Issue 21, 2013

Molecular dynamics investigation of the disordered crystal structure of hexagonal LiBH4

Abstract

The crystal structure of the hexagonal phase of solid lithium borohydride (LiBH4) is studied by ab initio molecular dynamics simulations of both the low and high-temperature phases. A temperature range of 200–535 K is simulated with the aim of characterising the disorder in the high-temperature structure in detail. The mechanism and kinetics of the reorientational motion of the borohydride units (BH4) are determined and are consistent with published neutron scattering experiments; it is found that rotational diffusivity increases by an order of magnitude at the phase transition temperature. The average equilibrium orientation is characterised by a broad distribution of orientations, and reorientational jumps do not occur between sharply defined orientations. In addition, split positions with partial occupancy for the lithium and boron atoms are found (in agreement with previous theoretical studies), which, together with the disordered BH4 orientational distribution in equilibrium, lead to the conclusion that the correct crystallographic space group of the high-temperature phase is P63/mmc rather than P63mc.

Graphical abstract: Molecular dynamics investigation of the disordered crystal structure of hexagonal LiBH4

Article information

Article type
Paper
Submitted
14 Dec 2012
Accepted
29 Jan 2013
First published
29 Jan 2013

Phys. Chem. Chem. Phys., 2013,15, 8081-8087

Molecular dynamics investigation of the disordered crystal structure of hexagonal LiBH4

P. C. Aeberhard, K. Refson and W. I. F. David, Phys. Chem. Chem. Phys., 2013, 15, 8081 DOI: 10.1039/C3CP44520H

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