Abstract

Magnesium is one of the potential candidates for on-board hydrogen storage, but slow hydrogenation kinetics and unfavourable thermodynamics limits its practical implementation. To improve the hydrogenation characteristics, nanocrystalline magnesium was prepared by a simple wet milling method without addition of heavy metal catalyst. Compared to micro-crystalline Mg, developed nanocrystalline Mg exhibits improved hydrogen storage properties showing extended plateau region in the pressure-composition-temperature curves with higher hydrogen storage capacity (6.24 wt% at 300°C). Hydrogenation and dehydrogenation kinetics is found to follow Kolmogorov−Johnson−Mehl−Avrami activation energy model confirming the involvement of nucleation-growth-impingement mechanism. Prolonged ball milling leads to quite fast hydrogenation kinetics (upto 90% of the saturation value in 15.5 minutes at 250°C) and leads to substantial decrease in the activation barrier. The activation energy for hydrogenation is found to be 68.88 kJ mol−1 for 8 hours ball milled sample. Present study established a simple and scalable method for nanocrystalline Mg, which can undergo reversible hydrogen absorption and desorption with improved performance without using any additional catalyst.

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