KR101921545B1 - Electrolyte and lithium secondary battery with the same - Google Patents

Abstract

The present invention relates to an electrolyte and a lithium secondary battery comprising the same, wherein the electrolyte comprises a first electrolyte system comprising a cyclic carbonate-based solvent and LiPF ₆ , and a second electrolyte system including a chain carbonate solvent, difluoro phosphate, methylene And a second electrolyte system comprising Methylene Methanedisulfonate and 4-Fluorotoluene.
The electrolyte has improved linear LSV (linear sweep voltametry) values, and does not lower the contact angle and Li ⁺ transference number on the surface of the anode relative to the commercial electrolyte.

Description

ELECTROLYTE AND LITHIUM SECONDARY BATTERY WITH THE SAME BACKGROUND OF THE INVENTION 1. Field of the Invention [0001]

The present invention relates to an electrolyte and a lithium secondary battery including the same, and more particularly, to a lithium secondary battery including an electrolyte having improved linear sweep voltametry (LSV) values, contact angle and Li- ^{+ < / RTI >} transference number), and a lithium secondary battery comprising the electrolyte.

Lithium secondary batteries can be used not only as portable power sources such as mobile phones, notebook computers, digital cameras and camcorders but also as power tools, electric bicycles, hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles HEV, PHEV), and the like. As the application field is expanded and demand is increased, the external shape and size of the battery are variously changed, and performance and stability are demanded more than the characteristics required in the conventional small batteries. In order to meet such a demand, the performance of the battery should be stabilized in a condition where battery components are flowing in a large current.

The lithium secondary battery is manufactured by using a material capable of inserting and desorbing lithium ions as a cathode and an anode, providing a porous separator between the two electrodes, and injecting a liquid electrolyte. The insertion and extraction of lithium ions in the cathode and the anode, Electricity is generated or consumed by the redox reaction due to desorption.

Various non-aqueous solvents and additives have been studied as electrolyte-containing components in order to improve battery characteristics such as output characteristics, cycle characteristics, and storage characteristics of lithium ion batteries. In addition, even when a specific compound is added to an electrolyte as an additive for improving battery performance, performance of some items of most battery performance can be expected to be improved, but the performance of other items is rather reduced.

An object of the present invention is to provide an electrolyte in which the contact angle and the lithium ion transfer number (Li ⁺ transference number) of the positive electrode surface are not lowered, while improving the value of the positive electrode LSV (linear sweep voltametry).

Another object of the present invention is to provide a lithium secondary battery comprising the electrolyte.

In order to achieve the above object, an electrolyte according to an embodiment of the present invention includes a first electrolyte system including a cyclic carbonate-based solvent and LiPF ₆ , and a first electrolyte system including a chain carbonate solvent, difluoro phosphate, A second electrolyte system comprising Methylene Methanedisulfonate and 4-Fluorotoluene.

The second electrolyte system may be included in an amount of 5 to 50 parts by weight based on 100 parts by weight of the first electrolyte system.

The first electrolyte system may include 6 to 30% by weight of the LiPF ₆ based on the entire first electrolyte system.

The second electrolyte system may include 0.1 to 10% by weight of the difluorophosphate based on the entirety of the second electrolyte system.

The second electrolyte system may include 0.1 to 10% by weight of the methylene methane disulfonate based on the entire second electrolyte system.

The second electrolyte system may include 0.1 to 10% by weight of the 4-fluorotoluene based on the entirety of the second electrolyte system.

The electron density value of the first electrolyte system may be 2.4 to 2.74 [Phi] * [Phi].

The electron density value of the second electrolyte system may be within ± 10% of the electron density value of the first electrolyte system.

The electron density value of the second electrolyte system may be 2.40 to 2.78? *?.

The electron density value of the electrolyte may be 2.44 to 2.81 [Phi] * [Phi].

The electrolyte may have a linear sweep voltametry (LSV) value that is greater than a positive LSV value of the first electrolyte system.

The electrolyte may have an anode LSV value of 4 V or higher.

The cyclic carbonate-based solvent may include any one selected from the group consisting of ethylene carbonate, propylene carbonate, butylene carbonate, fluoroethylene carbonate, and mixtures thereof.

