Abstract
In recent years, scientists have progressively recognized the role of electronic structures in the characterization of chemical properties for actinide containing materials. High-energy resolution X-ray spectroscopy at the actinide M4,5 edges emerged as a promising direction because this method can probe actinide properties at the atomic level through the possibility of reducing the experimental spectral width below the natural core-hole lifetime broadening. Parallel to the technical developments of the X-ray method and experimental discoveries, theoretical models, describing the observed electronic structure phenomena, have also advanced. In this feature article, we describe the latest progress in the field of high-energy resolution X-ray spectroscopy at the actinide M4,5 and ligand K edges and we show that the methods are able to (a) provide fingerprint information on the actinide oxidation state and ground state characters (b) probe 5f occupancy, non-stoichiometry, defects, and ligand/metal ratio and (c) investigate the local symmetry and effects of the crystal field. We discuss the chemical aspects of the electronic structure in terms familiar to chemists and materials scientists and conclude with a brief description of new opportunities and approaches to improve the experimental methodology and theoretical analysis for f-electron systems.
Highlights
Most of the radioactive chemical elements are situated at the bottom of the periodic table and form the actinide group
In this article we show how the X-ray absorption near edge structure (XANES), high-energy resolution fluorescence detection (HERFD) and RIXS methods at the actinide M4,5 edges and ligand K edge can provide an unprecedented amount of detail regarding the actinide oxidation state, speciation, defects, nature of the actinide chemical bonding, 5f occupation and degree of the 5f localization
We show the utility of the method by using an example of the mixed actinide oxide (MOX) study
Summary
Most of the radioactive chemical elements are situated at the bottom of the periodic table and form the actinide group.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.