Designing of Organic Bridging Linkers of Metal-Organic Frameworks for Enhanced Carbon Dioxide Adsorption

Abstract

The global rate of anthropogenic carbon dioxide (CO2) emission is rising, which urges the development of efficient carbon capture and storage (CCS) technologies. Among the various CO2 capture methods, adsorption by the Metal-Organic Frameworks (MOFs) linkers has received immense interest as an excellent CO2 adsorbent because of their important role in understanding the interaction mechanism for CO2 adsorption. Here, we have investigated the adsorption of a CO2 molecule at the center and side positions of eight MOF-linkers using molecular cluster models. The interaction between CO2 and the linkers is assessed by computing the binding enthalpy (ΔH) through the first principles-based Density Functional Theory (DFT) with Grimme’s dispersion corrections (i.e., B3LYP-D3) and second-order Møller Plesset Theory (MP2) methods. The results of our investigations revealed that the center and side positions of the FBDC, DFBDC-1, DFBDC-2, and TFBDC linkers, the side position of the DClBDC-2, and the center position of the NDC linkers exhibit favorable physisorption behavior for CO2 adsorption, with the values of ΔH ranging from -12.05 to -14.09 kJ/mol. After lithium (Li) decoration on the pure linkers, CO2 adsorption at the center position of the BDC, FBDC, DClBDC-1 and side position of the BDC, FBDC, DFBDC-1, and DFBDC-2 linkers reflects a strong physisorption behavior with the values of ΔH lying in the range of -34.64 to -35.30 kJ/mol but remains below the energy of a chemical bond (chemisorption), which is required for facile CO2 release. To support our computed results, the Energy Decomposition Analysis (EDA) has been performed and the EDA study reveals that among all the energy components, the contribution of electrostatic and polarization energy components to the ΔH value is the most dominant. The Frontier Molecular Orbital (FMO) analysis demonstrated the stability of the Li-decorated linkers. The results of our investigations will direct toward the development and synthesis of novel porous MOFs with enhanced CO2 adsorption.