Syntheses of alkali-metal carbazolides for hydrogen storage

摘要

Metalorganic hydrides are a new class of hydrogen storage materials. Replacing the H of N-H or O-H functional groups using metal hydrides have been recently reported, which substantially improved the dehydrogenation properties of heteroaromatic organic hydrides by lowering their enthalpies of dehydrogenation (DHd), enabling dehydrogenation at much lower temperatures. Among the reported metalorganic hydrides, lithium carbazolide and sodium carbazolide appear to be the most attractive hydrogen storage/delivery material owing to its high hydrogen capacity (6.0 wt%) and ideal DHd. Nevertheless, the interaction of carbazole and corresponding metal hydride to form metallo-carbazolide is a multistep process involving intensive ball milling and high temperature treatment, where the interaction was not investigated in detail. In this paper, both alkali metal hydrides and amides were employed to react with carbazole to synthesize corresponding carbazolides, aiming to broaden and optimize the synthetic method and understand the reaction mechanism. Our experimental results showed that around one equivalent of H-2 or NH3 could be released from the reactions of carbazole and corresponding hydrides or amides, respectively. Instrumental spectroscopic analyses proved that metallo-carbazolides were successfully synthesized from all precursors. It is found that the alkali metal amides (i.e., LiNH2 and NaNH2) with stronger Lewis basicities as metal precursors could synthesize the metallo-carbazolides under milder conditions. Furthermore, quasi in situ nuclear magnetic resonance results revealed that alkali metal could replace H (H-N) gradually, donating more electrons to carbazole ring. Additionally, the solubilized alkali cation may unselectively interact with n-electron of aromatic systems of both carbazole molecules and carbazolide anions via electrostatic cation-n interactions. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.