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In-situ synthesis of NiCo2S4@graphene composite for high-performance supercapacitor.

Authors :
Xu, Xiaojun
Xu, HuiZhong
Zhou, Qiannan
Liu, Weifeng
Gao, Jie
Zhuang, Ziqiushui
Zhou, Xin
Li, Wei
Source :
Ionics; Dec2023, Vol. 29 Issue 12, p5453-5463, 11p
Publication Year :
2023

Abstract

Binary transition metal sulfides have garnered widespread concentration result from their superior electrical conductivity and outstanding capacitance. However, their poor cycling stability hinders their applications in energy storage devices. The objective of this study is to devise and prepare graphene and NiCo<subscript>2</subscript>S<subscript>4</subscript> composite (NiCo<subscript>2</subscript>S<subscript>4</subscript>@graphene) using a simple one-step hydrothermal modality. Graphene is used as a conductive substrate, and NiCo<subscript>2</subscript>S<subscript>4</subscript> nanoparticles are formed in situ and homogeneously anchored on graphene nanosheets through C-S-C covalent bonds. For example, the NiCo<subscript>2</subscript>S<subscript>4</subscript>@graphene composite has a high specific capacitance of 918.0 C g<superscript>−1</superscript> at a current density of 1 A g<superscript>−1</superscript> and enhanced cycling stability (90.1% after 6000 cycles). In addition, the asymmetric supercapacitor was fabricated with NiCo<subscript>2</subscript>S<subscript>4</subscript>@graphene as the positive electrode and graphene (GR) as the negative electrode, and the device provided a maximum energy density of 49.8 Wh kg<superscript>−1</superscript> at a power density of 845.3 Wh kg<superscript>−1</superscript>. Besides, the capacitance retention rate was as high as 92.0% after 1000 cycles. The superior electrochemical properties of the NiCo<subscript>2</subscript>S<subscript>4</subscript>@graphene material verified its huge potential for realistic applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09477047
Volume :
29
Issue :
12
Database :
Complementary Index
Journal :
Ionics
Publication Type :
Academic Journal
Accession number :
173653620
Full Text :
https://doi.org/10.1007/s11581-023-05206-5