WO2016157551A1 - チタン酸化物粒子、チタン酸化物粒子の製造方法、チタン酸化物粒子を含む蓄電デバイス用電極、チタン酸化物粒子を含む電極を備えた蓄電デバイス - Google Patents
チタン酸化物粒子、チタン酸化物粒子の製造方法、チタン酸化物粒子を含む蓄電デバイス用電極、チタン酸化物粒子を含む電極を備えた蓄電デバイス Download PDFInfo
- Publication number
- WO2016157551A1 WO2016157551A1 PCT/JP2015/065204 JP2015065204W WO2016157551A1 WO 2016157551 A1 WO2016157551 A1 WO 2016157551A1 JP 2015065204 W JP2015065204 W JP 2015065204W WO 2016157551 A1 WO2016157551 A1 WO 2016157551A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- titanium oxide
- oxide particles
- particles according
- carbon
- crystallites
- Prior art date
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 150
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 title claims abstract description 144
- 239000002245 particle Substances 0.000 title claims abstract description 98
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 238000003860 storage Methods 0.000 title claims description 15
- 239000011148 porous material Substances 0.000 claims abstract description 30
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 82
- 239000010936 titanium Substances 0.000 claims description 78
- 229910052799 carbon Inorganic materials 0.000 claims description 66
- 229910052744 lithium Inorganic materials 0.000 claims description 57
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 55
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 52
- 238000010438 heat treatment Methods 0.000 claims description 48
- 239000012298 atmosphere Substances 0.000 claims description 26
- 229910052760 oxygen Inorganic materials 0.000 claims description 24
- 238000002156 mixing Methods 0.000 claims description 21
- 239000002131 composite material Substances 0.000 claims description 17
- 239000001301 oxygen Substances 0.000 claims description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
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- 239000000203 mixture Substances 0.000 claims description 6
- 229910052596 spinel Inorganic materials 0.000 claims description 4
- 239000011029 spinel Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 description 25
- 229910052719 titanium Inorganic materials 0.000 description 23
- 239000012467 final product Substances 0.000 description 22
- 239000000463 material Substances 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 239000003990 capacitor Substances 0.000 description 13
- -1 titanic acid compound Chemical class 0.000 description 13
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
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- 239000002243 precursor Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 230000005540 biological transmission Effects 0.000 description 9
- 238000000192 extended X-ray absorption fine structure spectroscopy Methods 0.000 description 8
- 238000000024 high-resolution transmission electron micrograph Methods 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
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- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 6
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- 230000015572 biosynthetic process Effects 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 2
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Chemical compound [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000011817 metal compound particle Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
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- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 229910000505 Al2TiO5 Inorganic materials 0.000 description 1
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- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
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Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/08—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances oxides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/003—Titanates
- C01G23/005—Alkali titanates
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
- C01G23/04—Oxides; Hydroxides
- C01G23/043—Titanium sub-oxides
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/50—Electrodes characterised by their material specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2027—Light-sensitive devices comprising an oxide semiconductor electrode
- H01G9/2031—Light-sensitive devices comprising an oxide semiconductor electrode comprising titanium oxide, e.g. TiO2
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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
- H01M4/04—Processes of manufacture in general
- H01M4/0471—Processes of manufacture in general involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis
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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
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- H01M4/02—Electrodes composed of, or comprising, active material
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Definitions
- the present invention relates to titanium oxide particles.
- Titanium oxide sintered particles such as titanium oxide represented by the general formula Ti n O 2n and lithium titanate represented by the general formula Li ⁇ Ti ⁇ O ⁇ are used in various applications due to the characteristics of the titanium oxide. Is expected to be used.
- titanium oxide (IV) is a dye-sensitized solar cell electrode, a storage battery that can be charged with light, a photoelectrode for hydrogen production by water decomposition, a pigment, a colorant, a photocatalyst, an antibacterial material, water treatment technology, cancer Expected to be used for treatment.
