WO2011105833A9 - 출력 향상을 위한 양극 활물질 및 이를 포함하는 리튬 이차전지 - Google Patents
출력 향상을 위한 양극 활물질 및 이를 포함하는 리튬 이차전지 Download PDFInfo
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- WO2011105833A9 WO2011105833A9 PCT/KR2011/001300 KR2011001300W WO2011105833A9 WO 2011105833 A9 WO2011105833 A9 WO 2011105833A9 KR 2011001300 W KR2011001300 W KR 2011001300W WO 2011105833 A9 WO2011105833 A9 WO 2011105833A9
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- 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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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/362—Composites
- H01M4/364—Composites as mixtures
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- 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
- H01M4/52—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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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- 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
- H01M4/5825—Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- 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
- H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- 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
- H01M10/052—Li-accumulators
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/625—Carbon or graphite
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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
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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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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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
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/60—Other road transportation technologies with climate change mitigation effect
- Y02T10/70—Energy storage systems for electromobility, e.g. batteries
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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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49108—Electric battery cell making
Definitions
- the present invention relates to a mixed cathode active material having an expanded SOC area and improved output characteristics at low voltage, a lithium secondary battery including the same, and a method of manufacturing the same.
- lithium secondary batteries having high energy density and voltage, long cycle life, and low self discharge rate are commercially used.
- electric vehicles and hybrid electric vehicles which can replace fossil fuel-based vehicles such as gasoline and diesel vehicles, which are one of the main causes of air pollution, are being conducted.
- Recently, researches using lithium secondary batteries having high energy density and discharge voltage have been actively conducted as power sources of such electric vehicles and hybrid electric vehicles, and some commercialization stages are in progress.
- LiCoO 2 a conventional cathode material, has reached the practical limit of increasing its energy density and output characteristics, and especially when used in high energy density applications, due to its structural instability, oxygen in the structure is changed along with structural modification at high temperature. Emissions cause exothermic reactions with the electrolyte in the battery, causing the battery to explode.
- This LiCoO has been the use of a lithium-containing manganese oxide and lithium nickel oxide (LiNiO 2), such as LiMn 2 O 4 of the layered crystal structure of LiMnO 2, spinel crystal structure is considered to improve the second instability of recently LiNi x
- LiNiO 2 lithium-containing manganese oxide and lithium nickel oxide
- Ni 1/3 Co 1/3 Mn 1/3 ] O 2 of the three-component layered oxide changes from Ni 2+ to Ni 3+ or Ni 4+ depending on the filling depth.
- Ni 3+ or Ni 4+ loses lattice oxygen due to instability and is reduced to Ni 2+ , which reacts with the electrolyte to alter the surface properties of the electrode. Or increase the charge transfer impedance of the surface to reduce capacity or high rate characteristics.
- a nonaqueous electrolyte used by mixing a first lithium compound containing lithium-containing olivine-type phosphate with a second lithium compound such as lithium-containing cobalt oxide or lithium-containing nickel cobalt oxide as a cathode active material
- a second lithium compound such as lithium-containing cobalt oxide or lithium-containing nickel cobalt oxide as a cathode active material
- the lithium secondary battery according to the present invention also has a portion of the voltage drop suddenly at the terminal end of the operating voltage of the second lithium compound due to the difference in the operating voltage of the two materials mixed There was still a problem that the output was reduced.
- the present invention is to solve the problems of the prior art as described above, Applicants of the present invention, after extensive research and various experiments, the sudden voltage of the positive electrode active material mixed with the three-component layered oxide and the metal oxide of the olivine structure Note that the drop occurs near the operating voltage boundary of the two oxides, and the output characteristics at the low voltage while solving the problems of the conventional invention when implementing the positive electrode active material in which the operating voltage region is not completely separated as described above. It was confirmed that the present invention can provide a secondary battery having a high capacity to improve the.
- an object of the present invention is to provide a mixed cathode active material in which a layered lithium manganese oxide having a voltage profile of 3 V or less and an olivine-structured metal oxide are mixed instead of the three-component layered oxide.
- Another object of the present invention is to provide a lithium secondary battery including the mixed cathode active material.
- Another object of the present invention is to provide a method for manufacturing a lithium secondary battery including the mixed cathode active material.
