KR101780094B1 - Non-aqueous liquid electrolyte and lithium secondary battery comprising the same - Google Patents

Abstract

The present invention relates to a non-aqueous electrolytic solution containing lithium bis (fluorosulfonyl) imide (LiFSI) and a fluorinated carbonate compound additive, a lithium-nickel-manganese-cobalt oxide as a cathode active material A lithium secondary battery comprising an anode, a cathode, and a separator.
According to the nonaqueous electrolyte solution for a lithium secondary battery of the present invention, a solid SEI film is formed at the cathode at the time of initial charging of the lithium secondary battery including the same, and the output characteristics of the lithium secondary battery are improved, Can be improved.

Description

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a non-aqueous electrolytic solution and a lithium secondary battery comprising the same.

The present invention relates to a non-aqueous electrolytic solution containing lithium bis (fluorosulfonyl) imide (LiFSI) and a fluorinated carbonate compound additive, a lithium-nickel-manganese-cobalt oxide as a cathode active material An anode, a cathode, and a separator.

As technology development and demand for mobile devices are increasing, the demand for secondary batteries as energy sources is rapidly increasing. Among these secondary batteries, lithium secondary batteries having high energy density and voltage have been commercialized and widely used.

Lithium metal oxide is used as the positive electrode active material of the lithium secondary battery, and lithium metal, lithium alloy, crystalline or amorphous carbon or carbon composite material is used as the negative electrode active material. The active material is coated on the current collector with an appropriate thickness and length, or the active material itself is coated in a film form and wrapped or laminated together with a separator as an insulator to form an electrode group. The electrode group is then placed in a can or similar container, Thereby manufacturing a secondary battery.

This lithium secondary battery is charged and discharged while repeating the process of intercalating lithium ions from the lithium metal oxide of the anode into the graphite electrode of the cathode and deintercalating the lithium ions. At this time, since lithium is highly reactive, it reacts with the carbon electrode to form Li ₂ CO ₃ , LiO, LiOH and the like to form a film on the surface of the cathode. This film is called Solid Electrolyte Interface (SEI) film. The SEI film formed at the beginning of charging prevents the reaction between lithium ion and carbon anode or other materials during charging and discharging. It also acts as an ion tunnel, allowing only lithium ions to pass through. This ion tunnel serves to prevent the collapse of the structure of the carbon anode by co-intercalating the organic solvent of the electrolyte having a large molecular weight moving together by solvation of the lithium ion together with the carbon anode.

Therefore, in order to improve the high-temperature cycle characteristics and the low-temperature output of the lithium secondary battery, a solid SEI film must always be formed on the cathode of the lithium secondary battery. Once the SEI membrane is formed at the time of initial charging, it is used as an ion tunnel to prevent the reaction between the lithium ion and the negative electrode or other materials during repetition of charging and discharging by using the battery and passing only lithium ions between the electrolyte and the negative electrode .

It has been difficult to expect improvement in low-temperature output characteristics due to the formation of a non-uniform SEI film in the case of an electrolyte solution which does not contain an electrolyte additive or contains an electrolyte additive having poor characteristics. Further, even when the amount of the electrolyte additive is included, if the amount of the electrolyte additive can not be adjusted to the required amount, the surface of the anode may be decomposed or the oxidation reaction may occur at the high temperature due to the electrolyte additive, thereby ultimately increasing the irreversible capacity of the secondary battery, There is a problem in that it is lowered.

The present invention provides a non-aqueous electrolyte for a lithium secondary battery and a lithium secondary battery including the same, which can improve not only low-temperature power characteristics but also high-temperature storage characteristics and stability.

In order to solve the above problems, the present invention provides a non-aqueous electrolytic solution containing lithium bis (fluorosulfonyl) imide (LiFSI) and a fluorinated carbonate compound additive, a lithium-nickel-manganese- A lithium secondary battery comprising a cathode, a cathode, and a separator including a cobalt-based oxide.

