Graphene-loaded nickel-vanadium bimetal oxides as hydrogen pumps to boost solid-state hydrogen storage kinetic performance of magnesium hydride

被引:5
作者
Gao, Dong-qiang [1 ]
Wu, Fu-ying [2 ]
Zhang, Zhi [1 ]
Lu, Zi-chuan [1 ]
Zhou, Ren [1 ]
Zhao, Hu [3 ]
Zhang, Liu-ting [1 ,3 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Energy & Power, Zhenjiang 212003, Peoples R China
[2] Jiangsu Univ Sci & Technol, Instrumental Anal Ctr, Zhenjiang 212003, Peoples R China
[3] Nanyang Technol Univ, Sch Mech & Aerosp Engn, Singapore 639798, Singapore
基金
中国国家自然科学基金;
关键词
hydrogen storage properties; MgH2; graphene-loaded Ni-V - V bimetal oxides; catalytic mechanism; DEHYDROGENATION; NANOPARTICLES; DIFFUSION; SIZE; MGH2;
D O I
10.1016/S1003-6326(24)66566-0
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
To modify the thermodynamics and kinetic performance of magnesium hydride (MgH2) for solid-state hydrogen storage, Ni3V2O8-rGO (rGO represents reduced graphene oxide) and Ni3V2O8 nanocomposites were prepared by hydrothermal and subsequent heat treatment. The beginning hydrogen desorption temperature of 7 wt.% Ni3V2O8-rGO modified MgH2 was reduced to 208 degrees C, while the additive-free MgH2 and 7 wt.% Ni3V2O8 doped MgH(2 )appeared to discharge hydrogen at 340 and 226 degrees C, respectively. A charging capacity of about 4.7 wt.% H-2 for MgH2 + 7 wt.% Ni3V2O8-rGO was achieved at 125 degrees C in 10 min, while the dehydrogenated MgH2 took 60 min to absorb only 4.6 wt.% H-2 at 215 degrees C. The microstructure analysis confirmed that the in-situ generated Mg2Ni/Mg2NiH4 and metallic V contributed significantly to the enhanced performance of MgH2. In addition, the presence of rGO in the MgH2 + 7 wt.% Ni3V2O8-rGO composite reduced particle aggregation tendency of Mg/MgH2, leading to improving the cyclic stability of MgH2 during 20 cycles.
引用
收藏
页码:2645 / 2657
页数:13
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