The hydrogen storage properties of Hf1-xTixNbVZr high entropy alloys (HEAs) synthesized by arc melting have been investigated. The first hydrogenation of the alloys was performed at room temperature under 20 bars of hydrogen pressure. Results show an increase in gravimetric hydrogen content with Ti substitutions. Upon hydrogenation, the multiphase alloys (x = 0 and x = 0.25) exhibit a combination of faces-centred-cubic (FCC) hydride and C15 Laves phases, while single-phase alloys (x = 0.5, 0.75, and 1) display FCC structures. The crystal structure evolution during dehydrogenation of HfNbVZr (x = 0) and TiNbVZr (x = 1) HEAs was examined using in-situ neutron diffraction. The analysis demonstrates temperature-dependent desorption behaviour, with HfNbVZr displaying lower desorption temperatures compared to TiNbVZr. Additionally, in-situ neutron diffraction experiments during deuterium desorption indicate a two-step phase transition from FCC dihydride to BCT monohydride, followed by a transition to BCC.@en

The hydride phase of Ti₅₀V₂₀Cr₃₀ alloy cast with 4 wt% of 7Zr+10Ni has been investigated. Pressure composition desorption isotherms were measured at 150 °C and 200 °C. These isotherms revealed same desorption of 1.5 wt% at 150 °C and 200 °C. The evolution of the crystal structure upon dehydrogenation was investigated by in-situ neutron diffraction. A sample was fully deuterated at room temperature under 2000 kPa pressure. Afterwards, the sample was heated from 120 °C to 266 °C under vacuum and neutron diffraction patterns were recorded as a function of temperature. It was found that the alloy started to desorb very quickly at 200 °C. The amount of fcc phase was monitored using the relative intensity of the fcc phase compared to a standard. At 266 °C only 10% hydride phase was seen, which was confirmed by X-ray diffraction. Besides the fcc phase, a minor aluminum phase due to the heating element was also observed in all patterns. Thermal expansion coefficient of Al and fcc phase were calculated. Using the aluminum peaks as reference, it was found that deuterium occupancy reflect the phase abundance of the fcc deuteride.

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Magnesium hydride has been studied extensively for applications as a hydrogen storage material owing to the favourable cost and high gravimetric and volumetric hydrogen densities. However, its high enthalpy of decomposition necessitates high working temperatures for hydrogen desorption while the slow rates for some processes such as hydrogen diffusion through the bulk create challenges for large-scale implementation. The present paper reviews fundamentals of the Mg–H system and looks at the recent advances in the optimisation of magnesium hydride as a hydrogen storage material through the use of catalytic additives, incorporation of defects and an understanding of the rate-limiting processes during absorption and desorption.

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