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

TLDR: In this paper, the formation mechanism of active sites on Cu/ZrO2 specific toward CO2-to-methanol hydrogenation was examined, and the authors concluded that the selective synthesis of CuaZr1-aOb, especially amorphous CuZr 1-aO2, is a key feature of the catalyst preparation.

Abstract: 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 (CuaZr1-aOb) The H2 reduction of the thus-formed CuaZr1-aOb 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 CuaZr1-aOb, especially amorphous CuaZr1-aOb, is a key feature of the catalyst preparation The preparation conditions of the amorphous CuaZr1-aOb 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) Vi