Flow battery systems and methods of using the same
Flow battery systems are provided, including flowing a liquid electrolyte from a storage tank of a flow battery system to an electrode chamber of the flow battery system, the liquid electrolyte comprising a solvent and a first active ion dissolved in the solvent, wherein the storage tank comprises the liquid electrolyte and a first solid composed of the active ion and an ion of the solvent; inducing an electrochemical reaction in the electrode chamber to convert the first active ion dissolved in the solvent to a second active ion dissolved in the solvent, wherein the first solid dissolves to provide more of the first active ion dissolved in the solvent; flowing the liquid electrolyte comprising the solvent and the second active ion dissolved in the solvent from the electrode chamber back to the storage tank; and precipitating a second solid composed of the second active ion and the ion of the solvent in the storage tank.
1 . A method of operating a flow battery system, the method comprising:
(a) flowing a liquid electrolyte from a storage tank of a flow battery system to an electrode chamber of the flow battery system, the liquid electrolyte comprising a solvent and a first active ion dissolved in the solvent, wherein the storage tank comprises the liquid electrolyte and a first solid composed of the first active ion and an ion of the solvent, wherein the storage tank further comprises a material comprising nucleation sites on which the first solid and a second solid composed of a second active ion and the ion of the solvent form;
(b) inducing an electrochemical reaction in the electrode chamber to convert the first active ion dissolved in the solvent to a second active ion dissolved in the solvent, wherein the first solid dissolves to provide more of the first active ion dissolved in the solvent;
(c) flowing the liquid electrolyte comprising the solvent and the second active ion dissolved in the solvent from the electrode chamber back to the storage tank; and
(d) precipitating the second solid composed of the second active ion and the ion of the solvent in the storage tank,
wherein the liquid electrolyte is passed to the electrode chamber without passing the first solid and the second solid to the electrode chamber, the storage tank further comprising a porous separating layer configured to divide the storage tank into compartments such that the liquid electrolyte is passed to the electrode chamber without passing the first solid and the second solid to the electrode chamber.
2 . The method of claim 1 , wherein the liquid electrolyte in the storage tank is at a storage temperature and the liquid electrolyte in the electrode chamber is at a different, operating temperature, wherein the first active ion's solubility in the liquid electrolyte and the second active ion's solubility in the liquid electrolyte are greater at the operating temperature than at the storage temperature.
3 . The method of claim 2 , wherein the operating temperature is higher than the storage temperature.
4 . The method of claim 1 , wherein the material is an undissolved form of the first active ion, an undissolved form of the second active ion, or combinations thereof.
5 . The method of claim 1 , wherein the liquid electrolyte in the electrode chamber is at an operating temperature and the second active ion dissolved in the solvent reaches a concentration greater than its saturation concentration at the operating temperature in the liquid electrolyte in the electrode chamber.
6 . The method of claim 5 , wherein the material is an undissolved form of the first active ion, an undissolved form of the second active ion, or combinations thereof.
7 . The method of claim 5 , wherein the liquid electrolyte in the storage tank is at a different, storage temperature, wherein the first active ion's solubility in the liquid electrolyte and the second active ion's solubility in the liquid electrolyte are greater at the operating temperature than at the storage temperature.
8 . The method of claim 1 , wherein the first active ion and the second active ion are each independently selected from a group consisting of V +2 , V +3 , VO +2 , and VO 2 + .
9 . The method of claim 1 , further comprising:
(e) flowing a second liquid electrolyte from a second storage tank of the flow battery system to a second electrode chamber of the flow battery system, the second liquid electrolyte comprising a second solvent and a third active ion dissolved in the second solvent, wherein the second storage tank comprises the second liquid electrolyte and a third solid composed of the third active ion and an ion of the second solvent;
(f) inducing an electrochemical reaction in the second electrode chamber to convert the third active ion dissolved in the second solvent to a fourth active ion dissolved in the second solvent, wherein the third solid dissolves to provide more of the third active ion dissolved in the second solvent;
(g) flowing the second liquid electrolyte comprising the second solvent and the third active ion dissolved in the second solvent from the second electrode chamber back to the second storage tank; and
(h) precipitating a fourth solid composed of the fourth active ion and the ion of the second solvent in the second storage tank.
