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dc.creatorLuo, Kai
dc.date.accessioned2012-06-07T23:00:06Z
dc.date.available2012-06-07T23:00:06Z
dc.date.created2000
dc.date.issued2000
dc.identifier.urihttps://hdl.handle.net/1969.1/ETD-TAMU-2000-THESIS-L834
dc.descriptionDue to the character of the original source materials and the nature of batch digitization, quality control issues may be present in this document. Please report any quality issues you encounter to digital@library.tamu.edu, referencing the URI of the item.en
dc.descriptionIncludes bibliographical references (leaves 85-91).en
dc.descriptionIssued also on microfiche from Lange Micrographics.en
dc.description.abstractMetal/oxide chemistry and metal cluster growth on oxides are fundamental to our understanding of the catalytic activity and selectivity of metal catalysts, thus considerable research recently has addressed the physical and chemical properties of metal clusters on well-defined oxide surfaces. In this work, the nucleation and growth modes of Ag on TiO₃(110)(1x1) and (1x2) surfaces, Ag on ultra-thin Al₂O₃ films, and Au on ultra-thin SiO₂ films were studied by scanning tunneling microscopy (STM), low energy ion scattering spectroscopy (LEIS) and X-ray photoelectron spectroscopy (XPS). In general, Ag grows three-dimensionally (3D) on both TiO₂(110) and Al₂O₃ film at 300 K. The growth mode of Au at fractional monolayer coverages is quasi-two dimensional (2D); at higher coverages, three-dimensional growth of Au was found. In these three systems, Ag/TiO₂, Ag/Al₂O₃, and Au/SiO₂, no strong chemical interaction was observed between metal clusters and substrates. Sintering was observed for all metal clusters upon annealing. A non-zero order desorption was observed for Ag/Al₂O₃ and Au/SiO₂ in temperature programmed desorption (TPD) studies. The desorption activation energies decrease with decreasing metal coverages.en
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.publisherTexas A&M University
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries in 2008. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.subjectchemistry.en
dc.subjectMajor chemistry.en
dc.titleSpectroscopic studies of metal growth on oxidesen
dc.typeThesisen
thesis.degree.disciplinechemistryen
thesis.degree.nameM.S.en
thesis.degree.levelMastersen
dc.type.genrethesisen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen


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