首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Role of bond strength on the lattice thermal expansion and oxide ion conductivity in quaternary pyrochlore solid solutions
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Role of bond strength on the lattice thermal expansion and oxide ion conductivity in quaternary pyrochlore solid solutions

机译:季铵盐固溶体中结合强度对晶格热膨胀和氧化物离子电导率的作用

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摘要

Quaternary pyrochlore-type solid solutions, CaGdZrNb _(1-x)Ta _xO _7 (x = 0, 0.2, 0.4, 0.6, 0.8, 1), were prepared by a high-temperature ceramic route. The pyrochlore phases of the compounds were confirmed by powder X-ray diffraction (XRD), Raman spectroscopy, and transmission electron microscopy. The crystallographic parameters of the pyrochlore compounds were accurately determined by Rietveld analysis of the powder XRD data. The isovalent substitution of Ta in place of Nb at the B site can reveal the effect of chemical bonding on lattice thermal expansion and oxide ion conductivity because both Nb and Ta have the same ionic radius (0.64 ?). Lattice thermal expansion coefficients of the samples were calculated from high-temperature XRD measurements, and it was found that the thermal expansion coefficient decreases with substitution of Ta. Oxide ion conductivity measured by a two-probe method also shows the same trend with substitution of Ta, and this can be attributed to the high bond strength of the Ta-O bond compared to that of the Nb-O bond. Microstructural characterization using scanning electron microscopy proves that the size of the grains has a small effect on the oxide ion conductivity. Our studies established the role of chemical bonding in deciding the conductivity of pyrochlore oxides and confirmed that the 48f-48f mechanism of oxide ion conduction is dominant in pyrochlore oxides.
机译:通过高温陶瓷路线制备季铵盐型固溶体CaGdZrNb _(1-x)Ta _xO _7(x = 0、0.2、0.4、0.6、0.8、1)。通过粉末X射线衍射(XRD),拉曼光谱和透射电子显微镜确认化合物的烧绿石相。通过粉末XRD数据的Rietveld分析准确地确定了烧绿石化合物的晶体学参数。 Ta的等价取代是在B位上代替Nb,因为Nb和Ta具有相同的离子半径(0.64Ω),因此可以揭示化学键合对晶格热膨胀和氧化物离子传导性的影响。通过高温XRD测量计算出样品的晶格热膨胀系数,发现热膨胀系数随着Ta的替代而降低。通过双探针法测量的氧化物离子电导率在取代Ta时也显示出相同的趋势,这可以归因于Ta-O键的键强度比Nb-O键的键强度高。使用扫描电子显微镜的显微结构表征证明,晶粒尺寸对氧化物离子电导率的影响很小。我们的研究建立了化学键在确定烧绿石氧化物电导率中的作用,并证实了48f-48f的氧化离子传导机理在烧绿石氧化物中占主导地位。

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