Journal
JOURNAL OF SOLID STATE CHEMISTRY
Volume 228, Issue -, Pages 189-198Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2015.04.029
Keywords
Lanthanide nickelates; Chemical stability; low pO(2); Shrinkage; Thermal expansion coefficient; Chemical expansion
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The chemical stability of lanthanide nickelates Ln(2)NiO(4+delta) (Ln=La, Pr or Nd) has been studied in the temperature range 25-1300 degrees C, either in air or at low pO(2) (down to 10(-4) atm). Thermal gravimetry analysis (TGA) measurements coupled with X-ray diffraction (XRD) characterization have shown that all compounds retain their K2NiF4-type structure in these conditions, while remaining over-stoichiometric in oxygen up to 1000 degrees C Only Nd2NiO4+delta starts to decompose into Nd2O3 and NiO above 1000 degrees C, at pO(2)=10(-4) atm. In addition, a careful analysis of the lanthanide nickelates structural features has been performed by in situ XRD, as a function of temperature and pO(2). For all compounds, a structural transition has been always observed in the temperature range 200-400 degrees C, in air or at pO(2)=10(-4) atm. In addition, their cell volume did not vary upon the variation of the oxygen partial pressure. Therefore, these materials do not exhibit a chemical expansion in these conditions, which is beneficial for a fuel cell application as cathode layers. Additional dilatometry measurements have revealed that a temperature as high as 950 degrees C for Pr2NiO4+delta or 1100 degrees C for La2NiO4+delta and Nd2NiO4+delta has to be reached in order to begin the sintering of the material particles, which is of primary importance to obtain an efficient electronic/ionic conduction in the corresponding designed cathode layers. Besides, excellent matching was found between the thermal expansion coefficients of lanthanide nickelates and SOFC electrolytes such as 8wt% yttria stabilized zirconia (8YSZ) or Ce0.8Gd0.2O2-delta(GDC), at least from 400 degrees C up to 1400 degrees C in air or up to 1200 degrees C at pO(2)=10(-4) atm. 2015 Elsevier Inc. All rights reserved.
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