The non-aqueous electrolytic solution may further include a lithium salt, wherein a mixing ratio of the lithium salt to lithium bisfluorosulfonylimide is 1: 0.01 to 1: 1 in a molar ratio, and the lithium bisfluorosulfonylimide is a non- And the concentration in the aqueous electrolytic solution is 0.01 mole / l to 2 mole / l.

The lithium-nickel-manganese-cobalt-based oxide may include an oxide represented by the following formula (1).

[Chemical Formula 1]

Li _{1 + x} (Ni _a Co _b Mn _c ) O ₂

0.55? A? 0.65, 0.18? B? 0.22, 0.18? C? 0.22, and -0.2? X? 0.2.

According to the nonaqueous electrolyte solution for a lithium secondary battery of the present invention and a secondary battery comprising the same, it is possible to form a solid SEI film in a negative electrode at the time of initial charging of the lithium secondary battery and suppress gas generation in a high temperature environment, , The decomposition of the surface of the anode and the oxidation reaction of the electrolyte are prevented so that the output characteristics of the lithium secondary battery can be improved and the output characteristics and stability after high temperature storage can be improved.

Hereinafter, the present invention will be described in detail in order to facilitate understanding of the present invention. The terms and words used in the present specification and claims should not be construed as limited to ordinary or dictionary terms and the inventor may appropriately define the concept of the term in order to best describe its invention It should be construed as meaning and concept consistent with the technical idea of the present invention.

The non-aqueous electrolytic solution according to an embodiment of the present invention includes lithium bisfluorosulfonylimide (LiFSI).

The lithium bisfluorosulfonylimide is added to a non-aqueous electrolyte as a lithium salt to improve the low-temperature output characteristics by forming a solid and thin SEI film on the cathode, and also to improve the decomposition of the anode surface And the oxidation reaction of the electrolytic solution can be prevented. Furthermore, since the SEI film formed on the cathode has a small thickness, it is possible to more smoothly move lithium ions in the cathode, thereby improving the output of the secondary battery.

According to an embodiment of the present invention, the concentration of the lithium bisfluorosulfonylimide in the non-aqueous electrolytic solution is preferably 0.01 mole / liter to 2 mole / liter, more preferably 0.01 mole / liter to 1 mole / liter Do. When the concentration of the lithium bisfluorosulfonylimide is less than 0.1 mole / l, the effect of improving the low-temperature power and improving the high-temperature cycle characteristics of the lithium secondary battery is insignificant, and when the lithium bisfluorosulfonylimide concentration is less than 0.1 mole / If it exceeds 2 mole / l, side reactions within the electrolyte may occur excessively during charging / discharging of the battery, causing swelling, and corrosion of the positive electrode made of metal or the negative electrode current collector in the electrolyte solution may be caused.

In order to prevent such side reactions, the non-aqueous electrolytic solution of the present invention may further include a lithium salt. Examples of the lithium salt include lithium salts such as LiPF ₆ , LiAsF ₆ , LiCF ₃ SO ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiBF ₄ , LiSbF ₆ , LiN (C _{2 F 5 SO 2) 2,} LiAlO 4, may be LiAlCl _4, LiClO _4, and any one group or a mixture of two or more of those selected from the consisting of.

The mixing ratio of the lithium salt to lithium bisfluorosulfonylimide is preferably 1: 0.01 to 1, in terms of the molar ratio. When the mixing ratio of the lithium salt and the lithium bisfluorosulfonyl imide is in the range of the above-mentioned molar ratio, a side reaction in the electrolytic solution during the charging / discharging of the battery may occur excessively and swelling may occur, , The output improvement of the generated secondary battery may be deteriorated. Specifically, when the mixing ratio of the lithium salt to the lithium bisfluorosulfonylimide is less than 1: 0.01, the process of forming the SEI film in the lithium ion battery and the process of forming the SEI film by solvating lithium ions by the carbonate solvent A large amount of irreversible reaction may occur during the process of inserting between the negative electrodes, and the deterioration of the negative electrode surface layer (for example, carbon surface layer) and the decomposition of the electrolyte may improve the low temperature output of the secondary battery, The effect of improving the capacity characteristics may be insufficient. When the mixing ratio of the lithium salt to the lithium bisfluorosulfonylimide is in a molar ratio of more than 1: 1, an excessive amount of lithium bis-fluorosulfonylimide is contained in the electrolytic solution and corrosion of the electrode current collector Thereby affecting the stability of the secondary battery.

