Abstract:
Ionic conductive chromophores can be used as the positive electrolytes for high-energy density, nonaqueous redox flow battery (NRFB) systems. The nonaqueous nature of the NRFB systems allow for high operation voltage (compared to aqueous systems). Furthermore, the structure modifications to chromophores described herein improve the solubility of the resultant ionic conductive chromophores, thereby allowing them to be used in flow cell configurations.
Abstract:
Disclosed are cathodes having electron-conductive high-surface-area materials, aqueous non-halide-containing electrolytes, secondary zinc-iodine energy storage devices using the same, and methods for assembling the same. The disclosed high-surface-area materials and the aqueous non-halide-containing electrolyte solutions can contribute together to the confinement of the active iodine species in the cathode and to the minimization of shuttle effects and self-discharging. The non-halide-containing electrolyte salts can facilitate preferential adsorption of the iodine species to the cathode material rather than dissolution in the aqueous electrolyte solution, thereby contributing to the confinement of the active iodine species.
Abstract:
A sodium-ion battery that includes an anode comprising hard carbon and lithium; and an electrolyte composition comprising an ether solvent and a sodium salt.
Abstract:
Improved metal-based redox flow batteries (RFBs) can utilize a metal and a divalent cation of the metal (M2+) as an active redox couple for a first electrode and electrolyte, respectively, in a first half-cell. For example, the metal can be Zn. The RFBs can also utilize a second electrolyte having I−, anions of Ix (for x≧3), or both in an aqueous solution, wherein the I− and the anions of Ix (for x≧3) compose an active redox couple in a second half-cell.
Abstract:
An aqueous redox flow battery system includes an aqueous catholyte and an aqueous anolyte. The aqueous catholyte may comprise (i) an optionally substituted thiourea or a nitroxyl radical compound and (ii) a catholyte aqueous supporting solution. The aqueous anolyte may comprise (i) metal cations or a viologen compound and (ii) an anolyte aqueous supporting solution. The catholyte aqueous supporting solution and the anolyte aqueous supporting solution independently may comprise (i) a proton source, (ii) a halide source, or (iii) a proton source and a halide source.
Abstract:
All-vanadium sulfate redox flow battery systems have a catholyte and an anolyte comprising an aqueous supporting solution including chloride ions and phosphate ions. The aqueous supporting solution stabilizes and increases the solubility of vanadium species in the electrolyte, allowing an increased vanadium concentration over a desired operating temperature range. According to one example, the chloride ions are provided by MgCl2, and the phosphate ions are provided by (NH4)2HPO4.
Abstract:
An energy storage device comprising a cathode comprising: (i) an Fe source; (ii) at least one sulfur species and (iii) NaCl, wherein the mol percent of S is less than 10, based on the total moles of (i), (ii) and (iii).
Abstract:
Composite separators having a porous structure and including acid-stable, hydrophilic, inorganic particles enmeshed in a substantially fully fluorinated polyolefin matrix can be utilized in a number of applications. The inorganic particles can provide hydrophilic characteristics. The pores of the separator result in good selectivity and electrical conductivity. The fluorinated polymeric backbone can result in high chemical stability. Accordingly, one application of the composite separators is in redox flow batteries as low cost membranes. In such applications, the composite separator can also enable additional property-enhancing features compared to ion-exchange membranes. For example, simple capacity control can be achieved through hydraulic pressure by balancing the volumes of electrolyte on each side of the separator. While a porous separator can also allow for volume and pressure regulation, in RFBs that utilize corrosive and/or oxidizing compounds, the composite separators described herein are preferable for their robustness in the presence of such compounds.
Abstract:
Sodium energy storage devices employing aspects of both ZEBRA batteries and traditional Na—S batteries can perform better than either battery alone. The hybrid energy storage devices described herein can include a sodium anode, a molten sodium salt catholyte, and a positive electrode that has active species containing sulfur. Additional active species can include a transition metal source and NaCl. As a product of the energy discharge process, Na2Sx forms in which x is less than three.
Abstract translation:采用ZEBRA电池和传统Na-S电池方面的钠能量储存装置可以比单独使用的电池性能更好。 本文所述的混合储能装置可包括钠阳极,熔融钠盐阴极电解液和具有含硫活性物质的正电极。 另外的活性物质可以包括过渡金属源和NaCl。 作为能量放电过程的产物,形成其中x小于3的Na 2 S x。
Abstract:
Sodium metal-halide energy storage devices utilizing a substituting salt in its secondary electrolyte can operate at temperatures lower than conventional ZEBRA batteries while maintaining desirable performance and lifetime characteristics. According to one example, a sodium metal-halide energy storage device operates at a temperature less than or equal to 200° C. and has a liquid secondary electrolyte having MxNa1-yAlCl4-yHy, wherein M is a metal cation of a substituting salt, H is an anion of the substituting salt, y is a mole fraction of substituted Na and Cl, and x is a ratio of y over r, where r is the oxidation state of M. The melting temperature of the substituting salt is less than that of NaCl.