催化作用
甲醇
锌
铜
立方氧化锆
无机化学
图层(电子)
二氧化碳
化学
材料科学
化学工程
冶金
纳米技术
有机化学
陶瓷
工程类
作者
Aitor Arandia,Jihong Yim,Hassaan Warraich,Emilia Leppäkangas,René Bès,Aku Lempelto,Lars Gell,Hua Jiang,Kristoffer Meinander,Tiia Viinikainen,Simo Huotari,Karoliina Honkala,Riikka L. Puurunen
标识
DOI:10.1016/j.apcatb.2022.122046
摘要
The development of active catalysts for carbon dioxide (CO2) hydrogenation to methanol is intimately related to the creation of effective metal-oxide interfaces. In this work, we investigated how the order of addition of copper and zinc on zirconia influences the catalytic properties, the catalytic activity and selectivity toward methanol. Regarding the carbon dioxide conversion and methanol production, the catalysts on which the promoter (zinc) was atomically deposited after copper impregnation (i.e., ZnO/Cu/ZrO2 and ZnO/Cu/ZnO/ZrO2) were superior catalysts compared to the reverse copper-after-zinc catalyst (Cu/ZnO/ZrO2). Temperature-programmed experiments and in situ diffuse reflectance infrared Fourier transform-spectroscopy (DRIFTS) experiments allowed us to elucidate the benefits of the zinc-after-copper pair to store CO2 as carbonate species and further convert them into formate species, key intermediates in the formation of methanol. This research provides insights into the potential of atomic layer deposition in the development of tailored heterogeneous catalysts for efficient CO2 valorization to methanol.
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