The chain carbonate-based solvent may include any one selected from the group consisting of dimethyl carbonate, diethyl carbonate, dipropyl carbonate, methylpropyl carbonate, ethylpropyl carbonate, methyl ethyl carbonate, ethyl methyl carbonate, and mixtures thereof .

A lithium secondary battery according to another embodiment of the present invention includes a cathode including a cathode active material, a cathode disposed opposite to the cathode, a cathode including the anode active material, and an electrolyte according to the present invention.

The electrolyte according to the present invention has an improved positive electrode LSV (linear sweep voltametry) value, and does not lower the contact angle and the lithium ion transfer number (Li ⁺ transference number) on the surface of the positive electrode relative to the commercial electrolyte. The higher the value of the positive electrode LSV is, the more the decomposition of the electrolyte can be suppressed and the high temperature performance can be improved.

1 is an exploded perspective view of a lithium secondary battery according to an embodiment of the present invention.

The present invention is capable of various modifications and various embodiments and is intended to illustrate and describe the specific embodiments in detail. It is to be understood, however, that the invention is not to be limited to the specific embodiments, but includes all modifications, equivalents, and alternatives falling within the spirit and scope of the invention.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. The singular expressions include plural expressions unless the context clearly dictates otherwise. In the present invention, terms such as comprise, having, or the like are intended to designate the presence of stated features, integers, steps, operations, elements, parts or combinations thereof, and may include one or more other features, , But do not preclude the presence or addition of one or more other features, elements, components, components, or combinations thereof.

The electrolyte according to an embodiment of the present invention includes a first electrolyte system including a cyclic carbonate-based solvent and LiPF ₆ , and a first electrolyte system including a chain carbonate solvent, difluoro phosphate, Methylene Methanedisulfonate , MMDS) and a second electrolyte system comprising 4-Fluorotoluene, 4-FT.

In the first electrolyte system, the cyclic carbonate-based solvent includes any one selected from the group consisting of ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate, fluoroethylene carbonate (FEC) And may preferably contain ethylene carbonate which is superior in terms of the characteristics of the cell.

In the first electrolyte system, the LiPF ₆ is dissolved in the carbonate-based solvent to function as a source of lithium ions in the lithium secondary battery and accelerate the movement of lithium ions between the positive electrode and the negative electrode. The LiPF ₆ may be contained in an amount of 6 to 30% by weight, preferably 8 to 20% by weight based on the total weight of the first electrolyte system. When the content of LiPF ₆ is less than 6% by weight, the conductivity of the electrolyte may be lowered to deteriorate the performance of the electrolyte. When the content of LiPF ₆ is more than 30% by weight, the viscosity of the electrolyte may increase and the mobility of lithium ions may be lowered.

The second electrolyte system may include at least one of dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate, methyl propyl carbonate, ethyl propyl carbonate, methyl ethyl carbonate, ethyl methyl carbonate (EMC) And mixtures thereof.

In the second electrolyte system, the counter cation of the difluorophosphate may be lithium, sodium, potassium, magnesium, calcium or NR ¹ R ² R ³ R ⁴ (the R ¹ To R < ⁴ > is an alkyl group having 1 to 10 carbon atoms), and lithium is particularly preferable. That is, the difluorophosphate is preferably lithium difluorophosphate (LiPO ₂ F ₂ ).

In the second electrolyte system, the difluorophosphate may be contained in an amount of 0.1 to 10% by weight, preferably 0.3 to 5% by weight based on the entirety of the second electrolyte system. If the content of the difluorophosphate is less than 0.1% by weight, the coating may not be formed, and if it exceeds 10% by weight, excessive coating may be formed and the resistance may be increased.

The first electrolyte system is a commonly used electrolyte system. However, in order to improve the positive electrode LSV value of the first electrolyte system, when the difluorophosphate is added directly to the first electrolyte system, the lithium ion transfer number of the first electrolyte system, There arises a problem that the contact angle of the contact surface is reduced.

