Graphite granules and their method of fabrication

Abstract

This invention discloses a type of improved graphite granules and the method for their fabrication. Each improved graphite granule includes an unimproved graphite granule whose electrochemical properties need to be improved, and a membrane of amorphous carbon enveloping said unimproved graphite granule forming the membrane. The thickness of said amorphous carbon membrane is between 0.05 μm and 1 μm. To fabricate said improved graphite granules, said unimproved graphite granules are immersed in a polymer surface modifying solution, stirred, separated, sifted, and then solidified and carbonized. Said improved graphite granules, when used as the negative electrode of a lithium ion rechargeable battery produces a battery with excellent high current characteristics, high reversible specific capacity, long cycle life, and can satisfy the performance demands on rechargeable batteries. The technology for the fabrication of this improved graphite granules is simple. Its cost of production is low. Therefore, it is easy to implement this technology for mass production.

Description

CROSS REFERENCE

[0001] This application claims priority from the following Chinese patent applications: “A Type of Improved Graphite and Its Method of Fabrication” filed on Aug. 16, 2003, having a Chinese Application No. 03140199.6; “The Fabrication Method of A Type of Improved Graphite” filed on May 16, 2003, having a Chinese Application No. 03126631.2; “Method for the Fabrication of a Carbon Containing Material for the Negative Electrode of A Type Lithium Ion Rechargeable Battery” filed on Jun. 20, 2003, having a Chinese Application No. 03 1 26961.3; and “A Type of Lithium Ion Rechargeable Battery” filed on Jul. 22, 2003, having a Chinese Application No. of 03132939.X. All of the above applications are incorporated herein by reference.

FIELD OF INVENTION

[0002] This invention relates to improved graphite granules and their method of fabrication. In particular, it relates to improved graphite granules used as the active material in the negative electrode of a battery.

BACKGROUND

[0003] With the rapid development of the electronic, communications, and information technology industries, market demands for power sources of electronic products have increased. During this last decade, lithium ion rechargeable batteries have seen rapid development and widespread use as a result of their excellent overall electrical properties.

[0004] Since electronic products, especially portable electronic products, are gradually becoming more complex and miniaturized, the demand for power sources of these products is also increasing. These power sources now require sufficiently high energy density per unit weight or volume, excellent high current characteristics, and suitable cycle life and reliable safety properties. Among these, the demand for power sources with dense energy capacity per body mass and high current characteristics is especially high.

[0005] Electrical and electronic products such as modem portable products, electrical tools, electric bicycles, and electric cars can have very high demand for electrical consumption per unit time. Examples include modem cell phones with color screens and with functions such as wireless internet connections and multimedia capabilities, notebook computers demanding the ability to use electricity for a long time, and, the starter mechanism for automobiles. For the lithium ion rechargeable batteries that are used as the power sources, these products high currents from these power sources. In other words, for many circumstances in recent years, greater demands are made on the high current characteristics of the lithium ion rechargeable batteries.

[0006] The high current characteristics of lithium ion rechargeable batteries mainly depend on the material for their positive and negative electrodes. Among these, the active material for the negative electrode is especially critical for improving the high current characteristics that are mainly dependent on the electrical conducting properties and the stability of the structure of the underlying active material.

[0007] At present, the most common active material for the negative electrode in a lithium ion rechargeable battery is a graphite type material as graphite has a lower discharging electricity platform and better cycle stability characteristics. Among these graphite type materials, natural graphite with a high degree of graphitization has higher specific capacity. However, in the process of attaching and detaching lithium, the structure of the crystallite in the natural graphite can easily be loosened or even destroyed resulting in the deterioration of the cycle and high current characteristics.

[0008] Chinese Patent CN1230159, entitled “Graphite Granules and Using Graphite Granules as the Negative Electrode for Lithium Rechargeable Batteries,” discloses a type of graphite granules. Lithium rechargeable batteries using those graphite granules have excellent rapid charge and discharge and cycle characteristics. The characteristics of this type of graphite granules are: lower directional property of the graphite granule resulting from the grouping or joining of many flat shaped granules together such that the directional position of the crystal surface of the neighboring flat shaped crystal granules are not parallel. The rate of attaching and detaching of the Li+ ion can then proceed more fully at a higher rate thereby obtaining a lithium rechargeable battery made from graphite with excellent high current characteristics. However, this method for fabricating graphite is actually is a type of man-made graphite treatment process that needs temperatures as high as 2800° C. for the graphitization treatment resulting in high cost and difficult technology, thus making it difficult to implement for industrial production as well.

