Developing red thermally activated delayed fluorescence (TADF) emitters for high‐performance OLEDs is still facing great challenge. Herein, three red TADF emitters, pDBBPZ‐DPXZ, pDTBPZ‐DPXZ, and ...oDTBPZ‐DPXZ, are designed and synthesized with same donor–acceptor (D‐A) backbone with different peripheral groups attaching on the A moieties. Their lowest triplet states change from locally excited to charge transfer character leading to significantly enhance reverse intersystem crossing process. In particular, oDTBPZ‐DPXZ exhibits efficient TADF feature and exciton utilization. It not only achieves an external quantum efficiency (EQE) of 20.1 % in red vacuum‐processed OLED, but also realize a high EQE of 18.5 % in a solution‐processed OLED, which is among the best results in solution‐processed red TADF OLEDs. This work provides an effective strategy for designing red TADF molecules by managing energy level alignments to facilitate the up‐conversion process and thus enhance exciton harvesting.
By introducing phenyl or o‐tolyl groups into different positions of the same acceptor backbone, the lowest triplet energy levels of red thermally activated delayed fluorescence emitters can be tuned from locally excited triplet (3LEA) to charge transfer triplet (3CT) states, resulting in enhancement of the rates of reverse intersystem crossing (RISC), and boosting efficiencies in both vacuum‐ and solution‐processed OLEDs.
Alternative polyadenylation (APA), which induces shortening of the 3′‐UTR, is emerging as an important feature in cancer development and progression. Nevertheless, the effects and mechanisms of ...APA‐induced 3′‐UTR shortening in nasopharyngeal carcinoma (NPC) remain largely unclear. Fibronectin type III domain containing 3B (FNDC3B) tended to use proximal polyadenylation site and produce shorter 3′‐UTR according to our previous sequencing study. Herein, we found that FNDC3B with shorter 3′‐UTR could escape from miRNA‐mediated gene repression, and caused its increased expression in NPC. Knocking down of FNDC3B inhibited NPC cell proliferation, migration, invasion, and metastasis in vitro and in vivo. Overexpression of FNDC3B, especially those with shorter 3′‐UTR, promoted NPC progression. Furthermore, the mechanism study revealed that FNDC3B could bind to and stabilize myosin heavy chain 9 (MYH9) to activate the Wnt/β‐catenin signaling pathway. In addition, MYH9 could reverse the inhibitory effects of FNDC3B knockdown in NPC. Altogether, our results suggested that the 3′‐UTR shortening of FNDC3B mRNA mediated its overexpression in NPC and promoted NPC progression by targeting MYH9. This newly identified FNDC3B‐MYH9‐Wnt/β‐catenin axis could represent potential targets for individualized treatment in NPC.
FNDC3B tended to use proximal polyadenylation site and produced shorter 3′‐UTR. FNDC3B with shorter 3′‐UTR could escape from microRNA‐mediated gene repression, and caused its increased expression in nasopharyngeal carcinoma (NPC) and promoted NPC progression by targeting MYH9.
Abstract
In radio-loud active galactic nuclei (AGNs), ultra-fast outflows (UFOs) were detected at the inclination angle of ∼10°–70° away from jets. Except for the inclination angle of UFOs, the UFOs ...in radio-loud AGNs have similar properties to that in radio-quiet AGNs. The UFOs with such low inclination cannot be explained in the line-force mechanism. The magnetic-driving mechanism is suggested to explain the UFOs based on a self-similar solution with radiative transfer calculations. However, the energetics of self-similar solution need to be further confirmed based on numerical simulations. To understand the formation and acceleration of UFOs in radio-loud AGNs, this paper presents a model of the disk winds driven by both line force and magnetic field and implements numerical simulations. Initially, a magnetic field is set to 10 times stronger than the gas pressures at the disk surface. Simulation results imply that the disk winds driven by both line force and magnetic field could describe the properties of UFOs in radio-loud AGNs. Pure magnetohydrodynamics (MHDs) simulation is also implemented. When the initial conditions are the same, the hybrid models of magnetic fields and line force are more helpful to form UFOs than the pure MHD models. It is worth studying the case of a stronger magnetic field to confirm this result.
Multiple resonance (MR) type thermally activated delayed fluorescence (TADF) material is currently a research hotspot in organic light‐emitting diodes (OLEDs) due to their high color purity and high ...exciton utilization. However, there are only a handful of MR‐TADF emitters with emissions beyond the blue‐to‐green region. The very limited emission colors for MR‐TADF emitters are mainly caused by the fact that so far molecular modifications of MR‐TADF do not offer much change in the emission colors. Here, we report a new approach to modifying a prototypical MR core of DABNA by fusing carbazoles to the MR framework. The carbazole‐fused molecule (TCZ‐F‐DABNA) basically maintains the MR‐dominated features of DABNA while red‐shifting the emission. Its OLED achieves an external quantum efficiency of 39.2 % with a peak at 588 nm, which is a record‐high efficiency for OLEDs with peaks beyond 560 nm. This work provides a new approach for significantly tunning emission colors of MR‐TADF emitters.
A new approach is reported by fusing carbazoles to a MR framework DABNA to significantly redshift emission while maintaining the MR‐dominated features. The carbazole‐fused molecule TCZ‐F‐DABNA can deliver a high PLQY of 99 %. Its OLEDs reached a record‐high EQE of 39.2 %.
