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Issue 22, 2016
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Morphology-controlled syntheses of α-MnO2 for electrochemical energy storage

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Abstract

Manganese dioxide (MnO2) nanoarchitectures including microspheres assembled by nanosheets and hollow urchins assembled by nanorods have been successfully synthesized using a facile and efficient hydrothermal method at 150 °C. The effects of concentrations of the reactants and reaction time on the structures and morphologies of MnO2 were systematically investigated. The experimental results showed that the morphologies of MnO2 transformed into nanosheet-assembled microspheres (10 min) from nanorod-assembled hollow urchins (5 min) by tuning the suitable reaction time. The nanorod-assembled hollow urchins experienced the morphology transformation cycle from urchin to a disordered structure to urchin with the extension of the reaction time. Furthermore, the nanorods with different diameters and lengths were formed with different concentrations of reactants at the same reaction time (8 h). The MnO2 nanorods fabricated with 0.59 g KMnO4 showed a maximum specific capacitance (198 F g−1) with a good rate capability and excellent cycling stability (maintained 94% after 2000 cycles). Furthermore, the nanosheet-assembled microspheres exhibited the higher specific capacitance of 131 F g−1 at 1 A g−1 with a long-term cycling stability for the samples at different reaction times. These results indicated their promising applications as high-performance supercapacitor electrodes and provided a generic guideline in developing different nanostructured electrode materials for electrochemical energy storage.

Graphical abstract: Morphology-controlled syntheses of α-MnO2 for electrochemical energy storage

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Publication details

The article was received on 19 Apr 2016, accepted on 09 May 2016 and first published on 10 May 2016


Article type: Paper
DOI: 10.1039/C6CP02548J
Citation: Phys. Chem. Chem. Phys., 2016,18, 15235-15243
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    Morphology-controlled syntheses of α-MnO2 for electrochemical energy storage

    W. He, W. Yang, C. Wang, X. Deng, B. Liu and X. Xu, Phys. Chem. Chem. Phys., 2016, 18, 15235
    DOI: 10.1039/C6CP02548J

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