Hydrogen Desorption Processes in Li-Mg-N-H Systems

Journal of Physics and Chemistry of Solids Volume 69 Issue 9 Page 2234-2236 published_at 2008-09
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Title ( eng )
Hydrogen Desorption Processes in Li-Mg-N-H Systems
Creator
Isobe Shigehito
Leng Haiyan
Fujii Hironobu
Source Title
Journal of Physics and Chemistry of Solids
Volume 69
Issue 9
Start Page 2234
End Page 2236
Abstract
Li-Mg-N-H systems composed of Mg(NH2)2 and LiH with various ratios can reversibly store a large amount of hydrogen under the temperature condition above 150 °C. These composites with 3:6, 3:8 and 3:12 ratio of Mg(NH2)2 and LiH have been independently reported by four groups as promising candidates of high performance hydrogen storage materials possessing the reversibility and the high capacity. In any cases, an interaction between NH3 and LiH plays an important role for the progress of hydrogen desorbing and absorbing reactions. For the hydrogen desorption process, the NH3 molecule generated from Mg(NH2)2 reacts with LiH, forming LiNH2 and H2. Especially, under an equilibrium condition, in-situ diffraction results indicated that the single phase of LiNH2•MgNH (LiMgN2H3) could be generated other than the separated two phases. As a next step, the NH3 molecule generated from LiNH2 reacts with LiH, desorbing H2. As a result, the dehydrogenated phase was evaluated to be Li2NH•MgNH (Li2MgN2H2) or separated two phases, in which the final phase should depend on the experimental conditions. Thus, if the amount of LiH is enough to react with NH3, the hydrogen desorption processes are described by the NH3 generation from the corresponding amides and the imide.
Keywords
Inorganic compounds
Chemical synthesis
Thermogravimetric analysis (TGA)
X-ray diffraction
Thermodynamic properties
NDC
Chemistry [ 430 ]
Language
eng
Resource Type journal article
Publisher
Pergamon
Elsevier Science Ltd.
Date of Issued 2008-09
Rights
Copyright (c) 2008 Elsevier Ltd
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0022-3697
[DOI] 10.1016/j.jpcs.2008.04.002
[NCID] AA00704949
[DOI] http://dx.doi.org/10.1016/j.jpcs.2008.04.002