[0009] Due to the limitation of the prior art, it is therefore desirable to have novel forms of improved graphite granules with better electrochemical properties such that batteries with negative electrodes made with these improved graphite granules -can have better performance characteristics. In addition, novel methods for the fabrication of such improved graphite granules are needed in order to produce said graphite granules in a low cost and simple manner.

SUMMARY OF INVENTION

[0010] An object of this invention is to provide improved graphite granules that have excellent electrochemical properties; such that when for negative electrodes in batteries such as lithium ion rechargeable batteries, it produces batteries with high current characteristics, higher reversible specific capacity, and longer cycle life.

[0011] Another object of this invention is to provide a method for fabricating said improved graphite granules with technology that is simple, of low cost and easy for mass production.

[0012] Briefly, the present invention relates to a type of improved graphite granules and the method of fabrication of said improved graphite granules. Each granule of said improved graphite granules comprises of an unimproved graphite granule, and a membrane of amorphous carbon enveloping said unimproved graphite granules to form the outer membrane. The thickness of the amorphous carbon membrane is between 0.05 μm and 1 μm. The unimproved graphite granule can be a natural, man-made, or even a modified graphite granule. To fabricate said improved graphite granules, the unimproved graphite granules is immersed in a surface modifying solution that is near saturation and the solution is produced by mixing a pre-determined amount of a surface modifying agent in a corresponding solvent. The unimproved graphite granules are stirred in the surface modifying solution at predetermined speed for a predetermined time period to form coated graphite granules. The coated graphite granules are then separated from the surface modifying solution, and heat to dry. The coated graphite granules are then sifted, and solidified in an inert environment at a predetermined temperature for a predetermined period of time. After solidification, said coated solidified graphite granules are carbonized in an inert environment at a predetermined temperature for a predetermined period of time to form the improved graphite granules.

[0013] The advantages of said improved graphite granules of the embodiments of this invention are: said improved graphite granules have excellent electrochemical properties, which, when used as the active material for the negative electrode in batteries (e.g. lithium ion batteries), produces batteries with excellent high current characteristics, higher reversible specific capacity, and longer cycle life that can satisfy the demands of practical application.

[0014] The advantages of said method for fabrication of said improved graphite granules of this invention is that the technology for the fabrication is simple and inexpensive, thus making it easy to use for commercial production.

DESCRIPTION OF DRAWINGS

[0015] FIG. 1 is the scanning electron micrograph of the unimproved graphite granules used in Embodiment 1.

[0016] FIG. 2 is the scanning electron micrograph of the improved graphite granules made by of Embodiment 1.

[0017] FIG. 3 is a graph of the result of the heat analysis (DSC—Differential Scanning Calorimetry and Thermal Gravimetric Analysis) of the improved graphite granules of Embodiment 1.

DETAILED DESCRIPTIONS OF THE PREFERRED EMBODIMENTS

[0018] An embodiment of said improved graphite granules can by made as follows. Immerse the unimproved graphite granules in a surface modifying solution that is almost saturated by mixing a pre-determined amount of a surface modifying agent in a corresponding solvent of said surface modifying solution. The surface modifying agent is one or more polymers selected from the group: coal pitch, coal tar, petroleum pitch, petroleum coke, benzene, naphthalene, copolymers of benzene and naphthalene copolymer, petroleum wax and petroleum resin. The corresponding solvent for the surface modifying agent is an organic solvent selected from the following group: acetone, anhydrous ethanol, N-methyl pyrrolidone, chloroform, tetrahydrofuran, carbon tetrachloride, and cyclohexane. The average granule diameter of said unimproved graphite granules is between 7 μm and 35 μm. 1.5 liters to 3 liters of said surface modifying solution is used for every 1 kg of unimproved graphite granules. The unimproved graphite granules are stirred in said surface modifying solution at 100 rpm to 2000 rpm for 0.5 hours to 10 hours to form coated graphite granules until the surface modifying solution is fully in contact with the surface of said unimproved core material of graphite granules. Then, the coated graphite granules are separated from the surface modifying solution, and heat to dry the excess surface correcting solution. The coated graphite granules is then sifted and solidified in an inert environment at 200° C. to 600° C. for 0.2 hours to 12 hours. During solidification, the temperature is increased at a rate of 0.5° C./min to 35° C./min. Lastly, said coated graphite is carbonized in an inert environment at 750° C. to 1300° C. for 1 hour to 24 hours to form said improved graphite granules. During carbonization, the rate of increase in temperature for carbonization is 0.1° C./min to 30° C./min.

