Suchergebnisse

This work combines new and earlier obtained results on electron hole and oxygen-ion transport in the La2NiO4-based solid solutions. The effect of lanthanum substitution with Ca/Sr and nickel with Fe, Mn, Co or Cu on transport properties of La2-xAxNi1-yMeyO4+δ was analyzed and discussed at different substitution levels. Besides the changes in concentration and mobility of electron holes induced by the doping with cations of different nature, the partial transformation of Ni3+ from low-spin to high-spin state was shown to have a profound effect on transport properties of these materials leading to a notable decrease in mobility of electron holes, especially in the strontium-rich oxides. The obtained results suggested that the size factor was the main driving force behind the observed transformation of Ni3+. The oxygen-ion transport in La2-xAxNi1-yMeyO4+δ was characterized by significant surface exchange limitations, which can be reduced only at relatively high concentrations of strontium and iron, and should be taken into account while evaluating the ionic conductivity by means of oxygen permeation or the modified Hebb-Wagner polarization method. © 2019 IUPAC and De Gruyter. ; This work was supported in parts by the Ministry of Education and Science of Russian Federation (State Task 4.2288.2017) and by Act 211 Government of the Russian Federation, agreement 02.A03.21.0006.

This paper discusses effects of different dopants, sintering technique and parameters on microstructure and properties of pure and Yb, Er-doped Na0.5Bi0.5TiO3 (NBT). All stoichiometric compositions follow the abnormal grain growth mechanism (AGG) and exhibit a bimodal grain size distribution. Bi over-stoichiometry, two step sintering and hot pressing are effective inhibitors of AGG. Microstructure of sintered NBT greatly influences such properties as dielectric permittivity and depolarization temperature. ; Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union's Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART²

The spin orientation in synthetic hematite-ilmenite samples and in a sample of natural hematite was studied from room temperature to above the antiferromagnetic-paramagnetic phase transition (the Néel temperature; $\textit{T}$$_{N}$ ≈ 600 − 950 K ) by neutron powder diffraction and at room temperature by Mö ssbauer spectroscopy. The usually assumed magnetic structure of hematite within this temperature range is antiferromagnetic with the spins confined to the basal plane of the hexagonal structure , however, an out-of-plane spin component is allowed by the symmetry of the system and has been observed in recent studies of synthetic hematite samples. We find the spins in the antifer romagnetic sublattices to be rotated out of the basal plane by an angle between 11 (2)° and 22.7(5)° in both synthetic hematite-ilmenite samples and in the natural hematite sample. The spin angle remains tilted out of the basal plane in the entire temperature range below the Néel temperature and does not depend systematically on Ti-content. The results indicate that the out-of-plane spin component is an intrinsic feature of hematite itself, with an origin not yet fully understood, but consistent with group theory. This represents a major shift in understanding of one of the two main mineral systems responsible for rock magnetism. ; This work was supported by the Danish Agency for Science, Technology and Innovation through DanScatt. The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013) ERC grant agreement 320750 and NERC Grant NE/D522203/1 .

Herein, single crystals of compounds In2S3, AgIn5S8 and solid solutions (In2S3)x·(AgIn5S8)1–x were grown by directional crystallization. The composition of the obtained single crystals was determined by microprobe X-ray spectral analysis. It is found that the content of the components in the grown single crystals is in satisfactory agreement with the specified composition in the initial charge. The structure of the obtained materials was determined by the X-ray method. It is shown that both the initial compounds and the solid solutions based on them were crystallized in the cubic structure of the spinel. The unit cell parameters of the In2S3, AgIn5S8 compounds and the solid solutions based on them, which vary linearly with the composition x, were calculated by the least squares method. The density was determined by the pycnometric method, and the microhardness of the In2S3 and AgIn5S8 compounds and the (In2S3)x·(AgIn5S8)1–x solid solutions was determined by the Knoop method. It is shown that the density, like the unit cell parameter, changes linearly with the composition x, but the dependence of microhardness on the x parameter has a maximum for x = 0.4. Using differential thermal analysis (DTA), the temperatures of phase transformations were determined and the phase diagram of the In2S3–AgIn5S8 system was constructed, which is characterized by a small crystallization interval and belongs to type III according to the Rosebom classification. The curves of liquidus and solidus are concave to the abscissa axis and have a common point.

The results of an experiment on studying the features of the crystal structure and magnetic studies of substitutional solid solutions of the Ni1–xCrxMnSb system (0 m х m 0.2) are presented. It was found that an increase in the concentration of chromium in solid solutions does not lead to significant changes in the size of the unit crystal cell. It was found that solid-phase quenching can be used to expand the limit of chromium solubility in Ni1–xCrxMnSb solid solutions. The temperature and field dependences of the specific magnetization of the synthesized compositions have been studied. It was found that the substitution of chromium for nickel in the NiMnSb compound leads to a decrease in the temperature of the "magnetic order – magnetic disorder" phase transformation with an increase in the concentration x from 0 to 20 mol.%. The values of specific magnetization and Curie temperature of hardened hard rasters are higher than those of slowly cooled ones. The results obtained contribute to the creation of a physical basis for the elemental base of spintronics.