A stable one-dimensional system in an orthorhombic α-V2O5 nanowires monocrystalline structure was obtained by a solvothermal method from a polymorphic V2O5 structure. The starting material was firstly submitted to ac...
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A stable one-dimensional system in an orthorhombic α-V2O5 nanowires monocrystalline structure was obtained by a solvothermal method from a polymorphic V2O5 structure. The starting material was firstly submitted to acid hydrolysis in H2O2 followed by a solvothermal treatment. The outcome of this procedure, a metastable phase of the one-dimensional system V10O24·12H2O/V3O7·H2O, was subsequently reoxidized by controlled heating in an open air system. The final product was an orange crystalline solid mainly formed by monocrystalline nanowires of α-V2O5 having lengths of tens of micrometers and widths of about 75 nm with a preferential [200] growth direction. It was found that the pH value of the initial solution plays an important role in the formation of the crystalline phase in the final products. Characterization was performed by X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). This study offers an alternate route for the synthesis of vanadium oxides and related compounds.
We present a study of their structure, morphology, electrical and magnetic properties on the (Ca1–xSrx) RuO3 system for x = 0.0, 0.07, 0.10, 0.15 and 1.0. The samples were prepared by the solidstate reaction method i...
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We present a study of their structure, morphology, electrical and magnetic properties on the (Ca1–xSrx) RuO3 system for x = 0.0, 0.07, 0.10, 0.15 and 1.0. The samples were prepared by the solidstate reaction method in air at ambient pressure and heat in the 700℃ - 800℃ range for 48 h. By X-ray powder diffraction (XRD), we determine a solid solution until x = 0.15. Scanning electron microscopy (SEM) indicates that the particle size is 77 - 266 nm. The resistance measurements, as a function of temperature measurements from 7 to 300 K the (Ca1–xSrx) RuO3 system for x = 0.0, 0.07, 0.10, 0.15 and 1.0 show a metallic behaviour. We can even observe that the resistance of the samples is due to the partial substitution of Sr2+ ions and Ru ion valence. Finally, the sample x = 0.07 has a magnetization applied high field to 10 K, whereas that to 300 K does not have a magnetization.
Studies of thermodynamic, electric and magnetic properties were conducted on the (KxSr1-x)CrOz, x = 0.10, 0.15 and 0.50system; adjusted for different crystal sizes (polycrystalline, nano-crystalline and single crys...
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Studies of thermodynamic, electric and magnetic properties were conducted on the (KxSr1-x)CrOz, x = 0.10, 0.15 and 0.50system; adjusted for different crystal sizes (polycrystalline, nano-crystalline and single crystals). For polycrystals, a solid-statereaction method was used (room temperature, TR, up to 665 °C). Nano-crystals, a crushing technique with a mechanical mortar wereprocessed at TR. Single crystals were acquired, through fusion method starting from polycrystals pre-manufactured (665 °C) over900 °C. For the methods described above, they all were worked at atmospheric pressure. Studying the thermodynamic in the crystalsmixture were obtained by TGA (thermogravimetric analysis) and DSC (differential scanning calorimetry). Powder XRD (X-raydiffraction) in the manual grinding mixture a SrCO3 solid solution, at TR was detected. When increasing the temperature, a solidsolution of K2Sr(CrO4)2 is formed. By HRTEM (high-resolution transmission electronic microscope), crystal sizes 4-12 nm were seen.(K0.50Sr0.50)CrOz composition presents a weak ferromagnetic and an insulating behavior.
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