Reverse water gas shift on interfacial sites formed by deposition of oxidized molybdenum moieties onto gold nanoparticles

R. Carrasquillo-Flores, I. Ro, M. Kumbhalkar, S. Burt, C. Carrero, A. Alba-Rubio, J. Miller, I. Hermans, G. Huber, J. Dumesic
J. Am. Chem. Soc. 137 (2015) 10317

Abstract

We show that MoOx-promoted Au/SiO2 catalysts are active for reverse water–gas shift (RWGS) at 573 K. Results from reactivity measurements, CO FTIR studies, Raman spectroscopy, and X-ray absorption spectroscopy (XAS) indicate that the deposition of Mo onto Au nanoparticles occurs preferentially on under-coordinated Au sites, forming Au/MoOx interfacial sites active for reverse water–gas shift (RWGS). Au and AuMo sites are quantified from FTIR spectra of adsorbed CO collected at subambient temperatures (e.g., 150–270 K). Bands at 2111 and 2122 cm–1 are attributed to CO adsorbed on under-coordinated Au0 and Auδ+ species, respectively. Clausius–Clapeyron analysis of FTIR data yields a heat of CO adsorption (ΔHads) of −31 kJ mol–1 for Au0 and −64 kJ mol–1 for Auδ+ at 33% surface coverage. Correlations of RWGS reactivity with changes in FTIR spectra for samples containing different amounts of Mo indicate that interfacial sites are an order of magnitude more active than Au sites for RWGS. Raman spectra of Mo/SiO2 show a feature at 975 cm–1, attributed to a dioxo (O═)2Mo(−O–Si)2 species not observed in spectra of AuMo/SiO2 catalysts, indicating preferential deposition of Mo on Au. XAS results indicate that Mo is in a +6 oxidation state, and therefore Au and Mo exist as a metal–metal oxide combination. Catalyst calcination increases the quantity of under-coordinated Au sites, increasing RWGS activity. This strategy for catalyst synthesis and characterization enables quantification of Au active sites and interfacial sites, and this approach may be extended to describe reactivity changes observed in other reactions on supported gold catalysts.

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