National Institute Of Materials Physics - Romania

Despite being the lightest element in the periodic table, hydrogen poses many risks regarding its production, storage, and transport, but it is also the one element promising pollution-free energy for the planet, energy reliability, and sustainability. Development of such novel materials conveying a hydrogen source face stringent scrutiny from both a scientific and a safety point of view: they are required to have a high hydrogen wt.% storage capacity, must store hydrogen in a safe manner (i.e., by chemically binding it), and should exhibit controlled, and preferably rapid, absorption-desorption kinetics. Even the most advanced composites today face the difficult task of overcoming the harsh re-hydrogenation conditions (elevated temperature, high hydrogen pressure). Traditionally, the most utilized materials have been RMH (reactive metal hydrides) and complex metal borohydrides M(BH4)(x) (M: main group or transition metal; x: valence of M), often along with metal amides or various additives serving as catalysts (Pd2+, Ti4+ etc.). Through destabilization (kinetic or thermodynamic), M(BH4)(x) can effectively lower their dehydrogenation enthalpy, providing for a faster reaction occurring at a lower temperature onset. The present review summarizes the recent scientific results on various metal borohydrides, aiming to present the current state-of-the-art on such hydrogen storage materials, while trying to analyze the pros and cons of each material regarding its thermodynamic and kinetic behavior in hydrogenation studies.

We report the mechanical behavior of a bulk boron ceramic prepared by spark plasma sintering of commercially available beta-boron powder. In order to fabricate polycrystalline boron ceramic, we used a protective tantalum foil reacted with carbon from the graphite die or graphite foil forming a thin layer of TaB2 and TaC covering the boron specimen. This is the first study to show the high-temperature flexural strength, toughness, and Young's moduli of boron up to 1400 degrees C. At 1600 degrees C and above, boron will react with testing environment forming an outer shell. The flexural strength and fracture toughness at room temperature reached an average of 340 MPa and 4.1 MPa m (1/2) , respectively. Despite showing clear signs of plastic deformation on the strain-stress curves, the yield strength of the monolithic boron ceramic exceed 1 GPa at 1200 degrees C. It was determined that fracture at elevated temperatures follows a quasi-transgranular mechanism, where the sub-grains of the boron fracture as plate-like structures. An interpretation for the observed fracture behavior was proposed.

This paper presents the effect of Mn2+ substitution for Co2+, in CoFe2O4 embedded in SiO2 matrix, on the structural, surface, morphological and magnetic properties. X-ray diffraction (XRD) and Mossbauer spectroscopy indicate the presence of a nanocrystalline mixed cubic spinel. In all cases, for the nanocomposites (NCs) heat-treated at 200 degrees C, a single, low crystalline ferrite phase was remarked, while for the other heat-treatment temperatures up to 1200 degrees C and with increasing Mn content, the secondary phase of alpha-Fe2O3 appears, accompanied also by the secondary phase of SiO2 at 1200 degrees C. The Fourier transform infrared (FT-IR) spectroscopy confirms the consumption of starting metallic nitrates, the formation of Co-O, Mn-O, Fe-O bonds in ferrites@SiO2 matrix. The Mossbauer spectra show the characteristic magnetic patterns of Co and Mn spinels. According to the atomic force microscopy (AFM) analysis, the particle size increases from 15 to 80 nm with the increase of Mn content. The specific surface area varies in the range 150-450 m(2)/g due to the substitution of Co2+ ion with Mn2+ ion and decreases with increasing heat treatment temperature, reaching values below 1 m(2)/g at 1200 degrees C. All NCs have pores within the mesoporous range, with high dispersion of pores' sizes. Furthermore, the release of fine nanoparticles in aqueous environment is facilitated by the powders' mesoporous structure preserved at 200, 500 and 800 degrees C heat treatment temperatures. The porous network collapse after heat treatment at 1200 degrees C leads to releasing of bigger nanoparticles, in good agreement with AFM observation. Magnetization, coercivity and anisotropy evolve proportionally with the particle size for the NCs heat-treated at 800 degrees C (M-s = 18.9-36.3 emu/g; M-R = 3.05-14.1 emu/g, H-c = 31.83-53.2 kA/m, K= 0.378.10(-3) -1.21.10(-3) erg/cm(-1)) and inverse proportionally for those heat-treated at 1200 degrees C (M-s = 30.7-19.4 emu/g; M-R = 11.60 7.20 emu/g, H-c= 127.3-15.9 kA/m, K= 2.45.10(-3)-0.19.10(-3) erg/cm(-1)). The NCs with high Mn content heat-treated at 1200 degrees C show superparamagnetic behavior, while those with low Mn content display ferrimagnetic behavior. (C) 2021 Elsevier B.V. All rights reserved.

In this work, thermoelectric properties of the nanocomposite materials produced via ball milling followed by spark plasma sintering from In0.2Yb0.2Co4Sb12 double filled skutterudite (SKT) with silicon and tungsten carbide inclusions are investigated. The nanocomposites with low volume ratios of beta-SiC and '-WC have a significantly increased power factor, while the lattice thermal conductivity is lowered only for beta-SiC composites. The power factor enhancement in '-WC/SKT composite compensates the increase of its thermal conductivity, and as a consequence, the maximum value of the figure of merit, 0.97, is attained for 0.33 v% 'WC at 450 degrees C, with 15% higher than that of the simple skutterudite sample. (c) 2021 Elsevier B.V. All rights reserved.

