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Crystal Structural Study of Ho-doped Ceria Using X-ray Powder Diffraction Data

机译:利用X射线粉末衍射数据研究Ho掺杂二氧化铈的晶体结构

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Crystal structural analysis of Ho-doped ceria (Ce_(0.7)Ho_(0.3)O_(1.85)) was performed using both conventional laboratory and synchrotron X-ray diffraction (XRD) data. In the laboratory XRD data, a poor refinement result was achieved based on a cubic phase (space group Fm-3m, No.225); weighted (R_(wp)) and profile (R_p) R-factors were 16.2 and 13.4%, respectively. However, the R-factors significantly decreased to 8.76 and 6.87% for the R_(wp) and R_p values, respectively, when a secondary cubic phase was added in the refinement model. While the phases were indistinguishable in the laboratory XRD data because of close peak positions, they were clearly separated in the synchrotron XRD data owing to monochromatic wavelength. The final Rietveld refinement results revealed that Ce_(0.7)Ho_(0.3)O_(1.85) consists of two cubic (Fm-3m) phases; major Ce-rich phase (Ce:Ho=78:22, with a lattice parameter of 5.4097(1) A) and minor Ho-rich phase (Ce:Ho=45:55, with a lattice parameter of 5.3877(1) A). The ratio between the major and minor phases was 66:34. The final converged R_(wp) and R_p obtained from the synchrotron XRD data were 12.9 and 10.8%, respectively.
机译:使用常规实验室和同步加速器X射线衍射(XRD)数据进行Ho掺杂二氧化铈(Ce_(0.7)Ho_(0.3)O_(1.85)的晶体结构分析。在实验室XRD数据中,基于立方相(空间群Fm-3m,编号225),精制效果不佳;加权(R_(wp))和曲线(R_p)R因子分别为16.2%和13.4%。但是,当在精炼模型中添加次立方相时,R_(wp)和R_p值的R因子分别显着降低至8.76和6.87%。尽管由于接近的峰位置在实验室XRD数据中无法区分这些相,但由于单色波长,它们在同步加速器XRD数据中明显分开。 Rietveld的最终精炼结果表明Ce_(0.7)Ho_(0.3)O_(1.85)由两个立方(Fm-3m)相组成。主富铈相(Ce:Ho = 78:22,晶格参数为5.4097(1)A)和次富硒相(Ce:Ho = 45:55,晶格参数为5.3877(1)A )。主相和次相之间的比例为66:34。从同步加速器XRD数据获得的最终收敛R_(wp)和R_p分别为12.9和10.8%。

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