Molten-salt battery, charge-discharge method, and charge-discharge system
US-2017025865-A1 · Jan 26, 2017 · US
US10622665B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10622665-B2 |
| Application number | US-201615764126-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 27, 2016 |
| Priority date | Oct 30, 2015 |
| Publication date | Apr 14, 2020 |
| Grant date | Apr 14, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method of operating a rechargeable sodium ion cell, wherein the cell comprises an anode material which is a disordered carbon and a nickel-containing sodium oxide cathode material comprises: in a formation charge phase, charging the cell to a first voltage at which sodium is irreversibly liberated from the cathode material; and in a subsequent charge-discharge cycle, charging the cell to a second voltage lower than the first voltage. The voltage to which the cell is charged in the formation charge phase may be selected such that the amount of sodium irreversibly liberated from the cathode material in the formation charge phase substantially equals the amount of sodium deposited in a surface electrolyte layer on the anode in the formation charge phase.
Opening claim text (preview).
The invention claimed is: 1. A method of operating a rechargeable sodium ion cell, wherein the cell comprises an anode material which is a disordered carbon and a cathode material A u M 1 v M 2 w M 3 x M 4 Y M 5 z O 2±c , wherein A comprises either sodium or a mixed alkali metal in which sodium is the major constituent; M 1 is nickel in an oxidation state between +2 and +4; M 2 comprises a metal in oxidation state +4 selected from one or more of manganese, titanium and zirconium; M 3 comprises a metal in oxidation state +2, selected from one or more of magnesium, calcium, copper, zinc and cobalt; M 4 comprises a metal in oxidation state +4, selected from one or more of titanium, manganese and zirconium; M 5 comprises a metal in oxidation state +3, selected from one or more of aluminium, iron, cobalt, molybdenum, chromium, vanadium, scandium and yttrium; U is in the range 0<U<1; V is in the range 0.25<V<1; W is in the range 0<W<0.75; X is in the range 0≤X<0.5; Y is in the range 0≤Y<0.5; Z is in the range 0≤Z<0.5; U+V+W+X+Y+Z≤3; and c≥0.0; wherein the method comprises: in a formation charge phase, charging the cell to a first voltage at which sodium is irreversibly liberated from the cathode material; and in a subsequent charge-discharge cycle, charging the cell to a second voltage lower than the first voltage. 2. A method as claimed in claim 1 wherein the first voltage is selected such that the amount of sodium irreversibly liberated from the cathode material in the formation charge phase substantially equals the amount of sodium deposited in a surface electrolyte layer on the anode in the formation charge phase. 3. A method as claimed in claim 1 or a wherein the first voltage is greater than 4.0V. 4. A method as claimed in claim 1 wherein the first voltage is less than 4.5V. 5. A method as claimed in claim 1 wherein the first voltage is between 4.1V and 4.3V. 6. A method as claimed in claim 1 wherein the second voltage is less than 4.0V. 7. A method as claimed in claim 1 wherein the second voltage is between 3.9V and 4.1V. 8. A method as claimed in claim 1 wherein the formation charge phase comprises charging the cell to the first voltage in at least two charge cycles. 9. A method as claimed in claim 1 , and comprising, before the formation charge phase, holding the temperature of the cell above room temperature. 10. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 30° C. for at least one hour. 11. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 50° C. for at least one hour. 12. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 70° C. for at least one hour. 13. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 50° C. for at least one day. 14. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 50° C. for less than 30 days. 15. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 70° C. for at least one day. 16. A method as claimed in claim 9 wherein holding the temperature of the cell above room temperature comprises holding the temperature of the cell above 70° C. for less than 30 days. 17. A method as claimed in claim 9 , and comprising applying a non-zero voltage across the cell while holding the temperature of the cell above room temperature. 18. A method as claimed in claim 17 wherein the non-zero voltage is greater than the open circuit voltage of the cell. 19. A method as claimed in claim 17 wherein the non-zero voltage is greater than 3V. 20. A method as claimed in claim 17 wherein the non-zero voltage is less than 4.5V.
of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title
containing carbon or carbonaceous materials as conductive part, e.g. graphite, carbon fibres · CPC title
of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy (H01M4/505, H01M4/525 take precedence) · CPC title
Processes for forming or storing electrodes in the battery container · CPC title
of manganese · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.