Enhanced Electrochemical Behavior of Peanut-Shell Activated Carbon/Molybdenum Oxide/Molybdenum Carbide Ternary Composites
Biomass-waste activated carbon/molybdenum oxide/molybdenum carbide ternary composites are prepared using a facile in-situ pyrolysis process in argon ambient with varying mass ratios of ammonium molybdate tetrahydrate to porous peanut shell activated carbon (PAC). The formation of MoO and Mo C nanost...
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Veröffentlicht in: | Nanomaterials (Basel, Switzerland) Switzerland), 2021-04, Vol.11 (4), p.1056 |
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Sprache: | eng |
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Zusammenfassung: | Biomass-waste activated carbon/molybdenum oxide/molybdenum carbide ternary composites are prepared using a facile in-situ pyrolysis process in argon ambient with varying mass ratios of ammonium molybdate tetrahydrate to porous peanut shell activated carbon (PAC). The formation of MoO
and Mo
C nanostructures embedded in the porous carbon framework is confirmed by extensive structural characterization and elemental mapping analysis. The best composite when used as electrodes in a symmetric supercapacitor (PAC/MoO
/Mo
C-1//PAC/MoO
/Mo
C-1) exhibited a good cell capacitance of 115 F g
with an associated high specific energy of 51.8 W h kg
, as well as a specific power of 0.9 kW kg
at a cell voltage of 1.8 V at 1 A g
. Increasing the specific current to 20 A g
still showcased a device capable of delivering up to 30 W h kg
specific energy and 18 kW kg
of specific power. Additionally, with a great cycling stability, a 99.8% coulombic efficiency and capacitance retention of ~83% were recorded for over 25,000 galvanostatic charge-discharge cycles at 10 A g
. The voltage holding test after a 160 h floating time resulted in increase of the specific capacitance from 74.7 to 90 F g
at 10 A g
for this storage device. The remarkable electrochemical performance is based on the synergistic effect of metal oxide/metal carbide (MoO
/Mo
C) with the interconnected porous carbon. The PAC/MoO
/Mo
C ternary composites highlight promising Mo-based electrode materials suitable for high-performance energy storage. Explicitly, this work also demonstrates a simple and sustainable approach to enhance the electrochemical performance of porous carbon materials. |
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ISSN: | 2079-4991 2079-4991 |
DOI: | 10.3390/nano11041056 |