Patent Application
20190288280
The present invention relates to electrode materials for a lithium-ion secondary battery.
In a lithium-ion secondary battery, a negative electrode may be formed using material capable of storing and releasing a lithium ion. The lithium-ion secondary battery may have less precipitation of dendrites than a lithium secondary battery having a negative electrode made of metal lithium. Because of this, the lithium-ion secondary battery has advantages that a high-capacity battery with an increased energy density can be provided while a short circuit in the battery is prevented to increase its safety.
Recently, a much higher capacity of this lithium-ion secondary battery has been sought. At the same time, it is required for a cell for high-power usage that cell resistance is reduced to increase performance of charging and discharging a large current. In this respect, the following considerations have been conventionally given: to increase a capacity of carbon-based negative electrode material and/or positive electrode material made of lithium metal oxide, a cell reactant; to miniaturize reactant particles; to increase an electrode surface area by increasing a specific surface area of the particles and/or by designing a cell; and to reduce liquid diffusion resistance by making a separator thinner, etc. However, in one hand, the particles are made smaller and the specific surface area is increased, which causes an increase in an amount of a binder. On the other hand, this increase is inconsistent with making the capacity higher. Further, positive and negative electrode materials are peeled and detached from a metal foil, which is a collector. This results in a short circuit inside a cell. Consequently, cell voltage is lowered and uncontrolled heating occurs, etc., so that the lithium-ion secondary battery sometimes becomes unsafe. Then, consideration has been made to modify a type of the binder so as to increase adhesion to the foil (see Patent Literature 1).
However, the modification of the type of the binder may increase the cell capacity, but insufficiently improves characteristics of charging and discharging a large current by decreasing its resistance. When the lithium-ion secondary batteries are compared with secondary batteries such as a nickel-cadmium battery and a nickel-hydrogen battery, it is difficult to develop application to an electric tool and a hybrid car. This is because in the application, a large current should be charged and discharged in a long period of time, which provides a big performance barrier for the lithium-ion secondary batteries.
In view of charging and discharging a large current in the lithium-ion secondary battery, a carbon conductive material has been devised so as to decrease its electrode resistance (see Patent Literatures 2 to 4). Unfortunately, when a large current is used to repeat a cycle of charge and discharge, positive and negative electrode materials are subject to expansion and contraction, which damages a conductive path of particles between positive and negative electrodes. As a result, a large current cannot be made to flow after a short period of time.
Meanwhile, metal oxide such as LiCoO2, LiNiO2, Li2MnO4, or LiCoxNiyMnzO2 (x+y+z=1) has been conventionally used as a positive electrode active substance for the lithium-ion secondary battery. Recently, much attention has been paid to lithium-containing phosphate such as LiFePO4, LiMnPO4, LiMnxFe(1-x)PO4, LiCoPO4, or Li3V2(PO4)3.
The first feature of the lithium-containing phosphate is that its anion is a polyanion (a phosphate ion: PO43−), which is more stable than an oxide ion (O2−). Differing from metal oxide, the lithium-containing phosphate generates no oxygen (O2), which is a combustion-supporting substance, after decomposition. Accordingly, use of the lithium-containing phosphate as a positive electrode active substance can increase safety of the lithium-ion secondary battery.
The second feature of the lithium-containing phosphate is that resistance of the material itself is large. Consequently, it is a big issue to make the battery highly conductive (see Patent Literatures 5 and 6). In order to provide possible solutions, various considerations have been made: to coat the surface of particles of the lithium-containing phosphate with carbon, a conductive material, to prepare positive electrode material; or to make a composite of the lithium-containing phosphate and carbon, etc., (see Patent Literatures 7 to 13). These considerations have improved performance of the positive electrode material using phosphate.
Patent Literature 1: JP05-226004A
Patent Literature 2: JP2005-19399A
Patent Literature 3: JP2001-126733A
Patent Literature 4: JP2003-168429A
Patent Literature 5: JP2000-509193A
Patent Literature 6: JP09-134724A
Patent Literature 7: JP2002-75364A
Patent Literature 8: JP2002-110162A
Patent Literature 9: JP2004-63386A
Patent Literature 10: JP2005-123107A
Patent Literature 11: JP2006-302671A
Patent Literature 12: JP2007-80652A
Patent Literature 13: JP2010-108889A
Patent Literature 14: JP2009-503182A
The above carbon coating of the positive electrode active substance may enhance electron conductivity. However, when contraction and expansion of the positive electrode active substance are repeated during cycles of charge and discharge, an electrical contact between the carbon coating and its surrounding conduction aid gradually deteriorates inside the positive electrode material. This likely causes a voltage drop and capacity reduction of a cell during a long period of the cycles. Accordingly, the above carbon coating has not radically improved the long-term cycle characteristics. Also, the above problems have not been resolved by a conventional technology in which lithium-containing phosphate and carbon are used to form a composite.
