Oh, H.; Tumanov, N.; Ban, V.; Li, X.; Richter, B.; Hudson, M.R.; Brown, C.M.; Iles, G.N.; Wallacher, D.; Jorgensen, S.W.; Daemen, L.; Balderas-Xicohténcatl, R.; Cheng, Y.; Ramirez-Cuesta, A.J.; Heere, M.; Posada-Pérez, S.; Hautier, G.; Hirscher, M.; Jensen, T.R.; Filinchuk, Y.: Small-pore hydridic frameworks store densely packed hydrogen. Nature Chemistry 16 (2024), p. 809-816
10.1038/s41557-024-01443-x
Open Accesn Version
Abstract:
Nanoporous materials have attracted great attention for gas storage, but achieving high volumetric storage capacity remains a challenge. Here, byusing neutron powder diffraction, volumetric gas adsorption, inelastic neutron scattering and first-principles calculations, we investigate a magnesium borohydride framework that has small pores and a partially negatively charged non-flat interior for hydrogen and nitrogen uptake. Hydrogen and nitrogen occupy distinctly different adsorption sites in the pores, with very different limiting capacities of 2.33 H2 and 0.66 N2 per Mg(BH4)2. Molecular hydrogen is packed extremely densely, with about twice the density of liquid hydrogen (144 g H2 per litre of pore volume). We found a penta-dihydrogen cluster where H2 molecules in one position have rotational freedom, whereas H2 molecules in another position have a well-defined orientation and a directional interaction with the framework. This study reveals that densely packed hydrogen can be stabilized in small-pore materials at ambient pressures.