Seuser, GrantStaffel, RaechelHocaoglu, YagmurUpton, Gabriel F.Garcia, Elijah S.Cronauer, Donald C.Kropf, A. JeremyMartinelli, MichelaJacobs, Gary2023-04-122023-04-122023-03-24Nanomaterials 13 (7): 1155 (2023)https://hdl.handle.net/20.500.12588/1812Sodium-promoted monoclinic zirconia supported ruthenium catalysts were tested for CO2 hydrogenation at 20 bar and a H2:CO2 ratio of 3:1. Although increasing sodium promotion, from 2.5% to 5% by weight, slightly decreased CO2 conversion (14% to 10%), it doubled the selectivity to both CO (~36% to ~71%) and chain growth products (~4% to ~8%) remarkably and reduced the methane selectivity by two-thirds (~60% to ~21%). For CO2 hydrogenation during in situ DRIFTS under atmospheric pressure, it was revealed that Na increases the catalyst basicity and suppresses the reactivity of Ru sites. Higher basicity facilitates CO2 adsorption, weakens the C–H bond of the formate intermediate promoting CO formation, and inhibits methanation occurring on ruthenium nanoparticle surfaces. The suppression of excessive hydrogenation increases the chain growth probability. Decelerated reduction during H2-TPR/TPR-MS and H2-TPR-EXAFS/XANES at the K-edge of ruthenium indicates that sodium is in contact with ruthenium. A comparison of the XANES spectra of unpromoted and Na-promoted catalysts after H2 reduction showed no evidence of a promoting effect involving electron charge transfer.Attribution 4.0 United Stateshttps://creativecommons.org/licenses/by/4.0/rutheniummonoclinic zirconiasodiumCO2 hydrogenationreverse water-gas shiftFischer-Tropsch synthesisArticle2023-04-12