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Pr2NiO(4+δ)的结构及与氧的反应性:原位同步辐射X射线粉末衍射研究

Structure and reactivity with oxygen of Pr2NiO(4+δ): an in situ synchrotron X-ray powder diffraction study.

作者信息

Broux Thibault, Prestipino Carmelo, Bahout Mona, Paofai Serge, Elkaïm Erik, Vibhu Vaibhav, Grenier Jean-Claude, Rougier Aline, Bassat Jean-Marc, Hernandez Olivier

机构信息

Institut des Sciences Chimiques de Rennes (ISCR), Equipe «Chimie du Solide et Matériaux», UMR CNRS N°6226, Université de Rennes 1, 263 Avenue du Général Leclerc, 35042 Rennes, France.

出版信息

Dalton Trans. 2016 Feb 21;45(7):3024-33. doi: 10.1039/c5dt03482e. Epub 2016 Jan 13.

Abstract

The promising SOFC cathode material Pr2NiO(4.22) has been studied in situ under a pure oxygen atmosphere from 25 to 950 °C by high resolution synchrotron X-ray powder diffraction. At room temperature (RT) δ = 0.22(1), the average crystal structure turns out to be monoclinic. The subtle monoclinic distortion (γ = 90.066(1)° at RT), retained up to 460 °C, is interpreted in terms of specific tilt schemes of the NiO6 octahedra. It is also shown that Pr2NiO(4.22) is incommensurately structurally modulated already at room temperature, in the same manner as the homologous cobaltate La2CoO(4.14). The phase transition to the High Temperature Tetragonal (HTT) phase was completed at 480 °C without any evidence for the Low Temperature Orthorhombic (LTO) phase allowing clarifying the phase diagram of this K2NiF4-type ternary oxide. Moreover, it turns out that above 800 °C, the HTT phase transforms reversibly into two coexisting isomorphous tetragonal phases. The incommensurate modulation subsists up to 950 °C, although modified concomitantly with the two abovementioned phase transformations. In addition, the role of kinetics on the decomposition process is highlighted through thermo-gravimetric analyses.

摘要

通过高分辨率同步辐射X射线粉末衍射,在25至950°C的纯氧气氛中对有前景的固体氧化物燃料电池(SOFC)阴极材料Pr2NiO(4.22)进行了原位研究。在室温(RT)下,δ = 0.22(1),平均晶体结构为单斜晶系。这种微妙的单斜畸变(室温下γ = 90.066(1)°)一直保持到460°C,可根据NiO6八面体的特定倾斜方案来解释。研究还表明,Pr2NiO(4.22)在室温下就已经存在非相称结构调制,与同族钴酸盐La2CoO(4.14)的方式相同。向高温四方(HTT)相的相变在480°C时完成,没有任何低温正交(LTO)相的证据,这有助于明确这种K2NiF4型三元氧化物的相图。此外,结果表明,在800°C以上,HTT相可逆地转变为两个共存的同构四方相。尽管与上述两个相变同时发生了变化,但非相称调制一直持续到950°C。此外,通过热重分析突出了动力学在分解过程中的作用。

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