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| Naji, M. |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Kočí, Jan | Prague |
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| Azam, Siraj |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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Hanna, John
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Publications (5/5 displayed)
- 2022Computational Modelling for the Effects of Capsular Clustering on Fracture of Encapsulation-Based Self-Healing Concrete Using XFEM and Cohesive Surface Techniquecitations
- 2018Final report: Understanding influence of thermal history and glass chemistry on kinetics of phase separation and crystallization in borosilicate glass-ceramic waste forms for aqueous reprocessed high level waste
- 2017Topotactic fluorine insertion into the channels of FeSb2O4-related materials.citations
- 2013Investigation into the effect of Si doping on the performance of Sr1−yCayMnO3−δ SOFC cathode materialscitations
- 2012(87)Sr solid-state NMR as a structurally sensitive tool for the investigation of materials: antiosteoporotic pharmaceuticals and bioactive glasses.citations
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article
Topotactic fluorine insertion into the channels of FeSb2O4-related materials.
Abstract
This paper discusses the fluorination characteristics of phases related to FeSb<sub>2</sub>O<sub>4</sub>, by reporting the results of a detailed study of Mg<sub>0.50</sub>Fe<sub>0.50</sub>Sb<sub>2</sub>O<sub>4</sub> and Co<sub>0.50</sub>Fe<sub>0.50</sub>Sb<sub>2</sub>O<sub>4</sub>. Reaction with fluorine gas at low temperatures (typically 230 °C) results in topotactic insertion of fluorine into the channels, which are an inherent feature of the structure. Neutron powder diffraction and solid state NMR studies show that the interstitial fluoride ions are bonded to antimony within the channel walls to form Sb – F – Sb bridges. To date, these reactions have been observed only when Fe<sup>2+</sup> ions are present within the chains of edge-linked octahedra (FeO<sub>6</sub> in FeSb<sub>2</sub>O<sub>4</sub>) that form the structural channels. Oxidation of Fe<sup>2+</sup> to Fe<sup>3+</sup> is primarily responsible for balancing the increased negative charge associated with the presence of the fluoride ions within the channels. For the two phases studied, the creation of Fe<sup>3+</sup> ions within the chains of octahedra modify the magnetic exchange interactions to change the ground-state magnetic symmetry to C-type magnetic order in contrast to the A-type order observed for the unfluorinated oxide parents.