Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/96001
Title: CO adsorption and hydrogenation on crystalline YBa2Cu3Ox. Thin films
Authors: Chen, L. 
Lin, J. 
Chen, H.Y.
Xu, S.
Li, K.
Ong, C.K. 
Tan, K.L.
Li, J.
Keywords: CO Hydrogenation
Infrared
Spectroscopy
Spectroscopy, Photoelectron
Thin Film
YBa2Cn3Ox
Issue Date: 1998
Source: Chen, 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.
Abstract: YBa2Cu3Ox (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.
Source Title: Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics
URI: http://scholarbank.nus.edu.sg/handle/10635/96001
ISSN: 0940483X
Appears in Collections:Staff Publications

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