KR20160077270A - Non-aqueous electrolyte solution for lithium secondary battery and lithium secondary battery comprising the same - Google Patents

Abstract

The present invention relates to an electrolyte solution for a lithium secondary battery including a lithium salt and an organic solvent and, more specifically, to an electrolyte solution for a lithium secondary battery in which the electrolyte solution further including a solid salt having one anion selected from a hexafluorophosphate anion (PF_6^-) and a tetrafluoroborate anion (BF_4^-), and a phosphonium-based cation; and a lithium secondary battery including the same. According to the present invention, an electrolyte solution including an additive is to provide a lithium secondary battery with improved high-temperature lifespan characteristics.

Description

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolyte for a lithium secondary battery, and a lithium secondary battery having the same. 2. Description of the Related Art [0002]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolyte for a lithium secondary battery and a lithium secondary battery having the same, and more particularly, to an electrolyte for a lithium secondary battery and a lithium secondary battery having the same.

As technology development and demand for mobile devices have increased, there has been a rapid increase in demand for secondary batteries as energy sources. Among such secondary batteries, lithium secondary batteries, which exhibit high energy density and operational potential, long cycle life, Batteries have been commercialized and widely used.

The lithium secondary battery has a structure in which an electrolyte solution containing a lithium salt is impregnated in an electrode assembly having a porous separator interposed between a positive electrode and a negative electrode coated with an active material on an electrode current collector. At the time of charging, lithium ions of the positive electrode active material are discharged and inserted into the active material layer of the negative electrode. During discharging, lithium ions of the negative electrode active material layer are discharged and inserted into the positive electrode active material. It plays a role.

The electrolytic solution generally includes an organic solvent and an electrolyte salt. For example, the electrolytic solution is mixed with a solvent mixture of a high-molecular cyclic carbonate such as propylene carbonate, ethylene carbonate, etc., and a low viscosity chain carbonate such as diethyl carbonate, ethyl methyl carbonate, dimethyl carbonate, etc. , LiPF ₆ , LiBF ₄ , LiClO ₄ Or the like is generally used.

Since the lithium-containing halogen salt such as lithium-containing flame retardant and lithium-containing chloride salt, which are mainly used as the electrolyte salt, reacts very sensitively to water, it reacts with moisture present in the battery or during the manufacturing process of the battery, (X = F, Cl, Br, I). In particular, LiPF ₆ lithium salts are unstable at high temperatures, so anions can be thermally decomposed to produce acidic substances such as hydrofluoric acid (HF). Such acidic substances are essentially accompanied by undesirable side reactions when they are present in the cell.

For example, a solid electrolyte interface (SEI) film present on the cathode surface can easily be destroyed due to the strong reactivity of HX (X = F, Cl, Br, I) And the increase in the coating amount of the negative electrode may lead to an increase in the interfacial resistance of the negative electrode. In addition, the anode interface resistance can be increased due to adsorption of lithium fluoride (LiF) on the anode surface, which is a by-product at the time of forming the hydrofluoric acid (HF). In addition, the HX causes a rapid oxidation reaction in the battery, dissolving and degenerating both electrode active materials, and in particular, the transition metal cations contained in the lithium metal oxide used as the cathode active material are eluted , These cations are electrodeposited to the negative electrode to form additional negative electrode coating, thereby further increasing the negative electrode resistance.

On the other hand, the SEI film reacts with lithium ions in the electrolytic solution and is formed on the surface of the negative electrode during the initial charging of the lithium secondary battery, so that decomposition of the carbonate-based electrolytic solution on the negative electrode surface is suppressed to stabilize the battery And serves as a protective film. However, the SEI film produced only by the organic solvent and the lithium salt is somewhat insufficient to serve as a continuous protective film, so that the charge and discharge of the battery are continuously carried out, and in particular, when stored at a high temperature in a fully charged state, And can be gradually collapsed by thermal energy. Due to the collapse of the SEI film, a side reaction in which the surface of the exposed negative electrode active material is reacted with the electrolyte solvent is continuously generated, which may cause an increase in resistance of the negative electrode.

In addition to the above-mentioned causes, the interface resistance between the electrode and the electrolyte can be increased by various causes, and when the interfacial resistance is increased, various performance deterioration of the battery such as charge / discharge efficiency and lifetime characteristics occurs.