[0019] The unimproved graphite granules that form the core of said improved graphite granules can be natural, man-made graphite, or graphite modified by other means.

[0020] The specifications for one of the preferred embodiments of said fabrication method are:

[0021] Said solidification proceeds at 300° C. to 500° C. where the temperature is held for 0.5 hours to 3 hours and the rate of increase in temperature is 5° C./min to 20° C./min.

[0022] Said carbonization proceeds at 800° C. to 1200° C. where the temperature is held for 2 hours to 10 hours and the rate of increase in temperature for said carbonization is 3° C./min to 20° C./min.

[0023] In said carbonization step, the rate of decrease in temperature is 5° C./min to 15° C./min.

[0024] This invention also discloses improved graphite granules where each improved graphite granule includes an unimproved graphite granule and a membrane of amorphous carbon enveloping said unimproved graphite granules forming the outer membrane. The thickness of said amorphous carbon membrane is between 0.05 μm and 1 μm.

[0025] In the embodiments of this invention, the crystallite interlayer spacing in said improved graphite granules, d002, is between 0.335 nm and 0.340 nm. The specific surface area of said improved graphite granules is between 1.3 m2/g and 4.2 m2/g. The average granule diameter of the improved graphite granules is between 8 μm and 35 μm.

[0026] Further preferable specifications of the embodiments for said improved graphite granules are: the crystallite interlayer spacing in said improved graphite granules, d002, is between 0.335 nm and 0.338 nm. The specific surface area of said improved graphite granules is 1.8 m2/g and 3.5 m2/g and the average granule diameter of said improved graphite granules is between 10 μm and 20 μm.

[0027] The average granule diameter is the D50 measured by using a particle size analyzer. The crystallite interlayer spacing, d002, is measured using an X-ray diffractometer. The specific area of the surface is obtained using the single-point BET method.

[0028] The amorphous carbon membrane that coats the surface of the core material of graphite granules can improve the surface morphology of the granule, lowering its specific surface area. When the improved graphite granules are used as active material for the negative electrode of lithium ion batteries, the improved surface morphology raises the compatibility between the granules and the electrical conducting solution in the battery, resulting in the improvement of the initial charge and discharge efficiency of the battery. The improve surface morphology can also compensate for the weakness of the boundary edges of the crystallite structure of the core material of unimproved graphite granules, lowering the directional characteristics of the crystallite, stabilizing the graphite crystallite, and further improving its electrical conduction and the uniformity of the electron distribution of the electrode. This results in raising the electrical mobility rate electrical migration rate of the Li+ s in the battery and increases the stability of the structure of the negative electrode during the process of charging and discharging and resulting in improving the high current characteristics.

[0029] In the embodiments of this invention, the average granule diameter of said improved graphite granules is between 8 μm and 35 μm. The preferred specification is between 10 μm and 20 μm. If the average granule diameter of the improved graphite granules is too small, then the improved graphite granules are too small and the specific surface area is too large. This can damage the reversibility discharge capacity in a battery with the negative electrode made from the improved graphite granules. If the average granule diameter is too large, then the distance between the improved graphite granule edge and the center is so large that the Li+ in the battery cannot fully attach and detach making the improved graphite granules not suitable as the active material for negative electrode of the lithium ion rechargeable battery.

[0030] In the embodiments of this invention, the crystallite interlayer spacing, d002, is between 0.335 nm and 0.340 nm. The preferred size is between 0.335 nm and 0.338 nm. The crystallite interlayer spacing, d002, of the graphite granules is mainly determined by the source of the unimproved graphite granules, i.e., whether said unimproved granules are made from natural graphite or man-made graphite with a high degree of graphitization. The surface modifying process does not greatly affect the crystallite layer interspacing, d002. Usually, the nearer the crystallite interlayer spacing, d002, is to the ideal graphite value of 0.3354 nm, the higher the degree of graphitization. The higher the degree of graphitzation, the higher is the reversible specific capacity of a battery made with the improved graphite granules as the active material for its negative electrode. Therefore, in order to assure that the discharge capacity of the lithium ion rechargeable battery, natural or man-made graphite with a high degree of graphitzation should be used as the source for the unimproved graphite granules.

