Sodium ion secondary battery and positive electrode active material particles
US-2018351197-A1 · Dec 6, 2018 · US
US12438151B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12438151-B2 |
| Application number | US-202117371231-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 9, 2021 |
| Priority date | Jan 11, 2019 |
| Publication date | Oct 7, 2025 |
| Grant date | Oct 7, 2025 |
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.
The present application discloses a positive electrode active material and its preparation method, a sodium ion battery and an apparatus containing the sodium ion battery. The positive electrode active material satisfies a chemical formula Na2+xCuhMnkMlO7-y, wherein M is one or more selected from Li, B, Mg, Al, K, Ca, Ti, V, Cr, Fe, Co, Ni, Zn, Ga, Sr, Y, Nb, Mo, Sn, Ba and W, 0≤x≤0.5, 0.1<h≤2, 1≤k≤3, 0≤l≤0.5, and 0≤y≤1, 2≤h+k+l≤3.5, and 0.57≤(2+x)/(h+k+l)≤0.9.
Opening claim text (preview).
What is claimed is: 1. A positive electrode active material, satisfying a chemical formula Na 2+x Cu h Mn k M l O 7-y , wherein Mis one or more selected from Li, B, Mg, Al, K, Ca, Ti, V, Cr, Fe, Co, Ni, Zn, Ga, Sr, Y, Nb, Mo, Sn, Ba and W, 0≤x≤0.5, 0.1<h≤2, 1≤k≤3, 0≤l≤0.5, and 0≤y≤1, 3.0≤h+k+l≤3.1, and 0.7≤(2+x)/(h+k+l)≤0.73, and wherein the positive electrode active material has a powder resistivity of from 10 Ω·cm to 3kΩ·cm at a pressure of 12 MPa, wherein the positive electrode active material has a specific surface area of from 0.01 m 2 /g to 3 m 2 /g; and, wherein the positive electrode active material has a mean particle size D V 50 of from 7 μm to 25 μm. 2. The positive electrode active material according to claim 1 , wherein in the chemical formula, 0.5≤h≤1.5, 1.5≤k≤2.5. 3. The positive electrode active material according to claim 1 , wherein in the chemical formula, k/(h+l)≥1.4. 4. The positive electrode active material according to claim 1 , wherein the positive electrode active material is of a triclinic phase crystal structure or a hexagonal phase crystal structure. 5. The positive electrode active material according to claim 4 , wherein the positive electrode active material comprises a first diffraction peak at an X-ray diffraction angle 2θ of from 15.8° to 16.0° and a second diffraction peak at an X-ray diffraction angle 2θ of from 32.0° to 32.2°, and an intensity ratio of the first diffraction peak to the second diffraction peak is from 5 to 30, the first diffraction peak has a full width at half maxima of from 0.02° to 0.5°, and the second diffraction peak has a full width at half maxima of from 0.02° to 0.5°. 6. The positive electrode active material according to claim 1 , wherein the positive electrode active material has a tap density of from 0.5 g/cm 3 to 3.5 g/cm 3 ; and/or, the positive electrode active material has a compaction density of from 2.5 g/cm 3 to 4.5 g/cm 3 at a pressure of 8 tons. 7. The positive electrode active material according to claim 1 , wherein the positive electrode active material has a first discharge voltage plateau of from 3.8V to 4.1V and a second discharge voltage plateau of from 3.4V to 3.7V. 8. The positive electrode active material according to claim 7 , wherein the positive electrode active material has a discharge capacity of Q 1 at the first discharge voltage plateau, a discharge capacity of Q 2 at the second discharge voltage plateau, and a full discharge capacity of Q, and Q 1 , Q 2 and Q satisfy: 30%≤( Q 1 +Q 2 )/ Q× 100%≤90%. 9. A method for preparing a positive electrode active material, comprising the following steps: providing a mixed solution, wherein the mixed solution comprises copper salts and manganese salts, and salts containing an M element are present in the mixed solution in an amount of 0 or more; adding a precipitant and a complexing agent into the mixed solution, and then subjecting it to coprecipitation to obtain a precursor; and mixing the precursor and a sodium source to obtain a mixture and sintering the mixture to obtain the positive electrode active material, wherein the positive electrode active material satisfies a chemical formula Na 2+x Cu h Mn k M l O 7-y , wherein M is one or more selected from of Li, B, Mg, Al, K, Ca, Ti, V, Cr, Fe, Co, Ni, Zn, Ga, Sr, Y, Nb, Mo, Sn, Ba and W; 0≤x≤0.5, 0.1<h≤2, 1≤k≤3, 0≤l≤0.5, 0≤y≤1, 3.0≤h+k+l≤3.1, and 0.7≤(2+x)/(h+k+l)≤0.73, and wherein the positive electrode active material has a powder resistivity of from 10 Ω·cm to 3 kΩ·cm at a pressure of 12 MPa, wherein the positive electrode active material has a specific surface area of from 0.01 m 2 /g to 3 m 2 /g; and, wherein the positive electrode active material has a mean particle size D V 50 of from 7 μm to 25 μm. 10. A sodium-ion battery, comprising a positive electrode plate, wherein the positive electrode plate comprises a positive electrode active material satisfying a chemical formula Na 2+x Cu h Mn k M l O 7-y , wherein M is one or more selected from Li, B, Mg, Al, K, Ca, Ti, V, Cr, Fe, Co, Ni, Zn, Ga, Sr, Y, Nb, Mo, Sn, Ba and W, 0≤x≤0.5, 0.1<h≤2, 1≤k≤3, 0≤l≤0.5, and 0≤y≤1, 3.0≤h+k+l≤3.1, and 0.7≤(2+x)/(h+k+l)≤0.73, and wherein the positive electrode active material has a powder resistivity of from 10 Ω·cm to 3kΩ·cm at a pressure of 12 MPa, wherein the positive electrode active material has a specific surface area of from 0.01 m 2 /g to 3 m 2 /g; and, wherein the positive electrode active material has a mean particle size D V 50 of from 7 μm to 25 μm. 11. The sodium-ion battery according to claim 10 , wherein in the chemical formula, 0.5≤h≤1.5, 1.5≤k≤2.5. 12. The sodium-ion battery according to claim 10 , wherein in the chemical formula, k/(h+l)≥1.4. 13. The sodium-ion battery according to claim 10 , wherein the positive electrode active material is of a triclinic phase crystal structure or a hexagonal phase crystal structure. 14. The sodium-ion battery according to claim 13 , wherein the positive electrode active material comprises a first diffraction peak at an X-ray diffraction angle 2θ of from 15.8° to 16.0° and a second diffraction peak at an X-ray diffraction angle 2θ of from 32.0° to 32.2°, and an intensity ratio of the first diffraction peak to the second diffraction peak is from 5 to 30, the first diffraction peak has a full width at half maxima of from 0.02° to 0.5°, and the second diffraction peak has a full width at half maxima of from 0.02° to 0.5°. 15. The sodium-ion battery according to claim 10 , wherein the positive electrode active material has a first discharge voltage plateau of from 3.8V to 4.1V and a second discharge voltage plateau of from 3.4V to 3.7V.
Positive electrodes · CPC title
Physical characteristics, e.g. porosity, surface area · CPC title
Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium · 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
involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.