脱氢
氢气储存
解吸
氢
镁
催化作用
反应性(心理学)
氢化镁
钝化
材料科学
氢氧化物
化学工程
无机化学
合金
化学
冶金
图层(电子)
纳米技术
物理化学
有机化学
吸附
工程类
医学
替代医学
病理
作者
Jinlian Ni,Yunfeng Zhu,Jiguang Zhang,Zhongliang Ma,Yana Liu,Aoqi Wang,Liquan Li
标识
DOI:10.1016/j.ijhydene.2023.03.120
摘要
It is well established that H2O and O2 have an inauspicious influence on hydrogen reactivity of hydrogen storage alloys. In this work, an unexpected improvement of the desorption behavior was discovered by just exposing the magnesium rich Mg–Ni hydrides into the air for a certain period. Upon an exposure duration of 4 months, the dehydrogenation peak and onset temperature were sharply lowered by 150 °C and 130 °C. Furthermore, the air-exposed sample could quickly absorb 3.08 wt% H2 and desorb 2.81 wt% H2 within 400 s at 300 °C. Besides the refinement of the powders due to the spontaneous hydrolysis reaction, the in-situ formed magnesium hydroxide layer and Ni are thought to be responsible for the remarkable improvement. This work gives interesting insights that the self-generating surface passivation is not necessarily harmful in the solid-state hydrogen storage area, especially for the cases where active sites of catalysis are present.
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