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Hydrogen content in doped and undoped BaPrO3 and BaCeO3 by cold neutron prompt-gamma activation analysis.

Authors :
Jones, Camille Y.
Wu, Jian
Li, LiPing
Haile, Sossina M.
Source :
Journal of Applied Physics; 6/1/2005, Vol. 97 Issue 11, p114908, 4p, 1 Chart, 3 Graphs
Publication Year :
2005

Abstract

Proton uptake in undoped and Y-doped BaPrO<subscript>3</subscript> has been measured by cold neutron prompt-gamma activation analysis, and compared to the proton uptake in Gd-doped BaCeO<subscript>3</subscript>, as determined by the same technique. The conventional proton incorporation model of perovskites in which oxygen ion vacancies, generated by the introduction of the trivalent dopant onto the tetravalent perovskite site, are filled with hydroxyl groups upon exposure of the sample to H<subscript>2</subscript>O containing atmospheres, predicts that the proton concentration in such materials should be no greater than the dopant concentration. In contradiction to this model, the proton concentration in BaPr<subscript>1-x</subscript>Y<subscript>x</subscript>O<subscript>3</subscript> after humidification is as much as three times greater than the dopant concentration, and even undoped samples contain a high concentration of protons. Moreover, x-ray photoemission spectra suggest that the Pr oxidation state is lowered upon hydration. In contrast, BaCe<subscript>0.9</subscript>Y<subscript>0.1</subscript>O<subscript>3</subscript> shows a typical hydrogen concentration, of close to 90% of the yttrium concentration. The results are interpreted in terms of the variable valence of Pr, which can become reduced from the 4<superscript>+</superscript> to the 3<superscript>+</superscript> oxidation state upon exposure to water, and effectively behaves as a self-dopant within the structure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00218979
Volume :
97
Issue :
11
Database :
Complementary Index
Journal :
Journal of Applied Physics
Publication Type :
Academic Journal
Accession number :
17392390
Full Text :
https://doi.org/10.1063/1.1922590