The inventors of the present invention have found that it is possible not to directly add the difluorophosphate to the first electrolyte system but to add the difluorophosphate to a second electrolyte system satisfying a specific condition, When the electrolyte is prepared by mixing the second electrolyte system, it is found that the addition of the difluorophosphate does not cause a problem of lowering the contact angle of the lithium ion transfer water or the surface of the anode while improving the positive electrode LSV value Thus completing the present invention.

Even when the second electrolyte system including the difluorophosphate is mixed with the first electrolyte system, in order that the contact angle of the electrolyte with respect to the lithium ion transfer water or the surface of the anode is not lowered, And the second electrolyte system should be adjusted so that the electron density values are substantially similar to each other.

In this case, when the organic solvent of the second electrolyte system is the chain carbonate-based solvent, the second electrolyte system may contain the methylene methane disulfonate and 4-fluorotoluene together with the difluorophosphate, The electron density value of the second electrolyte system can be adjusted to be substantially similar to the electron density value of the first electrolyte system.

In the second electrolyte system, the methylene methane disulfonate may be contained in an amount of 0.1 to 10% by weight, preferably 0.5 to 5% by weight, based on the total weight of the second electrolyte system. If the content of methylene methane disulfonate is less than 0.1% by weight, the film may not be formed, and if it exceeds 10% by weight, excess film may be formed and the resistance may be increased.

In addition, in the second electrolyte system, the 4-fluorotoluene may be contained in an amount of 0.1 to 10% by weight, preferably 0.5 to 5% by weight, based on the entirety of the second electrolyte system. When the content of 4-fluorotoluene is less than 0.1% by weight, a film may not be formed, and when it is more than 10% by weight, an excessive film may be formed and the resistance may be increased.

The electron density value of the electrolyte system can be measured by a Langmuir probe of Hiden Analytical ESPION. The Langmuir probe is a device for measuring plasma characteristics such as ion and electron density values or electron temperature or potential from an I-V curve obtained by changing the probe voltage. The probe can be a single probe rod with a diameter of 1.2 mm and a length of 6 mm.

The electron density value can be measured by gasifying the electrolyte system in a magnetic field, converting the gas into a plasma state, and measuring the relationship between current and voltage using the Langmuir probe. The relationship between the current and the voltage is determined by setting a copper tube antenna which is wound four times in a cylindrical shape so that the high frequency power is effectively absorbed into the plasma region outside the discharge tube and the RF frequency is 13.56 MHz and the power of the frequency generator is 20 W can do. For reference, when the RF power is 10 W or less, generation of plasma is weak and accurate discharge may not be exhibited.

The sheath potential ( VV _p ) and the current measured by the above method are substituted into the following equation (1), and the electron temperature ( T _e ) corresponding to the slope is obtained. Then, the saturation current ( I _e ) measured using the above method can be substituted into the following equation (2) to calculate the electron density value.

Where e , k, and T _e are the electron charge, the Boltzmann constant, and the electron temperature, respectively, and n _e , I _e , A _p And m _e are the electron density, the saturation current, the surface area of the probe, and the mass of the electron, respectively.

The electron density value of the first electrolyte system is about 2.4 to 2.74 [Phi] * [phi]. On the other hand, the electron density value of the third electrolyte system including only the chain carbonate solvent and LiPF ₆ is about 1.97 to 2.19 Φ * Φ, and the lower limit value thereof is -10 of the lower limit value of the electron density value of the first electrolyte system %. In this case, the electrolyte in which the first electrolyte system and the third electrolyte system are mixed has an insignificant improvement in the positive electrode LSV value, and the lithium ion transfer coefficient is remarkably lowered as compared with the first electrolyte system.

On the other hand, the electron density value of the second electrolyte system including the methylene methane disulfonate and the 4-fluorotoluene together with the difluorophosphate in the chain carbonate solvent is about 2.40 to 2.73? *? And the value is within +/- 10% of the electron density value of the first electrolyte system. In this case, the electrolyte in which the first electrolyte system and the second electrolyte system are mixed not only improves the positive electrode LSV value but also does not lower the contact angle at the surface of the positive electrode and the lithium ion transfer coefficient.

That is, the value of the electron density of the second electrolyte system is within ± 10%, preferably ± 5% of the value of the electron density of the first electrolyte system, that is, As the electron density value of the system is similar to that of the system, it is possible to prevent the contact angle on the surface of the anode and the decrease of the lithium ion transfer coefficient when the two electrolytic systems are mixed.

