Search

Composite sandwich structures are widely used in the aerospace field due to their advantages of high strength, lightweight, and fatigue resistance. However, these structures are prone to damage with very-low-energy impacts. In order to improve the impact resistance of aircraft skin structure, a low-velocity impact resistance of sandwich structure specimens was tested by means of drop hammer impact, and the impact damage area was scanned by ultrasonic C-scan, and obtains the impact damage of specimens with different impact energies and different ply sequences. Combined with the Hashin failure criterion, the finite element equivalent model of composite sandwich structure under low-velocity impact was established. The errors between the simulation results and the C-scan results of the test piece were less than 10%, in which the experimental measurements and numerical predictions were in close agreement. Finally, the finite element equivalent model was applied to optimize the application of model sandwich, which was used for fuselage skin of a certain electric aircraft. The total thickness of the laminate structure remains unchanged before and after optimization, but the impact resistance was significantly enhanced. The ±45° lay-up was beneficial for the structure to absorb the impact energy.

Zinc oxide (ZnO) has been widely acknowledged as a highly effective photocatalyst for the degradation of organic pollutants. In this study, we presented silver nanoparticles (AgNPs) embedded ZnO foam photocatalyst (Ag−ZnO) on glass substrates by the chemical bath in‐situ co‐deposition method. Our findings demonstrat that at low Ag‐loading content, metallic Ag0 NPs are embedded within the ZnO foam, while at high Ag‐loading content, they accumulates increasingly from inside to the surface of the foam. With the increase of AgNPs loading from 0.1 mM to 1.5 mM, the absorption of Ag−ZnO foams in the visible light region gradually enhances. The photocatalytic degradation efficiency of rhodamine B (RhB) is the highest in Ag−ZnO foams when the Ag loading concentration reaches 0.8 mM, suggesting an optimal content of Ag for enhanced performance. This trend is attributed to the photo‐induced charge transfer behavior of Ag−ZnO samples. The AgNPs embedded inside the ZnO foam enhance the separation of photo‐induced charges and prevent their recombination. As a result, Ag−ZnO(0.8 mM) foam with more photo‐induced holes participate in the photocatalytic reaction, leading to a remarkably high photocatalytic activity. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: Inverted perovskite solar cells (PerSCs) are a highly promising candidate in the photovoltaic field due to their low‐temperature fabrication process, negligible hysteresis, and easy integration with Si‐based solar cells. A cathode interlayer (CIL) is necessary in the development of inverted devices to reduce the trap density and energy barrier between the electron transport layer (ETL) and the electrode. However, most CILs are highly thickness‐sensitive due to low conductivity and poor film‐forming. In this study, we report on a self‐doping perylene imide‐based ionene polymer (PNPDIN) used as CIL material to modify electrode in inverted PerSCs. PNPDIN exhibits high conductivity and a good solubility in polar solvent, which results in an improved power conversion efficiency (PCE) from 10.05% (device without a CIL) to 16.97%. When the blend of PNPDIN and Bphen was used as a mixed CIL, the PCE of PerSCs can be further increased to 21.28% owing to the excellent morphology and matched energy level. More importantly, the PCE of the device is highly tolerant to the thickness of the mixed CIL, which benefited from the high conductivity of PNPDIN. This development is expected to provide an excellent mixed CIL material for roll‐to‐roll processing efficient and stable inverted PerSCs. [ABSTRACT FROM AUTHOR]

Photoelectrochemical (PEC) water splitting has attracted strong interest as sustainable technology by converting solar energy into hydrogen. The semiconductor photoelectrodes play an important role to increase the solar‐to‐hydrogen conversion efficiency. Bismuth vanadate (BiVO4) is an excellent candidate as a photoanode material for PEC water oxidation because of its visible light absorption, suitable band edge location, high stability and low cost. However, BiVO4 alone may undergo short carrier diffusion length, rapid recombination of photo‐induced charge carriers and photocorrosion. The heterojunction strategy established by combining two or more materials has provided an outstanding technique to address these issues. This Review focuses on recent important works with respect to BiVO4 heterojunction photoanodes for PEC water oxidation reactions, including interface junction and surface functional junction formation. Additionally, challenges faced and prospects for future research on BiVO4 heterojunction photoanodes in the field of solar‐to‐hydrogen conversion are proposed. [ABSTRACT FROM AUTHOR]

