Magnesium hydride
has long been regarded as a promising candidate
material for hydrogen and heat storage due to its high hydrogen capacity,
reversibility, and low cost. Catalytic doping has been demonstrated
as one of the most effective methods to improve hydrogen storage properties
of MgH2. In this study, amorphous Ti45Cu41Ni9Zr5 and Ti40Cu47Zr10Sn3 alloys are used as additives for MgH2. Nanostructured MgH2 doped with amorphous or crystalline
TiCu-based alloys are prepared by using a high-energy mechanochemical
synthesis method. Results show that the amorphous TiCu additives provide
enhanced catalytic effects compared to crystalline alloys of the same
composition. Doping MgH2 using an amorphous Ti45Cu41Ni9Zr5 alloy yielded improved
dehydrogenation kinetics compared to using crystalline Ti40Cu47Zr10Sn3 alloy. The analysis
using transmission electron microscopy reveals that there are nanostructured
catalytic particles uniformly distributed in the amorphous TiCu-catalyzed
MgH2. The MgH2 system catalyzed by amorphous
TiCu-based alloy shows little degradation during hydrogenation and
dehydrogenation cycling at 300 °C. The amorphous TiCu-based catalysts
are thermally stable at temperatures up to 360 °C. Heating the
amorphous Ti45Cu41Ni9Zr5-catalyzed MgH2 to temperatures above 360 °C led
to disproportionation of the catalyst alloy and the formation of MgCu2 and Ti2Cu. In addition, PCI analysis of the amorphous
Ti45Cu41Ni9Zr5-catalyzed
MgH2 shows a slight increase in hydrogen equilibrium pressure,
resulting in a reaction enthalpy of −78.7 kJ/mol·H2 and an entropy of 145.0 J/K·mol·H2.
The entropy calculated from this study is approximately 10 J/K·mol·H2 higher than values previously reported for undoped and catalyzed
Mg–H systems.