Synergic catalytic effect of Ti hydride and Nb nanoparticles for improving hydrogenation and dehydrogenation kinetics of Mg-based nanocomposite

被引:0
作者
Xiujuan Ma [1 ]
Xiubo Xie [1 ]
Peng Liu [1 ]
Li Xu [2 ]
Tong Liu [1 ]
机构
[1] Key Laboratory of Aerospace Materials and Performance (Ministry of Education), School of Materials Science and Engineering, Beihang University
[2] State Grid Smart Grid Research Institute, Future Science and Technology City Changping
关键词
Magnesium; Nanocomposite; Catalytic effect; Hydrogen storage;
D O I
暂无
中图分类号
TB33 [复合材料]; O643.36 [催化剂];
学科分类号
0805 ; 080502 ; 081705 ;
摘要
The Mg-9.3 wt%(TiH1.971-TiH)-0.7 wt% Nb nanocomposite has been synthesized by hydrogen plasma-metal reaction(HPMR) approach to enhance the hydrogen sorption kinetics of Mg at moderate temperatures by providing nanosizing effect of increasing H "diffusion channels" and adding transition metallic catalysts. The Mg nanoparticles(NPs) were in hexagonal shape range from 50 to 350 nm and the average size of the NPs was 177 nm. The small spherical TiH1.971, TiH and Nb NPs of about 25 nm uniformly decorated on the surface of the big Mg NPs. The Mg-TiH1.971-TiH-Nb nanocomposite could quickly absorb 5.6 wt% H2 within 5 min at 573 K and 4.5 wt% H2 within 5 min at 523 K, whereas the pure Mg prepared by HPMR could only absorb 4 and 1.5 wt% H2 at the same temperatures. TiH1.971, TiH and Nb NPs transformed into TiH2 and Nb H during hydrogenation and recovered after dehydrogenation process. The apparent activation energies of the nanocomposite for hydrogenation and dehydrogenation were 45.0 and 50.7 kJ mol-1, which are much smaller than those of pure Mg NPs, 123.8 and 127.7 kJ mol-1. The improved sorption kinetics of the Mg-based nanocomposite at moderate temperatures and the small activation energy can be interpreted by the nanostructure of Mg and the synergic catalytic effects of Ti hydrides and Nb NPs.
引用
收藏
页码:99 / 104
页数:6
相关论文
共 2 条
[1]  
J.Huot,G.Liang,S.Boily,A.Van Neste,R.Schulz. J.Alloy.Compd . 1999
[2]  
N.S.Norberg,T.S.Arthur,S.J.Fredrick,A.L.Prieto. J.Am.Chem.Soc . 2011