In order to solve such a problem, Patent Document 1 (Japanese Patent Laid-Open No. 5-13088) discloses a method of improving the resistance of a lithium secondary battery by adding vinylene carbonate (VC) to the electrolyte solution. However, since the coating formed by this method still shows a high resistance, it did not show sufficient effect in suppressing the increase in resistance of the battery.

Also, Patent Document 2 (Japanese Patent Laid-Open Publication No. 2012-0011209) discloses an electrolyte for a lithium secondary battery comprising an alkylene sulfate having a specific structure, an ammonium compound having a specific structure, and vinylene carbonate. According to this method, the SEI film produced by the above-mentioned sulfate compound has an advantage of reducing the resistance, so that it can improve the low-temperature output characteristics of the battery, but does not exhibit a significant improvement in terms of charging / discharging efficiency and life span of the battery , Further improvement is needed.

Japanese Patent Application Laid-Open No. 5-13088 KR 2012-0011209 A

The problem to be solved by the present invention is to provide a process for producing a solid electrolyte comprising a solid salt having one anion and a phosphonium cation selected from a hexafluorophosphate anion (PF ₆ ^- ) and a tetrafluoroborate anion (BF ₄ ^- ) as an additive Thereby improving the discharge efficiency and lifetime characteristics of the lithium secondary battery.

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

In order to solve this problem, in an electrolyte for a lithium secondary battery comprising a lithium salt and an organic solvent, the electrolyte is selected from the group consisting of hexafluorophosphate anion (PF ₆ ^- ) and tetrafluoroborate anion (BF ₄ ^- ) and a solid salt having a phosphonium-based cation represented by the following general formula (1): < EMI ID = 1.0 >

[Chemical Formula 1]

In Formula 1, R ₁ to R ₄ are each independently hydrogen, halogen, or an alkyl group having 1 to 8 carbon atoms.

Preferably, the content of the solid salt may be 0.01 to 5 parts by weight based on 100 parts by weight of the total amount of the lithium salt and the organic solvent.

The solid salt may be at least one selected from the group consisting of phosphonium hexafluorophosphate, tetramethylphosphonium hexafluorophosphate, tetraethylphosphonium hexafluorophosphate, tetrapropylphosphonium hexafluorophosphate, But are not limited to, Tetrapropylphosphonium hexafluorophosphate, Tetrapropylphosphonium hexafluorophosphate, Tetrahexylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, ), Ethyltrimethylphosphonium hexafluorophosphate, triethylmethylphosphonium hexafluorophosphate (Triethylmethylphosphonium hexafluorophosphate), triethylmethylphosphonium hexafluorophosphate but are not limited to, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, hexamethylphosphate, Phosphonium tetrafluoroborate, Tetramethylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, Tetrapropylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, , Tetrabutylphosphonium tetrafluoroborate, tetrahexylphosphonium tetrafluoroborate, tetraheptylphosphorus, tetrabutylphosphonium tetrafluoroborate, tetrahexylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, ethyltrimethylphosphonium tetrafluoroborate, triethylmethylphosphonium tetrafluoroborate, butyltrimethylphosphonium tetrafluoroborate (Tetraheptylphosphonium tetrafluoroborate), ethyltrimethylphosphonium tetrafluoroborate Butyltrimethylphosphonium tetrafluoroborate, diethyldimethylphosphonium tetrafluoroborate, and dibutyldimethylphosphonium tetrafluoroborate. In the present invention, at least one selected from the group consisting of dibutyldimethylphosphonium tetrafluoroborate, diethyldimethylphosphonium tetrafluoroborate and dibutyldimethylphosphonium tetrafluoroborate may be used.

The present invention also provides a lithium secondary battery comprising the electrolyte solution.

According to the present invention, there is provided an electrolyte solution for a lithium secondary battery comprising as an additive a solid salt having one anion selected from a hexafluorophosphate anion (PF ₆ ^- ) and a tetrafluoroborate anion (BF ₄ ^- ) and a phosphonium cation It is possible to provide a lithium secondary battery improved in high-temperature lifetime characteristics.

1 is a graph showing a comparison of discharge capacity retention ratios of lithium secondary batteries manufactured using the electrolytes of Examples 1 to 3 and Comparative Example 1 according to the present invention.

