Apr 11, 2025
11:30am - 11:45am
Summit, Level 3, Room 339
Shinhyo Bang1,Adrien Terricabras2,Xiaofeng Guo1,Joshua White2,Arjen van Veelen2
Washington State University1,Los Alamos National Laboratory2
Shinhyo Bang1,Adrien Terricabras2,Xiaofeng Guo1,Joshua White2,Arjen van Veelen2
Washington State University1,Los Alamos National Laboratory2
Chromia (CrO
x) doping has become a key method for promoting grain growth and enhancing fission gas retention in uranium dioxide (UO
2), leading to the commercial development of products like 'ADOPT' and 'PROtect.' While much of the research is focused on the local structure and valence of chromium, less attention has been given to the U environment in Cr-doped UO
2, which was assumed to have minimal changes after being introduced with dopant levels of Cr. In this work, we observed non-trivial changes in the U local structure of Cr-doped UO
2 using extended x-ray absorption fine structure (EXAFS) when the material was sintered under varying oxygen partial pressures at high temperatures. These changes are driven by the valence states of Cr susceptible to oxygen partial pressures and temperatures during the sintering. The structural change by the Cr dopant level was also systematically investigated. These findings offer new insights into the fundamental behavior governing the diffusion of species, which influences the grain growth of the Cr-doped UO
2. In the context of fuel performance, this understanding will contribute to the development of enhanced nuclear fuels.