Effect of the Addition of 4 wt% Zr to BCC Solid Solution Ti52V12Cr36 at Melting/Milling on Hydrogen Sorption Properties

The addition of 4 wt% Zr to Ti52V12Cr36 alloy was carried out in two different ways: arc-melting or ball-milling. The cast alloy showed rapid hydrogen absorption up to 3.6 wt% of hydrogen capacity within 15 min. Ball milling this sample worsened the kinetics, and no hydrogen absorption was registered when milling was carried out for 30 or 60 min. When zirconium is added by ball-milling, the kinetic is slower than that when addition is by arc-melting. This is due to the fact that when added by milling, zirconium does not form a ternary phase with Ti, V, and Cr but instead is just dispersed on the particles’ surface.

Resistivity Testing of Palladium Dilution Limits in CoPd Alloys for Hydrogen Storage

Palladium satisfies most of the requirements for an effective hydrogen storage material with two major drawbacks: it has a relatively low gravimetric hydrogen density and is prohibitively expensive for large scale applications. Pd-based alloys should be considered as possible alternatives to a pure Pd. The question is how much one can dilute the Pd concentration in a variety of candidate materials while preserving the hydrogen absorption capability. We demonstrate that the resistivity measurements of thin film alloy samples can be used for a qualitative high-throughput screening and study of the hydrogen absorbing properties over the entire range of palladium concentrations. Contrary to palladium-rich alloys where additional hydrogen scattering indicates a degree of hydrogen content, the diluted alloy films respond by a decrease in resistance due to their thickness expansion. Evidence of significant hydrogen absorption was found in thin CoPd films diluted to just 20% of Pd.

Combined Light and Electron Scattering for Exploring Proximity Effects on Hydrogen Absorption in Vanadium

We investigate proximity effects on hydrogen absorption in ultra-thin vanadium layers through combing light transmission and electron scattering. We compare the thermodynamic properties of the vanadium layers, which are based on the superlattice structure of Cr/V (001) and Fe/V (001). We find an influence of the proximity effects on the finite-size scaling of the critical temperatures, which can be explained by a variation of dead layers in the vanadium. In addition to this, the proximity effects on hydrogen absorption are also verified from the changes of excess resistivity.

The Crystal Structures in Hydrogen Absorption Reactions of REMgNi4-Based Alloys (RE: Rare-Earth Metals)

REMgNi4-based alloys, RE(2−x)MgxNi4 (RE: rare-earth metals; 0 < x < 2), with a AuBe5-type crystal structure, exhibit reversible hydrogen absorption and desorption reactions, which are known as hydrogen storage properties. These reactions involve formation of three hydride phases. The hydride formation pressures and hydrogen storage capacities are related to the radii of the RE(2−x)MgxNi4, which in turn are dependent on the radii and compositional ratios of the RE and Mg atoms. The crystal structures formed during hydrogen absorption reactions are the key to understanding the hydrogen storage properties of RE(2−x)MgxNi4. Therefore, in this review, we provide an overview of the crystal structures in the hydrogen absorption reactions focusing on RE(2−x)MgxNi4.