The present invention has been made to address the foregoing issues on positive electrode material for a lithium-ion secondary battery. It is an object of the present invention to provide positive electrode material for a lithium-ion secondary battery in which stable charge and discharge characteristics can be maintained over a long period of service life of the battery.
Specifically, in order to solve the above problems, the present invention has the following aspect (1):
(1) Composite particles comprising: particles of lithium-containing phosphate; and carbon coating comprising at least one carbon material selected from the group consisting of (i) fibrous carbon material, (ii) chain-like carbon material, and (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material, wherein each particle is coated with the carbon coating.
In addition, the present invention preferably provides the following aspects:
(2) The composite particles according to the aspect (1), wherein the fibrous carbon material is a carbon nanotube with an average fiber size of 5 to 200 nm;
(3) The composite particles according to the aspect (1) or (2), wherein the chain-like carbon material is carbon black produced by linking, like a chain, primary particles with an average particle size of 10 to 100 nm;
(4) The composite particles according to any one of the aspects (1) to (3), wherein the lithium-containing phosphate is LiFePO4, LiMnPO4, LiMnxFe(1-x)PO4, LiCoPO4, or Li3V2(PO4)3;
(5) The composite particles according to any one of the aspects (1) to (4), wherein primary particles have an average size of 0.02 to 20 μm;
(6) A process for producing the composite particles according to any one of the aspects (1) to (5), the process comprising: a first step of subjecting to surface treatment at least one carbon material selected from the group consisting of (i) fibrous carbon material, (ii) chain-like carbon material, and (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material; a second step of dispersing and mixing the at least one surface-treated carbon material in a solution having dissolved in a solvent a lithium ion (Li+), a phosphate ion (PO43−), and a metal ion other than from lithium, and a heat-degradable carbon source compound; a third step of heating the mixture as a solution state; and a fourth step of drying and further heating the mixture to form composite particles, wherein each particle of lithium-containing phosphate is coated with carbon coating comprising the at least one carbon material;
(7) A process for producing the composite particles according to any one of the aspects (1) to (5), the process comprising: a first step of subjecting to surface treatment at least one carbon material selected from the group consisting of (i) fibrous carbon material, (ii) chain-like carbon material, and (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material; a second step of heating a solution having dissolved in a solvent a lithium ion (Li+), a phosphate ion (PO43−), and a metal ion other than from lithium as a solution state to form particles of lithium-containing phosphate and/or particles of a precursor thereof; a third step of mixing the at least one surface-treated carbon material obtained in the first step, the particles obtained in the second step, and a heat-degradable carbon source compound; and a fourth step of heating the mixture to form composite particles, wherein each particle of lithium-containing phosphate is coated with carbon coating comprising the at least one carbon material;
(8) The process for producing composite particles according to the aspect (6) or (7), wherein the solvent is water, alcohol, or a mixed solvent of water and alcohol;
(9) The process for producing composite particles according to any one of the aspects (6) to (8), wherein a method using a pressured and heated solvent is used for the third step of the aspect (6) or the second step of the aspect (7);
(10) A process for producing the composite particles according to any one of the aspects (1) to (5), the process comprising: a first step of subjecting to surface treatment at least one carbon material selected from the group consisting of (i) fibrous carbon material, (ii) chain-like carbon material, and (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material; a second step of mixing the at least one surface-treated carbon material, particles of lithium-containing phosphate, and a heat-degradable carbon source compound; and a third step of heating the mixture to form composite particles, wherein each particle of lithium-containing phosphate is coated with carbon coating comprising the at least one carbon material;
(11) The process for producing composite particles according to any one of the aspects (6) to (10), wherein oxidation treatment is used for the surface treatment of the at least one carbon material;
(12) The process for producing composite particles according to any one of the aspects (6) to (10), wherein a method using a surfactant is used for the surface treatment of the at least one carbon material;
(13) The process for producing composite particles according to any one of the aspects (6) to (10), wherein a method using a polymer dispersant is used for the surface treatment of the at least one carbon material;
(14) Electrode material for a lithium-ion secondary battery, comprising 60 to 95% by mass of the composite particles according to any one of the aspects (1) to (5) and the remainder consisting of an conduction aid and a binder; and
(15) A lithium-ion secondary battery comprising: a positive electrode produced using the electrode material according to the aspect (14); a negative electrode; an electrolytic solution; and a separator that electrically insulates the positive electrode from the negative electrode and helps retain the electrolytic solution.
