Patent Application
20070099088
This application claims the benefit of the filing date of Korean Patent Application No. 10-2005-0101810, filed on Oct. 27, 2005, in the Korean Intellectual Property Office, the disclosure of which is incorporated herein in its entirety by reference.
(a) Field of the Invention
The present invention relates to an electrode active material for a secondary battery, and a secondary battery comprising the same electrode active material.
(b) Description of the Related Art
In general, a lithium secondary battery is obtained by using materials capable of lithium ion intercalation/deintercalation as a cathode and an anode, and by injecting an organic electrolyte or a polymer electrolyte between the cathode and the anode. Such a lithium secondary battery generates electric energy via redox reactions induced by the lithium ion intercalation/deintercalation at the cathode and the anode.
Currently, carbonaceous materials have been used as an electrode active material forming the anode of a lithium secondary battery. However, an electrode active material having a higher capacity is still required in order to further improve the capacity of a lithium secondary battery.
To satisfy such requirements, metals that show a higher charge/discharge capacity as compared to carbonaceous materials and are capable of forming an electrochemical alloy with lithium, such as Si, Al, etc., have been used as electrode active materials. However, such metal-based electrode active materials show a severe change in volume due to lithium intercalation/deintercalation, so that they are cracked and finely divided. Therefore, secondary batteries using such metal-based electrode active materials undergo a rapid drop in capacity during repeated charge/discharge cycles and show poor cycle life characteristics.
Japanese Laid-Open Patent No. 2001-297757 discloses an electrode active material having a structure based on an α phase comprising an element capable of lithium intercalation/deintercalation (e.g. Si) and a β phase essentially comprising an intermetallic compound or a solid solution of the above element with another element b.
However, the aforementioned electrode active materials are still insufficient in providing excellent cycle life characteristics, and thus cannot be used as practical electrode active materials for a lithium secondary battery.
Therefore, the present invention has been made in view of the above-mentioned problems. It is an object of the present invention to provide an electrode active material having excellent cycle life characteristics, and a secondary battery comprising the same electrode active material. The electrode active material according to the present invention comprises a core layer capable of repeating lithium intercalation/deintercalation, and an amorphous carbon layer and a crystalline carbon layer successively formed on a surface of the core layer. Such excellent cycle life characteristics are accomplished by the crystalline carbon layer, which is formed of sheet-like carbon layer units and is partially or totally formed of bilayer or multilayer sheet-like carbon layer units, so as to inhibit variations in volume of the core layer, such as a metal, during repeated charge/discharge cycles.
According to an aspect of the present invention, there is provided an electrode active material comprising: a core layer capable of repeating lithium intercalation/deintercalation; an amorphous carbon layer; and a crystalline carbon layer, successively, wherein the crystalline carbon layer comprises sheet-like carbon layer units and partially or totally comprises bilayer or multilayer sheet-like carbon layer units. A secondary battery comprising the above electrode active material is also provided.
According to another aspect of the present invention, there is provided a method for preparing the above electrode active material, the method comprising the steps of: mixing a metal or metalloid forming a core layer with crystalline carbon; and carrying out mechanical alloying of the mixture in a Mechano Fusion system in the presence of balls.
The foregoing and other objects, features and advantages of the present invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings in which:
Hereinafter, the present invention will be explained in more detail.
When the sheet-like carbon layer units 40 form a multilayer structure, interstitial volumes are formed among the layers of the sheet-like carbon layer units, and such interstitial volumes serve as buffers to variations in volume of the core layer 10 that may occur during charge/discharge cycles. Additionally, as shown in
In other words, it is possible to buffer variations in volume of the core layer by virtue of the interstitial volumes formed by the sheet-like carbon layer units that form a multilayer structure in the crystalline carbon layer. Hence, the electrode active material according to the present invention can be inhibited from variations in total volume thereof. As a result, a secondary battery using the electrode active material according to the present invention has a high charge/discharge capacity and excellent cycle life characteristics.
According to a preferred embodiment of the present invention, the core layer may be formed of a metal or metalloid capable of repeating lithium intercalation/deintercalation. A metal or metalloid having a higher charge/discharge capacity is more preferred.
Particular examples of the metal or metalloid include at least one metal or metalloid selected from the group consisting of Si, Al, Sn, Sb, Bi, As, Ge and Pb, or an alloy thereof. However, any metal or metalloid capable of electrochemical and reversible lithium intercalation/deintercalation can be used with no particular limitation.
