共 64 条
Superior hydrogen storage kinetics of MgH2 by in-situ generated α-Fe from the Fe-zeolitic imidazolate framework
被引:25
作者:
Yang, Huimin
[1
,2
]
Sun, Xuan
[3
,4
,5
]
Luo, Qun
[3
,4
,5
]
Lu, Yangfan
[1
,2
]
Li, Qian
[1
,2
,3
,4
,5
]
Pan, Fusheng
[1
,2
]
机构:
[1] Chongqing Univ, Natl Engn Res Ctr Magnesium Alloys, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China
[3] Shanghai Univ, State Key Lab Adv Special Steel, Shanghai 200444, Peoples R China
[4] Shanghai Univ, Sch Mat Sci & Engn, Shanghai 200444, Peoples R China
[5] Shanghai Univ, Shanghai Key Lab Adv Ferromet, Shanghai 200444, Peoples R China
关键词:
Hydrogen storage;
kinetics;
Fe-ZIF catalyst;
Magnesium;
HIGH-TEMPERATURE OXIDATION;
HYDRIDING KINETICS;
TRANSITION-METAL;
TM TM;
NI;
TI;
PERFORMANCE;
ALLOY;
CO;
DEHYDROGENATION;
D O I:
10.1016/j.scriptamat.2023.115782
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
While MgH2 is one of the promising hydrogen storage materials, its poor de/hydrogenation kinetics have hindered its potential applications. Here, we report that kinetic and cycle properties can be improved using Fe-doped zeolitic imidazolate framework (Fe-ZIF) as the catalysts. The synthesized MgH2@5 wt.% Fe-ZIF can absorb 5.0 wt.% hydrogen in 1 min at 200 degrees C and desorb 5.0 wt.% hydrogen within 16 min at 300 degrees C. No clear degradation of catalytic effects was observed over 30 cycles. Structural analysis revealed that the Fe-ZIF gradually decomposed into alpha-Fe, which strongly interacts with MgH2, realizing much higher catalytic activity and stability. Furthermore, the Fe-ZIF is characterized by a simple process and low cost nature, posing the metal-ZIF composite as a promising platform to disperse nano-catalysts in Mg-based hydrogen storage materials.
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页数:6
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