Compared to efficient green and near‐infrared light‐emitting diodes (LEDs), less progress has been made on deep‐blue perovskite LEDs. They suffer from inefficient domain various number of PbX6− ...layers (n) control, resulting in a series of unfavorable issues such as unstable color, multipeak profile, and poor fluorescence yield. Here, a strategy involving a delicate spacer modulation for quasi‐2D perovskite films via an introduction of aromatic polyamine molecules into the perovskite precursor is reported. With low‐dimensional component engineering, the n1 domain, which shows nonradiative recombination and retarded exciton transfer, is significantly suppressed. Also, the n3 domain, which represents the population of emission species, is remarkably increased. The optimized quasi‐2D perovskite film presents blue emission from the n3 domain (peak at 465 nm) with a photoluminescence quantum yield (PLQY) as high as 77%. It enables the corresponding perovskite LEDs to deliver stable deep‐blue emission (CIE (0.145, 0.05)) with an external quantum efficiency (EQE) of 2.6%. The findings in this work provide further understanding on the structural and emission properties of quasi‐2D perovskites, which pave a new route to design deep‐blue‐emissive perovskite materials.
A quasi‐two‐dimensional perovskite film with stable domain distribution is prepared based on a new spacer. The film containing pure bromide perovskite exhibits enhanced deep‐blue fluorescence with quantum yield of 77% by low‐dimensional component engineering. As a result, the corresponding light‐emitting diodes deliver stable deep‐blue emission with a peak external quantum efficiency of 2.6%.
Multi‐layer π‐stacked emitters based on spatially confined donor/acceptor/donor (D/A/D) patterns have been developed to achieve high‐efficiency thermally activated delayed fluorescence (TADF). In ...this case, dual donor moieties and a single acceptor moiety are introduced to form two three‐dimensional (3D) emitters, DM‐BD1 and DM‐BD2, which rely on spatial charge transfer (CT). Owing to the enforced face‐to‐face D/A/D pattern, effective CT interactions are realized, which lead to high photoluminescence quantum yields (PLQYs) of 94.2 % and 92.8 % for the two molecules, respectively. The resulting emitters exhibit small singlet–triplet energy splitting (ΔEST) and fast reverse intersystem crossing (RISC) processes. Maximum external quantum efficiencies (EQEs) of 28.0 % and 26.6 % were realized for devices based on DM‐BD1 and DM‐BD2, respectively, which are higher than those of their D/A‐type analogues.
Multi‐Layer π‐stacked molecules are designed to realize efficient thermally activated delayed fluorescence. Spatially confined molecules with stereochemical structures are constructed in donor/acceptor/donor architectures with different conformations. Their organic light‐emitting diode (OLED) devices exhibit high external quantum efficiencies (EQEs) of 28.0 %/26.6 %, respectively.
Dye and nitro-compound pollution has become a significant issue worldwide. The adsorption and degradation of dyes and nitro-compounds have recently become important areas of study. Different methods, ...such as precipitation, flocculation, ultra-filtration, ion exchange, coagulation, and electro-catalytic degradation have been adopted for the adsorption and degradation of these organic pollutants. Apart from these methods, adsorption, photocatalytic degradation, and chemical degradation are considered the most economical and efficient to control water pollution from dyes and nitro-compounds. In this review, different kinds of dyes and nitro-compounds, and their adverse effects on aquatic organisms and human beings, were summarized in depth. This review article covers the comprehensive analysis of the adsorption of dyes over different materials (porous polymer, carbon-based materials, clay-based materials, layer double hydroxides, metal-organic frameworks, and biosorbents). The mechanism and kinetics of dye adsorption were the central parts of this study. The structures of all the materials mentioned above were discussed, along with their main functional groups responsible for dye adsorption. Removal and degradation methods, such as adsorption, photocatalytic degradation, and chemical degradation of dyes and nitro-compounds were also the main aim of this review article, as well as the materials used for such degradation. The mechanisms of photocatalytic and chemical degradation were also explained comprehensively. Different factors responsible for adsorption, photocatalytic degradation, and chemical degradation were also highlighted. Advantages and disadvantages, as well as economic cost, were also discussed briefly. This review will be beneficial for the reader as it covers all aspects of dye adsorption and the degradation of dyes and nitro-compounds. Future aspects and shortcomings were also part of this review article. There are several review articles on all these topics, but such a comprehensive study has not been performed so far in the literature.