- the present invention provides the following means.
- the present invention includes a mixed cathode active material mixed with a lithium manganese oxide represented by the following [Formula 1] and a metal oxide of the olivine structure represented by the following [Formula 2], charged at a voltage of 4.45V or more based on the anode potential It provides a lithium secondary battery characterized in that.
- M may be any one element selected from the group consisting of Al, Mg, Mn, Ni, Co, Cr, V, Fe, or the like, or two or more elements may be simultaneously applied.
- the metal oxide of the olivine structure represented by the formula (2) is characterized in that LiFePO 4 .
- Charging at a voltage of 4.45V or more based on the anode potential is characterized in that it is charged in a number of cycles or every cycle after the formation step.
- the mixed cathode active material is characterized in that it comprises 5 to 50% by weight of the metal oxide of the olivine structure.
- the mixed cathode active material is characterized in that it comprises 10 to 40% by weight of the metal oxide of the olivine structure.
- the metal oxide of the olivine structure of the mixed cathode active material is characterized by being coated with a conductive material.
- the conductive material is characterized in that the carbon-based material.
- the mixed cathode active material may be lithium cobalt oxide, lithium nickel oxide, lithium manganese oxide, lithium cobalt-nickel oxide, lithium cobalt-manganese oxide, lithium manganese-nickel oxide, lithium cobalt-nickel-manganese oxide and ellipsoids thereof. It characterized in that it further comprises any one or two or more lithium-containing metal oxide selected from the group consisting of (s) substituted or doped oxide.
- the ellipsoid is characterized in that any one or two or more elements selected from the group consisting of Al, Mg, Mn, Ni, Co, Cr, V, Fe.
- the lithium-containing metal oxide is characterized in that it is included within 50% by weight relative to the total weight of the mixed cathode active material.
- the lithium secondary battery is characterized in that it comprises a positive electrode mixture further comprises a conductive material, a binder, a filler in addition to the mixed positive electrode active material.
- the lithium secondary battery is characterized in that it is used as a unit cell of the battery module which is the power source of the medium and large devices.
- the medium to large device includes a power tool; Electric vehicles including electric vehicles (EVs), hybrid electric vehicles (HEVs), and plug-in hybrid electric vehicles (PHEVs); Electric two-wheeled vehicles including E-bikes and E-scooters; Electric golf carts; Electric trucks; It is characterized in that the electric commercial vehicle or a system for power storage.
- Electric vehicles including electric vehicles (EVs), hybrid electric vehicles (HEVs), and plug-in hybrid electric vehicles (PHEVs); Electric two-wheeled vehicles including E-bikes and E-scooters; Electric golf carts; Electric trucks; It is characterized in that the electric commercial vehicle or a system for power storage.
- the present invention comprises the steps of preparing a mixed cathode active material mixed with a lithium manganese oxide represented by the following [Formula 1] and a metal oxide of the olivine structure represented by the following [Formula 2];
- a method of manufacturing a lithium secondary battery comprising a formation step of charging the lithium secondary battery at a voltage of 4.45V or more based on a cathode potential.
- M may be any one element selected from the group consisting of Al, Mg, Mn, Ni, Co, Cr, V, Fe, or the like, or two or more elements may be simultaneously applied.
- the metal oxide of the olivine structure represented by Formula 2 is characterized in that LiFePO 4 .
- the formation step may be performed every few cycles or every cycle.
- the mixed cathode active material is characterized in that it comprises 5 to 50% by weight of the metal oxide of the olivine structure.
- the mixed cathode active material manufacturing step may further include coating the metal oxide of the olivine structure with a conductive material.
- the conductive material is characterized in that the carbon-based material.
- the lithium secondary battery including the mixed cathode active material according to the present invention exhibits an even voltage profile continuously without sudden voltage drop in all SOC areas during discharge by using two oxides that can be connected without disconnecting the operating voltage region.
- the reduction in output power in the low SOC region can be improved, thereby providing a high capacity lithium secondary battery having excellent safety while expanding the available SOC region.
- the lithium secondary battery according to the present invention when used as a power source for medium and large devices such as electric vehicles, it is possible to sufficiently satisfy the requirements of the required output characteristics, capacity, safety and the like.
