This paper reports the electrochemical behaviour of supercapacitor carbon electrodes operating in different aqueous solutions modified by various redox-active species (hydroxybenzenes, bromine derivatives and iodide). Three dihydroxybenzenes with varying stereochemistry, i.e., -OH substitution, have been considered as electrolyte additives (0.38 mol L(-1)) in acidic, alkaline and neutral solutions. High capacitance values have been obtained, especially for the acidic and alkaline solutions containing 1,4-dihydroxybenzene (hydroquinone). Bromine derivatives of dihydroxybenzenes were also considered as the additive in alkaline solution for use as a supercapacitor electrolyte, and a significant increase in capacitance value was observed. The redox couple investigated next was an iodide/iodine system, where 2 mol L(-1) NaI aqueous electrolyte was utilized. In this case, the most promising faradaic contribution during capacitor operation was achieved. In particular, stable capacitance values from 300-400 F g(-1) have been confirmed by long-term galvanostatic cycling (over 100 000 cycles), cycling voltammetry and floating. The mechanism of pseudocapacitance phenomena was discussed and supported by electrochemical and physicochemical measurements, e.g., in situ Raman spectroscopy.

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