Patent Application
20070059233
This application claims priority to and the benefit of Korean Patent Application No. 10-2005-0080605 filed in the Korean Intellectual Property Office on Aug. 31, 2005, the entire content of which is incorporated herein by reference.
1. Field of the Invention
The present invention relates to a carbon material that has a high specific surface area and high conductivity, and a method for preparing the carbon material.
2. Description of the Related Art
Carbon materials may be divided into amorphous carbon and crystalline carbon according to their crystalline properties.
Amorphous carbon has a low graphitization degree or shows few diffraction lines in X-ray diffraction. Examples of amorphous carbon include petroleum-based pitch, soft carbon produced by firing petroleum-based pitch, and hard carbon produced by firing a polymer resin such as phenol resin.
Examples of crystalline carbon include natural graphite and artificial graphite.
Since the above-mentioned carbon materials have high conductivity, they are used as conductive materials for batteries, and they have recently been used as a catalyst supporter for a fuel cell.
One embodiment of the present invention provides a carbon material having a high specific surface area and high conductivity.
Another embodiment of the present invention provides a method for preparing a carbon material having a high specific surface area and high conductivity.
According to an embodiment of the present invention, a porous carbon material includes pores on the surface and pores inside, where the pores are connected by channels.
According to an embodiment of the present invention, a method for preparing a carbon material includes: mixing a carbon precursor and a pore-forming material in a solvent to produce a mixture; spinning the mixture to produce a fiber; treating the fiber with an acid or an alkali to remove the pore-forming material from the fiber and produce a porous fiber; and heat treating the porous fiber.
An embodiment of the present invention will hereinafter be described in detail with reference to the accompanying drawings.
Carbon materials with conductive properties are generally used as conductive materials in various fields. The present invention provides a method for preparing a carbon material with improved conductivity.
The porous carbon material has an X-ray diffraction pattern measured using a CuKα ray. In an embodiment, an X-ray diffraction intensity 2θ of a (002) plane ranges from 3.3 Å to 4.5 Å, and is preferably from 3.3 Å to 4.0 Å, more preferably from 3.3 Å to 3.6 Å, and even more preferably from 3.3 Å to 3.5 Å at 260. When the X-ray diffraction intensity of the carbon material is less than 3.3 Å, the carbon material cannot perform the role of the carbon material adequately. When it exceeds 4.5 Å, the conductivity of the carbon material tends to deteriorate to an undesirable level.
The carbon material may further include a pore-forming material. In such an embodiment, the XRD 20 has a peak of the pore-forming material at 26° together with a carbon peak.
In an embodiment, the carbon material of the present invention may have a Raman strength ratio D/G (I1360/I1580) of the peak value at 1360 cm−1 to the peak value at 1580 cm−1 ranging from 0.1 to 2.0.
In an embodiment, the carbon material of the present invention may have a very high specific surface area, and may have a Brunauer, Emmett, Teller Method (BET) value, of less than or equal to 2,500 m2/g, and the value preferably ranges from 100 m2/g to 2,500 m2/g, and more preferably ranges from 100 m2/g to 2,000 m2/g. Exemplary uses of such a carbon material include use as an electric double layer capacitor (EDLC), as a catalyst supporter for a fuel cell, as an electrode conductive material for a rechargeable lithium battery, and as an adsorption agent.
In an embodiment, the average diameter of the carbon material may range from 100 nm to 30 μm. It is difficult to prepare a carbon material having an average diameter of less than 100 nm, and when the average diameter of the carbon material exceeds 30 μm, the surface area generally becomes too small to be useful.
The carbon material of an embodiment of the present invention may be provided as a fiber or an amorphous micro fine powder prepared by pulverizing the carbon fiber.
In one embodiment, the carbon material of the present invention can be prepared as follows.
A carbon precursor is mixed with a pore-forming material. The mixing may be performed in a solvent, or it may be performed after dissolving the carbon precursor in a solvent first to form a solution and then adding the pore-forming material to the carbon precursor solution.
Examples of the carbon precursor include polyacrylonitrile, polybenzimidazole, polyvinylalcohol, polyimide, coal pitch, petroleum pitch, mesophase pitch, furfuryl alcohol, furan, phenol, cellulose, sucrose, polyvinyl chloride, and tar.
The pore-forming material may be a material that is not dissolved in the solvent but that may be removed after a spinning process as set forth in further detail below. Examples of the pore-forming material include Si oxides, Al oxides, NaCl, and microemulsion polymer beads. For an embodiment using microemulsion polymer beads, the polymer may be a material that can be prepared in the form of a fine powder. Representative examples of the polymer are styrene-based materials such as styrene butadiene rubber.
