Progress in Flow Battery Research and Development

Skyllas‐Kazacos, Maria; Chakrabarti, Mohammed Harun; Hajimolana, S.A.; Mjalli, Farouq S.; Saleem, Muhammad

doi:10.1149/1.3599565

Cited by 1,343 publications

(1,069 citation statements)

References 176 publications

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“…The conservation of ions is defined in the following equation: [4] where N i is the flux of species i in the electrolyte, and S i denotes the source term related to ion production/consumption in electrochemical reactions. Apparently, both S H + and S Cl − are equal to zero.…”

Section: Modelingmentioning

confidence: 99%

“…Owing to the exclusive advantage of decoupling power generation and energy storage, redox flow batteries (RFBs) have been considered as a critical candidate for large-scale electrical energy storage (EES). [1][2][3][4] Unlike the electrodes of conventional secondary batteries, the electrodes of RFBs do not participate in reactions but only provide electrochemical reaction sites for active ions and support electrons transfer. For numerous kinds of developed RFBs, the porous carbon felts, composed of randomly interlaced carbon fibers, are generally selected as electrodes.…”

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confidence: 99%

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The Dependence of Mass Transfer Coefficient on the Electrolyte Velocity in Carbon Felt Electrodes: Determination and Validation

You

Cheng

2017

J. Electrochem. Soc.

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In a flow battery, the salient impact of the electrolyte velocity on the mass transfer coefficient in carbon felt electrodes is demonstrated and quantified. A lab-scale flow battery, fed with identical electrolyte solutions containing Fe 2+ /Fe 3+ as active substances in both the anode and the cathode, is used to realize stable tests free from side reactions in a broad range of current densities. The electrolyte velocities ranging from 2.5 to 15 mm s −1 are selected in this work, which are typical in flow through electrodes in most flow batteries. By measuring limiting currents at various flow rates, a correlation between the mass transfer coefficient and the velocity in dimensionless form is obtained as Sh = 1.68 Re 0.9 . Meanwhile, a 2-D numerical model incorporating this correlation and the experimentally measured electrolyte conductivity is proposed. Voltage losses of the battery fed with adequate reactants at different velocities are both experimentally measured and numerically simulated. The agreement between simulated results and experimental data verifies the applicability of this correlation under normal operating conditions below limiting currents. Owing to the exclusive advantage of decoupling power generation and energy storage, redox flow batteries (RFBs) have been considered as a critical candidate for large-scale electrical energy storage (EES). [1][2][3][4] Unlike the electrodes of conventional secondary batteries, the electrodes of RFBs do not participate in reactions but only provide electrochemical reaction sites for active ions and support electrons transfer. For numerous kinds of developed RFBs, the porous carbon felts, composed of randomly interlaced carbon fibers, are generally selected as electrodes. [5][6][7] Obtaining high voltage efficiency at high current densities is one of the major challenges in the commercialization of RFBs. Much efforts have been devoted to diminishing the activation loss by modifying the carbon fiber surface. [8][9][10][11][12] In addition, ohmic loss and mass transfer loss also lead to the reduction of the voltage efficiency. It is generally recognized that supplying high flow rate of electrolyte for the RFB is the most feasible method to minimizing mass transfer loss, but more pumping power is inevitably required for increasing flow rates. Tang et al. 6 and Ma et al. 7 carried out special research on optimizing the operating strategy of electrolyte flow rate for kilowatts class allvanadium flow battery (VRFB) systems, in which the significant impact of flow rate on cell voltage was detected during the whole charge/discharge process. In a carbon felt electrode, the mass transfer loss is caused by the species transport between the bulk solution in the pore and the carbon fiber surface, which is usually quantified by the mass transfer coefficient k m . 13 For cells operating under high current densities, the mass transfer loss also contributes a significant proportion to the voltage loss, especially when approaching the end of charge/discharge process. Considerin...

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Section: Modelingmentioning

confidence: 99%

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confidence: 99%

The Dependence of Mass Transfer Coefficient on the Electrolyte Velocity in Carbon Felt Electrodes: Determination and Validation

You

Cheng

2017

J. Electrochem. Soc.

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“…8). Optimization of engineering and operating parameters such as the flow field geometry, electrode design, membrane separator and temperature-which have not yet even begun-should lead to significant performance improvements in the future, as it has for vanadium flow batteries, which took many years to reach the power densities we report here 6 . The use of redox processes in -aromatic organic molecules represents a new and promising direction for cost-effective, largescale energy storage.…”