- FIG. 1 is a graph showing a change in current-voltage and a slope of a profile during discharge of a lithium secondary battery according to an exemplary embodiment of the present invention.
- FIG. 2 is a graph showing a change in current-voltage and a slope of a profile during discharge of a lithium secondary battery according to Comparative Example 1 of the present invention.
- FIG 3 is a graph showing a change in current-voltage and a slope of a profile during discharge of a lithium secondary battery according to Comparative Example 2 of the present invention.
- FIG. 4 is a graph showing a change in current-voltage and a slope of a profile during discharge of a lithium secondary battery according to Comparative Example 3 of the present invention.
- the present invention relates to a metal oxide of olivine structure (hereinafter referred to as “olivine”) and a lithium manganese oxide of a layered structure having a flat state region when charged at a relatively high voltage (hereinafter referred to as “lithium).
- olivine metal oxide of olivine structure
- a mixed cathode active material mixed with "manganese oxide”
- a voltage profile is expressed up to a voltage of 3.5 V or less so as to be connected to the operating voltage region of the olivine.
- the positive electrode active material of the present invention is characterized by being a mixed positive electrode active material in which lithium manganese oxide and olivine are known to have a flat level voltage range when charged at a voltage of 4.45 V or higher based on the positive electrode potential.
- the lithium manganese oxide may be represented by the following [Formula 1].
- M may be any one element selected from the group consisting of Al, Mg, Mn, Ni, Co, Cr, V, Fe, or the like, or two or more elements may be simultaneously applied.
- the lithium manganese oxide represented by [Formula 1] includes Mn as an essential transition metal, and the content of Mn is higher than that of other metals except lithium.
- the lithium manganese oxide expresses a large capacity during overcharging at high voltage.
- the lithium manganese oxide shows a long voltage profile up to 3.5V voltage or less during discharge, the operating voltage region is not disconnected when mixed with olivine.
- Mn contained as an essential transition metal in the lithium manganese oxide represented by [Formula 1] is required to be included in a larger amount than other metals (except lithium), specifically, based on the total amount of metals except lithium It is preferable that it is 50-80 mol%.
- the lithium manganese oxide has a flat level of a certain period above the oxidation / reduction potential indicated by the change in the oxidation number of the component. Specifically, the lithium manganese oxide exhibits a flat level section with excess oxygen gas at about 4.5 V to 4.8 V when charged at a relatively high voltage of 4.45 V, more preferably 4.5 V or more, based on the anode potential. Large doses up to g are shown.
- Mn oxide, Ni oxide, or Co oxide may be solid-state reaction at a high temperature with Li 2 CO 3 , LiOH, or the like at the same time, or may be prepared by co-precipitation of lithium salt with co-precipitation of the metal salt.
- olivine used in the present invention may be represented by the following formula (2).
- LiFePO 4 having a relatively low charging potential is preferably used to assist the output of the 3V voltage band of the lithium manganese oxide of Formula 1 and to improve the output drop phenomenon at low voltage.
- the LiFePO 4 has a theoretical capacity of 170 mAh / g and a standard reduction potential of 3.4 V, and this voltage can maintain energy density without being high enough to decompose the electrolyte.
- LiFePO 4 its charging and discharging behavior is not sufficient due to low electrical conductivity.
- a form in which a conductive material is coated on a surface is widely used. Therefore, in the present invention, not only pure LiFePO 4 but also a conductive material on the surface thereof is used. This may include those that are in coated form.
- the conductive material is not particularly limited as long as it is excellent in electrical conductivity and does not cause side reactions in the internal environment of the secondary battery, but a carbon-based material having high conductivity is particularly preferable.
- the mixed cathode active material of the present invention is characterized by including the lithium manganese oxide of Formula 1 and the olivine of Formula 2, but may not be limited in content ratio, preferably the content of the olivine is 5 to 50% by weight based on the total amount, more preferably 10 to 40% by weight to be included.
- the content of the olivine is less than 5% by weight it may be difficult to fully play the role of the olivine, there may be a problem in the safety of the secondary battery, if more than 50% by weight, there may be a limit in the high capacity expression of the entire positive electrode.
- the mixed cathode active material of the present invention does not have a sharp operating voltage boundary, and there is no sudden voltage drop across the entire SOC region.
