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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