氢气储存
氢化镁
双金属片
纳米笼
催化作用
材料科学
氢化物
镁
氢
解吸
氧化物
无机化学
化学工程
复合数
化学
吸附
金属
冶金
复合材料
物理化学
有机化学
工程类
作者
Liuting Zhang,Changhao Zhao,Fuying Wu,Yijing Wang
标识
DOI:10.1016/j.jallcom.2023.170002
摘要
Carbon-wrapped Ti and Co bimetallic oxide nanocages (Ti-CoO@C) were successfully synthesized through a regulated hydrothermal method and then doped into magnesium hydride (MgH2) by mechanical ball milling to enhance its de/rehydrogenation performance. The hydrogen desorption of MgH2 with 5 wt% Ti-CoO@C started at 185.6 ºC, 160.2 ºC lower than that of pure MgH2. At 275 ºC, the composite rapidly released 6.3 wt% hydrogen within 5 min. The activation energy of hydrogen desorption/absorption of MgH2 + 5 wt%Ti-CoO@C composite was dropped from 169.19 kJ/mol and 83.61 kJ/mol of MgH2 to 137.76 kJ/mol and 35.17 kJ/mol, respectively. In addition, no significant performance degradation was observed in 20 cycles, indicating the excellent stability of the composite. The excellent hydrogen storage performance can be attributed to the homogeneous distribution of the catalyst and in situ generated titanium and MgO, as well as the promoting effect of Mg2Co/Mg2CoH5 as a hydrogen pump. Meanwhile, carbon played a key role in realizing catalyst nanosizing and weakening the Mg-H bond of MgH2, thus enabling the MgH2 + 5 wt%Ti-CoO@C composite to possess an excellent hydrogen storage property.
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