The present invention provides an electrolyte for a lithium secondary battery comprising a lithium salt and an organic solvent, wherein the electrolyte is selected from the group consisting of hexafluorophosphate anion (PF ₆ ^- ) and tetrafluoroborate anion (BF ₄ ^- ) And a solid salt having one anion and a phosphonium cation represented by the following general formula (1).

[Chemical Formula 1]

(Wherein R ₁ to R ₄ are each independently hydrogen, halogen or an alkyl group having 1 to 8 carbon atoms)

The performance of the battery depends largely on the basic electrolyte composition and the solid electrolyte interface (SEI) film formed by the reaction between the electrolyte and the electrode.

The SEI film refers to a coating formed on the cathode interface by the electrolyte reacting with the cathode when lithium ions deintercalated at the anode during the initial charging of the lithium secondary battery move and are intercalated into the cathode. The SEI film serves to prevent the organic solvent of the electrolyte having a large molecular weight, which is selectively passed through only lithium ions, from intercalating into the carbon anode to collapse the structure of the cathode, and in the subsequent charge / discharge process, Avoid side reactions between other materials. However, the conventional SEI film formed by a carbonate-based organic solvent, a fluoride salt, or other inorganic salt is weak, porous and dense, and thus fails to perform the above-mentioned function.

On the other hand, since the solid salt contained as an additive in the electrolyte solution of the present invention has a lower reduction potential than that of a carbonate-based electrolyte solution, it is reduced on the surface of the negative electrode prior to the electrolyte solvent at the time of initial charging of the battery, SEI film. Therefore, it is possible to prevent the side reaction in which the solvent of the electrolyte is co-intercalated into the negative electrode active material layer or decomposed on the surface of the negative electrode, thereby improving the charging / discharging efficiency of the battery. In addition, since the formed SEI film is a passivation layer having a low chemical reactivity, it can exhibit high stability even in a long-term cycle and can achieve long-life characteristics.

The content of the solid salt is preferably 0.01 to 5.0 parts by weight, more preferably 0.1 to 3.0 parts by weight based on 100 parts by weight of the total amount of the lithium salt and the organic solvent. When the content is less than 0.01 parts by weight, it may be difficult to obtain an effect of forming an SEI film having excellent stability. On the other hand, when the content is more than 5.0 parts by weight, charging and discharging efficiency may be lowered.

Preferable examples of the solid salt according to the present invention include phosphonium hexafluorophosphate, tetramethylphosphonium hexafluorophosphate, tetraethylphosphonium hexafluorophosphate, tetraethylphosphonium hexafluorophosphate, tetraethylphosphonium hexafluorophosphate, Tetrabutylphosphonium hexafluorophosphate, tetrabutylphosphonium hexafluorophosphate, tetrahexylphosphonium hexafluorophosphate, tetrahexylphosphonium hexafluorophosphate, tetrabutylphosphonium hexafluorophosphate, tetrabutylphosphonium hexafluorophosphate, tetrabutylphosphonium hexafluorophosphate, tetrabutylphosphonium hexafluorophosphate, (Tetraheptylphosphonium hexafluorophosphate), ethyltrimethylphosphonium hexafluorophosphate, triethylmethylphosphonium hexafluorophosphate (Triet but are not limited to, hylmethylphosphonium hexafluorophosphate, butyl trimethylphosphonium hexafluorophosphate, diethyldimethylphosphonium hexafluorophosphate, dibutyldimethylphosphonium hexafluorophosphate, phosphonium hexafluorophosphate, Phosphonium tetrafluoroborate, Tetramethylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, Tetrapropylphosphonium tetrafluoroborate, Tetramethylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, Tetraethylphosphonium tetrafluoroborate, ), Tetrabutylphosphonium tetrafluoroborate, tetrahexylphosphonium tetra (tetrabutylphosphonium tetrafluoroborate), tetrahexylphosphonium tetra fluoroborate, tetraheptylphosphonium tetrafluoroborate, ethyltrimethylphosphonium tetrafluoroborate, triethylmethylphosphonium tetrafluoroborate, butyltrimethylphosphonate, tetramethylphosphonium tetrafluoroborate, tetrabutylphosphonium tetrafluoroborate, At least one selected from the group consisting of Butyltrimethylphosphonium tetrafluoroborate, Diethyldimethylphosphonium tetrafluoroborate and Dibutyldimethylphosphonium tetrafluoroborate can be mentioned. But are not limited thereto.

