Cohesive assembly of carbon and its application

Patent metadata

Field	Value
Publication number	US-9617158-B2
Application number	US-201314106364-A
Country	US
Kind code	B2
Filing date	Dec 13, 2013
Priority date	Jun 20, 2011
Publication date	Apr 11, 2017
Grant date	Apr 11, 2017

Abstract

Cohesive carbon assemblies are prepared by obtaining a carbon starting material in the form of powder, particles, flakes, or loose agglomerates, dispersing the carbon in a selected organic solvent by mechanical mixing and/or sonication, and substantially removing the organic solvent, typically by evaporation, whereby the cohesive assembly of carbon is formed. The method is suitable for preparing free-standing, monolithic assemblies of carbon nanotubes in the form of films, wafers, or discs, having high carbon packing density and low electrical resistivity. The method is suitable for preparing adherent cohesive carbon assemblies on substrates comprising various materials. The assemblies have various potential applications, such as electrodes or current collectors in electrochemical capacitors, fuel cells, and batteries, or as electromagnetic interference shielding materials.

First claim

What is claimed:

1. A method of preparing a cohesive carbon assembly comprising:
(a) obtaining a carbon starting material in the form of powder, particles, flakes, or loose agglomerates,
(b) dispersing the carbon starting material in an organic solvent comprising toluene, o-dichlorobenzene (ODCB), isopropyl alcohol (IPA), N,N-dimethylformamide (DMF), benzene, chlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, bromobenzene, m-dibromobenzene, o-dibromobenzene, o-xylene, m-xylene, p-xylene, 1,2-dichloroethane, 1,2-dibromoethane, chloroform, formamide, N-methylformamide, N-vinylformamide, N-(phenethyl)formamide, N,N-diethylformamide, N,N-bis(1-methylethyl)formamide, dimethyl sulfoxide, or any combination thereof, in a prescribed ratio to form a dispersion,
(c) applying the dispersion to a hydrophobic surface, and
(d) substantially removing the organic solvent in a controlled manner to form a cohesive carbon assembly on the hydrophobic surface, wherein the hydrophobic surface comprises a dimethyl organosilane, a fluorinated dimethyl organosilane, a fluorinated polymer, or Teflon.

2. A method of preparing a cohesive carbon assembly comprising:
(a) obtaining a carbon starting material in the form of powder, particles, flakes, or loose agglomerates,
(b) dispersing the carbon starting material in an organic solvent comprising toluene, o-dichlorobenzene (ODCB), isopropyl alcohol (IPA), N,N-dimethylformamide (DMF), benzene, chlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, bromobenzene, m-dibromobenzene, o-dibromobenzene, o-xylene, m-xylene, p-xylene, 1,2-dichloroethane, 1,2-dibromoethane, chloroform, formamide, N-methylformamide, N-vinylformamide, N-(phenethyl)formamide, N,N-diethylformamide, N,N-bis(1-methylethyl)formamide, dimethyl sulfoxide, or any combination thereof, in a prescribed ratio to form a dispersion,
(c) applying the dispersion to a hydrophobic surface, and
(d) substantially removing the organic solvent in a controlled manner to form a cohesive carbon assembly on the hydrophobic surface, wherein the dispersion is applied to the hydrophobic surface by casting.

3. A method of preparing a cohesive carbon assembly comprising:
(a) obtaining a carbon starting material in the form of powder, particles, flakes, or loose agglomerates;
(b) dispersing the carbon starting material in an organic solvent comprising toluene, o-dichlorobenzene (ODCB), isopropyl alcohol (IPA), N,N-dimethylformamide (DMF), benzene, chlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, bromobenzene, m-dibromobenzene, o-dibromobenzene, o-xylene, m-xylene, p-xylene, 1,2-dichloroethane, 1,2-dibromoethane, chloroform, formamide, N-methylformamide, N-vinylformamide, N-(phenethyl)formamide, N,N-diethylformamide, N,N-bis(1-methylethyl) formamide, dimethyl sulfoxide, or any combination thereof in a prescribed ratio to form a dispersion;
(c) applying the dispersion to a hydrophilic surface; and
(d) substantially removing the organic solvent in a controlled manner to form a cohesive carbon assembly on the hydrophilic surface.

4. The method of claim 3 , wherein the hydrophilic surface is selected from the group consisting of metal, glass, silicon, plastic, ceramic, and any combinations thereof.

