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The Mn3Sb metastable compound is formed at high pressure and temperature and it decomposes upon heating above 420 K into Mn2Sb and Mn. It has a cubic crystalline structure describing the Pm-3m (№ 221) space group with a lattice parameter of a = 0.400 nm. In the present work, according to the results of neutron diffraction investigations and taking into account magnetometry data, it is shown that Mn3Sb is an antiferromagnet, and a model of the magnetic structure with a triangular configuration of equal magnetic moments in magnitude is proposed. The magnetic moments of manganese atoms, constituting the basis of a unit magnetic cell, lie in the (111) plane and form an equilateral triangle. According to neutron diffraction data, the magnetic moments of manganese atoms were determined at different temperatures.

Inorganic-based nanoelements such as nanoparticles (nanodots), nanopillars and nanowires, which have at least one dimension of 100 nm or less, have been extensively developed for biomedical applications. Furthermore, their properties can be varied by controlling such parameters as element shape, size, surface functionalization, and mutual interactions. In this study, Ni-alumina nanocomposite material was synthesized by the dc-Ni electrodeposition into a porous anodic alumina template (PAAT). The structural, morphological, and corrosion properties were studied using x-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and electrochemical techniques (linear sweep voltammetry). Template technology was used to obtain Ni nanopillars (NiNPs) in the PAAT nanocomposite. Low corrosion current densities (order of 0.5 μA/cm2) were indicators of this nanocomposite adequate corrosion resistance in artificial physiological solution (0.9% NaCl). A porous anodic alumina template is barely exposed to corrosion and performs protective functions in the composite. The results may be useful for the development of new nanocomposite materials technologies for a variety of biomedical applications including catalysis and nanoelectrodes for sensing and fuel cells. They are also applicable for various therapeutic purposes including targeting, diagnosis, magnetic hyperthermia, and drug delivery. Therefore, it is an ambitious task to research the corrosion resistance of these magnetic nanostructures in simulated body fluid. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. ; Government Council on Grants, Russian Federation ; Belarusian Republican Foundation for Fundamental Research, BRFFR: Ф18Д-007 ; 20163522 ; Funding: The work was performed with support of State Scientific and Technical Program "Nanotech" (ГБЦ No 20163522), Belarusian Republican Foundation for Fundamental Research (Grant No. Ф18Д-007), Act 211 of Government of Russian Federation (contract No. 02.A03.21.0011). Additionally, the work was partially supported by the Grant of World Federation of Scientists (Geneva, Switzerland).

Bi nanocrystalline films were formed from perchlorate electrolyte (PE) on Cu substrate via electrochemical deposition with different duration and current densities. The microstructural, morphological properties, and elemental composition were studied using scanning electron microscopy (SEM), atomic force microscopy (AFM), and energy-dispersive X-ray microanalysis (EDX). The optimal range of current densities for Bi electrodeposition in PE using polarization measurements was demonstrated. For the first time, it was shown and explained why, with a deposition duration of 1 s, co-deposition of Pb and Bi occurs. The correlation between synthesis conditions and chemical composition and microstructure for Bi films was discussed. The analysis of the microstructure evolution revealed the changing mechanism of the films' growth from pillar-like (for Pb-rich phase) to layered granular form (for Bi) with deposition duration rising. This abnormal behavior is explained by the appearance of a strong Bi growth texture and coalescence effects. The investigations of porosity showed that Bi films have a closely-packed microstructure. The main stages and the growth mechanism of Bi films in the galvanostatic regime in PE with a deposition duration of 1–30 s are proposed. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. ; Government Council on Grants, Russian Federation ; 2.34 ; Funding: The work was performed with support of State Scientific and Technical Program "Nanotech" (task No. 2.34), Branch Scientific and Technical Program "Nanotechnology and Nanomaterials" (task No. 1), Act 211 of Government of Russian Federation (contract No. 02.A03.21.0011). Additionally, the work was partially supported by the Grant of World Federation of Scientists (Geneva, Switzerland).