In use of electrode material for a lithium-ion secondary battery according to the present invention, particles of a positive electrode active substance contain at least one carbon material selected from the group consisting of (i) fibrous carbon material, (ii) chain-like carbon material, and (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material. As the first effect, this carbon material can enhance an electron conduction network, so that electrons can be smoothly transferred between lithium-containing phosphate particles and a conduction aid. Further, the at least one carbon material is included in the carbon coating of the particles of lithium-containing phosphate of the positive electrode active substance. As the second effect, this inclusion helps retain an electric contact between the at least one carbon material and the positive electrode active substance. Consequently, repeating contraction and expansion of the positive electrode active substance during cycles of charge and discharge fails to deteriorate the contact. These two effects help enhance cycle characteristics of the battery and enable stable charge and discharge characteristics to be maintained over a long period of service life of the battery.
The following details embodiments of the present invention.
In an embodiment of the present invention, composite particles comprise: particles of lithium-containing phosphate; and carbon coating comprising at least one carbon material selected from the group consisting of (i) fibrous carbon material, (ii) chain-like carbon material, and (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material, wherein each particle is coated with the carbon coating.
In an embodiment of the present invention, carbon material is (i) fibrous carbon material, (ii) chain-like carbon material, (iii) carbon material produced by linking together fibrous carbon material and chain-like carbon material, or a mixture thereof.
Examples of the fibrous carbon material include a carbon nanotube, carbon nanofiber, vapor-grown carbon fiber, polyacrylonitrile (PAN)-based carbon fiber, and pitch-based carbon fiber. Among them, a carbon nanotube with an average fiber size of 5 to 200 nm is preferable.
Examples of the chain-like carbon material include carbon black such as acetylene black (e.g., DENKA BLACK manufactured by DENKI KAGAKU KOGYO KABUSHIKI KAISHA) or furnace black (e.g., SUPER-P manufactured by TIMCAL GRAPHITE & CARBON, Inc.; Ketjenblack manufactured by Ketjen Black International Company). Among them, carbon black whose primary particles have an average size of 10 to 100 nm is preferable. Among the carbon black, particularly preferred is acetylene black.
Examples of a method for linking fibrous carbon material and chain-like carbon material include: but are not particularly limited to, a method for injecting fibrous carbon material during thermolysis of hydrocarbon to link the material and carbon black generated; a method for supplying and linking hydrocarbon containing a fibrous carbon-forming catalyst during thermolysis of acetylene gas and/or while acetylene gas is subjected to thermolysis (see Patent Literature 14); a method for dispersing fibrous carbon and carbon black into a liquid carbonization source such as hydrocarbon and alcohol to carbonize the liquid carbonization source by heating, etc., while keeping it in a liquid or gas phase; a method including: mixing beforehand a fibrous carbon-forming catalyst and carbon black; causing them to contact source gas for fibrous carbon; and linking the carbon black and the fibrous carbon while generating the fibrous carbon; and a method for linking fibrous carbon and carbon black by a mechanochemical process using a solid medium. Examples of the linking using a mechanochemical process include linking using a media mixing mill such as a bead mill, a vibrating mill, or a ball mill. For example, an SEM image can be examined to calculate an average fiber size of fibrous carbon material and an average particle size of primary particles of chain-like carbon material, which sizes may be a number average fiber size and a number average particle size, respectively. The average fiber size may be, for example, 5, 10, 15, 20, 30, 50, 100, 150, or 200 nm. The size may be between any two of the above values. The average particle size of primary particles of chain-like carbon material may be, for example, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100 nm. The size may be between any two of the above values.
