Iranian Journal of Materials Science and Engineering

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TiO2/SiO2 nanocomposite with molar ratio 1:1 was synthesized by a free calcination sol-gel method using titanium tetra chloride and tetraethylorthosilicate as raw materials. In the composite, TiO2 nanocrystals are highly dispersed in the amorphous SiO2 matrix and the mater showed size quantization effect arising from the presence of extremely small titanium oxide species having a low coordination number. Thermal phase transformation studies of the as-prepared composite were carried out by means of X-ray diffraction (XRD) patterns and thermogravimetry–differential scanning calorimetry (TG–DSC) analyses. The studies showed existence of anatase phase in all the tested temperatures. When temperature exceeds 400°C, brookite phase was formed beside anatase phase. At 950°C amorphous silica matrix was transformed to crystobalite and brookite phase disappeared. Finally, small peaks of rutile phase were detectable at 1100°C.

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The synthesis of mesoporous CuFe2O4 spinel by several nanocasting strategies (i.e., multi-step nanocasting, one step nanocasting, modified solid-liquid), in which copper and iron nitrates are used as precursors and Pluronic P123 as surfactant, is explored. We have also checked the effect of pH, citric acid and sodium citrate in multi-step nanocasting method. The modified solid-liquid method which contains impregnating mesoporous silica by molten state salts in a non-ionic solvent seems to be the best choice to obtain single phase ordered mesoporous copper ferrite. Other methods suffer from the presence of copper oxide or hematite as impurities or lack of integrity in the mesoporous structure. Increasing pH up to 9.5 does not enhance the phase formation inside the pores of the silica matrix. The citric acid yields a fine structure but does not facilitate the phase formation. Adding sodium citrate neither heals the phase formation nor the structure of the final product. Moreover, vinyl- functionalized mesoporous silica exploited in this study as a hard template entraps both metal nitrates in the pores, assisting impregnation procedure

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Mesoporous SiO₂ nanopowder was synthesized under an acidic condition by a sol-gel method using various amounts of cetyltrimethyl ammonium bromide (CTAB) as structure directing agent. The samples were investigated with XRD, SEM, FTIR, TEM and N₂ absorption-desorption analysis. Also, the incremental effect of surfactant were examined. The results obtained from the analysis suggested that an increase in the amount of surfactant resulted in increasing specific surface area, pore size and pore volume, of the synthesized particles up to 549 m².g^-1, 17.3 nm, and 2 cm³.g^-1, respectively. Absorption behavior of the mesoporous silica was investigated for degradation of methylene blue pigments (MB) in aqueous solutions. The samples SC0, SC0.5 and SC1 showed the maximum absorption capacities of 333, 454 and 526 mg/g, respectively

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The trimanganese tetraoxide (Mn₃O₄) nanostructured thin films doped with 2 mol % of nickel (Ni) and molybdenum (Mo) ions were deposited by a simple electrophoretic deposition technique. The structural, optical, and morphological studies of these doped thin films were compared with pure Mn₃O₄ thin films. X-ray diffraction (XRD) confirmed the tetragonal Hausmannite spinel structure. The Fourier transform infrared spectroscopy (FTIR) provided information about the molecular composition of the thin films and the presence of specific chemical bonds. The optical study and band gap energy values of all thin films were evaluated by the UV visible spectroscopy technique. The scanning electron microscopy (SEM) illustrated the morphological modifications of the Mn₃O₄ thin films due to doping of the nickel and molybdenum ions. The Brunauer Emmett Teller (BET) method has confirmed the mesoporous nanostructure and nanopores of the thin films. The supercapacitive performance of the thin films was studied by cyclic voltammetry (CV), and galvanostatic charge discharge (GCD) techniques using the three-electrode arrangement. An aqueous 1M Na₂SO₄ electrolyte was used for the electrochemical study. The 2 mol % Ni doped Mn₃O₄ thin film has shown maximum specific capacitance than pure and Mo doped Mn₃O₄ thin films. Hence, this study proved the validity of the strategy - metal ion doping of Mn₃O₄ thin films to develop it as a potential candidate for electrode material in the futuristic energy storage and transportation devices.