Wettability properties of porous Al2O3 coatings: effects of technological regimes and surface morphology

The comparative analysis of Al2O3 coatings and effect of surface morphology on the wettability properties were discussed. It was shown that it is possible to obtain high hydrophilic parameters with a contact angle value up to 17–20° using high values of current density, anodizing time, and electrolyte temperature by adjusting the electrochemical conditions. It was seen that this type of modified Al2O3 structures provides direct experimental evidence for the theory of threedimensional capillaries regarding superhydrophilicity

Studying the Thermodynamic Properties of Composite Magnetic Material Based on Anodic Alumina

Magnetic nanoparticles based on Fe3O4 and their modifications of surface with therapeutic substances are of great interest, especially drug delivery for cancer therapy includes boron-neutron capture therapy. In this paper we study the thermodynamic, morphological, structural, and chemical properties of a composite material consisting of nickel nanowires (NWs) electrochemically deposited in the pores of the membrane of porous anodic aluminum oxide (PAA) by methods of differential thermal analysis (DTA), scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), and dispersive X-ray spectroscopy (EDX)

Mechanisms of elastoplastic deformation and their effect on hardness of nanogranular Ni-Fe coatings

This article contains the study of correlation between the microstructure, mechanical properties and mechanisms of elastoplastic deformation of Ni-Fe coatings that were grown in five electrodeposition modes and had fundamentally different microstructures. A nonlinear change in hardness was detected using nanoindentation. Explanation of the abnormal change in hardness was found in the nature of the relaxation method of elastoplastic energy under load. It is shown that the deformation of coatings with a grain size of 100 nm or more occurs due to dislocation slip. A decrease in grain size leads to the predominance of deformation due to rotations and sliding of grains, as well as surface and grain boundary diffusion. The effect of deformation mechanisms on the nanoscale hardness of Ni-Fe coatings was established. Full hardening of the coatings (both in the bulk and on the surface) was achieved while maintaining the balance of three mechanisms of elastoplastic deformation in the sample. Unique coatings consisting of two fractions of grains (70% of nano-grains and 30% of their agglomerates) demonstrate high crack resistance and full-depth hardening up to H = 7.4 GPa due to the release of deformation energy for amorphization and agglomeration of nanograins. © 2021King Abdullah University of Science and Technology, KAUSTGovernment Council on Grants, Russian FederationFunding text 1: The work was supported by Act 211 Government of the Russian Federation, contract № 02.A03.21.0011. Dmitry Lyakhov and Dominik Michels are partially supported by KAUST (baseline funding).Funding text 2: The work was supported by Act 211 Government of the Russian Federation, contract ? 02.A03.21.0011. Dmitry Lyakhov and Dominik Michels are partially supported by KAUST (baseline funding)

Fe 3 O 4 nanoparticles for complex targeted delivery and boron neutron capture therapy

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)

Temperature induced structural and polarization features in BaFe12O19

We report the observation of a peculiar polarization behavior of BaFe12O19 in electric field where the linear polarization is detected at temperatures below 150 K whereas at higher temperatures a hysteresis-like polarization response is observed. At the same time, the performed neutron diffraction analysis shows no variations in crystal or magnetic structures with temperature. Based on the results of ab initio calculations we suggest the mechanism able to explain the experimentally observed behavior. We show that specific Fe atoms do not occupy the positions formally assigned to them by the conventional centrosymmetric P63/mmc (#194) space group (z = 0.25; 0.75) as these positions correspond to local energy maxima. Instead, these Fe atoms are shifted along the z-axis to positions z = 0.259 (0.241) and z = 0.759 (0.741), which correspond to local energy minima. To an inversion center move between these minima Fe atoms need to overcome an energy barrier. This barrier is rather insignificant for smaller volumes but it becomes larger for expanded volumes due to coupling between the displacements of these Fe atoms. Additionally, our analysis suggests that the non-centrosymmetric and polar P63mc (#186) space group could be appropriate for the description of the BaFe12O19 structure

