Metal organic framework-derived carbon aerogel, preparation method thereof and application in lithium ion batteries
US-12183924-B2 · Dec 31, 2024 · US
US2016197345A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016197345-A1 |
| Application number | US-201414911826-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 12, 2014 |
| Priority date | Aug 14, 2013 |
| Publication date | Jul 7, 2016 |
| Grant date | — |
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Provided is a production method for a composite active material for lithium secondary batteries which enables production of an electrode material in which volume expansion is suppressed even after repeated charging and discharging, and enables production of a lithium secondary battery exhibiting excellent cycle characteristics. A composite active material for lithium secondary batteries is produced using a mixing step of mixing graphite having a specific surface area of not less than 30 m 2 /g, silicon monoxide, and a carbon precursor to obtain a mixture; a conglobation step of performing conglobation treatment on the mixture and obtaining a spherical mixture; and a heating step of heat-treating the spherical mixture and producing a substantially spherical composite active material for lithium secondary batteries.
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1 . A composite active material for lithium secondary batteries comprising: a composite containing silicon and silicon dioxide; and a graphite component; an area ratio of the graphite component exposed on a surface observed by scanning electron microscope at acceleration voltage of not greater than 10 kV being not less than 95%. 2 . The composite active material for lithium secondary batteries according to claim 1 , wherein an average particle size of the silicon is from 1 to 100 nm. 3 . The composite active material for lithium secondary batteries according to claim 1 , wherein an average particle size of the composite is from 50 to 1000 nm. 4 . A production method for the composite active material for lithium secondary batteries described in claim 1 , comprising: a mixing step of mixing graphite having a specific surface area of not less than 30 m 2 /g, silicon monoxide, and a carbon precursor to obtain a mixture; a conglobation step of performing conglobation treatment on the mixture and obtaining a spherical mixture; and a heating step of heat-treating the spherical mixture and producing a substantially spherical composite active material for lithium secondary batteries. 5 . The production method for a composite active material for lithium secondary batteries according to claim 4 , wherein an average particle size of the silicon monoxide is not greater than 1 μm. 6 . The production method for a composite active material for lithium secondary batteries according to claim 4 , wherein the carbon precursor is at least one type selected from the group consisting of polymer compounds, coal-based pitch, petroleum-based pitch, mesophase pitch, coke, low-molecular-weight oil, and derivatives thereof. 7 . The production method for a composite active material for lithium secondary batteries according to claim 4 , wherein the graphite is expanded graphite. 8 . A lithium secondary battery comprising the composite active material for lithium secondary batteries described in claim 1 .
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for inserting or intercalating light metals · CPC title
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involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title
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