Developing red thermally activated delayed fluorescence (TADF) emitters, attainable for both high‐efficient red organic light‐emitting diodes (OLEDs) and non‐doped deep red/near‐infrared (NIR) OLEDs, ...is challenging. Now, two red emitters, BPPZ‐PXZ and mDPBPZ‐PXZ, with twisted donor–acceptor structures were designed and synthesized to study molecular design strategies of high‐efficiency red TADF emitters. BPPZ‐PXZ employs the strictest molecular restrictions to suppress energy loss and realizes red emission with a photoluminescence quantum yield (ΦPL) of 100±0.8 % and external quantum efficiency (EQE) of 25.2 % in a doped OLED. Its non‐doped OLED has an EQE of 2.5 % owing to unavoidable intermolecular π–π interactions. mDPBPZ‐PXZ releases two pyridine substituents from its fused acceptor moiety. Although mDPBPZ‐PXZ realizes a lower EQE of 21.7 % in the doped OLED, its non‐doped device shows a superior EQE of 5.2 % with a deep red/NIR emission at peak of 680 nm.
Two red emitters, BPPZ‐PXZ and mDPBPZ‐PXZ, with twisted donor–acceptor structures were designed and synthesized to study molecular design strategies of high‐efficiency red TADF emitters. BPPZ‐PXZ employs the strictest molecular restrictions to suppress energy loss and realizes red emission with a photoluminescence quantum yield (ΦPL) of 100±0.8 % and external quantum efficiency (EQE) of 25.2 % in a doped OLED.
Functionalization of hydrogen‐bonded organic frameworks (HOFs) for specific applications has been a long‐lasting challenge in HOF materials. Here, an efficient way to integrate functional species in ...the HOF structure through constructing an anionic framework is presented. The obtained HOFs, taking PFC‐33 (PFC = porous materials from FJIRSM,CAS) as an example, integrate a porphyrin photosensitizer as a porous backbone and a commercial biocide as counterions in the structure. The permanent channels and the electrostatic interaction between the framework and the counterions provide PFC‐33 ion‐responsive biocide‐release behavior in various physiological environments, thus exhibiting synergistic photodynamic and chemical antimicrobial efficiency. The unbonded carboxyl groups residing on the HOF surface further allow for manipulating the interfacial interaction between the PFC‐33 and the polymer matrix for membrane fabrication. Therefore, a polyHOF membrane with high stability, desired flexibility, and good permeability is obtained, which demonstrates noticeable bacterial inhibition toward Escherichia coli. This study may shed light on the functionalization of HOF materials for broad application potentials.
The functionalization of hydrogen‐bonded organic frameworks (HOFs) can be achieved in a porphyrin‐based anionic HOF structure, endowing the material with synergistic photodynamic and chemical antimicrobial efficacy. By further taking advantage of the unbonded carboxyl groups on the HOF particle surface, a freestanding flexible membrane that shows high permeability, good stability, and excellent antibacterial activity is successfully fabricated.
Multivalent-ion batteries have garnered significant attention due to their high energy density, low cost, and superior safety. Calcium-ion batteries (CIBs) are regarded as the next-generation energy ...storage systems for their abundant natural resources and bivalent characteristics. However, the absence of high-performance anode materials poses a significant obstacle to the progress of battery technology. Two-dimensional (2D) Dirac materials have excellent conductivity and abundant active sites, rendering them promising candidates as anode materials. A novel 2D Dirac material known as "graphene+" has been theoretically reported, exhibiting prominent properties including good stability, exceptional ductility, and remarkable electronic conductivity. By using first-principles calculations, we systematically investigate the performance of graphene+ as an anode material for CIBs. Graphene+ exhibits an ultra-high theoretical capacity (1487.7 mA h g
−1
), a small diffusion barrier (0.21 eV), and a low average open-circuit voltage (0.51 V). Furthermore, we investigate the impact of the electrolyte solvation on the performance of Ca-ion adsorption and migration. Upon contact with electrolyte solvents, graphene+ exhibits strong adsorption strength and rapid migration of Ca-ions on its surface. These results demonstrate the promising potential of graphene+ as a high-performance anode material for CIBs.
Two-dimensional graphene+ as an anode material for calcium-ion batteries with ultra-high capacity.
Nearly 100% triplet harvesting in conventional fluorophor‐based organic light‐emitting devices is realized through energy transfer from exciplex. The best C545T‐doped device using the exciplex host ...exhibits a maximum current efficiency of 44.0 cd A‐1, a maximum power efficiency of 46.1 lm W‐1, and a maximum external quantum efficiency of 14.5%.
A high‐performance hybrid white organic light‐emitting device (WOLED) is demonstrated based on an efficient novel thermally activated delayed fluorescence (TADF) blue exciplex system. This device ...shows a low turn‐on voltage of 2.5 V and maximum forward‐viewing external quantum efficiency of 25.5%, which opens a new avenue for achieving high‐performance hybrid WOLEDs with simple structures.
High‐efficiency, thermally activated delayed‐fluorescence organic light‐emitting diodes based on exciplex emitters are demonstrated. The best device, based on a TAPC:DPTPCz emitter, shows a high ...external quantum efficiency of 15.4%. Strategies for predicting and designing efficient exciplex emitters are also provided. This approach allow prediction and design of efficient exciplex emitters for achieving high‐efficiency organic light‐emitting diodes, for future use in displays and lighting applications.
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