WO2015064987A1 - 리튬 이차전지 - Google Patents
리튬 이차전지 Download PDFInfo
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- WO2015064987A1 WO2015064987A1 PCT/KR2014/010137 KR2014010137W WO2015064987A1 WO 2015064987 A1 WO2015064987 A1 WO 2015064987A1 KR 2014010137 W KR2014010137 W KR 2014010137W WO 2015064987 A1 WO2015064987 A1 WO 2015064987A1
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- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
- H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
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- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
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- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
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- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
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- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
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- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
- H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
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- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
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- H01M4/60—Selection of substances as active materials, active masses, active liquids of organic compounds
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- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
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- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
- H01M6/162—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
- H01M6/168—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by additives
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- H—ELECTRICITY
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- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0568—Liquid materials characterised by the solutes
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
- H01M2004/028—Positive electrodes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to a nonaqueous electrolyte and a positive electrode including a phosphate compound, and a lithium secondary battery including the same.
- Lithium secondary batteries are the batteries that can best meet these demands, and research on these is being actively conducted.
- a lithium secondary battery is a battery composed of a positive electrode, a negative electrode, and an electrolyte solution and a separator that provides a movement path of lithium ions between the positive electrode and the negative electrode, and is used for oxidation and reduction reactions when lithium ions are occluded and discharged from the positive electrode and the negative electrode. Thereby generating electrical energy.
- the average discharge voltage of the lithium secondary battery is about 3.6 to 3.7 V, which is one of the advantages of higher discharge voltage than other alkaline batteries, nickel-cadmium batteries, and the like.
- an electrochemically stable electrolyte composition is required in the charge and discharge voltage range of 0 to 4.2V.
- lithium ions derived from the positive electrode active material such as lithium metal oxide are moved to the negative electrode active material such as graphite and inserted into the interlayer of the negative electrode active material.
- the electrolyte and the carbon constituting the negative electrode active material react on the surface of the negative electrode active material such as graphite to generate a compound such as Li 2 CO 3 , Li 2 O, or LiOH.
- SEI Solid Electrolyte Interface
- the SEI membrane acts as an ion tunnel, passing only lithium ions.
- the SEI membrane is an effect of this ion tunnel, which prevents the breakdown of the negative electrode structure by intercalation of organic solvent molecules having a large molecular weight moving with lithium ions in the electrolyte between the layers of the negative electrode active material. Therefore, by preventing contact between the electrolyte solution and the negative electrode active material, decomposition of the electrolyte solution does not occur, and the amount of lithium ions in the electrolyte solution is reversibly maintained to maintain stable charge and discharge.
- the first technical problem to be solved by the present invention is to provide a nonaqueous electrolyte that can improve the life characteristics at high temperature and high voltage of the secondary battery by adding a small amount of an additive to the nonaqueous electrolyte of the lithium secondary battery.
- a second technical problem to be solved by the present invention is to provide a positive electrode that can improve the life characteristics at high temperature and high voltage of the secondary battery by adding a small amount of an additive to the positive electrode of the lithium secondary battery.
- Another object of the present invention is to provide a lithium secondary battery including the nonaqueous electrolyte or the positive electrode.
- the present invention is a lithium salt; Electrolyte solvents; And to provide a non-aqueous electrolyte containing a compound represented by the formula (1):
- Y 1 and Y 2 are each independently Si or Sn
- R 1 to R 6 are each independently hydrogen or a C 1 to C 10 alkyl group
- Y 3 is Si or Sn
- R 7 to R 9 are each independently hydrogen or a C 1 to C 10 alkyl group
- n 2-4.
- the present invention also provides a positive electrode comprising a lithium transition metal oxide and the compound represented by the formula (1).
- the life characteristics of a lithium secondary battery may be improved, and particularly, the life characteristics may be improved at a high temperature of 45 ° C. or higher and a high voltage of 4.3 V or higher. You can. In addition, it can exhibit stable and excellent life characteristics at high temperature and high voltage regardless of the moisture content of the electrode or the presence of drying and pressing.
