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Hydrogenation properties and kinetic study of MgH - x wt% AC nanocomposites prepared by ball milling. | LitMetric

AI Article Synopsis

  • The study addresses the challenge of high temperatures required for de/hydrogenation in magnesium hydride (MgH) used for hydrogen storage in automobiles.
  • Researchers used activated carbon/charcoal (AC) as a catalyst to create MgH-5 wt% AC nanocomposites, which showed improved hydrogen storage capacities through various synthesis and characterization techniques.
  • The results indicated that the MgH-AC nanocomposites achieved a maximum hydrogen storage capacity of ~6.312 wt% at 300 °C, significantly better than the 3.417 wt% of pure MgH, with lower onset temperatures and improved kinetics for hydrogen absorption.

Article Abstract

The high de-/hydrogenation temperature of magnesium hydride is still a challenge in solid-state hydrogen storage system for automobiles applications. To improve the hydrogenation properties of MgH we select activated carbon/charcoal (AC) as a catalyst. A systematic investigation was performed on the hydrogen storage behaviors of MgH and MgH - 5 wt% AC nanocomposites, which were prepared by a high-energy planetary ball mill. These synthesized nanocomposites were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscope (HRTEM) for phase identification, surface morphology and microstructural analysis. The pressure-composition-temperature (PCT) isotherm investigation shows the maximum hydrogen storage capacity ~ 6.312 wt% for MgH-AC nanocomposites, while 3.417 wt% for MgH at 300 °C. The onset temperature for MgH-AC nanocomposites is shifted towards lower side than the 50 h milled MgH. The HRTEM study show the activated carbon helps to reduce oxygen from MgO phase in MgH, so that significantly improvement achieved in the absorption capacity and kinetics also for the MgH-AC nanocomposites. The presence of β- and γ-phases of MgH in MgH-AC nanocomposites also supports the high hydrogenation properties and with the support of XRD data.

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Source
http://dx.doi.org/10.1007/s11356-020-08964-1DOI Listing

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