Facile fabrication of hierarchical porous carbon for a high-performance electrochemical capacitor
The template method is often used to synthesize porous materials. However, removing the template during post-processing is difficult and harsh reagents are frequently used, which is unfavorable for the carbon structure. In this paper, a facile and green synthesis route is developed for the synthesis...
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Veröffentlicht in: | RSC advances 2017-01, Vol.7 (73), p.46329-46335 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The template method is often used to synthesize porous materials. However, removing the template during post-processing is difficult and harsh reagents are frequently used, which is unfavorable for the carbon structure. In this paper, a facile and green synthesis route is developed for the synthesis of a 3D honeycomb-like hierarchical porous carbon based on rapid thermal decomposition of the mixture of a low-cost carbon precursor (typically starch) and Na
2
CO
3
followed by KOH activation, in which Na
2
CO
3
particles are employed as the water-soluble renewable macroporous template. Benefiting from the high specific surface area (1171 m
2
g
−1
) and the interconnected micro-, meso-, and macropores, the porous carbon exhibits superior capacitive performance, including high specific capacitance, good rate capability and excellent cycling stability. Moreover, the porous carbon-based symmetric supercapacitor delivers a maximum energy density of 33 W h kg
−1
at 100 W kg
−1
and presents excellent long-term cycling stability. Considering the easy-availability of the raw materials and the facile synthesis process, this environmentally friendly and cost-effective method can be expected to be widely applied, and we estimate that the obtained porous carbon could find additional applications in other fields.
A facile and rapid pyrolysis method is developed for the synthesis of 3D hierarchical porous carbon, which exhibits a high specific capacitance, good rate capability and good cycling performance. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c7ra08402a |