Abstract
AbstractAnthraquinone is one of the organic molecules that can potentially replace metal‐based electrodes due to its fast and reversible redox reaction as well as the abundance in nature. Here, we reported the redox activity of anthraquinone on N‐doped porous carbon electrodes derived from chemical activation of tea leaves with potassium carbonate. Electrochemical behavior was evaluated by cyclic voltammetry and galvanostatic charge/discharge in sulfuric acid, with X‐ray photoelectron spectroscopy providing insights into the surface chemistry of the electrodes. Anthraquinone on the composite electrode was able to achieve 97 % of its theoretical storage capacity. We found that nitrogen‐containing functional groups, especially graphitic and pyrrolic groups, had a major impact on the enhanced redox activity of anthraquinone.
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