Therefore, the electron density value of the second electrolyte system is 2.40 to 2.78 Is preferably? *?, More preferably 2.40 to 2.73 It is more preferable that? *? In addition, the electron density value of the electrolyte in which the first electrolyte system and the second electrolyte system are mixed may be 2.44 to 2.81? * ?.

As described above, since the first electrolyte system and the second electrolyte system have similar electron density values, even when the first electrolyte system and the second electrolyte system are mixed, the positive electrode LSV value of the electrolyte does not decrease Rather, the positive electrode LSV value of the electrolyte is greater than the positive electrode LSV value of the first electrolyte system. The anode LSV value of the first electrolyte system is about 3.86 V, but the anode LSV value of the electrolyte is 4 V or higher, preferably 4 to 6 V.

The second electrolyte system may be included in an amount of 5 to 50 parts by weight, and may be 10 to 30 parts by weight based on 100 parts by weight of the first electrolyte system. If the content of the second electrolyte system is less than 5 parts by weight, LSV may not be improved, and if the content of the second electrolyte system exceeds 30 parts by weight, swelling may occur.

Meanwhile, the electrolyte may further include an organic solvent and a lithium salt which are conventionally used.

The organic solvent may be any organic solvent that can act as a medium through which ions involved in an electrochemical reaction of a battery can move. Specifically, examples of the organic solvent include an ester solvent, an ether solvent, a ketone solvent, an aromatic hydrocarbon solvent, and an alkoxyalkane solvent. These solvents may be used alone or in combination of two or more.

Specific examples of the ester solvent include methyl acetate, ethyl acetate, n-propyl acetate, n-butyl acetate, dimethyl acetate, But are not limited to, methyl propionate, ethyl propionate, propyl propionate, butyl propionate,? -Butyrolactone, - fluoro? -Butyrolactone, 1,3-dioxolane, decanolide,? -Valerolactone, mevalonolactone, ),? -caprolactone,? -valerolactone,? -caprolactone, and the like.

Specific examples of the ether solvent include dibutyl ether, tetraglyme, 2-methyltetrahydrofuran, tetrahydrofuran, and the like.

Specific examples of the ketone solvent include cyclohexanone and the like. Specific examples of the aromatic hydrocarbon organic solvent include organic solvents such as benzene, fluorobenzene, chlorobenzene, iodobenzene, toluene, fluorotoluene, xylene). Examples of the alkoxyalkane solvent include dimethoxy ethane and diethoxy ethane.

The lithium salt can be used without particular limitation as long as it is a compound capable of providing lithium ions used in a lithium secondary battery. Specifically, LiClO _4, as to the lithium salt _{LiAsF 6, LiBF 4, LiSbF 6} , LiAl0 4, LiAlCl 4, LiCF 3 SO 3, LiC 4 F 9 SO 3, LiN (C 2 F 5 SO 3) 2, LiN ( C ₂ F ₅ SO ₂ ) ₂ , LiN (CF ₃ SO ₂ ) ₂ . _{LiN (C a F 2a + 1} SO 2) (C b F 2b + 1 SO 2) ( However, a and b is a natural number, preferably 1≤a≤20, 1≤b≤20 and Im), LiCl, LiI, LiB (C ₂ O ₄ ) _2, and mixtures thereof.

When the lithium salt is dissolved in the electrolyte, the lithium salt functions as a source of lithium ions in the lithium secondary battery, and can promote the movement of lithium ions between the cathode and the anode. Accordingly, the lithium salt is preferably contained in the electrolyte at a concentration of about 0.6 mol% to 2 mol%. If the concentration of the lithium salt is less than 0.6 mol%, the conductivity of the electrolyte may be lowered and the performance of the electrolyte may be deteriorated. If the concentration exceeds 2 mol%, the viscosity of the electrolyte may increase and the lithium ion mobility may be decreased. Considering the conductivity of the electrolyte and the mobility of lithium ions, it is more preferable that the lithium salt is controlled to be approximately 0.7 mol% to 1.6 mol% in the electrolyte.