- the LiFePo 4 is a low SOC region of lithium manganese oxide. It provides a cathode active material that can improve the output degradation phenomenon at low voltage by assisting the output from.
- the mixed positive electrode active material according to the present invention includes lithium manganese oxide and olivine having a flat level voltage region when charging at a high voltage of 4.45 V or higher and a voltage profile of 3.5 V or less, as described above. It may further include a lithium-containing metal oxide.
- lithium-containing metal oxides are various active materials known in the art, such as lithium cobalt oxide, lithium nickel oxide, lithium manganese oxide, lithium cobalt-nickel oxide, lithium cobalt-manganese oxide, lithium manganese-nickel oxide, lithium Cobalt-nickel-manganese oxides, oxides substituted or doped with ellipsoid (s), and the like may be included.
- the ellipsoid (s) may be Al, Mg, Mn, Ni, Co, Cr, V, or Fe. It may be any one or two or more elements selected from the group consisting of.
- the lithium-containing metal oxide which may be additionally included, may be included within 50 wt% of the total weight of the mixed positive electrode active material in order to exhibit the effects of the present invention.
- the lithium secondary battery including the mixed cathode active material according to the present invention at a voltage of 4.45V or more based on the anode potential to activate the lithium manganese oxide expressing a high capacity when charging at a voltage of 4.45V or more based on the cathode potential To be charged preferably may be to charge at a voltage of 4.5V or more.
- the lithium secondary battery according to the present invention has a flat level section in the vicinity of 4.45V through the activation process as described above, and exhibits a large capacity with generation of oxygen in the flat level section.
- lithium secondary battery that exhibits even discharge characteristics continuously without sudden voltage drop or output drop in the discharge process, and has an improved output reduction phenomenon by assisting the output of olivine even at low voltage.
- the activation process of charging at a relatively high voltage of 4.45 V or more based on the anode potential is not particularly limited, and a charging method known in the art is used.
- the charging treatment at the high voltage may be performed every operation cycle, but may be performed once or several times in the battery formation step in consideration of safety and fairness.
- an electrolyte that can operate stably at a high voltage is required, but it is not easy to implement such an electrolyte at the present technology stage.
- the present invention also provides a cathode mixture comprising a mixed cathode active material as described above.
- the positive electrode mixture may optionally include a conductive material, a binder, a filler, etc. in addition to the mixed positive electrode active material.
- the conductive material is typically added in an amount of 1 to 50 wt% based on the total weight of the mixed cathode active material.
- a conductive material is not particularly limited as long as it has conductivity without causing chemical change in the battery, and examples thereof include graphite such as natural graphite and artificial graphite; Conductive fibers such as carbon black such as carbon black, acetylene black, ketjen black, channel black, furnace black, lamp black and summer black, carbon fibers and metal fibers; Metal powders such as carbon fluoride powder, aluminum powder and nickel powder; Conductive whiskeys such as zinc oxide and potassium titanate; Conductive oxides such as titanium oxide; Conductive materials such as polyphenylene derivatives and the like can be used.
- addition of the conductive material may be omitted by adding a conductive second coating layer to the mixed positive electrode active material.
- the binder is a component that assists the bonding of the active material and the conductive material to the current collector, and is usually 1 to 50% by weight based on the total weight of the mixed cathode active material.
- binders include polyvinylidene fluoride, polyvinyl alcohol, carboxymethyl cellulose (CMC), starch, hydroxypropyl cellulose, regenerated cellulose, polyvinylpyrrolidone, tetrafluoroethylene, Polyethylene, polypropylene, ethylene-propylene-diene terpolymer (EPDM), sulfonated EPDM, styrene butylene rubber, fluorine rubber, various copolymers, and the like.
- the filler is optionally used as a component for inhibiting expansion of the positive electrode, and is not particularly limited as long as it is a fibrous material without causing chemical change in the battery.
- the filler include olefinic polymers such as polyethylene and polypropylene; Fibrous materials such as glass fibers and carbon fibers are used.
- the present invention also provides a cathode in which the cathode mixture is included on a current collector.