- FIG. 1 is a graph showing measurement results of life characteristics at 45 ° C. of secondary batteries in which the lithium secondary batteries of Examples 3 and 4 and Comparative Examples 6 to 8 do not have a roll press of the positive electrode.
- FIG. 2 is a graph showing measurement results of life characteristics at 45 ° C. of secondary batteries subjected to roll pressing of the positive electrode in the lithium secondary batteries of Examples 3 and 4 and Comparative Examples 6 to 8.
- FIG. 2 is a graph showing measurement results of life characteristics at 45 ° C. of secondary batteries subjected to roll pressing of the positive electrode in the lithium secondary batteries of Examples 3 and 4 and Comparative Examples 6 to 8.
- FIG. 3 is a graph showing measurement results of life characteristics at 45 ° C. of a secondary battery in Example 3 and the lithium secondary batteries of Comparative Examples 9 and 10, in which both drying and roll pressing of the positive electrode were not performed.
- FIG. 3 is a graph showing measurement results of life characteristics at 45 ° C. of a secondary battery in Example 3 and the lithium secondary batteries of Comparative Examples 9 and 10, in which both drying and roll pressing of the positive electrode were not performed.
- FIG. 4 is a graph showing measurement results of life characteristics at 45 ° C. of secondary batteries in Example 3 and Comparative Examples 9 and 10, in which the positive electrode was dried and the roll press was not performed.
- FIG. 5 is a graph showing measurement results of life characteristics at 45 ° C. of a secondary battery in which the positive electrode was dried and rolled in the lithium secondary batteries of Example 3 and Comparative Examples 9 and 10.
- FIG. 5 is a graph showing measurement results of life characteristics at 45 ° C. of a secondary battery in which the positive electrode was dried and rolled in the lithium secondary batteries of Example 3 and Comparative Examples 9 and 10.
- FIG. 6 is a graph showing measurement results of life characteristics at 45 ° C. according to the lithium secondary battery of Example 3, depending on whether the cathode is dried and roll press is performed.
- FIG. 7 is a graph illustrating a life characteristic measurement result at 45 ° C. according to drying of a positive electrode and whether roll press is performed in a lithium secondary battery of Comparative Example 9.
- FIG. 7 is a graph illustrating a life characteristic measurement result at 45 ° C. according to drying of a positive electrode and whether roll press is performed in a lithium secondary battery of Comparative Example 9.
- FIG. 8 is a graph illustrating a life characteristic measurement result at 45 ° C. according to drying of a positive electrode and whether roll press is performed in a lithium secondary battery of Comparative Example 10.
- FIG. 9 is a graph showing the results of measuring lifetime characteristics at 45 ° C. of the lithium secondary batteries of Examples 5 and 6 and Comparative Examples 11 and 12.
- FIG. 9 is a graph showing the results of measuring lifetime characteristics at 45 ° C. of the lithium secondary batteries of Examples 5 and 6 and Comparative Examples 11 and 12.
- a lithium salt comprising a compound represented by the formula (1):
- Y 1 and Y 2 are each independently Si or Sn
- R 1 to R 6 are each independently hydrogen or a C 1 to C 10 alkyl group
- Y 3 is Si or Sn
- R 7 to R 9 are each independently hydrogen or a C 1 to C 10 alkyl group
- n 2-4.
- A in A of Formula 1, when n is 3 or 4, A is linear or a ring by connecting O to another repeating unit adjacent to P of one repeating unit, or The linear and the ring may be connected together.
- the compound represented by Formula 1 may be preferably any one selected from the group consisting of the following compounds (1) to (6) or a mixture of two or more thereof:
- a nonaqueous electrolyte used in a lithium secondary battery has electrolyte stability decomposed at the surface of an electrode during charging and discharging of the battery, or co-intercalation between carbon material negative electrode layers to collapse the negative electrode structure, thereby ensuring stability of the battery. May inhibit.
- the SEI film formed on the surface of the negative electrode by reduction of the electrolyte solvent during the initial charging of the battery.
- the SEI film is insufficient to serve as a continuous protective film of the negative electrode, and as a result, when the battery is repeatedly charged and discharged, the life and performance thereof are deteriorated.