- Lithium titanate is expected to be used as an electrode active material for power storage devices such as storage batteries and capacitors.
- titanium oxides also have disadvantages such as low electrical conductivity and the ability to absorb only ultraviolet rays. Therefore, research on composites that combine the characteristics of titanium oxide with the characteristics of other substances to compensate for the disadvantages of titanium oxide is also progressing.
- an object of the present invention is to provide novel titanium oxide particles that can improve rate characteristics, do not require a conductive aid, or can minimize the conductive aid, a method for producing the same, and uses thereof Is to provide.
- the novel titanium oxide particles of the present invention have a three-dimensional network structure in which titanium oxide crystallites are connected, and a magnetic phase is formed on the surface of the crystallites. It is characterized by.
- the titanium oxide particles have an electron path including a magnetic phase, an energy storage space inside the particle, and an ion path to the energy storage space.
- the titanium oxide may be lithium titanate represented by a general formula Li ⁇ Ti ⁇ O ⁇ .
- the titanium oxide may be a spinel type lithium titanate represented by Li 4 Ti 5 O 12 .
- a titanium oxide particle can have the characteristics of both a lithium titanate and a Magneli phase.
- the magnetic phase is a titanium oxide represented by the general formula Ti n O 2n-1 (3 ⁇ n ⁇ 10).
- the magnetic phase may be Ti 4 O 7 .
- Ti 4 O 7 has an electrical conductivity that is 2.75 times that of carbon in particular.
- a plurality of pores connected to the inside of the three-dimensional network structure may be provided between the crystallites. As a result, an ion path that connects the pores to the space is formed.
- the crystallites may be bonded to each other without grain boundaries. Since the grain boundary resistance is reduced, the conductivity is improved.
- the carbon content is less than 5% by weight with respect to the whole particle, and it is not necessary to use a conductive aid, and the conductive aid can be minimized.
- the crystallite may have a flat plate shape, and the three-dimensional network structure may be a card house structure. It is more desirable that a magnetic phase is formed on the edge surface of the crystallite.
- This titanium oxide particle is most suitable for, for example, an electrode for an electricity storage device and an electricity storage device provided with this electrode.
- a composite of titanium oxide crystallites and carbon is heat-treated in an oxygen atmosphere to burn out the carbon and connect the titanium oxide crystallites to form particles with a three-dimensional network structure.
- a magnetic phase can be formed on the surface of the crystallite.
- the temperature of the heat treatment is preferably 400 to 600 ° C.
- the heat treatment time is preferably 0.5 to 10 hours. Thereby, it becomes easy to have the characteristics of the surface magnetic phase without impairing the characteristics of the titanium oxide constituting the entire crystallite.
- the composite may be generated by a mixing step of the titanium oxide source and the carbon source, and a step of heat-treating the mixture that has passed through the mixing step in an inert atmosphere.
- the temperature of the heat treatment under the inert atmosphere may be 600 to 950 ° C.
- the mixing step may include a mechanochemical treatment for the titanium oxide source and the carbon source in the solution.
- the titanium oxide particles of the present invention have an electron path including a magnetic phase, an energy storage space inside the particle, and an ion path to the energy storage space, and no conductive aid is required or the conductive aid is minimized. It is optimal for an electrode of an electricity storage device, an electrode of a dye-sensitized solar cell, a storage battery that can be charged with light, and a photoelectrode for hydrogen production by water splitting.
- FIG. 4 shows differential pore volume distributions in which the horizontal axis represents the pore diameter and the vertical axis represents the increase in the pore volume between measurement points in relation to the titanium oxide particles of Examples and Comparative Examples. It is the figure which showed the relationship between a rate and a capacity
- a novel titanium oxide particle 1 As shown in FIG. 1, a novel titanium oxide particle 1 according to the present invention has a three-dimensional network structure in which a plurality of crystallites 2 are continuously connected to each other. A granulated body having phase 2a. The crystallites 2 are randomly oriented and bonded to each other on a surface such as a table surface or an end surface. When the crystallite 2 has a flat plate shape, the three-dimensional network structure is a card house structure. A large number of nano-sized spaces 3 exist inside the titanium oxide particles 1. Grain boundaries are eliminated at the bonding interface of the crystallites 2, while many fine pores 4 exist between the crystallites 2.