In an embodiment, the average particle size of the pore-forming material is between 5 nm and 1 μm, which is larger than an average particle size of the carbon material.
The solvent is capable of dissolving the carbon precursor but not dissolving the pore-forming material. Examples of the solvent include organic solvents such as dimethylformaldehyde, N-methylpyrrolidone, tetrahydrofuran, and chloroform, and water.
In an embodiment, the mixing ratio of the carbon precursor to the pore-forming material may range from 99 to 5:1 to 95 by weight, and is preferably from 99 to 10:1 to 90 by weight, and more preferably from 70 to 30:30 to 70 by weight. When the carbon precursor is provided in a ratio greater than 99:1, the desired porosity may not be obtained. When the carbon precursor is provided in a ratio less than 5:1, the final product may not have the desired properties.
In an embodiment, a carbon precursor fiber is prepared by spinning the acquired mixture. The spinning process may be performed using an electrostatic spinning method, a melt spinning method, a melt blown carbon spinning method, an electrospray method, or a spray drying method.
In embodiments of the present invention, the carbon precursor may be selected to produce different shapes of the carbon precursor fiber which may include a spherical ball shape or a conventional long fiber shape.
The fiber may is treated with an acid or alkali to remove the pore-forming material. By removing the pore-forming material using an acid or alkali treatment, the pores are formed in the fiber. The pores are also connected to each other to form channels in order to produce a porous carbon fiber. An exemplary acid is hydrofluoric acid (HF), and an exemplary alkali is sodium hydroxide (NaOH). The acid or alkali treatment is performed by impregnating the fiber in an acid or alkali solution for from 1 to 48 hours.
Oxygen stabilization may be also performed prior to the acid or alkali treatment. Oxygen stabilization is a process of thermal oxidation treatment performed in the atmosphere at 200° C. to 400° C. for 1 to 24 hours. In the process, the molecular structure of the carbon precursor fiber molecules is stabilized by doping the carbon precursor fiber molecules with oxygen to maintain its fiber shape in the subsequent high-temperature heat treatment.
According to an embodiment of the invention, the acid or alkali treatment is followed by carbonization. The carbonization may be carried out in an inert gas at 800° C. to 1,500° C. for 1 to 12 hours. After the carbonization, a graphitization process may be further carried out. The graphitization process may be performed at 2,000° C. to 3,300° C. for 1 to 12 hours.
According to an embodiment, the resulting fiber-type carbon material may then be pulverized into a fine powder.
Hereinafter, examples and comparative examples of the present invention will be described. However, it is understood that the present invention is not limited by these examples.
A 10 wt % polyacrylonitrile solution was prepared by dissolving polyacrylonitrile in dimethylformaldehyde. Silica powder was added to the 10 wt % polyacrylonitrile solution in the same weight as the polyacrylonitrile. The solution was agitated, and carbon fiber was prepared by electrostatic spinning.
The prepared carbon fiber was stabilized using oxygen stabilization to produce a polyacrylonitrile structure. The oxygen stabilization was performed at about 250° C. for about 5 hours. The resultant material obtained from the oxygen stabilization was impregnated with HF acid and maintained for a day to remove silica from the carbon fiber. The carbon fiber with the silica removed was heated in a nitrogen atmosphere at 1,000° C. for one hour to produce porous carbon fiber.
The same process as in Example 1 was performed, except that 20 wt % polybenzimidazole solution was prepared by dissolving polybenzimidazole in dimethylacetamide and skipping the oxygen stabilization process.
The same process as in Example 1 was performed, except that a 20 wt % pitch solution was prepared by dissolving pitch in tetrahydrofuran.
The same process as in Example 1 was performed, except that a 20 wt % pitch solution was prepared by dissolving pitch in tetrahydrofuran, and silica powder was added to the pitch solution in an amount of 90 wt % of the pitch.
The same process as in Example 1 was performed, except that silica powder was added to pitch in the same weight and melt spinning was performed.
The same process as in Example 1 was performed except that silica powder was not added.
Since the carbon material of the present invention has a high specific surface area and high conductivity, it can be applied to diverse fields, such as an electric double layer capacitor (EDLC), a catalyst supporter of a fuel cell, an electrode conductive material of a rechargeable lithium battery, and an adsorption agent.
While this invention has been described in connection with what is presently considered to be practical exemplary embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2005-0080605 | Aug 2005 | KR | national |
