Enhanced hydrogen sorption kinetics of magnesium by destabilized MgH2−δ

The kinetics of the reversible reaction of hydrogen gas with magnesium forming MgH2 is enhanced significantly by the addition of transition metals oxide catalysts and by using nanostructured powders. Hydrogen absorption and desorption properties of such systems were studied by differential scanning calorimetry (DSC) under hydrogen atmosphere, from which the heat of hydride formation and decomposition is determined. Apart from Mg and stoichiometric MgH2, we find an additional, slightly destabilized phase, which is formed prior to MgH2 upon hydrogenation. The amount of this phase depends on the degree of nanostructuring and the used additive. X-ray diffraction measurements confirm the compared to MgH2 slightly different lattice parameters of the intermediate phase. The results correspond to recent neutron diffraction measurements, by which a new MgH2−δ phase was found. We propose that this destabilized phase acts as a gateway for de-hydrogenation of MgH2.