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An Electrochemical Approach toward the Metastable Type II Clathrate Germanium Allotrope

机译:稳定性型II型克拉尼锗锗型异化的电化学方法

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摘要

By using an anodic conversion process at 280 degrees C, the type II clathrates Na1.7(6)Ge136 and Na23.0(5)Ge136 were obtained from Na12Ge17 as the starting material. An alkali-metal iodide molten-salt electrolyte complied with the reaction conditions, allowing for the formation of microcrystalline products. Characterization by powder X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray spectroscopy also revealed Na4Ge13 as an intermediate and alpha-Ge and Cs8-xGe136 as byproducts, with the latter likely resulting from cation exchange between the starting material and electrolyte. Taking such minor side reactions and a small contribution of material without suitable electrical contact into account, anodic conversion of Na12Ge17 to Na1.7Ge136 proved to proceed without parasitic processes and to comprise the material bulk. The hitherto existing preparation method for Nax -> 0Ge136 by gas-solid oxidation of Na12Ge17 has thus been translated into a scalable high-temperature electrochemical approach with enhanced tools for reaction control, promising access to pure Ge(cF136) and Na24Ge136 after process optimization.
机译:通过使用280℃的阳极转化方法,从Na12Ge17获得II型Clathrates Na1.7(6)Ge136和Na23.0(5)Ge136作为起始材料。碱金属碘化物熔盐电解质符合反应条件,允许形成微晶产物。粉末X射线衍射,扫描电子显微镜和能量分散X射线光谱的表征还将Na4Ge13作为中间体和α-GE和CS8-XGE136作为副产物揭示,后者可能由起始材料之间的阳离子交换引起的电解质。在没有合适的电接触的情况下采取如此轻微的副反应和物质的小贡献,Na12Ge17至Na1.7ge136的阳极转化证明没有寄生过程并包含材料散装。因此,通过气体固体氧化Na12Ge17的NAX-> 0Ge136的现有制备方法已经转化为可伸缩的高温电化学方法,具有增强的反应控制工具,希望在工艺优化后对纯GE(CF136)和NA24GE136获得纯GCE(CF136)和NA24GE136。

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