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Abstract

Phytic acid-doped copolymers poly(aniline-co-pyrrole) have been synthesized by chemical polymerization for applications of supercapacitors. The results indicate that poly(aniline-co-pyrrole) copolymer delivered a high specific capacitance (639 F g−1) and 62.3% capacitance retention after 1000 cycles at 3 A g−1 in 1 M H2SO4. The good cycle stability was due to increased structural stability by the formation of cross-link between poly(aniline-co-pyrrole) backbones doped by phytic acid. The high capacitance may result from the formation of large specific surface area and effective conducting paths in the copolymer. A symmetrical supercapacitor device based on this copolymer was designed and provided a high energy density (12.2 Wh kg−1 at the power density of 500 W kg−1). Such results indicate that poly(aniline-co-pyrrole) might be a feasible candidate for electrocapacitive material of supercapacitors and this strategy can be extended to fabricate other conducting polymers for supercapacitor applications.

Details

Title
Phytic acid-doped poly(aniline-co-pyrrole) copolymers for supercapacitor electrodes applications
Author
Wang, Yao 1 ; Wen-Bin, Ma 1 ; Guo, Lin 1 ; Xiang-Zhu, Song 1 ; Xue-Yu, Tao 1   VIAFID ORCID Logo  ; Li-Tong, Guo 1 ; He-Liang, Fan 1 ; Zhang-Sheng, Liu 1 ; Ya-Bo, Zhu 1 ; Xian-Yong, Wei 2 

 China University of Mining and Technology, School of Materials and Physics, Xuzhou, China (GRID:grid.411510.0) (ISNI:0000 0000 9030 231X) 
 China University of Mining and Technology, School of Chemical Engineering and Technology, Xuzhou, China (GRID:grid.411510.0) (ISNI:0000 0000 9030 231X); China University of Mining and Technology, Key Laboratory of Coal Processing and Efficient Utilization, Ministry of Education, Xuzhou, China (GRID:grid.411510.0) (ISNI:0000 0000 9030 231X) 
Pages
6263-6273
Publication year
2020
Publication date
Apr 2020
Publisher
Springer Nature B.V.
ISSN
09574522
e-ISSN
1573482X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2388399986
Copyright
© Springer Science+Business Media, LLC, part of Springer Nature 2020.