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Pressure-induced amorphization of cubic ZrMo2O8 studied in situ by X-ray absorption spectroscopy and diffraction

机译:X射线吸收光谱和衍射原位研究立方ZrMo2O8的压力诱导非晶化

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A combination of in situ high-pressure X-ray diffraction and Mo K-edge XANES was used to examine the changes in local structure that occur as the negative thermal expansion material cubic zirconium molybdate becomes amorphous on compression and, hence, provide insight into the mechanism of amorphization. Amorphization started at similar to 1.7 and by 4.1 GPa the sample was glass like by diffraction. The XANES data shows that the pressure induced amorphization at 4.1 GPa does not involve a complete change of molybdenum coordination from tetrahedral, in the starting phase, to approximately octahedral as would be expected if the amorphous material were a metastable intermediate well advanced along the pathway towards decomposition into a mixture Of MoO3 and ZrO2. Recrystallization of the amorphous material at 600 degrees C and 4.1 GPa produced a sample that was not a simple mixture of known MoO3 and ZrO2 polymorphs nor a known polymorph of ZrMo2O8. (C) 2005 Elsevier Ltd. All rights reserved.
机译:原位高压X射线衍射和Mo K-edge XANES的组合用于检查局部结构的变化,这些变化是由于负热膨胀材料立方钼酸锆在压缩时变为非晶态而产生的,因此,我们可以了解非晶化机制。非晶化的开始时间接近1.7,到4.1 GPa时,样品像衍射一样是玻璃。 XANES数据表明,压力诱导的4.1 GPa非晶化不涉及钼配位从开始阶段的四面体到大约八面体的完全变化,如果非晶态材料是沿通向反应途径的亚稳中间井,则将是预期的。分解成MoO3和ZrO2的混合物。非晶材料在600摄氏度和4.1 GPa的条件下再结晶,产生的样品不是已知的MoO3和ZrO2多晶型物的简单混合物,也不是ZrMo2O8的已知多晶型物。 (C)2005 Elsevier Ltd.保留所有权利。

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