In addition to the above electrolyte components, the electrolyte may further include an additive (hereinafter, referred to as another additive) which can be generally used for an electrolyte for the purpose of improving lifetime characteristics of the battery, suppressing reduction of battery capacity, have.

Examples of the other additives include vinylene carbonate (vinylenecarbonate, VC), metal fluoride (metal fluoride, for example, LiF, RbF, TiF, AgF , AgF 2, BaF 2, CaF 2, CdF 2, FeF 2, HF ₂ , Hg ₂ F ₂ , MnF ₂ , NiF ₂ , PbF ₂ , SnF ₂ , SrF ₂ , XeF ₂ , ZnF ₂ , AlF ₃ , BF ₃ , BiF ₃ , CeF ₃ , CrF ₃ , DyF ₃ , EuF ₃ , _{GaF 3, GdF 3, FeF 3} , HoF 3, InF 3, LaF 3, LuF 3, MnF 3, NdF 3, PrF 3, SbF 3, ScF 3, SmF 3, TbF 3, TiF 3, TmF 3, YF 3 _{, YbF 3, TIF 3, CeF} 4, GeF 4, HfF 4, SiF 4, SnF 4, TiF 4, VF 4, ZrF4 4, NbF 5, SbF 5, TaF 5, BiF 5, MoF 6, ReF 6, SF ₆ , WF ₆ , CoF ₂ , CoF ₃ , CrF ₂ , CsF, ErF ₃ , PF ₃ , PbF ₃ , PbF ₄ , ThF ₄ , TaF ₅ and SeF ₆ ), glutaronitrile Succinonitrile (SN), adiponitrile (AN), 4-tolunitrile, 1,3,6-hexanetricarbonitrile (1,3,6-hexanetricarbonitrile) , Propylene sulfide (PS), 3,3'- (3,3'-thiodipropionitrile, TPN), vinylethylene carbonate (VEC), fluoroethylene carbonate (FEC), difluoroethylenecarbonate, fluorodimethyl carbonate fluoromethylcarbonate, fluorodimethylcarbonate, fluoroethylmethylcarbonate, lithium bis (trifluoromethylsulfonyl) imide, LiTFSI, lithium tetrafluoroborate (LiBF ₄ ), lithium tetrafluoroborate Lithium bis (oxalato) borate, LiBOB, Lithium difluoro (oxalate) borate, LiDFOB), lithium (malonate oxalate) borate malonato oxalato borate, LiMOB), LiPF ₂ C ₄ O ₈ , LiSO ₃ CF ₃ , LiPF ₄ (C ₂ O ₄ ), LiP (C ₂ O ₄ ) ₃ , LiC (SO ₂ CF ₃ ) ₃ , LiBF ₃ CF ₃ CF ₂ ), LiPF ₃ (CF ₃ CF ₂ ) ₃ , Li ₂ B ₁₂ F ₁₂ , 1,3-propane sultone, 1,3- propene sultone, biphenayl, cyclohexyl benzene, 4-fluorotoluene, succinic anhydride, ethylene sulfate anhydride, Tris (methylsilyl) borate, and the like. These may be used singly or in combination of two or more kinds.

The other additives may be included in an amount of 0.1 to 20% by weight, preferably 0.2 to 5% by weight based on the total weight of the electrolyte.

According to another embodiment of the present invention, there is provided a lithium secondary battery including the electrolyte. The lithium secondary battery according to an embodiment of the present invention can be classified into a lithium ion battery, a lithium ion polymer battery, and a lithium polymer battery depending on the type of the separator and the electrolyte used. The lithium secondary battery can be classified into a cylindrical shape, a square shape, Etc., and can be divided into a bulk type and a thin film type depending on the size. The electrolyte according to the embodiment of the present invention may be particularly excellent for application to a lithium ion battery, an aluminum laminated battery and a lithium polymer battery.

Specifically, the lithium secondary battery includes a cathode including a cathode active material disposed opposite to each other, a cathode including a cathode active material, and the electrolyte interposed between the anode and the cathode.

