Viologen-Decorated TEMPO for Neutral Aqueous Organic Redox Flow Batteries

Abstract
A novel electroactive organic molecule, viz., 1-(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)-1-(3-(trimethylammonio)propyl)-4,4-bipyridinium trichloride ((TPABPy)Cl3), is synthesized by decorating 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) with viologen, which is used as the positive electrolyte in neutral aqueous redox flow battery (ARFB). Extensive characterizations are performed to investigate the composition/structure and the electrochemical behavior, revealing the favorable effect of introducing the cationic viologen group on the electroactive TEMPO. Salient findings are as follows. First, the redox potential is elevated from +0.745 V for TEMPO to +0.967 V for decorated TEMPO, favoring its use as the positive electrolyte. Such an elevation originates from the electron-withdrawing effect of the viologen unit, as evidenced by the nuclear magnetic resonance and single crystal structure analysis. Second, linear sweep voltammetry reveals that the diffusion coefficient is <path d="M394 0V15C319 15 299 33 299 76V673L290 676L111 585V571L138 581C156 588 173 593 183 593C204 593 213 578 213 544V95C213 40 192 19 118...
Funding Information
  • National Natural Science Foundation of China (21905114, 21975081)

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