Understanding How Ligand Functionalization Influences CO₂ and N₂ Adsorption in a Sodalite Metal-Organic Framework

In this work, a detailed study is conducted to understand how ligand substitution influences the CO₂, and N₂ adsorption properties of two highly crystalline sodalite metal-organic frameworks (MOFs) known as Cu-BTT (BTT³ = 1,3,5-benzenetristetrazolate) and Cu-BTTri (BTTri^-3 = 1,3,5-benzenetristriazolate). The enthalpy of adsorption and observed adsorption capacities at a given pressure are significantly lower for Cu-BTTri compared to its tetrazole counterpart, Cu-BTT. In situ X-ray and neutron diffraction, which allow visualization of the CO₂ and N₂ binding sites on the internal surface of Cu-BTTri, provide insights into understanding the subtle differences. As expected, slightly elongated distances between the open Cu2+ sites and surface-bound CO, in Cu-BTTri can be explained by the fact that the triazolate ligand is a better electron donor than the tetrazolate. The more pronounced Jahn-Teller effect in Cu-BTTri leads to weaker guest binding. The results of the aforementioned structural analysis were complemented by the prediction of the binding energies at each CO₂ and N₂ adsorption site by density functional theory calculations. In addition, variable temperature in situ diffraction measurements shed light on the fine structural changes of the framework and CO₂ occupancies at different adsorption sites as a function of temperature. Finally, simulated breakthrough curves obtained for both sodalite MOFs demonstrate the materials' potential performance in dry postcombustion CO₂ capture. The simulation, which considers both framework uptake capacity and selectivity, predicts better separation performance for Cu-BTT. The information obtained in this work highlights how ligand substitution can influence adsorption properties and hence provides further insights into the material optimization for important separations.