Stabilized birnessite cathode for high power and high energy density applications

US11276877B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11276877-B2
Application numberUS-201816493966-A
CountryUS
Kind codeB2
Filing dateMay 4, 2018
Priority dateMar 15, 2017
Publication dateMar 15, 2022
Grant dateMar 15, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A battery comprises a housing, an electrolyte disposed in the housing, an anode disposed in the housing, a stabilized cathode disposed in the housing and comprising a cathode material. The cathode material comprises a composition selected from birnessite or layered-polymorph of manganese dioxide (δ-MnO 2 ), the composition being stabilized by bismuth and copper ions, a conductive carbon, and a binder. The anode can be at least 50% (m/m) lithium, magnesium, aluminum, or zinc.

First claim

Opening claim text (preview).

What is claimed is: 1. A battery comprising: a housing; an electrolyte disposed in the housing; an anode disposed in the housing, wherein the anode is at least 50% (m/m) lithium, magnesium, or aluminum; a stabilized cathode disposed in the housing and comprising a cathode material, the cathode material comprising: a composition selected from birnessite or layered-polymorph of manganese dioxide (δ-MnO 2 ), the composition being stabilized by bismuth and copper ions; a conductive carbon; and a binder. 2. The battery as recited in claim 1 , wherein the birnessite is synthesized through electrochemical, chemical, or heat treatment methods. 3. The battery as recited in claim 1 , wherein the stabilized cathode further comprises a metallic ion selected from the group consisting of tin, aluminum, nickel, iron, cobalt and lead. 4. The battery as recited in claim 1 , wherein the binder comprises a polytetrafluoroethylene, polyvinylidene fluoride, a cellulose-based hydrogel or a combination thereof. 5. The battery as recited in claim 1 , wherein the binder is a cellulose-based hydrogel selected from the group consisting of methyl cellulose (MC), carboxymethyl cellulose (CMC), hydroxypropyl cellulose (HPC), hydroxypropylmethyl cellulose (HPMC), hydroxyethylmethyl cellulose (HEMC), carboxymethylhydroxyethyl cellulose and hydroxyethyl cellulose (HEC). 6. The battery as recited in claim 5 , wherein the binder is a cellulose-based hydrogel crosslinked with a copolymer selected from the group consisting of polyvinyl alcohol, polyvinylacetate, polyaniline, polyvinylpyrrolidone, polyvinylidene fluoride and polypyrrole. 7. The battery as recited in claim 1 , wherein the conductive carbon is selected from the group consisting of TIMREX® Primary Synthetic Graphite, TIMREX® Natural Flake Graphite, TIMREX® MB, TIMREX® MK, TIMREX® MX, TIMREX® KC, TIMREX® B, TIMREX® LB, TIMREX® Dispersions; ENASCO 150G, ENASCO 210G, ENASCO 250G, ENASCO 260G, ENASCO 350G, ENASCO 150P, ENASCO 250P; SUPER P, SUPER P Li, carbon black, acetylene black, single walled carbon nanotubes, multi-walled carbon nanotubes, graphene, graphyne, graphene oxide, Zenyatta graphite and combinations thereof. 8. The battery as recited in claim 7 , wherein the conductive carbon further comprises a deposit of nickel, copper, tin, aluminum, cobalt, silver or nickel-phosphorous. 9. The battery as recited in claim 1 , where the cathode material is 1-98 wt. % stabilized birnessite, 1-98 wt. % conductive carbon and 1-10 wt. % binder. 10. The battery as recited in claim 1 , wherein the cathode material has a porosity between 5-95%. 11. The battery as recited in claim 1 , further comprising a current collector for the cathode material, the current collector selected from the group consisting of copper, aluminum, and nickel. 12. The battery as recited in claim 1 , wherein the electrolyte is an acidic electrolyte, an alkaline electrolyte, an ionic liquid, an organic-based electrolyte, a solid-phase electrolyte, a gelled electrolyte, or combinations thereof. 13. The battery as recited in claim 1 , wherein the electrolyte is selected from the group consisting of chlorides, sulfates, sodium hydroxide, potassium hydroxide, lithium hydroxide, a perchlorate, lithium perchlorate, magnesium perchlorate, aluminum perchlorate, lithium hexafluorophosphate, [M + ][AlCl 4 − ](M + )]-sulphonyl chloride, a phosphoryl chloride cation, 1-ethyl-3-methylimidazolium bis (trifluoromethyl sulfonyl)imide, 1-ethyl-3-methylimidazolium trifluoromethanesulfonate, 1-butyl-1-methylpyrrolidinium bis(trifluoromethyl sulfonyl)imide, 1-hexyl-3-methylimidazolium hexofluorophosphate, 1-ethyl-3-methylimidazolium dicyanamide, 11-methyl-3-octylimidazolium tetrafluoroborate, yttria-stabilized zirconia, beta-alumina solid, polyacrylamides, NASICON, lithium salts in mixed organic solvents, 1,2-dimethoxyethane, propylene carbonate, magnesium bis(hexamethyldisilazide) in tetrahydrofuran and combinations thereof. 