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Activation of Biomass-Derived Carbon Platelets for EDLC Symmetrical Devices.

Created on 12 Aug 2026

Authors

Vediyappan Thirumal, Perumal Rajivgandhi, Alagan Sekar, Jinho Kim

Published in

Nanomaterials (Basel, Switzerland). Volume 16. Issue 15. Aug 04, 2026. Epub Aug 04, 2026.

Abstract

The sustainable bio-activated carbon platelets were synthesized from tamarind (tamarind indicia) fruit seed shells (TFSs) by a pyrolysis approach with an inert gas atmosphere. The carbonization process was carried out at 800 °C under an inert argon atmosphere, yielding both pure TFS-AC and chemically activated TFS-AC (KOH) carbon materials. Microscopic surface morphological analysis confirmed the formation of thin, interconnected porous carbon platelet nanosheets with enhanced surface structural uniformity. Raman spectroscopy revealed characteristic D- and G-bands, signifying the presence of graphitic domains and partial structural disorder. BET surface area analysis indicated a significant improvement from 48.54 m2/g in TFS-AC to 124.72 m2/g in TFS-AC (KOH), suggesting enhanced pore development and surface accessibility due to KOH activation. Electrochemical two-electrode performance was evaluated in symmetric device configurations using 3M KOH aqueous electrolyte. The TFS-AC (KOH) device exhibited a remarkable specific capacitance, which delivered 129.03 F/g at 0.5A/g, compared to the pure TFS-AC device. Electrochemical impedance spectroscopy (EIS) further confirmed low internal resistance and favorable ion transport. These findings confirm that KOH-activated TFS-derived carbon nanosheets have higher electrochemical stability, retaining 98.2% capacitance over 10,000 cycles. These results are promising electrode materials for high-performance supercapacitor applications, owing to their superior electrochemical symmetric device performance of bio-mass carbon Tamarind seed shell platelet nanosheets for future energy storage symmetric device applications.

PMID:
42584350
Bibliographic data and abstract were imported from PubMed on 12 Aug 2026.

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