TY - JOUR
T1 - The thermal stability of non-stoichiometric Y-Zr-O nanoparticles in oxide dispersion strengthened (ODS) Mo alloys
AU - Yao, Liying
AU - Gao, Yimin
AU - Li, Yefei
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/11
Y1 - 2022/11
N2 - In our previous work, a nanostructured oxide dispersion strengthened (ODS) Mo alloy with a high density of non-stoichiometric Y-Zr-O nanoparticles was developed as fuel cladding material. Considering the hostile high-temperature condition, this study focuses on the thermal stability of non-stoichiometric Y-Zr-O nanoparticles at 1400 °C for 48 h. Results showed that non-stoichiometric Y-Zr-O nanoparticles appeared to coarsen, resulting in the loss of coherency with the Mo matrix. The core/shell structure with Y-rich Y-Zr-O oxide cores and Zr-rich shells was formed by Zr diffusion from the Mo matrix to the oxides/matrix interface. Together with Ostwald ripening, it contributed to the evolution from metastable non-stoichiometric Y-Zr-O oxides to equilibrium Y-Zr-O oxides with a partitioned Y2O3 concentration distribution. Further, the Zr addition accelerated the coarsening of Y-Zr-O oxides. Zr-rich Y-Zr-O oxides were more likely to coarsen due to the larger equilibrium solubility of the Zr element and diffusion activation energy than those of Y-rich Y-Zr-O oxides.
AB - In our previous work, a nanostructured oxide dispersion strengthened (ODS) Mo alloy with a high density of non-stoichiometric Y-Zr-O nanoparticles was developed as fuel cladding material. Considering the hostile high-temperature condition, this study focuses on the thermal stability of non-stoichiometric Y-Zr-O nanoparticles at 1400 °C for 48 h. Results showed that non-stoichiometric Y-Zr-O nanoparticles appeared to coarsen, resulting in the loss of coherency with the Mo matrix. The core/shell structure with Y-rich Y-Zr-O oxide cores and Zr-rich shells was formed by Zr diffusion from the Mo matrix to the oxides/matrix interface. Together with Ostwald ripening, it contributed to the evolution from metastable non-stoichiometric Y-Zr-O oxides to equilibrium Y-Zr-O oxides with a partitioned Y2O3 concentration distribution. Further, the Zr addition accelerated the coarsening of Y-Zr-O oxides. Zr-rich Y-Zr-O oxides were more likely to coarsen due to the larger equilibrium solubility of the Zr element and diffusion activation energy than those of Y-rich Y-Zr-O oxides.
KW - Core-shell structure
KW - Oxide dispersion strengthened (ODS) alloy
KW - Particle coarsening
KW - Y-Zr-O nanoparticles
UR - https://www.scopus.com/pages/publications/85136121584
U2 - 10.1016/j.jnucmat.2022.153984
DO - 10.1016/j.jnucmat.2022.153984
M3 - 文章
AN - SCOPUS:85136121584
SN - 0022-3115
VL - 570
JO - Journal of Nuclear Materials
JF - Journal of Nuclear Materials
M1 - 153984
ER -