摘要:
Titanium complexes containing at least one catecholate ligand can be desirable active materials for flow batteries and other electrochemical energy storage systems. Such complexes can be formed through reacting a catechol compound with a titanium reagent in an organic solvent, removing a byproduct species, and then obtaining an aqueous phase containing a salt form of the titanium catechol complex, particularly an alkali metal salt form. More specifically, the methods can include: forming a catechol solution containing a catechol compound and an organic solvent, contacting a titanium reagent with the catechol solution to form a reaction mixture, reacting the titanium reagent with the catechol compound to form an intermediate titanium catechol complex and a byproduct species, separating the byproduct species, and combining an alkaline aqueous solution containing a base with the intermediate titanium catechol complex to produce a salt form titanium catechol complex at least partially dissolved in an aqueous phase.
摘要:
Titanium catecholate complexes can be desirable active materials for flow batteries and other electrochemical energy storage systems, particularly when incorporated in aqueous electrolyte solutions. It can be desirable to avoid introducing even traces of certain organic solvents into aqueous electrolyte solutions. Neat methods for synthesizing titanium catecholate complexes can help avoid the unwanted introduction of trace organic solvents into aqueous electrolyte solutions and also provide further advantages. Methods for synthesizing titanium catecholate complexes can include: combining a catechol compound and a titanium reagent in an absence of solvent to produce a reaction mixture, and reacting the titanium reagent with the catechol compound in a neat state to form a titanium catecholate complex containing at least one catecholate ligand. The titanium catecholate complex can be further reacted with a base to produce a salt form titanium catecholate complex, which can be present in an aqueous phase.
摘要:
Provided are compositions having the formula MnTi(L1)(L2)(L3) wherein L1 is a catecholate, and L2 and L3 are each independently selected from catecholates, ascorbate, citrate, glycolates, a polyol, gluconate, glycinate, hydroxyalkanoates, acetate, formate, benzoates, malate, maleate, phthalates, sarcosinate, salicylate, oxalate, a urea, polyamine, aminophenolates, acetylacetone or lactate; each M is independently Na, Li, or K; n is 0 or an integer from 1-6. Also provided are energy storage systems.
摘要:
Titanium catecholate complexes can be desirable active materials for flow batteries and other electrochemical energy storage systems, particularly when incorporated in aqueous electrolyte solutions. It can be desirable to avoid introducing even traces of certain organic solvents into aqueous electrolyte solutions. Neat methods for synthesizing titanium catecholate complexes can help avoid the unwanted introduction of trace organic solvents into aqueous electrolyte solutions and also provide further advantages. Methods for synthesizing titanium catecholate complexes can include: combining a catechol compound and a titanium reagent in an absence of solvent to produce a reaction mixture, and reacting the titanium reagent with the catechol compound in a neat state to form a titanium catecholate complex containing at least one catecholate ligand. The titanium catecholate complex can be further reacted with a base to produce a salt form titanium catecholate complex, which can be present in an aqueous phase.
摘要:
Stable solutions comprising high concentrations of charged coordination complexes, including iron hexacyanides are described, as are methods of preparing and using same in chemical energy storage systems, including flow battery systems. The use of these compositions allows energy storage densities at levels unavailable by other iron hexacyanide systems.
摘要:
Electrolyte solutions for flow batteries and other electrochemical systems can contain an active material capable of transferring more than one electron per oxidation-reduction cycle. Such active materials can include coordination compounds containing a metal center and at least one redox non-innocent ligand. Accordingly, flow batteries can include a first half-cell having a first electrolyte solution therein, where the first electrolyte solution contains a coordination compound having at least one redox non-innocent ligand coordinated to a metal center. Particular redox non-innocent ligands can include those bearing a quinone functional group, such as substituted catecholates bearing a quinone functional group. Some active materials can include compositions containing a coordination compound having at least one redox non-innocent ligand coordinated to a metal center, where the at least one redox non-innocent ligand is a substituted catecholate or a salt thereof bearing a quinone functional group.
摘要:
Flow batteries and other electrochemical systems can contain an active material that is a coordination complex having at least one monosulfonated catecholate ligand or a salt thereof bound to a metal center. The monosulfonated catecholate ligand has a structure of More particularly, the coordination complex can be a titanium coordination complex with a formula of DgTi(L1)(L2)(L3), in which D is a counterion selected from H, NH4|, Li|, Na|, K|, or any combination thereof g ranges between 3 and 6; and L1, L2 and L3 are ligands, where at least one of L1, L2 and L3 is a monosulfonated catecholate ligand. Methods for synthesizing such monosulfonated catecholate ligands can include providing a neat mixture of catechol and up to about 1.3 stoichiometric equivalents of sulfuric acid, and heating the neat mixture at a temperature of about 80° C. or above to form 3,4-dihydroxybenzenesulfonic acid or a salt thereof.
摘要:
Solids can sometimes form in one or more electrolyte solutions during operation of flow batteries and related electrochemical systems. Over time, the solids can accumulate and compromise the integrity of flow pathways and other various flow battery components. Flow batteries configured for mitigating solids therein can include an autonomous solids separator, such as a lamella clarifier. Such flow batteries can include a first half-cell containing a first electrolyte solution, a second half-cell containing a second electrolyte solution, a first flow loop configured to circulate the first electrolyte solution through the first half-cell, a second flow loop configured to circulate the second electrolyte solution through the second half-cell, and at least one lamella clarifier in fluid communication with at least one of the first half-cell and the second half-cell. A hydrocyclone can be used as an alternative to a lamella clarifier in some instances.
摘要:
The invention concerns flow batteries comprising: a first half-cell comprising: (i) a first aqueous electrolyte comprising a first redox active material; and a first carbon electrode in contact with the first aqueous electrolyte; (ii) a second half-cell comprising: a second aqueous electrolyte comprising a second redox active material; and a second carbon electrode in contact with the second aqueous electrolyte; and (iii) a separator disposed between the first half-cell and the second half-cell; the first half-cell having a half-cell potential equal to or more negative than about −0.3 V with respect to a reversible hydrogen electrode; and the first aqueous electrolyte having a pH in a range of from about 8 to about 13, wherein the flow battery is capable of operating or is operating at a current density at least about 25 mA/cm2.
摘要翻译:本发明涉及流动电池,包括:第一半电池,包括:(i)第一含水电解质,其包含第一氧化还原活性材料; 和与第一含水电解质接触的第一碳电极; (ii)第二半电池,包括:包含第二氧化还原活性材料的第二含水电解质; 和与第二含水电解质接触的第二碳电极; 和(iii)设置在第一半电池和第二半电池之间的隔板; 所述第一半电池相对于可逆氢电极具有等于或大于约-0.3V的半电池电位; 并且所述第一含水电解质的pH在约8至约13的范围内,其中所述流动电池能够以至少约25mA / cm 2的电流密度操作或正在其操作。
摘要:
This invention is directed to aqueous redox flow batteries comprising redox-active metal ligand coordination compounds. The compounds and configurations described herein enable flow batteries with performance and cost parameters that represent a significant improvement over that previous known in the art.