[0031] In the embodiments of this invention, the specific surface area of the improved graphite granules is between 1.3 m2/g and 4.2 m2/g. A preferred specification is between 1.8 m2/g and 3.5 m2/g. The improved graphite that has undergone the surface modifying treatment effectively decreases the specific surface area of the unimproved graphite granules. (The specific surface area of the source for the unimproved graphite granules is approximately 5 m2/g.). The size of the specific surface area of the material for the negative electrode directly affects the amount of the irreversible capacity used by the SEI membrane that is formed during the initial charging process in a lithium ion battery. This directly affects the initial charge and discharge efficiency and the size of the reversible specific capacity of the battery. Therefore, in order to assure the highest reversible specific capacity in a battery, it is better to fabricate the negative electrode from a material that has as small a specific surface area as possible.

[0032] The thickness of the membrane of said amorphous carbon is between 0.05 μm and 1 μm. The thickness of the membrane of said amorphous carbon is calculated according to the volume of coating of the surface modifying agent on the surface of the graphite core material granules and the average diameter of the core material of graphite granules, the DSC (Differential Scanning Calorimetry and Thermal Gravimetric Analysis) graph of the improved graphite granules can be obtained by heat analysis.

[0033] In another embodiment of this invention, the improved graphite granules are obtained by treating and modifying the surfaces of natural or man-made graphite granules with high graphitization levels. The fabrication method is as follows: Immerse unimproved graphite granules in a polymer surface modifying solution that is saturated or almost saturated and prepared by dissolving a polymer surface modifying agent in its corresponding organic solvent; Stir at a speed of 100 rpm to 2000 rpm for 0.5 hours to 10 hours such that the surface modifying solution is fully in contact with the surface of said unimproved graphite granules to from coated graphite granules; Separate the coated graphite granules by filtering or centrifuge; Heat to dry excess surface modifying solution; Sift; Solidify and also carbonize the dried coated graphite granules in an inert environment. A crushing process is not needed to obtain the improved graphite granules in the embodiments of this invention.

[0034] In the embodiments of the fabrication method of this improved graphite granules, said surface modifying agent is a type of organic matter with high carbon content. It is one or more polymers selected from the following group: coal pitch, coal tar, petroleum pitch, petroleum coke, benzene, naphthalene, copolymers of benzene and naphthalene, petroleum wax, and petroleum resin. The corresponding solvent is an organic solvent selected from the following group: acetone, anhydrous ethanol, N-methyl pyrrolidone, chloroform, tetrahydrofuran, carbon tetrachloride, and cyclohexane.

[0035] In the fabrication method of said improved graphite granules of the embodiments of said invention, the effect of the surface modification is related to the stirring time in above described stirring step. If the stirring time is too long, the thickness of the organic membrane that is adhering to the surface of the core material of unimproved graphite granules is too thick and will affect the properties of the improved graphite granules such as lowering the initial charge/discharge efficiency the battery whose negative electrode is made from the improved graphite granules. If the stirring time is too short, then the membrane of organic material membrane adhering to the surface of the core material of unimproved graphite granule is too thin and not uniformly distributed on the surface of the core material of unimproved graphite granules thus affecting the properties of the improved graphite granules.

[0036] In the solidifying step of the fabrication method of the improved graphite granules of the embodiments of this invention, increase the temperature at the rate of 0.5° C./min to 35° C./min to reach the desired temperature for solidification. A better range is 5° C./min to 20° C./min. The solidification temperature is 200° C. to 600° C. A better range is 300° C. to 500° C. Hold the temperature for 0.2 hours to 12 hours. A better time is 0.5 hours to 3 hours. After solidification, increase the temperature at a rate of 0.1° C./min to 30° C./min to reach the desired temperature for carbonization. A better rate of increase is 3° C./min to 20° C./min. The carbonization temperature is 750° C. to 1300° C. A better range is 800° C. to 1200° C. Hold the temperature for 1 to 24 hours. A better time is 2 hours to 10 hours. After carbonization, lower the temperature at the rate of 1° C./min to 20° C./min. A better decrease rate is 5° C./min to 15° C./min. The temperature can also be lowered naturally.

