Catalytic effect of NiO/C derived from Ni-UMOFNs on the hydrogen storage performance of magnesium hydride

Abstract

Magnesium based solid hydrogen storage material (MgH2) has the advantages of good safety and high hydrogen storage capacity in the shipping field. However, the high hydrogen absorption and desorption temperature have not been well solved. Herein, this work proves that it is very effective to improve the hydrogen storage performance of MgH2 by doping nano NiO/C catalyst. Specifically, experimental results showed that MgH2 + 9 wt% NiO/C composite could dehydrogenate at 195 °C, which was 155 °C lower than pure MgH2. In addition, 6.21 wt% H2 could be released rapidly at 300 °C for 10 min. After complete dehydrogenation, the absorption rate of hydrogen is 50 °C, which is 80 °C lower than that of pure MgH2. Moreover, 5.13 wt% H2 could be absorbed within 1 h at 125 °C and 3 MPa hydrogen pressure. In addition, dehydrogenation and hydrogen absorption apparent activation energies of MgH2 + 9 wt% NiO/C composite are 70.26 kJ/mol and 25.55 kJ/mol lower than those of pure MgH2, respectively. The cycle experiment showed that MgH2 + 9 wt% NiO/C had excellent cycle stability and could maintain 98.8% hydrogen storage capacity after 20 cycles. Furthermore, the study of the catalytic mechanism indicated that NiO/C catalyst is evenly distributed on the surface of MgH2. More importantly, Mg2Ni/Mg2NiH4 is generated in situ, which acts as a "hydrogen pump" and speeds up hydrogen diffusion during the hydrogen absorption and desorption cycle.