Long life sealed alkaline secondary batteries

Patent metadata

Field	Value
Publication number	US-11611115-B2
Application number	US-201816957917-A
Country	US
Kind code	B2
Filing date	Dec 27, 2018
Priority date	Dec 29, 2017
Publication date	Mar 21, 2023
Grant date	Mar 21, 2023

Abstract

In an aspect, provided is an alkaline rechargeable battery comprising: i) a battery container sealed against the release of gas up to at least a threshold gas pressure, ii) a volume of an aqueous alkaline electrolyte at least partially filling the container to an electrolyte level; iii) a positive electrode containing positive active material and at least partially submerged in the electrolyte; iv) an iron negative electrode at least partially submerged in the electrolyte, the iron negative electrode comprising iron active material; v) a separator at least partially submerged in the electrolyte provided between the positive electrode and the negative electrode; vi) an auxiliary oxygen gas recombination electrode electrically connected to the iron negative electrode by a first electronic component, ionically connected to the electrolyte by a first ionic pathway, and exposed to a gas headspace above the electrolyte level by a first gas pathway.

First claim

What is claimed is:

1. Method of making a battery, comprising:
combining, in a battery container, an electrolyte, a positive electrode in contact with the electrolyte, a negative electrode in contact with the electrolyte, and a solid sparingly soluble sulfide-source material in contact with the electrolyte, the sulfide-source material being characterized by its dissociation into at least dissolved sulfide ions and dissolved counter-ions upon its dissolution in said electrolyte; and
adding a quantity of said counter-ions to the electrolyte in excess of counter-ions released by dissolution of the sulfide-source material.

2. The method of claim 1 , wherein adding a quantity of counter-ions to the electrolyte comprises adding a solid counter-ion source material into the battery container and in contact with the electrolyte.

3. The method of claim 1 , wherein adding a quantity of counter-ions to the electrolyte comprises combining the electrolyte with a liquid solution containing the counter-ions.

4. The method of claim 1 , wherein adding a counter-ion source material to the electrolyte comprises adding a sufficient quantity of the counter-ions to depress a solubility of the solid sulfide-source material below its solubility limit in a solution identical to the electrolyte but-for the added excess of counter-ions.

5. The method of claim 1 , wherein adding a counter-ion source material to the electrolyte comprises adding a sufficient quantity of the counter-ions to depress solubility of the sulfide-source material to less than 700 μM.

6. The method of claim 1 , wherein the sulfide-source material is an additive to the negative electrode.

7. The method of claim 1 , wherein the sulfide-source is in a sulfide reservoir electrically disconnected from the negative electrode.

8. The method of claim 1 , further comprising combining, in the container, an oxygen-reduction electrode and/or a hydrogen-oxidation electrode, and sealing the container against gas escape.

9. A battery comprising:
a battery container;
a liquid electrolyte in the battery container;
a positive electrode containing positive active material and operationally connected to the electrolyte;
an iron negative electrode operationally connected to the electrolyte, the iron negative electrode comprising an iron active material;
a solid sulfide-source material in contact with the electrolyte, the solid sulfide-source material being soluble in the electrolyte;
wherein a concentration of sulfide ions in the electrolyte is greater than 0.01 μM and less than 700 μM.

10. The battery of claim 9 , wherein the concentration of dissolved sulfide ions in the electrolyte is greater than a solubility limit of CuS or Bi2S3 in an identical electrolyte otherwise free of dissolved sulfide ions and less than a solubility limit of ZnS, FeS, or MnS in an identical electrolyte otherwise free of dissolved sulfide ions.

11. The battery of claim 9 wherein the solid sulfide-source material is characterized by its dissociation into at least dissolved sulfide ions and dissolved counter-ions upon its dissolution in said electrolyte.

