Guaiacol Hydrodeoxygenation over Iron-Ceria Catalysts with Platinum Single-Atom Alloy Clusters as a Promoter

A series of ceria-supported Fe catalysts with a trace amount of noble-metal modification (NM-Fe/CeO2, NM = Pt, Ir, Pd, Rh, and Ru) were prepared by the co-impregnation method and used for guaiacol hydrodeoxygenation (HDO) to phenolic compounds at 673 K and atmospheric pressure. In the absence of H2O, the addition of noble metal improved the initial activities but showed severer deactivation than Fe/CeO2. Conversely, the addition of water showed little effect on the initial activity and helped to improve the stability of NM-Fe/CeO2. Among all of the tested NM-Fe/CeO2 catalysts, Pt-Fe/CeO2 showed the highest guaiacol conversion. The X-ray absorption spectroscopy (XAS) characterization confirmed that the original structure of active FeOx species, probably Fe4O6, was mostly preserved after the addition of Pt. The Pt modifier was completely reduced to form Pt1Fe4 single-atom alloy (Pt(1)Fe(4)SAA) clusters during the guaiacol HDO reaction. These Pt(1)Fe(4)SAA clusters probably promoted the reduction of FeOx species to form the coordinatively unsaturated sites (CUS), which were the active sites for the HDO reaction. The presence of Pt(1)Fe(4)SAA dusters also encouraged the dissociation of H2O on Pt-Fe/CeO2 to maintain the catalytic activity under the H2O-containing conditions, as shown by the temperature-programmed surface reaction with H2O (H2O-TPSR). Characterization of spent catalysts with Raman spectroscopy, scanning transition electron microscopy (STEM), and XAS showed that the Pt-Fe/CeO2 catalyst was deactivated by coke deposition and carburization of Fe4O6 dusters in the absence of H2O, while the growth of coke species and the formation of inactive iron carbide were suppressed in the presence of H2O.

Automated summary

The study found that Fe/CeO2 catalysts modified with noble metals showed better catalytic performance in guaiacol hydrodeoxygenation reaction compared to unmodified catalysts, and the addition of water contributed to the stability of the catalytic reaction.