- the secondary battery positive electrode may be coated with a slurry prepared by mixing a positive electrode mixture such as a mixed positive electrode active material, a conductive material, a binder, and a filler in a solvent such as NMP on a positive electrode current collector, followed by drying and It can be produced by rolling.
- a positive electrode mixture such as a mixed positive electrode active material, a conductive material, a binder, and a filler in a solvent such as NMP on a positive electrode current collector, followed by drying and It can be produced by rolling.
- the positive electrode current collector is generally made to a thickness of 3 to 500 ⁇ m.
- a positive electrode current collector is not particularly limited as long as it has high conductivity without causing chemical changes in the battery.
- the surface of stainless steel, aluminum, nickel, titanium, calcined carbon, or aluminum or stainless steel Surface treated with carbon, nickel, titanium, silver, or the like can be used.
- the current collector may form fine irregularities on its surface to increase the adhesion of the positive electrode active material, and may be in various forms such as a film, a sheet, a foil, a net, a porous body, a foaming agent, and a nonwoven fabric.
- the present invention also provides a lithium secondary battery composed of the positive electrode, the negative electrode, the separator, and the lithium salt-containing nonaqueous electrolyte.
- the negative electrode may be manufactured by applying and drying a negative electrode mixture including a negative electrode active material on a negative electrode current collector, and the negative electrode mixture may further include components as described above as necessary.
- the negative electrode current collector is generally made of a thickness of 3 to 500 ⁇ m.
- the negative electrode current collector is not particularly limited as long as it has conductivity without causing chemical change in the battery.
- carbon on the surface of copper, stainless steel, aluminum, nickel, titanium, calcined carbon, copper or stainless steel , Surface treated with nickel, titanium, silver, or the like, an aluminum-cadnium alloy, or the like can be used.
- fine concavities and convexities may be formed on the surface to enhance the bonding strength of the negative electrode active material, and may be used in various forms such as a film, a sheet, a foil, a net, a porous body, a foam, and a nonwoven fabric.
- the separator is interposed between the cathode and the cathode, and an insulating thin film having high ion permeability and mechanical strength is used.
- the pore diameter of the separator is generally from 0.01 to 10 ⁇ m ⁇ m, thickness is generally 5 ⁇ 300 ⁇ m.
- a separator for example, olefin polymers such as chemical resistance and hydrophobic polypropylene; Sheets or non-woven fabrics made of glass fibers or polyethylene are used.
- a solid electrolyte such as a polymer
- the solid electrolyte may also serve as a separator.
- the said lithium salt containing non-aqueous electrolyte solution consists of a nonaqueous electrolyte solution and a lithium salt.
- a nonaqueous electrolyte a non-aqueous organic solvent, an organic solid electrolyte, an inorganic solid electrolyte, and the like are used.
- non-aqueous organic solvent examples include N-methyl-2-pyrrolidinone, propylene carbonate, ethylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, gamma-butylo lactone, and 1,2-dime Methoxy ethane, tetrahydroxy franc, 2-methyl tetrahydrofuran, dimethyl sulfoxide, 1,3-dioxolon, formamide, dimethylformamide, dioxoron, acetonitrile, nitromethane, methyl formate, Methyl acetate, phosphate triester, trimethoxy methane, dioxorone derivatives, sulfolane, methyl sulfolane, 1,3-dimethyl-2-imidazolidinone, propylene carbonate derivatives, tetrahydrofuran derivatives, ethers, pyrion
- An aprotic organic solvent such as methyl acid or ethyl
- organic solid electrolyte examples include polyethylene derivatives, polyethylene oxide derivatives, polypropylene oxide derivatives, phosphate ester polymers, polyedgetion lysine, polyester sulfides, polyvinyl alcohols, polyvinylidene fluorides, Polymers containing ionic dissociating groups and the like can be used.
- Examples of the inorganic solid electrolyte include Li 3 N, LiI, Li 5 NI 2 , Li 3 N-LiI-LiOH, LiSiO 4 , LiSiO 4 -LiI-LiOH, Li 2 SiS 3 , Li 4 SiO 4 , Nitrides, halides, sulfates and the like of Li, such as Li 4 SiO 4 -LiI-LiOH, Li 3 PO 4 -Li 2 S-SiS 2 , and the like, may be used.
