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The development of new functional materials based on metal–organic frameworks (MOFs) for adsorption and catalytic applications is one of the promising trends of modern materials science. The Zr-based MOFs, specifically UiO-66, are considered as the supports for metallic catalysts for the 5-hydroxymethylfurfural platform molecule reduction into valuable products. The present work focused on the effect of NH2 modification of UiO-66 on its structure and functional properties. The samples were prepared by a solvothermal method. The structure of the obtained materials was studied by X-ray diffraction, IR spectroscopy, UV–visible spectroscopy, and low-temperature nitrogen adsorption. Basic properties were investigated by HCl and CH3COOH adsorption, and electrokinetic properties were studied by electrophoretic light scattering. UiO-66-NH2 samples with different contents of aminoterephthalate linkers were successfully prepared. A gradual decrease in the specific surface area and the fraction of micropores with a diameter of ~0.9 nm was observed with an increase in the aminoterephthalate content. A proportional increase in the total number of basic sites in UiO-66-NH2 samples was established with an increase in the aminoterephthalate content up to 75%. At the same time, a noticeable decrease in the total number of basic sites and an increase in their strength with higher aminoterephthalate content was observed.

Three bismuth silicate-based photocatalysts (composites of Bi2SiO5 and Bi12SiO20) prepared via the hydro-/solvothermal approach were studied using electrochemical methods. The characteristic parameters of semiconductors, such as flat band potential, donor density, and mobility of their charge carriers, were obtained and compared with the materials’ photocatalytic activity. An attempt was made to study the effect of solution components on the semiconductor/liquid interface (SLI). In particular, the Mott–Schottky characterization was made in a common model electrolyte (Na2SO4) and with the addition of glycerol as a model organic compound for photocatalysis. Thus, a medium close to those in photocatalytic experiments was simulated, at least within the limits allowed by electrochemical measurements. Zeta-potential measurements and electrochemical impedance spectroscopy were used to reveal the processes taking place at the SLI. It was found that the medium in which measurements were carried out dramatically impacted the results. The flat band potential values (Efb) obtained via the Mott–Schottky technique were shown to differ significantly depending on the solution used in the experiment, which is explained by different processes taking place at the SLI. A strong influence of specific adsorption of commonly used sulfate ions and neutral molecules on the measured values of Efb was shown.

The present work is focused on nickel catalysts supported on La2O3-CeO2 binary oxides without and with the addition of Cu to the active component for the dry reforming of methane (DRM). The catalysts are characterized using XRD, XRF, TPD-CO2, TPR-H2, and low-temperature N2 adsorption–desorption methods. This work shows the effect of different La:Ce ratios (1:1 and 9:1) and the Cu addition on the structural, acid base, and catalytic properties of Ni-containing systems. The binary LaCeOx oxide at a ratio of La:Ce = 1:1 is characterized by the formation of a solid solution with a fluorite structure, which is preserved upon the introduction of mono- or bimetallic particles. At La:Ce = 9:1, La2O3 segregation from the solid solution structure is observed, and the La excess determines the nature of the precursor of the active component, i.e., lanthanum nickelate. The catalysts based on LaCeOx (1:1) are prone to carbonization during 6 h spent on-stream with the formation of carbon nanotubes. The Cu addition facilitates the reduction of the Cu-Ni catalyst carbonization and increases the number of structural defects in the carbon deposition products. The lanthanum-enriched LaCeOx (9:1) support prevents the accumulation of carbon deposition products on the surface of CuNi/La2O3-CeO2 9:1, providing high DRM activity and an H2/CO ratio of 0.9.

Hydrosphere pollution by organic pollutants of different nature (persistent dyes, phenols, herbicides, antibiotics, etc.) is one of the urgent ecological problems facing humankind these days. The task of water purification from such pollutants can be effectively solved with the help of modern photocatalytic technologies. This article is devoted to the study of photocatalytic properties of composite catalysts based on ZnO modified with plasmonic Ag nanoparticles. All materials were obtained by laser synthesis in liquid and differed by their silver content and preparation conditions, such as additional laser irradiation and/or annealing of produced powders. The prepared ZnO-Ag powders were investigated by electron microscopy, X-ray diffraction and UV-Vis spectroscopy. Photocatalytic tests were carried out with well- known test molecules in water (persistent dye rhodamine B, phenol and common antibiotic tetracycline) using LED light sources with wavelengths of 375 and 410 nm. The introduction of small concentrations (up to 1%) of plasmonic Ag nanoparticles is shown to increase the efficiency of the ZnO photocatalyst by expanding its spectral range. Both the preparation conditions and material composition were optimized to obtain composite photocatalysts with the highest efficiency. Finally, the operation mechanisms of the material with different distribution of silver are discussed.

