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Synthesis, characterization and study of electrochemical applicability of novel asymmetrically substituted 1,3-dialkyl-1,2,3-benzotriazolium salts for supercapacitor fabrication

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Here we report the successful synthesis, fabrication, and testing of novel asymmetrically substituted 1,3-dialkyl-1,2,3-benzotriazolium-based ionic liquids. Their applicability in energy storage is tested as gel polymer electrolytes (ILGPE) immobilized in… Click to show full abstract

Here we report the successful synthesis, fabrication, and testing of novel asymmetrically substituted 1,3-dialkyl-1,2,3-benzotriazolium-based ionic liquids. Their applicability in energy storage is tested as gel polymer electrolytes (ILGPE) immobilized in poly(vinylidene fluoride-co-hexa-fluoropropylene) (PVDF-HFP) copolymer as a solid-state electrolyte in electric double layer capacitors (EDLC). Asymmetrically substituted 1,3-dialkyl-1,2,3-benzotriazolium salts of tetrafluoroborates (BF4−) and hexafluorophosphates (PF6−) are synthesized by anion exchange metathesis reaction using 1,3-dialkyl-1,2,3-benzotriazolium bromide salts. N-Alkylation followed by quaternization reaction results in dialkyl substitution on 1,2,3-benzotriazole. The synthesized ionic liquids were characterized with 1H-NMR, 13C-NMR, and FTIR spectroscopy. Their electrochemical and thermal properties were studied using cyclic voltammetry, impedance spectroscopy, thermogravimetric analysis, and differential scanning calorimetry. The 4.0 V potential windows obtained for asymmetrically substituted 1,3-dialkyl-1,2,3-benzotriazolium salts of BF4− and PF6− are promising electrolytes for energy storage. ILGPE tested with symmetrical EDLC with a wide operating window from 0–6.0 V gave an effective specific capacitance of 8.85 F g−1 at a lower scan rate of 2 mV s−1, the energy density of 2.9 μW h and 11.2 mW g−1 power density. The fabricated supercapacitor was employed for lighting red LED (2 V, 20 mA).

Keywords: dialkyl benzotriazolium; benzotriazolium salts; spectroscopy; benzotriazolium; asymmetrically substituted; substituted dialkyl

Journal Title: RSC Advances
Year Published: 2023

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