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- J. Schnadt, J. N. O`Shea, L. Patthey, J. Schiessling, M. Shi, J. Krempasky, J. Åhlund, N. Mårtensson, and P. A, Brühwiler
(författare)
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Structural study of adsorption of isonicotinic acid and related molecules on rutile TiO2(110) II.: XPS
- 2003
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Ingår i: Surf. Sci.. ; :544, s. 74-
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Tidskriftsartikel (refereegranskat)
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- Schnadt, J, et al.
(författare)
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Excited-state charge transfer dynamics in systems of aromatic adsorbates on TiO2 studied with resonant core techniques
- 2003
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Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 119:23, s. 12462-12472
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Tidskriftsartikel (refereegranskat)abstract
- Resonant core spectroscopies are applied to a study of the excited electron transfer dynamics on a low-femtosecond time scale in systems of aromatic molecules (isonicotinic acid and bi-isonicotinic acid) adsorbed on a rutile TiO2(110) semiconductor surface. Depending on which adsorbate state is excited, the electron is either localized on the adsorbate in an excitonic effect, or delocalizes rapidly into the substrate in less than 5 fs (3 fs) for isonicotinic acid (bi-isonicotinic acid). The results are obtained by the application of a variant of resonant photoemission spectroscopy. (C) 2003 American Institute of Physics.
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- Schnadt, Joachim, et al.
(författare)
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Structural study of adsorption of isonicotinic acid and related molecules on rutile TiO2(110) I: XAS and STM
- 2003
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Ingår i: Surface Science. - 0039-6028. ; 540:1, s. 39-54
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Tidskriftsartikel (refereegranskat)abstract
- X-ray absorption spectroscopy (XAS) and scanning tunneling microscopy (STM) have been used to study the absorption of monolayers of the pyridinecarboxylic acid monomers (isonicotinic acid, nicotinic acid, and picolinic acid) and benzoic acid on a rutile TiO2(1 1 0) surface. We find that the pyridine and phenyl rings are oriented with their planes largely perpendicular to the surface. The azimuthal orientations are strongly influenced by adsorbate-adsorbate interactions, which in each case leads to at least two different molecular species. In order to reach this conclusion a detailed strategy has been developed for the interpretation of angle-dependent XAS data, which does not rely on any curve fitting procedures. (C) 2003 Elsevier B.V. All rights reserved.
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- O'Shea, J. N., et al.
(författare)
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Hydrogen-bond induced surface core-level shift in isonicotinic acid
- 2001
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1089-5647 .- 1520-6106 .- 1520-5207. ; 105:10, s. 1917-1920
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Tidskriftsartikel (refereegranskat)abstract
- 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.
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| 10. |
- O'Shea, J. N., et al.
(författare)
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Hydrogen-bond induced surface core-level shift in pyridine carboxylic acids
- 2001
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Ingår i: Surface Science. - 0039-6028 .- 1879-2758. ; 486:3, s. 157-166
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Tidskriftsartikel (refereegranskat)abstract
- Intermolecular hydrogen bonding in thick films of pyridine carboxylic acids (isonicotinic; picolinic and bi-isonicotinic acid) evaporated onto rutile TiO2(1 1 0) has been investigated with X-ray photoelectron spectroscopy and X-ray absorption spectroscopy. These molecules are shown to be strongly H-bonded in the condensed phase, and a surface core-level shift is observed due to the presence of non-H-bonded nitrogen atoms in the surface layer. Density functional theory calculations are used to relate the experimental data to the proposed bonding configurations based on the surface termination of the known equilibrium solid-state structure. A kinetic barrier, attributed to the high degree of molecular orientation required for the formation of extended H-bonding networks, has also been investigated.
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