[0037] If the carbonization temperature is too low, such as lower than 750° C., then the carbonization of the organic layer on the surface of the core material of unimproved graphite granule is insufficient to form a stable compact carbon membrane and minute pores may even be formed. A structure with minute holes and larger specific surface area may even be formed. This kind of structure does not improve the surface morphology. If the carbonization temperature is too high, such as higher than the 1200° C., there is no apparent improvement in the results. However, the energy usage is increased making this method uneconomical. The time for holding the temperature should not be too short or the carbonization will be insufficient to form a stable carbon membrane. If the temperature is held too long, then energy usage is increased and the method becomes uneconomical.

[0038] In the fabrication method of the improved graphite granules of the embodiments of said invention, furnaces such as: box-style electrical resistance furnace, tubular furnace, push pull tunnel furnace, or rotating tunnel furnace can be used for solidification and carbonization as long as the furnace can reach desired temperature, can be sealed and is able to aerate the inert environment. Said inert environment can be a mixture of one or more of the following: argon gas, helium gas, and nitrogen gas.

[0039] The embodiments discussed below provide further details about this invention. To test the electrochemical properties of the improved graphite granules made by the embodiments discussed below, the improved graphite granules is made into the active ingredient of the negative electrode of lithium ion rechargeable batteries and the performances of these batteries are tested against batteries with negative electrodes made from the unimproved graphite granules of two comparison examples discussed below.

[0040] To make the negative electrodes from the improved or improved graphite granules in the embodiments and comparison examples discussed below, add binder and de-ionized water to said improved or unimproved graphite granule. Stir the resultant mixture, then coat, heat to dry and compress to form the negative electrode plate.

[0041] To make lithium ion rechargeable batteries with existing battery technology using the negative electrodes made as described above, use LiCoO2 as the active material for the positive electrode, corresponding conducting agent, binder, and LiPF6 as the electrolyte salt. The solvent for the electrolyte solution is a mixture of the following organic solvent: ethylene carbonate, ethyl methyl carbonate, diethyl carbonate. The concentration is 1 mole per liter. The separator is polyethylene and polypropylene multiple separator.

Embodiment 1

[0042] The following steps comprise the method for the fabrication of Embodiment 1:

[0043] Dissolve 8 g of petroleum coke in carbon tetrachloride to formulate 200 ml of 4% surface modifying solution;

[0044] Immerse 100 g of unimproved dried natural graphite granules and immerse in the surface modifying agent organic solution;

[0045] Stir at 300 rpm speed for 1 hour to form a thin layer of surface modifying membrane on the surface of the unimproved graphite granules;

[0046] Filter the coated graphite granules that are obtained; Heat to dry and sift with 300 mesh;

[0047] Put sifted coated graphite granules into sealed tubular high temperature furnace. Pass highly pure nitrogen at 10 liters/min of flow volume and increase the temperature at 15° C./min to 400° C. and hold the temperature for 1 hour; and

[0048] Increase the temperature at 10° C./min to 1000° C. and hold the temperature for 3 hours. Lower the temperature naturally to room temperature to obtain the improved graphite granules with surface modification.

[0049] Using D50, the average granule diameter of said improved graphite granules of Embodiment is shown to be 13.8 μm. Its crystallite interlayer spacing, d002, is 0.3365 nm, and its specific surface area is 2.8 m2/g.

Embodiment 2

[0050] In this embodiment, the surface modifying solution is a 5% coal pitch in tetrahydrofuran. Other than this, all other steps and specifications are the same as Embodiment 1. The improved graphite granule obtained from this embodiment has fundamentally the same average granule diameter D50 and crystallite interlayer spacing, d002. as the improved graphite granules of Embodiment 1.

Embodiment 3

[0051] In this embodiment, the surface modifying solution is a 3% petroleum pitch and chloroform solution. Other than this all other steps and specifications are the same as Embodiment 1. The improved graphite granules obtained from this embodiment has fundamentally the same average granule diameter D50 and crystallite interlayer spacing, d002, as the improved graphite granules of Embodiment 1.

Embodiment 4

[0052] This Embodiment uses a carbonization temperature of 800° C. Other than this, all other steps and specifications are the same as Embodiment 1. The improved graphite granules obtained from this embodiment has fundamentally the same average granule diameter D50 and crystallite interlayer spacing, d002, as the improved graphite granules in Embodiment 1.

Embodiment 5

[0053] This Embodiment uses a carbonization temperature of 1200° C. Other than this, all other steps and specifications are the same as Embodiment 1. The improved graphite granules obtained from this embodiment has fundamentally the same average granule diameter D50 and crystallite interlayer spacing, d002, as the improved graphite granules in Embodiment 1.