- Crystallite 2 is the largest group that can be regarded as a single crystal of titanium oxide.
- the crystallite 2 has a shape formed by a triangular, square, or other polygonal flat plate shape, a polyhedron having a thickness, a sphere, an ellipsoid, or another curved surface.
- the surface of the crystallite 2 is an edge surface when the crystallite 2 is a flat plate or a polyhedron, and is a side portion or an end portion of the facet plane.
- One or more of the sides or ends of the crystallite 2 are transformed into the magnetic phase 2a.
- a part or the entire length of the side portion or end portion of the crystallite 2 is a Magneli phase 2a.
- the magnetic phase 2a may be included in a partial region of the facet surface.
- the surface of the crystallite 2 is a singular or plural partial region of the surface when the crystallite 2 has a curved surface.
- the titanium oxide constituting the crystallite 2 is a titanium oxide represented by the general formula Ti n O 2n and a titanic acid compound represented by the general formula M ⁇ Ti ⁇ O ⁇ .
- M is a metal.
- titanate compounds include lithium titanate, lead titanate, barium titanate, lead zirconate titanate, potassium titanate, vanadium titanate, strontium titanate, calcium titanate, magnesium titanate, and aluminum titanate. Can do.
- the titanium oxide is, for example, anatase type or rutile type titanium oxide (IV) represented by TiO 2 .
- the titanic acid compound is, for example, spinel type lithium titanate represented by Li 4 + w Ti 5 O 12 (0 ⁇ w ⁇ 3) or ramsdellite represented by Li 2 + y Ti 3 O 7 (0 ⁇ y ⁇ 3).
- Type of lithium titanate is, for example, spinel type lithium titanate represented by Li 4 + w Ti 5 O 12 (0 ⁇ w ⁇ 3) or ramsdellite represented by Li 2 + y Ti 3 O 7 (0 ⁇ y ⁇ 3).
- Type of lithium titanate is, for example, spinel type lithium titanate represented by Li 4 + w Ti 5 O 12 (0 ⁇ w ⁇ 3) or ramsdellite represented by Li 2 + y Ti 3 O 7 (0 ⁇ y ⁇ 3).
- the magnetic phase 2a is a titanium oxide represented by the general formula Ti n O 2n-1 (3 ⁇ n ⁇ 10).
- the magnetic phase 2a is selected from, for example, Ti 4 O 7 , a mixed phase of Ti 4 O 7 and Ti 5 O 9 , or a compound represented by the general formula Ti n O 2n-1 (3 ⁇ n ⁇ 10). Single or two or more mixed phases.
- the titanium oxide particles 1 have both the characteristics of lithium titanate and the characteristics of the magnetic phase 2a.
- Lithium titanate has an energy storage function by insertion / extraction of lithium ions. Since the volume change of the insertion / desorption is about 1%, there is little capacity deterioration. Since the charge / discharge potential is about 1.5 V (vs Li / Li +), side reactions such as decomposition of the electrolyte and precipitation of lithium metal due to rapid charge / discharge hardly occur, and the cycle characteristics are excellent.
- the crystallite 2 is lithium titanate
- the titanium oxide particles 1 have an advantage as an active material of such an electrode.
- lithium titanate has lower electrical conductivity than carbon.
- the magnetic phase 2a has high electrical conductivity
- Ti 4 O 7 has 2.75 times the electrical conductivity of carbon. That is, the titanium oxide particles 1 have a characteristic that high electrical conductivity is imparted by the magnetic phase 2a while maintaining the performance of the active material as lithium titanate.
