Highly Dispersed ZnO Sites in a ZnO/ZrO 2 Catalyst Promote Carbon Dioxide‐to‐Methanol Conversion

催化作用 单斜晶系 甲醇 四方晶系 选择性 材料科学 格式化 色散(光学) 化学工程 无机化学 相(物质) 化学 结晶学 晶体结构 有机化学 物理 工程类 光学
作者
Xibo Zhang,Xiang Yu,Rafael G. Mendes,Peter Matvija,Angela E. M. Melcherts,Chunning Sun,Xinwei Ye,Bert M. Weckhuysen,Matteo Monai
出处
期刊:Angewandte Chemie [Wiley]
卷期号:64 (4): e202416899-e202416899 被引量:23
标识
DOI:10.1002/anie.202416899
摘要

ZnO/ZrO2 catalysts have shown better activity in the CO2 hydrogenation to methanol compared with single component counterparts, but the interaction between ZnO and ZrO2 is still poorly understood. In particular, the effect of the ZrO2 support phase (tetragonal vs. monoclinic) was not systematically explored. Here, we have synthesized ZnO/ZrO2 catalysts supported on tetragonal ZrO2 (ZnO/ZrO2-t) and monoclinic ZrO2 (ZnO/ZrO2-m), which resulted in the formation of different ZnOx species, consisting of sub-nanometer ZnO moieties and large-sized ZnO particles, respectively. ZnO/ZrO2-t exhibited a higher methanol selectivity (81 vs. 39 %) and methanol yield (1.25 vs. 0.67 mmol g-1 h-1) compared with ZnO/ZrO2-m. The difference in performance was attributed to the redox state and degree of dispersion of Zn, based on spectroscopy and microscopy results. ZnO/ZrO2-t had a high density of ZnOx-ZrOy sites, which favored the formation of active HCOO* species and enhanced the yield and selectivity of methanol along the formate pathway. Such ZnO clusters were further dispersed on ZrO2-t during catalysis, while larger ZnO particles on ZnO/ZrO2-m remained stable throughout the reaction. This study shows that the phase of ZrO2 supports can be used to control the dispersion of ZnO and the catalyst surface chemistry, and lead to enhanced catalytic performance.
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