In an embodiment of the present invention, lithium-containing phosphate may be phosphate capable of storing and releasing a lithium ion. Specific examples of the lithium-containing phosphate include LiFePO4, LiMnPO4, LiMnxFe(1-x)PO4, LiCoPO4, and Li3V2(PO4)3. Particularly preferred are LiFePO4 and LiMnxFe(1-x)PO4.
In an embodiment of the present invention, the composite particles have an average primary particle size of preferably 0.02 to 20 μm and more preferably 0.05 to 5 μm. When the particle size is smaller than the above, it is difficult to coat the lithium-containing phosphate with the carbon coating containing the above carbon material because the particles are too small. When the particle size is larger than that, the positive electrode material has a reduced number of the particles. Also, the positive electrode active substance and the conduction aid have a reduced number of their contacts. Accordingly, the advantageous effects of the present invention as described in paragraph (0011) cannot be sufficiently achieved. The average particle size may be, for example, 0.02, 0.05, 0.1, 0.5, 1, 2, 3, 4, 5, 10, 15, or 20 μm. The size may be between any two of the above values. This average particle size can be calculated by examining, for example, an SEM image and may be a number average particle size. In an embodiment of the present invention, the coating includes a state in which the entire surface of the coated particles is coated. This coating may be carried out using carbon coating to cover 90, 95, 98, 99, 99.5, 99.9, or 100% of the particle surface. This ratio may be between any two of the above values. The coating of the particles may be observed with an SEM.
Composite particles produced by coating particles of lithium-containing phosphate with carbon coating containing the above carbon material may be prepared by any of the following methods: (a) a method for mixing and heating the above surface-treated carbon material, source material for lithium-containing phosphate, and a heat-degradable carbon source compound; (b) a method for mixing and heating the above surface-treated carbon material, particles of lithium-containing phosphate as obtained by heating source material for the lithium-containing phosphate and/or particles of a precursor thereof, and a heat-degradable carbon source compound; and (c) a method for mixing and heating the above surface-treated carbon material, particles of lithium-containing phosphate, and a heat-degradable carbon source compound. Note that in the method (c), commercially available particles of lithium-containing phosphate (including carbon-coated particles) may be used.
The carbon material is subjected to surface treatment. This process is, for example, oxidation treatment or treatment using a surfactant or a polymer dispersant. Carbon material without surface treatment is unsuitable for the present invention because the material is unlikely to be incorporated in carbon coating during formation of the coating. In the oxidation treatment, an oxidizer is used on a surface of the above carbon material to introduce a hydroxyl group (—OH), a carbonyl group (>C═O), a carboxyl group (—COOH), or a functional group containing an ether bond or an ester bond. Specific examples of the oxidation treatment include: (i) heating the carbon material under an oxygen-containing atmosphere (gas phase oxidation); (ii) retaining the carbon material under an ozone-containing atmosphere or in an ozone-containing solution (ozone oxidation); (iii) heating the carbon material in a solution containing an oxidizing compound (e.g., sulfuric acid, nitric acid, perchloric acid, hydrogen peroxide, potassium permanganate, osmic acid); and (iv) subjecting the carbon material to treatment using a wet jet mill in water, an organic solvent containing a functional group such as a hydroxy group (—OH) or a carbonyl group (>C═O) (e.g., ethanol, isopropyl alcohol, methyl ethyl ketone, methyl isobutyl ketone), or a mixed solution thereof. For example, a Star Burst manufactured by SUGINO MACHINE LIMITED, a Nano Jet Pal manufactured by JOKOH, Inc., a Nano Maker manufactured by Advanced Nano Technology Co., Ltd., or a microfluidizer manufactured by Powrex Corp. is suitable for the wet jet mill processor. Note that an SEM may be used to examine whether or not the carbon material is present in the carbon coating. In a surface image of the composite particles observed using the SEM, each composite particle may have, for example, 5, 10, 20, 30, or 50 pieces of the carbon material or a part thereof in its carbon coating. This number may be any one of the above values or higher, or may be between any two of the above values.
The treatment using a surfactant refers to a method for mixing the above carbon material and a surfactant in a polar solvent such as water or alcohol. Examples of the surfactant include: anionic surfactants such as sodium dodecyl sulfate (SDS); cationic surfactants such as dodecyltrimethylammonium chloride (C12TAC) or hexadecyltrimethylammonium bromide (C16TAB); amphoteric surfactants such as cocamidopropyl betaine or cocamidopropyl hydroxybetaine; and nonionic surfactants such as polyvinyl alcohol or polyoxyethylene octylphenylether (product name: Triton X-100). Note that paragraphs (0015) and (0028) of Patent Literature 10 (JP2005-123107A) disclose acetone as an example of a surfactant. When acetone is used as the surfactant, however, an object of the present invention cannot be achieved because of its volatile nature. Thus, acetone is excluded from the surfactant of the present invention.
