Positive electrode active material for sodium secondary battery, and method for preparing same
US-2017187039-A1 · Jun 29, 2017 · US
US10522828B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10522828-B2 |
| Application number | US-201715606800-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 26, 2017 |
| Priority date | May 26, 2016 |
| Publication date | Dec 31, 2019 |
| Grant date | Dec 31, 2019 |
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A method of fabricating a positive active material for a rechargeable sodium battery is provided. The method includes forming a metal hydroxide precursor including nickel, cobalt, and manganese, and fabricating a positive active material by mixing and firing the metal hydroxide precursor and a sodium source. A kind of the sodium source is changed depending on a content of nickel or manganese included in the metal hydroxide precursor.
Opening claim text (preview).
What is claimed is: 1. A method of fabricating a positive active material for a rechargeable sodium battery, the method comprising: forming a metal hydroxide precursor including nickel, cobalt, and manganese; and fabricating a positive active material by mixing and firing the metal hydroxide precursor and a sodium source, wherein the sodium source is selected from a first sodium source having a first melting point or a second sodium source having a second melting point which is lower than the first melting point, wherein a content of nickel included in the metal hydroxide precursor is selected from a first nickel content or a second nickel content which is higher than the first nickel content, and wherein when the first nickel content is selected, the first sodium source is selected in the method, and when the second nickel content is selected, the second sodium source is selected in the method. 2. The method of claim 1 , wherein the fabricating of the positive active material comprises: quenching the metal hydroxide precursor and the sodium source after the mixing and firing of the metal hydroxide precursor and the sodium source. 3. The method of claim 1 , wherein the positive active material is quenched in a vacuum state. 4. The method of claim 1 , wherein the fabricating of the positive active material comprises: melting the sodium source before the mixing of the sodium source and the metal hydroxide precursor. 5. The method of claim 1 , wherein the metal hydroxide precursor and the sodium source are fired at a temperature of 680 degrees Celsius to 720 degrees Celsius. 6. The method of claim 1 , wherein the forming of the metal hydroxide precursor comprises: preparing nickel sulfate, cobalt sulfate, and manganese sulfate; forming a core portion, in which concentrations of nickel, cobalt and manganese are constant, by using the nickel sulfate, the cobalt sulfate, and the manganese sulfate; and forming a concentration gradient portion, in which a concentration of at least one of nickel, cobalt or manganese is varied, by adjusting a mole percent ratio of the nickel sulfate, the cobalt sulfate and the manganese sulfate, wherein the concentration gradient portion surrounds the core portion. 7. The method of claim 6 , wherein the forming of the metal hydroxide precursor further comprises: forming a shell portion, in which concentrations of nickel, cobalt and manganese are constant, by using the nickel sulfate, the cobalt sulfate, and the manganese sulfate, wherein the shell portion surrounds the concentration gradient portion. 8. The method of claim 1 , wherein the second sodium source includes NaOH, and the first sodium source includes Na 2 CO 3 .
Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium · CPC title
of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy · CPC title
containing manganese · CPC title
Electric properties · CPC title
by d-values or two theta-values, e.g. as X-ray diagram · CPC title
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