文摘
Magnesium-based alloys show great potential for hydrogen storage because of their high capacity, excellent reversibility, and low cost. However, the sluggish hydrogen sorption kinetics and overhigh dehydrogenation temperature hinder their practical application. In this paper, we present the reversible de/hydriding reaction mechanism of two new Mg鈥揑n鈥揘i ternary intermetallic compounds, which shows improved thermodynamics and kinetics in comparison with pure Mg. These two new phases correspond to Mg2InNi and Mg14In3Ni3 stoichiometries, both with orthorhombic structure, as determined by combinational X-ray diffraction and electron diffraction tomography analysis. In the hydriding process, the Mg14In3Ni3 alloy decomposes into a mixture of MgH2 and Mg2InNi, which is fully reversible in the dehydrogenation with hydrogen storage capacity of 1.8 wt %. For the dehydriding of MgH2 and Mg2InNi, a decrease of the reaction enthalpy (70.1 kJ mol鈥? H2) is obtained compared with pure MgH2 (72.2 kJ mol鈥? H2), and the dehydrogenation activation energy is decreased to 78.5 kJ mol鈥? from 鈭?60 kJ mol鈥? for pure MgH2. Comparatively, the alloy Mg90In5Ni5 containing the Mg14In3Ni3 phase has higher reversible hydrogen storage capacity of 3.3 wt %, and the minimum dehydrogenation temperature is reduced to 220 掳C. This work demonstrates the potential of exploring new Mg-based intermetallic compounds for hydrogen storage applications.