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Tunable transport property of oxygen ion in metal oxide thin film: Impact of electrolyte orientation on conductivity

机译:氧离子在金属氧化物薄膜中的可调传输性能:电解质取向对电导率的影响

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摘要

Quest for efficient ion conducting electrolyte thin film operating at intermediate temperature (~600 °C) holds promise for the real-world utilization of solid oxide fuel cells. Here, we report the correlation between mixed as well as preferentially oriented samarium doped cerium oxide electrolyte films fabricated by varying the substrate temperatures (100, 300 and 500 °C) over anode/ quartz by electron beam physical vapor deposition. Pole figure analysis of films deposited at 300 °C demonstrated a preferential (111) orientation in out-off plane direction, while a mixed orientation was observed at 100 and 500 °C. As per extended structural zone model, the growth mechanism of film differs with surface mobility of adatom. Preferential orientation resulted in higher ionic conductivity than the films with mixed orientation, demonstrating the role of growth on electrochemical properties. The superior ionic conductivity upon preferential orientation arises from the effective reduction of anisotropic nature and grain boundary density in highly oriented thin films in out-of-plane direction, which facilitates the hopping of oxygen ion at a lower activation energy. This unique feature of growing an oriented electrolyte over the anode material opens a new approach to solving the grain boundary limitation and makes it as a promising solution for efficient power generation.
机译:寻求在中间温度(〜600 C)下运行的高效离子导电电解质薄膜,有望在现实世界中使用固体氧化物燃料电池。在这里,我们报告了混合和优先取向的do掺杂二氧化铈电解质薄膜之间的相关性,这些薄膜是通过电子束物理气相沉积通过改变阳极/石英上的基板温度(100、300和500 C)而制成的。在300°C下沉积的薄膜的极图分析表明,在偏外平面方向上具有优先(111)取向,而在100和500°C下观察到混合取向。根据扩展结构区模型,膜的生长机理随吸附原子的表面迁移率而异。优先取向比混合取向的薄膜具有更高的离子电导率,证明了生长对电化学性能的作用。优先取向时优越的离子电导率是由于有效降低了高取向薄膜在平面外方向上的各向异性和晶界密度而引起的,这有利于氧离子以较低的活化能跳跃。在阳极材料上生长定向电解质的独特功能为解决晶界限制开辟了新途径,使其成为有效发电的有前途的解决方案。

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