Influence of Y-substitution on phase composition and proton uptake of self-generated Ba(Ce,Fe)O3-δ-Ba(Fe,Ce)O3-δ composites
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in: Journal of Materials Chemistry A, Jahrgang 10.2022, Nr. 5, 15.11.2021, S. 2474-2482.
Publikationen: Beitrag in Fachzeitschrift › Artikel › Forschung › (peer-reviewed)
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TY - JOUR
T1 - Influence of Y-substitution on phase composition and proton uptake of self-generated Ba(Ce,Fe)O3-δ-Ba(Fe,Ce)O3-δ composites
AU - Berger, Christian
AU - Bucher, Edith
AU - Merkle, Rotraut
AU - Nader, Christina
AU - Lammer, Judith
AU - Grogger, Werner
AU - Maier, Joachim
AU - Sitte, Werner
PY - 2021/11/15
Y1 - 2021/11/15
N2 - Self-generated composites from the series BaCe1−(x+z)FexYzO3−δ with z = 0.2 for 0.1 ≤ x ≤ 0.6 and z = 0 for Ce : Fe = 1 were obtained by one-pot synthesis. The composites consist of proton and electron conducting phases and are interesting as electrode materials for protonic ceramic fuel and electrolyser cells. X-ray diffraction with quantitative phase analysis and scanning electron microscopy with energy-dispersive X-ray spectroscopy showed that the materials consist of Fe-rich phases and a Ce-rich perovskite phase, which are present in the corresponding proportion depending on the precursor composition (Ce–Fe ratio). Substitution with Y leads to a narrowing of the miscibility gap compared to BaCe1−xFexO3−δ composites, thus favouring transformation of the composites into single cubic phases at temperatures above 1000 °C. Further, Y influences the mutual solubility of Fe3+/4+ and Ce4+ in the Ce-rich and Fe-rich phase, respectively, as shown elemental mapping via scanning transmission electron microscopy. As only a small proportion of the Y dissolves in the electrolyte-type phase, the increased proton uptake resulting from the incorporation of Y in the Ce-rich phase is limited. Strategies to overcome this limitation by substitution with ions with similar ionic radii, but different basicity, are discussed.
AB - Self-generated composites from the series BaCe1−(x+z)FexYzO3−δ with z = 0.2 for 0.1 ≤ x ≤ 0.6 and z = 0 for Ce : Fe = 1 were obtained by one-pot synthesis. The composites consist of proton and electron conducting phases and are interesting as electrode materials for protonic ceramic fuel and electrolyser cells. X-ray diffraction with quantitative phase analysis and scanning electron microscopy with energy-dispersive X-ray spectroscopy showed that the materials consist of Fe-rich phases and a Ce-rich perovskite phase, which are present in the corresponding proportion depending on the precursor composition (Ce–Fe ratio). Substitution with Y leads to a narrowing of the miscibility gap compared to BaCe1−xFexO3−δ composites, thus favouring transformation of the composites into single cubic phases at temperatures above 1000 °C. Further, Y influences the mutual solubility of Fe3+/4+ and Ce4+ in the Ce-rich and Fe-rich phase, respectively, as shown elemental mapping via scanning transmission electron microscopy. As only a small proportion of the Y dissolves in the electrolyte-type phase, the increased proton uptake resulting from the incorporation of Y in the Ce-rich phase is limited. Strategies to overcome this limitation by substitution with ions with similar ionic radii, but different basicity, are discussed.
U2 - 10.1039/D1TA07208K
DO - 10.1039/D1TA07208K
M3 - Article
VL - 10.2022
SP - 2474
EP - 2482
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
SN - 2050-7488
IS - 5
ER -