材料科学
煅烧
氧化钇稳定氧化锆
兴奋剂
相(物质)
降水
热稳定性
微观结构
分析化学(期刊)
固溶体
半径
离子半径
化学工程
离子
立方氧化锆
冶金
化学
陶瓷
催化作用
有机化学
物理
气象学
工程类
光电子学
计算机科学
计算机安全
作者
Jianping Gong,Pengfei Gao,Guofeng Han,Qiang Ma,Lin Zhang,Xiaoming Wang,Baojun Yang
标识
DOI:10.1016/j.ceramint.2023.09.128
摘要
In this work, the Ce4+ and Ti4+ co-doped YSZ powders (Ce0.08-xTixY0.08Zr0.88O2.04) with various additions of Ti4+ substitution Ce4+ are prepared by the co-precipitation method. The microstructure, phase and chemical composition, phase transformation process, and phase stability after repeated calcination at 1300 °C of the powders have been investigated. The crystal structure of co-doping YSZ depends on the addition of Ti4+ substitution Ce4+ in the Ce0.08-xTixY0.08Zr0.88O2.04. When the doping molar ratio of Ce4+ to Ti4+ is 3:1 or 1:1, the ZrO2 can be stabilized to form the t′-phase and show better thermal stability, according to the TG-DSC and XRD results. Ti4+ enters the ZrO2 lattice in the form of substitution or interstitial. The oversized radius cation and undersized-radius cation co-stability can be induced by co-doping of Ti4+ and Ce4+. Thereby, the t′-ZrO2 is stabilized after repeated calcination at 1300 °C for 120 h. The co-doping of oversized radius cations and undersized-radius cations can further improve the t′-ZrO2 stability of YSZ, while the role of oversized radius cations is dominant.
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