Anode for lithium metal battery, and electrochemical device comprising same
US-12176528-B2 · Dec 24, 2024 · US
US2026018601A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2026018601-A1 |
| Application number | US-202519336537-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 23, 2025 |
| Priority date | Nov 1, 2023 |
| Publication date | Jan 15, 2026 |
| Grant date | — |
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 positive electrode material is disclosed, represented by the formula LiaNixCoyMn1-x-yMbO2-cQc, where 0.2≤a≤1.2, x≥0.6, y>0, b>0, and c>0. M comprises a high-valence cation and Q comprises an anion. The doping of a high-valence cation and an anion in a nickel-rich ternary material stabilizes the bulk structure during lithium deintercalation, reduces side reactions, lattice oxygen release, and transition metal dissolution, and improves cycling stability, high-temperature storage, and rate capability. The outer surface of the positive electrode material may further include a selenium-containing coating layer that reacts with residual lithium compounds and binds released lattice oxygen to suppress electrolyte oxidation. A conductive coating layer may be formed on the selenium-containing layer to prevent direct contact with the electrolyte and inhibit side reactions.
Opening claim text (preview).
What is claimed is: 1 . A positive electrode material, the positive electrode material having the following chemical formula: Li a Ni x Co y Mn 1-x-y M b O 2-c Q c , wherein 0.2≤a≤1.2, x≥0.6, y>0, b>0, c>0, M comprises a high-valence cation, Q comprises an anion, the high-valence cation comprises a tetravalent or higher cation, and the anion comprises at least one of S 2− , Se 2− , Te 2− and P 3− . 2 . The positive electrode material according to claim 1 , wherein the high-valence cation comprises at least one of Mo 6+ , Sb 5+ , Zr 4+ , Ti 4+ , Nb 5+ , W 6+ , Y 5+ and Ta 5+ . 3 . The positive electrode material according to claim 1 , wherein 0.0005≤b≤0.01, and/or 0.001≤c≤0.1. 4 . The positive electrode material according to claim 1 , wherein an outer surface of the positive electrode material further comprises a first coating layer which comprises a selenium-containing substance. 5 . The positive electrode material according to claim 4 , wherein the selenium-containing substance comprises at least one of elemental selenium (Se), selenium oxide (SeO 2 ), selenium sulfide (SeS 2 ) and tellurium selenide (TeSe). 6 . The positive electrode material according to claim 4 , wherein a content of selenium element in the positive electrode material containing the first coating layer is 0.03% to 5%. 7 . The positive electrode material according to claim 4 , wherein based on 100% of a total mass of the positive electrode material, an addition amount of the selenium-containing substance ranges from 0.1% to 5%. 8 . The positive electrode material according to claim 7 , wherein based on 100% of the total mass of the positive electrode material, the addition amount of the selenium-containing substance ranges from 0.5% to 2%. 9 . The positive electrode material according to claim 4 , wherein a particle size Dv50 of the selenium-containing substance is 100 nm to 1000 nm. 10 . The positive electrode material according to claim 4 , wherein the particle size Dv50 of the selenium-containing substance is 100 nm to 500 nm. 11 . The positive electrode material according to claim 4 , wherein the positive electrode material further comprises a second coating layer which is coated on a surface of the first coating layer and comprises a conductive polymer. 12 . The positive electrode material according to claim 11 , wherein the conductive polymer comprises at least one of polyaniline, polypyrrole, polypyridine and polythiophene, wherein the second coating layer has a thickness of 50 nm to 500 nm, wherein the second coating layer has a thickness of 50 nm to 200 nm. 13 . A preparation method for the positive electrode material according to claim 1 , the preparation method for the positive electrode material comprising the following steps: mixing a nickel-rich ternary positive electrode material precursor with a high-valence cation dopant, sintering same to obtain a high-valence cation-doped positive electrode material A, mixing the positive electrode material A with an anion dopant, sintering same to obtain the positive electrode material, and marking the positive electrode material as a positive electrode material C, wherein the positive electrode material C contains a high-valence cation and an anion, and the high-valence cation comprises a tetravalent or higher cation; or the preparation method for the positive electrode material comprising the following steps: mixing a nickel-containing positive electrode material precursor with an anion dopant, sintering same to obtain an anion-doped positive electrode material B, mixing the positive electrode material B with a high-valence cation dopant, sintering same to obtain the positive electrode material, and marking the positive electrode material as a positive electrode material C, wherein the positive electrode material C contains a high-valence cation and an anion, and the high-valence cation comprises a tetravalent or higher cation. 14 . The preparation method for the positive electrode material according to claim 13 , wherein in the step of preparing the positive electrode material A, the sintering comprises primary sintering and secondary sintering, a temperature of the primary sintering is 350 to 500° C., a time of the primary sintering is 2 to 7 h, the temperature of the secondary sintering is 600 to 800° C., and the time of the secondary sintering is 3 to 6 h. 15 . The preparation method for the positive electrode material according to claim 12 , wherein in the step of preparing the positive electrode material B, the temperature of the sintering is 400° C. to 650° C. 16 . A preparation method for a positive electrode material, comprising: mixing the positive electrode material C prepared by the preparation method according to claim 12 with a selenium-containing substance, heating same to obtain a positive electrode material, and marking the positive electrode material as a positive electrode material D, wherein a surface of the positive electrode material D has a selenium-containing substance coating layer. 17 . The preparation method for the positive electrode material according to claim 16 , wherein a heating temperature is 230° C. to 500° C.; and/or, the heating time is 15 min to 120 min. 18 . The preparation method for the positive electrode material according to claim 1 , wherein based on 100% of a total mass of the positive electrode material D, an addition amount of the conductive polymer is 0.5% to 10%. 19 . A lithium-ion battery, the lithium-ion battery comprising the positive electrode material according to claim 1 .
Safety or regulating additives or arrangements in electrodes, separators or electrolyte (H01M10/4242 takes precedence) · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
Inhibitors, e.g. gassing inhibitors, corrosion inhibitors · CPC title
Electric conductive fillers · CPC title
of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.