Show simple item record

dc.contributor.advisorHwang, Gyeong S.en
dc.identifier.oclc156913242en
dc.creatorPillay, Devinaen
dc.date.accessioned2008-08-28T23:09:01Zen
dc.date.accessioned2017-05-11T22:17:30Z
dc.date.available2008-08-28T23:09:01Zen
dc.date.available2017-05-11T22:17:30Z
dc.date.issued2006en
dc.identifierb65487060en
dc.identifier.urihttp://hdl.handle.net/2152/2791en
dc.descriptiontexten
dc.description.abstractCu, Ag, and Au nanoclusters dispersed on TiO2(110) surfaces are utilized in a wide variety of applications ranging from microelectronics to heterogeneous catalysis. The unique chemical reactivity of these clusters is largely dependent on their size, shape, spatial distribution, and interfacial interaction with the oxide support. This implies that atomic level control of these properties can offer great opportunities in the development of novel devices based on supported metal nanoclusters. It is therefore necessary to understand how formation and restructuring of these clusters alter their geometric and electronic characteristics. This thesis involves the development of a theoretical foundation for studying the growth, structure, and chemistry of Cu, Ag, and Au on TiO2(110) surfaces. Using density functional theory calculations, we have identified factors that control the chemical reactivity of these supported metal nanoclusters. First we investigated the electronic and geometric structures of the stoichiometric and reduced rutile TiO2(110) surfaces. Then we examined the surface chemistry of TiO2 towards gaseous CO and O2, as well as the structure and growth of 1B metal nanoclusters on TiO2(110). We also examined how the electronic and geometric properties of mixed metal nanoclusters, CuAun(n≤ 3), differ versus their single metal counterparts, Cum and Aum (m ≤ 4). Finally, we considered CO oxidation reactions on TiO2(110)-supported small Au clusters. While current experimental techniques are limited to providing complementary atomic-level real space information, first principles-based atomic level simulations greatly contribute to elucidating the fundamental behavior and properties of Cu, Ag, and Au nanoclusters on TiO2(110). First principles modeling has paved the way for new catalyst development by investigating how the geometric, electronic, and chemical properties of TiO2-supported 1B metal nanoclusters vary with surface defects, adsorbates, and metal dopants before valuable time and manpower is invested in experimental synthesis and characterization.
dc.format.mediumelectronicen
dc.language.isoengen
dc.rightsCopyright is held by the author. Presentation of this material on the Libraries' web site by University Libraries, The University of Texas at Austin was made possible under a limited license grant from the author who has retained all copyrights in the works.en
dc.subject.lcshTitanium dioxide--Surfacesen
dc.subject.lcshCopperen
dc.subject.lcshSilveren
dc.subject.lcshGolden
dc.subject.lcshSurface chemistryen
dc.subject.lcshReactivity (Chemistry)en
dc.titleGrowth, structure, and chemistry of 1B metal nanoclusters supported on TiO₂(110)en
dc.description.departmentChemical Engineeringen
dc.type.genreThesisen


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record