TY - JOUR
T1 - A new approach for nuclear forensics investigations of uranium dioxide: Application of laboratory-based photoelectron spectroscopy with hard and Soft X-ray sources
AU - Dunn, Stuart
AU - Harrison, Robert
AU - Gilbert, Matthew
AU - Middleburgh, Simon
PY - 2025/8/1
Y1 - 2025/8/1
N2 - Nuclear Forensic investigations rely on the analysis of the chemical and physical properties of nuclear materials. X-ray photoelectron spectroscopy (XPS) is a powerful tool that supports material assessment, typically analyzing the top few nanometers of the material. The onset of laboratory-based hard X-ray photoelectron spectroscopy (HAXPES) instrumentation provides the opportunity to probe deeper into the material’s bulk. The work presented in this study demonstrates the utility of a combined XPS and HAXPES analysis to isolate forensic signatures on the surface and into the bulk of uranium dioxide. A non-destructive depth profile, using the transitions observable with a 9.25 keV excitation source, highlighted an oxidized overlayer deeper than the XPS sampling depth. Peak fitting of high-resolution spectra allows identification of uranium oxidation states as well as inspection of secondary features, which provide insight into the material characteristics with an evolving chemistry from the surface to a more bulk like composition. Inelastic background analysis is performed to determine the in-depth distribution of atoms, developing a consistent model to describe the surface overlayer, correlated to the chemical and stoichiometric differences over the excitation range. Finally, the MNN X-ray excited Auger electron spectra are acquired from uranium dioxide for the first time for future use in the application of a Wagner chemical state plot to support nuclear forensics investigations.
AB - Nuclear Forensic investigations rely on the analysis of the chemical and physical properties of nuclear materials. X-ray photoelectron spectroscopy (XPS) is a powerful tool that supports material assessment, typically analyzing the top few nanometers of the material. The onset of laboratory-based hard X-ray photoelectron spectroscopy (HAXPES) instrumentation provides the opportunity to probe deeper into the material’s bulk. The work presented in this study demonstrates the utility of a combined XPS and HAXPES analysis to isolate forensic signatures on the surface and into the bulk of uranium dioxide. A non-destructive depth profile, using the transitions observable with a 9.25 keV excitation source, highlighted an oxidized overlayer deeper than the XPS sampling depth. Peak fitting of high-resolution spectra allows identification of uranium oxidation states as well as inspection of secondary features, which provide insight into the material characteristics with an evolving chemistry from the surface to a more bulk like composition. Inelastic background analysis is performed to determine the in-depth distribution of atoms, developing a consistent model to describe the surface overlayer, correlated to the chemical and stoichiometric differences over the excitation range. Finally, the MNN X-ray excited Auger electron spectra are acquired from uranium dioxide for the first time for future use in the application of a Wagner chemical state plot to support nuclear forensics investigations.
U2 - 10.1016/j.apsadv.2025.100782
DO - 10.1016/j.apsadv.2025.100782
M3 - Article
SN - 2666-5239
VL - 28
JO - Applied Surface Science Advances
JF - Applied Surface Science Advances
M1 - 100782
ER -