Vanadium solution, electrolyte comprising same, secondary battery comprising same, and method for preparing same

Patent metadata

Field	Value
Publication number	US-10096842-B2
Application number	US-201515316096-A
Country	US
Kind code	B2
Filing date	Jun 12, 2015
Priority date	Jun 13, 2014
Publication date	Oct 9, 2018
Grant date	Oct 9, 2018

Abstract

The present specification relates to a vanadium solution, an electrolyte including the same, a secondary battery including the same, and a method for preparing the same.

First claim

The invention claimed is:

1. A method for preparing a vanadium solution, the method comprising:
preparing a vanadium solution comprising a pentavalent vanadium ion (VO 2 + ), an acid, and deoxygenated distilled water; and
dissolving a vanadium precursor capable of forming a tetravalent vanadium ion (VO 2+ ) in the vanadium solution.

2. The method of claim 1 , wherein the preparing of the vanadium solution comprising the pentavalent vanadium ion, the acid, and the deoxygenated distilled water comprises:
dissolving a vanadium precursor capable of forming a tetravalent vanadium ion in distilled water in deoxygenated distilled water;
mixing the distilled water in which the vanadium precursor is dissolved with the acid to prepare a vanadium solution; and
oxidizing the tetravalent vanadium ion in the vanadium solution into the pentavalent vanadium ion.

3. The method of claim 1 , wherein the preparing of the vanadium solution comprising the pentavalent vanadium ion, the acid, and the deoxygenated distilled water comprises dissolving a vanadium precursor capable of forming a pentavalent vanadium ion in deoxygenated distilled water, an acid, or a mixture thereof.

4. The method of claim 3 , wherein the preparing of the vanadium solution comprising the pentavalent vanadium ion, the acid, and the deoxygenated distilled water comprises introducing a vanadium precursor capable of forming a pentavalent vanadium ion into deoxygenated distilled water, and then mixing the resulting mixture with the acid, or introducing a vanadium precursor capable of forming the pentavalent vanadium ion into the acid, and then mixing the resulting mixture with the deoxygenated distilled water.

5. The method of claim 1 , wherein the vanadium precursor is VOSO 4 .

6. The method of claim 1 , further comprising:
flowing an inert gas into distilled water to prepare deoxygenated distilled water before the preparing of the vanadium solution comprising the pentavalent vanadium ion (VO 2 + ), the acid, and the deoxygenated distilled water.

7. The method of claim 1 , wherein a concentration of the pentavalent vanadium ion (VO 2 + ) in the vanadium solution comprising the pentavalent vanadium ion (VO 2 + ), the acid, and the deoxygenated distilled water is 0.01 M to 2 M.

8. The method of claim 1 , wherein a concentration of the acid in the vanadium solution comprising the pentavalent vanadium ion (VO 2 + ), the acid, and the deoxygenated distilled water is 0.5 M to 7 M.

9. The method of claim 1 , further comprising:
heating the vanadium precursor at 80° C. or more before, while, or after the dissolving of the vanadium precursor.

10. The method of claim 3 , wherein the vanadium precursor capable of forming the pentavalent vanadium ion is V 2 O 5 .

11. A vanadium solution comprising a vanadium component which comprises a tetravalent vanadium ion, deoxygenated distilled water, and an acid, wherein the vanadium component comprises a pentavalent vanadium ion in a state where the vanadium solution is not used in a charge or discharge using electrodes.

12. The vanadium solution of claim 11 , wherein a concentration of oxygen in the vanadium solution is 0.1 ppm to 5 ppm.

13. The vanadium solution of claim 11 , wherein the vanadium solution displays a blackish blue color compared to a reference solution which comprises a tetravalent vanadium ion having the same concentration as that of the vanadium solution and does not comprise the pentavalent vanadium ion, an absorption wavelength present in at least a portion of 250 to 450 nm is shifted to a long wavelength, or an OCV is increased.

14. A vanadium solution comprising a vanadium component which comprises a tetravalent vanadium ion, deoxygenated distilled water, and an acid, wherein the vanadium solution comprises vanadium at a concentration of 1.5 to 3.5 M, and when the vanadium solution is left to stand at 5° C. for 100 hours in a state where the acid in the vanadium solution is at a concentration of 3 M, a molar percentage of the vanadium ion dissolved in the vanadium solution based on a content of vanadium in the entire vanadium solution is more than 95%.

15. The vanadium solution of claim 14 , wherein a concentration of oxygen in the vanadium solution is 0.1 ppm to 5 ppm.

16. An electrolyte comprising the vanadium solution of claim 11 .

17. A secondary battery comprising a positive electrode, a negative electrode, and an electrolyte comprising the vanadium solution of claim 16 provided between the positive electrode and the negative electrode.

18. An electrolyte comprising the vanadium solution of claim 14 .

Assignees

• Lg Chemical Ltd

Inventors

• Lee Jeongbae
• Noh Tae Geun
• Jeong Bong Hyun
• Min Geungi
• Moon Sikwon
• Byun Sujin

Classifications

• H01M8/20

  Indirect fuel cells, e.g. fuel cells with redox couple being irreversible (H01M8/18 takes precedence) · CPC title

• H01M8/02 Primary

  Details (electrodes H01M4/86 - H01M4/98) · CPC title

• H01M8/18

  Regenerative fuel cells, e.g. redox flow batteries or secondary fuel cells · CPC title

• H01M8/188 Primary

  by recharging of redox couples containing fluids; Redox flow type batteries · CPC title

• Y02E60/10

  Energy storage using batteries · CPC title