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Methanol Adsorption on V2O3(0001)

机译:甲醇在V2O3(0001)上的吸附

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Well ordered V2O3(0001) layers may be grown on Au(111) surfaces. These films are terminated by a layer of vanadyl groups which may be removed by irradiation with electrons, leading to a surface terminated by vanadium atoms. We present a study of methanol adsorption on vanadyl terminated and vanadium terminated surfaces as well as on weakly reduced surfaces with a limited density of vanadyl oxygen vacancies produced by electron irradiation. Different experimental methods and density functional theory are employed. For vanadyl terminated V2O3(0001) only molecular methanol adsorption was found to occur whereas methanol reacts to form formaldehyde, methane, and water on vanadium terminated and on weakly reduced V2O3(0001). In both cases a methoxy intermediate was detected on the surface. For weakly reduced surfaces it could be shown that the density of methoxy groups formed after methanol adsorption at low temperature is twice as high as the density of electron induced vanadyl oxygen vacancies on the surface which we attribute to the formation of additional vacancies via the reaction of hydroxy groups to form water which desorbs below room temperature. Density functional theory confirms this picture and identifies a methanol mediated hydrogen transfer path as being responsible for the formation of surface hydroxy groups and water. At higher temperature the methoxy groups react to form methane, formaldehyde, and some more water. The methane formation reaction consumes hydrogen atoms split off from methoxy groups in the course of the formaldehyde production process as well as hydrogen atoms still being on the surface after being produced at low temperature in the course of the methanol → methoxy + H reaction.
机译:可以在Au(111)表面上生长有序的V2O3(0001)层。这些膜被一层钒基封端,该钒基可通过电子辐照除去,从而导致表面被钒原子封端。我们目前对甲醇在钒基封端和钒封端的表面以及弱还原的表面上进行吸附的研究,通过电子辐照产生的钒氧空位密度有限。采用了不同的实验方法和密度泛函理论。对于钒基封端的V2O3(0001),仅发现发生分子甲醇吸附,而甲醇在钒封端和弱还原的V2O3(0001)上反应形成甲醛,甲烷和水。在两种情况下,均在表面上检测到甲氧基中间体。对于弱还原的表面,可以证明,甲醇在低温下吸附后形成的甲氧基的密度是表面上电子诱导的钒氧空位的密度的两倍,这归因于通过反应生成的其他空位。羟基形成水,该水在室温以下解吸。密度泛函理论证实了这一情况,并确定了甲醇介导的氢转移路径,这是表面羟基和水形成的原因。在较高温度下,甲氧基反应生成甲烷,甲醛和更多的水。甲烷形成反应消耗甲醛生产过程中从甲氧基分离出的氢原子,以及在甲醇→甲氧基+ H反应过程中在低温下生成后仍保留在表面上的氢原子。

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