Compositions and methods for silicon containing dry anode films
Dry process electrode films, and energy storage devices incorporating the same are described, including a silicon active material. The films may be free standing anode electrode films. Also provided are methods for fabricating such anode electrode films.
1. A dry electrode film of an energy storage device, comprising:
a dry active material comprising a Group 14 active material and a graphite active material; and
a dry binder, wherein the dry electrode film is free-standing,
wherein the graphite active material comprises primary graphite (PG) particles and secondary graphite (SG) particles distinct from the PG particles.
2. The dry electrode film of claim 1 , wherein the dry electrode film comprises about 1 wt % to 30 wt % the Group 14 active material.
3. The dry electrode film of claim 1 , wherein the Group 14 active material comprises at least one of silicon and tin.
4. The dry electrode film of claim 1 , wherein the Group 14 active material is selected from at least one of pristine silicon, silicon oxide (SiO), a silicon-carbon composite, a silicon alloy and SiH.
5. The dry electrode film of claim 4 , wherein the silicon-carbon composite is selected from at least one of silicon graphene (SiC), tin graphene, silicon graphite (Si/C), tin graphite, silicon oxide graphene (SiOC) and a silicon oxide graphite (SiO/C).
6. The dry electrode film of claim 4 , wherein the silicon alloy is selected from at least one of Si—Al and Si—Sn.
7. The dry electrode film of claim 1 , wherein the Group 14 active material is prelithiated.
8. The dry electrode film of claim 1 , wherein the Group 14 active material comprises particles with a D 50 primary particle size of about 1 μm to about 10 μm.
9. The dry electrode film of claim 1 , wherein the graphite active material is selected from at least one of artificial graphite and natural graphite.
10. The dry electrode film of claim 1 , wherein the PG particles have a D 50 primary particle size of about 15 μm to about 30 μm.
11. The dry electrode film of claim 1 , wherein the SG particles have a D 50 secondary particle size of about 2 μm to about 10 μm.
12. The dry electrode film of claim 1 , wherein a weight ratio of the PG particles to the SG particles is 10:1 to 1:10.
13. The dry electrode film of claim 1 , wherein the dry binder comprises a dry fibrillizable binder.
14. The dry electrode film of claim 13 , wherein the dry fibrillizable binder comprises polytetrafluoroethylene (PTFE).
15. An electrode comprising the dry electrode film of claim 1 in contact with a current collector.
16. A lithium ion battery comprising the electrode of claim 15 .
17. A method of fabricating a dry electrode film of an energy storage device, comprising:
a first mixing step comprising mixing a dry Group 14 active material with a dry graphite material to form a dry active material mixture, the dry graphite material comprises primary graphite (PG) particles and secondary graphite (SG) particles distinct from the PG particles;
a second mixing step comprising mixing the dry active material mixture with a dry binder to form a dry electrode film mixture; and
calendering the dry electrode film mixture to form a free-standing dry electrode film.
18. The method of claim 17 , further comprising a premixing step comprising mixing the dry Group 14 active material with a first dry binder prior to mixing the dry Group 14 active material with the dry graphite material, wherein mixing the dry active material mixture with the dry binder comprises mixing the dry active material mixture with a second dry binder.
19. The method of claim 18 , wherein the first dry binder and the second dry binder are different binder materials.
20. The method of claim 18 , wherein at least one of the premixing step, the first mixing step, and the second mixing step comprises a nondestructive mixing process.
21. The method of claim 20 , wherein the nondestructive mixing processes comprises a resonant acoustic mixing process.
22. The method of claim 18 , wherein at least one of the premixing step, the first mixing step, and the second mixing step comprises a high shear process.
23. The method of claim 22 , wherein the high shear process comprises a jet milling process.
24. The dry electrode film of claim 1 , wherein the PG particles have a D 50 primary particle size of about 15 μm to about 40 μm.