Magnesium-Based Materials for Hydrogen Storage: Microstructural Properties

R. Kondo, Takeshita T. Hiroyuki
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引用次数: 4

Abstract

Magnesium (Mg) is hydrogenated as core-shell-type hydride. Therefore, increase of absorption capacity to the theoretical hydrogen capacity is still one of the most important issues for the hydrogen storage materials. In this study, the procedure of the core-shell structure as well as effect of Al concentration in Mg on the growth MgH2 in Mg were investigated. MgH2 was formed on the surface as well as inside of unreacted Mg core. The inside MgH2 was formed in a granular form on Mg grain boundary and its size increased by applying plastic deformation. Thickness of the surface MgH2 and size of the internal MgH2 increased with an increase in hydrogenation time until the hydride surface was completely covered with MgH2. However, the growth of the surface and internal MgH2 came to a halt after the surface was covered with MgH2. From these results, supplying H from metal side was dominantly contributed for growth of the surface and internal MgH2 because diffusion rate of H in Mg was much higher than that in MgH2. In addi tion, the growth of internal MgH2 as well as control of surface MgH2 can contribute to the promotion of the complete hydrogenation of Mg-based hydrogen storage materials.
镁基储氢材料:微观结构性能
镁(Mg)氢化为核壳型氢化物。因此,将吸氢容量提高到理论储氢容量仍然是储氢材料研究的重要课题之一。本研究考察了核壳结构的形成过程以及镁中Al浓度对镁中MgH2生长的影响。MgH2在未反应的Mg核表面和内部形成。内部的MgH2在Mg晶界处呈粒状形成,通过塑性变形使其尺寸增大。表面MgH2的厚度和内部MgH2的尺寸随着加氢时间的增加而增加,直到氢化物表面完全被MgH2覆盖。然而,在表面被MgH2覆盖后,表面和内部的MgH2生长停止。从这些结果可以看出,由于H在Mg中的扩散速率远高于MgH2中的扩散速率,金属侧供给的H对表面和内部MgH2的生长起主要作用。此外,内部MgH2的生长和表面MgH2的控制有助于促进镁基储氢材料的完全加氢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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