5. The method of claim 3 , wherein the hydrophilic surface is a metal substrate selected from the group consisting of aluminum, nickel, copper, gold, silver, platinum, and any combination thereof.

6. The method of claim 3 , wherein the dispersion is applied to the hydrophilic surface by spin-coating, dip-coating, flow-coating, spray coating, casting, or any combination thereof.

7. A cohesive carbon assembly on a metal substrate prepared by the method of claim 5 .

8. The cohesive carbon assembly on a metal substrate of claim 7 , wherein the carbon starting material is carbon nanotubes, and the organic solvent is o-dichlorobenzene, toluene, IPA, DMF, or any combination thereof.

9. The method of claim 3 , wherein the carbon starting material is a carbon material selected from the group consisting of carbon nanotubes, graphene, graphite, expanded graphite, exfoliated graphite, amorphous carbon, and any combination thereof.

10. The method of claim 9 , wherein the carbon nanotubes are single-walled carbon nanotubes, double-walled carbon nanotubes, multi-walled carbon nanotubes, or any combination thereof.

11. The method of claim 10 , wherein the Raman G/D ratio of the formed cohesive carbon assembly is about the same or greater than the Raman G/D ratio of the carbon starting material.

12. The method of claim 3 , wherein the organic solvent is toluene, ODCB, IPA, DMF, or any combination thereof.

13. The method of claim 3 , wherein the carbon starting material is dispersed in the organic solvent in the presence of mechanical agitation in step (b).

14. The method of claim 13 , wherein the mechanical agitation comprises sonication, mechanical stirring, or a combination thereof.

15. The method of claim 3 , wherein the carbon starting material is single-walled carbon nanotubes, the organic solvent is toluene, ODCB, IPA, DMF, or any combination thereof, and the ratio of carbon starting material and the organic solvent is about 0.1 to about 20 mg carbon per gram of the organic solvent.

16. The method of claim 3 , wherein the organic solvent is substantially free of a binding material.

17. The method of claim 3 , further comprising collecting the removed organic solvent.

18. The method of claim 1 , wherein the carbon starting material is a carbon material selected from the group consisting of carbon nanotubes, graphene, graphite, expanded graphite, exfoliated graphite, amorphous carbon, and any combination thereof.

19. The method of claim 18 , wherein the carbon nanotubes are single-walled carbon nanotubes, double-walled carbon nanotubes, multi-walled carbon nanotubes, or any combination thereof.

20. The method of claim 19 , wherein the Raman G/D ratio of the formed cohesive carbon assembly is about the same or greater than the Raman G/D ratio of the carbon starting material.

21. The method of claim 1 , wherein the organic solvent is toluene, ODCB, IPA, DMF, or any combination thereof.

22. The method of claim 1 , wherein the carbon starting material is dispersed in the organic solvent in the presence of mechanical agitation in step (b).

23. The method of claim 1 , wherein the mechanical agitation comprises sonication, mechanical stirring, or a combination thereof.

24. The method of claim 1 , wherein the carbon starting material is single-walled carbon nanotubes, the organic solvent is toluene, ODCB, IPA, DMF, or any combination thereof, and the ratio of carbon starting material and the organic solvent is about 0.1 to about 20 mg carbon per gram of the organic solvent.

25. The method of claim 1 , wherein the organic solvent is substantially free of a binding material.

26. The method of claim 2 , wherein the carbon starting material is a carbon material selected from the group consisting of carbon nanotubes, graphene, graphite, expanded graphite, exfoliated graphite, amorphous carbon, and any combination thereof.

27. The method of claim 26 , wherein the carbon nanotubes are single-walled carbon nanotubes, double-walled carbon nanotubes, multi-walled carbon nanotubes, or any combination thereof.

28. The method of claim 27 , wherein the Raman G/D ratio of the formed cohesive carbon assembly is about the s

Assignees

• Yazaki Corp

Inventors

• Raychaudhuri Satyabrata
• Yan Yongan
• Grigorian Leonid

Classifications

• C01B32/159

  single-walled · CPC title

• H01M4/587

  for inserting or intercalating light metals · CPC title

• H01M4/0471

  involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title

• Y10S977/892

  Liquid phase deposition · CPC title

• C01B32/05

  Preparation or purification of carbon not covered by groups C01B32/15, C01B32/20, C01B32/25, C01B32/30 · CPC title