1999Journal of The Electrochemical SocietyOpen access

Stability of BaCeO3‐Based Proton Conductors in Water‐Containing Atmospheres

Sanjeevani V. Bhide, Anil V. Virkar

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Abstract

The stability of Gd‐doped and La‐doped in water‐containing atmospheres was examined. Samples containing up to 20 mol % Gd and 30 mol % La were synthesized by calcining the requisite mixtures of precursors. Three types of tests were performed: ( i ) thermal treatment in an atmosphere containing water vapor between 150 and 400°C, ( ii ) boiling in water, and ( iii ) simultaneous exposure to boiling water and water vapor at essentially the same temperature. Samples were characterized by X‐ray diffraction. All powders boiled in water decomposed within a few hours, whereas none of the powders decomposed when exposed to ∼1 atm water vapor pressure at the same temperature. This difference was rationalized on the premise that the mechanisms of decomposition depend upon the form of water, liquid or vapor. In liquid water, the decomposition kinetics appear to be interface‐controlled. By contrast, in water vapor, the kinetics appear to be dictated by bulk diffusion of water into the lattice. © 1999 The Electrochemical Society. All rights reserved.

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The stability of Gd‐doped and La‐doped in water‐containing atmospheres was examined. Samples containing up to 20 mol % Gd and 30 mol % La were synthesized by calcining the requisite mixtures of precursors. Three types of tests were performed: ( i ) thermal treatment in an atmosphere containing water vapor between 150 and 400°C, ( ii ) boiling in water, and ( iii ) simultaneous exposure to boiling water and water vapor at essentially the same temperature. Samples were characterized by X‐ray diffraction. All powders boiled in water decomposed within a few hours, whereas none of the powders decomposed when exposed to ∼1 atm water vapor pressure at the same temperature. This difference was rationalized on the premise that the mechanisms of decomposition depend upon the form of water, liquid or vapor. In liquid water, the decomposition kinetics appear to be interface‐controlled. By contrast, in water vapor, the kinetics appear to be dictated by bulk diffusion of water into the lattice. © 1999 The Electrochemical Society. All rights reserved.

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Available abstract

The stability of Gd‐doped and La‐doped in water‐containing atmospheres was examined. Samples containing up to 20 mol % Gd and 30 mol % La were synthesized by calcining the requisite mixtures of precursors. Three types of tests were performed: ( i ) thermal treatment in an atmosphere containing water vapor between 150 and 400°C, ( ii ) boiling in water, and ( iii ) simultaneous exposure to boiling water and water vapor at essentially the same temperature. Samples were characterized by X‐ray diffraction. All powders boiled in water decomposed within a few hours, whereas none of the powders decomposed when exposed to ∼1 atm water vapor pressure at the same temperature. This difference was rationalized on the premise that the mechanisms of decomposition depend upon the form of water, liquid or vapor. In liquid water, the decomposition kinetics appear to be interface‐controlled. By contrast, in water vapor, the kinetics appear to be dictated by bulk diffusion of water into the lattice. © 1999 The Electrochemical Society. All rights reserved.

Key concepts: Water vapor, Vapour pressure of water, Calcination, Vapor pressure, Chemistry, Boiling, Boiling point, Decomposition

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