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Synthesis and Characterization of the Aurivillius Phase CoBi2O2F4
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
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Number of Authors: 52018 (English)In: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 57, no 15, p. 9115-9121Article in journal (Refereed) Published
Abstract [en]

The new CoBi2O2F4 compound was synthesized by a hydrothermal method at 230 degrees C. Single-crystal X-ray diffraction data were used to determine the crystal structure. The compound is layered and belongs to the Aurivillius family of compounds. The present compound is the first oxo-fluoride Aurivillius phase containing Co2+. Inclusion of a d-block cation with such a low oxidation state as 2+ was achieved by partially replacing O2- with F- ions. The crystal structure is best described in the tetragonal noncentrosymmetric space group I<(4)overbar> with unit-cell parameters a = 3.843(2) angstrom and c = 16.341(8) angstrom. The crystal structure consists of two main building units: [BiO4F4] distorted cubes and [CoF6] octahedra. Interestingly, since the octahedra [CoF6] tilt between four equivalent positions, the F atoms occupy a 4-fold split position at room temperature. For the investigation of the structural disorder, Raman scattering data were collected in the range from 10 K to room temperature. As the temperature decreases, sharper phonon peaks appear and several modes clearly appear, which indicates a reduction of the disorder. Magnetic susceptibility and heat capacity measurements evidence long-range antiferromagnetic ordering below the Neel temperature of similar to 50 K. The magnetic susceptibility is in agreement with the Curie-Weiss law above 75 K with a Curie-Weiss temperature of theta(cw) = -142(2) K.

Place, publisher, year, edition, pages
2018. Vol. 57, no 15, p. 9115-9121
National Category
Chemical Sciences
Research subject
Inorganic Chemistry
Identifiers
URN: urn:nbn:se:su:diva-161142DOI: 10.1021/acs.inorgchem.8b01118ISI: 000441477100051PubMedID: 29995399OAI: oai:DiVA.org:su-161142DiVA, id: diva2:1256929
Available from: 2018-10-18 Created: 2018-10-18 Last updated: 2022-02-26Bibliographically approved
In thesis
1. Design of new materials with crystal structure-related properties: The role of lone pair cations
Open this publication in new window or tab >>Design of new materials with crystal structure-related properties: The role of lone pair cations
2020 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Non-centrosymmetry and low-dimensional arrangements, e.g. chains or layers, are very attractive structural characteristics of crystalline compounds since they are linked to some physical properties including nonlinear optical activity, ferroelectricity and magnetic frustration. The insertion of a lone-pair cation, equipped with a stereochemically active electron pair into a compound may increase its structural variety and induce the aforementioned characteristics.

In this thesis some novel oxide and oxohalide compounds are described. They contain a transition metal and also a p-element lone-pair cation. Relevant synthesis details, crystal structure and physical properties of the compounds will be presented.

Chemical systems containing iodate ions and either Cu2+ or Sc3+ have been explored in an effort to find new non-centrosymmetric compounds. The compounds contain also K+ due to its tendency to form highly coordinated asymmetric units. The new iodates are KCu(IO3)3 and the non-centrosymmetric compounds K3Sc(IO3)6 and KSc(IO3)3Cl.

Only a few oxofluoride compounds that contain lone-pair cations have been reported in the literature, mainly due to synthetic difficulties. In this work new oxofluoride compounds containing the transition metals Cu2+, Co2+, or Sc3+ and the lone pair cations Bi3+ or Se4+ have been synthesized, where the transition metal octahedra form low-dimensional arrangements in form of chains or layers. The electronegative F ̶ anions behave like O2 ̶  and bridge in between different building blocks. The new oxofluorides are Cu2SeO3F2, CoBi2O2F4 and ScBi2O3F3. The first is a framework-like compound and the latter two are layered and belong to the Aurivillius family with one perovskite like layer. The inclusion of F made it possible to broaden this Aurivillius family to contain low-oxidation state transition metals. 

The magnetic properties of the new compounds containing Cu2+ and Co2+ were characterised and the Sc3+ containing non-centrosymmetric iodates were found to show non-linear optical properties.

Place, publisher, year, edition, pages
Stockholm: Department of Materials and Environmental Chemistry, Stockholm University, 2020. p. 64
Keywords
Crystal structure determination, New oxohalide compounds, Lone-pair electrons, X-ray diffraction, Physical properties
National Category
Inorganic Chemistry
Research subject
Inorganic Chemistry
Identifiers
urn:nbn:se:su:diva-178526 (URN)978-91-7911-012-3 (ISBN)978-91-7911-013-0 (ISBN)
Public defence
2020-03-25, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, Stockholm, 10:00 (English)
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Note

At the time of the doctoral defense, the following paper was unpublished and had a status as follows: Paper 4: Accepted.

Available from: 2020-03-02 Created: 2020-02-10 Last updated: 2022-02-26Bibliographically approved

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Mitoudi Vagourdi, EleniKremer, Reinhard K.Johnsson, Mats

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