Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 5, Pages 1862-1870Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja806565t
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Funding
- National Natural Foundation of China [50631020, 50701040]
- National High-Technology Research and Development Plan (863 Program) [2006AA05Z127]
- Qianjiang Talent Project of Zhejiang Province [QJD0702005]
- State Education Ministry for Returned Overseas Chinese Scholars.
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High operating temperature and slow kinetics retard the practical applications of the Li-Mg-N-H system for hydrogen storage. To alleviate these problems, a first attempt was carried out by synthesizing Li2MgN2H2 through sintering a mixture of Mg(NH2)(2)-2LiNH(2) and investigating its size-dependent hydrogen storage performance. A dramatically enhanced kinetics for hydrogen absorption/desorption was achieved with a reduction in the particle size. For the dehydrogenation reaction, a three-dimensional diffusion-controlled kinetic mechanism was identified for the first time by analyzing isothermal hydrogen desorption curves with a linear plot method. The experimental improvement and mechanistic understanding on the dehydrogenation kinetics of the Li-Mg-N-H system shed light on how to further decrease the operating temperature and enhance the hydrogen absorption/desorption rate of the amide/hydride combined materials.
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