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
US9853284B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9853284-B2 |
| Application number | US-201715498113-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 26, 2017 |
| Priority date | Sep 30, 2011 |
| Publication date | Dec 26, 2017 |
| Grant date | Dec 26, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The loss of sulfur cathode material as a result of polysulfide dissolution causes significant capacity fading in rechargeable lithium/sulfur cells. Embodiments of the invention use a chemical approach to immobilize sulfur and lithium polysulfides via the reactive functional groups on graphene oxide. This approach obtains a uniform and thin (˜tens of nanometers) sulfur coating on graphene oxide sheets by a chemical reaction-deposition strategy and a subsequent low temperature thermal treatment process. Strong interaction between graphene oxide and sulfur or polysulfides demonstrate lithium/sulfur cells with a high reversible capacity of 950-1400 mAh g −1 , and stable cycling for more than 50 deep cycles at 0.1 C.
Opening claim text (preview).
What is claimed is: 1. A method of preparing a graphene oxide-sulfur (GO—S) nanocomposite comprising: providing a graphene oxide (GO) dispersion; adding a sodium polysulfide solution to the GO dispersion to form a blended solution; titrating the GO/sodium polysulfide blended solution into a HCOOH solution to form a precipitate; and heat treating, for a specified time and temperature, the precipitate in a sealed vessel utilizing a flowing gas at a specified gas flow rate. 2. The method of claim 1 , wherein the flowing gas is argon. 3. The method of claim 1 , wherein the gas flow rate is approximately 200 cc S −1 . 4. The method of claim 1 , wherein the temperature is approximately 155° C. 5. The method of claim 1 , wherein the time is approximately 12 hours. 6. The method of claim 1 , wherein the sodium polysulfide solution is added to the GO dispersion in the presence of 5 wt % surfactant cetyl trimethylammonium bromide (CTAB). 7. The method of claim 1 , wherein the sodium polysulfide solution is prepared by adding Na 2 S into a flask that has been filled with distilled water to form a Na 2 S solution, then elemental S is suspended in the Na 2 S solution, wherein the ratios of Na 2 S and elemental S, are adjusted to determine a value of x in Na 2 S x of the sodium polysulfide solution. 8. The method of claim 7 , wherein the GO after the heat treatment comprises approximately 50-90 wt % S. 9. The method of claim 8 , wherein the GO after the heat treatment comprises approximately 60-70 wt % S. 10. The method of claim 1 , wherein the graphene oxide (GO) dispersion is prepared by exfoliating GO from a graphite oxide. 11. The method of claim 10 , wherein the graphite oxide was prepared using a modified Hummers method.
Polyolefins · CPC title
Electric properties · CPC title
Chemistry & Metallurgy · mapped topic
obtained by TEM, STEM, STM or AFM · CPC title
obtained by SEM · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.