Meanwhile, the lithium salt contained in the electrolytic solution of the present invention can be used in a concentration range of 0.6M to 2.0M, more preferably in a range of 0.7M to 1.6M. If the concentration of the lithium salt is less than 0.6M, the conductivity of the electrolyte may be lowered to deteriorate the performance of the electrolyte. On the other hand, if the concentration exceeds 2.0M, the viscosity of the electrolyte may increase and the lithium ion mobility may decrease. The anion of the lithium salt may be, for example, F ^- , Cl ^- , Br ^- , I ^- , NO ₃ ^- , N (CN) _{2 ^{-, BF 4 -, ClO 4}} -, PF 6 -, (CF 3) 2 PF 4 -, (CF 3) 3 PF 3 -, (CF 3) 4 PF 2 -, (CF 3) 5 PF -, ( ^{_{CF 3) 6 P -, CF}} 3 SO 3 -, CF 3 CF 2 SO 3 -, (CF 3 SO 2) 2 N -, (FSO 2) 2 N -, CF 3 CF 2 (CF 3) 2 CO - _{, (CF 3 SO 2) 2} CH -, (SF 5) 3 C -, (CF 3 SO 2) 3 C -, CF 3 (CF 2) 7 SO 3 -, CF 3 CO 2 -, CH 3 CO 2 ^- , SCN ^-, and (CF ₃ CF ₂ SO ₂ ) ₂ N ^- .

The organic solvent contained in the electrolytic solution may be any of those conventionally used in an electrolyte for a lithium secondary battery. Examples of the organic solvent include ether, ester, amide, linear carbonate, cyclic carbonate, etc., Can be used.

Among them, a carbonate compound which is typically a cyclic carbonate, a linear carbonate, or a mixture thereof may be included. Specific examples of the cyclic carbonate compound include ethylene carbonate (EC), propylene carbonate (PC), 1,2-butylene carbonate, 2,3-butylene carbonate, 1,2-pentylene carbonate, 2,3-pentylene carbonate, vinylene carbonate, and halides thereof, or a mixture of two or more thereof. Specific examples of the linear carbonate compound include a group consisting of dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate, ethyl methyl carbonate (EMC), methyl propyl carbonate and ethyl propyl carbonate Any one selected, or a mixture of two or more thereof may be used as typical examples, but the present invention is not limited thereto.

In particular, ethylene carbonate and propylene carbonate, which are cyclic carbonates in the carbonate-based organic solvent, can be preferably used because they have high permittivity as a high viscosity organic solvent and dissociate the lithium salt in the electrolyte well, and dimethyl carbonate and diethyl carbonate When a low viscosity and a low dielectric constant linear carbonate are mixed in an appropriate ratio, an electrolyte having a high electric conductivity can be prepared, and thus it can be more preferably used.

As the ether in the organic solvent, any one selected from the group consisting of dimethyl ether, diethyl ether, dipropyl ether, methyl ethyl ether, methyl propyl ether and ethyl propyl ether or a mixture of two or more thereof may be used , But is not limited thereto.

Examples of the ester in the organic solvent include methyl acetate, ethyl acetate, propyl acetate, methyl propionate, ethyl propionate, propyl propionate,? -Butyrolactone,? -Valerolactone,? -Caprolactone,? -Valerolactone and? -Caprolactone, or a mixture of two or more thereof, but the present invention is not limited thereto.

The electrolyte solution for a lithium secondary battery of the present invention may further contain an additive for forming a known SEI film within the scope of the present invention. Examples of the additive for forming the SEI film that can be used in the present invention include vinylene carbonate, vinylethylene carbonate, fluoroethylene carbonate, cyclic sulfite, saturated sulphone, unsaturated sulphone and non-cyclic sulphone, But is not limited thereto.

