4.7 Article

Investigating the redox behavior of activated carbon supercapacitors with hydroquinone and p-phenylenediamine dual redox additives in the electrolyte

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 537, 期 -, 页码 295-305

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2018.11.026

关键词

Activated carbon, electrolyte; Hydroquinone; p-phenylenediamine; Redox additive; Supercapacitor

资金

  1. Ministry of Science and Technology (MOST) in Taiwan [MOST 106-2221-E-027-108, MOST 106-2119-M-027-001]
  2. MOST in Taiwan [MOST 107-2636-E-027-003]
  3. Research Center of Energy Conservation for New Generation of Residential, Commercial, and Industrial Sectors from The Featured Areas Research Center Program

向作者/读者索取更多资源

Activated carbon (AC) with large surface area and high electrical conductivity is widely applied on super-capacitors (SC), but the energy storage mechanism for the pure electrical double layer capacitor of carbon leads to a low energy density. Developing stable aqueous electrolytes with abundant redox reactions via incorporating more than one redox additive in the electrolyte is one of the efficient strategies to improve the energy storage capacity of the AC-based SC. In this study, the dual redox additives of hydroquinone (HQ) and p-phenylenediamine (PPD) are incorporated in the aqueous solution as the electrolyte for SC. The effects of the aqueous solution type as well as the total redox additive concentration and the relative amounts of HQ and PPD on the electrochemical performance of SC are carefully studied. Two binders are used for assembling the AC electrodes, and the binder-dependent electrochemical behaviors and energy storage capabilities for SC are obtained. The symmetric SC assembled with the optimized electrolyte and the AC electrode prepared using the LA132 binder shows the potential window of 1.6 V, the specific capacitance of 116.23 F/g at 2 A/g, and the maximum energy density of 1.85 W h/kg at the power density of 0.15 kW/kg. (C) 2018 Elsevier Inc. All rights reserved.

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