4.7 Article

Role of grain constraint on the martensitic transformation in ceria-doped zirconia

期刊

JOURNAL OF THE AMERICAN CERAMIC SOCIETY
卷 104, 期 2, 页码 1156-1168

出版社

WILEY
DOI: 10.1111/jace.17526

关键词

fracture; martensitic transformation; shape‐ memory ceramic; thermodynamics; zirconia

资金

  1. US Army Research Office through the Institute for Soldier Nanotechnologies [W911NF-18-2-0048]
  2. NSF [DMR-1419807, DGE-1745302]

向作者/读者索取更多资源

By conducting a comparative study on sintered pellets and powders, this research investigates the reasons behind decreased transformation temperatures and incomplete transformation in zirconia materials. The study finds that transformation temperatures are depressed in pellets due to grain constraint, while incomplete transformation in powders is attributed to insufficient driving force.
Zirconia polycrystals have historically suffered from catastrophic cracking during the tetragonal-monoclinic martensitic transformation. Recently, transformation-induced cracking has been avoided by doping to achieve crystallographic compatibility between the transforming phases. However, these materials showed depressed transformation temperatures and incomplete transformation, the causes for which are yet unknown. In this work, we probe these phenomena by performing a comparative study of sintered pellets and powders. We characterize the thermally induced transformation in a series of ZrO2-CeO2 compositions by in situ diffraction and calorimetry and develop a thermodynamic model of the system. In compositions exhibiting reduced cracking, we find that transformation temperatures are depressed in pellets but not in powders. Correspondingly, we measure significant compressive strains in pellets consistent with thermodynamically expected transformation temperature depression, demonstrating the influence of grain constraint and the resultant pressure build-up. However, we find that both pellets and powders exhibit incomplete transformation. In pellets, this is attributed to early exhaustion of autocatalysis caused by grain constraint, whereas in powders, this is attributed to insufficient driving force for distributed heterogeneous nucleation.

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