Negative electrode active material for nonaqueous electrolyte secondary batteries, and nonaqueous electrolyte secondary battery
US-2022344650-A1 · Oct 27, 2022 · US
US12424619B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12424619-B2 |
| Application number | US-202318392517-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 21, 2023 |
| Priority date | Jan 11, 2021 |
| Publication date | Sep 23, 2025 |
| Grant date | Sep 23, 2025 |
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An alloy anode for a seawater based aqueous battery and a universal strategy for preparing anodes for use in seawater based aqueous batteries. Zn-M alloys (where M can be manganese or other transition metal) were prepared by co-electrodeposition in the presence of hydrogen bubble formation to produce a porous nanostructured alloy that can serve as an anode for a seawater based aqueous battery. Exemplary Zn—Mn alloy anodes achieved stability over thousands of cycles even under harsh electrochemical conditions, including testing in seawater-based aqueous electrolytes and using a high current density of 80 mA cm−2. The anode design strategy allows for the production of durable electrodes for aqueous batteries and other applications.
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What is claimed: 1. A method of making an anode for an aqueous battery, comprising: co-electrodepositing ions of zinc and ions of a transition metal on a substrate; and simultaneously facilitating hydrogen bubble evolution at a solid/liquid interface of the substrate during the co-electrodeposition of the ions of zinc and the ions of the transition metal to form a coating on the substrate comprising a porous alloy of zinc and the transition metal forming an anode comprising the coated substrate, wherein the coating remains dendrite-free at current densities of up to 80 mA cm −2 in an aqueous battery. 2. The method of claim 1 , wherein the co-electrodepositing the ions of zinc and the ions of the transition metal occurs at a current density of 0.3 A cm −2 . 3. The method of claim 1 , wherein the co-electrodepositing the ions of zinc and the ions of the transition metal is performed for a time period of between 10 and 40 minutes. 4. The method of claim 1 , wherein the transition metal comprises manganese. 5. The method of claim 1 , wherein the transition metal comprises copper. 6. The method of claim 1 , wherein the alloy comprises Zn 3 Mn. 7. A method of making an anode for an aqueous battery, comprising: co-electrodepositing ions of zinc and ions of a transition metal on a substrate; and simultaneously facilitating hydrogen bubble evolution at a solid/liquid interface of the substrate during the co-electrodeposition of the ions of zinc and the ions of the transition metal to form a coating on the substrate comprising a porous alloy of zinc and the transition metal forming an anode comprising the coated substrate, wherein the coating comprises a plurality of pores having a diameter between five nanometers and 50 micrometers or between 1 nanometer and 10 nanometers. 8. The method of claim 7 , wherein the co-electrodepositing the ions of zinc and the ions of the transition metal occurs at a current density of 0.3 A cm −2 . 9. The method of claim 7 , wherein the co-electrodepositing the ions of zinc and the ions of the transition metal is performed for a time period of between 10 and 40 minutes. 10. The method of claim 7 , wherein the transition metal comprises manganese. 11. The method of claim 7 , wherein the transition metal comprises copper. 12. The method of claim 7 , wherein the alloy comprises Zn 3 Mn. 13. A method of making an anode for an aqueous battery, comprising: co-electrodepositing ions of zinc and ions of either copper or manganese on a substrate; and simultaneously facilitating hydrogen bubble evolution at a solid/liquid interface of the substrate during the co-electrodeposition of the ions of zinc and the ions of either copper or manganese to form a coating on the substrate comprising a porous alloy of zinc and either copper or manganese forming an anode comprising the coated substrate. 14. The method of claim 13 , wherein the co-electrodepositing the ions occurs at a current density of 0.3 A cm −2 . 15. The method of claim 13 , wherein the co-electrodepositing the ions is performed for a time period of between 10 and 40 minutes. 16. The method of claim 13 , wherein the coating comprises a plurality of pores having a diameter between five nanometers and 50 micrometers. 17. The method of claim 13 , wherein the coating comprises a plurality of pores having a diameter between 1 nanometer and 10 nanometers. 18. The method of claim 13 , wherein the coating comprises a plurality of pores having a diameter from 1.76 nanometers to 5.8 nanometers. 19. The method of claim 13 , wherein the alloy comprises Zn 3 Mn.
Aqueous electrolytes · CPC title
Electrochemical coating; Electrochemical impregnation · CPC title
Negative electrodes · CPC title
Physical characteristics, e.g. porosity, surface area · CPC title
Accumulators not provided for in groups H01M10/05-H01M10/34 · CPC title
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