Combination of two H-enriched B–N based hydrides towards improved dehydrogenation properties

Abstract

Abstract A new hydrogen storage system NaZn(BH 4 ) 3 ∙2NH 3 - n NH 3 BH 3 ( n = 1–5) was synthesized via a simple ball milling of NaZn(BH 4 ) 3 ∙2NH 3 and NH 3 BH 3 (AB) with a molar ratio from 1 to 5. Dehydrogenation results revealed that NaZn(BH 4 ) 3 ∙2NH 3 - n AB ( n = 1–5) showed a mutual dehydrogenation improvement in terms of significant decrease in the dehydrogenation temperature and preferable suppression of the simultaneous evolution of by-products (i.e. NH 3 , B 2 H 6 and borazine) compared to the unitary compounds (NaZn(BH 4 ) 3 ∙2NH 3 and AB). Specially, the NaZn(BH 4 ) 3 ∙2NH 3 -4AB sample is shown to reach the maximum hydrogen purity (99.1 mol %) and favorable dehydrogenation properties rapidly releasing 11.6 wt. % of hydrogen with a peak maximum temperature of 85 °C upon heating to 250 °C. Isothermal dehydrogenation results revealed that 9.6 wt. % hydrogen was liberated from NaZn(BH 4 ) 3 ∙2NH 3 -4AB within 80 min at 90 °C. High-resolution in-situ XRD and Fourier transform infrared (FT-IR) measurements indicated that the significant improvements on the dehydrogenation properties in NaZn(BH 4 ) 3 ∙2NH 3 -4AB can be attributed to the interaction between the NH 3 group from NaZn(BH 4 ) 3 ∙2NH 3 and AB in the mixture, resulting a more activated H δ+ ··· −δ H combination. The research on the reversibility of the spent fuels of NaZn(BH 4 ) 3 ∙2NH 3 -4AB showed that regeneration could be partly achieved by reacting them with hydrazine in liquid ammonia. These aforementioned favorable dehydrogenation properties demonstrate the potential of the combined systems to be used as solid hydrogen storage material.