Abstract

Ceria supported metal catalysts often exhibit high activity in the preferential oxidation (PROX) of CO in H2-rich stream and doping the ceria support with other metals proves to be rather effective in further enhancing their catalytic performance. Therefore, in this work, a series of ceria materials doped with Mn, Fe and Ni (CeM, where M = Mn, Fe and Ni; M/Ce = 1/8) were synthesized by a modified hydrothermal method; with the doped ceria materials (CeM) as the support, various supported gold catalysts (Au/CeM) were prepared by the colloidal deposition method. The influence of metal dopant on the performance of these ceria materials supported with gold catalysts in CO PROX was then investigated in detail with the help of various characterization measures such as N2 sorption, XRD, TEM, Raman spectroscopy, H2-TPR, XPS and XAS. The results indicate that the incorporation of Mn, Fe and Ni metal ions into ceria can remarkably increase the amount of oxygen vacancies in the doped ceria support, which is beneficial for enhancing the reducibility of ceria, the metal-support interaction and the dispersion of gold species. Although the gold catalysts supported on various doped ceria are similar in the size and state of Au nanoparticles, the CO conversions for CO PROX over Au/CeMn, Au/CeFe and Au/CeNi catalysts are 65.6%, 93.0% and 48.2%, respectively, much higher than the value of 33.6% over the undoped Au/CeO2 catalyst at ambient temperature. For CO PROX over the Au/CeNi catalyst, the conversion of CO remains near 100% at 60–130 °C, with a PROX selectivity to CO2 of higher than 50%. The excellent performance of Au/CeNi catalyst can be ascribed to its large amount of oxygen vacancies and high reducibility on account of Ni incorporation. The insight shown in this work helps to clarify the doping effect of other metals on the physicochemical properties of ceria, which is then beneficial to building a structure-performance relation for ceria supported gold catalyst as well as developing a better catalyst for removing trace CO in the hydrogen stream and producing high purity hydrogen.

Highlights

  • The catalytic oxidation of CO at lower temperatures is widely used in the removal of trace content of CO from various atmospheres; in particular, the preferential oxidation (PROX) of CO in H2 -richCatalysts 2018, 8, 469; doi:10.3390/catal8100469 www.mdpi.com/journal/catalystsCatalysts 2018, 8, 469 stream has received extensive attention, as it is rather effective in getting CO-free hydrogen sources (CO < 10 ppm) to feed the polymer electrolyte membrane fuel cell (PEMFC) [1,2,3,4]

  • The above results illustrate that the gold catalysts supported on the doped ceria (Au/ceria materials (CeM)), especially Au/CeNi, exhibit much better performance in CO PROX than that supported on undoped ceria (Au/CeO2 )

  • A series of ceria materials doped with Mn, Fe and Ni were synthesized by a modified hydrothermal method; with the doped ceria materials (CeM, M = Mn, Fe, and Ni; M/Ce = 1/8) as the support, gold catalysts (Au/CeM) were prepared by the colloidal deposition method

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Summary

Introduction

The catalytic oxidation of CO at lower temperatures is widely used in the removal of trace content of CO from various atmospheres; in particular, the preferential oxidation (PROX) of CO in H2 -richCatalysts 2018, 8, 469; doi:10.3390/catal8100469 www.mdpi.com/journal/catalystsCatalysts 2018, 8, 469 stream has received extensive attention, as it is rather effective in getting CO-free hydrogen sources (CO < 10 ppm) to feed the polymer electrolyte membrane fuel cell (PEMFC) [1,2,3,4]. The platinum group metal-based catalysts exhibited high activity, with a CO conversion of about 92–97% at 150–200 ◦ C, but the PROX selectivity (about 40%) in the presence of CO2 and H2 O was relatively low [18]. The Cu-based catalysts displayed high CO conversion (about 100%) and PROX stability (100%) at lower temperatures (about 90–170 ◦ C); their performance decreased obviously at high space velocities and the resistance towards. The gold-based catalysts were considered as a promising candidate for the selective removal of CO from reformate streams due to their high activity; over the gold-based catalysts, the conversion of CO reached almost 100% at low temperatures (

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