- the SEI film of the conventional lithium secondary battery is not thermally stable, and when the battery is operated or left at a high temperature, it is susceptible to collapse by increased thermal energy over time, and thus, the battery performance is further deteriorated under high temperature.
- gases such as CO 2 are continuously generated due to the collapse of the SEI film, decomposition of the electrolyte, and the like, thereby increasing the internal pressure and thickness of the battery.
- the compound represented by Chemical Formula 1 when added to the nonaqueous electrolyte or electrode of the lithium secondary battery, battery thickness increase and performance degradation due to destruction of the SEI film of the lithium secondary battery may be improved.
- the lithium secondary battery may improve life characteristics, particularly at high temperatures of 45 ° C. or higher and high voltages of 4.3 V or higher.
- the non-aqueous electrolyte including the addition may exhibit stable and excellent life characteristics at high temperature and high voltage regardless of the moisture content of the electrode or the drying and pressing of the electrode when the secondary battery is manufactured.
- the additive of Formula 1 may serve to stabilize anion of lithium salt.
- the electrolyte contains a material containing fluorine (F) such as LiPF 6
- the fluorine encounters moisture or lithium impurities during charge and discharge to generate HF (fluoric acid), and the corrosion caused by the HF leads to an electrode cycle.
- the additive may inhibit the generation of HF, which may be generated due to side reactions between the water generated during charge and discharge and the electrolyte.
- the structure of the compound of Formula 1 having a more unstable structure than the general phosphate compound having a simple structure for example, a phosphate compound having n of 2 or more in Chemical Formula 1 is electrochemically unstable and can easily be broken to participate in film formation of the electrode. In particular, a conductive film can be formed. These two factors can greatly affect the performance improvement when applying the secondary battery.
- the nonaqueous electrolyte may further include a compound represented by the following formula (2):
- R 10 to R 18 are each independently hydrogen or a C 1 to C 10 alkyl group.
- the compound represented by Chemical Formula 2 may be, for example, tris (trimethylsilyl) phosphate (TMSPa).
- the mixing ratio of the compound represented by the formula (1) and the compound represented by the formula (2) is 1: 0.1 to 2 by weight, preferably 1: 0.2 to 1 by weight, more preferably 1: 0.2 to 0.6 by weight.
- the compound represented by Formula 1 is 0.01 to 5% by weight based on the total amount of the non-aqueous electrolyte Wt%, preferably 0.1 wt% to 2 wt%.
- the secondary battery may be consumed during operation of the initial secondary battery, and thus, deterioration of life may occur during charge / discharge or long-term storage. May adversely affect stability characteristics.
- the lithium salt contained in the non-aqueous electrolyte may use a lithium salt commonly used in the art, for example, LiPF 6 , LiAsF 6 , LiCF 3 SO 3 , LiN (CF 3 SO 2 ) 2 , LiBF 4 , LiBF 6 , LiSbF 6 , LiN (C 2 F 5 SO 2 ) 2 , LiAlO 4 , LiAlCl 4 , LiSO 3 CF 3 and LiClO 4 , or any one selected from two It may be a mixture of the above.
- a lithium salt commonly used in the art for example, LiPF 6 , LiAsF 6 , LiCF 3 SO 3 , LiN (CF 3 SO 2 ) 2 , LiBF 4 , LiBF 6 , LiSbF 6 , LiN (C 2 F 5 SO 2 ) 2 , LiAlO 4 , LiAlCl 4 , LiSO 3 CF 3 and LiClO 4 , or any one selected from two It may be a mixture
- the electrolyte solvent used in the present invention can be used without limitation those conventionally used in the electrolyte for lithium secondary batteries, for example, ether, ester, amide, linear carbonate, cyclic carbonate and the like, each alone or two or more. It can be mixed and used.
- carbonate compounds which are typically cyclic carbonates, linear carbonates or mixtures thereof may be included.
- 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, any one selected from the group consisting of or mixtures of two or more thereof.
- linear carbonate compounds include dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate (DPC), ethylmethyl carbonate (EMC), methylpropyl carbonate (MPC) and ethylpropyl carbonate (EPC). Any one selected from the group consisting of, or a mixture of two or more thereof may be representatively used, but is not limited thereto.
