2020
DOI: 10.1039/d0dt02466j
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Structure and magnetism of the Rh4+-containing perovskite oxides La0.5Sr0.5Mn0.5Rh0.5O3and La0.5Sr0.5Fe0.5Rh0.5O3

Abstract: Synchrotron X-ray powder diffraction data indicate that La0.5Sr0.5Mn0.5Rh0.5O3 and La0.5Sr0.5Fe0.5Rh0.5O3 adopt distorted perovskite structures (space group Pnma) with A-site and B-site cation disorder. A combination of XPS and 57Fe Mössbauer...

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Cited by 2 publications
(6 citation statements)
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“…This is reasonable because the local environment of the Fe and Mn in perovskites might have the Fe 2+ -O2-Fe 3+ and Mn 3+ -O2-Mn 4+ double exchange interactions in reason for the increment in terms of the number of the d-d orbitals with oxygen. 58 These findings are consistent with the changes in the surface of the La 2 FeMnO 6 perovskite observed in the present work.…”
Section: Dalton Transactions Papersupporting
confidence: 93%
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“…This is reasonable because the local environment of the Fe and Mn in perovskites might have the Fe 2+ -O2-Fe 3+ and Mn 3+ -O2-Mn 4+ double exchange interactions in reason for the increment in terms of the number of the d-d orbitals with oxygen. 58 These findings are consistent with the changes in the surface of the La 2 FeMnO 6 perovskite observed in the present work.…”
Section: Dalton Transactions Papersupporting
confidence: 93%
“…8h) illustrates two main components for the doublet Mn 2 p 1/2 –Mn 2 p 3/2 at 652.8 and 640.9 eV, which is due to the Mn 3+ ions. 58 It is important to note that the multiplet associated with the Mn oxidation state is found with additional binding energies at 643.1 and 656.3 eV, which are due to the Mn 3+ and Mn 4+ species, respectively. This is reasonable because the local environment of the Fe and Mn in perovskites might have the Fe 2+ –O2–Fe 3+ and Mn 3+ –O2–Mn 4+ double exchange interactions in reason for the increment in terms of the number of the d–d orbitals with oxygen.…”
Section: Resultsmentioning
confidence: 96%
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