The cathode active material, which is the lithium-nickel-manganese-cobalt oxide, may include an oxide represented by Chemical Formula 1 below.

[Chemical Formula 1]

Li _{1 + x} (Ni _a Co _b Mn _c ) O ₂

0.55? A? 0.65, 0.18? B? 0.22, 0.18? C? 0.22, and -0.2? X? 0.2.

By using the positive electrode active material, which is the lithium-nickel-manganese-cobalt oxide, as the positive electrode, it can be combined with lithium bisfluorosulfonylimide to have a synergistic effect. Lithium-nickel-manganese-cobalt oxide cathode The positive electrode active material exhibits a phenomenon in which Li + ions and Ni +2 ions in the layered structure of the cathode active material in the charge / mixing, and the structure of the cathode active material is collapsed. As a result, the cathode active material causes a side reaction with the electrolyte or elution of transition metal. This is because Li + 1 ions and Ni +2 ions are similar in size to each other. As a result, the performance of the battery is easily deteriorated due to the depletion of the electrolyte in the secondary battery and the structural collapse of the cathode active material through the side reaction.

Therefore, a LiFSI-based layer is formed on the surface of the anode using a LiFSI-based electrolyte as a positive electrode active material according to an embodiment of the present invention, and cation mixing of Li + 1 + ions and Ni + A range capable of securing a sufficient amount of nickel transition metal for ensuring the capacity of the positive electrode active material has been found. According to the cathode active material containing the oxide of Formula 1 of the present invention, when the LiFSI-applied electrolyte is used, the electrolyte solution, the side reaction, and the metal elution phenomenon can be effectively suppressed.

Particularly, when the ratio of the oxide represented by the formula (1) to the Ni transition metal exceeds 0.65, excess Ni is contained in the cathode active material, and therefore Li + And Ni +2 may not suppress the cation mixing phenomenon of ions.

In addition, when the excess Ni transition metal is included in the cathode active material, the nickel transition metal having the d orbital in an environment such as high temperature has an octahedron structure in the environment of high temperature due to the variation of oxidation number of Ni, Or the oxidation number fluctuates (non-uniformization reaction) to form a warped octahedron. As a result, the crystal structure of the positive electrode active material including the nickel transition metal is deformed, and the probability of nickel metal in the positive electrode active material is increased.

As a result, the inventors of the present invention have found that high efficiency is obtained in high temperature stability and capacity characteristics while producing high output in combination with LiFSI salt and a cathode active material containing an oxide according to the range of Formula 1 above.

In addition, the electrolyte additive according to an embodiment of the present invention may include a fluorinated carbonate compound. Specifically, it may be at least one compound selected from the group consisting of compounds represented by the following formula (2).

(2)

R ₁ is an alkyl group having 1 to 3 carbon atoms, and hydrogen of the alkyl group may be substituted with at least two fluorine atoms. Specifically, R ₁ may be _{one selected} from a difluoromethyl group, a difluoroethyl group, a difluoropropyl group, a trifluoromethyl group, a trifluoroethyl group, and a trifluoropropyl group. According to an embodiment of the present invention, the fluorinated carbonate compound may be a compound represented by Formula (3).

