Passivated and/or protected silicon anode material slurries

Patent metadata

Field	Value
Publication number	US-11196039-B2
Application number	US-202016732587-A
Country	US
Kind code	B2
Filing date	Jan 2, 2020
Priority date	Jan 2, 2020
Publication date	Dec 7, 2021
Grant date	Dec 7, 2021

Abstract

Methods of preparing Si-based anode slurries and anode made thereof are provided. Methods comprise coating silicon particles within a size range of 300-700 nm by silver and/or tin particles within a size range of 20-500 nm, mixing the coated silicon particles with conductive additives and binders in a solvent to form anode slurry, and preparing an anode from the anode slurry. Alternatively or complementarily, silicon particles may be milled in an organic solvent, and, in the same organic solvent, coating agent(s), conductive additive(s) and binder(s) may be added to the milled silicon particles—to form the Si-based anode slurry. Alternatively or complementarily, milled silicon particles may be mixed, in a first organic solvent, with coating agent(s), conductive additive(s) and binder(s)—to form the Si-based anode slurry. Disclosed methods simplify the anode production process and provide equivalent or superior anodes.

First claim

We claim:

1. A method of preparing a Si-based anode slurry, the method comprising:
milling silicon particles in a first organic solvent that does not include water, to provide milled silicon particles;
following a completion of the milling, mixing the milled silicon particles, in the same first organic solvent and without adding any other solvent, with at least one coating agent, one or more added materials, wherein each of the one or more added materials differ from the first organic solvent, wherein the one or more added materials are configured to act as at least one conductive additive and at least one binder to form the Si-based anode slurry.

2. The method of claim 1 , wherein the first organic solvent comprises at least one of: butanol, dipropylene glycol methyl ether, NMP (N-methyl-2-pyrrolidone), DMF (dimethylformamide), ethanol, propanol, pentanol, hexanol and/or cyclohexanol.

3. The method of claim 1 , wherein the milled silicon particles are dried, following the mixing, in a second organic solvent.

4. The method of claim 3 , wherein the second organic solvent comprises at least one of: butanol, dipropylene glycol methyl ether and NMP (N-methyl-2-pyrrolidone).

5. The method of claim 3 , wherein the second organic solvent is the same as the first organic solvent.

6. The method of claim 3 , wherein the first and the second organic solvents comprise butanol.

7. The method of claim 1 , wherein the milled silicon particles have diameters between 100-1200 nm.

8. The method of claim 1 , wherein the milled silicon particles are passivated prior to the mixing.

9. The method of claim 1 , further comprising pre-mixing the milled silicon particles with at least one coating agent and/or at least one conductive additive.

10. The method of claim 9 , wherein the pre-mixing is further configured to passivate the milled silicon particles.

11. The method of claim 1 , further comprising adding tin particles to the first organic solvent.

12. The method of claim 11 , wherein the tin particles have diameters between 20-700 nm.

13. The method of claim 1 , wherein the at least one coating agent comprises graphite.

14. The method of claim 1 , wherein the at least one conductive additive comprises carbon, the at least one coating agent comprises graphite, and the at least one binder comprise is PAA-based.

15. The method of claim 1 , wherein the milled silicon particles have diameters between 100-500 nm.

16. The method according to claim 1 wherein the at least one coating agent is silver particles within a size range of 20-70 nm.

17. The method according to claim 1 wherein the at least one coating agent comprises silver particles and tin particles, the silver particles and the tin particles are within a size range of 20-70 nm.

18. The method according to claim 1 wherein the silicon particles are within a size range of between 100-500 nm, and the at least one coating agent comprises at least one of silver particles and tin particles, the at least one of silver particles and tin particles is within a size range of 20-70 nm.

19. The method according to claim 1 wherein the milling is wet ball milling.

Assignees

• Storedot Ltd

Inventors

• Sella Eran
• Matzner Eynat
• Kagan Maxim
• Ideses Yaron
• Koren Moria

Classifications

• H01M4/366

  as layered products · CPC title

• H01M4/386

  Silicon or alloys based on silicon · CPC title

• H01M4/625

  Carbon or graphite · CPC title

• H01M2004/027

  Negative electrodes · CPC title

• Y02E60/10

  Energy storage using batteries · CPC title