Implementation of a Core–Shell Design Approach for Constructing MOFs for CO₂ Capture

Abstract

Adsorption-based capture of CO₂ from flue gas and from air requires materials that have a high affinity for CO₂ and can resist water molecules that competitively bind to adsorption sites. Here, we present a core-shell metal-organic framework (MOF) design strategy where the core MOF is designed to selectively adsorb CO₂, and the shell MOF is designed to block H₂O diffusion into the core. To implement and test this strategy, we used the zirconium (Zr)-based UiO MOF platform because of its relative structural rigidity and chemical stability. Previously reported computational screening results were used to select optimal core and shell MOF compositions from a basis set of possible building blocks, and the target core-shell MOFs were prepared. Their compositions and structures were characterized using scanning electron microscopy, transmission electron microscopy, and powder X-ray diffraction. Multigas (CO₂, N₂, and H₂O) sorption data were collected both for the core-shell MOFs and for the core and shell MOFs individually. These data were compared to determine whether the core-shell MOF architecture improved the CO₂ capture performance under humid conditions. The combination of experimental and computational results demonstrated that adding a shell layer with high CO₂/H₂O diffusion selectivity can significantly reduce the effect of water on CO₂ uptake.