- the lithium salt is a material that is readily soluble in the non-aqueous electrolyte, for example, LiCl, LiBr, LiI, LiClO 4, LiBF 4, LiB 10 Cl 10, LiPF 6, LiCF 3 SO 3, LiCF 3 CO 2, LiAsF 6, LiSbF 6, LiAlCl 4, CH 3 SO 3 Li, CF 3 SO 3 Li, (CF 3 SO 2) 2 NLi, chloroborane lithium, lower aliphatic carboxylic acid lithium, lithium tetraphenyl borate and imide have.
- LiCl, LiBr, LiI, LiClO 4, LiBF 4, LiB 10 Cl 10, LiPF 6, LiCF 3 SO 3, LiCF 3 CO 2, LiAsF 6, LiSbF 6, LiAlCl 4, CH 3 SO 3 Li, CF 3 SO 3 Li, (CF 3 SO 2) 2 NLi, chloroborane lithium, lower aliphatic carboxylic acid lithium, lithium tetraphenyl borate and imide have.
- the non-aqueous electrolyte solution includes, for example, pyridine, triethyl phosphite, triethanolamine, cyclic ether, ethylene diamine, n-glyme, and hexaphosphate triamide.
- halogen-containing solvents such as carbon tetrachloride and ethylene trifluoride may be further included, and carbon dioxide gas may be further included to improve high temperature storage characteristics.
- Such a secondary battery according to the present invention can be used not only in a battery cell used as a power source of a small device, but also preferably used as a unit battery in a medium-large battery module including a plurality of battery cells.
- Preferred examples of the medium-to-large device include a power tool; Electric vehicles including electric vehicles (EVs), hybrid electric vehicles (HEVs), and plug-in hybrid electric vehicles (PHEVs); Electric two-wheeled vehicles including E-bikes and E-scooters; Electric golf carts; Electric trucks; Although an electric commercial vehicle or the system for electric power storage is mentioned, It is not limited only to these.
- Electric vehicles including electric vehicles (EVs), hybrid electric vehicles (HEVs), and plug-in hybrid electric vehicles (PHEVs); Electric two-wheeled vehicles including E-bikes and E-scooters; Electric golf carts; Electric trucks; Although an electric commercial vehicle or the system for electric power storage is mentioned, It is not limited only to these.
- LiFePO 4 and 0.5Li 2 MnO 3 -0.5Li (Mn0.33Ni0.33Co0.33) O 2 are mixed so that the weight ratio is 3: 7, which is 88% by weight based on the total weight of the positive electrode mixture, and Denka as a conductive material.
- Slurry was made by adding 6 wt% black and 6 wt% PVDF with binder to NMP. This was applied to a positive electrode current collector, rolled and dried to prepare a secondary battery positive electrode.
- a coin-type lithium secondary battery was manufactured by including a cathode prepared as described above, and injecting a lithium electrolyte solution through a separator of porous polyethylene between anodes made of lithium metal.
- Example 2 After the lithium ion secondary battery was manufactured in the same manner as in Example 1, the same procedure as in Example 1 was performed except that the lithium ion secondary battery was charged at 4.4 V based on the positive electrode potential.
- Example 1 except that a mixture of 0.5Li 2 MnO 3 -0.5Li (Mn0.33Ni0.33Co0.33) O 2 instead of Li (Mn0.33Ni0.33Co0.33) O 2 is in the same manner as in Example 1 Was carried out.
- FIG. 1 illustrates a change in current-voltage and a slope of a profile in a 3V to 4V region during discharge of a secondary battery according to an embodiment. The formation and the results of the second cycle are then described together.
- the lithium secondary battery of the example shows an even profile without a sudden drop in voltage over 2V to 4.5V, unlike the lithium secondary battery according to the comparative example.
- the present invention can provide a high capacity lithium secondary battery having excellent charge / discharge characteristics and safety and excellent output characteristics at low voltage, and particularly, when used as a medium-large battery used as a power source for an electric vehicle. It is possible to provide a medium-large-size lithium secondary battery capable of sufficiently satisfying conditions such as required output characteristics, capacity, and safety.