1 is an exploded perspective view of a lithium secondary battery 1 according to an embodiment of the present invention. 1, a lithium secondary battery 1 according to another embodiment of the present invention includes a separator 7 between a cathode 3, an anode 5, the cathode 3, and an anode 5, (5) and the separator (7) are impregnated into the electrolyte (15), and the electrolyte is injected to impregnate the negative electrode (3), the positive electrode (5) and the separator .

Conductive lead members 10 and 13 for collecting a current generated during a battery operation can be attached to the cathode 3 and the anode 5 respectively and the lead members 10 and 13 are respectively connected to the anode 5, And the current generated in the cathode (3) can be led to the positive electrode and the negative electrode terminal.

The anode 5 is prepared by mixing a cathode active material, a conductive agent and a binder to prepare a composition for forming a cathode active material layer, applying the composition for forming a cathode active material layer to a cathode current collector such as aluminum foil, can do.

As the cathode active material, a compound capable of reversibly intercalating and deintercalating lithium (a lithiated intercalation compound) can be used. Specifically, an olivine-type lithium metal compound represented by the following formula (3) can be used.

(3)

Li _x M _y M ' _z XO _4-w Y _w

M and M 'are independently Fe, Ni, Co, Mn, Cr, Zr, Nb, Cu, V, Mo, Ti, Zn, Al, Ga, Mg, B, And X is an element selected from the group consisting of P, As, Bi, Sb, Mo, and combinations thereof, and Y is selected from the group consisting of F, S, and combinations thereof 0 <x? 1, 0 <y? 1, 0 <z? 1, 0 <x + y + z? 2, and 0? W?

Among these compounds, LiCoO ₂ , LiMnO ₂ , LiMn ₂ O ₄ , LiNiO ₂ , LiNi _x Mn _(1-x) O ₂ (where 0 <x <1) and LiM _lx M _2y O ₂ (However, 0≤x≤1, 0≤y≤1, 0≤x + y≤1 , M 1 and M ₂ is one selected from the group consisting of Al, Sr, Mg and La are each independently One), and a mixture thereof.

The negative electrode 3 is prepared by mixing a negative electrode active material, a binder and an optional conductive agent in the same manner as the positive electrode 5 to prepare a composition for forming a negative electrode active material layer and then applying the composition to a negative electrode current collector such as a copper foil .

As the negative electrode active material, a compound capable of reversible intercalation and deintercalation of lithium may be used. Specific examples of the negative electrode active material include carbonaceous materials such as artificial graphite, natural graphite, graphitized carbon fiber and amorphous carbon. Further, in addition to the carbonaceous material, a compound including a metallic compound capable of alloying with lithium or a metallic compound and a carbonaceous material may be used as the negative electrode active material.

At least one of Si, Al, Sn, Pb, Zn, Bi, In, Mg, Ga, Cd, Si alloys, Sn alloys and Al alloys may be used as the metal capable of being alloyed with lithium. Further, a metal lithium thin film may be used as the negative electrode active material.

As the negative electrode active material, any one selected from the group consisting of crystalline carbon, amorphous carbon, carbon composite, lithium metal, lithium-containing alloy, and mixtures thereof may be used in view of high stability.

On the other hand, since the electrolyte is the same as described above with respect to the electrolyte, the description thereof will be omitted. Since the lithium secondary battery can be manufactured by a conventional method, a detailed description thereof will be omitted herein. Although the pouch type lithium secondary battery is described as an example in the present embodiment, the present invention is not limited to the pouch type lithium secondary battery, and any shape can be used as long as it can operate as a battery.

As described above, the lithium secondary battery including the electrolyte according to the embodiment of the present invention can exhibit low DC-IR characteristics, high-temperature storage characteristics, and improved output characteristics, It can be useful for portable devices such as computers, digital cameras, camcorders, electric vehicles such as hybrid electric vehicles (HEV), plug-in hybrid electric vehicles (HEV, PHEV) have.

Hereinafter, embodiments of the present invention will be described in detail so that those skilled in the art can easily carry out the present invention. The present invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein.

[Preparation Example 1: Preparation of electrolyte and lithium secondary battery]

Each of the electrolytes according to Examples and Comparative Examples was prepared with the composition shown in Table 1 below.

