The present disclosure relates to an electrode lead for a secondary battery having a gas release portion and a secondary battery including the same.
Due to the rapid increase in the use of fossil fuels, the demand for the use of alternative energy or clean energy is increasing, and the most actively studied field as a part thereof is the field of power generation and power storage using electrochemistry.
Currently, a typical example of electrochemical devices using electrochemical energy includes a secondary battery, and the area of use of secondary batteries is gradually expanding.
Recently, as technical development and demand for mobile instruments, such as portable computers, cellular phones and cameras, have been increased, secondary batteries as energy sources have been increasingly in demand Particularly, lithium secondary batteries which show high charge/discharge characteristics and life characteristics and are eco-friendly have been studied intensively, and have been commercialized and used widely.
However, as the application spectrum of lithium secondary batteries has been expanded as mentioned above, there is a need for an increase in energy density. Therefore, such lithium secondary batteries cause an increase in gases generated inside of the secondary batteries due to such increased energy density.
Moreover, when water infiltrates into secondary batteries, side reactions occur, and thus the problems of degradation of the performance of secondary batteries and gas generation are accelerated undesirably.
Under these circumstances, the above-mentioned safety problem has been solved by forming a gas release portion in a secondary battery so that the gases generated inside of the secondary battery may be released to the outside. However, when the secondary battery is vented, the life of the secondary battery is reduced significantly. Therefore, there is an imminent need for the solution of the above-mentioned problem.
The present disclosure is designed to solve the problems of the related art and the technical problems required to be solved from the past.
Particularly, the present disclosure is directed to providing an electrode lead for a secondary battery which has an efficiently structured gas release path to improve the safety of a secondary battery, and a secondary battery including the same.
In one aspect of the present disclosure, there is provided an electrode lead according to any one of the following embodiments.
According to the first embodiment, there is provided an electrode lead for a secondary battery, including a metal substrate, and a coating layer formed on the surface of the metal substrate, wherein at least one surface of the top surface and the bottom surface of the electrode lead has a gas release portion having a structure formed by surface-treatment with a non-adhesive material, or by removing the coating layer.
According to the second embodiment, there is provided the electrode lead for a secondary battery as defined in the first embodiment, wherein the coating layer has a thickness of 0.1-5 μm.
According to the third embodiment, there is provided the electrode lead for a secondary battery as defined in the first or the second embodiment, wherein the gas release portion has a structure formed by removing the coating layer partially or totally in the thickness direction through a physical or chemical etching process.
According to the fourth embodiment, there is provided the electrode lead for a secondary battery as defined in the third embodiment, wherein the gas release portion has a structure formed by removing the coating layer in the thickness direction to 50-100% based on the total thickness of the coating layer.
According to the fifth embodiment, there is provided the electrode lead for a secondary battery as defined in any one of the first to the fourth embodiments, wherein the gas release portion has a structure formed by coating with at least one non-adhesive material selected from the group consisting of a polyimide-based material, a fluorine-based material and polymethylpentene.
According to the sixth embodiment, there is provided the electrode lead for a secondary battery as defined in the fifth embodiment, wherein the fluorine-based material includes at least one selected from the group consisting of polytetrafluoroethylene and polyvinylidene fluoride.
According to the seventh embodiment, there is provided the electrode lead for a secondary battery as defined in any one of the first to the sixth embodiments, wherein the non-adhesive material is coated to a thickness of 30 nm to 10 μm.
According to the eighth embodiment, there is provided the electrode lead for a secondary battery as defined in any one of the first to the seventh embodiments, wherein the gas release portion has a planar shape selected from a circular shape, an oval shape and a polygonal shape.
According to the ninth embodiment, there is provided the electrode lead for a secondary battery as defined in any one of the first to the eighth embodiments, wherein the gas release portion is formed with an area corresponding to 10-70% based on the total area of the electrode lead.
According to the tenth embodiment, there is provided the electrode lead for a secondary battery as defined in any one of the first to the ninth embodiments, wherein the metal substrate includes at least one selected from the group consisting of nickel (Ni), aluminum (Al), copper (Cu) and stainless steel.