Optical Properties of Valve Metals Functional Thin Films Obtained by Electrochemical Anodization on Transparent Substrates

Nanostructured aluminum, tantalum, and vanadium oxide layers on glass substrates were obtained by electrochemical anodizing in oxalic and sulfuric–oxalic electrolytes. The morphological and optical properties of the obtained structures were investigated experimentally by scanning electron microscopy and transmission spectroscopy. Obtained oxide coatings are quasi-ordered arrays of vertical (aluminum oxide/tantalum oxide, aluminum oxide/vanadium oxide, and aluminum oxide obtained in the oxalic electrolyte) or non-ordered tree-like (aluminum oxide obtained in the sulfuric–oxalic electrolyte) pores depending on the initial film metal and anodizing technology. The light transmission in the range of 750–1200 nm is up to 60% for aluminum oxide/tantalum oxide/glass (annealed) and quasi-ordered aluminum oxide/glass structures, and around 40% for aluminum oxide/tantalum oxide/glass (not annealed) and aluminum oxide/vanadium oxide. Non-ordered aluminum oxide is characterized by low transmission (no more than 8%) but has a developed surface and may be of interest for the formation of films with poor adhesion on smooth substrates, for example, photocatalytic active xerogels. The refractive indices of dispersion of the obtained layers were calculated from the transmission spectra by the envelope method. The dispersion of the refractive indices of the obtained oxide films is insignificant in a wide range of wavelengths, and the deviation from the average value is assumed to be observed near the intrinsic absorption edges of the films. The glasses with proposed semi-transparent nanostructured oxide layers are promising substrate structures for subsequent sol–gel coating layers used in photocatalytic purification systems or up-conversion modules of tandem silica solar cells with forward and reverse illumination

Formation and corrosion properties of Ni-based composite material in the anodic alumina porous matrix

Ni nanopillars (Ni NPs) composite material formation technology embedded in porous anodic alumina by electrochemical deposition is presented in this paper. The morphological and structural properties of the composite material were investigated using scanning electron microscopy, atomic force microscopy, X-ray diffraction. The corrosion resistance of the nanocomposite materials has been studied by potentiodynamic polarization curves analysis and polarization resistance method. The composite represents the array of vertically ordered Ni NPs with the identical size in alumina matrix. XRD investigation indicates that Ni NPs are polynanocrystalline material with 18 nm crystallite size. It has been shown that Ni NPs and the composite material have sufficient corrosion resistance in a 0.9% aqueous NaCl solution. Porous alumina is the neutral and protective component of the composite. These nanocomposite materials can be excellent candidates for practical use in electronics, sensorics, biomedicine

Magnetic Properties of the Densely Packed Ultra-Long Ni Nanowires Encapsulated in Alumina Membrane

High-quality and compact arrays of Ni nanowires with a high ratio (up to 700) were obtained by DC electrochemical deposition into porous anodic alumina membranes with a distance between pores equal to 105 nm. The nanowire arrays were examined using scanning electron microscopy, X-ray diffraction analysis and vibration magnetometry at 300 K and 4.2 K. Microscopic and X-ray diffraction results showed that Ni nanowires are homogeneous, with smooth walls and mostly single-crystalline materials with a 220-oriented growth direction. The magnetic properties of the samples (coercivity and squareness) depend more on the length of the nanowires and the packing factor (the volume fraction of the nanowires in the membrane). It is shown that the dipolar interaction changes the demagnetizing field during a reversal magnetization of the Ni nanowires, and the general effective field of magnetostatic uniaxial shape anisotropy. The effect of magnetostatic interaction between ultra-long nanowires (with an aspect ratio of >500) in samples with a packing factor of ≥37% leads to a reversal magnetization state, in which a “curling”-type model of nanowire behavior is realized. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.Funding: An.T. (Andrei Turutin) acknowledges the financial support of the Russian Science Foundation (Grant No. 19-79-30062) in part of the experimental work. A.K. (Alexander Kislyuk) and I.K. (Ilya Kubasov) acknowledge the financial support of the Ministry of Science and Higher Education of the Russian Federation as a part of the State Assignment (basic research, Project No. 0718-2020-0031 “New magnetoelectric composite materials based on oxide ferroelectrics having an ordered domain structure: production and properties”) in part of the XRD study