Magnetic ceramic nanoparticles system xNd(2)O(3)-(1-x)alpha-Fe2O3 (x = 0.1, 0.3 and 0.5) was synthesized by mechanochemical activation starting from hematite and neodymium oxide precursors and characterized by X-ray diffraction (XRD) and Mossbauer spectroscopy. Rietveld refinement of XRD data evidenced the formation of neodymium orthoferrite NdFeO3 as an end-product with a particle size of about 22 nm, determined using the Scherrer method for x = 0.5. The Mossbauer spectra were typically analyzed considering 2 sextets, corresponding to hematite and neodymium orthoferrite and a doublet, representing superparamagnetic particles (SPM). The recoilless fractions were determined using our dual absorber method and were found consistent with a decrease in particle size as consequence of the ball milling process performed.

Zr0.8Sn0.2TiO3 (ZST) powders synthesized by solid-state reaction were subject to processing by spark plasma sintering (SPS). A single-phase ceramic with a high relative density of 95.7% and 99.6% was obtained for sintering temperatures of 1150 degrees C and 1200 degrees C, respectively, and for a dwell time of 3 min. In order to reduce the oxygen vacancies, as-sintered discs were annealed in air at 1000 degrees C. The dielectric loss of the annealed samples, expressed by the Q x f product, measured in the microwave (MW) domain, varied between 35 THz and 50 THz. The intrinsic losses (Q x f ~ 60 THz) were derived by using terahertz time-domain spectroscopy (THz-TDS).

Small multilayered laminated samples consisting of stacks of W (or K-doped W) foils without an interlayer or with interlayers from Cu, V, and Ti were exposed to a pulsed electron beam with an energy of 6 MeV in several irradiation sessions. All samples maintained their macroscopic integrity, suggesting that the W-metal laminate concept is compatible with high heat flux applications. The surface of the samples was analyzed using a scanning electron microscope (SEM) before and after each irradiation session. The experimental results indicate that electron beam irradiation induces obvious modifications on the surface of the samples. Morphological changes such as the appearance of nanodroplets, nanostructures, and melting and cracking, depending on the sample type and the electron beam fluence, are observed. The irradiation is carried out in a vacuum at a pressure of 2 to 4 x 10(-2) torr, without active cooling for the samples. The structures observed on the surface of the samples are likely due to electron beam heating and vaporization followed by vapor condensation in the volume adjacent to the surface.

This work reports on the influence of 5 MeV electron beam radiations on the morphological features and chemical structure of magnesium-doped hydroxyapatite/chitosan composite coatings generated by the magnetron sputtering technique. The exposure to ionizing radiation in a linear electron accelerator dedicated to medical use has been performed in a controllable manner by delivering up to 50 Gy radiation dose in fractions of 2 Gy radiation dose per 40 s. After the irradiation with electron beams, the surface of layers became nano-size structured. The partial detachment of irradiated layers from the substrates has been revealed only after visualizing their cross sections by scanning electron microscopy. The energy dispersive X-ray spectral analysis of layer cross-sections indicated that the distribution of chemical elements in the samples depends on the radiation dose. The X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and X-ray diffraction analysis have shown that the physicochemical processes induced by the ionizing radiation in the magnesium doped hydroxyapatite/chitosan composite coatings do not alter the apatite structure, and Mg remains bonded with the phosphate groups.

Bulk high density MgB2 and a composite material made of a PLA matrix and MgB2 powder inclusions were in vivo tested as candidates for biodegradable materials for orthopedic implants. A rat model was used. Implants were introduced into femoral bone, in transversal and longitudinal directions. Assessment of the implant-tissue interaction was performed by X-ray imaging, X-ray computer tomography, electron microscopy, cytology, and histopathology on samples at 40 and 90 days after surgery. Both materials are biocompatible, bone and adjacent soft tissue showing good tolerance of implants. Biodegradation of MgB2 is faster than for PLA-MgB2 composite, but in both cases, it is accompanied by bone regeneration. Results suggest that use of MgB2-containing composites can promote space and time control of degradation and promotes MgB2 as a promising material for fracture repair. (c) 2022 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/).

This work reports the effect of the rapid solidification technique and thermal treatment on the martensitic transformation (MT), magnetic and magnetostrictive properties on the off-stoichiometric Ni49Mn31Ga20 and Ni51Mn28Ga21 ferromagnetic shape memory ribbons. The samples were investigated by X-ray diffraction, differential scanning calorimetry, scanning electron microscopy, magnetic and magnetostrictive measurements. The temperature dependence of the X-ray phases analysis shows the presence of martensite structures, both tetragonal and monoclinic, at room temperature and allowed to study their evolution through MT. The thermal treatment induces changes in the microstructure with implications in MT and Curie temperatures evolution. The competition between the magnetization orientation and twin boundary motion within martensitic variants under magnetic field evidenced in the magnetic-strain curves was discussed and correlated with the magnetic data.