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      Remarkable capacitive behavior of a Co3O4–polyindole composite as electrode material for supercapacitor applications

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          Abstract

          A single step synthesized Co 3O 4–polyindole composite electrode exhibits high specific capacitance, rate performance and cyclability. This enhanced electrochemical supercapacitive behavior is mainly attributed to the synergistic effect between Co 3O 4 and polyindole.

          Abstract

          In this paper, we demonstrate a single step synthesis of cobalt oxide – conducting polyindole (Co 3O 4–Pind) composites by in-situ cathodic electrodeposition. The structural and morphological changes of the as-prepared Co 3O 4–Pind composites have been investigated using various techniques such as powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman analysis and X-ray photoelectron spectroscopy (XPS). Very interestingly, polyindole decoration over Co 3O 4 results in concomitant change in morphology leading to substantial improvement in the supercapacitor behavior. The electrochemical performance of Co 3O 4–Pind has been investigated by cyclic voltammetry, galvanostatic charge–discharge cycling and impedance analysis. The specific capacitance (SC) of Pind decorated Co 3O 4 is found to be 1805 F g −1 at a current density of 2 A g −1 with excellent rate capability (SC: 1625 F g −1 at a high current density of 25 A g −1) and cycling stability. This remarkable supercapacitive performance of the Co 3O 4–Pind composite is mainly attributed to the synergism that evolved between Co 3O 4 and Pind. More importantly, these electrodes are free from binders and conductive carbon which have significant impact over the gravimetric energy density of the devices.

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          Most cited references52

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          Hydrous Ruthenium Oxide as an Electrode Material for Electrochemical Capacitors

          J. Zheng (1995)
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            Nanomaterials for energy conversion and storage.

            Nanostructured materials are advantageous in offering huge surface to volume ratios, favorable transport properties, altered physical properties, and confinement effects resulting from the nanoscale dimensions, and have been extensively studied for energy-related applications such as solar cells, catalysts, thermoelectrics, lithium ion batteries, supercapacitors, and hydrogen storage systems. This review focuses on a few select aspects regarding these topics, demonstrating that nanostructured materials benefit these applications by (1) providing a large surface area to boost the electrochemical reaction or molecular adsorption occurring at the solid-liquid or solid-gas interface, (2) generating optical effects to improve optical absorption in solar cells, and (3) giving rise to high crystallinity and/or porous structure to facilitate the electron or ion transport and electrolyte diffusion, so as to ensure the electrochemical process occurs with high efficiency. It is emphasized that, to further enhance the capability of nanostructured materials for energy conversion and storage, new mechanisms and structures are anticipated. In addition to highlighting the obvious advantages of nanostructured materials, the limitations and challenges of nanostructured materials while being used for solar cells, lithium ion batteries, supercapacitors, and hydrogen storage systems have also been addressed in this review.
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              Multifunctional 3D nanoarchitectures for energy storage and conversion.

              The design and fabrication of three-dimensional multifunctional architectures from the appropriate nanoscale building blocks, including the strategic use of void space and deliberate disorder as design components, permits a re-examination of devices that produce or store energy as discussed in this critical review. The appropriate electronic, ionic, and electrochemical requirements for such devices may now be assembled into nanoarchitectures on the bench-top through the synthesis of low density, ultraporous nanoarchitectures that meld high surface area for heterogeneous reactions with a continuous, porous network for rapid molecular flux. Such nanoarchitectures amplify the nature of electrified interfaces and challenge the standard ways in which electrochemically active materials are both understood and used for energy storage. An architectural viewpoint provides a powerful metaphor to guide chemists and materials scientists in the design of energy-storing nanoarchitectures that depart from the hegemony of periodicity and order with the promise--and demonstration--of even higher performance (265 references).
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2015
                2015
                : 3
                : 48
                : 24338-24348
                Affiliations
                [1 ]Electroplating and Metal Finishing Technology Division
                [2 ]CSIR – Central Electrochemical Research Institute
                [3 ]Karaikudi-630003
                [4 ]India
                [5 ]Fuel Cells Section
                [6 ]Electrochemical Power Sources Division
                Article
                10.1039/C5TA07046E
                367bff1e-e127-418f-aafb-778ab23fdb51
                © 2015
                History

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