烧结
材料科学
萤石
陶瓷
三角晶系
相(物质)
大气温度范围
多孔性
衍射
晶体结构
微观结构
格子(音乐)
晶格常数
化学工程
结晶学
矿物学
复合材料
钽酸盐
冶金
结构稳定性
放松(心理学)
X射线晶体学
固溶体
立方晶系
作者
N. Korsunska,V. Prosolenko,O. Melnichuk,Krzysztof Pęcak,L. Melnichuk,A. Hryniszyn,O. Vrublevska,V. Alekseyenko,L. Khomenkova
标识
DOI:10.1002/pssa.202501023
摘要
The structural evolution of 1Ce10ScSZ and 0.5Ce0.5Gd10ScSZ ceramics is investigated as a function of sintering temperature in the range of 1100–1500°C. The ceramics are synthesized from commercial powders with compositions of 1 mol.% CeO 2 – 10 mol.% Sc 2 O 3 – 89 mol.% ZrO 2 (1Ce10ScSZ) and 0.5 mol.% CeO 2 – 0.5 mol.% Gd – 10 mol.% Sc 2 O 3 – 89 mol.% ZrO 2 (0.5Ce0.5Gd10ScSZ). X‐ray diffraction confirms that the initial powders possess a single‐phase cubic fluorite structure. After sintering, the 0.5Ce0.5Gd10ScSZ ceramics maintains the cubic phase at all temperatures investigated, indicating high structural stability. In contrast, the 1Ce10ScSZ one sintered at 1100°C contains both cubic and rhombohedral phases. These results demonstrate that the Ce/Gd ratio strongly influences phase stability in scandium‐stabilized zirconia. The rhombohedral phase formation in 1Ce10ScSZ is attributed to increased residual porosity, which promotes lattice relaxation and symmetry lowering at low sintering temperatures. A lower heating rate markedly reduces porosity and suppresses rhombohedral formation, leading to fully cubic ceramics.
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