Examples of the cyclic sulfite include ethylene sulfite, methyl ethylene sulfite, ethyl ethylene sulfite, 4,5-dimethylethylene sulfite, 4,5-diethyl ethylene sulfite, propylene sulfite, Diethyl propyl sulfite, 4,6-diethyl propyl sulfite, and 1,3-butylene glycol sulfite. The saturated sulphone includes, for example, 1,3-propane sultone, and 1,4-butane sultone. Examples of the unsaturated sultone include ethene sultone, 1,3-propene sultone, 1,4-butene sultone, Phenolsaltone, and the like. Examples of the non-cyclic sulfone include divinyl sulfone, dimethyl sulfone, diethyl sulfone, methyl ethyl sulfone, and methyl vinyl sulfone.

The additive for forming the SEI film may be contained in an appropriate amount depending on the specific kind of the additive, for example, 0.01 to 10 parts by weight based on 100 parts by weight of the electrolytic solution.

On the other hand, the present invention provides a lithium secondary battery comprising the electrolyte solution.

The lithium secondary battery is manufactured by injecting an electrolyte prepared according to the present invention into an electrode structure composed of a positive electrode, a negative electrode, and a separator interposed between the positive electrode and the negative electrode. The positive electrode and the negative electrode may be prepared by mixing the active material, the binder, and the conductive agent with a solvent to prepare a slurry, applying the slurry to a current collector such as aluminum, followed by drying and pressing.

As the cathode active material, a lithium-containing transition metal oxide may be preferably used. For example, Li _x CoO ₂ (0.5 <x <1.3), Li _x NiO ₂ (0.5 <x <1.3), Li _x MnO ₂ <x <1.3, 0 <a <1, 0 <b <1), Li _x Mn ₂ O ₄ (0.5 <x <1.3), Li _x (Ni _a Co _b Mn _c ) O ₂ , 0 <c <1, a + b + c = 1), Li x Ni 1-y Co y O 2 (0.5 <x <1.3, 0 <y <1), Li x Co 1 -y Mn y O 2 (0.5 <x <1.3, 0 = y <1), Li x Ni 1 -y Mn y O 2 (0.5 <x <1.3, O = y <1), Li x (Ni a Co b Mn c) O 4 (0.5 <x <1.3, 0 <a <2, 0 <b <2, 0 <c <2, a + b + c = 2), Li _x Mn _{2 -z} Ni _z O ₄ , 0 <z <2), Li x Mn 2 -z Co z O 4 (0.5 <x <1.3, 0 <z <2), Li x CoPO 4 (0.5 <x <1.3) and Li _x FePO ₄ (0.5 <x <1.3), or a mixture of two or more thereof. The lithium-containing transition metal oxide may be coated with a metal such as aluminum (Al) or a metal oxide. In addition to the lithium-containing transition metal oxide, sulfide, selenide and halide may also be used.

As the anode active material, a carbon material, lithium metal, silicon or tin, which lithium ions can be occluded and released, can be used, and metal oxides such as TiO ₂ and SnO ₂ having a potential with respect to lithium of less than ₂ V are also possible. Preferably, carbon materials can be used, and carbon materials such as low-crystalline carbon and highly-crystalline carbon can be used. Examples of low crystalline carbon include soft carbon and hard carbon. Examples of highly crystalline carbon include natural graphite, artificial graphite, Kishgraphite, pyrolytic carbon, High-temperature sintered carbon such as mesophase pitch based carbon fiber, meso-carbon microbeads, mesophase pitches and petroleum or coal tar pitch derived cokes are representative.

The binder serves to bind the active material and the conductive agent to bind to the current collector. The binder binds the active material and the conductive agent and binds the active material to the current collector. The binder includes a binder such as polyvinylidene fluoride, polypropylene, carboxymethylcellulose, polyvinylpyrrolidone, tetrafluoroethylene, polyethylene, polyvinyl alcohol, Rubber and the like which are conventionally used in a lithium ion secondary battery can be used.

Conductive agents such as artificial graphite, natural graphite, acetylene black, ketjen black, channel black, lamp black, thermal black, conductive fibers such as carbon fiber and metal fiber, conductive metal oxides such as titanium oxide, metal powders such as aluminum and nickel Can be used.

As the separator, a single olefin or olefin complex such as polyethylene (PE) and polypropylene (PP), polyamide (PA), polyacrylonitrile (PAN), polyethylene oxide (PEO), polypropylene oxide , Polyethyleneglycol diacrylate (PEGA), polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), polyvinyl chloride (PVC), and the like.

The external shape of the lithium secondary battery of the present invention is not particularly limited, but may be a cylindrical shape, a square shape, a pouch shape, a coin shape, or the like using a can.

