Hydrogen storage in MOF-5: A van der Waals density functional theory study

Abstract

Physisorption of hydrogen molecules in metal-organic frameworks (MOFs) provides a promising way for hydrogen storage, in which the van der Waals (vdW) interaction plays an important role but cannot described by the density functional theory (DFT). By using the vdW density functional (vdW-DF) method, we investigate systematically the binding energies of hydrogen molecules in MOF-5 crystal. We first examine the accuracy of this methodology by comparing its results with those from the correlated quantum chemistry methods for several fragment models cut out from the crystal. Good comparable accuracy is found. By performing calculations for the true crystal structure adsorbing one or multiple H$_2$ in the primitive cell, we show that these fragment models which have been focused previously cannot represent well the property of the crystal which cannot, however, be dealt with by the quantum chemistry methods. It is found that the binding energy with the organic linker is much smaller than with the metal oxide corner, which limits the H$_2$ loading. We show that this can be improved significantly (from 5.50 to 10.39 kJ/mol) by replacing the H atoms of the organic linker with F atoms which cause extra electrostatic interaction.