- the cyclic carbonate in the carbonate-based electrolyte solvent preferably includes propylene carbonate, ethylene carbonate, and mixtures thereof, and may be preferably used because it dissociates lithium salt in the electrolyte well because of high dielectric constant as a high-viscosity organic solvent.
- diethyl carbonate, dimethyl carbonate, ethylmethyl carbonate, and a linear carbonene, which is a mixture thereof, with the cyclic carbonate can be more preferably used because low viscosity, low dielectric constant linear carbonate can be mixed in an appropriate ratio to make an electrolyte having high electrical conductivity.
- ester in the electrolyte solvent is methyl acetate, ethyl acetate, propyl acetate, ethyl propionate (EP), methyl propionate (MP), ⁇ -butyrolactone, ⁇ -valerolactone, ⁇ -caprolactone , ⁇ -valerolactone and ⁇ -caprolactone, any one selected from the group consisting of, or mixtures of two or more thereof may be used, among which ethyl propionate (EP), methyl propionate (especially low viscosity) MP) and mixtures thereof.
- the present invention may provide a positive electrode comprising a lithium transition metal oxide and the compound represented by the formula (1) according to another embodiment:
- A in A of Formula 1, when n is 3 or 4, A is linear or a ring by connecting O to another repeating unit adjacent to P of one repeating unit, or The linear and the ring may be connected together.
- the preferred compound may be any one selected from the group consisting of compounds of the following (1) to (6) or a mixture of two or more thereof:
- the anode may further include a compound represented by Chemical Formula 2.
- the compound represented by Chemical Formula 2 may be, for example, tris (trimethylsilyl) phosphate (TMSPa).
- the mixing ratio of the compound represented by Formula 1 and the compound represented by Formula 2 is 1: 0.1 to 2 by weight, preferably 1: 0.2 to 1 by weight, more preferably 1: 0.2 to 0.6 by weight.
- the compound represented by the formula (1) in the case of including the compound represented by the formula (1) as an additive in the positive electrode, it is possible to improve the life characteristics of the lithium secondary battery, especially life characteristics at high temperature of 45 °C or higher and 4.3 V or higher Can improve. In addition, it can exhibit stable and excellent life characteristics at high temperature and high voltage regardless of the moisture content of the electrode or the presence of drying and pressing.
- the structure of the compound of Formula 1 having a more unstable structure than the general phosphate compound having a simple structure for example, a phosphate compound having n of 2 or more in Chemical Formula 1 is electrochemically unstable and can easily be broken to participate in film formation of the electrode. In particular, a conductive film can be formed.
- the compound represented by Formula 1 is 0.01% by weight to 5 based on the total amount of the positive electrode mixed slurry containing a positive electrode active material, an additive, a conductive agent and a binder Wt%, preferably 0.1 wt% to 2 wt%.
- the positive electrode active material for example, a lithium transition metal oxide may be a compound represented by Formula 3 below:
- a lithium secondary battery the positive electrode; cathode; A separator interposed between the positive electrode and the negative electrode; And a nonaqueous electrolyte, and the positive electrode or the nonaqueous electrolyte may include the compound of Formula 1.
- a carbon-based negative electrode active material such as crystalline carbon, amorphous carbon, or a carbon composite may be used alone or in combination of two or more thereof.
- the crystalline carbon is graphite such as natural graphite and artificial graphite. (graphite) carbon.
- the separator is a porous polymer film, for example, a porous polymer film made of a polyolefin-based polymer such as ethylene homopolymer, propylene homopolymer, ethylene / butene copolymer, ethylene / hexene copolymer and ethylene / methacrylate copolymer This may be a single or two or more laminated.
- a porous nonwoven fabrics such as high-melting glass fibers, polyethylene terephthalate fibers, and the like may be used, but are not limited thereto.
- Lithium secondary battery according to an embodiment of the present invention may be in the range of 4.3V to 5.0V in the charging voltage, even when charged at the high voltage is excellent in the life characteristics of the battery.
