Jump to main content
Jump to site search

Issue 34, 2015
Previous Article Next Article

Mechanochemistry of lithium nitride under hydrogen gas

Author affiliations


Hydrogen uptake during the mechanochemistry of lithium nitride under 9 MPa hydrogen pressure has been analyzed by means of in situ solid–gas absorption and ex situ X-ray diffraction (XRD) measurements. In situ hydrogenation curves show two H-sorption steps leading to an overall hydrogen uptake of 9.8 wt% H after 3 hours of milling. The milled end-products consist of nanocrystalline (∼10 nm) LiNH2 and LiH phases. The first reaction step comprises the transformation of the polymorph α-Li3N (S.G. P6/mmm) into the β-Li3N (S.G. P63/mmc) metastable phase and the reaction of the latter with hydrogen to form lithium imide: β-Li3N + H2 → Li2NH + LiH. Reaction kinetics of the first step is zero-order. Its rate-limiting control is assigned to the collision frequency between milling balls and Li3N powder. In the second absorption step, lithium imide converts to lithium amide following the reaction scheme Li2NH + H2 → LiNH2 + LiH. Reaction kinetics is here limited by one-dimensional nucleation and the growth mechanism, which, in light of structural data, is assigned to the occurrence of lithium vacancies in the imide compound. This study provides new insights into the reaction paths and chemical kinetics of light hydrogen storage materials during their mechanochemical synthesis.

Graphical abstract: Mechanochemistry of lithium nitride under hydrogen gas

Back to tab navigation

Supplementary files

Publication details

The article was received on 15 May 2015, accepted on 26 Jul 2015 and first published on 28 Jul 2015

Article type: Paper
DOI: 10.1039/C5CP02812D
Author version
Download author version (PDF)
Phys. Chem. Chem. Phys., 2015,17, 21927-21934

  •   Request permissions

    Mechanochemistry of lithium nitride under hydrogen gas

    Z. Li, J. Zhang, S. Wang, L. Jiang, M. Latroche, J. Du and F. Cuevas, Phys. Chem. Chem. Phys., 2015, 17, 21927
    DOI: 10.1039/C5CP02812D

Search articles by author