Mg-based
hydride materials (MgH2) are in the spotlight
of hydrogen storage due to their high gravimetric density. Yet, its
large-scale utilization is limited by the poor thermodynamic stability
and slow kinetics. Herein, we report a novel and straightforward way
to prepare MgH2 with amorphous carbon by cosintering 2-methylnaphthalene
(CMN) organics with pure Mg and a hydriding combustion synthesis method,
where the amorphous carbon formed from the CMN not only improves the
dehydrogenation/hydrogenation capacity but also enhances the kinetics
of the Mg/MgH2 system. The dehydrogenation capacity of
the CMN-MgH2 composite reaches 4.88 wt % of H2 at 623 K, nearly 2 times of pure MgH2, and its onset
dehydrogenation temperature decreases to 560 K, 90 K lower than that
of pure MgH2; in addition, at a lower temperature of 473
K, the composite remarkably absorbs 4.54 wt % of H2 within
42 s while the absorption is only 0.71 wt % H2 for the
pure MgH2. Moreover, the activation energy greatly decreases
from 165.35 to 101.52 kJ/mol. Further research reveals that the evolution
of hydrogenation changes from a three-dimensional diffusion process
to a one-dimensional diffusion process, attributed to the formation
of the amorphous carbon. This work is expected to provide inspiration
to design and prepare effective additives for the improvement of hydrogen
storage performance of Mg-based hydrides.