Fabrication of NiCo2O4@polyaniline heterostructure as positive electrode for asymmetrical supercapacitor

NiCo2O4, as a low‐cost and high‐performance binary transition metal oxide material, has been widely used in the fabrication of supercapacitor electrodes. However, the low energy density of binary metal oxides limits their large‐scale practical applications in supercapacitors, so it is highly desirab...

Full description

Saved in:
Bibliographic Details
Published in:Journal of applied polymer science 2023-11, Vol.140 (43)
Main Authors: Li, Xinxiu, Xie, Haidong, Feng, Yong, Qu, Yuqing, Zhai, Lidong, Sun, Hehang, Liu, Xiongfei, Hou, Chunping
Format: Article
Language:English
Subjects:
Asymmetry
Capacitance
Electrochemical analysis
Electrodes
Heterostructures
Materials science
Nickel compounds
Polyanilines
Polymers
Supercapacitors
Synergistic effect
Transition metal oxides
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:NiCo2O4, as a low‐cost and high‐performance binary transition metal oxide material, has been widely used in the fabrication of supercapacitor electrodes. However, the low energy density of binary metal oxides limits their large‐scale practical applications in supercapacitors, so it is highly desirable to design the structure of the NiCo2O4‐based supercapacitor. Therefore, in this paper, NiCo2O4 is compounded with polyaniline (PANI) to improve its electrochemical performance by exploiting the synergistic effect. The NiCo2O4@PANI composite electrode exhibits a specific capacitance of 561.2 F/g at 10 mV/s. In this study, asymmetric supercapacitors are assembled with NiCo2O4@PANI as the positive electrode and MXene as the negative electrode. The NiCo2O4@PANI‐CC//MXene‐CC supercapacitor has a specific capacitance of 31.95 F/g at a scan rate of 10 mV/s and a good cycle retention capacity of 86.2% after 3000 cycles. The excellent electrochemical performances are attributed to the dynamic equilibrium and fast redox kinetics of the two electrodes.
ISSN:0021-8995
1097-4628
DOI:10.1002/app.54580