2017
DOI: 10.1016/j.jallcom.2016.12.378
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Structural and magnetic phase transition observed in the YCrO3+γ compound

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Cited by 9 publications
(4 citation statements)
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“…Figure a shows the normalized X-ray adsorption near-edge structure (XANES) spectra of YCr 0.5 P 0.5 O 4 together with three references (Cr 2 O 3 , CrO 2 , and YCrO 4 ). Pristine YCr 0.5 P 0.5 O 4 reveals similar features to those of YCrO 4 (Cr 5+ ) in the XANES region, giving rise to the large pre-edge (approximately 5981 eV) peak due to the quadrupolar 1s → 3d transitions arising from the hybridization of the 3d levels of Cr in the presence of surrounding oxygen ligands. , This pre-edge feature is characteristic of tetrahedrally coordinated Cr atoms, , and so the octahedrally coordinated Cr 2 O 3 (corundum type) and CrO 2 (rutile type) do not show such a strong pre-edge peak. Heating at 700 °C lowers the intensity of the pre-edge peak slightly, disclosing that the local coordination environments around Cr atoms are modified by oxygen deficiency at elevated temperatures.…”
Section: Resultsmentioning
confidence: 88%
“…Figure a shows the normalized X-ray adsorption near-edge structure (XANES) spectra of YCr 0.5 P 0.5 O 4 together with three references (Cr 2 O 3 , CrO 2 , and YCrO 4 ). Pristine YCr 0.5 P 0.5 O 4 reveals similar features to those of YCrO 4 (Cr 5+ ) in the XANES region, giving rise to the large pre-edge (approximately 5981 eV) peak due to the quadrupolar 1s → 3d transitions arising from the hybridization of the 3d levels of Cr in the presence of surrounding oxygen ligands. , This pre-edge feature is characteristic of tetrahedrally coordinated Cr atoms, , and so the octahedrally coordinated Cr 2 O 3 (corundum type) and CrO 2 (rutile type) do not show such a strong pre-edge peak. Heating at 700 °C lowers the intensity of the pre-edge peak slightly, disclosing that the local coordination environments around Cr atoms are modified by oxygen deficiency at elevated temperatures.…”
Section: Resultsmentioning
confidence: 88%
“…In the true crystallographic cell of this structure, there has four distorted perovskite units. Fabian et al prepared YCrO 3+γ (γ = 0 and 1) compounds by the co-precipitation technique and performed studies with X-ray absorption near edge structure spectra and in situ XRPD [191]. The study indicates that (i) The onset of the crystallization process of the YCrO 4 phase (tetragonal, I41/amd space group) begins at ∼ 325 • C. (ii) At higher temperatures (680 ≤ T ≤ 720 • C), the phase of YCrO 3 (orthorhombic, Pbnm space group) gradually forms.…”
Section: Structuralmentioning
confidence: 99%
“…The Cr 5+ and Cr 3+ oxidation states depend on the preparation temperature. The temperature-dependent magnetic susceptibilities indicate that the zircon-like YCrO 4 phase undergoes a ferromagnetic phase transition at 9 K, and YCrO 3 displays an AFM transition at ∼ 120 K [191]. Poly-crystalline samples of YCrO 3 were prepared, and Mall et al measured temperature dependence of XRPD from 300 to 900 K [192].…”
Section: Structuralmentioning
confidence: 99%
“…The significance of studying these materials lies in their potential use as polyfunctional catalysts for neutralizing diesel exhaust emissions, offering several advantages over traditional catalysts, namely: low cost, resistance to inhibitors, and high thermal stability. The main interest in rare‐earth metal chromites with the general formula RCrO3 (where R=Y or a trivalent rare‐earth ion) is currently linked to their multiferroic properties, with strong correlation between structural, electrical, and magnetic properties [20–35]. Although there have been various publications exploring the relationship between the electronic structure of complex oxides and their catalytic properties [36–39], there have been a lack of studies on oxygen mobility within the crystal lattice.…”
Section: Introductionmentioning
confidence: 99%