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

机译:冷中子瞬发伽马活化分析法分析掺杂和未掺杂的BaPrO3和BaCeO3中的氢含量

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摘要

Proton uptake in undoped and Y-doped BaPrO3 has been measured by cold neutron prompt-gamma activation analysis, and compared to the proton uptake in Gd-doped BaCeO3, 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 H2O 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 BaPr1–xYxO3 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, BaCe0.9Y0.1O3 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+ to the 3+ oxidation state upon exposure to water, and effectively behaves as a self-dopant within the structure.
机译:已通过冷中子快速伽马活化分析测量了未掺杂和Y掺杂的BaPrO3中的质子吸收,并通过相同的技术将其与Gd掺杂的BaCeO3中的质子吸收进行了比较。钙钛矿的常规质子掺入模型中,通过将三价掺杂物引入四价钙钛矿位点而产生的氧离子空位在样品暴露于含H2O的气氛中时被羟基填充,预示着此类材料中的质子浓度不应大于掺杂剂浓度。与该模型相反,加湿后BaPr1-xYxO3中的质子浓度高达掺杂剂浓度的三倍,甚至未掺杂的样品也包含高浓度的质子。此外,X射线光发射光谱表明,水合后Pr的氧化态降低。相反,BaCe0.9Y0.1O3显示出典型的氢浓度,接近于钇浓度的90%。根据Pr的可变价来解释结果,Pr的可变价在暴露于水后可以从4+变为3+氧化态,并在结构内有效地表现为自掺杂。

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