On the other hand, LiCoO ₂ as a cathode active material, carbon black as a conductive agent, polyvinylidene fluoride (PVDF) as a binder, n-methyl-2-pyrrolidone as a solvent, 2-pyrrolidone, NMP) was coated on an aluminum (Al) substrate. As the negative electrode, a slurry prepared by mixing MCFC (mesocarbon microbead) and carbon black, PVDF as a binder, and NMP as a solvent was coated on a copper (Cu) substrate, .

An Al-pouch type lithium secondary battery was fabricated using the electrolyte prepared above, the positive electrode and the negative electrode.

The first electrolyte system The second electrolyte system The mixing ratio (weight ratio) of the first and second electrolyte systems Organic solvent (wt%) additive
(wt%) Sum
(wt%) Organic solvent (wt%) Additive 1
(wt%) Additive 2
(wt%) Sum
(wt%) Comparative Example 1 EC 84, LiPF ₆ (16) 100 - - - 100 - Comparative Example 2 EC 84, LiPF ₆ (16) 100 - LiPO ₂ F ₂ (100) - 100 95: 5 Comparative Example 3 - - - EMC (98) LiPO ₂ F ₂ (2) - 100 - Comparative Example 4 - - - EMC (92) LiPO ₂ F ₂ (4) MMDS (4) 100 - Comparative Example 5 - - - EMC (92) LiPO ₂ F ₂ (4) MMDS (2)
+
4-FT (2) 100 - Comparative Example 6 EC 84, LiPF ₆ (16) 100 EMC (98) LiPO ₂ F ₂ (2) - 100 80:20 Comparative Example 7 EC 84, LiPF ₆ (16) 100 EMC (92) LiPO ₂ F ₂ (4) MMDS (4) 100 80:20 Example 1 EC 84, LiPF ₆ (16) 100 EMC (92) LiPO ₂ F ₂ (4) MMDS (2)
+
4-FT (2) 100 80:20

[Experimental Example 1: Characteristic evaluation of the produced electrolyte]

The properties of the electrolytes prepared in the Examples and Comparative Examples were evaluated and the results are shown in Table 2 below.

In Table 2, the respective characteristics were measured by the following methods.

1) Electron density (Φ * Φ): Measured using Langmuir probe.

2) Contact angle (˚): The contact angle was measured by measuring the contact angle.

3) Anode LSV value (V): measured by lenear sweap voltammetry.

4) Lithium ion transition water: Electrochemical impedance spectroscopy (EIS) was measured. Specifically, the lithium ion transfer coefficient can be calculated by the following equation (3). However, I _o R _o and I _ss R _ss are negligible and can be calculated through I _ss / I _o . At this time, DC polarization induction was applied at 10 mV until the current value stabilized.

&Quot; (3) &quot;

t ₊ = I _SS (? VI _o R _o ) / I _o (? VI _SS R _SS )

t ₊ = lithium ion transference number, I _o = I polarization current, Iss = after polarization current

Electron density value Contact angle Positive LSV value Lithium ion transition number Comparative Example 1 2.4 ~ 2.74 14.7 3.86 0.38 to 0.43 Comparative Example 2 2.37-2.72 14.8 3.86 0.21 to 0.26 Comparative Example 3 1.97-2.19 - - - Comparative Example 4 1.98 ~ 2.21 - - - Comparative Example 5 2.40 ~ 2.73 - - - Comparative Example 6 2.32 ~ 2.64 14.9 3.84 0.21 to 0.24 Comparative Example 7 1.98 ~ 2.21 14 4 0.37-0.42 Example 1 2.44 ~ 2.81 15.2 4.06 0.45 to 0.49

Referring to Table 2, the second comparative example is a case where the difluorophosphate is directly added to the first electrolyte system, and the problem that the lithium ion transition number of the first electrolyte system is remarkably lowered occurs Able to know.

On the other hand, the electron density value of Comparative Example 3 containing only the chain carbonate solvent and the difluorophosphate was about 1.97 to 2.19? *?, And the value of the electron density value of the electrolytic solution of Comparative Example 1 There is a difference of over 10%. In this case, the electrolyte of Comparative Example 6 in which the electrolyte of Comparative Example 1 and the electrolyte of Comparative Example 3 were mixed had a slight improvement in the positive electrode LSV value, and the lithium ion transfer coefficient was remarkably higher than that of the electrolyte of Comparative Example 1 .

