Copper-zirconia interfaces in UiO-66 enable selective catalytic hydrogenation of CO2 to methanol
Yifeng Zhu1, Jian Zheng1, Jingyun Ye2,3
1Institute for Integrated Catalysis, and Physical and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.
Abstract:
Molecular interactions with both oxides and metals are essential for heterogenous catalysis, leading to remarkable synergistic impacts on activity and selectivity. Here, we show that the direct link between the two phases (and not merely being together) is required to selectively hydrogenate CO2 to methanol on catalysts containing Cu and ZrO2. Materials consisting of isolated Cu particles or atomically dispersed Cu-O-Zr sites only catalyze the reverse water-gas shift reaction. In contrast, a metal organic framework structure (UiO-66) with Cu nanoparticles occupying missing-linker defects maximizes the fraction of metallic Cu interfaced to ZrO2 nodes leading to a material with high adsorption capacity for CO2 and high activity and selectivity for low-temperature methanol synthesis.
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