Intrinsic defects and dopants in LiNH2: a first-principles study

• Published in: Physical chemistry chemical physics : PCCP 2011-04, Vol.13 (13), p.6043-6052
• Main Authors: HAZRATI, E, BROCKS, G, BUURMAN, B, DE GROOT, R. A, DE WIJS, G. A
• Format: Article
• Language: English
• Subjects: Amides; Chemistry; Crystal defects; Crystal lattices; Diffusion barriers; Dopants; Exact sciences and technology; General and physical chemistry; Magnesium; Nanostructure; Titanium
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/c0cp01540g

The lithium amide (LiNH(2)) + lithium hydride (LiH) system is one of the most attractive light-weight materials options for hydrogen storage. Its dehydrogenation involves mass transport in the bulk (amide) crystal through lattice defects. We present a first-principles study of native point defects and dopants in LiNH(2) using density functional theory. We find that both Li-related defects (the positive interstitial Li(i)(+) and the negative vacancy V(Li)(-)) and H-related defects (H(i)(+) and V(H)(-)) are charged. Li-related defects are most abundant. Having diffusion barriers of 0.3-0.5 eV, they diffuse rapidly at moderate temperatures. V(H)(-) corresponds to the [NH](2-) ion. It is the dominant species available for proton transport with a diffusion barrier of ∼0.7 eV. The equilibrium concentration of H(i)(+), which corresponds to the NH(3) molecule, is negligible in bulk LiNH(2). Dopants such as Ti and Sc do not affect the concentration of intrinsic defects, whereas Mg and Ca can alter it by a moderate amount. Ti and Mg are easily incorporated into the LiNH(2) lattice, which may affect the crystal morphology on the nano-scale.