Significant effort has been made to develop novel material systems to improve the efficiency of near‐infrared organic light‐emitting diodes (NIR OLEDs). Of those, fluorescent chromophores are mostly studied because of their advantages in cost and tunability. However, it is still rare for fluorescent NIR emitters to present good color purities in the NIR range and to have high external quantum efficiency (EQE). Here, a wedge‐shaped D‐π‐A‐π‐D emitter APDC‐DTPA with thermally activated delayed fluorescence property and a small single‐triplet splitting (ΔEst) of 0.14 eV is presented. The non‐doped NIR device exhibits excellent performance with a maximum EQE of 2.19% and a peak wavelength of 777 nm. Remarkably, when 10 wt% of APDC‐DTPA is doped in 1,3,5‐tris(1‐phenyl‐1H‐benzimidazol‐2‐yl)benzene host, an extremely high EQE of 10.19% with an emission peak of 693 nm is achieved. All these values represent the best result for NIR OLEDs based on a pure organic fluorescent emitter with similar device structure and color gamut.

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Blue phosphorescent organic light-emitting diode (PhOLED) with a high maximum external quantum efficiency (EQE) of 26.6% was achieved using a new material, 2,8-bis(9,9-dimethylacridin-10(9H)-yl)dibenzo[b,d]furan (DBF-DMS) with a small bandgap, as the host. The device with DBF-DMS showed improved performance compared with that with 1,3-di-9-carbazolylbenzene, which is ascribed to the enhancement in carrier injection and transporting abilities and material stability of DBF-DMS. A lifetime of more than 100 h (time to 50% of the initial luminance, 1000 cd/m(2) with an EQE of 19.6%) in the other DBF-DMS-based device is obtained by further utilizing better device structure. This is a report indicating that host material with a small bandgap like DBF-DMS can be successfully utilized toward blue PhOLEDs with high performance.

A novel exciplex-forming host is applied so as to design highly simplified reddish orange light-emitting diodes (OLEDs) with low driving voltage, high efficiency, and an extraordinarily low efficiency roll-off, by combining N,N-10-triphenyl-10H-spiro [acridine-9,9'-fluoren]-3'-amine (SAFDPA) with 4,7-diphenyl-1,10-phenanthroline (Bphen) doped with trivalent iridium complex bis(2-methyldibenzo[f,h]quinoxaline) (acetylacetonate)iridium(III) (Ir(MDQ)(acac)). The reddish orange OLEDs achieve a strikingly high power efficiency (PE) of 31.80 lm/W with an ultralow threshold voltage of 2.24 V which is almost equal to the triplet energy level of the phosphorescent reddish orange emitting dopant. The power efficiency of the device with the exciplex-forming host is enhanced, achieving 36.2% mainly owing to the lower operating voltage by the novel exciplex forming cohost, compared with the reference device (23.54 lm/W). Moreover, the OLEDs show extraordinarily low current efficiency (CE) roll-off to 1.41% at the brightness from 500 to 5000 cd/m with a maximal CE of 32.87 cd/A (EQE = 11.01%). The devices display a good reddish orange color (CIE of (0.628, 0.372) at 500 cd/m) nearly without color shift with increasing brightness. Co-host architecture phosphorescent OLEDs show a simpler device structure, lower working voltage, and a better efficiency and stability than those of the reference devices without the cohost architecture, which helps to simplify the OLED structure, lower the cost, and popularize OLED technology.

Hybrid single-emitting layer (SEML) white organic lightemitting diodes (WOLEDs) incorporating blue thermally activated delayed fluorescent (TADF) or fluorescent materials and yellow phosphors have been widely utilized for solid-state lighting. Nonetheless, developing appropriate host materials to reduce the large efficiency roll-off at high luminance is still an unsolved issue. Here, two TADF materials denoted as TRZ-CF and TRZ-CzF were synthesized, with electroluminescent emission peaking at 476 and 460 nm, respectively. In particular, TRZ-CF, using 7,7dimethyl-5,7-dihydroindeno[2,1-b]carbazole (CF) as donor moiety, maintained both highly efficient blue emission (EQE max = 20.0%) and excellent charge transport abilities. The WOLED utilizing TRZ-CF as host material, doped by 0.8 wt % iridium(III) bis(4-phenylthieno[3,2-c]pyridinato-N, C2′) (PO-01), has EQE max of 20.3%, realizing the lowest roll-off to date of less than 2% at a luminance of 10 000 cd/m 2 . The efficiency roll-off is alleviated through the reduction the exciton quenching and triplet−triplet annihilation (TTA) within the light-emitting layer, benefited from the TADF effect and bipolar property. The hybrid SEML WOLED exhibits Commission Internationale de L'Eclairage (CIE) coordinates of (0.38, 0.45), providing a practical way to simplify the production complexity and to reduce efficiency roll-off for solid-state lighting.

The C3 meta-position of fluorene is utilized to construct high-triplet energy compounds. Incorporating a spiroacridine structure, two new host materials SAFDPA and SAFCz were facilely obtained. Their thermal and photophysical properties are fully investigated. The best efficiencies of 19.4%/21.5% of blue/white devices are achieved by SAFCz.

The controlled fabrication of organic single-crystalline nanowires (OSCNWs) with a uniform diameter in the nanoscale via the bottom-up approach, which is just based on weak intermolecular interaction, is a great challenge. Herein, we utilize the synergy approach of the bottom-up and the top-down processes to fabricate OSCNWs with diameters of 120 ± 10 nm through stepwise evolution processes. Specifically, the evolution processes vary from the self-assembled organic micro-rods with a quadrangular pyramid-like end-structure bounded with {111}s and {11-1}s crystal planes to the "top-down" synthesized organic micro-rods with the flat cross-sectional {002}s plane, to the organic micro-tubes with a wall thickness of ∼115 nm, and finally to the organic nanowires. Notably, the anisotropic etching process caused by the protic solvent molecules (such as ethanol) is crucial for the evolution of the morphology throughout the whole top-down process. Therefore, our demonstration opens a new avenue for the controlled-fabrication of organic nanowires, and also contributes to the development of nanowire-based organic optoelectronics such as organic nanowire lasers.

Six homoleptic Ir(III) complexes bearing imidazo-[4,5-b]pyrazin-2-ylidene chelates were successfully designed and synthesized. Narrowband blue emission (λ max = 466−485 nm) and broadened green emission (λ max = 518−532 nm) in degassed toluene solution with high photoluminescent quantum yields in the range of 75−81 and 45−48% were observed for f-timpz, t2impz, and t2empz as well as m-timpz, t2impz, and t2empz, respectively. In addition, the tert-butylphenyl cyclometalate is more electron donating than N-phenyl cyclometalate and, hence, all tertbutylphenyl-substituted derivatives, that is, mand f-t2impz and mand f-t2empz, give more red-shifted emission in comparison to that of mand f-timpz. Moreover, solution-processed OLED with f-t2empz (20 wt %) as the dopant gave electrophosphorescence at 474 nm with maximum external quantum efficiency (max. EQE) of 5.1%, while hyper-OLED with assistant sensitizer f-t2empz (10 wt %) and the multi-resonance thermally activated delayed fluorescence emitter BCzBN (0.5 wt %) afforded narrowband emission centered at 485 nm and max. EQE up to 17.4%, confirming the high potential of this class of Ir(III) metal phosphors.