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail with reference to examples.

<Preparation of electrolytic solution>

Example  One

Ethylene carbonate, ethylmethylcarbonate and dimethylcarbonate were mixed in a volume ratio of 2: 4: 4 to prepare an organic solvent. Next, LiPF ₆ , which is a lithium salt, was dissolved in the organic solvent to prepare a LiPF ₆ mixed solution having a lithium salt concentration of 1.15 M. Tetraethylphosphonium tetrafluoroborate, which is a solid salt, was then added to the mixed solution in an amount of 0.5 part by weight based on 100 parts by weight of the mixed solution to prepare an electrolytic solution.

Example  2

In Example 1, instead of tetraethylphosphonium tetrafluoroborate, tetrabutylphosphonium tetrafluoroborate was used as a solid salt, and the other electrolytic solution was prepared in the same manner.

Example  3

In Example 1, tetraethylphosphonium hexafluorophosphate (Tetraethylphosphonium hexafluorophosphate) was used instead of tetraethylphosphonium tetrafluoroborate as a solid salt, and an electrolytic solution was prepared in the same manner as in the remainder.

Comparative Example  One

The electrolyte was prepared in the same manner as in Example 1, except that no solid salt was added.

<Manufacture of Battery>

As a cathode active material LiNi _{0 .5 Co 0 .2 Mn 0 .3 O} 2, the carbon black, polyvinylidene fluoride (PVdF) as a binder and a conductive material 91.5: 4.4: 4.1 were mixed in a weight ratio of, N- methyl Pyrrolidone to prepare a positive electrode slurry. The slurry was coated on an aluminum current collector, followed by drying and rolling to prepare a positive electrode. A graphite electrode was used as a negative electrode.

Then, a coin cell was prepared by using a porous polyethylene membrane (manufactured by Tonen Co., Ltd.) as a separator together with the prepared positive electrode and negative electrode, and injecting the prepared electrolyte solution.

<Evaluation method>

1. Cell Formation

The prepared coin cell was allowed to stand at a constant temperature of 25 DEG C for 12 hours and then subjected to a constant current of 0.1 C at a constant current of 4.3 V using a lithium secondary battery charge / discharge device (Toyo-System Co., LTD, TOSCAT-3600) C was charged to a constant voltage condition with a termination current and discharged at 0.1 C to 3.0 V under a constant current condition to complete the cell formation process.

2. Charging / discharging efficiency and high-temperature lifetime characteristics (%)

The cells having been subjected to the formation were charged at a constant current of 0.5 C to a constant current of 4.3 V and at a constant voltage of 0.05 C to a constant current of 0.5 V and discharged at a constant current of 3.0 V until the charge / Charging and discharging tests under these conditions were repeated 50 times. The charge-discharge efficiency and the capacity retention rate in each cycle were calculated in accordance with the following equations and are shown in Table 1. [

Charge / discharge efficiency (%) = discharge capacity / charge capacity × 100

Capacity retention rate [%] = (discharge capacity in 50 ^st cycles / discharge capacity in 1 ^st cycles)

 × 100

1 ^st cycle 50 ^st cycle Volume
Retention rate
(%) Charging capacity
(mAh / g) Discharge capacity
(mAh / g) efficiency
(%) Charging capacity
(mAh / g) Discharge capacity
(mAh / g) efficiency
(%) Example 1 154.5 150.5 97.5 137.3 136.9 99.8 91.0 Example 2 155.1 151.2 97.5 135.9 135.6 99.8 89.7 Example 3 157.3 153.4 97.5 138.0 137.8 99.8 89.8 Comparative Example 1 157.2 153.1 97.4 134.7 134.5 99.8 87.9

1 and FIG. 1, in the case of the coin cell manufactured using the electrolytic solution of Examples 1 to 3 according to the present invention, in comparison with the coin cell manufactured using the electrolytic solution of Comparative Example 1, And the discharge capacity retention ratio at 50 cycles was improved.

While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the scope of the present invention is not limited to the disclosed exemplary embodiments but is to be construed as being limited only by the appended claims. Should be construed as being included in the scope of the present invention.