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Abstract
Description
Claims (19)
- 아래 [화학식 1]로 표시되는 리튬망간산화물과 [하기 화학식 2]로 표시되는 올리빈 구조의 금속산화물을 혼합한 혼합 양극활물질을 포함하고, 양극전위를 기준으로 4.45V 이상의 전압에서 충전하는 것을 특징으로 하는 리튬 이차전지.[화학식 1] aLi2MnO3·(1-a)LiMO20<a<1이고, M은 Al, Mg, Mn, Ni, Co, Cr, V, Fe등으로 이루어진 군에서 선택되는 어느 하나의 원소, 또는 2 이상의 원소가 동시에 적용된 것일 수 있다.[화학식 2] LixMyM'zXO4(M, M'는 전이금속 원소 중 선택된 1종 이상, X는 P, Si, S, As, Sb 및 이들의 조합으로 이루어진 군에서 선택되는 어느 하나이며, x+y+z=2이다.)
- 제 1항에 있어서, 상기 화학식 2로 표시되는 올리빈 구조의 금속산화물은 LiFePO4인 것을 특징으로 하는 리튬이차전지.
- 제1항에 있어서, 상기 양극전위를 기준으로 4.45V 이상의 전압에서 충전하는 것은 포메이션 단계 혹은 그 이후 수 사이클 혹은 매 사이클에서 충전하는 것임을 특징으로 하는 리튬 이차전지.
- 제1항에 있어서, 상기 혼합 양극활물질은 올리빈 구조의 금속산화물을 5 내지 50 중량%로 포함하는 것을 특징으로 하는 리튬 이차전지.
- 제1항에 있어서, 상기 혼합 양극활물질은 상기 올리빈 구조의 금속산화물을 10 내지 40 중량%로 포함하는 것을 특징으로 하는 리튬 이차전지.
- 제1항에 있어서, 상기 혼합 양극활물질 중 올리빈 구조의 금속산화물은 전도성 물질로 코팅되어 있는 것을 특징으로 하는 리튬 이차전지.
- 제6항에 있어서, 상기 전도성 물질은 카본계 물질인 것을 특징으로 하는 리튬 이차전지.
- 제1항에 있어서, 상기 혼합 양극활물질은, 리튬 코발트 산화물, 리튬 니켈 산화물, 리튬 망간 산화물, 리튬 코발트-니켈 산화물, 리튬 코발트-망간 산화물, 리튬 망간-니켈 산화물, 리튬 코발트-니켈-망간 산화물 및 이들에 타원소(들)가 치환 또는 도핑된 산화물로 구성된 군에서 선택된 어느 하나 또는 2 이상의 리튬함유 금속 산화물이 더 포함되는 것을 특징으로 하는 리튬 이차전지.
- 제8항에 있어서, 상기 타원소는 Al, Mg, Mn, Ni, Co, Cr, V, Fe로 이루어진 군에서 선택되는 어느 하나 또는 2 이상의 원소인 것을 특징으로 하는 리튬 이차 전지.
- 제8항에 있어서, 상기 리튬함유 금속 산화물은 혼합 양극 활물질의 총 중량 대비 50중량% 이내로 포함되는 것을 특징으로 하는 리튬 이차전지.
- 제1항 내지 제10항 중 어느 한 항에 있어서, 상기 리튬 이차전지는 상기 혼합 양극활물질 이외에도 도전재, 바인더, 충진제가 더 포함되는 양극합제를 포함하는 것을 특징으로 하는 리튬 이차전지.
- 제1항에 있어서, 상기 리튬 이차전지는 중대형 디바이스의 전원인 전지모듈의 단위전지로 사용되는 것을 특징으로 하는 리튬 이차전지.
- 제12항에 있어서, 상기 중대형 디바이스는 파워 툴(power tool); 전기차(Electric Vehicle, EV), 하이브리드 전기차(Hybrid Electric Vehicle, HEV) 및 플러그인 하이브리드 전기차(Plug-in Hybrid Electric Vehicle, PHEV)를 포함하는 전기차; E-bike, E-scooter를 포함하는 전기 이륜차; 전기 골프 카트(Electric golf cart); 전기 트럭; 전기 상용차 또는 전력 저장용 시스템인 것을 특징으로 하는 리튬 이차전지.
