Magnesium
hydride is considered as a promising candidate for hydrogen
storage; however, the sluggish kinetics and thermodynamic stability
seriously obstruct its industrial applications. Hence, in order to
improve the hydrogen storage performances of magnesium hydride, NiS@C
additive was ball-milled with Mg powder to build NiS@C/Mg. The MgH2/Mg2NiH4 polyphase hydrides were in
situ formed after hydrogenated activation and turned into Mg/Mg2Ni phases during the dehydrogenation process, establishing
a cycle of hydrogen absorption and desorption. The NiS@C/Mg composite
showed enhanced de/hydrogenation rates: it could quickly absorb 6.02
wt % H2 within 5 min at 250 °C and desorb 5.34 wt
% H2 at 300 °C. Moreover, even at the temperature
of 50 °C, it could reach 3.23 wt % hydrogen absorption capacity,
and the apparent hydrogen desorption activation energy for MgH2 decreased to 60.45 kJ mol–1. It also delivered
a high cyclic stability performance of 98.9% for hydrogen absorption
and 98.5% for hydrogen desorption after 50 cycles. The enhanced de/absorption
kinetics of NiS@C/Mg were ascribed to the synergistic effects of multiple-phase
MgH2/Mg2NiH4 hydrides and the in
situ formed MgS catalyst, and the existence of C also effectively
prevented the passivation and agglomeration of multiple-phase particles.
The method of in situ generating of multiple-phase hydrides and catalysts
provides a new view for the preparation of high-performance hydrogen
storage materials.