Mg-Al mixed metal oxides (MMOs), derived from the decomposition of layered double hydroxides (LDHs), have been purposed as adsorbents for CO capture of industrial plant emissions. To aid in the design and optimization of these materials for CO capture at 200 °C, we have used a combination of solid-state nuclear magnetic resonance (ssNMR) and density functional theory (DFT) to characterize the CO gas sorption products and determine the various sorption sites in Mg-Al MMOs. A comparison of the DFT cluster calculations with the observed C chemical shifts of the chemisorbed products indicates that mono- and bidentate carbonates are formed at the Mg-O sites with adjacent Al substitution of an Mg atom, while the bicarbonates are formed at Mg-OH sites without adjacent Al substitution. Quantitative C NMR shows an increase in the relative amount of strongly basic sites, where the monodentate carbonate product is formed, with increasing Al/Mg molar ratios in the MMOs. This detailed understanding of the various basic Mg-O sites presented in MMOs and the formation of the carbonate, bidentate carbonate, and bicarbonate chemisorbed species yields new insights into the mechanism of CO adsorption at 200 °C, which can further aid in the design and capture capacity optimization of the materials.
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http://dx.doi.org/10.1021/acs.chemmater.1c03101 | DOI Listing |
ACS Cent Sci
December 2024
Department of Chemistry, Shanghai Stomatological Hospital & School of Stomatology, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433, P. R. China.
An efficient regiospecific co-assembly (RSCA) strategy is developed for general synthesis of mesoporous metal oxides with pore walls precisely decorated by highly dispersed noble metal nanocrystals with customized parameters (diameter and composition). It features the rational utilization of the specific interactions between hydrophilic molecular precursors, hydrophobic noble metal nanocrystals, and amphiphilic block copolymers, to achieve regiospecific co-assembly as confirmed by molecular dynamics simulations. Through this RSCA strategy, we achieved a controllable synthesis of a variety of functional mesoporous metal oxide composites (e.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Rates and selectivities for the partial oxidation of organic molecules on reactive electrodes depend on the identity and prevalence of reactive and spectator species. Here, we investigate the mechanism for the epoxidation of 1-hexene (CH) with reactive oxygen species formed by electrochemical oxidation of water (HO) on gold (Au) in an aqueous acetonitrile (CHCN) electrolyte. Cyclic voltammetry measurements demonstrate that oxygen (O) evolution competes with CH epoxidation, and the Au surface must oxidize before either reaction occurs.
View Article and Find Full Text PDFNanomaterials (Basel)
November 2024
Key Laboratory of Advanced Coating and Surface Engineering, Lingnan Normal University, Zhanjiang 524048, China.
Nanoscale Horiz
November 2024
Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Taipa, Macau, China.
MoS and related transition metal dichalcogenides (TMDs) have recently been reported as having extensive applications in nanoelectronics and catalysis because of their unique physical and chemical properties. However, one practical challenge for MoS-based applications arises from the easiness of oxygen contamination, which is likely to degrade performance. To this end, understanding the states and related energetics of adsorbed oxygen is critical.
View Article and Find Full Text PDFPhys Chem Chem Phys
November 2024
Department of Chemistry and Guangdong Provincial, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Interest in single-atom catalysts (SACs) has surged due to their potential to mitigate greenhouse NO gas from the environment. In this study, we explore the potential of NO reduction using porous 3D phosphorus graphdiyne decorated with an Al atom (3D-Al/PGDYN) through density functional theory. Results confirm the energetic stability of Al decorations on 3D-PGDYN and indicate that the Al atom plays an active role in catalysis.
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