Abstract

We studied the nucleation of gold clusters on TiO 2 (110) surfaces in three different oxidation states by high-resolution scanning tunneling microscopy. The three TiO 2 (110) supports chosen were (i) reduced (having bridging oxygen vacancies), (ii) hydrated (having bridging hydroxyl groups), and (iii) oxidized (having oxygen adatoms). At room temperature, gold nanoclusters nucleate homogeneously on the terraces of the reduced and oxidized supports, whereas on the hydrated TiO 2 (110) surface, clusters form preferentially at the step edges. From interplay with density functional theory calculations, we identified two different gold-TiO 2 (110) adhesion mechanisms for the reduced and oxidized supports. The adhesion of gold clusters is strongest on the oxidized support, and the implications of this finding for catalytic applications are discussed.

Keywords

NanoclustersScanning tunneling microscopeNucleationColloidal goldMaterials scienceDensity functional theoryOxygenChemical physicsNanoparticleNanotechnologyGold clusterCrystallographyCatalysisChemical engineeringChemistryPhotochemistryComputational chemistryOrganic chemistry

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Publication Info

Year
2007
Type
article
Volume
315
Issue
5819
Pages
1692-1696
Citations
475
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D. Matthey, J. G. Wang, Stefan Wendt et al. (2007). Enhanced Bonding of Gold Nanoparticles on Oxidized TiO <sub>2</sub> (110). Science , 315 (5819) , 1692-1696. https://doi.org/10.1126/science.1135752

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DOI
10.1126/science.1135752