Probing active sites for carbon oxides hydrogenation on Cu/TiO2 using infrared spectroscopy

The valorization of carbon oxides on metal/metal oxide catalysts has been extensively investigated because of its ecological and economical relevance. However, the ambiguity surrounding the active sites in such catalysts hampers their rational development. Here, in situ infrared spectroscopy in combination with isotope labeling revealed that CO molecules adsorbed on Ti3+ and Cu+ interfacial sites in Cu/TiO2 gave two disparate carbonyl peaks. Monitoring each of these peaks under various conditions enabled tracking the adsorption of CO, CO2, H-2,H- and H2O molecules on the surface. At room temperature, CO was initially adsorbed on the oxygen vacancies to produce a high frequency CO peak, Ti3+-CO. Competitive adsorption of water molecules on the oxygen vacancies eventually promoted CO migration to copper sites to produce a low-frequency CO peak. In comparison, the presence of gaseous CO2 inhibits such migration by competitive adsorption on the copper sites. At temperatures necessary to drive CO2 and CO hydrogenation reactions, oxygen vacancies can still bind CO molecules, and H-2 spilled-over from copper also competed for adsorption on such sites. Our spectroscopic observations demonstrate the existence of bifunctional active sites in which the metal sites catalyze CO2 dissociation whereas oxygen vacancies bind and activate CO molecules. The conversion of carbon oxides to products such as fuels is of high industrial relevance, but uncertainties regarding the catalytic mechanisms remain. Here, the authors use in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) to follow CO, CO2, H-2 and H2O molecules as they bind to a Cu/TiO2 surface, finding metallic copper sites serve as CO2 dissociation sites, whereas Cu+ and oxygen vacancies bind CO molecules for further reductions.

Automated summary

The study reveals the adsorption and reaction process of CO molecules on metal/metal oxide catalysts, providing new insights into the functional active sites in CO2 and CO reduction reactions.