Resin composition for lithium ion cell positive electrode
US-2015017534-A1 · Jan 15, 2015 · US
US2017170481A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017170481-A1 |
| Application number | US-201515039266-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 26, 2015 |
| Priority date | Aug 26, 2014 |
| Publication date | Jun 15, 2017 |
| Grant date | — |
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The present invention relates to a surface coated positive electrode active material, a preparation method thereof, and a lithium secondary battery including the same. More specifically, it relates to a positive electrode active material of which surface is coated with a nanofilm including polyimide (PI) and carbon black, a preparation method thereof, and a lithium secondary battery including the same. The positive electrode active material of which surface is coated with the nanofilm according to the present invention is capable of preventing direct contact of the positive electrode active material with an electrolyte thereby suppressing a side reaction between the positive electrode active material and the electrolyte, and as a result, a lifespan property of a lithium secondary battery using a positive electrode including the same may be significantly improved, and particularly, a lifespan property and conductivity are capable of being enhanced under a high temperature and high voltage condition.
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1 . A surface coated positive electrode active material comprising: a positive electrode active material; and a nanofilm including polyimide (PI) and carbon black coated on a surface of the positive electrode active material, wherein the nanofilm includes the polyimide and the carbon black in a weight ratio of 1:0.5 to 1:5. 2 . The surface coated positive electrode active material of claim 1 , wherein an iodine number of the carbon black measured in accordance with the ASTM D-1510 is from 200 mg/g to 400 mg/g. 3 . The surface coated positive electrode active material of claim 1 , wherein an oil absorption number of the carbon black measured in accordance with the ASTM D-2414 is from 100 cc/100 g to 200 cc/100 g. 4 . The surface coated positive electrode active material of claim 1 , wherein a surface of the carbon black is hydrophobized. 5 . The surface coated positive electrode active material of claim 1 , wherein the carbon black has an average particle diameter of less than 1000 nm. 6 . The surface coated positive electrode active material of claim 1 , wherein the nanofilm has a thickness range from 1 nm to 200 nm. 7 . The surface coated positive electrode active material of claim 1 , wherein content of the carbon black is from 0.05% by weight to 5% by weight with respect to 100% by weight of the total surface coated positive electrode active material. 8 . The surface coated positive electrode active material of claim 1 , wherein the positive electrode active material is any one selected from the group consisting an oxide of the following Chemical Formula 1 to Chemical Formula 3, V 2 O 5 , TiS and MoS, or a mixture of two or more types among these: Li 1+x [Ni a Co b Mn c ]O 2 [Chemical Formula 1] (−0.5≦x≦0.6, 0≦a, b, c≦1, x+a+b+c=1); LiMn 2-x M x O 4 [Chemical Formula 2] (M is one or more elements selected from the group consisting of Ni, Co, Fe, P, S, Zr, Ti and Al, 0≦x≦2); Li 1+a Fe 1-x M x (PO 4-b )X b [Chemical Formula 3] (M is one or more elements selected from the group consisting of Al, Mg, Ni, Co, Mn, Ti, Ga, Cu, V, Nb, Zr, Ce, In, Zn and Y, X is one or more elements selected from the group consisting of F, S and N, −0.5≦a≦+0.5, 0≦x≦0.5, 0≦b≦0.1). 9 . The surface coated positive electrode active material of claim 8 , wherein the positive electrode active material is any one selected from the group consisting of LiCoO 2 , LiNiO 2 , LiMnO 2 , LiMn 2 O 4 , Li[Ni a Co b Mn c ]O 2 (0<a, b, c≦1, a+b+c=1) and LiFePO 4 , or a mixture of two or more types among these. 10 . A method for preparing a surface coated positive electrode active material comprising: preparing a mixed solution mixing and dispersing carbon black into an organic solvent diluting polyamic acid; forming a film including the polyamic acid and the carbon black on a surface of a positive electrode active material by dispersing the positive electrode active material into the mixed solution; and imidization reacting the film-formed positive electrode active material, wherein the carbon black is used in an amount of 0.05% by weight to 5% by weight based on 100% by weight of the positive electrode active material. 11 . The method for preparing a surface coated positive electrode active material of claim 10 , wherein the imidization reaction is carried out while raising the temperature up to 300° C. to 400° C. with a rate of 3° C./minute at intervals of 50° C. to 100° C. 12 . The method for preparing a surface coated positive electrode active material of claim 11 , wherein the imidization reaction further includes maintaining the temperature for 10 minutes to 120 minutes in a range of 300° C. to 400° C. after raising the temperature. 13 - 15 . (canceled) 16 . The method for preparing a surface coated positive electrode active material of claim 10 , wherein the polyamic acid is used in an amount from 0.1% by weight to 1% by weight based on 100% by weight of the organic solvent. 17 . The method for preparing a surface coated positive electrode active material of claim 10 , wherein the polyamic acid is prepared by reacting an aromatic anhydride and diamine in the same equivalent. 18 . The method for preparing a surface coated positive electrode active material of claim 17 , wherein the aromatic anhydride is any one selected from the group consisting of phthalic anhydride, pyromellitic dianhydride, 3,3′4,4′-biphenyltetracarboxylic dianhydride, 4′4-oxydiphthalic anhydride, 3,3′4,4′-benzophenonetetracarboxylic dianhydride, trimellitic ethylene glycol, 4,4′-(4′4-isopropylbiphenoxy)biphthalic anhydride and trimellitic anhydride, or a mixture of two or more types among these. 19 . The method for preparing a surface coated positive electrode active material of claim 17 , wherein the diamine is any one selected from the group consisting of 4,4′-oxydianiline, p-phenyl diamine, 2,2-bis(4-(4-aminophenoxy)-phenyl)propane, p-methylene dianiline, propyltetramethyldisiloxane, polyaromatic amine, 4,4′-diaminodiphenyl sulfone, 2,2′-bis(trifluoromethyl)-4,4′-diaminobiphenyl and 3,5-diamino-1,2,4-triazole, or a mixture of two or more types among these. 20 . The method for preparing a surface coated positive electrode active material of claim 10 , wherein the polyamic acid includes 4 component polyamic acid. 21 . The method for preparing a surface coated positive electrode active material of claim 20 , wherein the 4 component polyamic acid is polyamic acid including pyromellitic dianhydride, biphenyl dianhydride, phenylenediamine and oxydianiline. 22 . The method for preparing a surface coated positive electrode active material of claim 10 , wherein the organic solvent is selected from the group consisting of cyclohexane, carbon tetrachloride, chloroform, methylene chloride, dimethylformamide, dimethylacetamide and N-methylpyrrolidone, or a mixture of two or more types among these. 23 - 25 . (canceled)
of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy · CPC title
Carbon or graphite · 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
Li-accumulators · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
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