The development of metal‐N‐C materials as efficient non‐precious metal (NPM) catalysts for catalysing the oxygen reduction reaction (ORR) as alternatives to platinum is important for the practical ...use of proton exchange membrane fuel cells (PEMFCs). However, metal‐N‐C materials have high structural heterogeneity. As a result of their high‐temperature synthesis they often consist of metal‐Nx sites and graphene‐encapsulated metal nanoparticles. Thus it is hard to identify the active structure of metal‐N‐C catalysts. Herein, we report a low‐temperature NH4Cl‐treatment to etch out graphene‐encapsulated nanoparticles from metal‐N‐C catalysts without destruction of co‐existing atomically dispersed metal‐Nx sites. Catalytic activity is much enhanced by this selective removal of metallic nanoparticles. Accordingly, we can confirm the spectator role of graphene‐encapsulated nanoparticles and the pivotal role of metal‐Nx sites in the metal‐N‐C materials for ORR in the acidic medium.
ORR inspiring: With a low‐temperature NH4Cl treatment graphene‐encapsulated nanoparticles (NPs) are etched out of metal‐N‐C catalysts. Removing these metallic NPs greatly enhances the catalytic oxygen reduction reaction (ORR) activity allowing the real catalytic centres to be identified.
► Analyze the effect of coplanar fissure angle on mechanical parameters of sandstone. ► Characterize crack coalescence behavior of sandstone by photographic monitoring. ► Obtain the sequence and type ...of crack coalescence in sandstone samples. ► Construct the relation between coplanar fissure angle and crack coalescence stress.
This investigation presents crack coalescence behavior of brittle sandstone samples containing two coplanar fissures in the process of deformation. On basis of experimental results, the influence of coplanar fissure angle on strength and deformation behavior of sandstone samples is firstly analyzed. By adopting photographic monitoring, the crack initiation and coalescence are all observed and characterized from the inner and outer tips of pre-existing coplanar fissures in brittle sandstone sample. Moreover, the sequence and type of crack coalescence in sandstone samples containing two coplanar fissures are analyzed. Finally, the relationship between coplanar fissure angle and crack coalescence stress is constructed.
Abstract
Supported metal nanoclusters consisting of several dozen atoms are highly attractive for heterogeneous catalysis with unique catalytic properties. However, the metal nanocluster catalysts ...face the challenges of thermal sintering and consequent deactivation owing to the loss of metal surface areas particularly in the applications of high-temperature reactions. Here, we report that sulfur—a documented poison reagent for metal catalysts—when doped in a carbon matrix can stabilize ~1 nanometer metal nanoclusters (Pt, Ru, Rh, Os, and Ir) at high temperatures up to 700 °C. We find that the enhanced adhesion strength between metal nanoclusters and the sulfur-doped carbon support, which arises from the interfacial metal-sulfur bonding, greatly retards both metal atom diffusion and nanocluster migration. In catalyzing propane dehydrogenation at 550 °C, the sulfur-doped carbon supported Pt nanocluster catalyst with interfacial electronic effects exhibits higher selectivity to propene as well as more stable durability than sulfur-free carbon supported catalysts.