Particular examples of the crystalline carbon include natural graphite, artificial graphite, etc., which have a high degree of graphitization. Particular examples of the graphite-based material include MCMB (MesoCarbon MicroBead), carbon fiber, natural graphite, or the like, but are not limited thereto.
Particular examples of the amorphous carbon include coal tar pitch, petroleum pitch, and carbonaceous materials obtained by heat treatment of various organic materials, but are not limited thereto.
According to a preferred embodiment of the present invention, the electrode active material comprising the core layer, the amorphous carbon layer and the crystalline carbon layer, successively, is provided in a ratio of [core layer:amorphous carbon layer:crystalline carbon layer] of 70-30 parts by weight:0.1˜50 parts by weight:29.9˜70 parts by weight.
If the core layer capable of repeating lithium intercalation/deintercalation is present in an amount less than 30 parts by weight, the electrode active material cannot be served as a high-capacity electrode active material due to its low reversible capacity. If the crystalline carbon layer is present in an amount less than 29.9 parts by weight, it is not possible to obtain conductivity sufficiently. Also, in this case, the crystalline carbon layer cannot be formed of bilayer or multilayer sheet-like carbon layer units. Additionally, if the amorphous carbon layer is present in an amount less than 0.1 parts by weight, it is not possible to inhibit a volume expansion sufficiently. On the other hand, if the amorphous carbon layer is present in an amount greater than 50 parts by weight, there is a possibility of degradation of capacity and conductivity.
Preferably, the amorphous carbon layer has an interlayer spacing d002 of 0.34 nm or more and a thickness of 5 nm or more. If the amorphous carbon layer has a thickness less than 5 nm, it is not possible to sufficiently inhibit variations in volume of the core layer. If the interlayer spacing is less than 0.34 nm, the amorphous carbon layer itself undergoes severe variations in volume during repeated charge/discharge cycles. Thus, it is not possible to sufficiently inhibit variations in volume of the core layer, resulting in degradation in cycle life characteristics.
Preferably, the crystalline carbon layer has an interlayer spacing d002 of 0.3354-0.35 nm. The lowest critical value is the theoretical minimum interlayer spacing of graphite, and thus any value smaller than the lowest critical value does not exist. Carbon having an interlayer spacing greater than the highest critical value has poor conductivity, so that the crystalline carbon layer using the same shows low conductivity. Thus, in this case, lithium intercalation/deintercalation cannot proceed smoothly.
Although there is no limitation in thickness of the crystalline carbon layer, the crystalline carbon layer preferably has a thickness of 110 microns. If the crystalline carbon layer has a thickness less than 1 micron, it is difficult to ensure sufficient conductivity among electrode active material particles. On the other hand, if the crystalline carbon layer has a thickness greater than 10 microns, proportion of the carbonaceous materials to the electrode active material is too high to obtain high charge/discharge capacity.
The electrode active material according to the present invention can be obtained by the method comprising the steps of: mixing a metal or metalloid forming a core layer with crystalline carbon; and carrying out mechanical alloying of the mixture in a Mechano Fusion system in the presence of balls. Herein, the term “mechanical alloying” refers to a process for forming an alloy having a uniform composition by applying a mechanical force.
In the first step, the metal or metalloid may be mixed with the crystalline carbon in a ratio of [metal or metalloid:crystalline carbon] of 70˜30 parts by weight:30˜70 parts by weight.
In the second step, the balls may be mixed with the mixture obtained from the first step in a ratio of [balls:mixture of the first step] of 50˜98 parts by weight:50˜2 parts by weight. If the ratio is less than 50:50, it is not possible to transfer compression stress to the mixture. On the other hand, if the ratio is greater than 98:2, the balls are used in an excessive amount, resulting in a drop in productivity.
Additionally, the balls that may be used in the second step include stainless steel balls or zirconia balls having a diameter of 0.1˜10 mm.
The electrode according to the present invention may be manufactured by a conventional method known to those skilled in the art. For example, the electrode active material according to the present invention may be mixed with a binder and a solvent, and optionally with a conductive agent and a dispersant, and the mixture is agitated to provide slurry. Then, the slurry is applied onto a metal collector, and the collector coated with the slurry is compressed and dried to provide an electrode.