- the moisture content or the press of the electrode for example, it can exhibit a stable and excellent life characteristics at high temperature and high voltage of 45 °C or more.
- the external shape of the lithium secondary battery of the present invention is not particularly limited, but may be cylindrical, square, pouch type, or coin type using a can.
- EC ethylene carbonate
- DMC dimethyl carbonate
- EMC ethylmethyl carbonate
- TMSPa tris (trimethylsilyl) phosphate
- a nonaqueous electrolyte was prepared by adding in an amount of 2% by weight based on the total amount.
- Example 1 In the preparation of the nonaqueous electrolyte of Example 1, a nonaqueous electrolyte was prepared in the same manner as in Example 1, except that tetra (trimethylsilyl) pyrophosphate was added alone as a nonaqueous electrolyte additive.
- Example 1 propane sultone (PS) and vinylene carbonate (VC) instead of a mixed additive of tetra (trimethylsilyl) pyrophosphate and tris (trimethylsilyl) phosphate (TMSPa) as a nonaqueous electrolyte additive ) was prepared in the same manner as in Example 1, except that 1.5: 1 by weight was added to prepare a nonaqueous electrolyte.
- PS propane sultone
- VC vinylene carbonate
- TMSPa tris (trimethylsilyl) phosphate
- Example 1 propane sultone (PS) and vinylene carbonate (VC) instead of a mixed additive of tetra (trimethylsilyl) pyrophosphate and tris (trimethylsilyl) phosphate (TMSPa) as a nonaqueous electrolyte additive ) And ethylene sulfate (ESa) was prepared in the same manner as in Example 1, except that 0.5: 3: 1 weight ratio was added to prepare a nonaqueous electrolyte.
- PS propane sultone
- VC vinylene carbonate
- TMSPa tris (trimethylsilyl) phosphate
- ESa ethylene sulfate
- Example 1 propane sultone (PS) and vinylene carbonate (VC) instead of a mixed additive of tetra (trimethylsilyl) pyrophosphate and tris (trimethylsilyl) phosphate (TMSPa) as a nonaqueous electrolyte additive ) was prepared in a weight ratio of 1.5: 3 and added, and a nonaqueous electrolyte was prepared in the same manner as in Example 1 except that LiPF 6 was used at a concentration of 1.3 M.
- PS propane sultone
- VC vinylene carbonate
- TMSPa tris (trimethylsilyl) phosphate
- Example 1 propane sultone (PS) and vinylene carbonate (VC) instead of a mixed additive of tetra (trimethylsilyl) pyrophosphate and tris (trimethylsilyl) phosphate (TMSPa) as a nonaqueous electrolyte additive ) And LiBF 4 were prepared in the same ratio as in Example 1, except that LiBF 4 was added in a weight ratio of 1.5: 1: 2 to prepare a nonaqueous electrolyte.
- PS propane sultone
- VC vinylene carbonate
- TMSPa tris (trimethylsilyl) phosphate
- TMSPa tris (trimethylsilyl) phosphate
- TMSPa tris (trimethylsilyl) phosphate
- TMSPa tris (trimethylsilyl) phosphate
- Li (Li 0.2 Mn 0.55 Ni 0.15 Co 0.1 ) O 2 94% by weight of Li (Li 0.2 Mn 0.55 Ni 0.15 Co 0.1 ) O 2 as a positive electrode active material, 3% by weight of carbon black as a conductive agent, 3% by weight of PVdF as a binder, N-methyl-2-pyrrolidone as a solvent (NMP) was added to prepare a positive electrode mixture slurry.
- the positive electrode mixture slurry was applied to a thin film of aluminum (Al), which is a positive electrode current collector having a thickness of about 20 ⁇ m, and dried to prepare a positive electrode.
- Al aluminum
- 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 at 96 wt%, 3 wt%, and 1 wt%, respectively, to NMP as a solvent.
- the negative electrode mixture slurry was applied to a copper (Cu) thin film, which is a negative electrode current collector having a thickness of 10 ⁇ m, dried to prepare a negative electrode, and then roll-rolled to prepare a negative electrode.
