Here, we conveniently designed and synthesized a self-host thermally activated delayed fluorescence (TADF) emitter, which can not only form a uniform thin film through wet-process, but also allow the subsequently deposition of electron transporting layer (ETL) by orthogonal solvent. By using this self-host material as emitter, the all-solution-processed multilayer TADF organic light emitting diodes (OLEDs) was successfully fabricated. The maximum current, power and external quantum efficiencies of this nondoped device are 46.3 cd A, 39.3 lm W and 15.5%, respectively, which are much higher than the values of all-solution-processed OLEDs based on tranditional fluorescence and even comparable to the TADF devices with vacuum-deposited ETL. Moreover, the device maintains the high efficiency of 42.9 cd A and 39.0 cd A at the luminance of 100 cd m for display and 1000 cd m for practical lighting. The high efficiency and small efficiency roll-off of the all-solution-processed fluorescent OLEDs can be attributed to the superiority of the newly designed self-host TADF emitter, which possesses the perfect electroluminescent property and sufficient solvent resistance at the same time.

The blue thermally activated delay fluorescence (TADF) emitters are highly attractive in the fields of constructing hybrid white organic light-emitting diodes (WOLEDs) due to its high efficiency and color stability. However, few blue TADF emitters can withstand sequential orthogonal solvents, making it impossible to fabricate the fully solution-processed hybrid WOLEDs. Here, two TADF materials, PCz-4CzCN and TPA-4CzCN, were designed and synthesized by equipping the emissive core with nonconjugated bulky units, which can effectively enhance the solvent resistance ability without disturbing the TADF feature. The photophysical investigation indicates that phenylcarbazole unit can efficiently block the electromer formation to enhance the energy transfer and exciton utilization of the emitter. Accordingly, the blue OLEDs of PCz-4CzCN shows higher external quantum efficiency (EQE) of 22.6%, which is the best performance recorded among the fully solution-processed blue OLEDs. Upon further doping, the yellow phosphor PO-01, the fully solution-processed TADF-phosphor (T–P) hybrid WOLEDs was successfully obtained with high performance for the first time. Thanks to the efficient exciplex formation, the turn-on voltage of the white device is only 2.8 V, and the maximum brightness and power efficiency are as high as 53 300 cd m–2 and 38.5 lm W–1, respectively, which are even higher than the previous reported T–P hybrid WOLEDs with a vacuum-deposited electron transfer layer.

A highly efficient solution-processible TADF blue host is developed by molecular encapsulation. Due to the steric shield effect of the peripheral units, the triplet–triplet and triplet–polaron quenching of the TADF blue host are restricted.

Fabrication of highly efficient all thermally activated delayed fluorescence (TADF) white organic light-emitting diodes (WOLEDs) through solution-process still remains a big challenge. Here, two encapsulated TADF molecules with a small singlet–triplet energy gap (ΔE ST) and high photoluminescence quantum yield (PLQY) were designed and synthesized as yellow emitters for solution-processed WOLEDs. The high current, power, and external quantum efficiencies of 41.6 cd A–1, 30.4 lm W–1, and 17.3% were achieved for the solution-processed all-fluorescence WOLEDs with a single-emission layer. In contrast, even with the same ΔE ST and PLQY, the corresponding unencapsulated parent emitters will account for nearly 50% loss of the potential device efficiency. This is for the first time that the small molecular TADF blue host and TADF yellow guest are used to construct solution-processed all-fluorescence WOLEDs, which exhibit high efficiency comparable with most of the vacuum-deposited all-fluorescence white devices. These results not only demonstrate the great potential of TADF emitters in achieving highly efficient solution-processed WOLEDs, but also testify the key role of molecular encapsulation in reducing polar-exciton quenching and enhancing electroluminescence performance.

The molecular aggregation and exciton-polaron interaction of the host-guest system were successfully restricted by efficient molecular encapsulation. The solution-processed blue and green TADF OLEDs have been realized with external quantum efficiencies above 23% by employing the encapsulated TADF host and guest as emission layers.