(3)

In the lithium secondary battery, the oxygen released from the anode in the high temperature environment promotes the exothermic decomposition reaction of the electrolyte solvent, causing so-called swelling phenomenon in which the battery is swollen, so that the life of the battery and the charging / discharging efficiency are rapidly lowered, The safety of the battery greatly deteriorates due to the explosion of the battery. Accordingly, the fluorinated carbonate compound is added to the electrolyte as a fluorine substituent as a flame retardant compound, so that the gas generated due to the decomposition of the electrolyte can be suppressed by the reaction between the cathode and the anode surface at high temperature and the electrolyte. Therefore, by adding the carbonate compound according to one embodiment of the present invention, lifetime characteristics at high temperature can be improved, and an increase in the cell thickness can be reduced and the stability can be increased.

At this time, the content of the fluorinated carbonate compound can be used without limitation as long as it is the amount required to achieve the effect of the present invention, such as high temperature storage output and stability improvement of the battery. For example, the fluorocarbonate compound may be used in an amount of 1 to 20 wt. %, And preferably from 3.0 wt% to 15 wt%. When the amount of the fluorinated carbonate compound is less than 1% by weight, it is difficult to sufficiently exhibit the effect of suppressing the generation of gas and the flame retardancy depending on the addition. When the amount of the fluorinated carbonate compound exceeds 20% by weight, However, it is possible to increase the irreversible capacity or to increase the resistance of the cathode. In particular, the fluorinated carbonate compound can be controlled according to the amount of lithium bisfluorosulfonylimide added. In order to more effectively prevent side reactions that may occur due to the addition of a large amount of lithium bisfluorosulfonylimide.

The non-aqueous organic solvent that can be included in the non-aqueous electrolyte solution is not limited as long as it can minimize decomposition due to oxidation reaction during charging and discharging of the battery, Such as a nitrile solvent, a cyclic carbonate, a linear carbonate, an ester, an ether or a ketone. These may be used alone, or two or more of them may be used in combination.

Among the above organic solvents, a carbonate-based organic solvent can be easily used. The cyclic carbonate may be any one selected from the group consisting of ethylene carbonate (EC), propylene carbonate (PC) and butylene carbonate (BC) (DMC), diethyl carbonate (DEC), dipropyl carbonate (DPC), ethyl methyl carbonate (EMC), methyl propyl carbonate (MPC) and ethyl propyl carbonate Or a mixture of two or more thereof.

The nitrile solvent may be at least one selected from the group consisting of acetonitrile, propionitrile, butyronitrile, valeronitrile, caprylonitrile, heptanenitrile, cyclopentanecarbonitrile, cyclohexanecarbonitrile, 2-fluorobenzonitrile , Difluorobenzonitrile, trifluorobenzonitrile, phenylacetonitrile, 2-fluorophenylacetonitrile, 4-fluorophenylacetonitrile, and may be one or more selected from the group consisting of one embodiment Examples of non-aqueous solvents include acetonitrile.

Meanwhile, the lithium secondary battery according to an embodiment of the present invention may include a cathode, a cathode, a separator interposed between the anode and the cathode, and the non-aqueous electrolyte. The positive electrode and the negative electrode may include the positive electrode active material and the negative electrode active material, respectively, according to an embodiment of the present invention.

On the other hand, examples of the negative electrode active material include amorphous carbon or regular carbon, specifically carbon such as non-graphitized carbon or graphite carbon; _{LixFe 2 O 3 (0≤x≤1),} LixWO 2 (0≤x≤1), SnxMe 1 - x Me 'y O z (Me: Mn, Fe, Pb, Ge; Me': Al, B, P , Si, Group 1, Group 2, and Group 3 elements of the periodic table, halogen, and 0 < x? 1; 1? Y? 3; 1? Z? 8); Lithium metal; Lithium alloy; Silicon-based alloys; Tin alloy; _{SnO, SnO 2, PbO, PbO} 2, Pb 2 O 3, Pb 3 O 4, Sb 2 O 3, Sb 2 O 4, Sb 2 O 5, GeO, GeO 2, Bi 2 O 3, Bi 2 O 4, And Bi ₂ O ₅ ; Conductive polymers such as polyacetylene; Li-Co-Ni-based materials and the like can be used.

