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首页> 外文期刊>The journal of physics and chemistry of solids >Structural stability of anhydrous proton conducting SrZr0.9Er0.1O3-delta perovskite ceramic vs. protonation/deprotonation cycling: Neutron diffraction and Raman studies
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Structural stability of anhydrous proton conducting SrZr0.9Er0.1O3-delta perovskite ceramic vs. protonation/deprotonation cycling: Neutron diffraction and Raman studies

机译:无水质子传导SrZr0.9Er0.1O3-δ钙钛矿陶瓷的结构稳定性与质子/去质子循环的关系:中子衍射和拉曼研究

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摘要

Long-term chemical and structural stability of an ion conducting ceramic is one of the main criteria for its selection as an electrolytic membrane in energy plant devices. Consequently, medium density SrZr0.9Er0.1O3-delta (SZE) anhydrous proton conducting ceramic - a potential electrolyte of SOFC/PCFC, was analysed by neutron diffraction between room temperature and 900 degrees C. After the first heating/cooling cycle, the ceramic pieces were exposed to water vapour pressure in an autoclave (500 degrees C, 40 bar, 7 days) in order to incorporate protonic species; the protonated compound was then again analysed by neutron diffraction. This procedure was repeated two times. At each step, the sample was also controlled by TGA and Raman spectroscopy. These studies allow the first comprehensive comparison of structural and chemical stability during the protonation/deprotonation cycling. The results reveal good structural stability, although an irreversible small contraction of the unit-cell volume and local structure modifications near Zr/ErO5[] octahedra are detected after the first protonation. After the second protonation easy ceramic crumbling under a stress is observed because of the presence of secondary phases (SrCO3, Sr(OH)(2)) well detected by Raman scattering and TGA. The role of crystallographic purity, substituting element and residual porosity in the proton conducting perovskite electrolyte stability is discussed. (C) 2015 Elsevier Ltd. All rights reserved.
机译:离子导电陶瓷的长期化学和结构稳定性是在能源设备中选择其作为电解膜的主要标准之一。因此,通过室温和900摄氏度之间的中子衍射分析了中等密度SrZr0.9Er0.1O3-δ(SZE)无水质子传导陶瓷-SOFC / PCFC的潜在电解质。在第一个加热/冷却循环后,陶瓷在高压釜中(500摄氏度,40巴,7天)将碎片暴露于水蒸气压力中,以吸收质子物质。然后再次通过中子衍射分析质子化的化合物。将该过程重复两次。在每个步骤中,还通过TGA和拉曼光谱控制样品。这些研究允许在质子化/去质子化循环过程中进行结构和化学稳定性的首次全面比较。结果显示了良好的结构稳定性,尽管在第一次质子化之后检测到Zr / ErO5 []八面体附近的晶胞体积不可逆小收缩和局部结构修饰。在第二次质子化之后,由于存在通过拉曼散射和TGA很好地检测到的次生相(SrCO3,Sr(OH)(2)),在应力下容易观察到陶瓷破裂。讨论了晶体纯度,取代元素和剩余孔隙率在质子传导钙钛矿电解质稳定性中的作用。 (C)2015 Elsevier Ltd.保留所有权利。

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