Correlation of the chemical composition, phase content, structural characteristics and magnetic properties of the Bi-substituted M-type hexaferrites

Bi-substituted M-type hexaferrites, BaFe12-xBixO19 (0.1 ≤ x ≤ 1.2), or Bi-BaM, were produced by the solid-state reactions. The correlation between the phase content, chemical composition, crystal structure features, and peculiarities of the magnetic properties of Bi-BaM was established using XRD (X-ray diffraction), SEM (scanning electron microscopy), and VSM (vibrational sample magnetometry). XRD phase analysis made it possible to establish the limit of substitution of Fe3+ ions by Bi3+ ions. It was shown that at a low substitution level (x ≤ 0.3), no impurity phases were detected, and the samples are characterized by a single-phase state with the space group (SG) P63/mmc. As the degree of substitution (x ≥ 0.6) increases, the formation of impurity phases was observed, which can be explained by the difficulties of ion diffusion in the process of solid-phase synthesis as well as the formation of defects in the magnetoplumbite structure due to the large ionic radius of Bi3+. As impurity phases in the studied compositions (x ≥ 0.6) the following were noted: BiFeO3 (SG: Pnma); BiO2 (SG: Fm-3m); BaBi2O6 (SG: R-3); and Ba0.5Bi1.5O2.16 (SG: Im-3m). The content of the main phase (SG: P63/mmc) decreases from 95.11 to 88.27 vol% with an increase in x from 0.6 to 1.2, respectively. Analysis of SEM images showed the growth of particles up to 10 μm, depending on the concentration of bismuth oxide during hexaferrite synthase. The Bi-BaM magnetic characteristics were examined using VSM in the range of 3 T at 300 K. Due to the magnetic structure's frustration, with increased x a decrease in saturation magnetization (Ms) was found. There were two concentration diapasons with different speeds of Ms decrease. In the first diapason, the main contribution belong to the magnetic structure frustration in the frame of the main phase (P63/mmc) due to the long-range Fe-O-Fe exchange interaction weakening (under Bi substitution). In the second diapason, the main contribution belong to the impurity phase formation and decrease of the main magnetic phase concentration in samples

Magnetic Properties of the Densely Packed Ultra-Long Ni Nanowires Encapsulated in Alumina Membrane

High-quality and compact arrays of Ni nanowires with a high ratio (up to 700) were obtained by DC electrochemical deposition into porous anodic alumina membranes with a distance between pores equal to 105 nm. The nanowire arrays were examined using scanning electron microscopy, X-ray diffraction analysis and vibration magnetometry at 300 K and 4.2 K. Microscopic and X-ray diffraction results showed that Ni nanowires are homogeneous, with smooth walls and mostly single-crystalline materials with a 220-oriented growth direction. The magnetic properties of the samples (coercivity and squareness) depend more on the length of the nanowires and the packing factor (the volume fraction of the nanowires in the membrane). It is shown that the dipolar interaction changes the demagnetizing field during a reversal magnetization of the Ni nanowires, and the general effective field of magnetostatic uniaxial shape anisotropy. The effect of magnetostatic interaction between ultra-long nanowires (with an aspect ratio of >500) in samples with a packing factor of ≥37% leads to a reversal magnetization state, in which a “curling”-type model of nanowire behavior is realized. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.Funding: An.T. (Andrei Turutin) acknowledges the financial support of the Russian Science Foundation (Grant No. 19-79-30062) in part of the experimental work. A.K. (Alexander Kislyuk) and I.K. (Ilya Kubasov) acknowledge the financial support of the Ministry of Science and Higher Education of the Russian Federation as a part of the State Assignment (basic research, Project No. 0718-2020-0031 “New magnetoelectric composite materials based on oxide ferroelectrics having an ordered domain structure: production and properties”) in part of the XRD study