4.7 Article

Effect of LiH on hydrogen storage property of MgH2

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 39, Issue 25, Pages 13622-13627

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2014.02.131

Keywords

Hydrogen storage materials; MgH2; LiH; Ball milling; H-H exchange

Funding

  1. Instrumental Analysis and Research Center of Shanghai University
  2. National Natural Science Foundation of China [51222402, 21071149]
  3. Innovation Program of Shanghai Municipal Education Commission [12YZ012]
  4. Shu Guang project
  5. Shanghai Municipal Education Commission
  6. Shanghai Education Development Foundation [13SG39]

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Recent works showed that the addition of LiBH4 significantly improves the sorption kinetics of MgH2, and LiH decomposed from LiBH4 was supposed to play the catalytic effect on MgH2. In order to clarify this mechanism, the effect of LiH on the hydriding/dehydriding kinetics and thermodynamics of MgH2 was systematically investigated. The hydrogenation kinetics of LiH-doped samples, as well as the morphology after several cycles, was similar to those of pure MgH2, which indicate that Li+ had no catalytic effect on the hydrogenation of Mg. Moreover, the addition of LiH strongly retarded the hydrogen desorption of MgH2 doped with/without Nb2O5, and resulted in higher starting temperature of desorption, larger activation energy and larger pressure hysteresis of PCI curves of MgH2. H-2, HD and D-2 were observed in the desorption products of MgH2-2LiD, which confirms that H-H exchange indeed occurs between MgH2 and LiH, hence deteriorate desorption kinetics/thermodynamics of MgH2. The results implied that the additives containing H- could retard the hydrogen desorption of MgH2 by H-H exchange effect. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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