Characterization of H2 Binding Sites in Prototypical Metal−Organic Frameworks by Inelastic Neutron Scattering

Abstract

The hindered rotor transitions of H₂ adsorbed in the chemically related and prototypical porous metal−organic frameworks IRMOF-1, IRMOF-8, IRMOF-11, and MOF-177 were studied by inelastic neutron scattering to gain information on the specifics of H₂ binding in this class of adsorbents. Remarkably sharp and complex spectra of these materials signify a diversity of well-defined binding sites. Similarities in the spectral features as a function of H₂ loading and correlations with recent crystallographic studies were used to assign transitions ranging in rotational barrier from 2 at the inorganic cluster sites is affected by the nature of the organic link and is strongest in IRMOF-11 in accord with our adsorption isotherm data. The sites on the organic link have lower binding energies, but a much greater capacity for increases in H₂ loading, which demonstrates their importance for hydrogen uptake by these materials.