The separation membrane may be a porous polymer film such as a porous polymer film made of a polyolefin-based polymer such as an ethylene homopolymer, a propylene homopolymer, an ethylene / butene copolymer, an ethylene / hexene copolymer and an ethylene / methacrylate copolymer Or may be a laminate of two or more kinds. In addition, nonwoven fabrics made of conventional porous nonwoven fabrics, for example, glass fibers having a high melting point, polyethylene terephthalate fibers, or the like can be used, but the present invention is not limited thereto.

The secondary battery may have a variety of shapes depending on purposes such as a cylindrical shape, a square shape, a pouch shape, and the like, and is not limited to the structure known in the art. The lithium secondary battery according to an embodiment of the present invention may be a pouch type secondary battery.

EXAMPLES The present invention will be further illustrated by the following examples and experimental examples, but the present invention is not limited by these examples and experimental examples.

Example

Example 1

[Preparation of electrolytic solution]

Aqueous organic solvent having a composition of ethylene carbonate (EC): ethylmethyl carbonate (EMC) = 3: 7 (volume ratio) and LiPF ₆ based on the total amount of non-aqueous electrolytic solution as a lithium salt 0.9 mole / liter of lithium bisfluorosulfonylimide and 0.1 mole / liter of lithium bisfluorosulfonylimide, and 10% by weight based on the total weight of the nonaqueous electrolytic solution as the additive, the fluorinated carbonate compound of Formula 3 was added to prepare a nonaqueous electrolytic solution .

 [Production of lithium secondary battery]

As a positive electrode active material Li (Ni Co _{0 .6 0 0 .2 .2} Mn) O ₂ 92% by weight, 4 wt% carbon black conductive agent (carbon black), polyvinylidene fluoride (PVdF) as a binder, 4 wt% Was added to the solvent N-methyl-2-pyrrolidone (NMP) to prepare a positive electrode mixture slurry. The positive electrode mixture slurry was applied to an aluminum (Al) thin film having a thickness of about 20 탆 and dried to produce a positive electrode, followed by a roll press to prepare a positive electrode.

Further, a negative electrode mixture slurry was prepared by adding carbon powder as a negative electrode active material, PVdF as a binder and carbon black as a conductive agent to 96 wt%, 3 wt% and 1 wt%, respectively, as a solvent. The negative electrode mixture slurry was applied to a copper (Cu) thin film as an anode current collector having a thickness of 10 mu m and dried to prepare a negative electrode, followed by roll pressing to produce a negative electrode.

The thus prepared positive electrode and negative electrode were fabricated by polymerizing a polymer type cell with a separator composed of three layers of polypropylene / polyethylene / polypropylene (PP / PE / PP), and then the prepared non-aqueous electrolyte was injected, The preparation of the battery was completed.

Example 2

The lithium salt is added to LiPF ₆ based on the total amount of the non-aqueous electrolytic solution Aqueous electrolyte and a lithium secondary battery were prepared in the same manner as in Example 1, except that the lithium secondary battery was used in an amount of 0.3 mole / liter and lithium bisfluorosulfonylimide 0.3 mole / liter.

Example 3

The lithium salt is added to LiPF ₆ based on the total amount of the non-aqueous electrolytic solution , And 0.4 mole / liter of lithium bis-fluorosulfonylimide were used in place of the non-aqueous electrolyte and lithium secondary battery.

Example 4

The lithium salt is added to LiPF ₆ based on the total amount of the non-aqueous electrolytic solution Aqueous electrolyte solution and a lithium secondary battery were prepared in the same manner as in Example 1, except that 0.5 mole / liter of lithium bisfluorosulfonylimide and 0.5 mole / liter of lithium bisfluorosulfonylimide were used.

Comparative Example 1

The lithium salt is added to LiPF ₆ based on the total amount of the non-aqueous electrolytic solution A nonaqueous electrolytic solution and a lithium secondary battery were prepared in the same manner as in Example 1, except that 0.4 mole / liter of lithium bisfluorosulfonylimide and 0.6 mole / liter of lithium bisfluorosulfonylimide were used.

