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The effect of Al addition on the structure, microstructure and hydrogen storage properties of the ternary TiVNb alloy was investigated from small amounts to equimolar composition. Alx(TiVNb)1−x (x = 0.05, 0.175 and 0.25) alloys are bcc single-phase materials with decreasing lattice parameters with increasing Al content. Al addition progressively decreases the hydrogen storage capacity but also destabilizes fcc dihydride formation for alloys with x ≤ 0.10. Among the different compositions, the most promising alloy was found to be that with x = 0.05 Al content that exhibited high initial storage capacity (2.96 wt.%), a less stable hydride (ΔH = −52 kJ/mol H2 and ΔS = −141 J/K∙mol H2), better desorption properties (desorption onset temperature around 100 °C) and enhanced reversible capacity during cycling (2.83 wt.%) compared to the ternary TiVNb. In situ and ex situ synchrotron X-ray powder diffraction, together with thermal desorption experiments, showed improved desorption properties with Al addition, together with a two-step reaction with hydrogen. These findings highlight the use of small quantities of lightweight Al in refractory multi-principal element alloys as a promising approach for enhancing the solid-state hydrogen storage performance of bcc-type alloys.

Data-driven predictions of metal hydride thermodynamic properties elucidate the Pareto optimal front of high entropy alloy candidates for hydrogen storage.