Abstract
Density functional theory calculations were adopted to systematically investigate the adsorption and diffusion behaviors of sodium and aluminum over TiB2 surfaces or in TiB2 crystal to characterize the interaction mechanism between sodium and TiB2 cathode in aluminum reduction cells. Results suggest that Na and Al will stably adsorbe on the low-index TiB2 (0 0 0 1) surface, and the presence of vacant defects can significantly strengthen this adsorption. The migration of Na and Al over pristine TiB2 is anisotropic, with the largest energy barrier of 0.024/0.32 eV for Na and 0.28/1.57 eV for Al over Ti/B-terminated surfaces. The Ti vacancy in Ti-terminated surface is more effective to hinder Na and Al migration with the large diffusion barriers of 0.36 eV for Na and 2.07 eV for Al. Specially, for the B-terminated surface, B vacancy will promote the Na and Al diffusion with the lower barriers. Additionally, it is difficult for Na and Al to form interstitial defects and diffuse in covalent TiB2 crystal. Given these results, compared to graphite cathode, the sodium prefers to deposit on TiB2 surface, and the strong interaction between sodium and TiB2 promotes the early process of sodium penetration. On the other hand, the smoother landscape for Na diffusion on the TiB2 surface suggests the decreased stability of aluminum liquid, so that the current efficiency of aluminum reduction cell will decrease.
NSTL
Elsevier