Comparative Example 2

A nonaqueous electrolytic solution and a lithium secondary battery were prepared in the same manner as in Example 2, except that the above additives were not used.

Comparative Example 3

Wherein as a positive electrode active material Li (Ni Co _{0 .5 0 0 .2 .3} Mn) O _2, and is in the same manner as Example 2, except to prepare a non-aqueous electrolytic solution and a lithium secondary battery.

Experimental Example

<Low Temperature Output Characteristics>

Outputs were calculated using the voltage difference generated when the secondary batteries manufactured in Examples 1 to 4 and Comparative Examples 1 to 3 were charged and discharged for 10 seconds at -30 ° C to 0.5 ° C. At this time, the output of Comparative Example 1 was 3.7W. The outputs of Examples 1 to 4 and Comparative Examples 2 to 3 were calculated on the basis of Comparative Example 1 as a percentage. The results are shown in Table 1 below. The test was performed at 50% SOC (state of charge).

<Output characteristics after high temperature storage>

Outputs were calculated using the voltage difference generated when the secondary batteries manufactured in Examples 1 to 4 and Comparative Examples 1 to 3 were charged and discharged at 23 ° C and 5 ° C for 10 seconds after storage at 60 ° C for 24 weeks. (24 watt power (W) / initial power (W) * 100 (%)) after 24 weeks based on the initial output power are shown in Table 1 below. The test was performed at 50% SOC (state of charge).

<Capacity characteristics after high temperature storage>

The secondary batteries manufactured in Examples 1 to 4 and Comparative Examples 1 to 3 were charged at 1 C to 4.2 V / 38 mA under constant current / constant voltage (CC / CV) conditions and discharged at 3 C to 2.5 V under constant current (CC) And the discharge capacity thereof was measured. Then, the secondary batteries prepared in Examples 1 to 4 and Comparative Examples 1 to 3 were stored at 60 DEG C for 24 weeks. Then, the secondary batteries were stored at 23 DEG C under constant current / constant voltage (CC / CV) , And discharged at 3 C to 2.5 V under a constant current (CC) condition, and the discharge capacity thereof was measured. The discharge capacity after 24 weeks based on the initial discharge capacity was calculated as a percentage (discharge capacity after 24 weeks / initial discharge capacity * 100 (%)), and the results are shown in Table 1 below.

&Lt; Measurement of cell thickness &

The thickness of the secondary batteries prepared in Examples 1 to 4 and Comparative Examples 1 to 3 was measured at 60 ° C for 24 weeks. The results are shown in Table 1 below.

<Nail test>

The secondary batteries prepared in Examples 2 and 4 and Comparative Example 2 were charged up to 4.2 V and subjected to a nail test through the battery at a speed of 1 m / min to evaluate the safety. The thermocouple was attached to the battery The temperature rise of the battery was confirmed. The maximum rising temperature of the cell during each nail test is shown in Table 1 below.

Low temperature output (%)
Comparative Example 1 Preparation Properties after high temperature storage Nail test rising temperature (℃) Output Characteristics (%) Capacity characteristics (%) Cell Thickness Growth Rate (%) Example 1 2.06 89.9 96.1 7.9 - Example 2 5.29 94.5 98.6 6.4 30 Example 3 3.89 92.9 96.9 6.8 - Example 4 2.11 92.1 95.8 7.1 32 Comparative Example 1 - 89.2 93.2 8.9 - Comparative Example 2 -3.24 80.4 88.5 18.5 118 Comparative Example 3 -2.87 76.8 91.9 12.2 -

As shown in Table 1, it can be seen that the secondary batteries of Examples 1 to 4 exhibit excellent output at a low temperature output of about 8% or more, compared with the secondary batteries of Comparative Examples 1 to 3. In particular, the secondary batteries of Examples 1 to 4 were improved in stability at high temperature by using a fluorinated carbonate compound as an additive, and were combined with LiFSI, which is a lithium salt, in the properties (capacity, output characteristics) To 3 &lt; th &gt; secondary batteries. In addition, since the fluorinated carbonate compound of Comparative Example 2 was not added, the rate of increase in thickness after storage at high temperature was remarkable to 18.5.

