Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Redox properties of titanium oxides on Pt3Ti
KTH, Superseded Departments, Physics.
Show others and affiliations
1995 (English)In: Journal of Physical Chemistry, ISSN 00223654 (ISSN), Vol. 99, no 34, 12892-12895 p.Article in journal (Refereed) Published
Abstract [en]

The morphology and electronic structure of surface-segregated titanium oxides on Pt3Ti(111) are presented. Core level photoemission spectra at grazing emission reveal two states of oxidation: a dominant and reducible four-valent oxide together with a small amount of a three-valent oxide is produced by oxidation in O2 at and below 400°C; an irreducible three-valent oxide by oxidation in O2 at and above 450°C. The ratio between the active four-valent and the inactive three-valent oxides decreases with increasing oxidation temperature. The probability for reduction by CO is almost unity for the Ti4+ oxide, and the conclusion must be that the four-valent oxide plays an active role for catalytic reactions. Scanning tunneling measurements relate these observations to changes in the dispersion and nucleation of the oxide overlayer. The four-valent oxide grows as islands with remaining areas open for CO adsorption while the three-valent oxide spreads on and blocks the crystal surface. Photoemission spectra relate these dispersion effects to an electronic interaction between the Ti3+ oxide and adjacent Pt atoms. The above observations are in accordance with the common picture of dispersion effects in titania-supported SMSI catalysts and prove that interfacial energies play a crucial role whether the dominant phase is metallic or an oxide. © 1995 American Chemical Society.

Place, publisher, year, edition, pages
1995. Vol. 99, no 34, 12892-12895 p.
National Category
Condensed Matter Physics
Identifiers
URN: urn:nbn:se:kth:diva-83031OAI: oai:DiVA.org:kth-83031DiVA: diva2:502767
Note
Correspondence Address: Paul, J.; KTH/Royal Institute of Technology, Physics III, 100 44 Stockholm, Sweden NR 20140805Available from: 2012-02-14 Created: 2012-02-12 Last updated: 2012-02-14Bibliographically approved

Open Access in DiVA

No full text

Other links

http://www.scopus.com/inward/record.url?eid=2-s2.0-6244285601&partnerID=40&md5=711f95f62d55b4ba8a86255fce2b122e
By organisation
Physics
Condensed Matter Physics

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 15 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf