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Catalytic effect of a novel MgC0.5Co3 compound on the dehydrogenation of MgH2
被引:17
|作者:
Fu, Yaokun
[1
]
Ding, Zhenmin
[1
]
Zhang, Lu
[1
,2
]
Zhang, Hongming
[1
]
Wang, Wenfeng
[1
]
Li, Yuan
[1
,2
]
Han, Shumin
[1
,2
]
机构:
[1] Yanshan Univ, Hebei Key Lab Appl Chem, Sch Environm & Chem Engn, Qinhuangdao 066004, Hebei, Peoples R China
[2] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Hebei, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Hydrogen storage materials;
Magnesium hydride;
Dehydrogenation performance;
MgC0;
5Co3 alloy compound;
HYDROGEN-STORAGE PROPERTIES;
SORPTION;
NI;
KINETICS;
MECHANISM;
ALLOY;
SIZE;
RGO;
D O I:
10.1016/j.pnsc.2021.01.009
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
The application of magnesium hydride (MgH2) is limited due to the high reaction temperature and slow kinetics during dehydrogenation. In order to ameliorate the dehydrogenation property of MgH2, MgC0.5Co3 compound with induction and catalytic effects was introduced into the Mg/MgH2 system via ball-milling and hydriding combustion methods in present study. Compared to the pure MgH2, the initial hydrogen desorption temperature of MgH2?MgC0.5Co3 composite lowered to 237 ?C, decreasing by 141 ?C. At 325 ?C the MgH2?MgC0.5Co3 composite could release 4.38 wt% H2 within 60 min, which is 4.5 times the capacity of hydrogen released by as milled-MgH2. Besides, the hydrogen desorption activation energy of the MgH2?MgC0.5Co3 composite was dramatically reduced to 126.7 ? 1.4 kJ/mol. It was observed that MgC0.5Co3 was chemically stable and no chemical transformation occurred after cycling, which not only inhibited the nucleation and growth of composite particles, but also had a positive effect on the hydrogen desorption reaction of MgH2 due to its catalytic effect. This study may provide references for designing and synthesizing Mg?C?Co alloy compound for the Mg-based hydrogen storage area.
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页码:264 / 269
页数:6
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