10 . A flow battery system comprising:
a storage tank comprising a liquid electrolyte comprising a solvent and a first active ion dissolved in the solvent, the storage tank further comprising a first solid composed of the first active ion and an ion of the solvent, wherein the storage tank further comprises a material comprising nucleation sites on which the first solid and a second solid composed of a second active ion and the ion of the solvent forms;
an electrode chamber in fluid communication with the storage tank;
a second electrode chamber in fluid and electrical communication with the electrode chamber; and
optionally, a membrane between the electrode chambers,
wherein the storage tank is configured so that the liquid electrolyte is passed to the electrode chamber without passing the first solid and the second solid to the electrode chamber, the storage tank further comprising a porous separating layer configured to divide the storage tank into compartments such that the liquid electrolyte is passed to the electrode chamber without passing the first solid and the second solid to the electrode chamber.
11 . The flow battery system of claim 10 , further comprising a heat exchanger in fluid communication with the storage tank and the electrode chamber and configured to adjust the liquid electrolyte's temperature.
12 . The flow battery system of claim 11 , wherein the heat exchanger is configured to maintain the temperature of the liquid electrolyte at a storage temperature in the storage tank and at a different, operating temperature in the electrode chamber.
13 . The flow battery system of claim 12 , wherein the operating temperature is greater than the storage temperature.
14 . The flow battery system of claim 10 , wherein the second electrode chamber is a hydrogen electrode chamber or an oxygen electrode chamber.
15 . The flow battery system of claim 10 , wherein the active ion is selected from a group consisting of V +2 , V +3 , VO +2 , and VO 2+ .
16 . The flow battery system of claim 10 , further comprising a second storage tank in fluid communication with the second electrode chamber, the second storage tank comprising a second liquid electrolyte comprising a second solvent and a third active ion dissolved in the second solvent, the second storage tank further comprising a third solid composed of the third active ion and an ion of the second solvent.
17 . The method of claim 4 , wherein the material is VOSO 4 , (VO 2 ) 2 SO 4 , or combinations thereof.
18 . The method of claim 17 , wherein the VOSO 4 is hydrated and the (VO 2 ) 2 SO 4 is hydrated.
19 . The method of claim 4 , wherein the undissolved form of the first active ion is a precipitate formed from an oversaturated solution of the first active ion and the undissolved form of the second active ion is a precipitate formed from an oversaturated solution of the second active ion.
20 . The flow battery system of claim 10 , wherein the material is an undissolved form of the first active ion, an undissolved form of the second active ion, or combinations thereof.
21 . The flow battery system of claim 20 , wherein the material is VOSO 4 , (VO 2 ) 2 SO 4 , or combinations thereof.
22 . The flow battery system of claim 21 , wherein the VOSO 4 is hydrated and the (VO 2 ) 2 SO 4 is hydrated.
23 . The flow battery system of claim 20 , wherein the undissolved form of the first active ion is a precipitate formed from an oversaturated solution of the first active ion and the undissolved form of the second active ion is a precipitate formed from an oversaturated solution of the second active ion.
24 . A storage tank for a flow battery system, the storage tank comprising a first solid composed of a first active ion and an ion of a solvent, wherein the storage tank further comprises a material comprising nucleation sites on which the first solid forms, wherein the material is an undissolved form of the first active ion, and further wherein the storage tank is configured so that a liquid electrolyte is passed to an electrode chamber of the flow battery system without passing the first solid to the electrode chamber, the storage tank further comprising a porous separating layer configured to divide the storage tank into compartments such that the liquid electrolyte is passed to the electrode chamber without passing the first solid to the electrode chamber.
25 . The storage tank of claim 24 , wherein the material is VOSO 4 , (VO 2 ) 2 SO 4 , or combinations thereof.
26 . The storage tank of claim 25 , wherein the VOSO 4 is hydrated and the (VO 2 ) 2 SO 4 is hydrated.
27 . The storage tank of claim 24 , wherein the undissolved form of the first active ion is a precipitate formed from an oversaturated solution of the first active ion.
28 . The storage tank of claim 24 , wherein the storage tank is in fluid communication with the electrode chamber of the flow battery system.