材料科学
氢气储存
氢化物
合金
氧化物
Laves相
电化学
相(物质)
金属
扩散
氢
兴奋剂
化学工程
透射电子显微镜
冶金
纳米技术
物理化学
热力学
化学
电极
光电子学
物理
有机化学
金属间化合物
工程类
作者
K. Young,T. Ouchi,Jean Nei,Dhanashree Moghe
出处
期刊:Batteries
[MDPI AG]
日期:2016-07-11
卷期号:2 (3): 25-25
被引量:27
标识
DOI:10.3390/batteries2030025
摘要
Effects of substitutions of rare earth (RE) elements (Y, La, Ce, and Nd) to the Zr-based AB2 multi-phase metal hydride (MH) alloys on the structure, gaseous phase hydrogen storage (H-storage), and electrochemical properties were studied and compared. Solubilities of the RE atoms in the main Laves phases (C14 and C15) are very low, and therefore the main contributions of the RE additives are through the formation of the RENi phase and change in TiNi phase abundance. Both the RENi and TiNi phases are found to facilitate the bulk diffusion of hydrogen but impede the surface reaction. The former is very effective in improving the activation behaviors. −40 °C performances of the Ce-doped alloys are slightly better than the Nd-doped alloys but not as good as those of the La-doped alloys, which gained the improvement through a different mechanism. While the improvement in ultra-low-temperature performance of the Ce-containing alloys can be associated with a larger amount of metallic Ni-clusters embedded in the surface oxide, the improvement in the La-containing alloys originates from the clean alloy/oxide interface as shown in an earlier transmission electron microscopy study. Overall, the substitution of 1 at% Ce to partially replace Zr gives the best electrochemical performances (capacity, rate, and activation) and is recommended for all the AB2 MH alloys for electrochemical applications.
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