAT, and TABAT using triphenylamine (TPA) as the donor, benzothiadiazole (BT) as the acceptor, and anthracene (AN) as a bridge. We found that the emission peaks of TBAN, TBT, TBAT and TABAT are located at 596, 615, 580 and 546 nm, respectively. We successfully applied them to non-doped OLEDs, and the resulting devices exhibited excellent performance. For example, the optimal TBAN-based OLEDs showed a maximum luminance of 74 820 cd m⁻², a current efficiency of 12.1 cd A⁻¹ and a maximum EQE of 5.7% with low roll-off. Additionally, the device with TBAN as both the emitter and hole-transport material also exhibited high efficiency that is comparable to that of an NPB-based device. This work demonstrates that it is feasible to obtain excellent orange and red emitters by employing BT- and TPA-based D–A architectures.