Functional Pyrene-Pyridine-Integrated Hole-Transporting Materials for Solution-Processed OLEDs with Reduced Efficiency Roll-Off.

A series of new functional pyridine-appended pyrene derivatives, viz., 2,6-diphenyl-4-(pyren-1-yl)pyridine (Py-03), 2,6-bis(4-methoxyphenyl)-4-(pyren-1-yl)pyridine (Py-MeO), 4-(pyren-1-yl)-2,6-di-p-tolylpyridine (Py-Me), and 2,6-bis(4-bromophenyl)-4-(pyren-1-yl)pyridine (Py-Br) were designed, developed, and studied as the hole-transporting materials (HTMs) for organic light-emitting diode (OLED) application. The crystal structures of two molecules revealed to have a large dihedral angle between the pyrene and pyridine units, indicating poor π-electronic communication between them due to ineffective orbital overlap across the pyrene-pyridine systems as the two p-orbitals of pivotal atoms are twisted at 66.80° and 68.75° angles to each other in Py-03 and Py-Me, respectively. The influence of variedly functionalized pyridine units on the electro-optical properties and device performance of the present integrated system for OLED application was investigated. All of the materials have suitable HOMO values (5.6 eV) for hole injection by closely matching the HOMOs of indium tin oxide (ITO) and the light-emitting layer. All of the synthesized molecules have suitable triplet energies, glass transition temperatures, and melting temperatures, which are highly desirable for good HTMs. The pyrene-pyridine-based devices demonstrated stable performance with low-efficiency roll-off. The device with Py-Br as HTM showed a maximum luminance of 17300 cd/m2 with a maximum current efficiency of 22.4 cd/A and an EQE of 9% at 3500 cd/m2 with 7% roll-off from 1000 to 10 000 cd/m2. Also, the devices with Py-Me and Py-03 showed performance roll-up while moving from 1000 to 10 000 cd/m2.

AIE-active mechanoluminescent discotic liquid crystals for applications in OLEDs and bio-imaging.

A multifunctional molecular design of fluorescent discotic liquid crystal (DLC) consisting of a tetraphenylethylene core is reported, which is found to serve as an excellent solid-state emitter in OLED devices with EQE of 4.4% and tunable mechanochromism. X-ray diffraction studies unveiled that change in supramolecular self-assembly is the physical origin of mechanochromism. The luminescent DLC molecule has been shown to act as a highly selective probe for labelling acidic cellular compartments (such as lysosomes) in bio-imaging using HeLa cells.

Versatile Exciplex-Forming Co-Host for Improving Efficiency and Lifetime of Fluorescent and Phosphorescent Organic Light-Emitting Diodes.

We report a new efficient exciplex-forming system consisting of a biscarbazole donor and a triazine-based acceptor. The new exciplex was characterized with a high photoluminescence quantum yield up to 68% and effective thermally activated delayed fluorescence behavior. The BCzPh:3P-T2T (2:1, 30 nm) blend was examined not only as an emitting layer (device D1) but also a reliable co-host of fluorescent and phosphorescent emitters for giving highly efficient exciplex-based organic light-emitting diodes (OLEDs) with a high maximum external quantum efficiency of 15.5 and 29.7% for devices doped with 1 wt % C545T (device D2) and 8 wt % Ir(ppy)2(acac) (device D4), respectively. More strikingly, a strongly enhanced lifetime ( T75 = 16 927 min.) of the C545T-doped device was obtained. The transient electroluminescence measurement as well as capacitance-voltage and impedance-voltage correlations were utilized to explore the factors governing the high efficiency and stability. The obtained results clearly show that the energy transfer and charge transport is highly efficient; they also show the photoelectric semiconducting characteristics of exciplex-based OLEDs, which are significantly different from those of unipolar host-based reference devices D3 (Alq3: 1 wt % C545T) and D5 (CBP: 8 wt % Ir(ppy)2(acac)). Our works have established a systematic protocol to shed light on the mechanisms behind exciplex-based devices. The combined results also confirm the bright prospect of the exciplex-forming system as the co-host for highly efficient and stable OLEDs.