Embodiment 6

[0054] This Embodiment uses natural graphite with smaller average granule diameter as the unimproved graphite granules. Other than this, all other steps and specifications are the same as Embodiment 1. The improved graphite granules obtained from this Embodiment has an average granule diameter D50 of 8.2 μm and its crystallite interlayer spacing, d002, is fundamentally the same as the improved graphite granules in Embodiment 1.

Embodiment 7

[0055] This Embodiment uses natural graphite with larger average granule diameter as the unimproved graphite granules. Other than this, all other steps and specifications are the same as Embodiment 1. The improved graphite granules obtained from this Embodiment has an average granule diameter D50 of 35.0 μm and its crystallite interlayer spacing, d002, is fundamentally the same as the improved graphite granules in Embodiment 1

[0056] In order to investigate the electrochemical properties of the embodiments of said invention in Embodiments 1 though 7, the properties of batteries whose negative electrodes are made from above described embodiments are compared with the properties of batteries whose negative electrodes are made from graphite granules that has not undergone the improvement described in the embodiments of this invention. The examples of unimproved graphite granules that are used for comparison includes the following:

COMPARISON EXAMPLE 1

[0057] Directly use the natural graphite granules of Embodiment 1 as the active material for the negative electrode to make battery. Other than that, all other steps and processes for fabricating the lithium ion battery remains the same as Embodiment 1.

COMPARISON EXAMPLE 2

[0058] This Embodiment uses a carbonization temperature of 700° C., holding the temperature for 5 hours. Therefore, the graphite granules in this comparison example are modified but are not improved. Other than that, all other steps and specifications remains the same as Embodiment 1.

[0059] The following operating characteristics of the batteries made from the Embodiments 1 through 7 and Comparison Examples 1 and 2 are measured and compared:

[0060] For high current characteristics, C3C/C0.5C, the ratio of discharging capacity using 3C of current to discharge from 4.2V to 3.0V and from 0.5C of current from 4.2V to 3.0V;

[0061] For high current characteristics, C2C/C0.5C, the ratio of discharging capacity using 2C of current to discharge from 4.2V to 3.0V and from 0.5C of current from 4.2V to 3.0V.

[0062] Reversible specific capacity, the discharge capacity of the initial discharge of from 0.1C of current from 4.2V to 3.0V after it had been initially charged with 0.1C of current to 4.2V)/the weight of the active material of the negative electrode; and

[0063] Cycle life; a cycle is the process of using 1C of electricity to charge to 4.2V and then to discharge the electricity to 3.0V. For each cycle, the discharge capacity is the capacity of that cycle. In the measuring of electrochemical properties of the embodiments of this invention, the cycle life is the number of cycles its takes for the discharge capacity of that cycle to reach 80% of the discharge capacity of the initial cycle.

[0064] The methodology for obtaining the electrochemical properties of the improved graphite granules in Embodiments 1 to 7 and Comparison Examples 1 and 2 are as follows:

[0065] The specific surface area is obtained using the single-point BET method.

[0066] The conditions for heat analysis testing are:

[0067] Instrument model and number of instrument used are: NETSCH STA 449C

[0068] The method used is the Differential Scanning Calorimetry and Thermal Gravimetric analysis, that is, DSC-TG

[0069] The weight of the sample of unimproved graphite granules is 6.824 mg

[0070] The crucible material is: Al2O3

[0071] The furnace environment is gas with flow speed of 25 Nml/min

[0072] The temperature of the furnace environment is to start from toom temperature and increase the temperature at 10° C./min to 1000° C.

[0073] The results of the testing of the above described electrochemical characteristics are shown in the following table:

		High Current	Reversible
	Specific	Characteristics	Specific
	Surface Area	C3C/	C2C/	Capacity	Cycle Life
Number	m2/g	C0.5C	C0.5C	mAh/g	Span
Embodiment 1	1.8	86.2	96.4	340	280
Embodiment 2	2.8	86.1	96.9	351	312
Embodiment 3	2.6	82.6	96.4	338	264
Embodiment 4	3.5	80.5	95.8	330	320
Embodiment 5	2.3	88.4	96.7	350	277
Embodiment 6	4.2	82.8	95.1	332	320
Embodiment 7	1.5	80.2	94.6	340	245
Comparison	5.7	57.4	88.1	337	76
Example 1
Comparison	4.8	72.2	94.5	332	253
Example 2

[0074] The above table shows that the specific surface area of the improved graphite granules from Embodiments 1 to 7 is smaller that those of Comparison Examples 1 to 2. The batteries made from Embodiment 1 through 7 has excellent high current characteristics, higher reversible specific capacity and longer cycle life.

