Molybdenum carbide nanoparticle-decorated 3D nitrogen-doped carbon flowers as an efficient electrode for high-performance, all-solid-state symmetric supercapacitors
Electrode materials with high electro-catalytic activity and tailored nanostructures are of great importance for high performance energy storage devices. We develop a novel 3D nanostructured electrode with highly stable, and catalytically-active molybdenum carbide nanoparticles decorated on nitrogen...
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Published in | Journal of alloys and compounds Vol. 748; pp. 134 - 144 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier B.V
05.06.2018
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | Electrode materials with high electro-catalytic activity and tailored nanostructures are of great importance for high performance energy storage devices. We develop a novel 3D nanostructured electrode with highly stable, and catalytically-active molybdenum carbide nanoparticles decorated on nitrogen-doped carbon flowers (Mo2C/NCF). The controlled synthesis of Mo2C/NCF provides a uniform distribution of Mo2C nanoparticles of ∼80 nm on carbon microflowers with a self-assembled petal-like structure. The Mo2C/NCF achieves excellent electrochemical performance, with a specific capacitance of 1250 F/g at the current density of 1 A/g in a liquid electrolyte. A device consisting of all-solid-state symmetric supercapacitors (SSC) that used this novel electrode exhibits a high energy density of 54 Wh/kg along with remarkable cycling stability (100% retention after 5000 cycles). We believe that these results provide a new way for carbide materials to be used in high-performance energy storage devices.
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•Nanostructured Mo2C/NCF electrodes are developed via simple reflux reactions.•The Mo2C/NCF achieves an excellent specific capacitance of 1250 F/g at 1 A/g.•An all-solid-state symmetric supercapacitor exhibits an energy density of 54 Wh/kg.•After 5000 cycles, the specific capacitance retention of the Mo2C/NCF is 100%. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2018.03.139 |