English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Photoelectron spectroscopy of polycrystalline platinum catalysts

MPS-Authors
/persons/resource/persons22071

Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21498

Ertl,  Gerhard
Physical Chemistry, 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)

929592.pdf
(Any fulltext), 2MB

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

Paál, Z., Schlögl, R., & Ertl, G. (1992). Photoelectron spectroscopy of polycrystalline platinum catalysts. Journal of the Chemical Society, Faraday Transactions, 88(8), 1179-1189. doi:10.1039/FT9928801179.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-2255-8
Abstract
Pt black catalysts have been characterized by X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS). The spectra measured after standard purification (O2 and H2 at 600 K) compared well with those of a purified reference Pt foil. All samples exhibited pronounced Fermi-edge intensities in UPS although only 60–70% Pt was detected on their surfaces by XPS, the remainder being C and O. Line analysis of the C 1s XPS, region showed the presence of partly oxidized graphite and hydrocarbon polymer, likely in three-dimensional islands. OH/H2O species attached to the metallic Pt sites were detected by UPS bands, in agreement with O 1s XPS line analysis. Similar spectral features are recorded at 600 K. Carbon could not be removed entirely by O2 up to 850 K; hydrogen did not remove surface oxygen even up to 750 K. UPS features of C on Pt used in hydrocarbon reactions were similar to those reported for amorphous hydrogenated carbon overlayers. Consequences of the present findings for the catalytic properties of Pt in n-hexane reactions and the quantification of H2–O2 titration are discussed briefly.