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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]