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Oxygen Ion Diffusion and Surface Exchange Properties of the phases of Bi2O3

机译:Bi2O3相的氧离子扩散和表面交换性质

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Fast oxide ion conduction is a highly desirable property for materials in a wide range of applications. The fastest reported ionic conductor, representing the current state of the art and an oft-proposed effective limit of oxide ion conductivity, is the high temperature fluorite-structured δ phase of Bi2O3. Here, the ionic nature of this conduction is, for the first time, directly determined through oxygen tracer diffusion measurements. This phase also presents a remarkably high oxygen surface exchange coefficient, competitive with the highest performance solid oxide fuel cell (SOFC) cathodes yet counterintuitively in a material with negligible electronic conduction. The low temperature -Bi2O3 polymorph is also investigated, revealing a remarkable drop in diffusivity of over 7 orders of magnitude with a temperature drop of just ≈150 °C. Surprisingly, the diffusion studies also reveal a secondary, significantly faster migration pathway in the phase. This is attributed to grain boundary conduction and shown to be 3–4 orders of magnitude higher than in the bulk. This previously unobserved property could present an exciting opportunity to tailor ionic conductivity levels through manipulating microstructure down to the nanoscale.
机译:快速氧化物离子传导是材料在广泛应用中的高度期望的性能。报告最快的离子导体是Bi2O3的高温萤石结构δ相,代表了目前的技术水平和经常提出的氧化物离子电导率的有效极限。在此,首次通过氧示踪剂扩散测量直接确定这种传导的离子性质。该相还具有非常高的氧表面交换系数,可与性能最高的固体氧化物燃料电池(SOFC)阴极竞争,但在电子传导性可忽略的材料中却相反。还研究了低温-Bi2O3多晶型物,发现扩散率显着下降了7个数量级以上,而温度下降仅为≈150°C。出人意料的是,扩散研究还揭示了该阶段的第二条明显更快的迁移途径。这归因于晶界传导,显示出比整体高3-4个数量级。这种以前无法观察到的特性可能会提供一个令人兴奋的机会,可以通过将微观结构控制到纳米级来调整离子电导率水平。

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