Claims (7)

1. An electrolyte for a lithium secondary battery comprising a lithium salt and an organic solvent,
Wherein the electrolytic solution contains one anion selected from hexafluorophosphate anion (PF ₆ ^- ) and tetrafluoroborate anion (BF ₄ ^- ) and phosphonium cations represented by the following formula (1) &Lt; / RTI &gt; wherein the solid salt further comprises: &lt; RTI ID = 0.0 &gt;
[Chemical Formula 1]

In Formula 1, R ₁ to R ₄ are each independently hydrogen, halogen, or an alkyl group having 1 to 8 carbon atoms. The method according to claim 1,
The solid salt may be selected from the group consisting of phosphonium hexafluorophosphate, tetramethylphosphonium hexafluorophosphate, tetraethylphosphonium hexafluorophosphate, tetrapropylphosphonium hexa But are not limited to, Tetrapropylphosphonium hexafluorophosphate, Tetrabutylphosphonium hexafluorophosphate, Tetrahexylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, Tetraheptylphosphonium hexafluorophosphate, Ethyl trimethylphosphonium hexafluorophosphate, triethylmethylphosphonium hexafluorophosphate, triethylmethylphosphonium hexafluorophosphate, But are not limited to, butyltrimethylphosphonium hexafluorophosphate, diethyldimethylphosphonium hexafluorophosphate, dibutyldimethylphosphonium hexafluorophosphate, phosphonium tetrafluoroborate, phosphonium tetrafluoroborate, tetramethylphosphonium tetrafluoroborate, tetraethylphosphonium tetrafluoroborate, tetrapropylphosphonium tetrafluoroborate, tetrabutylphosphorus, tetrabutylphosphonium tetrafluoroborate, tetrabutylphosphonium tetrafluoroborate, Tetrabutylphosphonium tetrafluoroborate, tetrahexylphosphonium tetrafluoroborate, tetraheptylphosphonium bromide, tetrahexylphosphonium tetrafluoroborate, But are not limited to, tetrafluoroborate, tetrafluoroborate, ethyltrimethylphosphonium tetrafluoroborate, triethylmethylphosphonium tetrafluoroborate, butyltrimethylphosphonium tetrafluoroborate, ), Diethyldimethylphosphonium tetrafluoroborate, and dibutyldimethylphosphonium tetrafluoroborate. The electrolytic solution for a lithium secondary battery according to claim 1, wherein the electrolyte is at least one selected from the group consisting of lithium diisopropylphosphonium tetrafluoroborate, diethyldimethylphosphonium tetrafluoroborate, and dibutyldimethylphosphonium tetrafluoroborate. The method according to claim 1,
Wherein the content of the solid salt is 0.01 to 5 parts by weight based on 100 parts by weight of the total amount of the lithium salt and the organic solvent. The method according to claim 1,
The anion of the lithium salt is selected from the group consisting of F ^- , Cl ^- , Br ^- , I ^- , NO ₃ ^- , N (CN) ₂ ^- , BF ₄ ^- , ClO ₄ ^- , PF ₆ ^- , (CF ₃ ) ₂ PF ₄ ^{- _{CF 3) 3 PF 3 -,}} (CF 3) 4 PF 2 -, (CF 3) 5 PF -, (CF 3) 6 P -, CF 3 SO 3 -, CF 3 CF 2 SO 3 -, (CF 3 ^{_{SO 2) 2 N -, (}} FSO 2) 2 N -, CF 3 CF 2 (CF 3) 2 CO -, (CF 3 SO 2) 2 CH -, (SF 5) 3 C -, (CF 3 SO 2 ) ₃ C ^- , CF ₃ (CF ₂ ) ₇ SO ₃ ^- , CF ₃ CO ₂ ^- , CH ₃ CO ₂ ^- , SCN ^- and (CF ₃ CF ₂ SO ₂ ) ₂ N ^- And an electrolyte solution for a lithium secondary battery. The method according to claim 1,
Wherein the organic solvent is at least one selected from the group consisting of ether, ester, amide, linear carbonate and cyclic carbonate. The method according to claim 1,
Wherein the electrolytic solution further comprises at least one selected from the group consisting of vinylene carbonate, vinylethylene carbonate, fluoroethylene carbonate, cyclic sulfite, saturated sulphone, unsaturated sulphone, and acyclic sulphone. A lithium secondary battery comprising the electrolyte according to any one of claims 1 to 6.

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