The binder and the conductive agent may be used in an amount of 1˜10 parts by weight and 1˜30 parts by weight, respectively, based on the weight of the electrode active material.
Particular examples of the binder that may be used in the present invention include polytertrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), or the like.
In general, the conductive agent that may be used in the present invention includes carbon black. Commercially available conductive agents include acetylene black-based conductive agents (available from Chevron Chemical Company or Gulf Oil Company), Ketjen Black EC series (available from Armak Company), Vulcan XC-72 (available from Cabot Company) and Super P
(available from MMM Co.)
The metal collector includes a metal with high conductivity. Any metal to which the electrode active material slurry can be adhered with ease can be used as long as it shows no reactivity in the drive voltage range of a battery using the same. Typical examples of the collector include mesh, foil, etc., obtained from aluminum, copper, gold, nickel, aluminum alloy or a combination thereof.
Also, there is no particular limitation in methods of applying the slurry onto the collector. For example, the slurry may be applied onto the collector via a doctor blade coating, dip coating or brush coating process. There is no particular limitation in the amount of the slurry applied onto the collector. However, it is preferred that the slurry is applied in such an amount that the active material layer formed after removing a solvent or a dispersant can be in a range of generally 0.005˜5 mm, and preferably 0.05˜2 mm.
Further, there is no particular limitation in methods of removing the solvent or the dispersant. However, it is preferred that the solvent or the dispersant is allowed to evaporate as quickly as possible, provided that no cracking occurs in the active material layer due to stress concentration, and no separation occurs between the active material layer and the collector. For example, the collector coated with the active material slurry may be dried in a vacuum oven at 50˜200° C. for 0.5˜3 days.
The secondary battery according to the present invention can be manufactured by using the electrode active material of the present invention according to a conventional method known to those skilled in the art. For example, the secondary battery may be obtained by interposing a porous separator between a cathode and an anode to form an electrode assembly, and then by injecting an electrolyte thereto. The secondary battery includes a lithium ion secondary battery, a lithium polymer secondary battery or a lithium ion polymer secondary battery.
The electrolyte may comprise a non-aqueous solvent and an electrolyte salt.
Any non-aqueous solvent currently used for a non-aqueous electrolyte may be used with no particular limitation. Particular examples of such non-aqueous solvents include cyclic carbonates, linear carbonates, lactones, ethers, esters, and/or ketones.
Particular examples of the cyclic carbonates include ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), or the like. Particular examples of the linear carbonates include diethyl carbonate (DEC), dimethyl carbonate (DMC), dipropyl carbonate (DPC), ethylmethyl carbonate (EMC), methyl propyl carbonate (MPC), or the like. Particular examples of the lactone include gamma-butyrolactone (GBL). Particular examples of the ether include dibutyl ether, tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, or the like. Additionally, particular examples of the ester include methyl acetate, ethyl acetate, methyl propionate, methyl pivalate, or the like. Further, particular examples of the ketone include polymethylvinyl ketone. Such non-aqueous solvents may be used alone or in combination.
Any electrolyte salt currently used for a non-aqueous electrolyte may be used in the present invention with no particular limitation. Non-limiting examples of the electrolyte salt include a salt represented by the formula of A+B−, wherein A+ represents an alkali metal cation selected from the group consisting of Li+, Na+, K+ and combinations thereof, and B− represents an anion selected from the group consisting of PF6−, BF4−, Cl−, Br−, I−, ClO4−, AsF6−, CH3CO3−, CF3SO3−, N(CF3SO2)2−, C(CF2SO2)3− and combinations thereof. A lithium salt is particularly preferred. Such electrolyte salts may be used alone or in combination.
The secondary battery according to the present invention may further comprise a separator. Although there is no particular limitation in the separator that may be used in the present invention, it is preferable to use a porous separator. Non-limiting examples of the separator that may be used include a polypropylene-based, polyethylene-based or polyolefin-based porous separator.
There is no particular limitation in the outer shape of the secondary battery according to the present invention. The secondary battery may be a cylindrical battery using a can, a prismatic battery, a pouch-type battery or a coin-type battery.
Reference will now be made in detail to the preferred embodiments of the present invention. It is to be understood that the following examples are illustrative only and the present invention is not limited thereto.