- Cu copper
- the positive electrode and the negative electrode prepared as described above were manufactured in a conventional manner with a PE separator, and then the non-aqueous electrolyte prepared in Example 1 was injected to complete the production of a lithium secondary battery.
- a lithium secondary battery was manufactured in the same manner as in Example 3, except that the nonaqueous electrolyte prepared in Example 2 was used.
- a lithium secondary battery was manufactured in the same manner as in Example 3, except that the nonaqueous electrolyte prepared in Comparative Example 1 was used.
- a lithium secondary battery was manufactured in the same manner as in Example 3, except that the nonaqueous electrolytes prepared in Comparative Examples 2 to 5 were used.
- the lithium secondary batteries prepared in Examples 3 and 4 and Comparative Examples 6 to 8 (based on 3.26 mAh of battery capacity) were charged at 45 ° C. at a constant current of 1 C until they reached 4.35 V, and then charged at a constant voltage of 4.35 V. Charging was terminated when the charging current became 0.163 mAh. Thereafter, it was left for 10 minutes and then discharged until it became 2.94V with a constant current of 2 C. This was repeated with 1 to 100 cycles and 200 cycles. The results are shown in FIGS. 1 and 2, respectively.
- FIG. 1 shows the life characteristics of a lithium secondary battery using a positive electrode that does not perform a roll press when manufacturing a positive electrode
- FIG. 2 shows a lithium secondary battery using a positive electrode that performs a roll press. The lifetime characteristics of the result.
- the lithium secondary batteries of Examples 3 and 4 of the present invention containing tetra (trimethylsilyl) pyrophosphate (Compound (1)) as an additive of a non-aqueous electrolyte have a roll press during the production of the positive electrode Regardless, the slope was slow up to 100 cycles.
- TMSPa tris (trimethylsilyl) phosphate
- Figure 3 is a result of the life characteristics of the lithium secondary battery using a positive electrode that did not perform both drying and roll press in the production of the positive electrode (A)
- Figure 4 is a positive electrode that does not perform the drying, roll press It is a result of the life characteristics of the used lithium secondary battery (B)
- Figure 5 is a result of the life characteristics of the lithium secondary battery using the positive electrode that performed both drying and roll press (C).
- Example 3 the life characteristic results of the lithium secondary battery using the positive electrode that did not perform both drying and roll press (roll press), Example 3 was a graph of the life characteristic results up to 30 cycles.
- the secondary batteries of Comparative Examples 9 and 10 can be seen that the slope is significantly reduced from the tenth cycle.
- the lithium secondary battery of Comparative Example 10 using only TMSPa as the electrolyte additive drops rapidly from the fifth cycle.
- the lithium secondary battery of Example 3 showed a stable life characteristics, regardless of the drying and roll press performed.
- the drying performance and the roll press were affected, and the life performance was lower than that in Example 3.
- 6 to 8 are graphs illustrating the graphs of FIGS. 3 to 5 separated by lithium secondary batteries.
- the lithium secondary battery of Example 3 is a graph for the presence of drying and roll pressing. It can be seen that the lithium secondary battery of Example 3 has excellent life characteristics up to 30 cycles regardless of drying and roll pressing.
- FIG. 7 is a graph showing whether drying and roll pressing are performed on the lithium secondary battery of Comparative Example 9.
- FIG. The lithium secondary battery of Comparative Example 9 had excellent life characteristics up to 30 cycles when both dry and roll press were performed, but when the dry or roll press was not performed, the life characteristics decreased.
- FIG. 8 is a graph for the presence or absence of drying and roll press for the lithium secondary battery of Comparative Example 10.
- the lithium secondary battery of Comparative Example 10 had excellent life characteristics up to 30 cycles when both drying and roll pressing were performed, but life characteristics were decreased when drying or roll pressing was not performed.
- the lithium secondary battery of Comparative Example 10 is further affected by the presence or absence of drying and roll pressing, compared to Comparative Example 9.
- Tetra (trimethylsilyl) pyrophosphate (Compound (1)) and tris (trimethylsilyl) phosphate (TMSPa) were mixed at a weight ratio of 3: 1 to prepare an additive mixture, which was then added to the total weight of the positive electrode mixture slurry.
