Experimental and molecular simulation study of CO2 adsorption in ZIF-8: Atomic heat contributions and mechanism

Abstract

We successfully synthesised ZIF-8 using the solvothermal method at room temperature to study CO₂ adsorption storage at 273 and 298 K up to 35 bar. Characterisation methods such as BET, SEM-EDS, XRD, and TGA were used to measure the physical and composition properties of ZIF-8. Grand canonical Monte Carlo (GCMC) simulation was conducted to compare with experimental data and get inside of the CO₂ adsorption mechanism by calculating the isosteric heat and its fluid–fluid and solid–fluid contributions. The second was also split into fluid–solid atom contributions to understand in detail the interaction between CO₂ and ZIF-8. The analyses revealed that there are three main stages during the CO₂ adsorption gas–solid atom contributions, developing, pore-filling and densification. During the developing and pore-filling stages the largest fluid–solid atom contribution to the isosteric heat is CO₂-C2 interactions, indicating that the CO₂ is adsorbed close to the hexagonal windows of the ZIF-8 structure, while during the densification stage the largest contribution is CO₂-N interactions. Where C2 and N refers to C-atom and N-atom, respectively in NCH group of the solid framework. This is because CO₂ changes its orientation to be able to accommodate more molecules in the pore cavity. This work provides a better understanding of the adsorption mechanism of CO₂ on ZIF-8 and shows how molecular simulation can be used to improve the understanding gas adsorption storage on metal–organic frameworks.