Uncovering the Effects of Non-Hydrostaticity on Pressure-Induced Phase Transformation in Xenotime-Structured TbPO4

Solids Pub Date : 2024-02-16 DOI:10.3390/solids5010008
Jai Sharma, C. Packard
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Abstract

The pressure-induced phase transformations of rare earth orthophosphates (REPO4s) have become increasingly relevant in ceramic matrix composite (CMC) research; however, understanding of the shear-dependence of these transformations remains limited. This study employs diamond anvil cell experiments with three pressure media (neon, KCl, sample itself/no medium) to systematically assess the effect of shear on the phase transformations of TbPO4. Results show a lowering of the TbPO4 transformation onset pressure (Ponset) as well as an extension of the xenotime–monazite phase coexistence range under non-hydrostatic conditions. The TbPO4 Ponset under no medium (4.4(3) GPa) is the lowest REPO4 Ponset reported to date and represents a ~50% drop from the hydrostatic Ponset. Enthalpic differences likely account for lower Ponset values in TbPO4 compared to DyPO4. Experiments also show scheelite may be the post-monazite phase of TbPO4; this phase is consistent with observed and predicted REPO4 transformation pathways.
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揭示非静力学对氙结构 TbPO4 中压力诱导相变的影响
稀土正磷酸盐(REPO4)的压力诱导相变在陶瓷基复合材料(CMC)研究中的重要性日益凸显;然而,对这些相变的剪切依赖性的了解仍然有限。本研究采用三种压力介质(氖、氯化钾、样品本身/无介质)进行金刚石砧室实验,系统评估剪切力对 TbPO4 相变的影响。结果表明,在非流体静力学条件下,TbPO4 转变起始压力(Ponset)降低,氙-蒙脱石相共存范围扩大。无介质条件下的 TbPO4 起始压(4.4(3) GPa)是迄今为止报告的最低的 REPO4 起始压,与静水压起始压相比下降了约 50%。与 DyPO4 相比,TbPO4 中较低的 Ponset 值可能与邻苯二甲酸盐的差异有关。实验还显示白钨矿可能是 TbPO4 的后蒙脱石相;该相与观察到的和预测的 REPO4 转化途径一致。
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