Werner, Josephina
- Institutionen för kemi och bioteknologi, Sveriges lantbruksuniversitet
- Uppsala universitet
Sammanfattning
X-ray photoelectron spectroscopy (XPS) is widely used to probe properties such as molecular stoichiometry, microscopic distributions relative to the surface by so-called depth-profiling, and molecular orientation. Such studies usually rely on the core-level photoionization cross sections being independent of molecular composition. The validity of this assumption has recently been questioned, as a number of gas-phase molecules have been shown to exhibit photon-energy-dependent nonstochiometric intensity oscillations arising from EXAFS-like modulations of the photoionization cross section. We have studied this phenomenon in trichloroethanol in both gas phase and dissolved in water. The gas-phase species exhibits pronounced intensity oscillations, similar to the ones observed for other gas-phase molecules. These oscillations are also observed for the dissolved species, implying that the effect has to be taken into account when performing depth-profiling experiments of solutions and other condensed matter systems. The similarity between the intensity oscillations for gas phase and dissolved species allows us to determine the photoelectron kinetic energy of maximum surface sensitivity, approximate to 100 eV, which lies in the range of pronounced intensity oscillations.
Publicerad i
Journal of Physical Chemistry C
2014, volym: 118, nummer: 50, sidor: 29333-29339
Utgivare: AMER CHEMICAL SOC
SLU författare
UKÄ forskningsämne
Fysikalisk kemi
Publikationens identifierare
- DOI: https://doi.org/10.1021/jp505569c
Permanent länk till denna sida (URI)
https://res.slu.se/id/publ/67120