- this titanium oxide particle 1 has a three-dimensional network structure in which a highly electrically conductive magnetic phase 2a is present on the surface of the crystallite 2 and the crystallite 2 is continuous on the surface such as a table surface or an end surface. Therefore, each crystallite 2 is partially connected via the magnetic phase 2a.
- a connection mode there are a case where the magnetic phases 2a are connected to each other, a case where the magnetic phases 2a and the surface other than the magnetic phase 2a are connected, or a mixture thereof. Therefore, an electron path including the magnesium phase 2a is formed in the titanium oxide particles 1 even without a conductive auxiliary agent such as carbon, and the titanium oxide particles 1 as a whole have high electrical conductivity. Since carbon is unnecessary or less carbon is used, a decrease in energy density can be suppressed.
- the titanium oxide particles 1 have nano-sized spaces 3 and serve as a reservoir for the electrolyte. Since a large number of pores 4 are formed between the crystallites 2 in the nano-sized space portion 3, an ion path for lithium ions is also secured. Furthermore, there is no grain boundary at the bonding interface between the crystallites 2, and the grain boundary resistance is low. Therefore, the titanium oxide particles 1 are optimal for, for example, an electrode of an electricity storage device, an electrode of a dye-sensitized solar cell, a storage battery that can be charged with light, and a photoelectrode for hydrogen production by water splitting.
- the crystallite 2 preferably has an average size of 5 to 100 nm.
- the crystallite 2 has a thickness of 1 nm or less at the 2 to 5 atomic layer level, and one side of the two-dimensional surface expands to 5 to 100 nm.
- the titanium oxide particles 1 preferably have a size of about 500 nm to 5 ⁇ m by combining a plurality of crystallites 2. This size is easy to handle as an electrode material.
- the sizes of the crystallites 2 and the titanium oxide particles 1 can be adjusted by the temperature and time in the heat treatment step.
- Each pore is preferably about 5 to 100 nm.
- the differential pore volume in the pore diameter in the range of 10 to 40 nm has a value of 0.01 cm 3 / g or more, In particular, by having a value of 0.02 cm 3 / g or more, it becomes an ion path of fine lithium ions, the area of the crystallite 2 in contact with the electrolytic solution is increased, and the rate characteristics when used for the electrode are improved.
- the remaining amount of carbon is ideally zero, but is preferably less than 5% by weight with respect to the titanium oxide particles 1.
- the titanium oxide particles 1 can be obtained by heat-treating a titanium oxide crystallite 2 and a carbon composite in an oxygen atmosphere. As shown in FIG. 2, by heat-treating the composite in an oxygen atmosphere, carbon is burned out from the composite and the crystallites 2 are sintered together. Furthermore, by heat-treating the composite in an oxygen atmosphere, the surface of the crystallite 2 is transformed into the magnetic phase 2a, whereby the titanium oxide particles 1 are generated.
- carbon is combined with oxygen in the atmosphere and burned. Further, although not limited to this mechanism, carbon becomes carbon monoxide Co or carbon dioxide CO 2 by desorbing oxygen atoms of titanium oxide from the bonding interface, and titanium is reduced, It is thought that lithium takes the oxygen atom of titanium oxide and gasifies it into Li 2 O. Through these reactions, oxygen is desorbed until Ti: O is changed from n: 2n + 2 to n: 2n ⁇ 1, lithium is gasified, and lithium titanate constituting the surface of the crystallite 2 is transformed into the magnetic phase 2a. it is conceivable that.
- the degree of bonding between carbon and crystallites, oxygen concentration, firing temperature and firing time are the same as the size of titanium oxide particles, the degree of carbon removal, the transformation into the magnetic phase 2a due to the above reaction, and the alteration.
- the percentage can be determined.
- the heat treatment temperature is preferably in the range of 400 to 600 ° C.
- the heat treatment time is preferably maintained between 0.5 and 10 hours.
- the temperature is less than 400 ° C. and the heat treatment time is less than 0.5 hours, the carbon is not sufficiently removed and the energy density is significantly reduced.