In addition, the electron density value of the electrolyte of Comparative Example 4 containing only the methylene methane disulfonate together with the difluorophosphate in the chain carbonate solvent was about 1.98 to 2.21 Φ * Φ, and in this case, the electron density value of Comparative Example 1 The electrolyte of Comparative Example 7 in which the electrolyte of Comparative Example 4 is mixed with the electrolyte of Comparative Example 4 is improved in the positive electrode LSV value but the lithium ion transfer number is not improved.

On the other hand, the electron density value of the electrolyte of Comparative Example 5 including the methylene methane disulfonate and the 4-fluorotoluene together with the difluorophosphate in the chain carbonate solvent is about 2.40 to 2.73? *? , And the value is within ± 10% of the electron density value of the first electrolyte system. In this case, the electrolyte of Embodiment 1 in which the electrolyte of Comparative Example 1 and the electrolyte of Comparative Example 5 are mixed has an unexpected effect that not only the positive electrode LSV value is improved but also the contact angle at the positive electrode surface is remarkably improved .

That is, the value of the electron density of the second electrolyte system is within ± 10%, preferably ± 5% of the value of the electron density of the first electrolyte system, that is, It can be seen that the contact angle on the surface of the anode and the decrease in the lithium ion transition number can be prevented when the two electrolyte systems are mixed.

While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed exemplary embodiments, Of the right.

1: Lithium secondary battery
3: cathode 5: anode
7: separator 9: electrode assembly
10, 13: lead member 15: case

Claims (15)

A first electrolyte system comprising a cyclic carbonate-based solvent and LiPF ₆ , and
A second electrolyte system comprising a chain carbonate type solvent, difluoro phosphate, Methylene Methanedisulfonate and 4-Fluorotoluene,
&Lt; / RTI &gt; The method according to claim 1,
Wherein the second electrolyte system is included in an amount of 5 to 50 parts by weight based on 100 parts by weight of the first electrolyte system. The method according to claim 1,
Wherein the first electrolyte system comprises 6 to 30% by weight of the LiPF ₆ based on the entire first electrolyte system. The method according to claim 1,
Wherein the second electrolyte system comprises 0.1 to 10% by weight of the difluorophosphate based on the total of the second electrolyte system. The method according to claim 1,
Wherein the second electrolyte system comprises 0.1 to 10% by weight of methylene methane disulfonate based on the total of the second electrolyte system. The method according to claim 1,
Wherein the second electrolyte system comprises 0.1 to 10% by weight of the 4-fluorotoluene based on the total of the second electrolyte system. The method according to claim 1,
Wherein the first electrolyte system has an electron density value of 2.4 to 2.74 [Phi] * [phi]. 8. The method of claim 7,
Wherein an electron density value of the second electrolyte system is within +/- 10% of an electron density value of the first electrolyte system. 9. The method of claim 8,
And the second electrolyte system has an electron density value of 2.40 to 2.78? *?. The method according to claim 1,
Wherein the electrolyte has an electron density value of 2.44 to 2.81? *?. The method according to claim 1,
Wherein the electrolyte has a linear sweep voltametry (LSV) value greater than a positive LSV value of the first electrolyte system. 12. The method of claim 11,
Wherein the electrolyte has an anode LSV value of at least 4 volts. The method according to claim 1,
Wherein the cyclic carbonate-based solvent comprises any one selected from the group consisting of ethylene carbonate, propylene carbonate, butylene carbonate, fluoroethylene carbonate, and mixtures thereof. The method according to claim 1,
Wherein the chain carbonate-based solvent includes any one selected from the group consisting of dimethyl carbonate, diethyl carbonate, dipropyl carbonate, methylpropyl carbonate, ethylpropyl carbonate, methyl ethyl carbonate, ethyl methyl carbonate, Electrolyte. An anode including a cathode active material,
A negative electrode disposed opposite to the positive electrode and including a negative electrode active material, and
A lithium secondary battery comprising the electrolyte according to claim 1.

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