4.6 Article

Super long-life supercapacitor electrode materials based on hierarchical porous hollow carbon microcapsules

Journal

RSC ADVANCES
Volume 5, Issue 106, Pages 87077-87083

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra15594k

Keywords

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Funding

  1. National Natural Science Foundation of China [51203071, 51363014, 51463012, 51362018]
  2. China Postdoctoral Science Foundation [2014M552509, 2015T81064]
  3. Opening Project of State Key Laboratory of Polymer Materials Engineering (Sichuan University) [sklpme2014-4-25]
  4. Program for Hongliu Distinguished Young Scholars in Lanzhou University of Technology [J201402]
  5. University Scientific Research Project of Gansu Province [2014B-025]

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Remarkable supercapacitor electrodes with a high specific supercapacitance and a super long cycle life were achieved by using hierarchical porous hollow carbon microcapsules (HPHCMs) as active materials. HPHCMs were prepared by a facile chemical route based on pyrolysis of a soft sacrificial template involving a non-crosslinked core of poly(styrene-r-methylacrylic acid) and a crosslinked shell of poly(styrene-r-divinylbenzene-r-methylacrylic acid), which were synthesized by using traditional radical polymerization and emulsion polymerization. The results of scanning electron microscopy, transmission electron microscopy and Brunauer-Emmett-Teller characterizations revealed that HPHCM possessed the desired pore structure with apparent macro-/meso- and micropores, which not only provided a continuous electron-transfer pathway to ensure good electrical contact, but also facilitated ion transport by shortening diffusion pathways. As electrode materials for supercapacitor, a high specific capacitance of 278.0 F g(-1) was obtained at the current density of 5 mA cm(-2). Importantly, after 5000 potential cycles in 2 M KOH electrolyte at the discharge current density of 20 mA cm(-2), the capacitance actually increased from 125 to 160 F g(-1) and then remained 151 F g(-1), corresponding to a capacitance retention of 120%, likely due to electrochemical self-activation.

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