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Experimental thermoelectric power of liquid silver-germanium alloys interpreted with an analytical energy-dependent calculation

机译:液态银锗合金的实验热电功率通过与能量相关的解析计算进行解释

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The absolute thermoelectric power of liquid Ag-Ge alloys has been measured as a Function of temperature over the whole phase diagram in 10 at.% steps, from the liquidus to 1150 degrees C. To interpret these original measurements we present an analytical expression of the thermoelectric power of the liquid alloys within the extended Faber-Ziman formalism in terms of partial structure factors and t-matrix formulation including, for the first time to our knowledge, an analytical expression of the energy-dependent contribution. The experimental first peak asymmetry of both germanium and silver structure factors cannot be reproduced with hard spheres. The Silbert-Young (1976, Phys. Lett. A, 58, 469) square-well potential describes them better for pure metal. To minimize the uncertainty in the knowledge of the partial structure factors in the electronic transport properties of liquid metals, we used the same model extended to alloys by Gopala Rao and Das (1987, Phys. Rev. B, 36, 6325). The muffin-tin potential used in this calculation to determine the t matrix is derived both from a screened ionic and from a neutral atomic potential. [References: 39]
机译:从液相线到1150摄氏度,已在整个相图中以10 at。%的步长测量了液态Ag-Ge合金的绝对热电功率作为温度的函数。为解释这些原始测量值,我们提供了解析式在扩展的Faber-Ziman形式主义内,液态合金的热电功率在局部结构因子和t矩阵公式方面均包括,据我们所知,这首次是能量依赖性贡献的分析表达式。硬球无法重现锗和银结构因子的实验性第一峰不对称性。 Silbert-Young(1976,Phys。Lett。A,58,469)的方阱势能更好地描述了纯金属。为了使液态金属的电子传输特性中的部分结构因子的知识的不确定性最小化,我们使用了Gopala Rao和Das(1987,Phys。Rev. B,36,6325)扩展到合金的相同模型。在此计算中用于确定t矩阵的松饼-锡电势既来自筛选的离子电势,也来自中性原子电势。 [参考:39]

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