- the temperature is less than 400 ° C. and the heat treatment time is less than 0.5 hours, the transformation into the magnetic phase 2a may not proceed easily, and satisfactory high electrical conductivity cannot be imparted to the titanium oxide particles 1.
- the temperature exceeds 600 ° C. and the heat treatment exceeds 10 hours the aggregation of the titanium oxide proceeds and the voids of the titanium oxide particles 1 are reduced.
- the transformation to the magnetic phase 2a proceeds excessively and high electrical properties are imparted, but the properties of the titanium oxide may be impaired.
- the crystallite 2 obtained by setting the temperature range and time as described above is maintained at an average size of 5 to 100 nm, and particle growth from the average size of titanium oxide before the heat treatment is suppressed.
- the oxygen atmosphere may be a mixed atmosphere with nitrogen or the like, and is preferably an atmosphere in which oxygen is present at 15% or more, such as in the air.
- the amount of oxygen decreases due to carbon burnout, so that oxygen may be appropriately supplied into the heat treatment furnace to the extent that oxygen desorption is not inhibited.
- the composite of titanium oxide crystallites 2 and carbon can be obtained, for example, through a mixing process of a titanium oxide material source and a carbon source and a heat treatment process in an inert atmosphere of the mixture.
- the titanium oxide particles 1 generally comprise a mixing step of a titanium oxide material source and a carbon source, a first heat treatment step in an inert atmosphere of the mixture, and a first The heat-treated mixture is obtained by a second heat treatment step under an oxygen atmosphere.
- carbon is burned out and accompanied by oxygen desorption or lithium desorption, it may be combined with titanium oxide instead of carbon.
- a lithium titanate precursor and a lithium titanate precursor are formed by a composite method such as mechanochemical treatment, spray drying treatment, or stirring treatment.
- the compounding of the body and the carbon source is advanced.
- the precursor of lithium titanate is Ti ⁇ O ⁇ or a constituent compound thereof.
- Ti ⁇ O ⁇ or a constituent compound thereof may be in accordance with the stoichiometric ratio of titanium oxide. For example, if Li 4 Ti 5 O 12 is lithium titanate, the atomic ratio of Ti and O can be 5:12. That's fine.
- a titanium source such as titanium oxide or titanium alkoxide that can be a precursor of lithium titanate is added to the solvent.
- the mixing step the composite of titanium oxide and the carbon source is advanced by a composite method such as mechanochemical treatment, spray drying treatment, or stirring treatment.
- a composite method such as mechanochemical treatment, spray drying treatment, or stirring treatment.
- titanium oxide itself is added to the solvent together with the carbon source.
- Carbon source means carbon (powder) itself or a material that can be converted to carbon by heat treatment.
- carbon (powder) any carbon material having electrical conductivity can be used without particular limitation.
- carbon black such as ketjen black, acetylene black, channel black, fullerene, carbon nanotube, carbon nanofiber, amorphous carbon, carbon fiber, natural graphite, artificial graphite, graphitized ketjen black, mesoporous carbon, gas phase method Carbon fiber etc. can be mentioned.
- a carbon material having a nano-sized particle size is preferable.
- the material that can be converted to carbon by the heat treatment is an organic material that is deposited on the surface of the material source of the crystallite 2 and is converted into carbon in the subsequent heat treatment step.
- organic substances include polyhydric alcohols (such as ethylene glycol), polymers (such as polyvinyl alcohol, polyethylene glycol, and polyvinylpyrrolidone), sugars (such as glucose), and amino acids (such as glutamic acid).
- the mixing ratio of carbon is preferably in the range of 95: 5 to 30:70 by weight ratio of titanium oxide particles 1 and carbon. Within this range, the pores and spaces of the finally obtained titanium oxide particles 1 can be increased.
- the solvent can be used without particular limitation as long as it does not adversely affect the reaction, and water, methanol, ethanol, isopropyl alcohol, and the like can be suitably used. Two or more solvents may be mixed and used.
