Significantly improved hydrogen storage properties of Mg90Al10 catalyzed by TiF3

Magnesium hydride (MgH2) is one of the most promising materials for solid state hydrogen storage, but overly stable thermodynamics and sluggish kinetics of hydrogenation and dehydrogenation hinders its application. In this study, Mg90Al10 was prepared by hydriding combustion synthesis (HCS), and then various Ti-based compounds (Ti, TiH2, TiO2 and TiF3) were introduced into Mg90Al10 by ball milling. Mg90Al10 + 10 wt% TiF3 displays the most excellent dehydrogenation property compared with those doped with other Ti-based compounds. For instance, due to the addition of 10 wt% TiF3, the peak dehydrogenation temperature and the apparent dehydrogenation activation energy of the composite are 86 degrees C and 77.1 kJ/mol lower than those of Mg90Al10 (364 degrees C and 155.95 kJ/mol). In addition, the catalytic effect of TiF3 on the hydrogen storage properties of Mg90Al10 has been investigated in detail. Except for the unreacted TiF3, Al3Ti and MgF2 can be found during the first dehydrogenation process and remain stable in the subsequent de/ hydrogenation cycles, which can act as the active sites to accelerate the hydrogen dissociation and recombination. Therefore, the excellent hydrogen storage properties of Mg90Al10 + 10 wt% TiF3 can be attributed to the catalytic effect of TiF3, in-situ formed Al3Ti and MgF2. Our result is very significant to emphasize the practical application of the Mg-Al hydrogen storage alloys. (c) 2022 Elsevier B.V. All rights reserved.

Automated summary

In this study, the dehydrogenation performance of magnesium hydride was improved by introducing TiF3 as a catalyst, resulting in lower peak dehydrogenation temperature and apparent dehydrogenation activation energy. The catalytic effect of TiF3 and the formation of Al3Ti and MgF2 were found to play a crucial role in hydrogen dissociation and recombination.