Abstract

Ceria-supported gold catalyst has drew much research interest owing to its high reactivity on CO oxidation and water-gas shift (WGS) reactions. However, till now, there were relatively limited studies on the effect of secondary metal/metal oxide component into gold-ceria system to enhance its catalytic performance. In this work, we synthetized the ceria supported gold-nickel samples via a deposition-precipitation method with the base of NaHCO3 to adjust final pH value of 8~9. We found that the addition of nickel oxide drove off the gold species from the stock solution during synthesis, and thus resulted in a dramatical decrease on doped Au concentration. No crystallized phases of gold and nickel were observed on the surface of ceria nanorods in both X-ray diffraction (XRD) and transmission electron microscopy (TEM). The valence of nickel was maintained as Ni2+ for all the measured samples by X-ray photoelectron spectroscopy (XPS), while gold was oxidized with the increased nickel amount after analysis of X-ray absorption near edge spectroscopy (XANES). The corresponding catalytic tests showed that with the introduction of nickel oxide, the activity of gold-ceria catalyst was promoted for the WGS reaction, but inhibited for the CO oxidation reaction.

Highlights

  • There are considerable research have ascertained that supported metal catalysts, especially to gold catalysts, are extraordinarily active for oxidation of carbon monoxide (2CO + O2 = 2CO2 ) [1,2,3,4,5,6] and water-gas shift (CO + H2 O = CO2 + H2 ) [7,8,9,10,11,12] reaction

  • We investigated three different precipitating agents: ammonium carbonate ((NH4 )2 CO3 ), sodium carbonate (Na2 CO3 ) and sodium hydrogen carbonate (NaHCO3 ), and found that: (1) (NH4 )2 CO3 is very suitable for gold deposition onto pure ceria [7], but nickel ion was complexed with molecular ammonia, which is prejudicial to the deposition of nickel; (2) When

  • We hypothesized that the as-formed Ni(OH)x(H2O)y nucleation in stock solution can cover part of ceria ceria-supported pure gold (AuCe) and gold-nickel (AuNiCe) samples, respectively

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Summary

Introduction

There are considerable research have ascertained that supported metal catalysts, especially to gold catalysts, are extraordinarily active for oxidation of carbon monoxide (2CO + O2 = 2CO2 ) [1,2,3,4,5,6] and water-gas shift (CO + H2 O = CO2 + H2 ) [7,8,9,10,11,12] reaction. Carrettin et al reported that nanocrystalline CeO2 supported gold nanoparticles are more active than those anchored on other oxides (TiO2 , Fe2 O3 ) for CO oxidation [1]. Fu et al confirmed that gold nanoparticles are essential for some oxidation reactions, but unimportant in WGS reaction over Au-ceria [22]. On the basis of these findings, we can see the significant importance of physical and chemical properties of Au modified by the matrix

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