Grabow, Lars C.Fleming, Kevin2023-07-032023-07-032023-04-13https://hdl.handle.net/10657/14748Metal-organic frameworks (MOFs) are porous organometallic compounds that are of high interest to many researchers due to their capability to trap industrial greenhouse gases, such as CO2, that contribute to anthropogenic global warming. A promising MOF that has gained the attention of the research community in recent years is the CO2 adsorbent MIL-100 (Cr). This compound consists of Cr3-μ3-oxo clusters referred to as secondary building units (SBU) and organic linkers derived from trimesic acid. Thermally activated SBUs possess coordinatively unsaturated sites Cr sites – or open metal sites (OMS) – that possess oxidation states of +2 or +3. Previous experimental work indicated that CO2 molecules bind more strongly to +2 OMS than to +3 OMS at low adsorptive pressures. In this study, two central questions were addressed. Firstly, can the experimentally observed OMS selectivity be verified through density functional theory (DFT) simulations? Secondly, what electronic processes are responsible for OMS selectivity? DFT computations of the binding energy, enthalpy, and free energy of CO2 adsorption onto +2 and +3 OMS verify that CO2 exhibits a significantly greater affinity for the +2 OMS. Furthermore, a comparison of the adsorption charge transfer and optimized binding geometries reveal that this selectivity arises from the energetically favorable chemisorption of CO2 onto +2 OMS – relative to the weaker physisorption of the greenhouse gas onto +3 OMS. The novel methodology utilized for this study can be implemented in computational investigations of other MOFs that can be used for carbon capture applications.enThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).Chemical engineeringPoster