First-principles study of CO2 hydrogenation on Cd-doped ZrO2: Insights into the heterolytic dissociation of H2

Cd-doped ZrO2 catalyst has been found to have high selectivity and activity for CO2 hydrogenation to methanol. In this work, density functional theory calculations were carried out to investigate the microscopic mechanism of the reaction. The results show that Cd doping effectively promotes the generation of oxygen vacancies, which significantly activate the CO2 with stable adsorption configurations. Compared with CO2, gaseous H-2 adsorption is more difficult, and it is mainly dissociated and adsorbed on the surface as [H-Cd-H-O]* or [H-Zr-H-O]* compact ion pairs, with [H-Cd-H-O]* having the lower energy barrier. The reaction pathways of CO2 to methanol has been investigated, revealing the formate path as the dominated pathway via HCOO* to H2COO* and to H3CO*. The hydrogen anions, H-Cd* and H-Zr*, significantly reduce the energy barriers of the reaction.

Automated summary

In this study, density functional theory calculations were performed to investigate the microscopic mechanism of CO2 hydrogenation to methanol over Cd-doped ZrO2 catalyst. The results showed that Cd doping promoted the generation of oxygen vacancies and activated the stable adsorption configurations of CO2. Additionally, the dominant reaction pathway from CO2 to methanol via formate intermediate was revealed.