Hydrogen tracer diffusion in LiBH4 measured by spatially resolved Raman spectroscopy.

The hydrogen tracer diffusion in LiBH(4) has been determined by spatially resolved Raman spectroscopy. The measurements give direct evidence of a macroscopic diffusion of BH ions as well as atomic exchange of hydrogen between the anions. An effective tracer diffusion coefficient of deuterium in LiBH(4) of D approximately 7 x 10(-14) m(2) s(-1) at 473 K is derived. The direct exchange rate of hydrogen between BH(4) units is 10 orders of magnitude slower, i.e. the relatively fast effective hydrogen diffusion has its origin in the fast diffusion of BH(4) units.

Structural stability and decomposition of Mg(BH(4))(2) isomorphs-an ab initio free energy study.

We present the first comprehensive comparison between free energies, based on a phonon dispersion calculation within density functional theory, of theoretically predicted structures and the experimentally proposed α (P6(1)) and ß (Fddd) phases of the promising hydrogen storage material Mg(BH(4))(2). The recently proposed low-density [Formula: see text] ground state is found to be thermodynamically unstable, with soft acoustic phonon modes at the Brillouin zone boundary. We show that such acoustic instabilities can be detected by a macroscopic distortion of the unit cell. Following the atomic displacements of the unstable modes, we have obtained a new F 222 structure, which has a lower energy than all previously experimentally and theoretically proposed phases of Mg(BH(4))(2) and is free of imaginary eigenmodes. A new meta-stable high-density I4(1)/amd structure is also derived from the [Formula: see text] phase. Temperatures for the decomposition are found to be in the range of 400-470 K and largely independent of the structural complexity, as long as the primary cation coordination polyhedra are properly represented. This opens a possibility of using simple model structures for screening and prediction of finite temperature stability and decomposition temperatures of novel borohydride systems.

High-resolution Raman spectroscopy study of phonon modes in LiBH4 and LiBD4.

We have performed micro Raman measurements on LiBH4 and LiBD4 powders for temperatures between 5 and 300 K. At the lowest temperature, the peak energies agree very well with the results of a calculation within the density functional theory for the orthorhombic structure. The spectra are dominated by three separated bands: the external modes, the internal bending, and the internal stretching vibrations. Internal refers to vibrations within the BH 4 tetrahedrons, whereas external modes imply motions of Li and BH 4. The temperature dependence of the observed phonons corroborates the strong anharmonicity of the system. Due to the anharmonicity, Fermi resonances occur between the first order stretching modes and the second order bending modes of LiBH4. Moreover, the linewidths of the observed modes in LiBH4 have an Arrhenius-like component, with activation energies ranging from 250 to 500 K.

Structure of Ca(BD4)2 beta-phase from combined neutron and synchrotron X-ray powder diffraction data and density functional calculations.

We have investigated the crystal structure of Ca(BD4)2 by combined synchrotron radiation X-ray powder diffraction, neutron powder diffraction, and ab initio calculations. Ca(BD4)2 shows a variety of structures depending on the synthesis and temperature of the samples. An unknown tetragonal crystal of Ca(BD4)2, the beta phase has been solved from diffraction data measured at 480 K on a sample synthesized by solid-gas mechanochemical reaction by using MgB2 as starting material. Above 400 K, this sample has the particularity to be almost completely into the beta phase of Ca(BD4)2. Seven tetragonal structure candidates gave similar fit of the experimental data. However, combined experimental and ab initio calculations have shown that the best description of the structure is with the space group P4(2)/m based on appropriate size/geometry of the (BD4)tetrahedra, the lowest calculated formation energy, and real positive vibrational energy, indicating a stable structure. At room temperature, this sample consists mainly of the previously reported alpha phase with space group Fddd. In the diffraction data, we have identified weak peaks of a hitherto unsolved structure of an orthorombic gamma phase of Ca(BD4)2. To properly fit the diffraction data used to solve and refine the structure of the beta phase, a preliminary structural model of the gamma phase was used. A second set of diffraction data on a sample synthesized by wet chemical method, where the gamma phase is present in significant amount, allowed us to index this phase and determine the preliminary model with space group Pbca. Ab initio calculations provide formation energies of the alpha phase and beta phase of the same order of magnitude (delta H < or = 0.15 eV). This indicates the possibility of coexistence of these phases at the same thermodynamical conditions.

Suppression of the order parameter correlation length by inhomogeneous strains

Very recently we presented puzzling results of diffuse neutron scattering experiments on KSCN and RbSCN. The data yield an increase of the diffuse intensity with increasing temperature below T(c), whereas the width remains constant. Using molecular dynamics and 3D Monte Carlo simulations, we have shown that below T(c) the width of the correlation functions can be stabilized by strain fields originating from the order parameter strain interactions. Here we construct a novel analytic model which predicts the existence of a second characteristic length scale and explains the suppression of the growth of precursor clusters by the influence of inhomogeneous strain fields.