2016
DOI: 10.1039/c6cc04325a
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Ion transfer battery: storing energy by transferring ions across liquid–liquid interfaces

Abstract: A battery in which the cell voltage is generated or enhanced by a Galvani potential difference between two liquid–liquid interfaces.

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Cited by 27 publications
(35 citation statements)
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“…In most of the above systems, the cell voltage of the battery is attributed to the difference in the redox potentials of the redox couples. Peljo et al [111] proposed an ion-transfer battery based on the potential differences of the two phases. The proposed battery consists of two organic redox electrolytes of decamethylferrocene (DMFc, C20H30Fe) and decaethylferrocene tetrakis (penta-fluorophenyl)borate (DMFcTB, C44H30BF20Fe) (0.1 mol dm -3 ), which are separated by an immiscible aqueous phase (1 mol dm -3 LiClO4 and 0.1 mol dm -3 LiOH).…”
Section: Organometallic Based Immiscible Electrolyte Batteriesmentioning
confidence: 99%
“…In most of the above systems, the cell voltage of the battery is attributed to the difference in the redox potentials of the redox couples. Peljo et al [111] proposed an ion-transfer battery based on the potential differences of the two phases. The proposed battery consists of two organic redox electrolytes of decamethylferrocene (DMFc, C20H30Fe) and decaethylferrocene tetrakis (penta-fluorophenyl)borate (DMFcTB, C44H30BF20Fe) (0.1 mol dm -3 ), which are separated by an immiscible aqueous phase (1 mol dm -3 LiClO4 and 0.1 mol dm -3 LiOH).…”
Section: Organometallic Based Immiscible Electrolyte Batteriesmentioning
confidence: 99%
“…In those hybrid systems it is not possible to fully decouple power and energy, being one of the most important advantage of RFBs . Girault and co‐workers reported an ion transfer battery utilizing the Galvani potential difference between liquid–liquid interphases in a nonaqueous/aqueous/nonaqueous triphasic system. Unlikely, our membrane‐free battery is based on two immiscible phases and the voltage of this battery exclusively depends on the difference of redox potential of active species dissolved in catholyte and anolyte, as in any type of RFB.…”
Section: Introductionmentioning
confidence: 99%
“…However, as long as the anolyte and catholyte molecules on the interface are constantly in contact, this strategy still leads to higher indexes of self-discharge, which currently is one of the major drawbacks to be surpassed [228][229][230]. Despite there being some more advanced strategies to use the immiscible membraneless configuration, e.g., two nonaqueous phases separated by an aqueous phase, these devices are still on the laboratory scale due to their low energy density, solvent evaporation (which leads to unstable CDC), high ohmic resistance, and reliance on flammable organic solvents [231].…”
Section: Membranelessmentioning
confidence: 99%