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Abstract: Tin oxide coated molybdenum oxide nanowires (SnO2/MoO3) are synthesized by a combination of hydrothermal and wet chemical routes. The electrochemical capacitance properties of the SnO2/MoO3 core shell composite nanowires are measured by cyclic voltammetry (CV) and galvanostatic charge–discharge method in 1M Na2SO4 aqueous solutions. The results showed that specific capacitance of SnO2/MoO3 core shell composite nanowires is 295Fg−1, which is much higher than the specific capacitance of pure individual MoO3 (69Fg−1) and SnO2 (96.6Fg−1). Moreover the synthesized core shell composite nanowires has also exhibited excellent long-term cycling stability (only 3% loss of its initial specific capacitance after 1000 cycles) which may lead to its multifarious usage in high-performance energy storage devices for future potential applications. [Copyright &y& Elsevier]

A ternary nanocomposite of molybdenum trioxide (α-MoO 3 ) nanowires coated with a thin layer of carbon, which is intertwined with graphene oxide is synthesized by hydrothermal and ultrasonication route. It is found that high conductivity of carbon coated MoO 3 nanowires is further increased by introducing the graphene sheets. The ternary nanocomposite (rGO/MoO 3 @C) exhibits high specific capacitance, excellent cyclic stability compared to the carbon coated MoO 3 (MoO 3 @C) and virginal MoO 3 nanowires due to the synergistic effect of carbon layer and graphene. The electrochemical impedance measurements show that rGO/MoO 3 @C nanocomposite have lower charge transfer resistance as compared to MoO 3 @C and MoO 3 nanowires electrodes. Two probe electrical conductivity ( I–V ) measurements confirm the enhanced conductivity of rGO/MoO 3 @C nanocomposite relative to MoO 3 @C and bare MoO 3 nanowires. The electrical and electrochemical measurements indicate that the rGO/MoO 3 @C nanocomposite is promising candidate for energy storage applications. [ABSTRACT FROM AUTHOR]

Novel graphitic material containing chromium oxide (Cr 2 O 3 ) nanoribbons is obtained by carbonizing a mixture of polyfurfuryl alcohol and MIL–101(Cr) at 900 °C. Morphological, structural, and chemical analysis of the product is carried out with HR–TEM, SEM, XPS, XRD, and BET surface area. The maximum BET surface area recorded for the nanocomposite is 438 m 2 g −1 . The nanocomposite exhibits a specific capacitance as high as 300 F g −1 at 2 mV s −1 and 291 F g −1 at 0.25 A g −1 , and presents 95.5% long–term cycling stability over 3000 cycles. The pseudo-capacitive role of Cr 2 O 3 nanoribbons is found to be important towards total capacitance of nanocomposite material. [ABSTRACT FROM AUTHOR]