1994
DOI: 10.1103/physrevb.50.5074
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Crystal-structure effects in the CeL3-edge x-ray-absorption spectrum ofCeO2

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Cited by 210 publications
(152 citation statements)
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“…The intense peaks B and C can be interpreted as transitions toward O 2p state hybridized with Ce ͑or dopant͒ 5d-e g and 5d-t 2g states that are split under the crystalfield effects. 25,26 Therefore, the relative intensity of peaks B and C is sensitive to the change in crystal structure. Particularly, in nonstoichiometric oxides, it has been suggested that the enhancement of peak B could be introduced by the local ordering of oxygen vacancies.…”
Section: Resultsmentioning
confidence: 99%
“…The intense peaks B and C can be interpreted as transitions toward O 2p state hybridized with Ce ͑or dopant͒ 5d-e g and 5d-t 2g states that are split under the crystalfield effects. 25,26 Therefore, the relative intensity of peaks B and C is sensitive to the change in crystal structure. Particularly, in nonstoichiometric oxides, it has been suggested that the enhancement of peak B could be introduced by the local ordering of oxygen vacancies.…”
Section: Resultsmentioning
confidence: 99%
“…Among these characteristics, peak A is obvious in pure ceria but weaker in doped ceria, which could be explained by the decrease of Ce concentration in doped ceria since this preedge peak is related to the hybridization between oxygen and Ce 4+ cations. 15,16 Inversely, the relative intensity of peak B in doped ceria is considerably higher than that of pure ceria. Previous studies had shown that the intensities of peaks B and C can be influenced by the crystal structure 16,17 and particularly, the enhancement of peak B could be introduced by the ordering of oxygen vacancies in nonstoichiometric oxides.…”
mentioning
confidence: 99%
“…15,16 Inversely, the relative intensity of peak B in doped ceria is considerably higher than that of pure ceria. Previous studies had shown that the intensities of peaks B and C can be influenced by the crystal structure 16,17 and particularly, the enhancement of peak B could be introduced by the ordering of oxygen vacancies in nonstoichiometric oxides. 14 In our samples, the increase in peak B is different with a sequence of SmϾ DyϾ Y Ͼ Yb, which agrees with the extra diffraction spots on SAED patterns ͑Fig.…”
mentioning
confidence: 99%
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“…Peak A results from the hybridization between oxygen and Ce 4+ cations, 30,31 which is obvious in pure ceria and becomes weak in doped ceria because of the decrease of the Ce concentration in doped ceria. As for the case of peaks B and C, previous studies have shown that the relative intensities of the peaks can be influenced by the crystal structure 30,31 and the enhancement of peak B could be due to the ordering of oxygen vacancies in nonstoichiometric oxides. 19,29 To compare the relative intensities of peaks B and C, the spectra in Fig.…”
Section: B Ordering Of Oxygen Vacancies In the Domainsmentioning
confidence: 99%