The treatment using a polymer dispersant refers to a method for mixing the above carbon material and a polymer dispersant in water or an organic solvent. Examples of the polymer dispersant include polyvinylpyrrolidone (PVP) and poly(allylamine hydrochloride) (PAH).
Examples of the source material for lithium-containing phosphate include: lithium carbonate (Li2CO3), lithium hydroxide monohydrate (LiOH.H2O), lithium sulfate monohydrate (Li2SO4.H2O), lithium formate monohydrate (Li(HCOO).H2O), and/or lithium nitrate (LiNO3); ferric phosphate dihydrate (FePO4.2H2O), ferrous oxalate dihydrate (FeC2O4.2H2O), ferric sulfate heptahydrate (FeSO4.7H2O), and/or ferrous chloride tetrahydrate (FeCl2.4H2O); and phosphoric acid (H3PO4), ammonium dihydrogen phosphate ((NH4)H2PO4) or ammonium monohydrogen phosphate ((NH4)2HPO4), and/or ammonium phosphate ((NH4)3PO4).
In addition, lithium manganese phosphate (LiMnPO4) may be produced. In this case, as source material, manganese carbonate (MnCO3), manganese dioxide (MnO2), manganese sulfate monohydrate (MnSO4.H2O), manganese nitrate tetrahydrate (Mn(NO3)2.4H2O), and/or manganese acetate tetrahydrate ((CH3COO)2Mn.4H2O), for example, may be used to substitute the iron compound such as ferrous oxalate dihydrate, ferric phosphate dihydrate, ferric sulfate heptahydrate, and/or ferrous chloride tetrahydrate in the case of the lithium iron phosphate. Further, lithium manganese iron phosphate (LiMnxFe(1-x)PO4) may be produced. In this case, source material for the lithium iron phosphate and source material for the lithium manganese phosphate may be used at the same time.
Furthermore, lithium cobalt phosphate (LiCoPO4) may be produced. In this case, as source material, cobalt sulfate heptahydrate (CoSO4.7H2O), for example, may be used to substitute the iron compound in the case of the lithium iron phosphate. Moreover, lithium vanadium phosphate (Li3V2(PO4)3) may be produced. In this case, as source material, divanadium pentoxide (V2O5) and/or vanadium oxide sulfate hydride (VOSO4.xH2O)(x=3 to 4), for example, may be used to substitute the iron compound in the case of the lithium iron phosphate.
In an embodiment of the present invention, examples of the heat-degradable carbon source compound include glucose (C5H12O6), sucrose (C12H22O11), dextrin ((C6H12O5)n), ascorbic acid (C6H8O6), carboxymethyl cellulose, and coal pitch.
In an embodiment of the present invention, a mixer may be used for the mixing. Examples of the mixer include a tank with a mixer, a sonicator, and a homogenizer. In this case, water, alcohol, or a mixed solvent of water and alcohol is suitable for the solvent. Note that when a surfactant or a polymer dispersant is used for surface treatment, pretreatment may be carried out before the source material is mixed or treatment may be carried out at the same time when the source material is mixed.
In an embodiment of the present invention, it is preferable to perform a method for heating a solution having dissolved therein a lithium ion (Li+), a phosphate ion (PO43−), and a metal ion other than from lithium, and/or a heat-degradable carbon source compound, etc., as a solution state while stirring in a tank with a mixer, etc. The heating temperature is preferably from 60 to 100° C. In order to increase a reaction rate, however, it is preferable to use a method using a pressured and heated solvent at from 100 to 250° C. (i.e., a hydrothermal synthesis method). In this case, the heating is carried out using a pressure-resistant vessel such as an autoclave. This heating temperature may be, for example, 60, 80, 100, 150, 200, or 250° C. The temperature may be between any two of the above values. In this case, depending on the need, a pH modifier such as ammonia (NH3), phosphoric acid (H3PO4), or sulfuric acid (H2SO4) may be added to a solution having dissolved therein a lithium ion (Lit), a phosphate ion (PO43−), and a metal ion other than from lithium, and/or a heat-degradable carbon source compound, etc.