- 아래 [화학식 1]로 표시되는 리튬망간산화물과 [하기 화학식 2]로 표시되는 올리빈 구조의 금속산화물을 혼합한 혼합 양극활물질을 제조하는 단계;상기 혼합 양극활물질을 포함하는 리튬이차전지의 제조단계; 및상기 리튬이차전지를 양극전위 기준으로 4.45V 이상의 전압에서 충전하는 포메이션 단계를 포함하는 리튬 이차전지의 제조방법.[화학식 1] aLi2MnO3·(1-a)LiMO20<a<1이고, M은 Al, Mg, Mn, Ni, Co, Cr, V, Fe등으로 이루어진 군에서 선택되는 어느 하나의 원소, 또는 2 이상의 원소가 동시에 적용된 것일 수 있다.[화학식 2] LixMyM'zXO4(M, M'는 전이금속 원소 중 선택된 1종 이상, X는 P, Si, S, As, Sb 및 이들의 조합으로 이루어진 군에서 선택되는 어느 하나이며, x+y+z=2이다.)
- 제 14항에 있어서, 상기 화학식 2로 표시되는 올리빈 구조의 금속산화물은 LiFePO4인 것을 특징으로 하는 리튬이차전지 제조방법.
- 제14항에 있어서, 상기 포메이션 단계는 수 사이클 혹은 매 사이클마다 수행하는 것을 특징으로 하는 리튬 이차전지 제조방법.
- 제14항에 있어서, 상기 혼합 양극활물질은 올리빈 구조의 금속산화물을 5 내지 50 중량%로 포함하는 것을 특징으로 하는 리튬 이차전지 제조방법.
- 제14항에 있어서, 상기 혼합 양극활물질 제조단계는 올리빈 구조의 금속산화물은 전도성 물질로 코팅하는 단계를 더 포함하는 것을 특징으로 하는 리튬 이차전지 제조방법.
- 제18항에 있어서, 상기 전도성 물질은 카본계 물질인 것을 특징으로 하는 리튬 이차전지 제조방법.
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CA2791187A CA2791187C (en) | 2010-02-24 | 2011-02-24 | Positive electrode active material for improving output, and lithium secondary battery comprising same |
JP2012554933A JP5861208B2 (ja) | 2010-02-24 | 2011-02-24 | 出力向上のための正極活物質およびこれを含むリチウム二次電池 |
CN201180020504.4A CN102859763B (zh) | 2010-02-24 | 2011-02-24 | 用于改善输出的正极活性材料和包含所述正极活性材料的锂二次电池 |
EP11747723.2A EP2541655B1 (en) | 2010-02-24 | 2011-02-24 | Positive electrode active material for improving output, and lithium secondary battery comprising same |
US13/167,475 US9240592B2 (en) | 2010-02-24 | 2011-06-23 | Positive-electrode active material for elevation of output and lithium secondary battery including the same |
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2011
- 2011-02-24 WO PCT/KR2011/001300 patent/WO2011105833A2/ko active Application Filing
- 2011-02-24 KR KR1020110016544A patent/KR101139972B1/ko active IP Right Grant
- 2011-02-24 JP JP2012554933A patent/JP5861208B2/ja active Active
- 2011-02-24 CA CA2791187A patent/CA2791187C/en active Active
- 2011-02-24 CN CN201180020504.4A patent/CN102859763B/zh active Active
- 2011-02-24 EP EP11747723.2A patent/EP2541655B1/en active Active
- 2011-06-23 US US13/167,475 patent/US9240592B2/en active Active
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CA2791187C (en) | 2015-10-27 |
US20110311872A1 (en) | 2011-12-22 |
EP2541655A2 (en) | 2013-01-02 |
CA2791187A1 (en) | 2011-09-01 |
JP5861208B2 (ja) | 2016-02-16 |
CN102859763B (zh) | 2016-08-24 |
EP2541655A4 (en) | 2014-08-06 |
EP2541655B1 (en) | 2017-09-06 |
US9240592B2 (en) | 2016-01-19 |
KR101139972B1 (ko) | 2012-04-30 |
KR20110097718A (ko) | 2011-08-31 |
JP2013520783A (ja) | 2013-06-06 |
WO2011105833A2 (ko) | 2011-09-01 |
WO2011105833A3 (ko) | 2012-03-01 |
CN102859763A (zh) | 2013-01-02 |
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