Aluminium complexes of B- and N-based hydrides: synthesis, structures and hydrogen storage properties

The storage of hydrogen in a solid state is one of the main challenges for stationary and mobile applications. Light metal hydrides have attracted significant attention as potential candidates for energy storage. Remarkably, Al-containing hydrides, namely AlH3 and M(AlH4)n, are among the most fascinating classes of materials, able to cycle up to 5.5 wt% of hydrogen at moderate temperatures. This review covers the recent research on the families of Al-based complex hydrides involving other light elements such as B and N. They were classified according to the charge of the Al-based complexes, as anionic, molecular, cationic or “autoionized” where Al is centering both the cation and the anion. The factors influencing the stability and the hydrogen purity of the series of anionic aluminium amides M[Al(NH2)4]n, borohydrides M[Al(BH4)4] and amidoboranes M[Al(NH2BH3)4], as well as molecular [Al(L)(BH4)3] (L ¼ molecular ligands) and cation [Al(NH3)6]3þ-based complexes are discussed. In particular, the ability of the strong Lewis acid Al3þ to coordinate both the initial hydrogenated species as well as their dehydrogenation products makes it a good template for chemical transformations involving light chemical and complex hydrides