According to the eleventh embodiment, there is provided the electrode lead for a secondary battery as defined in any one of the first to the tenth embodiments, wherein the coating layer includes at least one selected from the group consisting of chrome (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), titanium (Ti), columbium (Cb), silicon oxide, tin oxide and titanium oxide.
In another aspect of the present disclosure, there is provided a secondary battery according to any one of the following embodiments.
According to the twelfth embodiment, there is provided a secondary battery, which includes an electrode assembly including a positive electrode, a negative electrode and a separator interposed between the positive electrode and the negative electrode, and received in a battery casing together with an electrolyte,
According to the thirteenth embodiment, there is provided the secondary battery as defined in the twelfth embodiment, wherein the coating layer has a thickness of 0.1-5 μm.
According to the fourteenth embodiment, there is provided the secondary battery as defined in the twelfth or the thirteenth embodiment, wherein the gas release portion has a structure formed by removing the coating layer partially or totally in the thickness direction through a physical or chemical etching process.
According to the fifteenth embodiment, there is provided the secondary battery as defined in the fourteenth embodiment, wherein the gas release portion has a structure formed by removing the coating layer in the thickness direction to 50-100% based on the total thickness of the coating layer.
According to the sixteenth embodiment, there is provided the secondary battery as defined in any one of the twelfth to the fifteenth embodiments, wherein the gas release portion has a structure formed by coating with at least one non-adhesive material selected from the group consisting of a polyimide-based material, a fluorine-based material and polymethylpentene.
According to the seventeenth embodiment, there is provided the secondary battery as defined in the sixteenth embodiment, wherein the fluorine-based material includes at least one selected from the group consisting of polytetrafluoroethylene and polyvinylidene fluoride.
According to the eighteenth embodiment, there is provided the secondary battery as defined in any one of the twelfth to the seventeenth embodiments, wherein the non-adhesive material is coated to a thickness of 30 nm to 10 μm.
According to the nineteenth embodiment, there is provided the secondary battery as defined in any one of the twelfth to the eighteenth embodiments, wherein the gas release portion has a planar shape selected from a circular shape, an oval shape and a polygonal shape.
According to the twentieth embodiment, there is provided the secondary battery as defined in any one of the twelfth to the nineteenth embodiment, wherein the gas release portion is formed with an area corresponding to 20-90% based on the total area in which the electrode lead is in contact with the insulation film.
According to the twenty-first embodiment, there is provided the secondary battery as defined in any one of the twelfth to the twentieth embodiments, wherein the adhesion strength between the gas release portion and the insulation film is 20-80% based on the adhesion strength between the electrode lead, except the gas release portion, and the insulation film.
The electrode lead for a secondary battery according to an embodiment of the present disclosure has a gas release portion to provide an increased utility value.
In addition, the gas release portion may be formed by a simplified process of providing a non-adhesive surface to an insulation film to be adhered with the electrode lead subsequently, and thus may be formed rapidly and efficiently.
Hereinafter, preferred embodiments of the present disclosure will be described in detail with reference to the accompanying drawings.
Prior to the description, it should be understood that the terms used in the specification and the appended claims should not be construed as limited to general and dictionary meanings, but interpreted based on the meanings and concepts corresponding to technical aspects of the present disclosure on the basis of the principle that the inventor is allowed to define terms appropriately for the best explanation.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the present disclosure. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise.
It will be further understood that the terms “comprises” and/or “comprising”, “includes” and/or “including”, or “has” and/or “having” when used in this specification, specify the presence of stated features, numbers, steps, elements, or combinations thereof, but do not preclude the presence or addition of one or more other features, numbers, steps, elements, or combinations thereof.
In one aspect of the present disclosure, there is provided an electrode lead for a secondary battery, including a metal substrate, and a coating layer formed on the surface of the metal substrate, wherein at least one surface of the top surface and the bottom surface of the electrode lead has a gas release portion having a structure formed by surface-treatment with a non-adhesive material, or by removing the coating layer.
Herein, the coating layer may include a coating layer for improving the adhesion to an insulation film, while preventing the electrode lead from corrosion caused by a strong acid, or the like.
