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Hydrogen-bond induced surface core-level shift in isonicotinic acid

O'Shea, J. N. (author)
Schnadt, J. (author)
Bruhwiler, P. A. (author)
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Hillesheimer, H. (author)
Martensson, N. (author)
Patthey, L. (author)
Krempasky, J. (author)
Wang, C. K. (author)
Luo, Yi (author)
KTH,Bioteknologi
Ågren, Hans (author)
KTH,Bioteknologi
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 (creator_code:org_t)
2001-02-20
2001
English.
In: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1089-5647 .- 1520-6106 .- 1520-5207. ; 105:10, s. 1917-1920
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Intermolecular hydrogen-bonding in thick films of isonicotinic acid evaporated onto rutile TiO2(110) has been investigated with X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS). The rate of deposition is found to be a key factor in overcoming the kinetic barriers to extensive hydrogen-bond formation, which, when present, gives rise to large energy shifts between bulk and surface in both the N1s XPS and XAS. The origin of the surface core-level shift is attributed to the presence of non-hydrogen-bonded nitrogen atoms in the surface layer.

Keyword

molecular-beam deposition
organic thin-films
rutile tio2(110)
spectroscopy
clusters

Publication and Content Type

ref (subject category)
art (subject category)

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