Electrochemical behaviour of Ti/Al2O3/Ni nanocomposite material in artificial physiological solution: Prospects for biomedical application

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 FederationBelarusian Republican Foundation for Fundamental Research, BRFFR: Ф18Д-00720163522Funding: 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)

Electrochemical behaviour of Ti/Al2O3/Ni nanocomposite material in artificial physiological solution: Prospects for biomedical application

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 FederationBelarusian Republican Foundation for Fundamental Research, BRFFR: Ф18Д-00720163522Funding: 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)

The effect of heat treatment on the microstructure and mechanical properties of 2d nanostructured au/nife system

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

Peculiarities of the crystal structure evolution of Bifeo3-batio3 ceramics across structural phase transitions

Evolution of the crystal structure of ceramics BiFeO3-BaTiO3 across the morphotropic phase boundary was analyzed using the results of macroscopic measuring techniques such as X-ray diffraction, differential scanning calorimetry, and differential thermal analysis, as well as the data obtained by local scale methods of scanning probe microscopy. The obtained results allowed to specify the concentration and temperature regions of the single phase and phase coexistent regions as well as to clarify a modification of the structural parameters across the rhombohedral-cubic phase boundary. The structural data show unexpected strengthening of structural distortion specific for the rhombohedral phase, which occurs upon dopant concentration and temperature-driven phase transitions to the cubic phase. The obtained results point to the non-monotonous character of the phase evolution, which is specific for metastable phases. The compounds with metastable structural state are characterized by enhanced sensitivity to external stimuli, which significantly expands the perspectives of their particular use. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.Instituto Nacional de Ciência e Tecnologia para Excitotoxicidade e Neuroproteção, INCT-EN: UID/04564/2020, UIDB/50011/2020, UIDP/50011/2020Russian Science Foundation, RSF: 18-19-00307Funding: This work was supported by the RSF (project #18-19-00307). Investigations performed at the Center for Physics of the University of Coimbra were supported by Fundação para a Ciência e a Tecnologia (project UID/04564/2020). M.V.S. acknowledges Russian academic excellence project “5-100” for Sechenov University. Part of work done at the University of Aveiro was developed within the scope of the project CICECO-Aveiro Institute of Materials, refs. UIDB/50011/2020 & UIDP/50011/2020, financed by national funds through the FCT/MEC

Magnetic and microwave properties of SrFe12O19/MCe0.04Fe1.96O4 (M = Cu, Ni, Mn, Co and Zn) hard/soft nanocomposites

This paper reports the synthesis, structural characteristics and magnetism of SrFe12O19/MCe0.04Fe1.96O4 (M = Cu, Ni, Mn, Co and Zn) hard/soft nanocomposites. The hard/soft compositions were manufactured via a one-pot reactions citrate sol-gel approach. The hard/soft phases formation was confirmed using XRD, SEM, TEM and HRTEM techniques. M vs. H (Magnetization measurements) were done at unbent temperature and 10 K. Smoothed M against H loops and single peaks in dM/dH vs. H curves were noticed in SrFe12O19/MnCe0.04Fe1.96O4, SrFe12O19/CuCe0.04Fe1.96O4 and SrFe12O19/ZnCe0.04Fe1.96O4 hard/soft nanocomposites. This indicated the manifestation of well exchange-coupled effect among hard and soft phases in these composites. However, SrFe12O19/CoCe0.04Fe1.96O4 and SrFe12O19/NiCe0.04Fe1.96O4 hard/soft nanocomposites showed non-well smoothed M against H loops and two peaks in dM/dH versus H plots, indicating that the dipolar interactions are unimportant compared to exchange-coupling behavior. Among all prepared nanocomposites, the SrFe12O19/MnCe0.04Fe1.96O4 hard/soft nanocomposite showed the highest exchange-coupling behavior. Microwave properties of the SrFe12O19/MCe0.04Fe1.96O4 (M = Cu, Ni, Mn, Co and Zn) hard/soft nanocomposites were investigated using coaxial method with applied frequency values fall between 2 and 18 GHz. Reflection losses were calculated from frequency dependences of the imaginary and real parts of permeability and permittivity. The correlation between the chemical composition of the spinel phase (A-cation) and microwave properties of composites. Most intensive electromagnetic absorption was observed for Ni- and Mn-spinels. This is can be a result of the differences in electron shell configuration and radii for A-site ions in the spinel phase. Change of the absorption mechanisms (transition from ionic polarization to dipole polarization) was observed. © 2020 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).The work was supported by the Russian Science Foundation (agreement number 19-72-10071 ). Also Authors are thank to the Institute for Research & Medical Consultations (Projects Application No. 2018-IRMC-S-2 ) of Imam Abdulrahman Bin Faisal University (IAU – Saudi Arabia) for financial and technical supports

A-site Randomness Effect on Structural and Physical Properties of Ba-based Perovskite Manganites

The discovery of novel structural and physical properties in the $A$-site ordered manganite $R$BaMn$_{2}$O$_{6}$ ($R$ = Y and rare earth elements) has demanded new comprehension about perovskite manganese oxides. In the present study, the $A$-site disordered form, $R_{0.5}$Ba$_{0.5}$MnO$_{3}$, has been investigated and compared with both $R$BaMn$_{2}$O$_{6}$ and $R_{0.5}A_{0.5}$MnO$_{3}$ ($A$: Sr, Ca) in the structures and electromagnetic properties. $R_{0.5}$Ba$_{0.5}$MnO$_{3}$ has a primitive cubic perovskite cell in the structure and magnetic glassy states are dominant as its ground state, in contrast to the ordinary disordered $R_{0.5}A_{0.5}$MnO$_{3}$ ($A$: Sr, Ca). In Pr-compounds with various degrees of Pr/Ba randomness at the $A$-sites, the $A$-site disorder gradually suppresses both ferromagnetic and A-type antiferromagnetic transitions and finally leads to a magnetic glassy state in Pr$_{0.5}$Ba$_{0.5}$MnO$_{3}$. A peculiar behavior, multi-step magnetization and resistivity change, has been observed in Pr$_{0.5}$Ba$_{0.5}$MnO$_{3}$. These properties could be closely related to any spatial heterogeneity caused by the random distribution of Ba$^{2 +}$ and $R^{3 +}$ with much different ionic radius.Comment: 9 pages, to be published in J. Phys. Soc. Jpn. 73 Aug. (2004

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

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)