Вимоги до матеріалів, що приймаються до друку в збірнику наукових праць «Сучасна українська політика. Політики і політологи про неї»

Whereas bulk zinc oxide (ZnO) exhibits the wurtzite crystal structure, nanoscale ZnO was recently synthesized in the rock salt structure by addition of Mg. Using first-principles methods, we investigated two stabilization routes for accessing rock salt ZnO. The first route is stabilization by Mg addition, which was investigated by considering ZnO-MgO mixed phases. The second route is through size effects, as surface energies become dominant for small nanocrystal sizes. We discovered that the surface energy of rock salt ZnO is surprisingly low at 0.63 J m-2, which is lower than those of wurtzite and zinc blende ZnO and lower than that of rock salt MgO. We predict that pure rock salt ZnO is stable for nanocrystals smaller than 1.6 nm, and that Mg additions can greatly extend the size range in which the rock salt phase is stable. Both mixed-phase and core-shell models were considered in the calculations. The present approach could be applied to predict the stabilization of many other nanocrystal phases in deviating crystal structures

Рифма в рамках средневекового крымскотатарского силлабического стиха

В предложенной статье представлен теоретический материал, который раскрывает сущность и особенности рифмы, подкреплённый необходимым материалом из крымскотатарской литературы.У запропонованій статті представлений теоретичний матеріал, що розкриває сутність і особливості рими, підкріплений необхідним матеріалом із кримськотатарської літератури.In offered article the theoretical material which opens essence and features of the rhyme, supported by a necessary material from crimean tatars literatures is submitted

Nanoscale Porosity of High Surface Area Gadolinium Oxide Nanofoam Obtained With Combustion Synthesis

Nanoscale gadolinium oxide (Gd2O3) is a promising nanomaterial with unique physicochemical properties that finds various applications ranging from biomedicine to catalysis. The preparation of highly porous Gd2O3 nanofoam greatly increases its surface area thereby boosting its potential for functional use in applications such as water purification processes and in catalytic applications. By using the combustion synthesis method, a strong exothermic redox reaction between gadolinium nitrate hexahydrate and glycine causes the formation of crystalline nanoporous Gd2O3. In this study, the synthesis of Gd2O3 nanofoam is achieved with combustion synthesis at large scale (grams). Its nanoscale porosity is investigated by nitrogen physisorption and its nanoscale 3D structure by electron tomography, and the formation process is investigated as well by means of in situ heating inside the transmission electron microscope. The bulk nanofoam product is highly crystalline and porous with a surface area of 67 m2 g−1 as measured by physisorption, in good agreement with the electron tomographic 3D reconstructions showing an intricate interconnected pore network with pore sizes varying from 2 to 3 nm to tens of nanometers. In situ heating experiments point to many possibilities for tuning the porosity of the Gd2O3 nanofoam by varying the experimental synthesis conditions

Thermal Reduction of MoO₃ Particles and Formation of MoO₂ Nanosheets Monitored by In Situ Transmission Electron Microscopy

Nanoscale forms of molybdenum trioxide have found widespread use in optoelectronic, sensing, and battery applications. Here, we investigate the thermal evolution of micrometer-sized molybdenum trioxide particles during in situ heating in vacuum using transmission electron microscopy and observed drastic structural and chemical changes that are strongly dependent on the heating rate. Rapid heating (flash heating) of MoO3 particles to a temperature of 600 °C resulted in large-scale formation of MoO2(001) nanosheets that were formed in a wide area around the reducing MoO3 particles, within a few minutes of time frame. In contrast, when heated more gently, the initially single-crystal MoO3 particles were reduced into hollow nanostructures with polycrystalline MoO2 shells. Using density functional theory calculations employing the DFT-D3 functional, the surface energy of MoO3(010) was calculated to be 0.187 J m-2, and the activation energy for exfoliation of the van der Waals bonded MoO3 (010) layers was calculated to be 0.478 J m-2. Ab initio molecular dynamics simulations show strong fluctuations in the distance between the (010) layers, where thermal vibrations lead to additional separations of up to 1.8 Å at 600 °C. This study shows efficient pathways for the generation of either MoO2 nanosheets or hollow MoO2 nanostructures with very high effective surface areas beneficial for applications.</p

Thermal Reduction of MoO₃ Particles and Formation of MoO₂ Nanosheets Monitored by In Situ Transmission Electron Microscopy

