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

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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.