Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/96001
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dc.titleCO adsorption and hydrogenation on crystalline YBa2Cu3Ox. Thin films
dc.contributor.authorChen, L.
dc.contributor.authorLin, J.
dc.contributor.authorChen, H.Y.
dc.contributor.authorXu, S.
dc.contributor.authorLi, K.
dc.contributor.authorOng, C.K.
dc.contributor.authorTan, K.L.
dc.contributor.authorLi, J.
dc.date.accessioned2014-10-16T09:18:21Z
dc.date.available2014-10-16T09:18:21Z
dc.date.issued1998
dc.identifier.citationChen, L.,Lin, J.,Chen, H.Y.,Xu, S.,Li, K.,Ong, C.K.,Tan, K.L.,Li, J. (1998). CO adsorption and hydrogenation on crystalline YBa2Cu3Ox. Thin films. Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics 102 (1) : 103-110. ScholarBank@NUS Repository.
dc.identifier.issn0940483X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/96001
dc.description.abstractYBa2Cu3Ox (YBCO, x=6-7) is shown to have catalytic activity for methanol synthesis from syngas in this work. In order to get more details about the nature of the reactive site and reaction mechanism, CO adsorption and hydrogenation on a high quality YBCO thin film were studied by using in situ Fourier transform infrared spectroscopy (FTIR), angle-resolved X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and atomic force microscopy (AFM). Carbonate-like species, aldehyde, formate and methoxy were detected as reaction intermediates. After the CO hydrogenation reaction Cu2+ ions were reduced to Cul+, and the orthorhombic structures of YBCO was transformed to the tetragonal phase with the formation of carbonatelike complexes. The degradation of some YBCO to amorphous surface phases was also observed. Based on these studies, carbonate-formate-dioxymethylene-methoxy (or carbonate-aldehyde-carnene-methane) reaction scheme is proposed. © WILEY-VCH Verlag GmbH, 1998.
dc.sourceScopus
dc.subjectCO Hydrogenation
dc.subjectInfrared
dc.subjectSpectroscopy
dc.subjectSpectroscopy, Photoelectron
dc.subjectThin Film
dc.subjectYBa2Cn3Ox
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.description.sourcetitleBerichte der Bunsengesellschaft/Physical Chemistry Chemical Physics
dc.description.volume102
dc.description.issue1
dc.description.page103-110
dc.description.codenBBPCA
dc.identifier.isiutNOT_IN_WOS
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