Thanks to the unique properties of graphite oxides and graphene oxide (GO), this material has become one of the most promising materials that are widely studied. Graphene oxide is not only a precursor for the synthesis of thermally or chemically reduced graphene: researchers revealed a huge amount of unique optical, electronic, and chemical properties of graphene oxide for many different applications. In this review, we focus on the structure and characterization of GO, graphene derivatives prepared from GO and GO applications. We describe GO utilization in environmental applications, medical and biological applications, freestanding membranes, and various composite systems.

We report the direct observation of strong coupling between magnons and phonons in a two-dimensional antiferromagnetic semiconductor ${\mathrm{FePS}}_3$, via magneto-Raman spectroscopy at magnetic fields up to 30 Tesla. A Raman-active magnon at $121{\mathrm{cm}}^{-1}$ is identified through Zeeman splitting in an applied magnetic field. At a field-driven resonance with a nearby phonon mode, a hybridized magnon-phonon quasiparticle is formed due to strong coupling between the two modes. We develop a microscopic model of the strong coupling in the two-dimensional magnetic lattice, which enables us to elucidate the nature of the emergent quasiparticle. Our polarized Raman results directly show that the magnons transfer their spin angular momentum to the phonons and generate phonon spin through the strong coupling.

In this work, carbon dioxide uptake by magnesium oxychloride cement (MOC) based materials is described. Both thermodynamically stable magnesium oxychloride phases with stoichiometry 3Mg(OH)₂∙MgCl₂∙8H₂O (Phase 3) and 5Mg(OH)₂∙MgCl₂∙8H₂O (Phase 5) were prepared. X-ray diffraction (XRD) measurements were performed to confirm the purity of the studied phases after 7, 50, 100, 150, 200, and 250 days. Due to carbonation, chlorartinite was formed on the surface of the examined samples. The Rietveld analysis was performed to calculate the phase composition and evaluate the kinetics of carbonation. The SEM micrographs of the sample surfaces were compared with those of the bulk to prove XRD results. Both MOC phases exhibited fast mineral carbonation and high maximum theoretical values of CO₂ uptake capacity. The materials based on MOC cement can thus find use in applications where a higher concentration of CO₂ in the environment is expected (e.g., in flooring systems and wall panels), where they can partially mitigate the harmful effects of CO₂ on indoor air quality and contribute to the sustainability of the construction industry by means of reducing the carbon footprints of alternative building materials and reducing CO₂ concentrations in the environment overall.

We have performed a detailed analysis of the magnetic (collinear and non-collinear) order and the atomic and electron structures of UO₂, PuO₂ and UN on the basis of density functional theory with the Hubbard electron correlation correction (DFT + U). We have shown that the 3-k magnetic structure of UO₂ is the lowest in energy for the Hubbard parameter value of U = 4.6 eV (and J = 0.5 eV) consistent with experiments when Dudarev's formalism is used. In contrast to UO₂, UN and PuO₂ show no trend for a distortion towards rhombohedral structure and, thus, no complex 3-k magnetic structure is to be anticipated in these materials.

Today, low-energy and low-carbon footprint alternatives to Portland cement are searched because of huge CO₂ emissions coming from Portland clinker calcination. Because of some superior properties of magnesium oxychloride cement (MOC) and the lower carbon footprint of its production, MOC became an intensively studied material with high application potential for the design and development of construction products. In this contribution, magnesium oxychloride with stoichiometry 5Mg(OH)₂∙MgCl₂∙8H₂O (Phase 5) was prepared and characterized. The kinetics of formation and the phase composition of the material were determined using X-ray diffraction and consequent Rietveld analysis. The morphology was studied by scanning electron microscopy, and the chemical composition was determined by both energy-dispersive spectroscopy and X-ray fluorescence. Moreover, the simultaneous thermal analysis in combination with mass spectroscopy and Fourier-transform infrared spectroscopy was employed to study the thermal stability. Using mass spectroscopy, we were able to clarify the mechanism of water and hydrochloric acid release, which was not previously reported. The observed structural and chemical changes induced by exposure of studied samples to elevated temperatures were linked with the measured residual macro and micro parameters, such as bulk density, specific density, porosity, water absorption, compressive strength, and pore size distribution. The Phase 5 revealed a needle-like crystalline morphology which formed rapidly and was almost completed after 96 h, resulting in relatively high material strength. The four-day compressive strength of magnesium oxychloride cement was similar to the 28-day compressive strength of Portland cement. The thermal stability of Phase 5 was low as the observed disruptive thermal processes were completed at temperatures lower than 470 °C.

Nanoparticles with controllable sizes of ferrite spinel CoFe₂O₄ were formed by thermal treatment of cobalt-iron glycerolate. Thermal behavior during the heating was studied by differential thermal analysis combined with thermogravimetry. The precursor, as well as the prepared nanoparticles, were analyzed by a broad spectrum of analytic techniques (X-Ray photoelectron spectroscopy (XPS), X-Ray diffraction (XRD), Energy dispersive spectroscopy (EDS), Atomic absorption spectroscopy (AAS), Scanning electron microscopy (SEM), and Raman spectroscopy). The particle size of nanoparticles was obtained from Transmission electron microscopy and also calculated using Scherrer formula. A vibrating sample magnetometer (VSM) in a Physical Property Measurement System was used to analyze the magnetic properties of nanoparticles.