NiO has been incorporated into the Pr0.5Ba0.5MnO3−δ perovskite to produce in situ exsolved Ni-catalyst on the PrBaMn2O5 anode material upon heating under a hydrogen atmosphere.
HAL is a multi-disciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers. L'archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d'enseignement et de Exsolution of Ni nanoparticles from A-site deficient layered double perovskites for dry reforming of methane and as anode material for solid oxide fuel cell
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.
International audienceThe chemical reduction of the K2NiF4-type oxides, Ln2Sr2CrNiO8−δ (Ln = La, Nd) and Nd2.25Sr1.75CrNiO8−δ, has been investigated in situ under a dynamic hydrogen atmosphere at high temperature using neutron powder diffraction. The high count-rate and high resolution of the D20 diffractometer at ILL, Grenoble allowed real-time data collection and structure refinement by full-pattern Rietveld analysis with a temperature resolution of 1 °C. Excellent agreement was obtained with the results of thermogravimetric analysis of these materials, which are potential fuel-cell electrodes. The neutron study revealed that oxygen is lost only from the equatorial anion site; the reduction of La2Sr2CrNiO8−δ yields a pure Ni(II) phase, La2Sr2CrNiO7.5en route to a mixed Ni(II,I) oxide, La2Sr2CrNiO7.40, whereas hydrogen reduction of Nd2Sr2CrNiO8−δ and Nd2.25Sr1.75CrNiO8−δ proceeds continuously from Ni(III) to an average oxidation state of 1.80 for the nickel ion. The data collected throughout a subsequent heating/cooling cycle in air indicated that the reduced phases intercalate oxygen reversibly into the equatorial vacancies of the K2NiF4-type structure. The retention of I4/mmm symmetry, along with the absence of the formation of any impurities throughout the heating/cooling cycles under reducing and oxidizing atmospheres, demonstrates both the reversibility and the strongly topotactic character of the oxygen deintercalation/intercalation chemical redox process and establishes the excellent structural stability of these layered mixed-metal oxides over a wide range of oxygen partial pressures
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