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Composition-graded solid electrolyte for determination of the Gibbs energy of formation of lanthanum zirconate

Jacob, Thomas K and Dasgupta, Niladri and Waseda, Yoshio (1998) Composition-graded solid electrolyte for determination of the Gibbs energy of formation of lanthanum zirconate. In: Journal of the American Ceramic Society, 81 (7). pp. 1926-1930.

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Abstract

A composition-graded solid electrolyte has been used to determine the standard Gibbs free energy of formation of lanthanum zirconate (La2Zr2O7) from the component oxides lanthana (La2O3) (A-rare earth) and zirconia (ZrO2) (monoclinic) in the temperature range of 870-1240 K. The cell used for measurement can be represented as Pt, O-2, CaO + CaF(2)parallel to CaF2 (x=0) (LaF3)(x)(CaF2)(1-x) parallel to(x=0.32) LaF3 + La2Zr2O7 + ZrO2, O-2, Pt A composition-graded electrolyte has been introduced to compensate the solubility effects of the electrode material (lanthanum fluoride, LaF3) in the solid electrolyte (calcium fluoride, CaF2), The ability of the graded electrolyte to generate a Nernstian response is demonstrated, using electrodes with known fluorine chemical potentials. For the reaction La2O3 (A-rare earth) and (ZrO2) (monoclinic) La2Zr2O7 (pyrochlore), the Gibbs free energy change (Delta G(f,ox)degrees) is given by the formula -133800 - 10.32T (+/-4500) (in units of J/mol), The enthalpy and entropy of formation of La2Zr2O7 obtained in this study are in good agreement with calorimetric data. The "third-law" enthalpy of formation of La2Zr2O7, from the component oxides at 298.15 K, is -133.8 +/- 5 kJ/mol.

Item Type: Journal Article
Publication: Journal of the American Ceramic Society
Publisher: American Ceramic Society
Additional Information: Copyright of this article belongs to American Ceramic Society.
Department/Centre: Division of Chemical Sciences > Materials Research Centre
Division of Mechanical Sciences > Materials Engineering (formerly Metallurgy)
Date Deposited: 28 May 2009 11:08
Last Modified: 19 Sep 2010 05:01
URI: http://eprints.iisc.ac.in/id/eprint/18298

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