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Defect Structure and Oxide Ion Conduction of Potassium Ion Substituted CaWO(4)

We have prepared Ca(1−x)K(x)WO(4−x/2) solid solutions with the Scheelite-type structure to investigate high-temperature electrochemical properties. Room-temperature X-ray diffraction suggested the solid solution range was x ≤ 0.2, since the second phase presumably of K(2)WO(4) was detected for x = 0...

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Detalles Bibliográficos
Autores principales: Takai, Shigeomi, Shitaune, Shinya, Sano, Toshifumi, Kawaji, Hitoshi, Yabutsuka, Takeshi, Esaka, Takao, Yao, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073822/
https://www.ncbi.nlm.nih.gov/pubmed/29954067
http://dx.doi.org/10.3390/ma11071092
Descripción
Sumario:We have prepared Ca(1−x)K(x)WO(4−x/2) solid solutions with the Scheelite-type structure to investigate high-temperature electrochemical properties. Room-temperature X-ray diffraction suggested the solid solution range was x ≤ 0.2, since the second phase presumably of K(2)WO(4) was detected for x = 0.3. For all the substituted samples up to x = 0.4, a large jump in conductivity has been observed around 500 °C. At higher temperatures, oxide ion conduction is found to be predominant even for x = 0.4, exceeding the solution limit estimated from the room-temperature XRD. The conductivity at high temperature is essentially proportional to the amount of substituted potassium ions up to x = 0.4, indicating that oxide ion conduction is associated with the formed oxide ion vacancy. High-temperature X-ray diffraction detected no apparent change in lattice parameters around 500 °C for x = 0.1, and the remaining second phase seems to be incorporated into the Scheelite lattice at high temperatures.