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| Naji, M. |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Ali, M. A. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Albrecht, R.
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Publications (5/5 displayed)
- 2021Hydrothermal Synthesis, Crystal Structure, and Magnetism of Na2[Ir(OH)6] and its Dehydration to Na2IrO3citations
- 2021Tunable Potassium Ion Conductivity and Magnetism in Substituted Layered Ferratescitations
- 2021Ba3[Rh(OH)6]2 ⋅ H2O – a Precursor to Barium Oxorhodates with One-dimensional Hydrogen Bonding Systemscitations
- 2020The Hydrogarnets Sr3[RE(OH)6]2 (RE = Sc, Y, Ho – Lu): Syntheses, Crystal Structures, and their Thermal Decomposition to Ternary Rare-Earth Metal Oxidescitations
- 2020CaNa[Cr(OH)6] – A Layered Hydroxochromate(III) with Ordered Brucite Structure and its Thermal Decompositioncitations
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article
The Hydrogarnets Sr3[RE(OH)6]2 (RE = Sc, Y, Ho – Lu): Syntheses, Crystal Structures, and their Thermal Decomposition to Ternary Rare-Earth Metal Oxides
Abstract
Seven rare-earth metal hydrogarnets Sr3[RE(OH)6]2 (RE = Sc, Y, Ho-Lu) were synthesized at about 200 °C starting from the respective RE2O3 and Sr(NO3)2 in a KOH hydroflux with a water-to-base ratio of 1.6. All seven hydrogarnets crystallize in the acentric variant (space group I43d) of the cubic garnet structure. The crystal structures of the hydrogarnets Sr3[RE(OH)6]2, the differences between both structural variants including a simple method to distinguish between them, and the crystal-chemical classification with respect to other known strontium hydrogarnets are discussed. The rare-earth hydrogarnets can be used as carbon-free precursors for magnetic oxides. Starting at about 300 °C, the hydrogarnets decompose in a two- or three-step dehydration to SrRE2O4 and SrO. The decomposition of Sr3[Sc(OH)6]2 follows a different mechanism and was studied by in-situ temperature-dependent powder X-ray diffraction up to 1000 °C. The final decomposition products were SrO and an unknown strontium scandium oxide, with an X-ray pattern similar to BaSc2O4. Magnetic measurements of the erbium and ytterbium hydrogarnets revealed paramagnetic behavior down to 1.8 K.