- TMSPa tris (trimethylsilyl) phosphate
- a positive electrode mixture slurry was prepared by addition to 2-pyrrolidone (NMP).
- the positive electrode mixture slurry was applied to a thin film of aluminum (Al), which is a positive electrode current collector having a thickness of about 20 ⁇ m, and dried to prepare a positive electrode.
- 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 at 96 wt%, 3 wt%, and 1 wt%, respectively, to NMP as a solvent.
- the negative electrode mixture slurry was applied to a copper (Cu) thin film, which is a negative electrode current collector having a thickness of 10 ⁇ m, dried to prepare a negative electrode, and then roll-rolled to prepare a negative electrode.
- Cu copper
- EC ethylene carbonate
- DMC dimethyl carbonate
- EMC ethyl methyl carbonate
- VMC vinylene carbonate
- PS propane sultone
- the positive electrode and the negative electrode prepared as described above were manufactured in a conventional method with a PE separator, and then the non-aqueous electrolyte was prepared by pouring the prepared lithium secondary battery.
- Example 5 In preparing the positive electrode of Example 5, a positive electrode and a lithium secondary battery were manufactured in the same manner as in Example 5, except that tetra (trimethylsilyl) pyrophosphate alone was used instead of the additive mixture.
- a positive electrode and a lithium secondary battery were manufactured in the same manner as in Example 5, except that the additive mixture was not used when preparing the positive electrode of Example 5.
- Example 5 In preparing the positive electrode of Example 5, a positive electrode and a lithium secondary battery were manufactured in the same manner as in Example 5, except that TMSPa alone was used instead of the additive mixture.
- the lithium secondary batteries prepared in Examples 5 and 6 and Comparative Examples 11 and 12 (based on 3.26 mAh of battery capacity) were charged at 45 ° C. with a constant current of 1 C until they reached 4.35 V, and then charged at a constant voltage of 4.35 V. Charging was terminated when the charging current became 0.163 mAh. Thereafter, it was left for 10 minutes and then discharged until it became 2.94V with a constant current of 2 C. This was repeated for 1 to 100 cycles.
- the lithium secondary batteries of Examples 5 and 6 of the present invention including tetra (trimethylsilyl) pyrophosphate (Compound (1)) as an additive had a gentle slope up to 100 cycles.
- Example 5 using an additive mixture in which tetra (trimethylsilyl) pyrophosphate (compound (1)) and TMSPa were mixed as an additive for the positive electrode were tetra (trimethylsilyl) pyrophosphate (compound (1)). Although it was superior to 100 cycles compared to Example 6, which was used alone, it showed a remarkable difference compared to Comparative Examples 11 and 12 without the tetra (trimethylsilyl) pyrophosphate in the positive electrode.
- Examples 5 and 6 of the present invention showed about 25% improvement in the 90th cycle compared to Comparative Example 11 without using the positive electrode additive, and did not include tetra (trimethylsilyl) pyrophosphate, and added only TMSPa. Compared to Comparative Example 12, the discharge capacity was improved by about 150% or more at the 100th cycle.
- the life characteristics of a lithium secondary battery may be improved, and particularly, the life characteristics may be improved at a high temperature of 45 ° C. or higher and a high voltage of 4.3 V or higher. You can. Therefore, the nonaqueous electrolyte and the positive electrode according to the exemplary embodiment of the present invention may be usefully used in the lithium secondary battery field.
Abstract
Description
건조 | 롤 프레스 | |
(A) Set | X | X |
(B) Set | O | X |
(C) Set | O | O |
Claims (20)
- 제 1 항에 있어서,상기 화학식 1의 A에서, n이 3 또는 4인 경우, 상기 A는 하나의 반복단위의 P와 인접하는 다른 반복단위의 O가 서로 연결되어 선형 또는 고리, 또는 선형과 고리가 함께 연결되어 형성되는 것을 특징으로 하는 비수 전해액.
- 제 4 항에 있어서,상기 화학식 2로 표시되는 화합물은 트리스(트리메틸실릴)포스페이트(TMSPa)인 것을 특징으로 하는 비수 전해액.
