NO Adsorption and Optical Detection in Rare Earth Metal-Organic Frameworks

Acid gases (e.g., NO and SO), commonly found in complex chemical and petrochemical streams, require material development for their selective adsorption and removal. Here, we report the NO adsorption properties in a family of rare earth (RE) metal-organic frameworks (MOFs) materials. Fundamental understanding of the structure-property relationship of NO adsorption in the RE-DOBDC materials platform was sought via a combined experimental and molecular modeling study. No structural change was noted following humid NO exposure. Density functional theory (DFT) simulations indicated that H₂O has a stronger affinity to bind with the metal center than NO₂, while NO₂ preferentially binds with the DOBDC ligands. Further modeling results indicate no change in binding energy across the RE elements investigated. Also, stabilization of the NO₂ and H₂O molecules following adsorption was noted, predicted to be due to hydrogen bonding between the framework ligands and the molecules and nanoconfinement within the MOF structure. This interaction also caused distinct changes in emission spectra, identified experimentally. Calculations indicated that this is due to the adsorption of NO₂ molecules onto the DOBDC ligand altering the electronic transitions and the resulting photoluminescent properties, a feature that has potential applications in future sensing technologies.