Atomically ordered intermetallic nanoparticles are promising for catalytic applications but are difficult to produce because the high-temperature annealing required for atom ordering inevitably ...accelerates metal sintering that leads to larger crystallites. We prepared platinum intermetallics with an average particle size of <5 nanometers on porous sulfur-doped carbon supports, on which the strong interaction between platinum and sulfur suppresses metal sintering up to 1000°C. We synthesized intermetallic libraries of small nanoparticles consisting of 46 combinations of platinum with 16 other metal elements and used them to study the dependence of electrocatalytic oxygen-reduction reaction activity on alloy composition and platinum skin strain. The intermetallic libraries are highly mass efficient in proton-exchange-membrane fuel cells and could achieve high activities of 1.3 to 1.8 amperes per milligram of platinum at 0.9 volts.
Metal-support interaction is of great significance for catalysis as it can induce charge transfer between metal and support, tame electronic structure of supported metals, impact adsorption energy of ...reaction intermediates, and eventually change the catalytic performance. Here, we report the metal size-dependent charge transfer reversal, that is, electrons transfer from platinum single atoms to sulfur-doped carbons and the carbon supports conversely donate electrons to Pt when their size is expanded to ~1.5 nm cluster. The electron-enriched Pt nanoclusters are far more active than electron-deficient Pt single atoms for catalyzing hydrogen evolution reaction, exhibiting only 11 mV overpotential at 10 mA cm
and a high mass activity of 26.1 A mg
at 20 mV, which is 38 times greater than that of commercial Pt/C. Our work manifests that the manipulation of metal size-dependent charge transfer between metal and support opens new avenues for developing high-active catalysts.
Uniaxial compression experiments were performed for brittle sandstone samples containing a single fissure by a rock mechanics servo-controlled testing system. Based on the experimental results of ...axial stress-axial strain curves, the influence of single fissure geometry on the strength and deformation behavior of sandstone samples is analyzed in detail. Compared with the intact sandstone sample, the sandstone samples containing a single fissure show the localization deformation failure. The uniaxial compressive strength, Young’s modulus and peak axial strain of sandstone samples with pre-existing single fissure are all lower than that of intact sandstone sample, which is closely related to the fissure length and fissure angle. The crack coalescence was observed and characterized from tips of pre-existing single fissure in brittle sandstone sample. Nine different crack types are identified based on their geometry and crack propagation mechanism (tensile, shear, lateral crack, far-field crack and surface spalling) for single fissure, which can be used to analyze the failure mode and cracking process of sandstone sample containing a single fissure under uniaxial compression. To confirm the subsequence of crack coalescence in sandstone sample, the photographic monitoring and acoustic emission (AE) technique were adopted for uniaxial compression test. The real-time crack coalescence process of sandstone containing a single fissure was recorded during the whole loading. In the end, the influence of the crack coalescence on the strength and deformation failure behavior of brittle sandstone sample containing a single fissure is analyzed under uniaxial compression. The present research is helpful to understand the failure behavior and fracture mechanism of engineering rock mass (such as slope instability and underground rock burst).
Epstein-Barr virus (EBV)-associated epithelial cancers, including nasopharyngeal carcinoma (NPC) and approximately 10% of gastric cancers, termed EBVaGC, represent 80% of all EBV-related ...malignancies. However, the exact role of EBV in epithelial cancers remains elusive. Here, we report that EBV functions in vasculogenic mimicry (VM). Epithelial cancer cells infected with EBV develop tumor vascular networks that correlate with tumor growth, which is different from endothelial-derived angiogenic vessels and is VEGF-independent. Mechanistically, activation of the PI3K/AKT/mTOR/HIF-1α signaling cascade, which is partly mediated by LMP2A, is responsible for EBV-induced VM formation. Both xenografts and clinical samples of NPC and EBVaGC exhibit VM histologically, which are correlated with AKT and HIF-1α activation. Furthermore, although anti-VEGF monotherapy shows limited effects, potent synergistic antitumor activities are achieved by combination therapy with VEGF and HIF-1α-targeted agents. Our findings suggest that EBV creates plasticity in epithelial cells to express endothelial phenotype and provides a novel EBV-targeted antitumor strategy.
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