In an embodiment of the present invention, the final heating is preferably carried out in vacuo under an inert atmosphere, reducing atmosphere, or mixed atmosphere of an inert gas and a reducing gas to form composite particles coated with carbon coating containing carbon material. Examples of the inert gas include argon (Ar), helium (He), and nitrogen (N2). Examples of the reducing gas include hydrogen (H2) and ammonia (NH3). The heating temperature is preferably from 400 to 900° C. and more preferably from 500 to 800° C. This heating temperature may be, for example, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, or 900° C. The temperature may be between any two of the above values.
Composite particles according to an embodiment of the present invention, a conduction aid, and a binder may be mixed to form an electrode material for a lithium-ion secondary battery. Examples of the conduction aid used include: carbon black such as acetylene black or furnace black, and/or a carbon nanotube or carbon nanofiber. Polyvinylidene fluoride (PVDF) may be used as the binder. With regard to a mixing ratio in an embodiment of the present invention, the composite particles have, for example, 60 to 95% by mass and the remainder consists of the conduction aid and the binder. When the composite particles are less than 60% by mass, the lithium-ion secondary battery has a reduced charge/discharge capacity. In addition, when the composite particles are more than 95% by mass, the amount of the conduction aid is insufficient. This increases the electric resistance of a positive electrode. In addition, the insufficient amount of the binder causes insufficient firmness of the positive electrode. Unfortunately, this results in a problem that the positive electrode material is likely to detach from a collector (mostly made of aluminum) during charge and discharge.
In an embodiment of the present invention, a positive electrode material is used for a positive electrode formed on a collector and the positive electrode may be used for a lithium-ion secondary battery. Examples of other components used for the lithium-ion secondary battery include a separator, an electrolytic solution, and a negative electrode material. The separator electrically insulates the positive electrode from the negative electrode and helps retain the electrolytic solution. Separators made of synthetic resin such as polyethylene and polypropylene may be used. In order to increase retention of the electrolytic solution, a porous film is preferably used for the separators.
In addition, in a lithium secondary battery using a positive electrode according to an embodiment of the present invention, a lithium salt-containing nonaqueous electrolytic solution or ion conductive polymer may be preferably used as an electrolytic solution in which a group of the electrodes is soaked. Examples of a nonaqueous solvent for a nonaqueous electrolyte in the lithium salt-containing nonaqueous electrolytic solution include ethylene carbonate (EC), propylene carbonate (PC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and methylethyl carbonate (MEC). In addition, examples of the lithium salt capable of being dissolved in the above nonaqueous solvent include lithium hexafluorophosphate (LiPF6), lithium tetrafluoroborate (LiBF4), and lithium trifluoromethanesulfonate (LiSO3CF3).
A preferable active substance of a negative electrode is a material that can reversibly store and release a Li ion in the same manner as in the case of the positive electrode, has poor reactivity with the electrolyte, and has a less redox potential than the positive electrode material. Examples include graphite, lithium titanate, silicon (Si), and tin (Sn). Two or more of them may be combined depending on the need. These compounds may be combined with a conduction aid and a binder in the same manner as in the case of the positive electrode, and may be practically used as a negative electrode material formed on a collector (in the case of the negative electrode, copper is mainly used).
The material members disclosed in paragraphs (0027) to (0029) are combined. Then, in order to prevent damage, deformation, and contact with an ambient air, the members are sealed in a container to form a lithium-ion secondary battery. The shape and material of the container are appropriately selected depending on its usage. For example, when charge and discharge characteristics, for example, are tested in a simple way, it is preferable to form a coin cell using a disk container made of metal such as stainless for sealing.
A high capacity and long service life may be required for industrial or consumer use. In this case, a positive electrode material, a separator, and a negative electrode material are alternately wound to form a wound cell using a metal cylinder-type or rectangular-type container for sealing. In the case of intermediate usage, a positive electrode material, a separator, and a negative electrode material are alternately stacked to form a laminated cell (aluminum pouch cell) using an aluminum-laminated package, etc., for sealing.
The following details composite particles, a process for producing the same, electrode material for a secondary battery and a secondary battery according to the present invention by referring to Examples and Comparative Examples. The present invention, however, is not limited to the following Examples without departing from the scope of the present invention.
