Hyperfine interactions of ⁵⁷Fe nuclei in Fe_100-xNi_x nanostructures synthesized in polymer ion-track membranes were studied by Mössbauer spectroscopy. The main part of obtained nanostructures was Fe_100-xNi_x nanotubes with bcc structure for 0 ≤ x ≤ 40, and with fcc structure for 50 ≤ x ≤ 90. The length, outside diameter and wall thickness of nanotubes were 12 μm, 400 ± 10 nm and 120 ± 5 nm respectively. For the studied nanotubes a magnetic texture is observedalong their axis. The average value of the angle between the direction of the Fe atom magnetic moment and the nanotubes axis decreases with increasing of Ni concentration for nanotubes with bcc structure from ~50° to ~40°, and with fcc structure from ~55° to ~46°. The concentration dependences of the hyperfine parameters of nanotubes Mössbauer spectra are qualitatively consistent with the data for bulk polycrystalline samples. With Ni concentration increasing the average value of the hyperfine magnetic field increases from ~328 kOe to ~335 kOe for the bcc structure and drops to ~303 kOe in the transition to the fcc structure and then decreases to ~290 kOe at x = 90. Replacing the Fe atom with the Ni atom in the nearest environment of Fe atom within nanotubes with bcc structure lead to an increase in the hyperfine magnetic field by “6–9 kOe”, and in tubes with fcc structure—to a decrease in the hyperfine magnetic field by “11–16 kOe”. The changes of the quadrupole shift and hyperfine magnetic field are linearly correlated with the coefficient −(15 ± 5)·10⁻⁴ mm/s/kOe.

The aim of this work is to study the effect of lanthanum doping on the phase formation processes in ceramics based on CaTiO₃, as well as to evaluate the effectiveness of the ceramics as photocatalysts for the decomposition of the organic dye Rhodamine B. The methods used were scanning electron microscopy to evaluate the morphological features of the synthesized ceramics, X-ray diffraction to determine the phase composition and structural parameters, and UV-Vis spectroscopy to determine the optical properties of the ceramics. During the experiments it was found that an increase in the lanthanum dopant concentration from 0.05 to 0.25 mol leads to the formation of the orthorhombic phase La_0.3Ca_0.7TiO₃ and the displacement from the ceramic structure of the impurity phase TiO_2, which presence is typical for the synthesized ceramics by solid-phase synthesis. On the basis of the data of the X-ray phase analysis the dynamics of phase transformations depending on concentration of lanthanum was established: CaTiO₃/TiO₂ → CaTiO₃/La₂TiO₅ → CaTiO₃/La_0.3Ca_0.7TiO₃ → La_0.3Ca_0.7TiO₃. During the determination of photocatalytic activity it was found that the formation of La_0.3Ca_0.7TiO₃ phase leads to an increase in the decomposition rate as well as the degree of mineralization.

The luminescence of Kr-Xe, Ar-Kr, and Ar-Xe mixtures was studied in the spectral range 300–970 nm when excited by ⁶Li (n, α)³ H nuclear reaction products in the core of a nuclear reactor. Lithium was deposited on walls of experimental cell in the form of a capillary-porous structure, which made it possible to measure up to a temperature of 730 K. The temperature dependence of the radiation intensity of noble gas atoms, alkali metals, and heteronuclear ionic noble gas molecules was studied. Also, as in the case of single-component gases, the appearance of lithium lines and impurities of sodium and potassium is associated with vaporization during the release of nuclear reaction products from the lithium layer. The excitation of lithium atoms occurs mainly as a result of the Penning process of lithium atoms on noble gas atoms in the 1s states and subsequent ion-molecular reactions. Simultaneous radiation at transitions of atoms of noble gases and lithium, heteronuclear ion molecules of noble gases allows us to increase the efficiency of direct conversion of nuclear energy into light.