Phase segregation in hydride-forming alloys may persist under the action of multiple hydrogenation/dehydrogenation cycles. We use this effect to destabilize metal hydrides in the immiscible Mg-Mn system. Here, in the MgxMn1-x thin films, the Mg and Mn domains are chemically segregated at the nanoscale. In Mn-rich compositions, the desorption pressure of hydrogen from MgH2 is elevated at a given temperature, indicating a thermodynamic destabilization. The increase in the desorption pressure of hydrogen reaches ∼2.5 orders in magnitude for x = 0.30 at moderate temperatures. Such large thermodynamic destabilization allows the MgH2 to reversibly absorb and desorb hydrogen even at room temperature. Our strategy to use immiscible elements for destabilization of MgH2 is effective and opens up the possibility for the development of advanced and low-cost hydrogen storage and supply systems. @en

Thin films often exhibit fascinating properties, but the understanding of the underlying mechanism behind such properties is not simple. This is partially because of the limited structural information available. The hurdle in obtaining such information is especially high for textured thin films such as Mg-rich MgxTi1-x, a promising switchable smart coating material. Although these metastable thin films are seen as solid solution alloys by conventional crystallographic methods, their hydrogen-induced optical transition is hardly understood by a solid solution model. In this study, we collect atomic pair distribution function (PDF) data for a Mg0.7Ti0.3Hy thin film in situ on hydrogenation and successfully resolve TiH2 clusters of an average size of 30 Å embedded in the Mg matrix. This supports the chemically segregated model previously proposed for this system. We also observe the emergence of a previously unknown intermediate face-centered tetragonal phase during hydrogenation of the Mg matrix. This phase appears between Mg and MgH2 to reduce lattice mismatch, thereby preventing pulverization and facilitating rapid hydrogen uptake. This work may shed new light on the hydrogen-induced properties of Mg-rich MgxTi1-x thin films. ©@en