14. The battery as recited in claim 1 , further comprising a polymeric or ceramic separator between the anode and the cathode material. 15. A method of operating a battery comprising: discharging a battery, wherein the battery comprises: a housing; an electrolyte disposed in the housing; an anode disposed in the housing, wherein the anode is at least 50% (m/m) lithium, magnesium, or aluminum; a stabilized cathode disposed in the housing and comprising a cathode material, the cathode material comprising: a composition selected from birnessite or layered-polymorph of manganese dioxide (δ-MnO 2 ), the composition being stabilized by bismuth and copper ions; a conductive carbon; and a binder; charging the battery; and stabilizing the cathode with the bismuth and copper ions during the discharging and charging. 16. The method as recited in claim 15 , wherein the birnessite is synthesized through electrochemical, chemical, or heat treatment methods. 17. The method as recited in claim 15 , wherein the bismuth and copper ions are included directly after making birnessite. 18. The method as recited in claim 15 , wherein the stabilized cathode further comprises a metallic ion selected from the group consisting of tin, aluminum, nickel, iron, cobalt and lead. 19. The method as recited in claim 15 , wherein the binder comprises a polytetrafluoroethylene, polyvinylidene fluoride, a cellulose-based hydrogel or a combination thereof. 20. The method as recited in claim 15 , wherein the binder is a cellulose-based hydrogel selected from the group consisting of methyl cellulose (MC), carboxymethyl cellulose (CMC), hydroxypropyl cellulose (HPC), hydroxypropylmethyl cellulose (HPMC), hydroxyethylmethyl cellulose (HEMC), carboxymethylhydroxyethyl cellulose and hydroxyethyl cellulose (HEC). 21. The method as recited in claim 20 , wherein the binder is a cellulose-based hydrogel crosslinked with a copolymer selected from the group consisting of polyvinyl alcohol, polyvinylacetate, polyaniline, polyvinylpyrrolidone, polyvinylidene fluoride and polypyrrole. 22. The method as recited in claim 15 , wherein the conductive carbon is selected from the group consisting of TIMREX® Primary Synthetic Graphite, TIMREX® Natural Flake Graphite, TIMREX® MB, TIMREX® MK, TIMREX® MX, TIMREX® KC, TIMREX® B, TIMREX® LB, TIMREX® Dispersions; ENASCO 150G, ENASCO 210G, ENASCO 250G, ENASCO 260G, ENASCO 350G, ENASCO 150P, ENASCO 250P; SUPER P, SUPER P Li, carbon black, acetylene black, single walled carbon nanotubes, multi-walled carbon nanotubes, graphene, graphyne, graphene oxide, Zenyatta graphite and combinations thereof. 23. The method as recited in claim 22 , where in the conductive carbon further comprises a deposit of nickel, copper, tin, aluminum, cobalt, silver or nickel-phosphorous. 24. The method as recited in claim 15 , where the cathode material is 1-98 wt. % stabilized birnessite, 1-98 wt. % conductive carbon and 1-10 wt. % binder. 25. The method as recited in claim 15 , wherein the cathode material has a porosity between 5-95%. 26. The method as recited in claim 15 , further comprising a current collector for the cathode material, the current collector selected from the group consisting of copper, aluminum and nickel. 27. The method as recited in claim 15 , wherein the electrolyte is an acidic electrolyte, an alkaline electrolyte, an ionic liquid, an organic-based electrolyte, a solid-phase electrolyt

Assignees

Inventors

Classifications

  • Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title

  • one element only · CPC title

  • involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title

  • H01M4/525Primary

    of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title

  • Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium · CPC title

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What does patent US11276877B2 cover?
A battery comprises a housing, an electrolyte disposed in the housing, an anode disposed in the housing, a stabilized cathode disposed in the housing and comprising a cathode material. The cathode material comprises a composition selected from birnessite or layered-polymorph of manganese dioxide (δ-MnO 2 ), the composition being stabilized by bismuth and copper ions, a conductive carbon, and a …
Who is the assignee on this patent?
Univ City New York Res Found
What technology area does this patent fall under?
Primary CPC classification H01M10/0525. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Mar 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).