Combining Atomic Layer Deposition with Surface Organometallic Chemistry to Enhance Atomic-Scale Interactions and Improve the Activity and Selectivity of Cu-Zn/SiO2 Catalysts for the Hydrogenation of CO2 to Methanol

The direct synthesis of methanol via the hydrogenation of CO2, if performed efficiently and selectively, is potentially a powerful technology for CO2 mitigation. Here, we develop an active and selective Cu-Zn/SiO2 catalyst for the hydrogenation of CO2 by introducing copper and zinc onto dehydroxylated silica via surface organometallic chemistry and atomic layer deposition, respectively. At 230 degrees C and 25 bar, the optimized catalyst shows an intrinsic methanol formation rate of 4.3 g h(-1) g(Cu) (-1) and selectivity to methanol of 83%, with a space-time yield of 0.073 g h(-1) g(cat) (-1) at a contact time of 0.06 s g mL(-1). X-ray absorption spectroscopy at the Cu and Zn K-edges and X-ray photoelectron spectroscopy studies reveal that the CuZn alloy displays reactive metal support interactions; that is, it is stable under H-2 atmosphere and unstable under conditions of CO2 hydrogenation, indicating that the dealloyed structure contains the sites promoting methanol synthesis. While solid-state nuclear magnetic resonance studies identify methoxy species as the main stable surface adsorbate, transient operando diffuse reflectance infrared Fourier transform spectroscopy indicates that mu-HCOO*(ZnOx) species that form on the Cu-Zn/SiO2 catalyst are hydrogenated to methanol faster than the mu-HCOO*(Cu) species that are found in the Zn-free Cu/SiO2 catalyst, supporting the role of Zn in providing a higher activity in the Cu-Zn system.

Automated summary

A Cu-Zn/SiO2 catalyst was developed for the efficient and selective hydrogenation of CO2 to methanol. The optimized catalyst exhibited an intrinsic methanol formation rate of 4.3 g h(-1) g(Cu) (-1) and a selectivity to methanol of 83% at 230 degrees C and 25 bar.