2015
DOI: 10.1016/j.elecom.2015.07.013
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Electrochemical properties of a non-aqueous redox battery with all-organic redox couples

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Cited by 60 publications
(39 citation statements)
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“…[9] Another encouraging research line is the substitution of aqueous electrolytes by non-aqueous electrolytes [10] or even ionic liquids, [11] which are more electrochemically stable and would allow achieving higher battery voltages and energy densities. [12,13] In the last few years, RFBs based on organic redox molecules, such as quinones, phenothiazine, nitroxides, viologens, and pyridines [14][15][16][17] have experienced a great deal of interest, becoming one of the hottest topics in electrochemical energy storage (see Table S1 in the Supporting Information). [18,19] Regardless of the chemical nature of the electroactive species and the type of electrolytes, most RFBs rely on ion-selective membranes to separate the two redox electrolytes and to prevent the crossover of active compounds while allowing the migration of charge carriers.…”
mentioning
confidence: 99%
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“…[9] Another encouraging research line is the substitution of aqueous electrolytes by non-aqueous electrolytes [10] or even ionic liquids, [11] which are more electrochemically stable and would allow achieving higher battery voltages and energy densities. [12,13] In the last few years, RFBs based on organic redox molecules, such as quinones, phenothiazine, nitroxides, viologens, and pyridines [14][15][16][17] have experienced a great deal of interest, becoming one of the hottest topics in electrochemical energy storage (see Table S1 in the Supporting Information). [18,19] Regardless of the chemical nature of the electroactive species and the type of electrolytes, most RFBs rely on ion-selective membranes to separate the two redox electrolytes and to prevent the crossover of active compounds while allowing the migration of charge carriers.…”
mentioning
confidence: 99%
“…Before analyzing the origin of battery fading, we assembled a similar battery but employing more concentrated redox electrolytes; 0.1m H 2 Q in 0.1m HCl for the catholyte and 0.1m pBQ in PYR 14 TFSI for the anolyte. The higher concentration of the active species causes an improvement in the discharge capacity reaching 90 % of the theoretical one at the lowest current density (Figure 4 a).…”
mentioning
confidence: 99%
“…Thepeak current shows agood linear response to the square root of the sweep rates (Supporting Information, Figure S1b). [14] According to the Randles-Sevcik equation, the diffusion coefficient of Fe 2+ (Gly) 2 (the complex of iron ions and glycine) was estimated to be about 1.85 10 À5 cm 2 s À1 and that of Fe 3+ (Gly) 2 was 2.05 10 À5 cm 2 s À1 ,w hich is somewhat higher than the experimentally evaluated diffusion coefficient. [13] Thed iffusion coefficient of Fe 3+ was about 2.13 10 À5 cm 2 s À1 and that of Fe 2+ was about 2.89 10 À5 cm 2 s À1 , based on the same method (Supporting Information, Figure S1c,d).…”
mentioning
confidence: 88%
“…+0.3 V vs. Ag) and its chemical stability [188]. For these reasons, another TEMPO-based non-aqueous system has been proposed by Park and co-workers [189]. In this system camphoquinone and oxo-TEMPO were used at the negative and positive electrodes, respectively, resulting in an open-circuit voltage of up to 2.12 V, compared to ca.…”
Section: Camphoquinone-oxo-tempo Redox Flow Batterymentioning
confidence: 99%