Design of Interfacial Sites between Cu and Amorphous ZrO2 Dedicated to CO2‑to-Methanol Hydrogenation

We examined the formation mechanism of active sites on Cu/ZrO2 specific toward CO2-to-methanol hydrogenation. The active sites on Cu/a-ZrO2 (a-: amorphous) were more suitable for CO2-to-methanol hydrogenation than those on Cu/t-ZrO2 (t-: tetragonal) and Cu/m-ZrO2 (m-: monoclinic). When a-ZrO2 was impregnated with a Cu­(NO3)2·3H2O solution and then calcined under air, most of the Cu species entered a-ZrO2, leading to the formation of a Cu–Zr mixed oxide (Cu a Zr1‑a O b ). The H2 reduction of the thus-formed Cu a Zr1‑a O b led to the formation of Cu nanoparticles on a-ZrO2, which can be dedicated to CO2-to-methanol hydrogenation. We concluded that the selective synthesis of Cu a Zr1‑a O b , especially amorphous Cu a Zr1‑a O b , is a key feature of the catalyst preparation. The preparation conditions of the amorphous Cu a Zr1‑a O b specific toward CO2-to-methanol hydrogenation is as follows: (i) Cu­(NO3)2·3H2O/a-ZrO2 is calcined at low temperature (350 °C in this study) and (ii) the Cu loading is low (6 and 8 wt % in this study). Via these preparation conditions, the characteristics of a-ZrO2 for the catalysts remained unchanged during the reaction at 230 °C. The latter preparation condition is related to the solubility limit of Cu species in a-ZrO2. Accordingly, we obtained the amorphous Cu a Zr1‑a O b without forming crystalline CuO particles.