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      Synthesis of 3D-Nanonet Hollow Structured Co3O4 for High Capacity Supercapacitor

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          Abstract

          A 3D-nanonet structured cobalt-basic-carbonate precursor has been obtained by a facile, low cost and eco-friendly route under ambient temperature and pressure. After calcination in air, the as-prepared precursor was converted to a 3D-nanonet hollow structured Co3O4 with its original frame structure almost preserved. Encouragingly, by alternating experimental parameters (Table S1 in the Supporting Information ), such as concentration of the starting reagents and calcination temperature, we got the optimized condition for the final product with desirable electrochemical performance (Figure S1 in the Supporting Information ). The pseudocapacitive properties of the obtained Co3O4 were evaluated by cyclic voltammetry (CV), galvanostatic charge-discharge measurement and electrochemical impedance spectroscopy in 6.0 M KOH solution. At different scan rates of 5, 10, 20, and 30 mV s(-1), the corresponding specific capacitances were 820, 755, 693, and 656 F g(-1), respectively. The material also exhibited superior charge-discharge stability and maintained 90.2% of its initial capacitance after 1000 continuous charge-discharge cycles at a current density of 5 A g(-1). From a broad view, our research and the outstanding results not only present a feasible access to nanostructured Co3O4 but also remind us of paying more attention to the simple synthetic methods without complex processes and sophisticated instruments.

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          Author and article information

          Journal
          ACS Applied Materials & Interfaces
          ACS Appl. Mater. Interfaces
          American Chemical Society (ACS)
          1944-8244
          1944-8252
          May 2014
          May 14 2014
          May 2014
          May 14 2014
          : 6
          : 9
          : 6739-6747
          Affiliations
          [1 ]College of Chemical Engineering and ‡College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu 610064, People’s Republic of China
          Article
          10.1021/am500464n
          24745604
          031b61f1-3876-4889-b78f-d737319de366
          © 2014
          History

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