The coating layer may have a thickness of 0.1-5 μm.
When the thickness of the coating layer satisfies the above-defined range, it is possible to prevent an excessive increase in thickness of the electrode lead, while preventing the electrode lead from corrosion caused by a strong acid generated inside of a secondary battery.
Meanwhile, according to the related art, there have been developed various methods for forming a gas release portion for releasing gases generated inside of a secondary battery to the outside. For example, there has been an attempt to ensure the safety of a secondary battery by releasing the gases inside of the secondary battery through the formation of a notch in a pouch, formation of a separate gas release member between lead portions, or the like.
However, the above-mentioned methods cannot have an advantage in processing efficiency and cost competitiveness, since a secondary battery may not be used any longer, when being vented, resulting in significant degradation of the life of the battery and a need for a separate member.
On the contrary, according to the present disclosure, a gas release portion may be formed on the electrode lead for a secondary battery by a simplified process. Thus, it is possible to improve the life of a secondary battery, while ensuring the safety of the secondary battery.
Particularly, the gas release portion formed on at least one surface of the electrode lead may be formed through a very simple and economical process.
For example, the gas release portion may be formed by removing the coating layer partially or totally in the thickness direction through a physical or chemical etching process, wherein the gas release portion may have a structure formed by removing the coating layer in the thickness direction to 50-100% based on the total thickness of the coating layer.
When the removal of the coating layer satisfies the above-defined range, it is possible to ensure an effect of vent and to prevent the electrode lead itself from being damaged.
Herein, the physical or chemical etching process is not particularly limited, as long as it can remove the coating layer. For example, the physical or chemical etching may be carried out by a wet etching process through ultraviolet ozone (UVO) treatment and exposure to an acidic solution, a sputtering etching process, a plasma etching process, or the like. In other words, the gas release portion may be formed by disposing a mask on the electrode lead, wherein the mask has an opening corresponding to the shape of a gas release portion to be formed on the electrode lead, and removing the coating layer of the electrode lead through various etching processes.
The method will be explained in more detail hereinafter.
In a variant, the gas release portion may be formed by coating a polymer having a melting point of 220° C. or higher. In addition, the gas release portion may be formed by coating a polymer having a glass transition temperature of 100° C. or higher. When the gas release portion uses a polymer having the above-defined range of glass transition temperature, it is possible to form a gas release portion more easily, when the electrode lead is attached to the insulation film as described hereinafter.
The melting point may be determined by using a differential scanning calorimeter (DSC). For example, after the temperature of a sample is increased from 30° C. to 280° C. at a rate of 10° C./min, the sample is allowed to stand at 280° C. for 10 minutes, cooled to 30° C. at a rate of 10° C./min, and is allowed to stand at 30° C. for 10 minutes. Then, the temperature of the sample is increased from 30° C. to 280° C. at a rate of 10° C./min, is allowed to stand at 280° C. for 10 minutes to measure the temperature of each of melting peaks, and the top of the DSC curve is taken as a melting point.
The glass transition temperature may be determined by using a differential scanning calorimeter (DSC). For example, after the temperature of a sample is increased from 30° C. to 280° C. at a rate of 10° C./min, the sample is allowed to stand at 280° C. for 10 minutes, cooled to 30° C. at a rate of 10° C./min, and is allowed to stand at 30° C. for 10 minutes. Then, the glass transition temperature may be determined by measuring the intersection point of heat absorption amount when maintaining the temperature, and the tangent at the knee point of the enthalpy curve obtained by increasing the temperature of the sample from 30° C. to 280° C. at a rate of 10° C./min and allowing the sample to stand at 280° C. for 10 minutes.
According to an embodiment of the present disclosure, the gas release portion may be formed by coating with at least one non-adhesive material selected from the group consisting of a polyimide-based material, polytetrafluoroethylene, a polyvinylidene fluoride-based material and polymethylpentene.
The non-adhesive material is one that is not adhered to the insulation film attached to the electrode lead subsequently.
