Positive electrode active material and preparation method thereof, positive electrode plate, secondary battery, battery module, battery pack, and electric apparatus
US-2024429384-A1 · Dec 26, 2024 · US
US10297822B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10297822-B2 |
| Application number | US-201615362103-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 28, 2016 |
| Priority date | Dec 27, 2010 |
| Publication date | May 21, 2019 |
| Grant date | May 21, 2019 |
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An object of the present invention is to provide a positive active material for a nonaqueous electrolyte secondary battery which has a large discharge capacity and is superior in charge-discharge cycle performance, initial efficiency and high rate discharge performance, and a nonaqueous electrolyte secondary battery using the positive active material. The present invention pertains to a positive active material for a nonaqueous electrolyte secondary battery containing a lithium transition metal composite oxide which has a crystal structure of an α-NaFeO2 type, is represented by a compositional formula Li1+αMe1−αO2 (Me is a transition metal element including Co, Ni and Mn, α>0), and has a molar ratio Li/Me of Li to the transition metal element Me of 1.2 to 1.6, wherein a molar ratio Co/Me of Co in the transition metal element Me is 0.02 to 0.23, a molar ratio Mn/Me of Mn in the transition metal element Me is 0.62 to 0.72, and the lithium transition metal composite oxide is observed as a single phase attributed to a space group R3-m on an X-ray diffraction chart when it is electrochemically oxidized up to a potential of 5.0 V (vs. Li/Li+).
Opening claim text (preview).
The invention claimed is: 1. A positive active material for a nonaqueous electrolyte secondary battery containing a lithium transition metal composite oxide which has a crystal structure of an α-NaFeO 2 type, is represented by a compositional formula Li 1+α Me 1−α O 2 , wherein Me is a transition metal element including Co, Ni and Mn, and α>0, a molar ratio Li/Me of Li to the transition metal element Me is 1.2 to 1.6, a molar ratio Co/Me of Co in the transition metal element Me is 0.02 to 0.23, a molar ratio Mn/Me of Mn in the transition metal element Me is 0.625 to 0.707, the lithium transition metal composite oxide is a single phase attributed to a space group R3-m on an X-ray diffraction chart under a condition in which the lithium transition metal composite oxide is electrochemically oxidized up to a potential of 5.0 V (vs. Li/Li + ), and an oxygen position parameter of the lithium transition metal composite oxide is 0.260 or less, the oxygen position parameter being determined in a state of a discharge end, by crystal structure analysis by a Rietveld method, using a space group R3-m as a crystal structure model based on an X-ray diffraction pattern. 2. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein a BET specific surface area is 1.24 to 5.87 m 2 /g. 3. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein a tapped density is 1.25 g/cm 3 or more. 4. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein a ratio between the diffraction peak intensity I (003) of (003) line and the diffraction peak intensity I (114) of (114) line based on X-ray diffraction measurement before charge-discharge satisfies I (003) /I (114) ≥1.20. 5. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein the lithium transition metal composite oxide is obtained by mixing/sintering a coprecipitated precursor of compounds of the transition metal elements including Co, Ni and Mn, and a lithium compound. 6. A method of manufacturing the positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , comprising the steps of coprecipitating compounds of transition metal elements including Co, Ni and Mn in a solution to produce a coprecipitated precursor; and mixing/sintering the coprecipitated precursor and a lithium compound. 7. The method of manufacturing a positive active material for a nonaqueous electrolyte secondary battery according to claim 6 , wherein a pH in the step of coprecipitating compounds of transition metal elements including Co, Ni and Mn in a solution to produce a coprecipitated precursor is 8.5 to 11.0. 8. The method of manufacturing a positive active material for a nonaqueous electrolyte secondary battery according to claim 6 , wherein a sintering temperature in the step of mixing/sintering the coprecipitated precursor and a lithium compound is 800 to 940° C. 9. An electrode for a nonaqueous electrolyte secondary battery containing the positive active material for a nonaqueous electrolyte secondary battery according to claim 1 . 10. A nonaqueous electrolyte secondary battery including the electrode for a nonaqueous electrolyte secondary battery according to claim 9 . 11. A nonaqueous electrolyte secondary battery comprising the positive active material of claim 1 , wherein a volume ratio of oxygen to a total of nitrogen and oxygen contained in a gas in the battery is 0.2 to 0.25 under a condition in which the battery is charged so that a maximum potential of a positive electrode of the battery is 4.5 to 4.6 V (vs. Li/Li + ). 12. A positive active material for a nonaqueous electrolyte secondary battery containing a lithium transition metal composite oxide which has a crystal structure of an α-NaFeO 2 type, is represented by a compositional formula Li 1+α Me 1−α O 2 , wherein Me is a transition metal element including Co, Ni and Mn, and α>0, a molar ratio Li/Me of Li to the transition metal element Me is of 1.2 to 1.6, a molar ratio Co/Me of Co in the transition metal element Me is 0.02 to 0.23, a molar ratio Mn/Me of Mn in the transition metal element Me is 0.625 to 0.707, the lithium transition metal composite oxide is a single phase attributed to a space group R3-m on an X-ray diffraction chart under a condition in which the lithium transition metal composite oxide is electrochemically oxidized up to a potential of 5.0 V (vs. Li/Li + ), and a tapped density is 1.25 g/cm 3 or more. 13. A nonaqueous electrolyte secondary battery comprising the positive active material of claim 12 , wherein a volume ratio of oxygen to a total of nitrogen and oxygen contained in a gas in the battery is 0.2 to 0.25 under a condition in which the battery is charged so that a maximum potential of a positive electrode of the battery is 4.5 to 4.6 V (vs. Li/Li + ). 14. A positive active material for a nonaqueous electrolyte secondary battery containing a lithium transition metal composite oxide which has a crystal structure of an α-NaFeO 2 type, is represented by a compositional formula Li 1+α Me 1−α O 2 , wherein Me is a transition metal element including Co, Ni and Mn, and α>0, a molar ratio Li/Me of Li to the transition metal element Me is of 1.2 to 1.6, a molar ratio Co/Me of Co in the transition metal element Me is 0.02 to 0.23, a molar ratio Mn/Me of Mn in the transition metal element Me is 0.625 to 0.707, and the lithium transition metal composite oxide is a single phase attributed to a space group R3-m on an X-ray diffraction chart under a condition in which the lithium transition metal composite oxide is electrochemically oxidized up to a potential of 5.0 V (vs. Li/Li + ). 15. The positive active material for a nonaqueous electrolyte secondary battery according to claim 14 , wherein a BET specific surface area is 1.24 to 5.87 m 2 /g. 16. A nonaqueous electrolyte secondary battery comprising the positive active material of claim 14 , wherein a volume ratio of oxygen to a total of nitrogen and oxygen contained in a gas in the battery is 0.2 to 0.25 under a condition in which the battery is charged so that a maximum potential of a positive electrode of the battery is 4.5 to 4.6 V (vs. Li/Li + ).
Positive electrodes · CPC title
of the type (MnO2)-, e.g. LiMnO2 or Li(MxMn1-x)O2 · CPC title
Micrometer sized, i.e. from 1-100 micrometer · CPC title
Li-accumulators · CPC title
involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
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