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CO 的回收:用常压 X 射线光电子能谱法探测甲烷化反应过程中 Ni(111) 表面的化学状态。

Recycling of CO: Probing the Chemical State of the Ni(111) Surface during the Methanation Reaction with Ambient-Pressure X-Ray Photoelectron Spectroscopy.

机构信息

Department of Materials Science and Engineering, University of California , Berkeley, California 94720, United States.

出版信息

J Am Chem Soc. 2016 Oct 12;138(40):13246-13252. doi: 10.1021/jacs.6b06939. Epub 2016 Sep 28.

Abstract

Using ambient-pressure X-ray photoelectron spectroscopy (AP-XPS), we studied the adsorption and reactions of CO and CO + H on the Ni(111) surface to identify the surface chemical state and the nature of the adsorbed species during the methanation reaction. In 200 mTorr CO, we found that NiO is formed from CO dissociation into CO and atomic oxygen. Additionally, carbonate (CO) is present on the surface from further reaction of CO with NiO. The addition of H into the reaction environment leads to reduction of NiO and the disappearance of CO. At temperatures >160 °C, CO adsorbed on hollow sites, and atomic carbon and OH species are present on the surface. We conclude that the methanation reaction proceeds via dissociation of CO, followed by reduction of CO to atomic carbon and its hydrogenation to methane.

摘要

使用常压 X 射线光电子能谱 (AP-XPS),我们研究了 CO 和 CO+H 在 Ni(111)表面上的吸附和反应,以确定甲烷化反应过程中表面化学状态和吸附物种的性质。在 200 毫托 CO 中,我们发现 CO 离解成 CO 和原子氧形成 NiO。此外,CO 与 NiO 进一步反应生成碳酸盐 (CO)。向反应环境中添加 H 会导致 NiO 还原和 CO 消失。在温度>160°C 时,CO 吸附在空位上,表面上存在原子碳和 OH 物种。我们得出结论,甲烷化反应通过 CO 的解离进行,然后将 CO 还原为原子碳,并将其加氢成甲烷。

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