Electromagnetic wave absorbing particles, electromagnetic wave absorbing particle dispersion liquid, electromagnetic wave absorbing particle dispersion, and electromagnetic wave absorbing laminate
US-2024052135-A1 · Feb 15, 2024 · US
US9997779B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9997779-B2 |
| Application number | US-201514972574-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 17, 2015 |
| Priority date | Jul 30, 2013 |
| Publication date | Jun 12, 2018 |
| Grant date | Jun 12, 2018 |
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In at least one embodiment, a rechargeable battery is provided comprising an anode having an active material including MSb 2 O 4 having a purity level of greater than 93 percent by weight, wherein M is a metal. The metal may have an oxidation state of 2+ and may include transition metals and/or alkali-earth metals. The anode active material may be synthesized using metal acetates or metal oxides. The synthesis may include heating at a first temperature to remove oxygen and water and reacting at a second temperature to form the MSb 2 O 4 structure, which may be a spinel crystal structure.
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What is claimed is: 1. A method of forming an anode active material comprising: mixing a metal oxide of the formula MO with antimony oxide, where M is one of Zn, Mn, or Mg and has an oxidation state of 2+; heating the mixture to a first temperature to remove oxygen and water from the mixture; and reacting the mixture at a second temperature to form MSb 2 O 4 . 2. The method of claim 1 , wherein the first temperature is from 80° C. to 200° C. 3. The method of claim 1 , wherein the mixture is reacted to form MSb 2 O 4 with a purity of at least 95 percent by weight. 4. The method of claim 1 , wherein the second temperature is from 450° C. to 650° C. 5. The method of claim 1 , wherein the mixture is held at the second temperature for 5 to 25 hours. 6. The method of claim 1 , wherein the mixing includes ball milling stoichiometric ratios of the MO and antimony oxide to form an intermixed powder. 7. The method of claim 1 , wherein the heating and reacting are done in an argon gas atmosphere. 8. The method of claim 1 , wherein the mixture is held at the first temperature for 10 minutes to 2 hours. 9. The method of claim 1 , wherein the mixing further includes mixing a metal oxide of the formula M2O, where M2 is different from M and has an oxidation state of 2+, and the reacting forms M x M2 y Sb 2 O 4 with x and y summing to 1. 10. The method of claim 9 , wherein the mixing further includes mixing a metal oxide of the formula M3O, where M3 is different from M and M2 and has an oxidation state of 2+, and the reacting forms M x M2 y M3 z Sb 2 O 4 with x, y, and z summing to 1. 11. The method of claim 1 , wherein the antimony oxide includes Sb 2 O 3 . 12. The method of claim 1 , wherein the second temperature is from 525° C. to 575° C. 13. A method of forming an anode active material comprising: mixing a metal (M) acetate or acetate hydrate with an antimony oxide, where M has an oxidation state of 2+and is one of Zn, Fe, Mg, or Mn; heating the mixture to a first temperature to remove oxygen and water from the mixture; and reacting the mixture at a second temperature to form MSb 2 O 4 . 14. The method of claim 13 , wherein the mixing includes ball milling stoichiometric ratios of the M acetate or acetate hydrate and antimony oxide to form an intermixed powder. 15. The method of claim 13 , further comprising forming an anode with the MSb 2 O 4 as an active material. 16. The method of claim 13 , wherein the second temperature is from 450° C. to 750° C. and the mixture is held at the second temperature for a period of 5 to 25 hours. 17. The method of claim 13 , wherein the mixing further includes mixing a metal (M2) acetate or acetate hydrate, where M2 is different from M and has an oxidation state of 2+, and the reacting forms M x M2 y Sb 2 O 4 with x and y summing to 1. 18. The method of claim 17 , wherein the mixing further includes mixing a metal (M3) acetate or acetate hydrate, where M3 is different from M and M2 and has an oxidation state of 2+, and the reacting forms M x M2 y M3 z Sb 2 O 4 with x, y, and z summing to 1. 19. The method of claim 13 , wherein the second temperature is from 575° C. to 625° C.
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