4.8 Article

Redox Poly-Counterion Doped Conducting Polymers for Pseudocapacitive Energy Storage

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 1, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202006203

关键词

conducting polymers; high mass loading; permanent doping; redox dopants; supercapacitors

资金

  1. National Natural Science Foundation of China [21673035, 51804066, 51974070]
  2. 111 Project [B16009]
  3. China Postdoctoral Science Foundation [2019T120214]
  4. Fundamental Research Funds for the Central Universities of China [N170504022]
  5. LiaoNing Revitalization Talents Program [XLYC1907069]

向作者/读者索取更多资源

This study introduces a redox-active poly-counterion doping concept to enhance the electrochemical performance of conducting polymers (CPs), especially under ultra-high mass loadings. By doping with poly-counterions, the dopants undergo redox reactions during charge/discharge processes to provide additional capacitance and improve the electrical conductivity of CPs. Additionally, poly-counterions with steric hindrance can act as structural pillars and facilitate ion transport in CPs.
Conducting polymers (CPs) have been widely studied for electrochemical energy storage. However, the dopants in CPs are often electrochemically inactive, introducing dead-weight to the materials. Moreover, commercial-level electrode materials with high mass loadings (e.g., >10 mg cm(-2)) often encounter the problems of inferior electrical and ionic conductivity. Here, a redox-active poly-counterion doping concept is proposed to improve the electrochemical performance of CPs with ultra-high mass loadings. As a study prototype, heptamolybdate anion (Mo7O246-) doped polypyrrole (PPy) is synthesized by electro-polymerization. A 2 mm thick PPy electrode with mass loading of approximate to 192 mg cm(-2)reaches a record-high areal capacitance of approximate to 47 F cm(-2), competitive gravimetric capacitance of 235 F g(-1), and volumetric capacitance of 235 F cm(-3). With poly-counterion doping, the dopants also undergo redox reactions during charge/discharge processes, providing additional capacitance to the electrode. The interaction between polymer chains and the poly-counterions enhances the electrical conductivity of CPs. Besides, the poly-counterions with large steric hindrance could act as structural pillars and endow CPs with open structures for facile ion transport. The concept proposed in this work enriches the electrochemistry of CPs and promotes their practical applications.

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