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首页> 外文期刊>Physical review. B, Condensed Matter And Materials Physics >Characterization of La_(0.8)Sr_(0.2)FeO_(3-δ) and La_(0.7)Sr_(0.2)FeO_(3-δ) as a function of temperature by x-ray absorption spectroscopy
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Characterization of La_(0.8)Sr_(0.2)FeO_(3-δ) and La_(0.7)Sr_(0.2)FeO_(3-δ) as a function of temperature by x-ray absorption spectroscopy

机译:X射线吸收光谱法表征La_(0.8)Sr_(0.2)FeO_(3-δ)和La_(0.7)Sr_(0.2)FeO_(3-δ)随温度的变化

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A temperature-dependent x-ray absorption spectroscopy (XAS) study was performed to investigate the changes in electronic and atomic structure of La-deficient La_(0.7)Sr_(0.2)FeO_(3-δ) (L7S2FO3) and stoichiometric La_(0.8)Sr_(0.2)FeO_(3-δ) (L8S2FO3). La_(0.8)Sr_(0.2)FeO_(3-δ) is a promising cathode material for intermediate operating temperature (700-800℃) solid oxide fuel cells. Performance improvements have been shown by increasing the La- or A-site deficiency in this material but a clear understanding of the mechanisms responsible for this improvement are still needed. Here we report an x-ray absorption spectroscopy (XAS) study as a function of temperature to investigate electronic and atomic structure changes of La-deficient La_(0.7)Sr_(0.2)FeO_(3-δ) (L7S2FO3) and stoichiometric La_(0.8)Sr_(0.2)FeO_(3-δ) (L8S2FO3). In particular we have measured the temperature-dependent changes in oxidation state, bond distance, Fe coordination number, and oxygen vacancies for both compounds. L7S2FO3 contains 10% A-site vacancies compared to stoichiometric L8S2FO3, which has a fully occupied A site and thus some form of charge compensation is necessary in the former to maintain charge neutrality. X-ray absorption near edge spectroscopy shows the presence of Fe~(3+) and Fe~(4+) in both L7S2FO3 and L8S2FO3 (mixed valence) as established by comparison with model compounds. Studies from room temperature to 850℃ show that Fe~(3+) dominates over Fe~(4+) in both materials with increasing dominance as the temperature is increased. Furthermore, the temperature-dependent study revealed the La-deficiency in L7S2FO3 leads to a higher concentration of both electron holes (i.e., more Fe~(4+) created) and oxygen vacancies, compared to the stoichiometric L8S2FO3. Analysis of the extended x-ray absorption fine structure shows that the Fe-O bond increases with the increase in temperature for both the systems.
机译:进行了温度依赖性X射线吸收光谱(XAS)研究,以研究La不足的La_(0.7)Sr_(0.2)FeO_(3-δ)(L7S2FO3)和化学计量La_(0.8)的电子和原子结构的变化Sr_(0.2)FeO_(3-δ)(L8S2FO3)。 La_(0.8)Sr_(0.2)FeO_(3-δ)是用于中等工作温度(700-800℃)固体氧化物燃料电池的有希望的阴极材料。通过增加此材料中La或A位点的缺乏已显示出性能的改善,但仍需要对造成这种改善的机理有清楚的了解。在这里,我们报告了X射线吸收光谱(XAS)研究作为温度的函数,以研究缺乏La的La_(0.7)Sr_(0.2)FeO_(3-δ)(L7S2FO3)和化学计量La_( 0.8)Sr_(0.2)FeO_(3-δ)(L8S2FO3)。特别是,我们已经测量了两种化合物的氧化态,键距,Fe配位数和氧空位的温度依赖性变化。与化学计量的L8S2FO3具有完全占据的A位点相比,L7S2FO3包含10%的A位空位,因此前者需要某种形式的电荷补偿来保持电荷中性。通过与模型化合物比较确定,L7S2FO3和L8S2FO3中的Fe〜(3+)和Fe〜(4+)均存在X射线吸收(近价)。从室温到850℃的研究表明,两种材料中的Fe〜(3+)都比Fe〜(4+)占主导地位,并且随着温度的升高,Fe〜(3+)的占位性增加。此外,温度依赖性研究表明,与化学计量的L8S2FO3相比,L7S2FO3中的La缺乏会导致更高的电子空穴浓度(即,产生更多的Fe〜(4+))和氧空位。对扩展的X射线吸收精细结构的分析表明,两个系统的Fe-O键均随温度的升高而增加。

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