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
US2017040602A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017040602-A1 |
| Application number | US-201615229999-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 5, 2016 |
| Priority date | Aug 7, 2015 |
| Publication date | Feb 9, 2017 |
| Grant date | — |
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The present invention relates to a negative electrode for a secondary battery and a method for manufacturing the negative electrode, and more particularly, to a negative electrode for a secondary battery which exhibits excellent charge/discharge characteristics and lifespan characteristics by including a carbon-silicon composite and graphite at a predetermined particle size ratio.
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What is claimed is: 1 . A negative electrode for a secondary battery, the negative electrode comprising a negative electrode active material that comprises: a carbon-silicon composite having a Si-block copolymer core-shell particle in a carbonaceous material; and graphite, wherein the negative electrode comprises a plurality of pores therein, and when a 50% accumulated weight particle size distribution diameter in particle distribution in the negative electrode is D50, D50 of the carbon-silicon composite is D Si—C , and D50 of graphite is D G , D Si—C and D G satisfy 1.0≦D G /D Si—C ≦1.8. 2 . The negative electrode of claim 1 , wherein D Si—C satisfies 3 μm≦D Si—C ≦12 μm. 3 . The negative electrode of claim 1 , wherein D G satisfies 8 μm≦D G ≦20 μm. 4 . The negative electrode of claim 1 , wherein an electrode porosity of the negative electrode is in a range of about 25% to about 45%. 5 . The negative electrode of claim 1 , wherein when pores having a particle diameter less than 100 nm among the pores are referred to as fine pores, a porosity of the fine pores is in a range of about 30% to about 50%. 6 . The negative electrode of claim 1 , wherein a tap density (D T ) of the negative electrode active material is in a range of about 1.0 g/cc to about 1.2 g/cc. 7 . The negative electrode of claim 1 , wherein an electrode density (D R ) of the negative electrode is in a range of about 1.35 g/cc to about 1.85 g/cc. 8 . The negative electrode of claim 1 , wherein a weight ratio of the carbon-silicon composite and the graphite in the negative electrode is in a range of about 50:50 to about 1:99. 9 . The negative electrode of claim 1 , wherein the carbon-silicon composite and the graphite have a spherical shape. 10 . A method for manufacturing a negative electrode for a secondary battery, the method comprising: (a) mixing a slurry solution including Si-block copolymer core-shall particles and a carbonaceous raw material to prepare a mixture; (b) performing heat-treatment on the mixture; (c) carbonizing and pulverizing the heat-treated mixture to prepare a carbon-silicon composite; (d) mixing the carbon-silicon composite and graphite to prepare a negative electrode active material; and (e) coating a current collector with a mixture of the negative electrode active material, a conducting agent, a binder, and a thickener, wherein the (c) carbonizing and pulverizing are repeated at least twice, and when a 50% accumulated weight particle size distribution diameter in particle distribution in the negative electrode is D50, D50 of the carbon-silicon composite is D Si—C , and D50 of graphite is D G , D Si—C and D G satisfy 1.0≦D G /D Si—C ≦1.8. 11 . The method for claim 10 , wherein D Si—C satisfies 3 μm≦D Si—C ≦12 μm. 12 . The method for claim 10 , wherein D G satisfies 8 μm≦D G ≦20 μm. 13 . The method for claim 10 , wherein (b) the performing heat-treatment on the mixture is performed at a temperature in a range of about 100° C. to about 200° C. 14 . The method for claim 10 , wherein (c) the mixing the carbon-silicon composite and graphite is repeated at least twice at temperatures different from each other. 15 . The method for claim 14 , wherein (c) the mixing the carbon-silicon composite and graphite comprises a primary carbonization process which comprises heat-treating the mixture at a temperature in a range of about 400° C. to about 600° C. for about 1 hour to about 24 hours and then pulverizing the mixture; and a secondary carbonization process which comprises heat-treating the resultant of the primary carbonization process at a temperature in a range of about 700° C. to about 1400° C. for about 1 hour to about 24 hours and then pulverizing the resultant. 16 . The method for claim 15 , wherein the pulverizing of the primary carbonization process or the secondary carbonization process is performed at a pressure of 13 bar or lower. 17 . The method for claim 10 , wherein a weight ratio of the carbon-silicon composite and graphite in (d) the mixing the carbon-silicon composite and graphite is in a range of about 50:50 to about 1:99.
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