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Open AccessArticle

Rapid Microwave Synthesis, Characterization and Reactivity of Lithium Nitride Hydride, Li4NH

1
WestCHEM, School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK
2
Ecole Nationale Supérieure de Chimie de Clermont-Ferrand, Université Blaise Pascal, BP 187, Aubière Cedex 63174, France
*
Author to whom correspondence should be addressed.
Materials 2013, 6(11), 5410-5426; https://doi.org/10.3390/ma6115410
Received: 8 October 2013 / Revised: 23 October 2013 / Accepted: 11 November 2013 / Published: 21 November 2013
(This article belongs to the Section Manufacturing Processes and Systems)
Lithium nitride hydride, Li4NH, was synthesised from lithium nitride and lithium hydride over minute timescales, using microwave synthesis methods in the solid state for the first time. The structure of the microwave-synthesised powders was confirmed by powder X-ray diffraction [tetragonal space group I41/a; a = 4.8864(1) Å, c = 9.9183(2) Å] and the nitride hydride reacts with moist air under ambient conditions to produce lithium hydroxide and subsequently lithium carbonate. Li4NH undergoes no dehydrogenation or decomposition [under Ar(g)] below 773 K. A tetragonal–cubic phase transition, however, occurs for the compound at ca. 770 K. The new high temperature (HT) phase adopts an anti-fluorite structure (space group Fm 3̅ m; a = 4.9462(3) Å) with N3− and H ions disordered on the 4a sites. Thermal treatment of Li4NH under nitrogen yields a stoichiometric mixture of lithium nitride and lithium imide (Li3N and Li2NH respectively). View Full-Text
Keywords: nitride; hydride; structure; microwaves; synthesis; hydrogen storage; diffraction; thermal analysis; reactivity nitride; hydride; structure; microwaves; synthesis; hydrogen storage; diffraction; thermal analysis; reactivity
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Tapia-Ruiz, N.; Sorbie, N.; Vaché, N.; Hoang, T.K.A.; Gregory, D.H. Rapid Microwave Synthesis, Characterization and Reactivity of Lithium Nitride Hydride, Li4NH. Materials 2013, 6, 5410-5426.

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