- the reactor is composed of a concentric cylinder of an outer cylinder and an inner cylinder, as shown in FIG. 1 of JP-A-2007-160151.
- a reactor in which a dam plate is disposed in the part is preferably used.
- the distance between the inner cylinder outer wall surface and the outer cylinder inner wall surface is preferably 5 mm or less, and more preferably 2.5 mm or less.
- the centrifugal force required to produce on the thin film is 1500 N (kgms -2) or more, preferably 70000N (kgms -2) or more.
- a reaction inhibitor may be added to the solution.
- a predetermined compound that forms a complex with the titanium alkoxide as a reaction inhibitor, it is possible to suppress the chemical reaction from being accelerated too much.
- the reaction is suppressed and controlled by adding 1 to 3 moles of a predetermined compound such as acetic acid which forms a complex with titanium alkoxide to 1 mole of the titanium alkoxide to form a complex.
- Substances capable of forming a complex with titanium alkoxide include acetic acid, citric acid, succinic acid, formic acid, lactic acid, tartaric acid, fumaric acid, succinic acid, propionic acid, carboxylic acid such as propionic acid, and aminopolyester such as EDTA.
- Examples include complexing agents represented by amino alcohols such as carboxylic acid and triethanolamine.
- carbon powder may be dispersed in a solvent.
- a dispersion method it is preferable to highly disperse carbon powder in a solvent by ultracentrifugation (treatment of applying shear stress and centrifugal force to powder in a solution), bead mill, homogenizer, or the like.
- a solution obtained by dissolving a material source of titanium oxide in a solvent in which the carbon powder is dispersed is spray-dried on a substrate.
- the spray drying process is performed at a temperature at which the carbon powder is not burned out at a pressure of about 0.1 MPa.
- the material source of the titanium oxide is titanium alkoxide
- the titanium alkoxide is oxidized to produce a lithium titanate precursor, and the lithium titanate precursor and the carbon powder are combined.
- the solution is stirred.
- the powder is preferably pulverized in advance to form nano-level fine particles.
- a titanium oxide material source is added to a solvent to which a polymer has been added in advance, and the solution is stirred.
- the polymer may be adjusted to be in the range of 0.05 to 5 when the weight of the powder that is a material source of titanium oxide is 1.
- the lithium titanate precursor or titanium oxide is presumed to be adsorbed to the carbon source by intermolecular chemical bonds such as ionic bonds, metal bonds, hydrogen bonds, and van der Waals bonds. .
- the first heat treatment step after the mixing treatment generation of lithium titanate and crystal growth of titanium oxide are caused on the carbon.
- a titanium source is charged in the mixing step, a lithium source is added before this heat treatment step.
- the lithium source include lithium acetate, lithium nitrate, lithium oxide, lithium carbonate, and lithium hydroxide.
- the lithium source and the titanium source may be in accordance with the stoichiometric ratio of lithium titanate. For example, if Li 4 Ti 5 O 12 is lithium titanate, the atomic ratio of Li and Ti is 4: 5.
- the source and the lithium source may be added to the solvent. In the mixing step, not only the titanium source but also a lithium source may be charged in advance.
- the composite obtained in the mixing step is heat-treated in a vacuum and in an inert atmosphere such as a nitrogen or argon atmosphere.
- an inert atmosphere such as a nitrogen or argon atmosphere.
- the lithium titanate precursor is melted and lithium is taken in, so that titanium oxide is generated and crystal growth occurs, or titanium oxide is crystallized.
- the carbon source is carbonized to become carbon.
- Carbon and titanium oxide are lattice-bonded at the bonding interface by the growth of titanium oxide on the carbon.
- the inert atmosphere is used to prevent carbon from being burned out by which oxygen atoms are desorbed from the titanium oxide in the second heat treatment step.
- This heat treatment is held in an inert atmosphere at a temperature in the range of 600 to 950 ° C. for 1 to 20 minutes in order to prevent the carbon source from being burned out.
