English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

V-doped TiO2(110): Quantitative structure determination using energy scanned photoelectron diffraction

MPS-Authors
/persons/resource/persons21761

Kreikemeyer-Lorenzo,  Dagmar
Chemical Physics, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21973

Primorac,  Elena
Chemical Physics, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21699

Karslıoğlu,  Osman
Chemical Physics, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21907

Naschitzki,  Matthias
Chemical Physics, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22188

Unterberger,  Werner
Chemical Physics, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21774

Kuhlenbeck,  Helmut
Chemical Physics, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

Mixed_Oxide_preprint.pdf
(Any fulltext), 3MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Duncan, D., Kreikemeyer-Lorenzo, D., Primorac, E., Karslıoğlu, O., Naschitzki, M., Unterberger, W., et al. (2014). V-doped TiO2(110): Quantitative structure determination using energy scanned photoelectron diffraction. Surface Science, 630, 64-70. doi:10.1016/j.susc.2014.07.002.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0024-5260-F
Abstract
The surface structure of a novel vanadium–titanium dioxide epitaxial film (Ti1−xVxO2, x ~ 0.2) has been explored using V4+ 2p and Ti4+ 2p energy-scanned photoelectron diffraction (PhD). The determined structure is a rutile TiO2(110)-like surface, with V atoms substitutionally replacing some Ti atoms. The results show no evidence for significant preferential occupation by V atoms of any specific surface or sub-surface sites. LEED shows a (1 × 2) reconstruction to be present on the surface, and the PhD simulations do favour this being the dominant surface termination, although the reliability factor for simulations for a (1 × 1) termination falls just within the variance of the value for the preferred (1 × 2) structure. The V3+ and Ti3+ species were observed to occupy the same sites as the V4+ and Ti4+ species; V5+ species do not appear to occupy a single well-defined structural site.