Herein, we investigated the correlation between the chemical composition, microstructure, and microwave properties of composites based on lightly Tb/Tm-doped Sr-hexaferrites (SrTb0.01Tm0.01Fe11.98O19) and spinel ferrites (AFe2O4, A = Co, Ni, Zn, Cu, or Mn), which were fabricated by a one-pot citrate sol-gel method. Powder XRD patterns of products confirmed the presence of pure hexaferrite and spinel phases. Microstructural analysis was performed based on SEM images. The average grain size for each phase in the prepared composites was calculated. Comprehensive investigations of dielectric properties (real (ε′) and imaginary parts (ε′′) of permittivity, dielectric loss tangent (tan(δ)), and AC conductivity) were performed in the 1-3 × 106Hz frequency range at 20-120 °C. Frequency dependency of microwave properties were investigated using the coaxial method in frequency range of 2-18 GHz. The non-linear behavior of the main microwave properties with a change in composition may be due to the influence of the soft magnetic phase. It was found that Mn- and Ni-spinel ferrites achieved the strongest electromagnetic absorption. This may be due to differences in the structures of the electron shell and the radii of the A-site ions in the spinel phase. It was discovered that the ionic polarization transformed into the dipole polarization. © The Royal Society of Chemistry 2020. ; 2020-164-IRMC ; 2018-IRMC-S-2 ; Ministry of Science and Higher Education of the Russian Federation ; The authors highly acknowledged the nancial supports provided by the Institute for Research and Medical Consultations (Project application No. 2018-IRMC-S-2) and by the Deanship for Scientic Research (Project application No. 2020-164-IRMC) of Imam Abdulrahman Bin Faisal University (Saudi Arabia). M. S. acknowledges the Ministry of Science and Higher Education of the Russian Federation State assignment 2020– 2022 No. FSMR-2020-0018 (Proposal mnemonic code 0719-2020-0018). The work was partially supported by Act 211 Government of the Russian Federation, contract No. 02.A03.21.0011.

Nanostructured NiFe film was obtained on silicon with a thin gold sublayer via pulsed electrodeposition and annealed at a temperature from 100 to 400◦C in order to study the effect of heat treatment on the surface microstructure and mechanical properties. High-resolution atomic force microscopy made it possible to trace stepwise evolving microstructure under the influence of heat treatment. It was found that NiFe film grains undergo coalescence twice—at ~100 and ~300°C—in the process of a gradual increase in grain size. The mechanical properties of the Au/NiFe nanostructured system have been investigated by nanoindentation at two various indentation depths, 10 and 50 nm. The results showed the opposite effect of heat treatment on the mechanical properties in the near-surface layer and in the material volume. Surface homogenization in combination with oxidation activation leads to abnormal strengthening and hardening-up of the near-surface layer. At the same time, a nonlinear decrease in hardness and Young's modulus with increasing temperature of heat treatment characterizes the internal volume of nanostructured NiFe. An explanation of this phenomenon was found in the complex effect of changing the ratio of grain volume/grain boundaries and increasing the concentration of thermally activated diffuse gold atoms from the sublayer to the NiFe film. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. ; Funding: The work was supported by Act 211 Government of the Russian Federation, contract № 02.A03.21.0011.

Indium-substituted strontium hexaferrites were prepared by the conventional solid-phase reaction method. Neutron diffraction patterns were obtained at room temperature and analyzed using the Rietveld methods. A linear dependence of the unit cell parameters is found. In3+ cations are located mainly in octahedral positions of 4fVI and 12 k. The average crystallite size varies within 0.84-0.65 μm. With increasing substitution, the TC Curie temperature decreases monotonically down to ~ 520 K. ZFC and FC measurements showed a frustrated state. Upon substitution, the average and maximum sizes of ferrimagnetic clusters change in the opposite direction. The Mr remanent magnetization decreases down to ~ 20.2 emu/g at room temperature. The Ms spontaneous magnetization and the keff effective magnetocrystalline anisotropy constant are determined. With increasing substitution, the maximum of the ε/ real part of permittivity decreases in magnitude from ~ 3.3 to ~ 1.9 and shifts towards low frequencies from ~ 45.5 GHz to ~ 37.4 GHz. The maximum of the tg(α) dielectric loss tangent decreases from ~ 1.0 to ~ 0.7 and shifts towards low frequencies from ~ 40.6 GHz to ~ 37.3 GHz. The low-frequency maximum of the μ/ real part of permeability decreases from ~ 1.8 to ~ 0.9 and slightly shifts towards high frequencies up to ~ 34.7 GHz. The maximum of the tg(δ) magnetic loss tangent decreases from ~ 0.7 to ~ 0.5 and shifts slightly towards low frequencies from ~ 40.5 GHz to ~ 37.7 GHz. The discussion of microwave properties is based on the saturation magnetization, natural ferromagnetic resonance and dielectric polarization types. ; Investigations were performed under financial support from the Russian Science Foundation (Agreement No. 19-19-00694 of 06 May 2019). ; With funding from the Spanish government through the 'Severo Ochoa Centre of Excellence' accreditation (CEX2019-000917-S). ; Peer reviewed

Magnetic Fe 3 O 4 nanoparticles (NPs) and their surface modification with therapeutic substances are of great interest, especially drug delivery for cancer therapy, including boron-neutron capture therapy (BNCT). In this paper, we present the results of boron-rich compound (carborane borate) attachment to previously aminated by (3-aminopropyl)-trimethoxysilane (APTMS) iron oxide NPs. Fourier transform infrared spectroscopy with Attenuated total reflectance accessory (ATR-FTIR) and energy-dispersive X-ray analysis confirmed the change of the element content of NPs after modification and formation of new bonds between Fe3O4 NPs and the attached molecules. Transmission (TEM) and scanning electron microscopy (SEM) showed Fe3O4 NPs' average size of 18.9 nm. Phase parameters were studied by powder X-ray diffraction (XRD), and the magnetic behavior of Fe 3 O 4 NPs was elucidated by Mössbauer spectroscopy. The colloidal and chemical stability of NPs was studied using simulated body fluid (phosphate buffer-PBS). Modified NPs have shown excellent stability in PBS (pH = 7.4), characterized by XRD, Mössbauer spectroscopy, and dynamic light scattering (DLS). Biocompatibility was evaluated in-vitro using cultured mouse embryonic fibroblasts (MEFs). The results show us an increasing of IC50 from 0.110 mg/mL for Fe 3 O 4 NPs to 0.405 mg/mL for Fe 3 O 4 -Carborane NPs. The obtained data confirm the biocompatibility and stability of synthesized NPs and the potential to use them in BNCT. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. ; Funding: This study was funded by the Ministry of Education and Science of the Republic of Kazakhstan (grant No AP05130947 "Setting the stage for boron neutron capture therapy of cancer in the Republic of Kazakhstan") and Nazarbayev University "Social Policy Grant" (project title: "Research and development of the new Nano-Optical Sensor based on Polymer Optical Fiber for Near-Field Scanning Optical Microscopy", PI: Kanat Dukenbayev). The authors also gratefully acknowledge the financial support of the Ministry of Education and Science of the Russian Federation in the framework of Increase Competitiveness Program of NUST «MISiS» (NoK4-2018-036, P02-2017-2-4), implemented by a governmental degree dated 16th of March 2013, No 211. The work was partially supported by Act 211 Government of the Russian Federation, contract No 02.A03.21.0011. This work was partially supported by the Ministry of Education and Science of the Russian Federation (Government task in SUSU 5.5523.2017/8.9).

The modern development of nanotechnology requires the discovery of simple approaches that ensure the controlled formation of functional nanostructures with a predetermined morphology. One of the simplest approaches is the self-assembly of nanostructures. The widespread implementation of self-assembly is limited by the complexity of controlled processes in a large volume where, due to the temperature, ion concentration, and other thermodynamics factors, local changes in diffusion-limited processes may occur, leading to unexpected nanostructure growth. The easiest ways to control the diffusion-limited processes are spatial limitation and localized growth of nanostructures in a porous matrix. In this paper, we propose to apply the method of controlled self-assembly of gold nanostructures in a limited pore volume of a silicon oxide matrix with submicron pore sizes. A detailed study of achieved gold nanostructures' morphology, microstructure, and surface composition at different formation stages is carried out to understand the peculiarities of realized nanostructures. Based on the obtained results, a mechanism for the growth of gold nanostructures in a limited volume, which can be used for the controlled formation of nanostructures with a predetermined geometry and composition, has been proposed. The results observed in the present study can be useful for the design of plasmonic-active surfaces for surface-enhanced Raman spectroscopy-based detection of ultra-low concentration of different chemical or biological analytes, where the size of the localized gold nanostructures is comparable with the spot area of the focused laser beam. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. ; 3.1.5.1 ; Ministry of Education and Science of the Russian Federation, Minobrnauka: К-2018-036, N 211 ; Russian Foundation for Fundamental Investigations, RFFI: 19-32-50058 ; European Commission, EC ; Ministry of Science and Technology, MOST ; Funding: This research was funded by H2020-MSCA-RISE2017-778308-SPINMULTIFILM Project, the scientific– technical program, 'Technology-SG' [project number 3.1.5.1], Ministry of Education and Science of the Russian Federation in the framework of Increase Competitiveness Program of NUST «MISiS» [№ К-2018-036], implemented by a governmental decree dated 16th of March 2013, N 211 and Russian Foundation for Fundamental Investigations [project number 19-32-50058]. ; Acknowledgments: D.V.Y. greatly acknowledges the World Federation of Scientists National Scholarship Program. E.Yu.K., D.V.Y., V.D.B., and V.S. greatly acknowledge the European Union program Mobility Scheme for Targeted People-to-People-Contacts (MOST) for supporting research visits.