The role of differently distributed vanadium nanocatalyst in the hydrogen storage of magnesium nanostructures

被引:21
作者
He, Yuping [1 ,2 ]
Fan, Jianguo [1 ,2 ,3 ]
Zhao, Yiping [1 ,2 ]
机构
[1] Univ Georgia, Dept Phys, Nanoscale Sci & Engn Ctr, Athens, GA 30602 USA
[2] Univ Georgia, Dept Astron, Nanoscale Sci & Engn Ctr, Athens, GA 30602 USA
[3] Univ Georgia, Ctr Adv Ultrastruct Res, Athens, GA 30602 USA
基金
美国国家科学基金会;
关键词
Vanadium; Magnesium nanostructures; Hydrogen storage; Contact area; Porosity; TRANSITION-METALS; PARTICLE-SIZE; HYDRIDE; SORPTION;
D O I
10.1016/j.ijhydene.2010.02.103
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using a glancing angle (co)deposition technique, similar to 4.6 at.% V has been coated on the surface of individual Mg nanoblades and doped into Mg nanostructures fabricated at different deposition angles. The hydrogen storage properties of the formed V-decorated and V-doped Mg nanostructures depend strongly on how the nanocatalyst V is surrounded by the host Mg. The V-doped Mg sample has lower activation energies for hydrogen absorption (E-a(a) =35.3 +/- 0.9 kJ/molH(2)) and hydrogen desorption (E-a(d) = 38.9 +/- 0.3 kJ/mol H-2) than the V-decorated Mg sample when deposited at the same deposition angle of theta = 70 degrees. The activation energies of the doped samples increase gradually with the decrease of the theta angle. We also find that the porosity of the Mg nanostructures plays a secondary role. A phenomenological model based on a heterogeneous reaction is proposed to explain the different hydrogen desorption activation energies obtained for different V-Mg nanostructured samples. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4162 / 4170
页数:9
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