A highly regioselective reaction of 2-indolylmethanols with enamides has been developed at room temperature by using AlCl3 as a catalyst. A wide range of hybrids (40 examples) of indoles and enamides were obtained in moderate to good yields (up to 98% yield). This transformation represents the efficient way to introduce biologically important indoles and enamides skeleton into structurally complex hybrids. [ABSTRACT FROM AUTHOR]

Flow chemistry technology innovatively integrates the traditional independent experimental operation processes, speeds up reaction rates and, especially, can be applied in special reactions that are hazardous or under difficult reaction conditions, being beneficial for the development of green chemistry and laboratory automation. In flow chemistry, the application of traditional pipeline microreactors is usually limited by blockage, corrosion and difficult maintenance. The micro/nanomaterials-based microreactors for flow chemistry are supposed to solve these problems. Herein, we report a novel solid–liquid composite microreactor (BiOBr@ILG-microspheres) with ionic liquid compartments based on ionic liquid gel microspheres (ILG-microspheres) and a typical photocatalyst, BiOBr. The BiOBr@ILG-microspheres show high photodegradation performance, which is attributed to the enrichment of organic substrates by the ILG-microspheres, the efficient charge transfer microenvironment of the internal ionic liquids (ILs), and the flower-like heterostructure of the microspheres that hosts abundant active sites. Furthermore, the BiOBr@ILG-microspheres are embedded in a poly(vinyl alcohol) (PVA) hydrogel to build a multi-liquid phase membrane, which exhibits promising performance in removing pollutants continuously from flowing water with an ∼100% removal rate of ciprofloxacin for a long time, due to the synergic effect of the enrichment and catalytic degradation of the pollutants by the BiOBr@ILG-microspheres. This work provides a new research strategy for constructing liquid compartment microreactors with a synergistic effect of extraction–catalysis using the novel developed ILG-microspheres, which will attract widespread interest because it is in accordance with the concept of green chemistry. [ABSTRACT FROM AUTHOR]

The regular structure provided by two-dimensional (2D) structural colloidal crystals is widely accepted to provide an ideal template that ensures that plasmonic bimetallic composite nanostructures are uniform. Herein, we report an effective method for fabricating bimetallic Au–Ag composite films loaded on the surfaces of 2D polystyrene@polyacrylic acid (PS@PAA) colloidal crystals. PS@PAA particles coated with uniform Ag particle layers (AgFON) were produced by a simple and effective sputtering-deposition technique, after which the galvanic replacement (GR) reaction was used to produce a bimetallic (Au–Ag)FON composite film at the liquid/solid interface in aqueous HAuCl4. The morphology and relative contents of the bimetallic (Au–Ag)FON composite film can be regulated by changing the kinetic factors that control the GR reaction, including the concentration and pH of the HAuCl4 solution, and the reaction time. We demonstrated that the fabricated bimetallic (Au–Ag)FON composite has localized surface plasmon resonance (LSPR) properties that can be regulated by varying the composite structure and Ag/Au composition. On the one hand, the regular 2D colloidal crystal structure provides an ideal template for preparing Au–Ag composite films, which ensures that the optical signals of plasmonic Au–Ag composite films are reproducible. On the other hand, the synergy between Ag and Au in the bimetallic alloy composite film ensures stable and tunable LSPR performance. Furthermore, the prepared 2D ordered (Au–Ag)FON Au–Ag bimetallic material is expected to be used in sensing and catalysis applications. [ABSTRACT FROM AUTHOR]