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首页> 外文期刊>Journal of Catalysis >Oxidative dehydrogenation of methanol at ceria-supported vanadia oligomers
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Oxidative dehydrogenation of methanol at ceria-supported vanadia oligomers

机译:Ceria载体钒寡聚体甲醇的氧化脱氢

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We study the adsorption and partial oxidation of methanol at a trimeric VOx species supported on ceria, which was found to be the thermodynamically most stable species under slightly reducing conditions. Results for the oxidation of methanol obtained using dispersion-corrected PBE+U and HSE are compared with a metastable monomeric VO2 species. The intrinsic barriers for monomers (103 kJ/mol), trimers (133 kJ/mop, and the pristine surface (136 kJ/mol) are compared with the corresponding values derived from temperature-programmed desorption experiments, i.e. 100, 125, and 150 kJ/mol, respectively. It was found that the VO2 trimer is more active than the pristine ceria (1 1 1) surface due to entropic effects, showing up in a higher pre-exponential factor. However, the VO2 trimer is less active than the monomer due to structural relaxation in the surface O layer of the latter. (C) 2017 Elsevier Inc. All rights reserved.
机译:我们研究了在二氧化铈中负载的三聚体VOX物种下甲醇的吸附和部分氧化,发现在略微降低条件下是热力学上最稳定的物种。 将使用分散校正的PBE + U和HSE获得的甲醇氧化的结果与亚稳定的单体VO2物种进行比较。 与从温度编程的解吸实验的相应值进行比较,将单体(103kJ / mol),三聚体(133kJ /橡木和原始表面(136kJ / mol)进行固氮屏障(133kJ / mop,以及原始表面(136kJ / mol),即100,125和150 分别kj / mol。发现VO2三聚体比熵效应更高的原始二氧化铈(111)表面更活跃,在更高的预指数因子中出现。然而,VO2三聚体较小 由于后者的表面o层结构松弛导致的单体。(c)2017 Elsevier Inc.保留所有权利。

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