Nanocomposites with polymer matrix offer excellent opportunities to explore new functionalities beyond those of conventional materials. TiO2, as a reinforcement agent in polymeric nanocomposites, is a viable strategy that significantly enhanced their mechanical properties. The size of the filler plays an essential role in determining the mechanical properties of the nanocomposite. A defining feature of polymer nanocomposites is that the small size of the fillers leads to an increase in the interfacial area compared to traditional composites. The interfacial area generates a significant volume fraction of interfacial polymer, with properties different from the bulk polymer even at low loadings of the nanofiller. This review aims to provide specific guidelines on the correlations between the structures of TiO2 nanocomposites with polymeric matrix and their mechanical properties. The correlations will be established and explained based on interfaces realized between the polymer matrix and inorganic filler. The paper focuses on the influence of the composition parameters (type of polymeric matrix, TiO2 filler with surface modified/unmodified, additives) and technological parameters (processing methods, temperature, time, pressure) on the mechanical strength of TiO2 nanocomposites with the polymeric matrix.

The presence of toxic, non-biodegradable and harmful organic pollutants in soils, wastewater, and atmosphere has become an indisputable, and global fact as a significant environmental problem. The heterogeneous photocatalysis, an advanced oxidation process (AOP) using semiconductor materials as catalysts, is a topic of great interest considering the possibility of the pollutants removal from water. The photocatalytic degradation of organic contaminants (i.e., dyes, pesticides, phenolic compounds) present in water using semiconductor materials depends on a number of parameters such as: the bandgap energy, phase composition, crystallinity, morphology and surface area of catalyst, electron-hole recombination rate, intensity of light, and adsorption capacity of the dye on the photocatalyst surface. One of the important constraints related to the catalyst photocatalytic efficiency is the fast recombination of the photogenerated electrons and holes. Therefore, various strategies have been involved in promoting the charge separation, including the development of heterojunction between two semiconductor materials, by tailoring the photocatalysts properties. This mini-review deals with the recent developments on dyes photodegradation using as catalysts various heterojunctions based on copper sulfide nanostructures, such as copper sulfide/metal oxide, copper sulfide/metal sulfide, copper sulfide/graphene, copper sulfide/organic semiconductors etc. The effects of different parameters, such as synthesis parameters, particle size, bandgap energy, surface area, and morphology on the photocatalytic activity of copper sulfide heterojunctions for dyes degradation is also highlighted.

Titanium oxide/graphene oxide nanocomposite thin films were grown by ultraviolet (UV) matrix‐assisted pulsed laser evaporation (MAPLE) technique in controlled oxygen or nitrogen atmospheres. The effect of graphene oxide addition and laser‐induced reduction as well as nitrogen doping on the wetting behavior and photoactive properties of titanium oxide thin films was investigated. Hydrophobic to hydrophilic conversion of titanium oxide films takes place progressively as the relative amount of graphene oxide in the MAPLE composite target increases. Nitrogen doping leads to further decrease of the static contact angle of the composite films. The photoactive properties of the synthesized materials were investigated through the evolution of contact angle under UV light irradiation. Wetting properties of both TiO2 and TiO2/GO nanocomposite thin films improved upon exposure to UV light.

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