[0075] With respect to the drawings, FIG. 1 is the scanning electron micrograph of the unimproved graphite granules used in Embodiment 1. FIG. 2 is the scanning electron micrograph of the improved graphite granules made by of Embodiment 1. The micrographs of FIGS. 1 and 2 are made using the equipment from JOEL equipment with model number JSM-5160. The micrograph shows that the shape of the improved graphite granules is potato shaped or spherical shaped.

[0076] FIG. 3 is the result of the heat analysis (DSC—Differential Scanning Calorimetry and Thermal Gravimetric Analysis) of the improved graphite granules in Embodiment 1. The peak corresponding to 592.1° C. is the amorphous carbon membrane. The peak corresponding to 821.2° C. is the unimproved graphite granules core material. Under customary conditions, the peak corresponding to 500° C. to 650° C. should be the amorphous carbon membrane. The peak corresponding to 750° C. to 850° C. should be the graphite granules core material.

[0077] The detailed data relating to the complex peak of the unimproved graphite granules core material are listed below:

Area:   15600 J/g
Peak:   821.2° C.
Onset:  727.5° C.
End:    874.7° C.
Width:  122.8° C. (37.000%)
Height: 23.2 mW/mg.

[0078] The detailed data relating to the complex peak of the amorphous carbon membrane are listed below:

Area:   117.2 J/g
Peak:   592.1° C.
Onset:  564.1° C.
End:    617.1° C.
Width:  40.0° C. (37.000%)
Height: 0.5611 mW/mg.

[0079] The improved graphite granules in the embodiments of this invention have excellent high current characteristics with great practical potential and superiority in conditions that require a high demand for rapid charging and discharging. Such active material for the negative electrode retains higher reversible specific capacity, and possesses longer cycle life, is stable and reliable and can satisfy the demands of practical applications. The fabrication method of this improved graphite granules in the embodiments of this invention has simple technology, is low cost, and easy for industrial production.

[0080] While the present invention has been described with reference to certain preferred embodiments, it is to be understood that the present invention is not limited to such specific embodiments. Rather, it is the inventor's contention that the invention be understood and construed in its broadest meaning as reflected by the following claims. Thus, these claims are to be understood as incorporating and not only the preferred embodiments described herein but all those other and further alterations and modifications as would be apparent to those of ordinary skilled in the art.

Claims

1. A method for fabricating improved graphite granules, comprising the steps of: preparing a surface modifying solution by mixing a pre-determined amount of a surface modifying agent in a corresponding solvent of said surface modifying agent; immersing unimproved graphite granules in said surface modifying solution; stirring said unimproved graphite granules in said surface modifying solution at predetermined speed for a predetermined time period to form coated graphite granules; separating said coated graphite granules from said surface modifying solution; heating to dry said coated graphite granules; sifting said coated graphite granules; solidifying said coated graphite granules in an inert environment at a predetermined temperature for a predetermined period of time; and carbonizing said solidified graphite in an inert environment at a predetermined temperature for a predetermined period of time to form said improved graphite granules.

2. The method of claim 1 wherein the average granule diameter of said unimproved graphite granules is between 7 μm and 35 μm.

3. The method of claim 1 wherein 1.5 liters to 3 liters of said surface modifying solution is used for every 1 kg of said unimproved graphite granules.

4. The method of claim 1 wherein said surface modifying agent is one or more polymers selected from the group consisting of: coal pitch, coal tar, petroleum pitch, petroleum coke, benzene, naphthalene, copolymers of benzene and naphthalene copolymer, petroleum wax and petroleum resin.

5. The method of claim 1 wherein said corresponding solvent is an organic solvent selected from the group consisting of: acetone, anhydrous ethanol, N-methyl pyrrolidone, chloroform, tetrahydrofuran, carbon tetrachloride, and cyclohexane.

6. The method of claim 1 wherein said unimproved graphite granules is stirred in said surface modifying solution at 100 rpm to 2000 rpm for 0.5 hours to 10 hours.

7. The method in claim 1 wherein said in solidifying step, solidification proceeds at 200° C. to 600° C. for 0.2 hour to 12 hours.

