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Published on: February 13, 2017
4,4'-Hydrazobis(1-methylpyridinium) as a Two-Electron Posolyte Molecule for Aqueous Organic Redox Flow Batteries
Hélène Lebel1, Dominic Rochefort1, Calvine Lai1
1Département de Chimie, Center for Green Chemistry and Catalysis, Quebec Center for Advanced Materials, Institut Courtois, Université de Montréal, C.P. 6128, Succursale Centreville, Montréal, Québec, Canada, H3C 3J7.
Abstract:
Aqueous organic redox flow batteries (AORFBs) are a safe and sustainable solution for the storage of intermittent renewable energy. While several highly soluble two-electron organic molecule negolytes have been developed for AORFBs, most reported organic posolyte species exchange only one electron. Herein, readily available 4,4'-hydrazobis(1-methylpyridinium) dichloride (HydBPyMeCl) is described as a novel two-electron posolyte molecule for AORFBs. The synthesis of HydBPyMeCl was accomplished by a three-step process, yielding multiple grams of the compound. HydBPyMeCl exhibited a reversible two-electron transfer at high redox potential (+0.64 V vs Ag/AgCl reference electrode, pH = 0). When evaluated at 1 M concentration and low pH (2 M HCl) with V3+/V2+ on the negative side, HydBPyMeCl showed high stability. A capacity retention of 99.997% per cycle (99.980% per day measured over 70 days) was achieved, coupled with a high volumetric specific capacity of 47.1 Ah/L (87.2% of capacity utilization at 80 mA/cm2).
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Spontaneous redox reactions occur abundantly in nature. The chemical reaction occurring in a disposable AA battery powering our remote controls is one such example of a spontaneous redox reaction. Another example is the immersion of coiled copper wire into an aqueous silver nitrate solution. The reaction shows a gradual, visually impressive color change from colorless to bright blue and the formation of a grey precipitate on the copper wire. In this experiment,...