Due to the relatively low photoluminescence quantum yield (PLQY) and horizontal dipole orientation of doped films, anthracene-based fluorescent organic light-emitting diodes (F-OLEDs) have faced a great challenge to achieve high external quantum efficiency (EQE). Herein, a novel approach is introduced by incorporating penta-helicene into anthracene, presented as linear-shaped 3-(4-(10-phenylanthracen-9-yl)phenyl)dibenzo[c,g]phenanthrene (BABH) and 3-(4-(10-(naphthalen-2-yl)anthracen-9-yl)phenyl)dibenzo[c,g]phenanthrene (NABH). These blue hosts exhibit minimal intermolecular overlap of π-π stacking, effectively suppressing excimer formation, which facilitates the effective transfer of singlet energy to the fluorescent dopant for PLQY as high as 90%. Additionally, the as-obtained two hosts of BABH and NABH have effectively demonstrated major horizontal components transition dipole moments (TDM) and high thermal stability with glass transitional temperature (Tg) surpassing 188 °C, enhancing the horizontal dipole orientation of their doped films to be 89% and 93%, respectively. The OLEDs based on BABH and NABH exhibit excellent EQE of 10.5% and 12.4% at 462 nm and device lifetime up to 90% of the initial luminance over 4500 h at 100 cd m-2, which has firmly established them as among the most efficient blue F-OLEDs based on anthracene to date to the best knowledge. This work provides an instructive strategy to design an effective host for highly efficient and stable F-OLEDs.
In the field of active-matrix organic light emitting display (AMOLED), large-size and ultra-high-definition AMOLED applications have escalated the demand for the integration density of driver chips. However, as Moore's Law approaches the limit, the traditional technology of improving integration density that relies on scaling down device dimension is facing a huge challenge. Thus, developing a multifunctional and highly integrated device is a promising route for improving the integration density of pixel circuits. Here, a novel nonvolatile memory ferroelectric organic light-emitting transistor (Fe-OLET) device which integrates the switching capability, light-emitting capability and nonvolatile memory function into a single device is reported. The nonvolatile memory function of Fe-OLET is achieved through the remnant polarization property of ferroelectric polymer, enabling the device to maintain light emission at zero gate bias. The reliable nonvolatile memory operations are also demonstrated. The proof-of-concept device optimized through interfacial modification approach exhibits 20 times improved field-effect mobility and five times increased luminance. The integration of nonvolatile memory, switching and light-emitting capabilities within Fe-OLET provides a promising internal-storage-driving paradigm, thus creating a new pathway for deploying storage capacitor-free circuitry to improve the pixel aperture ratio and the integration density of circuits toward the on-chip advanced display applications.
We designed and synthesized a new class of six phosphorescent [3 + 2 + 1] iridium(III) complexes [(pbib)Ir(C^C)CN] bearing a tridentate 1,3-bis(1-butylimidazolin-2-ylidene) phenyl N-heterocyclic carbene (NHC)-based pincer ligand (pbib), bidentate imidazole-based NHC ligands (C^C), and a monodentate cyano group and investigated their photophysical, electrochemical, and thermal stabilities and electroluminescent properties. The extended π-conjugation of the imidazole-based C^C ligand is found to be the key to fine-tune the emission energies from ultraviolet blue (λ = 378 nm) to saturated blue (λ = 482 nm), as shown by electrochemical and photophysical studies, which is also revealed by the density functional theory (DFT) and time-dependent DFT calculations. Vacuum-deposited organic light-emitting diode devices have been fabricated with these newly synthesized emitters and exhibited the best external quantum efficiency of 6.4% and Commission International de L'Éclairage (CIE) coordinates of (0.163, 0.096), where the CIE y is very similar to the National Television System Committee standard blue CIE (x, y) coordinates of (0.149, 0.085). These results indicate that the novel [3 + 2 + 1] coordinated iridium(III) complexes [(pbib)Ir(C^C)CN], having a saturated blue emission, not only could alleviate the photodegradation of the emitters when compared to [(pbib)Ir(pmi)CN] but also provide new design strategies of saturated-blue-emitting iridium(III) complexes.
