Characterized by its strength, durability, and thermal properties, epoxy resin has been widely used as an adhesive, paint, and coating in many applications in the aerospace, civil and automotive industries. Despite this, the thermoset polymer resin has been known for its brittleness and low fracture resistance. This study focuses on the reinforcement of an epoxy resin system (diglycidyl ether of bisphenol A) with zinc oxide (ZnO) nanoparticles in their pristine form and a further modified form. The modification took place in two ways: coating with polydopamine (PDA) and covalently functionalizing them with (3‐aminopropyl)triethoxysilane (APTES) and (3‐glycidoxypropyl)trimethoxysilane (GPTMS). Therefore, four different types of nanoparticles were used: pristine ZnO, ZnO/PDA, ZnO/GPTMS, and ZnO/APTES aiming to improve the interfacial bonding between the polymeric matrix and the reinforcement. Thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy, and scanning electron microscopy characterization and imaging techniques were used to prove that the ZnO nanoparticles were successfully modified prior to manufacturing the epoxy composites. While tensile testing showed that using pristine ZnO increases the composite's strength by 32.14%, the fracture toughness of the resin was improved by 9.40% when reinforced with ZnO functionalized with APTES. TGA showed that the addition of functionalized nanoparticles increases the material's degradation temperature by at most 7.31 ± 4.9°C using ZnO/APTES. Differential scanning calorimetry and dynamic mechanical analysis testing proved that the addition of any type of nanoparticles increases the resin's glass transition temperature by as much as 7.83°C (ZnO/APTES).

Epoxy polymers, having good mechanical properties and thermal stability, are often used for engineering applications. Their properties can be further enhanced by the addition of iron oxide (Fe3O4) nanoparticles (NPs) as fillers to the resin. In this study, pristine Fe3O4 NPs were functionalized with polydopamine (PDA), (3‐glycidoxypropyl)trimethoxysilane (GPTMS), and (3‐aminopropyl)trimethoxysilane (APTES). X‐ray diffraction and scanning electron microscopy (SEM) were used to study any changes in the crystal structure and size of the NPs while Fourier‐Transform Infrared Spectroscopy (FTIR) and Thermogravimetric Analysis (TGA) were used to ensure the presence of functional groups on the surface. The mechanical properties of the Fe3O4‐based nanocomposites generally improved except when reinforced with Fe3O4/PDA. The maximum improvement in tensile strength (∼34%) and fracture toughness (∼13%) were observed for pristine Fe3O4‐based nanocomposites. Dynamic mechanical analysis (DMA) showed that the use of any of the treated NPs improved the material's initial storage modulus and had a substantial impact on its dissipation potential. Also, it was observed that the glass transition temperature measurements by DMA and differential scanning calorimetry were below that of pure epoxy. SEM of the cracked surfaces shows that the incorporation of any NPs leads to an enhancement in its thermal and mechanical properties.

A growing number of research articles have been published on the use of halide perovskite materials for photocatalytic reactions. These articles extend these materials' great success from solar cells to photocatalytic technologies such as hydrogen production, CO 2 reduction, dye degradation, and organic synthesis. In the present review article, we first describe the background theory of photocatalysis, followed by a description on the properties of halide perovskites and their development for photocatalysis. We highlight key intrinsic factors influencing their photocatalytic performance, such as stability, electronic band structure, and sorption properties. We also discuss and shed light on key considerations and challenges for their development in photocatalysis, such as those related to reaction conditions, reactor design, presence of degradable organic species, and characterization, especially for CO 2 photocatalytic reduction. This review on halide perovskite photocatalysts will provide a better understanding for their rational design and development and contribute to their scientific and technological adoption in the wide field of photocatalytic solar devices.

Numerous ways to reinforce epoxy resin and improve its thermomechanical properties have been attempted using organic and inorganic nanoparticles. In this paper, graphitic carbon nitride (g‐C3N4) nanoparticles were synthesized and used to improve the mechanical properties and thermal stability of epoxy composites. The g‐C3N4 was synthesized from cheap melamine powder using a simple one‐step thermal treatment, then was used to reinforce the resin at different weight percentages (wt%). X‐ray diffraction, scanning electron microscopy (SEM), and Fourier infrared spectroscopy were used to characterize the g‐C3N4 and ensure its successful synthesis by studying the changes in its crystal structure, morphology, and chemical structure. The filler was dispersed in the resin using a combination of ultrasonication and high shear mixing. The results showed that the mechanical properties were optimum when 0.5 wt% g‐C3N4 was used. The tensile strength and fracture toughness of the resulting epoxy composite improved by 21.8% and 77.3%, respectively. SEM was used to investigate the morphologies of cracks formed in epoxy composite specimens after the tensile testing. The SEM micrographs of the fracture surface showed a transition from a brittle to a rough morphology, signifying the enhancement in the composites' toughness. Thermogravimetric analysis showed a good improvement in degradation temperature of up to 8.86% while dynamic mechanical analysis showed that the incorporation of g‐C3N4 did not affect the material's glass transition temperature.

CO2 photocatalytic conversion into value-added fuels through solar energy is a promising way of storing renewable energy while simultaneously reducing the concentration of CO2 in the atmosphere. Lead-based halide perovskites have recently shown great potential in various applications such as solar cells, optoelectronics, and photocatalysis. Even though they show high performance, the high toxicity of Pb2+ along with poor stability under ambient conditions restrains the application of these materials in photocatalysis. In this respect, we developed an in situ assembly strategy to fabricate the lead-free double perovskite Cs2AgBiBr6 on a 2D bismuthene nanosheet prepared by a ligand-assisted reprecipitation method for a liquid-phase CO2 photocatalytic reduction reaction. The composite improved the production and selectivity of the eight-electron CH4 pathway compared with the two-electron CO pathway, storing more of the light energy harvested by the photocatalyst. The Cs2AgBiBr6/bismuthene composite shows a photocatalytic activity of 1.49(±0.16) μmol g–1 h–1 CH4, 0.67(±0.14) μmol g–1 h–1 CO, and 0.75(±0.20) μmol g–1 h–1 H2, with a CH4 selectivity of 81(±1)% on an electron basis with 1 sun. The improved performance is attributed to the enhanced charge separation and suppressed electron–hole recombination due to good interfacial contact between the perovskite and bismuthene promoted by the synthesis method.