(Surface Treatment of Carbon Material)
Tables 1 and 2 list carbon materials used for treatment and treatment methods. Note that organic functional groups introduced onto a surface of the carbon materials by oxidation treatment were determined by temperature-programmed desorption gas chromatography/mass spectrometry (a TDS-GC/MS method) using a temperature-programmed desorption device (Double-Shot Pyrolyzer 7683B manufactured by Agilent Technologies Inc.), gas chromatography equipment (HP6890 manufactured by Hewlett-Packard Development Company, L.P.), and a mass spectrometer (5973 manufactured by Hewlett-Packard Development Company, L.P.). Qualitative analysis was performed by examining whether or not there were mass spectral peaks of water (mass number=18), carbon monoxide (mass number=28), and carbon dioxide (mass number=44). Note that a mass spectrum detected below 200° C. was considered to be due to detachment of adsorbed gas. Accordingly, the mass spectrum was neglected. In addition, the same condition as of the temperature-programmed desorption device (i.e., heating in vacuo at a temperature increasing rate of 25° C./min from 200° C. to 1000° C.) was applied to heat 10 g of the carbon materials in an electric furnace and to determine a change in mass before and after the heating. The following equation was used to calculate an amount of decrease in mass and the amount was defined as a content of the organic functional groups.
[Organic functional group content (% by mass)]=[{(Mass of carbon material after heating at 200° C.)−(Mass of carbon material after heating at 1000° C.)}/(Mass of carbon material after heating at 200° C.)]×100
(Mixing and Heating of Surface-Treated Carbon Material, Source Material for Lithium-Containing Phosphate, and Heat-Degradable Carbon Source Compound)
The surface-treated carbon material as prepared in Examples 1 to 3, source material, and a carbon source compound were mixed and heated under conditions designated in Table 3.
(Method for Forming Particles of Lithium-Containing Phosphate and/or Particles of Precursor Thereof and Mixing of Surface-Treated Carbon Material, Particles of Lithium-Containing Phosphate and/or Particles of Precursor Thereof, and Carbon Source Compound)
Table 4 shows a method for forming particles of lithium-containing phosphate and/or particles of a precursor thereof from source material. The particles formed, the surface-treated carbon material, and a carbon source compound were mixed under conditions designated in Table 4.
(Mixing of Surface-Treated Carbon Material, Particles of Lithium-Containing Phosphate, and Carbon Source Compound)
The surface-treated carbon material as prepared in Example 7, Particles of lithium-containing phosphate, and a carbon source compound were mixed under conditions designated in Table 4.
(Further Heating)
The mixture containing the surface-treated carbon material, a lithium-containing phosphate precursor and/or lithium-containing phosphate, and a carbon source compound, which mixture was produced in Examples 8 to 14, was further heated under conditions designated in Table 5 to prepare composite particles according to an example of the present invention. The crystal phase of the composite particles was identified by powder X-ray diffraction (using an X-ray diffractometer RU-200A manufactured by Rigaku Corporation; an X-ray source: Cu-Kα; a voltage: 40 kV; a current: 30 mA). In addition, a scanning electron microscope (a scanning electron microscope (SEM) JSM-6301F manufactured by JEOL Ltd.; an acceleration voltage: 1 kV; magnification: 10,000 to 50,000 x) was used to measure an average primary particle size of the composite particles and to inspect whether or not the carbon material was included in the carbon coating on the particle surface.
The carbon material was not subjected to surface treatment and the same as of Examples 1 to 21 applied to the other processes to prepare particles of Comparative Examples 15 to 21.
Tables 5 to 9 show these conditions and results together.
