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High-performance asymmetric pseudocapacitor based on NiCo2O4@MnO2 cathode and N-doped graphene anode.

Authors :
Liu, Weiwei
Shi, Pan
Tian, Xueni
He, Xihong
Li, Linbo
Source :
Journal of Electroanalytical Chemistry. May2024, Vol. 960, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

• N -doped graphene is prepared from mechanical exfoliation process and nitrogen plasma irradiation. • MnO 2 nanoflakes are successfully electrodeposited on hydrothermal prepared NiCo 2 O 4 nanowires. • Asymmetric supercapacitor based on NiCo 2 O 4 @MnO 2 nanowires and N -doped graphene exhibits competitive performance. The design and fabrication of scalable energy storage systems are crucial for portable applications, demanding advanced materials through large-scale and facile processing. In this report, an asymmetric solid-state pseudocapacitor (ASPC) is assembled using a core–shell NiCo 2 O 4 @MnO 2 composite and solution-processed nitrogen-doped graphene (N -GP) as the positive and negative electrodes, respectively. With interconnected porous structures, the electrodes based on N -GP and NiCo 2 O 4 @MnO 2 offer high specific capacitance and rate capability, broad operation voltage, and a binder-free design with no added conductive agent. With these benefits, the ASPC with a PVA-KOH electrolyte exhibits a specific capacitance of 103.3F g−1 at 1 A/g and exceptional energy density of 36.73 Wh kg−1 at a power density of 792 W kg−1. In addition, the specific capacitance retention reaches 90.9 % after 5000 cycles, indicating excellent cycling stability. In the broader context of solid-state supercapacitors based on solution-processed graphene, this ASPC exhibits highly competitive performance, establishing it as a promising candidate for advanced energy storage. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15726657
Volume :
960
Database :
Academic Search Index
Journal :
Journal of Electroanalytical Chemistry
Publication Type :
Academic Journal
Accession number :
176760111
Full Text :
https://doi.org/10.1016/j.jelechem.2024.118216