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Structure of semiconducting versus fast-ion conducting glasses in the Ag–Ge–Se system

机译:Ag-Ge-Se系统中的半导电和快速离子导电玻璃的结构

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摘要

The transition from a semiconductor to a fast-ion conductor with increasing silver content along the Agx(Ge0.25Se0.75)(100−x) tie line (0≤x≤25) was investigated on multiple length scales by employing a combination of electric force microscopy, X-ray diffraction, and neutron diffraction. The microscopy results show separation into silver-rich and silver-poor phases, where the Ag-rich phase percolates at the onset of fast-ion conductivity. The method of neutron diffraction with Ag isotope substitution was applied to the x=5 and x=25 compositions, and the results indicate an evolution in structure of the Ag-rich phase with change of composition. The Ag–Se nearest-neighbours are distributed about a distance of 2.64(1) Å, and the Ag–Se coordination number increases from 2.6(3) at x=5 to 3.3(2) at x=25. For x=25, the measured Ag–Ag partial pair-distribution function gives 1.9(2) Ag–Ag nearest-neighbours at a distance of 3.02(2) Å. The results show breakage of Se–Se homopolar bonds as silver is added to the Ge0.25Se0.75 base glass, and the limit of glass-formation at x≃28 coincides with an elimination of these bonds. A model is proposed for tracking the breakage of Se–Se homopolar bonds as silver is added to the base glass.
机译:通过结合使用以下方法在多个长度尺度上研究了沿着Agx(Ge0.25Se0.75)(100-x)连接线(0≤x≤25)从半导体到具有更高银含量的快速离子导体的过渡电动显微镜,X射线衍射和中子衍射。显微镜结果表明,分离为富银相和贫银相,其中富银相在快速离子电导率开始时发生渗滤。将具有银同位素取代的中子衍射方法应用于x = 5和x = 25组成,结果表明富Ag相的结构随组成的变化而变化。 Ag-Se最近邻居的分布距离为2.64(1)Å,Ag-Se配位数从x = 5的2.6(3)增加到x = 25的3.3(2)。对于x = 25,测得的Ag-Ag部分对分布函数给出1.9(2)Ag-Ag最近邻居,距离为3.02(2)Å。结果表明,当向Ge0.25Se0.75基玻璃中添加银时,Se-Se同质键断裂,并且在x≃28处形成玻璃的极限与这些键的消除相吻合。提出了一种模型,用于在向基础玻璃中添加银时追踪Se-Se同极性键的断裂。

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