Abstract

Research was carried out on the incorporation of divalent cobalt cations into the crystalline structure of MgF2 to form MgxCo1−xF2 binary fluorides, which had not been investigated before. The above fluorides were obtained by the precipitation from aqueous solution of magnesium and cobalt nitrates with ammonium fluoride. Binary fluorides containing 0.6, 7.5 and 37.7 mol% CoF2 were prepared. The effects of treatment temperature (300, 400 °C) and atmosphere (oxidizing or reducing) on the structure (XRD, TPR-H2, UV-Vis), texture (low-temperature N2 adsorption), surface composition (XPS) and surface acidity (NH3-TPD) of the binary fluorides were determined. It has been found that in MgxCo1−xF2 an isomorphic substitution occurs of Mg2+ cations by Co2+ cations which results in the formation of a rutile-type solid solution. The obtained binary fluorides are characterized by a mesoporous structure and relatively large surface area. It has been found that thermal treatment of the binary fluorides in oxidizing conditions results in the oxidation of CoF2 to Co3O4 even at 300 °C; therefore it is not possible to obtain pure MgxCo1−xF2 binary fluorides in the presence of air. The preparation of the latter requires reducing conditions, namely thermal treatment of dry precipitate at 300 °C in an atmosphere of hydrogen. If the treatment is conducted at a higher temperature (400 °C), CoF2 undergoes a partial reduction to metallic cobalt. An XPS study has shown the presence of hydroxyl groups in the investigated samples. However, these are solely surface groups because their presence was not detected by XRD measurements. The binary fluorides obtained by our method are characterized by a very narrow optical energy gap (5.31–3.50 eV), considerably narrower than that recorded for bulk fluorides. Measurements of temperature-programmed desorption of ammonia have shown that the incorporation of cobalt cations into the crystal structure of MgF2 results in a decrease in the surface acidity of the binary fluorides.

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