The non-adhesive material may be coated through a conventional known coating process with no particular limitation. For example, the non-adhesive material may be coated through a spin coating process, a blade coating process, a spray coating process, or an ink jet printing process, wherein a mask having an opening corresponding to the shape of the gas release portion may be used in order to form a gas release portion having a specific shape, similarly to the above-mentioned method. In a variant, the non-adhesive material may be transferred through a roll pressing process.
The method will be explained in more detail hereinafter.
Herein, the non-adhesive material may be coated to a thickness of 30 nm to 10 μm.
When the thickness of the non-adhesive material satisfies the above-defined range, there is no difficulty in processing, and a problem, such as electrolyte leakage caused by insufficient sealing of the other portions, may be prevented with ease.
In other words, the gas release portion may be formed by a very simple process of forming a portion where the insulation film is not attached to the electrode lead, when the insulation film is attached to the electrode lead subsequently during the manufacture of a secondary battery.
Therefore, the gases inside of a secondary battery may be released to the outside through the portion not attached to the insulation film.
In this manner, the gas release portion may be formed through a very simple and economical process of removing the coating layer of the electrode lead showing high adhesiveness to the insulation film, or coating a material having no adhesiveness to the insulation film, according to the present disclosure. Therefore, it is possible to realize the desired effects of the present disclosure with high processing and cost efficiency.
Herein, the gas release portion may be formed with an area corresponding to 10-70%, particularly 20-50%, based on the total planar area of the electrode lead, considering the area where the insulation film is attached subsequently.
When the area of the gas release portion satisfies the above-defined range, it is possible to form a gas release portion at the insulation film-attached portion and to prevent a sealability-related problem, such as excessive peeling of the coating layer and electrolyte leakage.
Meanwhile, the gas release portion has any planar shape with no particular limitation, and may have various shapes, such as a circular, oval or polygonal shape. However, the gas release portion may be formed with a pattern capable of releasing gases efficiently, while preventing a problem, such as electrolyte leakage.
However, the shapes shown in
Meanwhile, the electrode lead according to the present disclosure includes a metal substrate and a coating layer coated on the metal substrate.
Herein, the metal substrate may include at least one selected from the group consisting of nickel (Ni), aluminum (Al), copper (Cu) and stainless steel. More particularly, preferred materials for the metal substrate may vary depending on whether the electrode lead is a positive electrode lead or negative electrode lead. For example, in the case of a positive electrode lead, aluminum, nickel or alloy containing at least one of them may be used. In the case of a negative electrode lead, copper, nickel or alloy containing at least one of them may be used.
Meanwhile, the electrode lead according to the present disclosure may have a coating layer formed on the metal substrate, and the coating layer prevents infiltration of water to a secondary battery and reaction thereof with an electrolyte to generate a strong acid causing corrosion of the secondary battery, and improves the adhesion with the insulation film. Herein, the coating layer may include a metal or metal oxide, particularly at least one selected from the group consisting of chrome (Cr), nickel (Ni), iron (Fe), molybdenum (Mo), silicon (Si), titanium (Ti), columbium (Cb), silicon oxide, tin oxide and titanium oxide.
Herein, the coating layer may have a thickness of 5 μm or less, particularly, 0.1-5 μm, more particularly 0.1-0.5 μm, and most particularly 0.2-0.3 μm.
When the coating layer thickness satisfies the above-defined range, it is possible to prevent corrosion of the electrode lead, caused by the strong acid generated in the secondary battery, and to inhibit an excessive increase in thickness of the electrode lead.
In addition, the coating layer may be formed by using a conventional method well known to those skilled in the art and is not particularly limited. For example, the coating layer may be formed through electroplating, or the like.
The gas release portion according to the present disclosure is formed by removing the coating layer partially or totally in the thickness direction, or by surface-treatment on the coating layer with a non-adhesive material.
In another aspect of the present disclosure, there is provided a secondary battery, which includes an electrode assembly including a positive electrode, a negative electrode and a separator interposed between the positive electrode and the negative electrode, and received in a battery casing together with an electrolyte,
The secondary battery will be explained in more detail with reference to
Referring to
Herein, when enlarging the negative electrode lead 100 to review the structure thereof (portion A), it can be seen that a gas release portion 101 is formed partially in the portion where the insulation film 206 is attached to the negative electrode lead 100.
