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Amorphous mesoporous nickel phosphate/reduced graphene oxide with superior performance for electrochemical capacitors.

Authors :
Yuan, Jingjing
Zheng, Xiaoke
Yao, Dachuan
Jiang, Ling
Li, Ya
Che, Jianfei
He, Guangyu
Chen, Haiqun
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry. 10/7/2018, Vol. 47 Issue 37, p13052-13062. 11p.
Publication Year :
2018

Abstract

Nickel phosphate (Ni3(PO4)2) is a promising electrode material for electrochemical capacitors, but the low intrinsic electrical conductivity and poor rate capability of Ni3(PO4)2 are the main challenges. To tackle these problems, amorphous mesoporous Ni3(PO4)2 with a pore diameter of 2–10 nm is grown on reduced graphene oxide (rGO), and a Ni3(PO4)2/rGO composite is obtained via a facile hydrothermal-calcination method in this work. The Ni3(PO4)2/rGO composite calcined at 300 °C (Ni3(PO4)2/rGO-300) possesses a uniform particle size and a high specific surface area of 198.72 m2 g−1. Benefiting from the structural characteristics, the synergistic effect of components and the high specific surface area, the Ni3(PO4)2/rGO-300 composite exhibits an extremely high specific capacitance of 1726 F g−1 at 0.5 A g−1 and an excellent rate capability of 850 F g−1 at 25 A g−1. In addition, the assembled Ni3(PO4)2/rGO-300//activated carbon asymmetric electrochemical capacitor delivers a good energy density of 57.42 W h kg−1 at a power density of 160 W kg−1. Compared with Ni3(PO4)2/rGO composites calcined at other temperatures and other nickel–phosphorus compounds reported in the literature, the Ni3(PO4)2/rGO-300 composite containing amorphous mesoporous Ni3(PO4)2 exhibits superior electrochemical performance, representing a new kind of electrode material for electrochemical capacitors. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
47
Issue :
37
Database :
Academic Search Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
131971664
Full Text :
https://doi.org/10.1039/c8dt02304b