MgH2 with different morphologies synthesized by thermal hydrogenolysis method for enhanced hydrogen sorption

被引:49
作者
Setijadi, Eki J. [1 ,2 ]
Boyer, Cyrille [2 ]
Aguey-Zinsou, Kondo-Francois [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn, MERLin Grp, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Chem Engn, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
Hydrogen storage; Magnesium; Organomagnesium; Hydrogenolysis; Nanoparticles; Kinetics; STORAGE PROPERTIES; MAGNESIUM HYDRIDE; CATALYTIC SYNTHESIS; KINETICS; BEHAVIOR; NB2O5; SIZE; MGO;
D O I
10.1016/j.ijhydene.2013.02.128
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
Magnesium hydride (MgH2) with a range of morphologies has been synthesized via a simple hydrogenolysis route involving the decomposition of di-n-butylmagnesium. As the synthetic medium evolved from an inert atmosphere of argon to hydrogen pressure, the morphology shifted from rod like to small particles (25-170 nm). In cyclohexane, a solvent relative inert toward magnesium, smaller particles (15-50 nm) were formed. However in diethyl ether, which is more reactive toward magnesium, flakes organized in large microstructures were obtained. Remarkably in all cases beta-MgH2 was readily obtained with some residual carbon contamination. Hydrogen release from these structures occurred at a relatively low temperature (300 degrees C), with desorption kinetics faster or equivalent to that of ball milled magnesium. In particular, hydrogen desorption from the smallest particles of MgH2 produced via the hydrogenolysis of di-n-butylmagnesium under hydrogen pressure or cyclohexane was impressive with the full desorption achieved in less than 10 min without any catalyst. These remarkable hydrogen storage properties are believed to result from an appropriate stabilization of the nanoparticles generated. Crown Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5746 / 5757
页数:12
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