Herein, the gas release portion 101 is not adhered with the insulation film 205 to provide a gas release path.
Although it is not shown in the drawing, a gas release portion may be formed in the positive electrode lead 110, or formed in both of the positive electrode lead 110 and the negative electrode lead 120.
Meanwhile, the gas release portion 101 may be formed with an area corresponding to 20-90%, particularly 30-80%, based on the area where the electrode lead is in contact with the insulation film.
When the area of the gas release portion 101 satisfies the above-defined range, it is possible to ensure a vent effect, while ensuring such an area that the sealability between the electrode lead and the insulation film may be retained.
In addition, the structure, shape, material, or the like, of the gas release portion 101 is the same as described above. Further, the other constitutional elements of the electrode lead are the same as described above.
Referring to
Referring to
Referring to
In addition, referring to
Reference will be made to the known contents about the other specification of the insulation film.
The adhesion strength between the gas release portion 101 of the electrode lead 100 formed according to the present disclosure and the insulation film 206 may be 20-30%, particularly 30-70%, of the adhesion strength between the electrode lead 100, except that gas release portion 101, and the insulation film 206.
Herein, the adhesion strength may be obtained by carrying out melt fusion of an electrode lead in which the gas release portion 101 is formed with an insulation film 206 made of polypropylene, storing the resultant structure in a chamber including 30 g of an electrolyte and 1.3 g of dry ice at 60° C. and 90% RH for 2 weeks, partially peeling the electrode lead from the insulation film, and measuring the strength loaded depending on strain by using UTM, while drawing the electrode lead and the insulation film at 180°.
Meanwhile, the battery casing is not particularly limited, but may be a pouch-type battery casing which allows utilization of the above-described constitution suitably.
Since the other constitutional elements, such as the positive electrode, negative electrode, separator, positive electrode tab, negative electrode tab, battery casing and electrolyte, are known to those skilled in the art, detailed description thereof will be omitted herein.
Meanwhile, as described above, the gas release portion 101 has a structure formed by removing the coating layer or by surface-treatment with a non-adhesive material. Hereinafter, such structures will be explained in more detail with reference to
According to an embodiment of the present disclosure, the gas release portion may be formed by removing the coating layer.
Particularly, the gas release portion may be formed by the method including the steps of:
Particular embodiments of the method for partially removing the coating layer are shown in
First, referring to
Particularly, a mask 310 including an opening 311 corresponding to the shape of a gas release portion 301 to be formed is disposed on a preliminary electrode lead 300, and impact is applied thereto through the opening 311 of the mask 310 by using a gas ionized by a sputter 320 to remove the coating layer with a shape corresponding to the opening 311 from the preliminary electrode lead 300, thereby forming the gas release portion 301.
In addition, referring to
Particularly, a mask 410 including an opening 411 is disposed on a preliminary electrode lead 400, an acidic solution 420 is introduced through the opening 411 to carry out chemical etching treatment so that the coating layer of the preliminary electrode lead 400 may be removed, thereby forming a gas release portion 401.
Herein, the acidic solution 420 is not particularly limited, as long as it is acidic and is capable of removing the coating layer. For example, the acidic solution may be a mixed solution of perchloric acid with ammonium nitrate.
According to another embodiment, the gas release portion on the electrode lead may be formed by surface-treating the electrode lead with a non-adhesive material that is not adhesive to the insulation film.
Particularly, the gas release portion may be formed by the method including the steps of:
Particular embodiments of the method are shown in
Referring to
Particularly, a mask 510 including an opening 511 corresponding to the shape of a gas release portion 501 to be formed is disposed on at least one surface of the top surface and the bottom surface of a preliminary electrode lead 500, and a non-adhesive material 521 is applied through the opening 511 of the mask 510 by using various methods, such as a spray coater 520, to form the gas release portion 501.
In a variant,
Particularly, a gas release portion 601 is formed by transferring and coating a non-adhesive material 611 onto the surface of a preliminary electrode lead 600 through a pressing process using a roll 610 having the non-adhesive material 611 formed thereon with a shape corresponding to the shape of the gas release portion 601.