Nanoscale forms of molybdenum trioxide have found widespread use in optoelectronic, sensing, and battery applications. Here, we investigate the thermal evolution of micrometer-sized molybdenum trioxide particles during in situ heating in vacuum using transmission electron microscopy and observed drastic structural and chemical changes that are strongly dependent on the heating rate. Rapid heating (flash heating) of MoO3 particles to a temperature of 600 °C resulted in large-scale formation of MoO2(001) nanosheets that were formed in a wide area around the reducing MoO3 particles, within a few minutes of time frame. In contrast, when heated more gently, the initially single-crystal MoO3 particles were reduced into hollow nanostructures with polycrystalline MoO2 shells. Using density functional theory calculations employing the DFT-D3 functional, the surface energy of MoO3(010) was calculated to be 0.187 J m-2, and the activation energy for exfoliation of the van der Waals bonded MoO3 (010) layers was calculated to be 0.478 J m-2. Ab initio molecular dynamics simulations show strong fluctuations in the distance between the (010) layers, where thermal vibrations lead to additional separations of up to 1.8 Å at 600 °C. This study shows efficient pathways for the generation of either MoO2 nanosheets or hollow MoO2 nanostructures with very high effective surface areas beneficial for applications.</p

Stabilization of Rock Salt ZnO Nanocrystals by Low-Energy Surfaces and Mg Additions: A First-Principles Study

Whereas bulk zinc oxide (ZnO) exhibits the wurtzite crystal structure, nanoscale ZnO was recently synthesized in the rock salt structure by addition of Mg. Using first-principles methods, we investigated two stabilization routes for accessing rock salt ZnO. The first route is stabilization by Mg addition, which was investigated by considering ZnO–MgO mixed phases. The second route is through size effects, as surface energies become dominant for small nanocrystal sizes. We discovered that the surface energy of rock salt ZnO is surprisingly low at 0.63 J m^–2, which is lower than those of wurtzite and zinc blende ZnO and lower than that of rock salt MgO. We predict that pure rock salt ZnO is stable for nanocrystals smaller than 1.6 nm, and that Mg additions can greatly extend the size range in which the rock salt phase is stable. Both mixed-phase and core–shell models were considered in the calculations. The present approach could be applied to predict the stabilization of many other nanocrystal phases in deviating crystal structures

Solution-mediated inversion of SnSe to Sb₂Se₃ thin-films

Abstract New facile and controllable approaches to fabricating metal chalcogenide thin films with adjustable properties can significantly expand the scope of these materials in numerous optoelectronic and photovoltaic devices. Most traditional and especially wet-chemical synthetic pathways suffer from a sluggish ability to regulate the composition and have difficulty achieving the high-quality structural properties of the sought-after metal chalcogenides, especially at large 2D length scales. In this effort, and for the first time, we illustrated the fast and complete inversion of continuous SnSe thin-films to Sb₂Se₃ using a scalable top-down ion-exchange approach. Processing in dense solution systems yielded the formation of Sb₂Se₃ films with favorable structural characteristics, while oxide phases, which are typically present in most Sb₂Se₃ films regardless of the synthetic protocols used, were eliminated. Density functional theory (DFT) calculations performed on intermediate phases show strong relaxations of the atomic lattice due to the presence of substitutional and vacancy defects, which likely enhances the mobility of cationic species during cation exchange. Our concept can be applied to customize the properties of other metal chalcogenides or manufacture layered structures

Tandem catalysis with double-shelled hollow spheres

Metal-zeolite composites with metal (oxide) and acid sites are promising catalysts for integrating multiple reactions in tandem to produce a wide variety of wanted products without separating or purifying the intermediates. However, the conventional design of such materials often leads to uncontrolled and non-ideal spatial distributions of the metal inside/on the zeolites, limiting their catalytic performance. Here we demonstrate a simple strategy for synthesizing double-shelled, contiguous metal oxide@zeolite hollow spheres (denoted as MO@ZEO DSHSs) with controllable structural parameters and chemical compositions. This involves the self-assembly of zeolite nanocrystals onto the surface of metal ion-containing carbon spheres followed by calcination and zeolite growth steps. The step-by-step formation mechanism of the material is revealed using mainly in situ Raman spectroscopy and X-ray diffraction and ex situ electron microscopy. We demonstrate that it is due to this structure that an Fe2O3@H-ZSM-5 DSHSs-showcase catalyst exhibits superior performance compared with various conventionally structured Fe2O3-H-ZSM-5 catalysts in gasoline production by the Fischer-Tropsch synthesis. This work is expected to advance the rational synthesis and research of hierarchically hollow, core-shell, multifunctional catalyst materials