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System Bi–Sr–O: Synergistic measurements of thermodynamic properties using oxide and fluoride solid electrolytes

Published online by Cambridge University Press:  31 January 2011

K. T. Jacob  and
K. P. Jayadevan
K. T. Jacob
Affiliation:
Materials Research Centre and Department of Metallurgy, Indian Institute of Science, Bangalore 560 012, India
K. P. Jayadevan
Affiliation:
Materials Research Centre and Department of Metallurgy, Indian Institute of Science, Bangalore 560 012, India
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Extract

Phase equilibrium and electrochemical studies of the ternary system Bi–Sr–O indicate the presence of six ternary oxides (Bi2SrO4, Bi2Sr2O5, Bi2Sr3O6, Bi4Sr6O15, Bi14Sr24O52, and Bi2Sr6O11) and three solid solutions (δ, β, and γ). An isothermal section of the phase diagram is established at 1050 K by phase analysis of quenched samples. Three compounds, Bi4Sr6O15, Bi14Sr24O52, and Bi2Sr6O11, contain Bi5+ ions. The stability of these phases is a function of oxygen partial pressure. The chemical potentials of SrO in two-phase fields are determined as a function of temperature using solid-state cells based on single crystal SrF2 as the electrolyte. Measurement of the emf of cells based on SrF2 as a function of oxygen partial pressure in the gas at constant temperature gives information on oxygen content of the compounds present at the electrodes. The chemical potentials of Bi2O3 in two-phase fields of the pseudobinary Bi2O3–SrO are measured using cells incorporating (Y2O3)ZrO2 as the solid electrolyte. The standard free energies of formation of the ternary oxides are calculated independently using emfs of different cells. The independent assessments agree closely; the maximum difference in the value of of component binary oxides. The results are discussed in the light of the phase diagram and compared with calorimetric and chemical potential measurements reported in the literature. The combined use of emf data from cells incorporating fluoride and oxide electrolytes enhances the reliability of derived data.

Type
Articles
Information
Journal of Materials Research , Volume 13 , Issue 7 , July 1998 , pp. 1905 - 1918
Copyright
Copyright © Materials Research Society 1998

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