Herein, particular examples of the non-adhesive material 521, 611 are the same as described above.
Hereinafter, the present disclosure will be explained with reference to preferred examples, comparative examples and test examples. However, it should be understood that the specific examples are given by way of illustration only, since various changes and modifications within the scope of the disclosure will become apparent to those skilled in the art from this detailed description.
A preliminary electrode lead including aluminum (Al) foil having a thickness of 200 μm and coated with chrome (Cr) to a thickness of 0.2 μm was irradiated with laser (output: 70 W, wavelength: 300 nm) to carry out etching of Cr in the rectangular shape as shown in
Then, a polypropylene film (thickness: 100 μm) as an insulation film was stacked on the corresponding portion and fused thereto in such a manner that it might cover the corresponding portion to prepare an electrode lead/insulation film laminate.
An electrode lead/insulation film laminate was obtained in the same manner as Example 1, except that a preliminary electrode lead including copper (Cu) foil having a thickness of 200 μm and coated with nickel (Ni) to a thickness of 1 μm and chrome (Cr) coated to the surface of nickel to a thickness of 0.2 μm was used.
To the surface of a preliminary electrode lead 100 including aluminum (Al) foil having a thickness of 200 μm and coated with chrome (Cr) to a thickness of 0.2 μm, a copolymer of vinylidene monomer, hexafluoropropylene monomer and tetrafluoroethylene monomer was applied by using a dispenser in a T-like shape as shown in
Then, a polypropylene film (thickness: 100 μm) as an insulation film 205 was stacked and fused in such a manner that it might cover the corresponding portion to prepare an electrode lead/insulation film laminate, as shown in
Each of the laminate according to Example 1 and the laminate according to Example 2 was stored in a chamber including 30 g of a solution containing fluoroethylene carbonate (FEC) and ethyl methyl carbonate (EMC) at a volume ratio of 3:7 and 1 M LiFSI dissolved therein, and 1.3 g of dry ice, at 60° C. and 90% RH for 2 weeks.
After 2 weeks, each laminate was mounted to a UTM system (LLOYD Instrument LF Plus) and force was applied thereto at a rate of 300 mm/min at 180° to determine the separation strength (i.e. adhesion strength) required for separating the insulation film and the electrode lead from each other. The results are shown in
Referring to
Each of the laminate according to Example 1 and the laminate according to Example 2 was dipped in a solution containing fluoroethylene carbonate (FEC) and ethyl methyl carbonate (EMC) at a volume ratio of 3:7 and 1 M LiFSI dissolved therein in an oven at 25° C. (RT), 60° C., 80° C. or 100° C. for 1 day. Then, the laminate was taken out and mounted to a UTM system (LLOYD Instrument LF Plus), and force was applied thereto at a rate of 300 mm/min at 180° to determine the separation strength (i.e. adhesion strength) required for separating the insulation film and the electrode lead from each other. The results are shown in
Referring to
The gas release amount with the lapse of time was determined by preparing three secondary batteries each including the electrode lead/insulation film laminate according to Example 3 and a gas line capable of gas injection from the outside, injecting gas from the outside through the gas line at a rate of 50 sc/cm to a pressure of 1, 1.5 or 2 atm, observing how the pressure is changed with the lapse of time, and calculating the gas release amount according to the correlation equation between pressure and gas injection amount.
It can be seen from
It should be understood that various changes and modifications within the scope of the disclosure will become apparent to those skilled in the art from this detailed description.
Number | Date | Country | Kind |
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10-2020-0184482 | Dec 2020 | KR | national |
10-2021-0148398 | Nov 2021 | KR | national |
The present application is a national phase entry under 35 U.S.C. § 371 of the International Application No. PCT/KR2021/019781 filed on Dec. 23, 2021, which claims priority to Korean Patent Application No. 10-2020-0184482 filed on Dec. 28, 2020 and Korean Patent Application No. 10-2021-0148398 filed on Nov. 2, 2021, the disclosures of which are incorporated herein by reference in their entireties.
Filing Document | Filing Date | Country | Kind |
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PCT/KR2021/019781 | 12/23/2021 | WO |