Structural and hydrogen storage characterization of nanocrystalline magnesium synthesized by ECAP and catalyzed by different nanotube additives

Ball-milled nanocrystalline Mg powders catalyzed by TiO2 powder, titanate nanotubes and carbon nanotubes were subjected to intense plastic deformation by equal-channel angular pressing. Microstructural characteristics of these nanocomposites have been investigated by X-ray diffraction. Microstructural parameters, such as the average crystallite size, the average dislocation density and the average dislocation distance have been determined by the modified Williamson–Hall analysis. Complementary hydrogen desorption and absorption experiments were carried out in a Sieverts’ type apparatus. It was found that the Mg-based composite catalyzed by titanate nanotubes exhibits the best overall H-storage performance, reaching 7.1 wt% capacity. The hydrogenation kinetic curves can be fitted by the contracting volume function for all the investigated materials. From the fitted parameters, it is confirmed that the titanate nanotube additive results in far the best kinetic behavior, including the highest hydride front velocity

Hydrogen storage of nanocrystalline Mg-Ni alloy processed by equal-channel angular pressing and cold rolling

Ball-milled nanocrystalline Mg2Ni powders were subjected to intense plastic straining by cold rolling or equal-channel angular pressing. Morphological and microstructural evolution during these processes has been investigated by scanning electron-microscopy and X-ray diffraction line profile analysis, respectively. Complementary hydrogen absorption experiments in a Sieverts’ type apparatus revealed that there exists some correlation between the micro- and nanostructure and hydrogen storage properties of the severely deformed materials

Reactive Sputter Deposition of Ga2O3 Thin Films Using Liquid Ga Target

Ga2O3 is a promising material in the optoelectronics and semiconductor industry. In this work, gallium oxide thin films were deposited via radio frequency (RF) sputtering, using a liquid Ga target. The reactive sputtering was carried out using different oxygen flow rates and DC target potentials induced via the RF power. The thickness of the samples varied between 160 nm and 460 nm, depending on the preparation conditions. The composition and the refractive index of the layers were investigated via energy-dispersive spectroscopy, X-ray photoelectron spectroscopy, and spectroscopic ellipsometry, respectively. It was found that, through the use of a lower DC target potential, a better film quality and higher oxygen content can be achieved. The reactive sputtering was modeled based on the Berg model, with the aim of determining the sputtering yields and the sticking coefficient. It was shown that an increase in DC target potential leads to the preferential sputtering of gallium

Thermal, Microstructural and Electrochemical Hydriding Performance of a Mg65Ni20Cu5Y10 Metallic Glass Catalyzed by CNT and Processed by High-Pressure Torsion

A Mg65Ni20Cu5Y10 metallic glass was produced by melt spinning and was mixed with a 5 wt.% multiwall carbon nanotube additive in a high-energy ball mill. Subsequently, the composite mixture was exposed to high-pressure torsion deformation with different torsion numbers. Complimentary XRD and DSC experiments confirmed the exceptional structural and thermal stability of the amorphous phase against severe plastic deformation. Combined high-resolution transmission electron microscopy observations and fast Fourier transform analysis revealed deformation-induced Mg2Ni nanocrystals, together with the structural and morphological stability of the nanotubes. The electrochemical hydrogen discharge capacity of the severely deformed pure metallic glass was substantially lower than that of samples with the nanotube additive for several cycles. It was also established that the most deformed sample containing nanotubes exhibited a drastic breakdown in the electrochemical capacity after eight cycles

High-Pressure Torsion of Non-Equilibrium Hydrogen Storage Materials: A Review

As the most abundant element in the world, hydrogen is a promising energy carrier and has received continuously growing attention in the last couple of decades. At the very moment, hydrogen fuel is imagined as the part of a sustainable and eco-friendly energy system, the “hydrogen grand challenge”. Among the large number of storage solutions, solid-state hydrogen storage is considered to be the safest and most efficient route for on-board applications via fuel cell devices. Notwithstanding the various advantages, storing hydrogen in a lightweight and compact form still presents a barrier towards the wide-spread commercialization of hydrogen technology. In this review paper we summarize the latest findings on solid-state storage solutions of different non-equilibrium systems which have been synthesized by mechanical routes based on severe plastic deformation. Among these deformation techniques, high-pressure torsion is proved to be a proficient method due to the extremely high applied shear strain that develops in bulk nanocrystalline and amorphous materials

Microstructure and Hydrogen Storage Performance of Ball-Milled MgH2 Catalyzed by FeTi

A high-energy ball-milling method was applied for different milling times (1 h, 3 h, and 10 h) to synthetize nanocrystalline MgH2 powder samples catalyzed by Fe2Ti. Morphology and microstructure of the powders were characterized by scanning electron microscopy and X-ray diffraction. The recorded diffraction profiles were evaluated by the convolutional multiple whole profile fitting algorithm, in order to determine microstructural parameters of the composites, such as average crystallite size and average dislocation density. Differential scanning calorimetry was performed to investigate the dehydrogenation characteristics of the alloys. It was obtained that there exists an optimal milling time (3 h) when desorption occurs at the lowest temperature. X-ray diffraction of partially dehydrided states confirmed a two-step H-release, including the subsequent desorption of γ-MgH2 and α-MgH2. The effect of milling time on the H-sorption performance was investigated in a Sievert-type apparatus. The best overall hydrogenation performance was obtained for the composite milled for 3 h