- 제 4 항에 있어서,상기 화학식 1로 표시되는 화합물과 상기 화학식 2로 표시되는 화합물의 혼합비는 1: 0.1 내지 2 중량비인 것을 특징으로 하는 비수 전해액.
- 제 1 항에 있어서,상기 화학식 1로 표시되는 화합물은 비수 전해액 총량을 기준으로 0.01 중량% 내지 5 중량%인 것을 특징으로 하는 비수 전해액.
- 제 1 항에 있어서,상기 리튬염은 LiPF6, LiAsF6, LiCF3SO3, LiN(CF3SO2)2, LiBF4, LiBF6, LiSbF6, LiN(C2F5SO2)2, LiAlO4, LiAlCl4, LiSO3CF3 및 LiClO4로 이루어진 군에서 선택된 어느 하나 또는 이들 중 2종 이상의 혼합물인 것을 특징으로 하는 비수 전해액.
- 제 1 항에 있어서,상기 전해액 용매는 선형 카보네이트, 환형 카보네이트, 에스테르, 또는 이들의 조합을 포함하는 것을 특징으로 하는 비수 전해액.
- 제 9 항에 있어서,상기 선형 카보네이트는 디메틸 카보네이트, 디에틸 카보네이트, 디프로필 카보네이트, 에틸메틸 카보네이트, 메틸프로필 카보네이트 및 에틸프로필 카보네이트로 이루어진 군에서 선택되는 어느 하나 또는 이들 중 2종 이상의 혼합물을 포함하고; 상기 환형 카보네이트는 에틸렌 카보네이트, 프로필렌 카보네이트, 1,2-부틸렌 카보네이트, 2,3-부틸렌 카보네이트, 1,2-펜틸렌 카보네이트, 2,3-펜틸렌 카보네이트, 비닐렌 카보네이트, 및 이들의 할로겐화물로 이루어진 군에서 선택되는 어느 하나 또는 이들 중 2종 이상의 혼합물을 포함하고; 상기 에스테르는 메틸 아세테이트, 에틸 아세테이트, 프로필 아세테이트, 에틸 프로피오네이트(EP), 메틸 프로피오네이트(MP), γ-부티로락톤, γ-발레로락톤, γ-카프로락톤, σ-발레로락톤 및 ε-카프로락톤으로 이루어진 군에서 선택되는 어느 하나 또는 이들 중 2종 이상의 혼합물을 포함하는 것을 특징으로 하는 비수 전해액.
- 제 11 항에 있어서,상기 화학식 1의 A에서, n이 3 또는 4인 경우, 상기 A는 하나의 반복단위의 P와 인접하는 다른 반복단위의 O가 서로 연결되어 선형 또는 고리, 또는 선형과 고리가 함께 연결되어 형성되는 것을 특징으로 하는 양극.
- 제 14 항에 있어서,상기 화학식 2로 표시되는 화합물은 트리스(트리메틸실릴)포스페이트(TMSPa)인 것을 특징으로 하는 양극.
- 제 14 항에 있어서,상기 화학식 1로 표시되는 화합물과 상기 화학식 2로 표시되는 화합물의 혼합비는 1: 0.1 내지 2 중량비인 것을 특징으로 하는 양극.
- 제 11 항에 있어서,상기 화학식 1로 표시되는 화합물은 리튬 전이금속 산화물 총량을 기준으로 0.01 중량% 내지 5 중량%인 것을 특징으로 하는 양극.
- 제 11 항에 있어서,상기 리튬 전이금속 산화물은 하기 화학식 3으로 표시되는 화합물인 것을 특징으로 하는 양극:<화학식 3>Li[LixNiaCobMnc]O2 (-0.05 ≤ x ≤ +0.5, 0 < a, b, c ≤1, x+a+b+c=1, 0.4 < c < 1).
- 제 1 항 또는 제 11 항의 양극을 포함하는 리튬 이차전지.
- 제 19 항에 있어서,상기 리튬 이차전지의 충전 전압은 4.3V 내지 5.0V 범위인 것을 특징으로 하는 리튬 이차전지.
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