Active sites and structure–activity relationships for methanol synthesis from a stoichiometric mixture of CO2 and H2 were investigated for a series of coprecipitated Cu-based catalysts with temperature-programmed reduction (TPR), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and N2O decomposition. Experiments in a reaction chamber attached to an XPS instrument show that metallic Cu exists on the surface of both reduced and spent catalysts and there is no evidence of monovalent Cu+ species. This finding provides reassurance regarding the active oxidation state of Cu in methanol synthesis catalysts because it is observed with 6 compositions possessing different metal oxide additives, Cu particle sizes, and varying degrees of ZnO crystallinity. Smaller Cu particles demonstrate larger turnover frequencies (TOF) for methanol formation, confirming the structure sensitivity of this reaction. No correlation between TOF and lattice strain in Cu crystallites is observed suggesting this structural parameter is not responsible for the activity. Moreover, changes in the observed rates may be ascribed to relative distribution of different Cu facets as more open and low-index surfaces are present on the catalysts containing small Cu particles and amorphous or well-dispersed ZnO. In general, the activity of these systems results from large Cu surface area, high Cu dispersion, and synergistic interactions between Cu and metal oxide support components, illustrating that these are key parameters for developing fundamental mechanistic insight into the performance of Cu-based methanol synthesis catalysts.

A series of CdSe quantum dot (QD)-sensitized TiO2 heterostructures have been synthesized, characterized, and tested for the photocatalytic reduction of CO2 in the presence of H2O. Our results show that these heterostructured materials are capable of catalyzing the photoreduction of CO2 using visible light illumination (λ > 420 nm) only. The effect of removing surfactant caps from the CdSe QDs by annealing and using a hydrazine chemical treatment have also been investigated. The photocatalytic reduction process is followed using infrared spectroscopy to probe the gas-phase reactants and gas chromatography to detect the products. Gas chromatographic analysis shows that the primary reaction product is CH4, with CH3OH, H2, and CO observed as secondary products. Typical yields of the gas-phase products after visible light illumination (λ > 420 nm) were 48 ppm g−1 h−1 of CH4, 3.3 ppm g−1 h−1 of CH3OH (vapor), and trace amounts of CO and H2.

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