Distributing conductive carbon black on active material in lithium battery electrodes
US-2017098817-A1 · Apr 6, 2017 · US
US10141564B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10141564-B2 |
| Application number | US-201615087435-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 31, 2016 |
| Priority date | Mar 31, 2016 |
| Publication date | Nov 27, 2018 |
| Grant date | Nov 27, 2018 |
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A method is provided in which a lithium titanate precursor structure is subjected to element selective sputtering to form a lithium titanate structure including a lithium titanate core and a conformal layer on the lithium titanate core, wherein the conformal layer includes titanium oxide. A method of preparing an electrode for a lithium ion battery, wherein the electrode includes lithium titanate structures, is also provided.
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The invention claimed is: 1. A method, comprising: subjecting a lithium titanate precursor structure to element selective sputtering to form a lithium titanate structure including a lithium titanate core and a conformal layer on the lithium titanate core, wherein the conformal layer includes titanium oxide and the lithium titanate structure has a surface essentially devoid of lithium. 2. The method as defined in claim 1 wherein the element selective sputtering is performed by any of electron sputtering, plasma sputtering, laser sputtering, and X-ray sputtering. 3. The method as defined in claim 2 wherein the element selective sputtering is performed by plasma sputtering in a rotary plasma system. 4. The method as defined in claim 1 wherein the conformal layer has substantially no lithium. 5. The method as defined in claim 1 , further comprising heat-treating the lithium titanate structure. 6. The method as defined in claim 5 wherein the lithium titanate structure is heat-treated at a temperature ranging from about 400° C. to about 800° C. for a period of time ranging from about 1 hour to about 24 hours. 7. The method as defined in claim 1 , further comprising reducing gas production in a lithium ion battery by: incorporating a plurality of the lithium titanate structures into a negative electrode; incorporating the negative electrode into a lithium ion battery; and cycling the lithium ion battery. 8. A method, comprising: subjecting a lithium titanate precursor structure to element selective sputtering to form a lithium titanate structure including a lithium titanate core and a conformal layer on the lithium titanate core, wherein the conformal layer includes titanium oxide and the lithium titanate structure has a surface essentially devoid of lithium; incorporating a plurality of the lithium titanate structures into a negative electrode; incorporating the negative electrode into a lithium ion battery; and cycling the lithium ion battery. 9. The method as defined in claim 8 wherein the element selective sputtering is performed by any of electron sputtering, plasma sputtering, laser sputtering, and X-ray sputtering. 10. The method as defined in claim 9 wherein the element selective sputtering is performed by plasma sputtering in a rotary plasma system. 11. The method as defined in claim 8 wherein the conformal layer has substantially no lithium. 12. The method as defined in claim 8 , further comprising heat-treating the lithium titanate structure. 13. The method as defined in claim 12 wherein the lithium titanate structure is heat-treated at a temperature ranging from about 400° C. to about 800° C. for a period of time ranging from about 1 hour to about 24 hours. 14. The method as defined in claim 8 wherein: the lithium titanate structures are recovered from the element selective sputtering as lithium titanate powder; the powder is mixed with conductive carbon and polymer binder in a solvent to form a slurry; and the slurry is coated onto a current collector material and dried to form the negative electrode. 15. The method as defined in claim 8 wherein the negative electrode includes the lithium titanate structures in an amount ranging from about 70 wt. % to about 95 wt. % based on a composition of the negative electrode. 16. The method as defined in claim 8 wherein an average particle size of the lithium titanate structures is 5 μm or less and a surface area of the lithium titanate structures is less than 16 m 2 /g, and wherein the lithium titanate structures have a capacity ranging from about 150 mAh/g to about 170 mA/g. 17. The method as defined in claim 8 wherein the conformal layer has a thickness from about 0.5 nm to about 100 nm. 18. The method as defined in claim 8 wherein the lithium titanate precursor structure is subjected to element selective sputtering for a time of about 1 minute to about 10 minutes. 19. The method as defined in claim 1 wherein the conformal layer has a thickness from about 0.5 nm to about 100 nm. 20. The method as defined in claim 1 wherein the lithium titanate precursor structure is subjected to element selective sputtering for a time of about 1 minute to about 10 minutes.
as layered products · CPC title
of alkaline earth metals · CPC title
Submicrometer sized, i.e. from 0.1-1 micrometer · CPC title
Oxidic · 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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