催化作用
氧化钒
脱氢
拉曼光谱
化学
氧化物
无机化学
氧化还原
光化学
多相催化
吸附
钒
材料科学
化学工程
物理化学
有机化学
物理
光学
工程类
作者
Patrick Ober,Simone Rogg,Christian Heß
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-02-03
卷期号:10 (5): 2999-3008
被引量:42
标识
DOI:10.1021/acscatal.9b05174
摘要
Ceria-supported vanadia is catalytically active in oxidative dehydrogenation (ODH) reactions. Here, we provide direct spectroscopic evidence for the participation of the ceria support in the redox catalysis. To unravel the structural dynamics of vanadia/ceria (VOx/CeO2) catalysts during ethanol ODH, we have applied a combination of operando multiwavelength Raman and operando UV–vis spectroscopy. Our approach consists of the targeted use of different Raman excitation wavelengths, enabling the selective enhancement of ceria (at 385 nm) and vanadia (at 515 nm) vibrational features. As part of the support dynamics, ceria lattice oxygen is shown to directly participate in the ODH reaction, while V–O–Ce interface bonds are broken during substrate adsorption, resulting in ethoxide formation. The presence of V–O–Ce bonds is considered to be crucial for the observed synergy effect in catalytic performance, allowing ceria to act as an oxygen buffer stabilizing the vanadium center. By providing an experimental basis for a detailed understanding of working VOx/CeO2 catalysts, our results highlight the importance of active support participation in oxide catalysis.
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