Si was mixed with natural graphite in a ratio of 50 wt %:50 wt % to provide a mixture, and stainless steel balls having a diameter of 3 mm and the mixture were introduced into a Mechano Fusion system available from Hosokawa Micron Co. in a weight ratio of 5:1. Next, the resultant mixture was subjected to mechanical alloying at a rotation speed of 600 rpm for 30 minutes to provide an electrode active material having a core layer, an amorphous carbon layer and a crystalline carbon layer having multilayer-structured sheet-like carbon layer units.
Then, 100 parts by weight of the electrode active material powder obtained as described above, 10 parts by weight of PVDF as a binder and 10 parts by weight of acetylene black as a conductive agent were mixed, NMP was further added to the above mixture as a solvent, and then the resultant mixture was mixed thoroughly to provide uniform slurry. Next, the slurry was coated onto copper foil with a thickness of 20 micron, followed by drying and rolling. The coated foil was cut into a desired size via punching to provide an electrode.
As an electrolyte, a non-aqueous solvent comprising ethylene carbonate (EC) and ethyl methyl carbonate (EMC) in a ratio of 1:2 (v:v) and containing 1M LiPF6 dissolved therein was used.
The electrode obtained as described above was used as an anode, and lithium metal was used as a counter electrode. Then, a polyolefin-based separator was interposed between both electrodes and the electrolyte was injected thereto to provide a coin-type battery according to the present invention.
A battery was provided in the same manner as described in Example 1, except that Si was mixed with natural graphite in a ratio of 50 wt %:50 wt % to provide a mixture, zirconia balls having a diameter of 5 mm and the mixture were introduced into a Mechano Fusion system available from Hosokawa Micron Co. in a weight ratio of 10:1, and then the resultant mixture was subjected to mechanical alloying at a rotation speed of 600 rpm for 30 minutes to provide an electrode active material having a core layer, an amorphous carbon layer and a crystalline carbon layer having multilayer-structured sheet-like carbon layer units.
A battery was provided in the same manner as described in Example 1, except that Si was mixed with natural graphite in a ratio of 80 wt %:20 wt % to provide a mixture, stainless steel balls having a diameter of 3 mm and the mixture were introduced into a Mechano Fusion system available from Hosokawa Micron Co. in a weight ratio of 5:1, and then the resultant mixture was subjected to mechanical alloying at a rotation speed of 600 rpm for 30 minutes to provide an electrode active material having a core layer, an amorphous carbon layer and a crystalline carbon layer having monolayer-structured sheet-like carbon layer units.
A battery was provided in the same manner as described in Example 1, except that Si was mixed with natural graphite in a ratio of 80 wt %:20 wt % to provide a mixture, zirconia balls having a diameter of 5 mm and the mixture were introduced into a Mechano Fusion system available from Hosokawa Micron Co. in a weight ratio of 10:1, and then the resultant mixture was subjected to mechanical alloying at a rotation speed of 600 rpm for 30 minutes to provide an electrode active material having a core layer, an amorphous carbon layer and a crystalline carbon layer having monolayer-structured sheet-like carbon layer units.
Experimental Results
Each of the batteries according to Examples 1 and 2 and Comparative Examples 1 and 2 was subjected to three charge/discharge cycles, and measured for variations in volume. As shown in the following Table 1, the battery according to Example 1 shows a variation in volume of about 51% (33 μm→50 μm), while the battery according to Comparative Example 1 shows a variation in volume of about 124% (29 μm→65 μm). This indicates that the electrode active material according to the present invention has an effect of inhibiting a volume expansion.
In addition, each of the batteries obtained by using the electrode active materials according to Examples 1 and 2 shows little variation in volume of the core layer after being subjected to charge/discharge cycles. As shown in the following Table 1, each battery maintains the initial capacity to a ratio of 98% or more even after fifty charge/discharge cycles (see
As can be seen from the foregoing, the electrode active material according to the present invention can inhibit variations in volume of the core layer that may occur during repeated charge/discharge cycles, by virtue of the interstitial volumes formed by the multilayer sheet-like carbon layer units in the crystalline carbon layer. Therefore, the battery using the electrode active material according to the present invention can provide improved cycle life characteristics.
While this invention has been described in connection with what is presently considered to be the most practical and preferred embodiment, it is to be understood that the invention is not limited to the disclosed embodiment and the drawings. On the contrary, it is intended to cover various modifications and variations within the spirit and scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2005-0101810 | Oct 2005 | KR | national |