8. The method of claim 1 wherein the rate of increase in temperature in said solidifying step is 0.5° C./min to 35° C./min.

9. The method of claim 1 wherein in said carbonizing step, carbonizing proceeds at 750° C. to 1300° C. for 1 hour to 24 hours.

10. The method of claim 1 wherein the rate of increase in temperature for said carbonizing step is 0.1° C./min to 30° C./min.

11. The method of claim 6 wherein 1.5 liters to 3 liters of said surface modifying solution is used for every 1 kg of said unimproved graphite granules.

12. The method of claim 6 wherein the average granule diameter of said unimproved graphite granules is between 7 μm and 35 μm, and 1.5 liters to 3 liters of said surface modifying solution is used for every 1 kg of said unimproved graphite granules.

13. The method of claim 7 wherein in said solidifying step, the rate of increase in temperature for solidification is 0.5° C./min to 35° C./min.

14. The method of claim 9 and, in said carbonizing step, the rate of increase in temperature for said carbonization is 0.1° C./min to 30° C./min.

15. The method of claim 13 wherein in said carbonizing step, carbonization proceeds at 750° C. to 1300° C. for 1 to 24 hours and the rate of increase in temperature for said carbonization is 0.1° C./min to 30° C./min.

16. A method for fabricating improved graphite granules, comprising the steps of: preparing a surface modifying solution by mixing a pre-determined amount of a surface modifying agent in a corresponding solvent of said surface modifying solution wherein said surface modifying agent is one or more polymers selected from the group consisting of: coal pitch, coal tar, petroleum pitch, petroleum coke, benzene, naphthalene, copolymers of benzene and naphthalene copolymer, petroleum wax and petroleum resin; and said corresponding solvent is an organic solvent selected from the group consisting of: acetone, anhydrous ethanol, N-methyl pyrrolidone, chloroform, tetrahydrofuran, carbon tetrachloride, and cyclohexane; immersing said unimproved graphite granules in said surface modifying solution wherein the average granule diameter of said unimproved graphite granules is between 7 μm and 35 μm and 1.5 liters to 3 liters of said surface modifying solution is used for every 1 kg of said unimproved graphite granules; stirring said unimproved graphite granules in said surface modifying solution at 100 rpm to 2000 rpm for 0.5 hours to 10 hours to form coated graphite granules; separating said coated graphite granules from said surface modifying solution; heating to dry said coated graphite granules; sifting said coated graphite granules; solidifying said coated graphite granules in an inert environment at 200° C. to 600° C. for 0.2 to 12 hours wherein the rate of increase in temperature for solidification is 0.5° C./min to 35° C./min; and carbonizing said coated solidified graphite in an inert environment at 750° C. to 1300° C. for 1 to 24 hours to form said improved graphite granules wherein the rate of increase in temperature for carbonization is 0.1° C./min to 30° C./min.

17. An improved graphite granule, comprising: an unimproved graphite granule; and a membrane of amorphous carbon enveloping said unimproved graphite granule, wherein the thickness of said amorphous carbon membrane is between 0.05 μm and 1 μm.

18. Said improved graphite of claim 17 wherein the crystallite interlayer spacing in said improved graphite granules, d002, is between 0.335 nm and 0.340 nm; the specific surface area of said improved graphite granules is between 1.3 m2/g and 4.2 m2/g; and the average granule diameter of said improved graphite granules is between 8 μm and 35 μm.

19. Said improved graphite of claim 17 wherein said improved graphite granules are fabricated using the method, comprising the steps of: preparing a surface modifying solution by mixing a pre-determined amount of a surface modifying agent in a corresponding solvent of said surface modifying solution; immersing said unimproved graphite granules in said surface modifying solution; stirring said unimproved graphite granules in said surface modifying solution at predetermined speed for a predetermined time period to form coated graphite granules; separating said coated graphite granules from said surface modifying solution; heating to dry said coated graphite granules; sifting said coated graphite granules; solidifying said coated graphite granules in an inert environment at a predetermined temperature for a predetermined period of time; and carbonizing said coated solidified graphite in an inert environment at a predetermined temperature for a predetermined period of time to form said improved graphite granules.

20. Said improved graphite of claim 19 wherein said the interlayer spacing of the said graphite granules, d002, is between 0.335 and 0.340 nm; the specific surface area of said improved graphite granules is between 1.3 m2/g and 4.2 m2/g; the average granule diameter of said improved graphite granules is between 8 and 35 μm.