SearcharxivSearch

arXiv · 2403.03958

Size, nanostructure, and composition dependence of bimetallic Au-Pd supported on ceria-zirconia mixed oxide catalysts for selective oxidation of benzyl alcohol

Abstract

A bimetallic Au-Pd catalyst supported on ceriazirconia with Au:Pd molar ratio 0.8 has been synthesized using a simultaneous deposition-precipitation method and oxidized at 250, 450, and 700 $^\circ$C in order to modify its particle size, nanostructure, and composition. Combined Xray energy dispersive spectroscopy and Xray photoelectron spectroscopy analysis clearly evidence that the bimetallic Au-Pd catalyst oxidized at 250 $^\circ$C is made up of a mixture of monometallic Au and Pd and bimetallic Au-Pd nanoparticles with Au:Pd ratios varying over a wide range. Increasing oxidation temperature leads to a stronger interaction between Au and Pd. Meanwhile, a slight increase of particle size and a narrowing of the Au:Pd ratio in the bimetallic nanoparticles take place. Compared with titania and activated carbon supports, the resistance against sintering at high temperatures of Au-Pd metal particles supported on ceriazirconia is proven to be higher. A synergistic effect has been observed for selective oxidation of benzyl alcohol on these catalysts. The catalytic activity decreases only slightly after oxidation at 450 $^\circ$C. However, oxidation at 700 $^\circ$C results in much lower catalytic activity. Migration of Pd onto Au particles during oxidation of benzyl alcohol enhances the catalytic activity of a physical mixture of monometallic Au and Pd supported on ceriazirconia catalysts. This fact, jointly with an analysis of the intrinsic activity, reveals the influence of the actual nature of Au-Pd interactions in the bimetallic particles, which points to higher activity of Au@Pd or Au@Pd@Pd nanostructures on ceria-zirconia support.

Explore related subjects

Keep this discovery

BibTeXRIS

Carol Olmos, Lidia Esther Chinchilla, Alberto Villa, Juan José Delgado, Ana Belén Hungría, Ginesa Blanco, Laura Prati, José Juan Calvino, Xiaowei Chen. 2024-02-02. Size, nanostructure, and composition dependence of bimetallic Au-Pd supported on ceria-zirconia mixed oxide catalysts for selective oxidation of benzyl alcohol. https://doi.org/10.1016/j.jcat.2019.05.002

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Breaking Water at Graphene Defects

Water dissociation at solid surfaces underpins processes ranging from corrosion and catalysis to electrochemistry and photovoltaics. Defects often serve as reactive sites for dissociation, yet how solvation influences water dissociation at such sites remains poorly understood. Here, we use state-of-the-art machine-learned interatomic potentials to explore water dissociation at defective graphene-water interfaces. We show that solvation qualitatively changes the reaction mechanism at a graphene single vacancy (SV), opening pathways that are absent for an isolated water molecule. Whereas the gas-phase process proceeds via a single concerted channel, the solvated SV splits water through two competing pathways: a basic route forming SV-H and OH-(aq), and an acidic route forming SV-OH and H3O+(aq). These lower-barrier pathways produce distinct chemisorbed intermediates that enhance graphene-water adsorption. Accordingly, even a simple carbon vacancy gives rise to unexpectedly rich interfacial chemistry, coupling surface chemistry to interfacial charge and wettability, with implications for carbon functionalization and nanofluidic transport.

physics.chem-ph

Comprehensive Study of L-Menthol and Octanoic Acid as a Hydrophobic Eutectic Solvent

Hydrophobic eutectic solvents (HES) based on natural compounds represent promising green alternatives to conventional solvents. In this work, we investigate the physicochemical, structural, and dynamical properties of an ES formed by L-menthol and octanoic acid using a combined experimental and molecular dynamics simulation approach. Five compositions with molar ratios from 1:3 to 3:1 were studied with molecular dynamics simulation in the temperature range 15 degrees C to 35 degrees C. Experimental measurements of density and viscosity in the temperature range from 5 degrees C to 35 degrees C were complemented with results obtained from MD simulations employing the OPLS force field. Structural analyses based on radial distribution functions and Kirkwood-Buff integrals reveal that the dominant interactions in the mixture are hydrogen bonds between L-menthol and octanoic acid molecules. Dynamic properties, including self-diffusion coefficients and hydrogen-bond lifetimes, indicate that intermolecular hydrogen bonds between the two components are stronger and longer-lived than bonds between identical species. These findings provide molecular-level insight into the structure and transport properties of menthol-based ESs relevant for green solvent applications.

physics.chem-ph

More is not always better: Dissociative photoionization limits the EUV absorbing photacid generator pentafluorophenyl triflate in photolithography

Pentafluorophenyl triflate has been explored as a highly absorbing neutral photoacid generator (PAG) candidate for next generation chemically amplified resists used in extreme ultraviolet (EUV) lithography. Although increased fluorination enhances EUV absorption, this study demonstrates that such an approach does not necessarily improve photoacid generation efficiency. Using photoelectron-photoion coincidence (PEPICO) spectroscopy at the 92 eV photon energy of the EUV scanners in combination with quantum chemical calculations, the dissociative photoionization of pentafluorophenyl triflate was systematically investigated. The photoionization mass spectrum reveals extensive fragmentation, with the parent ion contributing only 3.1 % of the total signal and CF$_3^+$ representing the dominant product ion. Computed appearance energies align well with experimental trends and support a sequential fragmentation pathway involving loss of SO$_2$, CF$_3$, and CO. Crucially, none of the major dissociation channels yield precursors capable of forming triflic acid, the strong photoacid required for efficient deprotection reactions in chemically amplified resists. Combined with previous dissociative electron attachment studies indicating similarly unfavorable fragmentation, the results demonstrate that despite its high EUV absorption cross section, pentafluorophenyl triflate is unsuitable as a PAG for EUV lithography. The findings highlight the importance of understanding fundamental photoionization and electron interaction mechanisms to guide the rational design of next generation high performance EUV photoresists.

physics.chem-ph