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
US2016248084A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016248084-A1 |
| Application number | US-201514630406-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 24, 2015 |
| Priority date | Feb 24, 2015 |
| Publication date | Aug 25, 2016 |
| Grant date | — |
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The disclosure provides methods for producing uniformly sized lithium sulfide materials which are coated with one or more durable and conductive carbon shells that impede the polysulfide shuttle. The disclosure further provides for the carbon coated lithium sulfide materials made therefrom, and the use of these materials in lithium sulfide batteries.
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What is claimed is: 1 . A method to synthesize a Li 2 S core material having a uniform size, comprising: adding a first solution comprising elemental sulfur in a nonpolar organic solvent to a second solution comprising a strong lithium based reducing agent to make a reaction mixture; precipitating the Li 2 S core material from the reaction mixture by heating the reaction mixture at an elevated temperature for 2 to 30 minutes. 2 . The method of claim 1 , wherein the method further comprises: collecting the precipitated Li 2 S core material from the reaction mixture; washing the Li 2 S core material; and drying the Li 2 S core material. 3 . The method of claim 2 , wherein the nonpolar organic solvent is selected from pentane, cyclopentane, hexane, cyclohexane, benzene, toluene, chloroform, 1,4-dioxane, tetrahydrofuran (THF), and diethyl ether. 4 . The method of claim 3 , wherein precipitating the Li 2 S core material from the reaction mixture comprises heating the reaction mixture at an elevated temperature of between approximately 80° C. to 100° C. for 2 to 30 minutes. 5 . The method of claim 4 , wherein the strong lithium based reducing agent is selected from lithium triethylborohydride, n-butyl-lithium, and lithium aluminum hydride. 6 . The method of claim 5 wherein the first solution comprises 64 mg of sulfur dissolved in 6 mL of the nonpolar organic solvent. 7 . The method of claim 6 , wherein 6 mL of the first solution is added to a second solution which comprises 1.0 M lithium triethylborohydride in 4.2 mL of tetrahydrofuran. 8 . The method of claim 6 , wherein 3 mL of the first solution is added to a second solution which comprises 1.0 M lithium triethylborohydride in 4.2 mL of tetrahydrofuran. 9 . The method of claim 6 , wherein 3.5 mL of the first solution is added to a second solution which comprises 1.0 M lithium triethylborohydride in 4.2 mL of tetrahydrofuran. 10 . The method of claim 9 , wherein the reaction mixture is heated at about 90° C. 11 . The method of claim 10 , wherein the reaction mixture is heated for 7 minutes. 12 . The method of claim 10 , wherein the reaction mixture is heated for 10 minutes. 13 . The method of claim 12 , wherein the Li 2 S core material is substantially spherical in shape. 14 . The method of claim 13 , wherein the Li 2 S core material is uniformly size particles from 500 nm to 2 μm in diameter. 15 . The method of claim 14 , wherein the Li 2 S core material is 1 μm in diameter. 16 . A uniformly sized Li 2 S core material made by the method of claim 14 . 17 . A method of forming one or more durable and conductive carbon shells on a Li 2 S core material comprising: placing the uniformly sized Li 2 S core material of claim 16 under an atmosphere comprising a carbon based precursor compound and an inert gas; and pyrolyzing the precursor compound by heating at an elevated temperature for a period between 15 minutes to 3 hours. 18 . The method of claim 17 , wherein during the pyrolyzing step the Li 2 S core material was periodically ground to break up any agglomerations. 19 . The method of claim 18 , wherein the carbon based precursor compound is selected from methane, ethylene, acetylene, benzene, xylene, carbon monoxide, or combinations thereof. 20 . The method of claim 19 , wherein the carbon based precursor compound is acetylene. 21 . The method of claim 20 , wherein the inert gas is argon. 22 . The method of claim 21 , wherein the inert gas to the carbon based precursor compound is introduced at a Standard Cubic Centimeters per Minute (SCCM) flow rate ratio of 1:10 to 10:1. 23 . The method of claim 22 , wherein the carbon based precursor compound is pyrolyzed by heating at a temperature between 400° C. to 700° C. 24 . The method of claim 23 , wherein carbon based precursor compound is pyrolyzed by heating at 450° C. for 1.5 hours. 25 . A Li 2 S core material comprising one or more carbon shells (Li 2 S@C material) made by the method of claim 24 . 26 . An electrode comprising the Li 2 S@C material of claim 25 . 27 . A lithium/sulfur battery comprising the electrode of claim 26 .
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