In this paper, we report an investigation of adding a non-hydride forming element in the multicomponent Ti-V-Nb-M system. By the Calculation of Phase Diagrams approach (CALPHAD), the thermodynamic phase stability of the TiVNbT (T = Cr, Mn, Fe, Co, and Ni) was investigated, and Cr was selected as the fourth alloying element due its high tendency to stabilize body-centered cubic solid solutions (BCC). The (TiVNb)_100−xCr_x alloys (with x = 15, 25, and 35 at.% Cr) were synthesized by arc-melting. The structural characterization reveals that the three alloys were composed of a major BCC phase, which agrees with the thermodynamic calculations. The three alloys absorb hydrogen at room temperature without any activation treatment, achieving a hydrogen uptake of about H/M = 2. The Pressure-Composition-Isotherms curves (PCI) has shown that increasing the Cr amount increases the equilibrium pressures, indicating that tunable H storage properties can be achieved by controlling the alloys’ Cr content.

This paper reports the effect of high-pressure torsion (HPT) on the first hydrogenation of LaNi₅. We found that, for loose powder, reduction of particle size has an effect of increasing the incubation time and decreasing the hydrogen capacity. A higher amount of HPT turns only marginally reduce the incubation time but has no effect on hydrogen capacity. In all cases, the first dehydrogenation and subsequent hydrogenation have the same kinetics, irrespective of the particle size or number of HPT turns. Therefore, for LaNi₅, HPT has a beneficial effect only for the first hydrogenation.