Abstract:Controlling the orientation of the emissive dipole has led to a renaissance of organic light-emitting diode (OLED) research, with external quantum efficiencies (EQEs) of >30% being reported for phosphorescent emitters. These highly efficient OLEDs are generally manufactured using evaporative methods and are comprised of small-molecule heteroleptic phosphorescent iridium(III) complexes blended with a host and additional layers to balance charge injection and transport. Large area OLEDs for lighting and display … Show more
“…The EL spectra coincided well with the PL profiles of the EML in a thin film, indicating that emission originates from the same chromophore and suggestive that there were no strong optical cavity effects. The absence of the emission peaks at lower wavelengths due to the CBP host molecule at 385 nm [42] and TmPyPB layer at 396 nm [38] denotes a sole emitter emission. Besides, for each device, the EL spectra's shape and maximum wavelength remained unchanged under different applied voltages.…”
A series of axially linked pyrene‐naphthalimide fluorophores (N2Py, N4Py, and BNPy) bearing a different number of 1,8‐naphthalimide units substituted on pyrene and bis‐pyrene cores were designed and synthesized using palladium‐catalyzed cross‐coupling reactions in a stepwise synthetic manner. These molecules were chemically characterized, and their photoelectric properties were explored by spectroscopy, electrochemical and theoretical studies. They exhibited push‐pull characteristics with intense fluorescence in solutions, strong solvatochromic behaviors, good thermal and electrochemical stabilities. N2Py, N4Py, and BNPy were successfully applied as emitters in solution‐processed OLED devices, which resulted in blue‐green emissions with promising device performance. Particularly, the BNPy‐based device achieved the best EL results with a maximum brightness of 3389 cd m−2, a maximum EQE of 3.98 %, a maximum LE of 3.22 cd A−1, and a low turn‐on voltage of 3.2 V.
“…The EL spectra coincided well with the PL profiles of the EML in a thin film, indicating that emission originates from the same chromophore and suggestive that there were no strong optical cavity effects. The absence of the emission peaks at lower wavelengths due to the CBP host molecule at 385 nm [42] and TmPyPB layer at 396 nm [38] denotes a sole emitter emission. Besides, for each device, the EL spectra's shape and maximum wavelength remained unchanged under different applied voltages.…”
A series of axially linked pyrene‐naphthalimide fluorophores (N2Py, N4Py, and BNPy) bearing a different number of 1,8‐naphthalimide units substituted on pyrene and bis‐pyrene cores were designed and synthesized using palladium‐catalyzed cross‐coupling reactions in a stepwise synthetic manner. These molecules were chemically characterized, and their photoelectric properties were explored by spectroscopy, electrochemical and theoretical studies. They exhibited push‐pull characteristics with intense fluorescence in solutions, strong solvatochromic behaviors, good thermal and electrochemical stabilities. N2Py, N4Py, and BNPy were successfully applied as emitters in solution‐processed OLED devices, which resulted in blue‐green emissions with promising device performance. Particularly, the BNPy‐based device achieved the best EL results with a maximum brightness of 3389 cd m−2, a maximum EQE of 3.98 %, a maximum LE of 3.22 cd A−1, and a low turn‐on voltage of 3.2 V.
“…The investigation of novel CDs with different passivation agents has improved their photophysical properties while maintaining their low toxicity. For example, the application of CDs in light-emitting diode (LED) technology is an area of increasing interest due to its efficiency in energy consumption [37][38][39]. The most important component of LED devices is a sandwich-type structure known as the emitting layer, which is made of different organic and organic-inorganic materials with extraordinary emission properties, high photostability, and optimal external quantum efficiency (EQE) [3,40].…”
Section: Figure 2 Schematic Example Of Top-down and Bottom-up Methodologies For Producing Cdsmentioning
The design of nanomaterials for application in diverse fields ranging from photovoltaic to fluorescence sensing is a research area of increasing interest. Recently, Quantum Dots (QDs), which are classified as semiconductor quantum dots (SQDs) and Carbon dots (CDs), have become a hot topic of investigation, owing to their extraordinary tunable fluorescence emission properties that render them excellent candidates for sensing metal ions. The detection of metal ions in aqueous solutions with high sensitivity is very important as these ions have toxicological and environmental impacts. In this short review, we have described the fluorescence emission properties of CDs and their application for the detection of different metal ions, such as Hg2+, Pb2+, Cu2+, Fe3+, Cd2+, and Cr6+.
“…The reason that the efficiency of the device is approximately four times different is due to three reasons as follows: First, the improved device efficiencies in 2,6-PhPMAF doped device is caused by fast upconverted triplet excitons to the singlet state with relatively smaller E ST of 0.17 eV compared to 0.27 eV in 4,6-PhPMAF dopant. Second is that it is believed to be due to improved internal quantum efficiency by the relatively higher PLQY value of the 2,6-PhPMAF (29.5%) emitter than 4,6-PhPMAF (16.9%) because the device efficiency is depends on the solid-state PLQY of the emitter, as discussed in literatures (de Sá Pereira et al, 2017;Maasoumi et al, 2018). As mentioned in the azimuthal intensity distributions, finally, it can be explained because the relatively narrow FWHM of DPEPO:2,6-PhPMAF film compared with the DPEPO:4,6-PhPMAF film has relatively horizontal plane-on orientation to the substrate, resulting in improved outcoupling efficiency in the emitting layer.…”
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