In the nail test, the nail penetrates into the cell, tears the separator, and when the anode and the cathode are short-circuited, a large amount of current flows instantaneously as the temperature rises instantaneously, resulting in ignition or explosion. According to Table 1, the batteries manufactured in Examples 2 and 4 suppressed the maximum temperature of the battery from 30 to 32 ° C, which was higher than the normal operation temperature of the battery, compared with the battery manufactured in Comparative Example 2 . Accordingly, it has been found that the safety of the secondary battery according to the present invention is improved.

Claims (13)

A non-aqueous electrolytic solution comprising a non-aqueous organic solvent, a first lithium salt, a second lithium salt, lithium bis (fluorosulfonyl) imide (LiFSI), and a fluorinated carbonate compound additive;
A positive electrode comprising an oxide represented by the following formula (1) as a positive electrode active material;
cathode; And
Comprising a separator,
Wherein the mixing ratio of the first lithium salt to the lithium bisfluorosulfonylimide as the second lithium salt is 1: 0.01 to 1: 1 in a molar ratio.
[Chemical Formula 1]
Li _{1 + x} (Ni _a Co _b Mn _c ) O ₂
0.55? A? 0.65, 0.18? B? 0.22, 0.18? C? 0.22, and -0.2? X? 0.2.
delete delete delete The method according to claim 1,
Wherein the concentration of the lithium bisfluorosulfonylimide in the non-aqueous electrolytic solution is 0.01 mole / l to 2 mole / l.
The method according to claim 1,
Wherein the first lithium salt is selected from the group consisting of LiPF ₆ , LiAsF ₆ , LiCF ₃ SO ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiBF ₄ , LiSbF ₆ , LiN (C ₂ F ₅ SO ₂ ) ₂ , LiAlO ₄ , LiAlCl ₄ , LiClO ₄ , or a mixture of two or more thereof.
The method according to claim 1,
Wherein the fluorinated carbonate compound is a compound represented by the following formula (2).
(2)

(Wherein,
R ₁ is an alkyl group having 1 to 3 carbon atoms, and the hydrogen of the alkyl group is substituted with at least two fluorine atoms.)
The method according to claim 1,
Wherein the fluorinated carbonate compound is a compound represented by the general formula (3).
(3)

The method according to claim 1,
Wherein the content of the fluorinated carbonate compound additive is 1 to 20% by weight based on the total weight of the nonaqueous electrolyte solution.
The method according to claim 1,
Wherein the non-aqueous organic solvent includes a nitrile solvent, a linear carbonate, a cyclic carbonate, an ester, an ether, a ketone, or a combination thereof.
11. The method of claim 10,
The cyclic carbonate is any one selected from the group consisting of ethylene carbonate (EC), propylene carbonate (PC) and butylene carbonate (BC), or a mixture of two or more thereof. The linear carbonate is selected from the group consisting of dimethyl carbonate (DMC) Wherein the lithium secondary carbonate is one selected from the group consisting of diphenyl carbonate (DEC), dipropyl carbonate (DPC), ethyl methyl carbonate (EMC), methyl propyl carbonate (MPC) and ethyl propyl carbonate (EPC) battery.
11. The method of claim 10,
The nitrile solvent may be at least one selected from the group consisting of acetonitrile, propionitrile, butyronitrile, valeronitrile, caprylonitrile, heptanenitrile, cyclopentanecarbonitrile, cyclohexanecarbonitrile, 2-fluorobenzonitrile At least one selected from the group consisting of fluorobenzonitrile, difluorobenzonitrile, trifluorobenzonitrile, phenylacetonitrile, 2-fluorophenylacetonitrile, and 4-fluorophenylacetonitrile.
The method according to claim 1,
Wherein the lithium secondary battery is a pouch type lithium secondary battery.