Activated carbon derived from tree bark biomass with promising material properties for supercapacitors
Activated carbon from tree bark (ACB) has been synthesized by a facile and environmentally friendly activation and carbonization process at different temperatures (600, 700 and 800 °C) using potassium hydroxide (KOH) pellets as an activation agent with different mass loading. The physicochemical and...
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Veröffentlicht in: | Journal of solid state electrochemistry 2017-03, Vol.21 (3), p.859-872 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Activated carbon from tree bark (ACB) has been synthesized by a facile and environmentally friendly activation and carbonization process at different temperatures (600, 700 and 800 °C) using potassium hydroxide (KOH) pellets as an activation agent with different mass loading. The physicochemical and microstructural characteristics of the as-obtained material revealed interconnected microporous/mesoporous architecture with increasing trend in specific surface area (SSA) as carbonization temperatures rises. The SSA values of up to 1018 m
2
g
−1
and a high pore volume of 0.67 cm
3
g
−1
were obtained. The potential of the ACB material as suitable supercapacitor electrode was investigated in both a three and two-electrode configuration in different neutral aqueous electrolytes. The electrodes exhibited electric double-layer capacitor (EDLC) behaviour in all electrolytes with the Na
2
SO
4
electrolyte working reversibly in both the negative (−0.80 V to −0.20 V) and positive (0.0 V to 0.6 V) operating potentials. A specific capacitance (
C
s
) of up to 191 F g
−1
at a current density of 1 A g
−1
was obtained for the optimized ACB electrode material in 1 M Na
2
SO
4
electrolyte. A symmetric device fabricated exhibited specific
C
s
of 114 F g
−1
at 0.3 A g
−1
and excellent stability with a coulombic efficiency of a 100 % after 5000 constant charge–discharge cycles at 5.0 A g
−1
and a low capacitance loss for a floating time of 70 h.
Graphical abstract
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ISSN: | 1432-8488 1433-0768 |
DOI: | 10.1007/s10008-016-3432-z |