Electrolyte-Assisted Hydrogen Cycling In Lithium And Sodium Alanates At Low Pressures And Temperatures

An investigation of electrolyte-assisted hydrogen storage reactions in complex aluminum hydrides (LiAlH4 and NaAlH4) reveals significantly reduced reaction times for hydrogen desorption and uptake in the presence of an electrolyte. LiAlH4 evolves similar to 7.8 wt% H-2 over similar to 3 h in the presence of a Li-KBH4 eutectic at 130 degrees C compared to similar to 25 h for the same material without the electrolyte. Similarly, NaAlH4 exhibits 4.8 wt% H-2 evolution over similar to 4 h in the presence of a diglyme electrolyte at 150 degrees C compared to 4.4 wt% in similar to 15 h for the same material without the electrolyte. These reduced reaction times are composed of two effects, an increase in reaction rates and a change in the reaction kinetics. While typical solid state dehydrogenation reactions exhibit kinetics with rates that continuously decrease with the extent of reaction, we find that the addition of an electrolyte results in rates that are relatively constant over the full desorption window. Fitting the kinetics to an Avrami-Erofe'ev model supports these observations. The desorption rate coefficients increase in the presence of an electrolyte, suggesting an increase in the velocities of the reactant-product interfaces. In addition, including an electrolyte increases the growth parameters, primarily for the second desorption steps, resulting in the observed relatively constant reaction rates. Similar effects occur upon hydrogen uptake in NaH/Al where the presence of an electrolyte enables hydrogenation under more practical low temperature (75 degrees C) and pressure (50 bar H-2) conditions.