12. The battery of claim 11 , wherein the electrolyte comprises dissolved counter-ions capable of forming a sulfide compound with dissolved sulfide ions; and wherein the counter-ions are present in a concentration sufficient to depress a solubility of the solid sulfide-source material below its solubility limit in a counter-ion free electrolyte otherwise identical to the electrolyte.

13. The battery of claim 11 , wherein a total concentration of dissolved counter-ions in the electrolyte is at least 10% greater than a concentration of dissolved counter-ions derived from dissolution of said solid sulfide-source material during at least 1% of the charge-discharge cycles throughout the lifetime of said battery.

14. The battery of claim 11 , further comprising a solid counter-ion source material exposed to the electrolyte; said solid counter-ion source material being soluble in said electrolyte and being characterized by its dissociation into at least said dissolved counter-ions upon its dissolution in said electrolyte.

15. The battery of claim 11 wherein a ratio of total moles of dissolved and undissolved counter-ions in the battery to total moles of dissolved and undissolved sulfur species in the battery is greater than the stoichiometric ratio of counter-ions to sulfide ions in said solid sulfide-source material, wherein the counter-ion is a metal ion other than iron.

16. The battery of claim 15 , wherein a ratio of total concentration of dissolved counter-ions in the electrolyte to concentration of dissolved sulfide ions in the electrolyte is at least 10% greater than a stoichiometric ratio of counter-ions to sulfide ions in said solid sulfide-source material during at least 1% of the charge-discharge cycles throughout the lifetime of said battery.

17. The battery of claim 9 , wherein a concentration of dissolved sulfide ions in the electrolyte is selected from the range of 0.1 μM to 300 μM.

18. The battery of claim 9 wherein the solid sulfide-source material is one or more metal sulfides selected from the group consisting of bismuth sulfide, iron sulfide, iron disulfide, iron-copper sulfide, zinc sulfide, manganese sulfide, tin sulfide, copper sulfide, cadmium sulfide, silver sulfide, titanium disulfide, lead sulfide, molybdenum sulfide, nickel sulfide, antimony sulfide, any polymorph of these, and any combination thereof.

19. The battery of claim 9 , wherein said solid sulfide-source material is a first sulfide-source material characterized by its dissociation into at least dissolved sulfide ions and dissolved first counter-ions upon its dissolution in said electrolyte; said battery further comprising a second sulfide-source material operationally connected to the electrolyte; said second sulfide-source material being soluble in said electrolyte and characterized by its dissociation into at least dissolved sulfide ions and dissolved second counter-ions upon its dissolution in said electrolyte; and wherein a solubility product constant (“Ksp”) of said first solid sulfide-source material is greater than a Ksp of said second solid sulfide-source material.

20. The battery of claim 9 , wherein the solid sulfide-source material is contained within a sulfide reservoir operationally coupled to the electrolyte for delivering a quantity of sulfide ions to the electrolyte at a rate slower than a rate of dissolution of the sulfide-source material in the electrolyte.

21. The battery of claim 9 , wherein the battery is an alkaline rechargeable battery and wherein the electrolyte is an aqueous alkaline electrolyte.

22. The battery of claim 9 , wherein the solid sulfide-source material is an additive in the iron negative electrode.

23. The battery of claim 9 , wherein the solid sulfide-source material is electrically disconnected from the iron negative electrode.

Assignees

• Form Energy Inc

Inventors

• Pham Ai Quoc
• Nijhawan Sandeep
• Manohar Aswin K
• Galloway Kevin Van
• Yang Chenguang
• Benson Eric E
• Mchardy Lang
• Rackers Tim

Classifications

• H01M10/52

  Removing gases inside the secondary cell, e.g. by absorption (vent plugs or other mechanical arrangements for facilitating escape of gases H01M50/30) · CPC title

• H01M10/24

  Alkaline accumulators · CPC title

• H01M10/4242

  Regeneration of electrolyte or reactants · CPC title

• H01M4/5815

  Sulfides · CPC title

• H01M4/623

  fluorinated polymers · CPC title