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Yttrium manganite (YMnO3) is a compound belonging to the hexagonal rare earth manganites family, which demonstrates multiferroic properties. This material can be prepared by several synthetic approaches, with the most common one being the solid-state synthesis. In this work, we show a possibility of preparing this material via molten salt synthesis using the NaCl-KCl mixture as the reaction medium and yttrium and manganese nitrates as the starting materials. We demonstrate that, by varying the reaction temperature and the nitrates-to-chlorides ratio, it is feasible to synthesize hexagonally shaped particles of microscopic dimensions. A similar synthesis procedure can be successfully applied for the preparation of other hexagonal manganites—ErMnO3, TmMnO3, and YbMnO3. [ABSTRACT FROM AUTHOR]

In this study, an environmentally friendly sol-gel synthetic approach was used for the preparation of yttrium-doped MgFe2O4. Two series of compounds with different iron content were synthesized and A-site substitution effects were investigated. In the first series, the iron content was fixed and the charge balance was suggested to be compensated by a partial reduction of Fe3+ to Fe2+ or formation of interstitial O2− ions. For the second series of samples, the iron content was reduced in accordance with the substitution level to compensate for the excess of positive charge, which accumulates due to replacing divalent Mg2+ with trivalent Y3+ ions. Structural, morphological and magnetic properties were inspected. It was observed that single-phase compounds can only form when the substitution level reaches 20 mol% of Y3+ ions and iron content is reduced. The coercivity as well as saturation magnetization decreased with the increase in yttrium content. Mössbauer spectroscopy was used to investigate the iron content in both tetrahedral and octahedral positions. [ABSTRACT FROM AUTHOR]

In the present work, polycrystalline Bi0.67La0.33Fe0.5Sc0.5O3 thin films were synthesized using a simple and cost-effective chemical solution deposition process employing the spin coating technique. In order to check the feasibility of the fabrication of thin films on various types of substrates, the films were deposited on Pt-coated silicon, silicon, sapphire, corundum, fused silica and glass. Based on the results of thermogravimetric analysis of precursor and thermal stability study, it was determined that the optimal annealing temperature for the formation of perovskite structure is 600 °C. It was observed that the relative intensity of the pseudocubic peaks (001)p and (011)p in the XRD patterns is influenced by the nature of substrates, suggesting that the formed crystallites have some preferred orientation. Roughness of the films was determined to be dependent on the nature of the substrate. [ABSTRACT FROM AUTHOR]

In this study, the aqueous sol-gel method was employed for the synthesis of (1−x)SrTiO3-xBiMnO3 solid solutions. Powder X-ray diffraction analysis confirmed the formation of single-phase perovskites with a cubic structure up to x = 0.3. A further increase of the BiMnO3 content led to the formation of a negligible amount of neighboring Mn3O4 impurity, along with the major perovskite phase. Infrared (FT-IR) analysis of the synthesized specimens showed gradual spectral change associated with the superposition effect of Mn-O and Ti-O bond lengths. By introducing BiMnO3 into the SrTiO3 crystal structure, the size of the grains increased drastically, which was confirmed by means of scanning electron microscopy. Magnetization studies revealed that all solid solutions containing the BiMnO3 component can be characterized as paramagnetic materials. It was observed that magnetization values clearly correlate with the chemical composition of powders, and the gradual increase of the BiMnO3 content resulted in noticeably higher magnetization values. [ABSTRACT FROM AUTHOR]

Vacuum ultraviolet and thermal activation spectroscopies were used to study the nature of intrinsic emission and the mechanisms of the formation of electron and hole trapping centres in irradiated Li2SO4 powders and crystals. The obtained results along with excitation spectra showed that recombination emission at 3.8–4.2 eV and 4.5–5.5 eV occurs when an electron passes from the second and third sub-bands of the valence band formed from the 2p state of oxygen to the conduction band. It has been determined that Li2SO4 electron and hole trapping centres are created when electrons are trapped in the SO42– anionic sites. The holes are localised in the form of SO4 – radicals. The spectral position and intensity of individual emission bands are dependent on the crystallographic arrangement of localised holes. [ABSTRACT FROM AUTHOR]

Rare-earth manganese pyrochlores (R 2 Mn 2 O 7 ) are frustrated magnetic materials, which previously have only been accessed using expensive high-pressure and high-temperature synthesis. In the present work, we demonstrate a convenient synthetic approach to synthesize R 2 Mn 2 O 7 pyrochlores at ambient pressure. A series of pyrochlores (R = Y, Ho-Lu) were prepared by a simple and cost-effective molten salt method using NaCl and KCl as the flux. Moreover, phase-selectivity was demonstrated for yttrium manganese oxides (YMnO 3 and Y 2 Mn 2 O 7 ) by a simple variation of synthesis temperature and precursors-to-chlorides ratio. The synthetic procedure does not require high pressures or temperatures nor oxygen flow. All synthesized pyrochlores demonstrated ferromagnetic behavior at low temperature, and the magnetic properties were in good agreement with those of high-pressure-synthesized materials. The versatility of the method was confirmed by the preparation of a mixed-rare earth Y 0.4 Er 0.4 Tm 0.4 Yb 0.4 Lu 0.4 Mn 2 O 7 solid solution─a compositionally complex high-entropy oxide.