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Nanostructured cobalt sulfide-on-fiber with tunable morphology as electrodes for asymmetric hybrid supercapacitors
Porous cobalt sulfide (Co 9 S 8 ) nanostructures with tunable morphology, but identical crystal phase and composition, have been directly nucleated over carbon fiber and evaluated as electrodes for asymmetric hybrid supercapacitors. As the morphology is changed from two-dimensional (2D) nanoflakes t...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2014-01, Vol.2 (38), p.16190-16198 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Porous cobalt sulfide (Co
9
S
8
) nanostructures with tunable morphology, but identical crystal phase and composition, have been directly nucleated over carbon fiber and evaluated as electrodes for asymmetric hybrid supercapacitors. As the morphology is changed from two-dimensional (2D) nanoflakes to 3D octahedra, dramatic changes in supercapacitor performance are observed. In three-electrode configuration, the binder-free Co
9
S
8
2D nanoflake electrodes show a high specific capacitance of 1056 F g
−1
at 5 mV s
−1
vs.
88 F g
−1
for the 3D electrodes. As sulfides are known to have low operating potential, for the first time, asymmetric hybrid supercapacitors are constructed from Co
9
S
8
nanostructures and activated carbon (AC), providing an operation potential from 0 to 1.6 V. At a constant current density of 1 A g
−1
, the 2D Co
9
S
8
, nanoflake//AC asymmetric hybrid supercapacitor exhibits a gravimetric cell capacitance of 82.9 F g
−1
, which is much higher than that of an AC//AC symmetric capacitor (44.8 F g
−1
). Moreover, the asymmetric hybrid supercapacitor shows an excellent energy density of 31.4 W h kg
−1
at a power density of 200 W Kg
−1
and an excellent cycling stability with a capacitance retention of ∼90% after 5000 cycles. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C4TA03341H |