The synthesis of surface-active structures is important for creating many applications. The structural formation of SnO${}_2$ thin films in the range from 1.4 to 1.53 pH is studied in this work. This process occurs on the surface of the sample in the range of 1.4 to 1.49 and in the volume in the range of 1.51 to 1.53. SnO${}_2$ is formed after annealing at 400 ${}^{\circ }$C, according to XRD. Doping NH${}_4$OH to solution stimulates particle coagulation and gel formation. All of these have an impact on the transparency of samples investigated by spectrophotometric methods. By increasing the pH, the resistance raises at room temperature. The E${}_g$ calculation along the fundamental absorption edge shows that it is greater than 3.6 eV’ for SnO${}_2$ films. According to the Burstein–Moss effect, a change of the bandgap is related to the increased concentration of the free charge carriers. Elemental analysis has shown that chlorine ions are considered to be additional sources of charge carriers. The value pH = 1.49 is critical since there is a drastic change in the structure of the samples, the decrease in transparency is replaced by its increase, and the energy of activation of impurity levels is changed.

The formation of complex surface morphology of a multilayer structure, the processes of which are based on quantum phenomena, is a promising domain of the research. A hierarchy of pore of various sizes was determined in the initial sample of porous silicon by the atomic force microscopy. After film deposition by spray pyrolysis, ZnO nanoclusters regularly distributed over the sample surface were formed. Using the electron paramagnetic resonance (EPR) method it was determined that the localization of paramagnetic centers occurs more efficiently as a result of the ZnO deposition. An increase in the number of deposited layers, leads to a decrease in the paramagnetic center relaxation time, which is probably connected with the formation of ZnO nanocrystals with energetically stable properties. The nucleation and formation of nanocrystals is associated with the interaction of particles with an uncompensated charge. There is no single approach to determine the mechanism of this process. By the EPR method supplemented with the signal cyclic saturation, spectral manifestations from individual centers were effectively separated. Based on electron paramagnetic resonance and photoluminescence studies it was revealed that the main transitions between energy levels are due to oxygen vacancies and excitons.

This article presents the results of the formation of hierarchical micro–nano structures in nanostructured tin dioxide films obtained from the lyophilic film-forming system SnCl₄/EtOH/NH₄OH. The classification of the shape and size of the synthesized structures, in relation to the pH of the solution, is presented. Measurements were carried out on an X-ray diffractometer to study the crystal structure of the samples analyzed. It was found that SnO₂ and NH₄Cl crystallites participate in the formation of the synthesized hierarchical structures. It is shown that the mechanism of the formation of hierarchical structures depends on the amount of ammonium hydroxide added. This makes it possible to control the shape and size of the synthesized structures by changing the ratio of precursors.

In this paper, we investigated fractal cluster structures of colloidal particles in tin dioxide films obtained from lyophilic film-forming systems SnCl₄/EtOH/NH₄OH with different pH levels. It was revealed that at the ratio Sn > Cl₂ > O₂, N₂ = 0, and pH = 1.42, the growth of cross-shaped and flower-shaped structures of various sizes from several μm to tens of μm is observed. At the ratio Cl₂ > Sn > O₂ > N₂ and pH = 1.44, triangular and hexagonal structures are observed, the sizes of which are on the order of several tens of micrometers. The growth of hexagonal structures is probably affected by the presence of nitrogen in the film, according to the elemental analysis data. At the ratio Sn > Cl₂ > O₂ > N₂ and solution pH of 1.49, the growth of hexagonal and cross-shaped structures is observed, whereas flower-shaped structures are not observed. Hierarchical flower-like and cross-shaped structures are fractal. The shape of microstructures is directly related to the shape of the elementary cells of SnO₂ and NH₄Cl. A direct dependence of the formation of hierarchical structures on the volume of ammonium hydroxide additive was found. This allows for controlling the shape and size of the synthesized structures when changing the ratio of the initial precursors and influencing the final physicochemical characteristics of the obtained samples.

The detection of particles with uncompensated charge and the determination of the features of their interaction during the formation of nanocrystals on substrates with a developed surface are an interesting area of research. The porous surface formed via the electrochemical etching of silicon acquired fractal properties as a result of the deposition of zinc oxide layers. Microscopy methods using different resolutions revealed a hierarchical structure of the surface, where each of the three consecutive levels contains uniformly distributed formations. The deposition of 20 layers of ZnO maximizes the concentration of nanocrystals at the pore boundaries, while the deposition of 25 layers leads to the formation of a continuous layer. The increase in photoluminescence intensity with an increase in the number of deposited layers is due to the saturation of surface nanostructures with electrons through several mechanisms. Electron paramagnetic resonance (EPR) studies have shown that the main mechanism of radiation recombination is the capture of electrons on oxygen vacancies. The different nature of the EPR saturation of the signal of interconnected paramagnetic centers revealed the formation of zinc oxide particles at the boundaries of pores with different sizes. The results of these studies of surface-active structures effectively complement the knowledge about sensory materials.

Antimony oxychloride compounds represent a distinct class of inorganic materials that combine structural features characteristic of both oxides and halides. Their compositional flexibility and anisotropic properties make them promising candidates for use in photocatalytic systems, optoelectronic devices, flame-retardant coatings, and energy storage technologies. This review provides an overview of the structural characteristics and synthesis strategies associated with key members of the Sb_xO_yCl_z family, including SbOCl, Sb₄O₅Cl₂, and Sb₈O₁₁Cl₂. Emphasis is placed on how synthesis parameters—such as temperature, pH, and precursor composition—govern phase formation, morphology, and resulting properties. Recent advances in composite engineering, controlled doping, and surface modification are discussed as effective routes to overcome limitations such as low conductivity and chemical instability. The broader significance of antimony as a strategic element is also addressed in the context of global resource availability and its role in sustainable technologies. Overall, these materials provide a versatile platform for the design of multifunctional systems tailored to meet future demands in materials science and applied engineering.