Issue 7, 2018

NiMoO4 nanorod deposited carbon sponges with ant-nest-like interior channels for high-performance pseudocapacitors

Abstract

The mounting challenges of global energy shortage and climate change call for the development of low-cost and high performance energy storage systems. Here, we propose the facile preparation of a 3D sponge electrode material by the uniform deposition of NiMoO4 nanorods on a carbonized melamine sponge (CMS) during a solvothermal reaction. Under the templating of a macroporous CMS backbone, the obtained 3D hierarchical NiMoO4/CMS composite sponge can offer numerous electrochemical sites for faradaic redox reactions and also provide interconnected conducting carbon networks for direct and rapid charge transfer. Particularly, the unique ant-nest-like interior channels in the NiMoO4/CMS composite sponge can ensure fast ion transportation and also buffer the volume change of NiMoO4 during the long-term cycling. Benefiting from these advantages, the NiMoO4/CMS composite electrode exhibits a high specific capacitance of 1689 F g−1 at 1 A g−1, which outperforms most of the previously reported NiMoO4-based electrodes. Moreover, the asymmetric supercapacitor device fabricated utilizing the composite sponge as a binder-free positive electrode also delivers a superior cycling stability (91.9% capacity retention after 2500 cycles) and a high energy density of 48.8 W h kg−1 at a power density of 800 W kg−1. Hence, the current study provides a new protocol for the low-cost fabrication of 3D sponge-like electrodes towards practical supercapacitor applications.

Graphical abstract: NiMoO4 nanorod deposited carbon sponges with ant-nest-like interior channels for high-performance pseudocapacitors

Supplementary files

Article information

Article type
Research Article
Submitted
20 Mar 2018
Accepted
18 Apr 2018
First published
21 Apr 2018

Inorg. Chem. Front., 2018,5, 1594-1601

NiMoO4 nanorod deposited carbon sponges with ant-nest-like interior channels for high-performance pseudocapacitors

Y. Huang, F. Cui, Y. Zhao, J. Lian, J. Bao, T. Liu and H. Li, Inorg. Chem. Front., 2018, 5, 1594 DOI: 10.1039/C8QI00247A

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