BROUX, Thibault; PRESTIPINO, Carmelo; BAHOUT, Mona; PAOFAI, Serge; ELKAIM, Erik; VIBHU, Vaibhav; GRENIER, Jean-Claude; ROUGIER, Aline; BASSAT, Jean-Marc.; HERNANDEZ, Olivier

doi:10.1039/c5dt03482e

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BROUX, Thibault
Institut des Sciences Chimiques de Rennes [ISCR]

PRESTIPINO, Carmelo
Institut des Sciences Chimiques de Rennes [ISCR]

BAHOUT, Mona
Institut des Sciences Chimiques de Rennes [ISCR]

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Dalton Transactions. 2016-01, vol. 45, n° 7, p. 3024-3033

Royal Society of Chemistry

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The promising SOFC cathode material Pr2NiO4.22 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 Pr2NiO4.22 is incommensurately structurally modulated already at room temperature, in the same manner as the homologous cobaltate La2CoO4.14. 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< Réduire

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Structure and reactivity with oxygen of Pr2NiO4+δ: an in situ synchrotron X-ray powder diffraction study

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