2008
DOI: 10.1016/j.jiec.2008.02.011
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Characteristics of mixed conducting perovskites (Ba1−xNdx)Fe3+1−tFe4+tO3−y

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Cited by 9 publications
(4 citation statements)
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“…The TPR-H 2 results (see below) indicate that Fe(IV) and Fe(III) oxidation states co-exist in the BaFe 1−x Cu x O 3 catalysts, as it is observed that the experimental H 2 consumption is in between the nominal (calculated) H 2 consumption expected, considering that iron as Fe(III) or Fe(IV) is reduced to Fe(II). The presence of Fe(IV) in BaFe 1−x Cu x O 3 catalysts is additionally supported by the well-known stabilization of high oxidation state for B cation, as Fe(IV), in perovskites [19,39,48,49,50]. On the basis of the BaFeO 3 stoichiometric formula, Fe(IV) must be the oxidation state for Fe in the perovskite, and, in the presence of copper, a rise in the Fe(IV) amount and /or the generation of additional oxygen vacancies into the perovskite structure would be expected to compensate the deficiency of positive charge due to the partial iron substitution [19].…”
Section: Resultsmentioning
confidence: 90%
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“…The TPR-H 2 results (see below) indicate that Fe(IV) and Fe(III) oxidation states co-exist in the BaFe 1−x Cu x O 3 catalysts, as it is observed that the experimental H 2 consumption is in between the nominal (calculated) H 2 consumption expected, considering that iron as Fe(III) or Fe(IV) is reduced to Fe(II). The presence of Fe(IV) in BaFe 1−x Cu x O 3 catalysts is additionally supported by the well-known stabilization of high oxidation state for B cation, as Fe(IV), in perovskites [19,39,48,49,50]. On the basis of the BaFeO 3 stoichiometric formula, Fe(IV) must be the oxidation state for Fe in the perovskite, and, in the presence of copper, a rise in the Fe(IV) amount and /or the generation of additional oxygen vacancies into the perovskite structure would be expected to compensate the deficiency of positive charge due to the partial iron substitution [19].…”
Section: Resultsmentioning
confidence: 90%
“…The deconvolution of the main band shows two significant contributions at around 709 eV and 711 eV. Even though the identification of iron oxidation states by XPS is very difficult [46], according to literature [39,46,47,48,49,50], the first peak corresponds to Fe(III) species, and the second one could be assigned to Fe(IV) species [48,49,50]. It has been established that the position of the satellite peak is the key finger to detect the oxidation state of Fe [46,48].…”
Section: Resultsmentioning
confidence: 99%
“…This volume decrease is well-known for bulk powders of Fe systems [28,29], for ultra-thin films and also found in the present work for 250 nm thick films of BFO. By creating mixed Fe 3+ /Fe 4+ oxidation states an additional electronic conductivity component might be induced (small polaron hopping), in addition to reducing the concentration of the protonic charge carriers, which is why an investigation into the conducting properties, depending on atmosphere and temperature was performed and analyzed in Section 3.4 [30]. To illustrate the process of creating mixed Fe 3+ /Fe 4+ in more detail the following equilibrium reaction in Kröger-Vink notation can be used VO+12O2+2FeFex OOx+2FeFe where FeFex represents Fe ions in the 3+ valence state and FeFe denotes Fe ions in the 4+ valence state (similar to holes), both on Fe lattice sites.…”
Section: Resultsmentioning
confidence: 99%
“…With Fe present in Fe 3+ /Fe 4+ mixed oxidation states the mechanism of conduction can fundamentally change, which was shown for ultrathin films compared to bulk powders [21]. In addition Lee investigated the change in electrochemical impedance response in different atmospheres and correlated the results with the Fe 4+ ratio contained in the bulk samples [30]. With respect to these findings the measurements in this study were conducted in oxidizing (air) and inert (Ar) atmospheres, as well as under wet and dry conditions.…”
Section: Resultsmentioning
confidence: 99%