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confidence: 94%

A metal-free organic–inorganic aqueous flow battery

Huskinson

Marshak

Suh

et al. 2014

Nature

1,400

1,331

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This paper can be cited as: B. Huskinson, M.P. Marshak, C. Suh, S. Er, M.R. Gerhardt, C.J. Galvin, X. Chen, A. Aspuru-Guzik, R.G. Gordon and M.J. Aziz, "A metal-free organicinorganic aqueous flow battery", Nature 505, 195-198 (2014).The formatted version of this manuscript can be found at the following link: http://www.nature.com/nature/journal/v505/n7482/full/nature12909.html A metal-free organic-inorganic aqueous flow batteryBrian Huskinson 1 *, Michael P. Marshak 1,2 *, Changwon Suh 2 , Süleyman Er 2,3 , Michael R. *These authors contributed equally to this work.As the fraction of electricity generation from intermittent renewable sources-such as solar or wind-grows, the ability to store large amounts of electrical energy is of increasing importance. Solid-electrode batteries maintain discharge at peak power for far too short a time to fully regulate wind or solar power output 1,2 . In contrast, flow batteries can independently scale the power (electrode area) and energy (arbitrarily large storage volume) components of the system by maintaining all of the electro-active species in fluid form 3-5 . Wide-scale utilization of flow batteries is, however, limited by the abundance and cost of these materials, particularly those using redox-active metals and precious metal electrocatalysts 6,7 . Here we describe a class of energy storage materials that exploits the favourable chemical and electrochemical properties of a family of molecules known as quinones. The example we demonstrate is a metal-free flow battery based on the redox chemistry of 9,10-anthraquinone-2,7-disulphonic acid (AQDS). AQDS undergoes extremely rapid and reversible two-electron two-proton reduction on a glassy carbon electrode in sulphuric acid. An aqueous flow battery with inexpensive carbon electrodes, combining the quinone/hydroquinone couple with the Br 2 /Br  redox couple, yields a peak galvanic power density exceeding 0.6 W cm Solutions of AQDS in sulphuric acid (negative side) and Br 2 in HBr (positive side) were pumped through a flow cell as shown schematically in Fig. 1a. The quinone-bromide flow battery (QBFB) was constructed using a Nafion 212 membrane sandwiched between Toray carbon paper electrodes (six stacked on each side) with no catalysts; it is similar to a cell described elsewhere (see figure 2 in ref. 7). We report the potential-current response (Fig. 1b) and the potential-power relationship ( measured with respect to the quinone side of the cell). As the SOC increased from 10% to 90%, the open-circuit potential increased linearly from 0.69 V to 0.92 V. In the galvanic direction, peak power densities were 0.246 W cm 2 and 0.600 W cm 2 at these same SOCs, respectively ( Fig. 1c). In order to avoid significant water splitting in the electrolytic direction, we used a cutoff voltage of 1.5 V, at which point the current densities observed at 10% and 90% SOCs were −2.25 A cm −2 and −0.95 A cm −2 , respectively, with corresponding power densities of −3.342 W cm −2 and −1.414 W cm −2 .In Fig. 2 we report the results of initial cy...

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“…Cycled negative electrolyte was also collected and characterized by the same method; both studies showed no degradation product at the sensitivity level of 1% (Fig S3). Membrane crossover contamination has been a common challenge in acid-based redox flow batteries where most electro-active molecules are either neutral or positive and tend to migrate through proton-conductive membranes (5). In this alkaline system, however, all the electro-active molecules remain negatively charged in all charge states, leading to a dramatic decrease in the degree of crossover during cell cycling.…”

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confidence: 99%

Alkaline quinone flow battery

Lin

Chen

Gerhardt

et al. 2015

Science

963

910

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Abstract:Storage of photovoltaic and wind electricity in batteries could solve the mismatch problem between the intermittent supply of these renewable resources and variable demand. Flow batteries permit more economical long-duration discharge than solid-electrode batteries by using liquid electrolytes stored outside of the battery. We report an alkaline flow battery based on redox-active organic molecules that are composed entirely of earth-abundant elements and are non-toxic, non-flammable, and safe for use in residential and commercial environments. The battery operates efficiently with high power density near room temperature. These results demonstrate the stability and performance of redox-active organic molecules in alkaline flow batteries, potentially enabling cost-effective stationary storage of renewable energy. Main Text:The cost of photovoltaic (PV) and wind electricity has dropped so much that one of the largest barriers to getting the vast majority of our electricity from these renewable sources is their intermittency (1-3). Batteries provide a means to store electrical energy; however, traditional, enclosed batteries maintain discharge at peak power for far too short a duration to adequately regulate wind or solar power output (1, 2). In contrast, flow batteries can independently scale the power and energy components of the system by storing the electro-active species outside the battery container itself (3)(4)(5). In a flow battery, the power is generated in a device resembling a fuel cell, which contains electrodes separated by an ion-permeable membrane. Liquid solutions of redox-active species are pumped into the cell where they can be charged and discharged, before being returned to storage in an external storage tank. Scaling the amount of energy to be stored thus involves simply making larger tanks ( Fig 1A). Existing flow batteries are based on metal ions in acidic solution but there are challenges with corrosivity, hydrogen evolution, kinetics, material cost and abundance, and efficiency that thus far have prevented large-scale commercialization. The use of anthraquinones in an acidic aqueous flow battery can dramatically reduce battery costs (6, 7); however, the use of bromine in the other half of the system precludes deployment in residential communities due to toxicity concerns.We demonstrate that quinone-based flow batteries can be adapted to alkaline solutions, where hydroxylated anthraquinones are highly soluble and bromine can be replaced with the non-toxic ferricyanide ion (8, 9) -a food additive (10). Functionalization of 9,10-anthraquinone (AQ) with electron-donating groups such as OH has been shown to lower the reduction potential and expand the battery voltage (6). In alkaline solution, these OH groups are deprotonated to provide solubility and greater electron donation capability, which results in an increase in the open circuit voltage of 47% over the previously reported system. Because functionalization away from the ketone group provides molecules with the highest solubility...

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Progress in Flow Battery Research and Development

Cited by 1,343 publications

References 176 publications

The Dependence of Mass Transfer Coefficient on the Electrolyte Velocity in Carbon Felt Electrodes: Determination and Validation

The Dependence of Mass Transfer Coefficient on the Electrolyte Velocity in Carbon Felt Electrodes: Determination and Validation

A metal-free organic–inorganic aqueous flow battery

Alkaline quinone flow battery

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