In this work, a new approach to the preparation of heterostructured nanoparticles (NPs) based on bismuth silicates Bi2SiO5/Bi12SiO20 is proposed and implemented. This approach is based on solid-phase synthesis by annealing of a pre-homogenized mixture of β-Bi2O3 and SiO2 powders in different ratios. For this purpose, industrial silica nanopowder and β-bismuth oxide NPs powder obtained by pulsed laser ablation (PLA) in air are used. The morphology, phase composition and optical properties of the obtained materials are studied. By changing the ratio of precursors, the powders similar in structure to single-phase bismuth silicates Bi2SiO5 and Bi12SiO20 was well as heterostructured NPs on their basis are obtained. The activity of the photocatalysts in the reactions of Rhodamine B (Rh B) decomposition and selective oxidation of 5-hydroxymethylfurfural (5-HMF) is estimated. The best photocatalytic activity is demonstrated by powders with a similar Bi2SiO5/Bi12SiO20 (or 4Bi: 1Si) phase ratio. As a result of the analysis of the data obtained, the formation of a type II heterojunction is proposed.

Photocatalysis offers a powerful approach for water purification from toxic organics, hydrogen production, biosolids processing, and the conversion of CO2 into useful products. Further advancements in photocatalytic technologies depend on the development of novel, highly efficient catalysts and optimized synthesis methods. This study aimed to develop a laser synthesis technique for bismuth oxyhalide nanoparticles (NPs) as efficient and multifunctional photocatalysts. Laser ablation of a Bi target in a solution containing halogen salt precursors, followed by laser plasma treatment of the resulting colloid, yielded crystalline bismuth oxyhalides (BixOyXz, where X = Cl, Br, or I) NPs without the need for additional annealing. The composition, structure, morphology, and optical properties of the synthesized BixOyXz (X = Cl, Br, I) NPs were characterized using XRD analysis, electron microscopy, Raman spectroscopy, and UV-Vis spectroscopy. The effect of the halogen on the photocatalytic activity of the double oxides was investigated. The materials exhibited high photocatalytic activity in the degradation of persistent model pollutants like Rhodamine B, tetracycline, and phenol. Furthermore, the BixOyXz NPs demonstrated good efficiency and high yield in the selective oxidation of 5-hydroxymethylfurfural (5-HMF) to 2,5-furandicarboxylic acid (FDCA). The obtained results highlight the promising potential of this laser synthesis approach for producing high-performance bismuth oxyhalide photocatalysts.

Novel yttrium-doped CeO2, MnOx, and CeMnOx composites are investigated as catalysts for low-temperature NH3-SCR. The study involves the preparation of unmodified oxide supports using a citrate method followed by modification with Y (2 wt.%) using two approaches, including the one-pot citrate method and incipient wetness impregnation of undoped oxides. The NH3-SCR reaction is studied in a fixed-bed quartz reactor to test the ability of the prepared catalysts in NO reduction. The gas reaction mixture consists of 800 ppm NO, 800 ppm NH3, 10 vol.% O2, and He as a balance gas at a WHSV of 25,000 mL g−1 h−1. The results indicate that undoped CeMnOx mixed oxide exhibits significantly higher deNOx performance compared with undoped and Y-doped MnOx and CeO2 catalysts. Indeed, yttrium presence in CeMnOx promotes the competitive NH3-SCO reaction, reducing the amount of NH3 available for NO reduction and lowering the catalyst activity. Furthermore, the physical-chemical properties of the prepared catalysts are studied using nitrogen adsorption/desorption, XRD, Raman spectroscopy, temperature-programmed reduction with hydrogen, and temperature-programmed desorption of ammonia. This study presents a promising approach to enhancing the performance of NH3-SCR catalysts at low temperatures that can have significant implications for reducing NO emissions.

