Sulfur-containing carbon nanotube arrays as electrodes
US-2018183041-A1 · Jun 28, 2018 · US
US11239465B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11239465-B2 |
| Application number | US-201716304806-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 26, 2017 |
| Priority date | Aug 11, 2016 |
| Publication date | Feb 1, 2022 |
| Grant date | Feb 1, 2022 |
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A sulfur-carbon composite including a carbon-based material of which surface is modified by acid treatment is provided, as well as a method for preparing the same, and a lithium-sulfur battery including the same. A sulfur-carbon composite suppresses polysulfide elution when used as a positive electrode active material of a lithium-sulfur battery by including a carbon-based material of which surface is modified to have a hydroxyl group and a carboxyl group capable of adsorbing polysulfide on the surface. Accordingly, capacity property and life time property of the battery may be enhanced. In addition, a surface of the carbon-based material can be modified using a simple process of treating with a mixed solution of nitric acid and sulfuric acid, and a content of functional groups on the surface can be controlled depending on a mixing ratio of the nitric acid and the sulfuric acid.
Opening claim text (preview).
The invention claimed is: 1. A lithium-sulfur battery comprising: a positive electrode comprising a sulfur-carbon composite as an active material; a negative electrode; and an electrolyte present therebetween, wherein the sulfur-carbon composite, comprises: a carbon-based material, wherein a surface of the carbon-based material is modified with a hydroxyl group and a carboxyl group; and sulfur, wherein the hydroxyl group and the carboxyl group are included in an amount of 7.3% to 10% by weight based on the total weight of the carbon-based material, and the sulfur-carbon composite has a core-shell structured coating form or a loaded form, wherein if the sulfur-carbon composite has a core-shell structured coating form, then the carbon-based material coats the sulfur, and wherein if the sulfur-carbon composite has a loaded form, then the carbon-based material is porous, and the sulfur is loaded inside the carbon-based material. 2. The lithium-sulfur battery of claim 1 , wherein the carbon-based material is at least one selected from the group consisting of carbon nanotubes, graphene, graphite, amorphous carbon, carbon black and active carbon. 3. The lithium-sulfur battery of claim 1 , wherein, in the sulfur-carbon composite, a ratio of the carbon-based material and the sulfur is from 1:1 to 1:9. 4. The lithium-sulfur battery of claim 1 , wherein the sulfur-carbon composite has a diameter of 0.1 μm to 20 μm. 5. A method for preparing the sulfur carbon composite the lithium-sulfur battery according to claim 1 , comprising assembling the positive electrode comprising the sulfur-carbon composite as an active material, the negative electrode and the electrolyte; wherein the sulfur-carbon composite is prepared by: S1) preparing a surface-modified carbon-based material by treating the carbon-based material with a mixed solution of nitric acid and sulfuric acid, or sulfuric acid under ultrasonication conditions; S2) drying the surface-modified carbon-based material; and S3) preparing the sulfur-carbon composite by compositing the dried surface-modified carbon-based material with sulfur (S 8 ) powder by ball mixing, wherein the surface-modified carbon-based material of S1 has the hydroxyl group and the carboxyl group on the surface thereof in an amount of 7.3% to 10% by weight based on the total weight of the carbon-based material. 6. The method according to claim 5 , wherein the mixed solution of S1 is a solution prepared by mixing a 70% by weight aqueous nitric acid solution and sulfuric acid in a volume ratio of 1:1 to 0:1. 7. The method according to claim 6 , wherein in S1, the mixed solution is added in 50 ml to 150 ml per 1 g of the carbon-based material. 8. The method according to claim 5 , wherein S1 includes ultrasonication at room temperature. 9. The method according to claim 5 , wherein S1 includes heating at a temperature of 90° C. to 120° C.
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