The composite particles of Examples 15 to 21, carbon as a conduction aid, and polyvinylidene fluoride (a KF polymer solution manufactured by KUREHA CORPORATION) as a binder were combined at predetermined ratios designated in Table 9. N-methylpyrrolidone (catalog No. 328634 manufactured by Sigma-Aldrich Co. LLC.) was added thereto as a dispersion solvent. Then, the mixture was kneaded to prepare a positive electrode combination (slurry). This combination was used as positive electrode material to manufacture a laminated cell. After that, its charge and discharge characteristics were evaluated. The following shows an example of a method for manufacturing a positive electrode and a laminated cell. First, the composite particles of Examples 15 to 21 were used as a positive electrode combination slurry. Next, an aluminum foil with a thickness of 20 μm was coated with this slurry and dried. Then, the foil was pressed and cut at 40 mm×40 mm to prepare a positive electrode for a lithium secondary battery. Graphite (synthetic graphite MCMB6-28 manufactured by OSAKA GAS CO., Ltd.) was used for a negative electrode. Polyvinylidene fluoride as a binder was mixed at a predetermined ratio. Then, a slurry was prepared in the same manner as in the case of the positive electrode. Subsequently, a copper foil with a thickness of 10 μm was coated with this slurry and dried. After that, the foil was pressed and cut at 45 mm×45 mm to manufacture a negative electrode for a lithium secondary battery. An olefin fiber nonwoven fabric with a size of 50 mm×50 mm was used as a separator that electrically separate the positive electrode from the negative electrode. An electrolytic solution was a solution prepared by mixing EC (ethylene carbonate manufactured by Aldrich Inc.) and MEC (methylethyl carbonate manufactured by Aldrich Inc.) at a volume ratio of 30:70 and by dissolving lithium hexafluorophosphate (LiPF6 manufactured by Stella Chemifa Corporation) at 1 mol/L in the solution. After terminals were connected to the positive and negative electrodes, the whole body was enclosed in an aluminum-laminated package to form a laminated cell with a size of 60 mm×60 mm.
Discharge performance of the cell was tested as follows. First, a cell was initially charged. Next, its charge/discharge efficiency was verified to be at or near 100%. Then, a constant current was discharged at a current density of 0.7 mA/cm2 until the voltage reached 2.1 V. At that time, the discharge capacity was measured. After that, the discharge capacity was divided by an amount of positive electrode active substance to calculate a capacity density (mAh/g). A current level that can charge and discharge this capacity (mAh) in 1 hour was defined as “1C”.
After the initial charge and discharge, its charge was conducted at 4.2 V (4.8 V was used for Examples 25 and 26 and Comparative Examples 25 and 26)(at a constant current of 0.2 C; terminated when a current was 0.05 C). With regard to the discharge, a current level in each cycle was gradually increased from 0.2 C, 0.33 C, 0.5 C, 1 C, to 3 C (at a constant current; terminated when the voltage was 2.1 V). A 10-min interval was placed between the cycles, and the cycle was then repeated while keeping a current level of 3 C. A cycle characteristic was defined as a ratio of a charge/discharge capacity at cycle 1000 of 3 C to a charge/discharge capacity at the initial cycle (0.2 C). Further, I-V characteristics at a SOC (charge depth) of 50% were used to calculate direct current resistance (DCR) of the cell. The direct current resistance during charge was defined as “charge DCR” and the direct current resistance during discharge was defined as “discharge DCR”. Table 9 lists these results.
Except using the composite particles of Comparative Examples 15 to 21 as alternatives for those of Examples 15 to 21, the same procedure as in Examples 22 to 28 was applied to form a laminated cell. Then, the discharge performance of the cell was tested. Table 9 shows the results.
It has been found from Examples and Comparative Examples that cells using composite particles according to the present invention have remarkable improvements in the cycle characteristic determined by the discharge performance test.
Positive electrode material for a lithium-ion secondary battery according to the present invention has excellent electron conductivity while using lithium-containing phosphate as a positive electrode active substance and overcoming its drawback. The lithium-containing phosphate should be heat-stable and highly safe, but has the drawback that its resistance is high. The positive electrode material of the present invention has resolved the drawback of the lithium-containing phosphate. As a result, it is possible to manufacture a highly safe lithium-ion secondary battery capable of maintaining stable charge and discharge characteristics over a long period of service life. A lithium-ion secondary battery using positive electrode material of the present invention can be suitably used for application such as an electric tool and a hybrid car, which require stable charge and discharge over a long period.
Although a few embodiments of the present invention have been shown and described, it would be appreciated by those skilled in the art that changes may be made in this embodiment without departing from the principles and spirit of the invention, the scope of which is defined in the claims and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2011-250184 | Nov 2011 | JP | national |
This application is a divisional of U.S. application Ser. No. 14/358,016 filed Jun. 2, 2014, which is a national stage of International Application No. PCT/JP2012/079484 filed Nov. 14, 2012, which claims the benefit of Japanese Application No. 2011-250184, filed Nov. 15, 2011, in the Japanese Patent Office. All disclosures of the documents named above are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14358016 | Jun 2014 | US |
| Child | 16429716 | US |
