Enhanced Hydrogen Storage Performance of MgH2 by the Catalysis of a Novel Intersected Y2O3/NiO Hybrid

MgH2 is one of the most promising hydrogen storage materials due to its high hydrogen storage capacity and favorable reversibility, but it suffers from stable thermodynamics and poor dynamics. In the present work, an intersected Y2O3/NiO hybrid with spherical hollow structure is synthesized. When introduced to MgH2 via ball-milling, the Y2O3/NiO hollow spheres are crushed into ultrafine particles, which are homogenously dispersed in MgH2, showing a highly effective catalysis. With an optimized addition of 10 wt% of the hybrid, the initial dehydrogenation peak temperature of MgH2 is reduced to 277 degrees C, lowered by 109 degrees C compared with that of the bare MgH2, which is further reduced to 261 degrees C in the second cycle. There is ca. 6.6 wt% H-2 released at 275 degrees C within 60 min. For the fully dehydrogenation product, hydrogenation initiates at almost room temperature, and a hydrogenation capacity of 5.9 wt% is achieved at 150 degrees C within 150 min. There is still 5.2 wt% H-2 desorbed after 50 cycles at a moderate cyclic condition, corresponding to the capacity retention of 79.2%. The crystal structure and morphology of the Y2O3/NiO hybrid is well preserved during cycling, showing long-term catalysis to the hydrogen storage of MgH2. The Y2O3/NiO hybrid also inhibits the agglomeration of MgH2 particles during cycling, favoring the cyclic stability.

Automated summary

A Y2O3/NiO hybrid with spherical hollow structure was synthesized and introduced into MgH2 through ball-milling, showing significantly improved catalytic performance and hydrogen desorption rate. The hybrid also enhanced the adsorption velocity and stability of hydrogen, indicating potential for efficient hydrogen storage applications.