Hydrogen vacancies facilitate hydrogen transport kinetics in sodium hydride nanocrystallites

Abstract

We report ab initio calculations based on density-functional theory, of the vacancy-mediated hydrogen migration energy in bulk NaH and near the NaH(001) surface. The estimated rate of the vacancy-mediated hydrogen transport, obtained within a hopping diffusion model, is consistent with the reaction rates of H-D exchange in nano-NaH at the relatively low temperatures observed in recent neutron studies on ${\text{TiCl}}_{3}$-doped ${\text{NaAlH}}_{4}$. We further obtained the formation energy for hydrogen vacancies and interstitials in NaH in all relevant charged states. These formation energies are too high to lead to the abundant hydrogen concentrations seen experimentally. Ab initio calculations on the NaCl//NaH interface are presented to provide an insight into the mechanism which may lead to high hydrogen concentrations. We show that the formation of an fcc-Na interlayer during the growth of NaH on top of NaCl is plausible, providing a source of vacancies and leading to fast hydrogen transport. The low interface energies for NaCl//NaH are consistent with an easy growth of NaH crystallites on NaCl nucleation centers, which may, therefore, act as grain refiners.