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Crystal Growth Mechanism of Highly c-Axis-Oriented Apatite-Type Lanthanum Borosilicate Using B(2)O(3) Vapor
[Image: see text] Apatite-type lanthanum silicate (LSO) exhibits high oxide-ion conductivity and has recently garnered attention as a potential solid electrolyte for high-temperature solid oxide fuel cells and oxygen sensors that operate in the low- and intermediate-temperature ranges (300–500 °C)....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745409/ https://www.ncbi.nlm.nih.gov/pubmed/33344848 http://dx.doi.org/10.1021/acsomega.0c04846 |
Sumario: | [Image: see text] Apatite-type lanthanum silicate (LSO) exhibits high oxide-ion conductivity and has recently garnered attention as a potential solid electrolyte for high-temperature solid oxide fuel cells and oxygen sensors that operate in the low- and intermediate-temperature ranges (300–500 °C). LSO exhibits anisotropic oxide-ion conduction along with high c-axis-oriented oxide-ion conductivity. To obtain solid electrolytes with high oxide-ion conductivity, a technique for growing crystals oriented along the c-axis is required. For mass production and upscaling, we have thus far focused on the vapor-phase synthesis of c-axis-oriented apatite-type LSO and successfully grew polycrystals of highly c-axis-oriented boron-substituted apatite-type lanthanum silicate (c-LSBO) using B(2)O(3) vapor. Here, we investigated the mechanism of c-LSBO crystal growth to determine why the utilization of B(2)O(3) vapor resulted in such a strong c-axis crystal orientation. The synthesis of c-LSBO by the B(2)O(3) vapor-phase method results in crystal growth accompanied by the diffusion of B(2)O(3) supplied from another new compound that formed on the surface of the La(2)SiO(5) disk, LaBO(3). In addition, c-LSBO crystals are formed not only by vapor–solid reactions but also by solid–solid and liquid–solid reactions. The increase in the c-axis orientation degree might be due to the increase in the amount of the liquid-phase interface. |
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