IP Library › Granted Patent US 7,670,582
Granted Patent B2
US 7,670,582 · App. 11/434,113 · Granted Mar 2, 2010

Mesoporous carbon and method of producing the same

Assignee: Samsung SDI Co., Ltd.
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Quick Facts
Patent No.
US 7,670,582
App. No.
11/434,113
Granted
Mar 2, 2010
Kind
B2
Abstract

Provided are a mesoporous carbon and a method of preparing the same, where the mesoporous carbon is prepared using phenanthrene as a carbon source and a mesoporous silica as a template. The mesoporous carbon has a significantly low plane resistance, which can be obtained without sacrificing other physical properties, and thus obtains a high conductivity and effectively transfers electrical energy. Accordingly, a fuel cell electrode or a fuel cell which is produced using the mesoporous carbon as a conductive material has high efficiency. Furthermore, the mesoporous carbon may be used in various electrochemical devices as a conductive material.

Claims (45)

1. A method of preparing a mesoporous carbon, the method comprising:

preparing a precursor mixture that contains 5-15 parts by weight of phenanthrene, 10-35 parts by weight of an acid, and 55-80 parts by weight of a solvent based on 100 parts by weight of the precursor mixture;

impregnating a mesoporous silica with the precursor mixture;

heat treating the impregnated mesoporous silica;

carbonizing the heat treated, impregnated mesoporous silica; and

removing the mesoporous silica from the carbonized, heat treated, impregnated mesoporous silica by using a solution that is capable of selectively dissolving the mesoporous silica only.

2. The method of claim 1 , wherein the acid is one of an organic acid or an inorganic acid.

3. The method of claim 1 , wherein the acid is a sulfuric acid, a nitric acid, a phosphoric acid, an organic acid thereof, a hydrochloric acid, or combinations thereof.

4. The method of claim 1 , wherein the solvent is water, acetone, methanol, ethanol, isopropylalcohol, n-propylalcohol, butylalcohol, dimethylacetamid(DMAc), dimethylformamid, dimethylsulfoxide (DMSO), N-methyl-2-pyrrolidone (NMP), tetrahydrofurane (THF), tetrabutylacetate, n-butylacetate, m-crezole, toluene, ethyleneglycol (EG), γ-butyrolactone, hexafluoroisopropanol (HFIP) or combinations thereof.

5. The method of claim 1 , wherein a weight ratio of the phenanthrene to the acid is in a range at or between 1:2.5 and 1:3.5.

6. The method of claim 1 , wherein the amount of the mesoporous silica is in a range at or between 5 and 15 parts by weight based on the 100 parts by weight of the precursor mixture.

7. The method of claim 1 , wherein the preparing of the impregnated mesoporous silica comprises drying the impregnated mesoporous silica.

8. The method of claim 1 , wherein the heat treatment is performed at a temperature at or between 50 and 250° C.

9. The method of claim 8 , wherein the heat treatment comprises a first heat treatment and a second heat treatment sequentially performed, wherein the first heat treatment is performed at a temperature at or between 50 and 150° C. and a second heat treatment is performed at a temperature at or between 150 and 250° C.

10. The method of claim 1 , wherein the preparing of the impregnated mesoporous silica comprises:

again impregnating the heat treated, impregnated mesoporous silica with the precursor mixtures;

again heat treating the impregnated, heat treated, impregnated mesoporous silica to prepare a repeatedly heat treated, impregnated mesoporous silica; and

repeating the again impregnating and the again heat treating zero to nine times.

11. The method of claim 1 , wherein the carbonization is performed at a temperature at or between 700 and 1500° C.

12. The method of claim 1 , wherein the mesoporous silica is removed using one of HF and NaOH solutions.

13. A method of producing a mesoporous carbon, the method comprising:

preparing a precursor mixture of 5-15 parts by weight of phenanthrene, 10-35 parts by weight of an acid, and 55-80 parts by weight of a solvent based on 100 parts by weight of the precursor mixture;

impregnating a mesoporous silica with the precursor mixture;

carbonizing the impregnated mesoporous silica to prepare mesoporous carbon; and

separating the mesoporous carbon from the mesoporous silica.

14. The method of producing a mesoporous carbon as claimed in claim 13 , further comprising:

heat treating the impregnated mesoporous silica prior to carbonizing to prepare a dried impregnated mesoporous silica; and

impregnating the dried impregnated mesoporous silica with the precursor mixture.

15. The method of claim 1 , wherein the precursor mixture consists of 5-15 parts by weight of phenanthrene, 10-35 parts by weight of an acid, and 55-80 parts by weight of a solvent based on 100 parts by weight of the precursor mixture.

16. The method of claim 13 , wherein the precursor mixture consists of 5-15 parts by weight of phenanthrene, 10-35 parts by weight of an acid, and 55-80 parts by weight of a solvent based on 100 parts by weight of the precursor mixture.

17. The method of claim 1 , further comprising:

after removing the mesoporous silica, impregnating the mesoporous carbon with a metal catalyst precursor; and

reducing the metal catalyst precursor to form a supported catalyst comprising metal catalyst particles supported by the mesoporous carbon.

18. The method of claim 17 , comprising:

applying the supported catalyst on an electrode support to form a first electrode; and

sequentially stacking the first electrode, an electrolyte membrane, and a second electrode.

19. The method of claim 13 , further comprising:

after removing the mesoporous silica, impregnating the mesoporous carbon with a metal catalyst precursor; and

reducing the metal catalyst precursor to form a supported catalyst comprising metal catalyst particles supported by the mesoporous carbon.

20. The method of claim 19 , comprising:

applying the supported catalyst on an electrode support to form a first electrode; and

sequentially stacking the first electrode, an electrolyte membrane, and a second electrode.

21. The method of claim 7 , further comprising cooling the dried impregnated mesoporous silica to room temperature before the heat treating of the impregnated mesoporous silica.

22. The method of claim 8 , wherein the heat treatment further comprises slowly heating the impregnated mesoporous silica from room temperature to the temperature at or between 50 and 250° C. over a period of about 1 hour and then maintaining such temperature for about 6 hours to prepare the heat treated, impregnated mesoporous silica.

23. The method of claim 11 , wherein the carbonization further comprises slowly heating the heat treated, impregnated mesoporous silica to the temperature at or between 700 and 1500° C. over a period of about 4 hours and then maintaining such temperature for about 2 hours to prepare the carbonized, heat treated, impregnated mesoporous silica.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2006
From: PAK, CHAN-HO; JOO, SANG-HOON; CHANG, HYUK; KIM, JI-MAN; LEE, HYUNG-IK
To: SAMSUNG SDI CO., LTD.
Reel/Frame 018024/0597 →
Priority Claims (1)
KR 10-2005-0041655 · May 18, 2005 · national
Continuity (1)
Related Publication 20060263288A1 · Nov 23, 2006