In the present study CeO2, MnO2 and CeMnOx mixed oxide (with molar ratio Ce/Mn = 1) were prepared by sol-gel method using citric acid as a chelating agent and calcined at 500 °C. The silver catalysts (1 wt.% Ag) over the obtained supports were synthesized by the incipient wetness impregnation method with [Ag(NH3)2]NO3 aqueous solution. The selective catalytic reduction of NO by C3H6 was investigated in a fixed-bed quartz reactor using a reaction mixture composed of 1000 ppm NO, 3600 ppm C3H6, 10 vol.% O2, 2.9 vol.% H2 and He as a balance gas, at WHSV of 25,000 mL g−1 h−1.The physical-chemical properties of the as-prepared catalysts were studied by several characterization techniques, such as X-ray fluorescence analysis, nitrogen adsorption/desorption, X-ray analysis, Raman spectroscopy, transmission electron microscopy with analysis of the surface composition by X-ray energy dispersive spectroscopy and X-ray photo-electron spectroscopy. Silver oxidation state and its distribution on the catalysts surface as well as the support microstructure are the main factors determining the low temperature activity in NO selective catalytic reduction. The most active Ag/CeMnOx catalyst (NO conversion at 300 °C is 44% and N2 selectivity is ~90%) is characterized by the presence of the fluorite-type phase with high dispersion and distortion. The characteristic “patchwork” domain microstructure of the mixed oxide along with the presence of dispersed Ag+/Agnδ+ species improve the low-temperature catalyst of NO reduction by C3H6 performance compared to Ag/CeO2 and Ag/MnOx systems.

In this work, we studied the catalytic performance of a β-Bi2O3/Bi12SiO20 nanocomposite material in the reactions involving the photodecomposition of rhodamine B and selective photooxidation of 5-hydroxymethylfurfural (HMF). The semiconductor composite nanomaterial was obtained by means of the mechanical grinding of a mixture of nanopowders of β-Bi2O3 and sillenite, both individually produced via pulsed laser ablation. The crystal structure of the prepared composite particles was confirmed by means of X-ray diffraction, while the optical properties of both individual components and their composite (with different ratios of Bi2O3 and Bi12SiO20) were also studied. The photocatalytic activity of the composite particles was studied in the course of their decomposition of rhodamine B under LED excitation at wavelengths of 375, 410 and 470 nm. It was shown that the optimal β-Bi2O3/Bi12SiO20 ratio in the composite particles resulted in their photocatalytic activity exceeding those of both single-phase β-Bi2O3 and Bi12SiO20, as well as that of their mixtures (by ~2.3 times for the excitation of an LED with λ = 375 nm). The novel composite particles were also found to perform better in the selective photocatalytic oxidation of HMF: at a conversion of ~5%, the selectivity toward DFF of the nanocomposite was significantly higher (10.3%) than that of sample Bi2O3 (−4.2%). A model was proposed that explains the increase in activity of the newly prepared photocatalyst due to the formation of a type II heterojunction in its particles.

The development of new functional materials based on metal-organic frameworks (MOFs) for adsorption and catalytic applications is one of the promising trends of modern materials science. The Zr-based MOFs, specifically UiO-66, are considered as the supports for metallic catalysts for the 5-hydroxymethylfurfural platform molecule reduction into valuable products. The present work focused on the effect of NH[sub.2] modification of UiO-66 on its structure and functional properties. The samples were prepared by a solvothermal method. The structure of the obtained materials was studied by X-ray diffraction, IR spectroscopy, UV-visible spectroscopy, and low-temperature nitrogen adsorption. Basic properties were investigated by HCl and CH[sub.3]COOH adsorption, and electrokinetic properties were studied by electrophoretic light scattering. UiO-66-NH[sub.2] samples with different contents of aminoterephthalate linkers were successfully prepared. A gradual decrease in the specific surface area and the fraction of micropores with a diameter of ~0.9 nm was observed with an increase in the aminoterephthalate content. A proportional increase in the total number of basic sites in UiO-66-NH[sub.2] samples was established with an increase in the aminoterephthalate content up to 75%. At the same time, a noticeable decrease in the total number of basic sites and an increase in their strength with higher aminoterephthalate content was observed.