- the heat treatment temperature is less than 600 ° C. because the generation of lithium titanate is not sufficient, and when the heat treatment temperature exceeds 950 ° C., the lithium titanate aggregates. And since lithium titanate itself decomposes
- heat treatment in a nitrogen atmosphere is particularly preferable under an inert atmosphere, and the titanium oxide particles are doped with nitrogen to increase the conductivity of the metal compound particles.
- the crystallites 2 of the titanium oxide When undergoing a heat treatment step under an inert atmosphere, the crystallites 2 of the titanium oxide preferably include a range of 5 to 100 nm. By using such nano-sized fine particles, the porosity of titanium oxide particles described later can be increased, and the number of fine pores present in the titanium oxide particles 1 can be increased. In order to obtain such a range, the mixing ratio of the titanium oxide material source and the carbon source may be adjusted in advance.
- a preheat treatment in which the composite that has undergone the mixing step is held at a temperature range of 200 to 500 ° C. for 1 to 300 minutes.
- impurities present in the composite can be removed, and a state in which the precursor of titanium oxide is uniformly attached to the carbon source can be obtained. It also has the effect of promoting the formation of a titanium oxide precursor.
- Example 1 of this invention is shown, this invention is not limited to Example 1.
- FIG. 1 the mixing process was first performed. 20 g of carbon nanofibers and 245 g of tetraisopropoxy titanium were added to 1300 g of isopropyl alcohol, and tetraisopropoxy titanium was dissolved in isopropyl alcohol. The weight ratio between the titanium alkoxide and the carbon nanofiber was selected so that the weight ratio between the lithium titanate and the carbon nanofiber after the first heat treatment step was about 8: 2.
- the obtained liquid was introduced into the inner cylinder of the reactor, which was composed of a concentric cylinder of an outer cylinder and an inner cylinder, a through hole was provided on the side surface of the inner cylinder, and a shed plate was arranged at the opening of the outer cylinder.
- the inner cylinder was swung for 300 seconds so that a centrifugal force of 35000 kgms-2 was applied to the liquid, and the carbon nanofibers were highly dispersed in the liquid.
- the reactor contents were collected, the solvent was evaporated in air, and further dried at 100 ° C. for 17 hours.
- the resulting product obtained by drying was subjected to preliminary heat treatment in nitrogen at 400 ° C. for 30 minutes, and then heat treated in nitrogen at 900 ° C. for 3 minutes.
- a final product was obtained by subjecting 100 g of the resulting product obtained by heat treatment in a nitrogen atmosphere to 500 ° C. for 6 hours.
- FIG. 3 is a TEM image obtained by photographing the cross section of the final product, and the magnification is 10,000 times.
- FIG. 4 is an HRTEM image in which the crystallite portion of the final product is focused by a high-resolution transmission electron microscope, and the magnification is 50,000 times.
- FIG. 5 is a STEM image in which the crystallite portion of the final product is focused by a transmission electron microscope.
- FIG. 6 is an HRTEM image in which the crystallite portion of the final product is focused by a high-resolution transmission electron microscope, and the magnification is 100,000 times.
- FIG. 7 is an HRTEM image in which the crystallite portion of the final product is focused by a high-resolution transmission electron microscope, and the magnification is 300,000 times.
- FIG. 8 is an HRTEM image in which the crystallite portion of the final product is focused by a high-resolution transmission electron microscope, and the magnification is 400,000 times.
- the final product has a size of about 1.7 ⁇ m, has a three-dimensional network structure as a whole, and has many space portions 3.
- the final product is a sintered body of a large number of primary particles.
- the primary particle size was most preferably about 40 nm. It can also be seen that a large number of pores 4 are formed between the primary particles.
- FIG. 5 it can be seen that the grain boundaries are hardly visible between the primary particles.
- the primary particles have a flake shape, and the primary particles are bonded to each other on the table surface or the end surface.
- the lattice of the primary particles is clear, and it can be seen that the primary particles are crystallites.
- the edges E1 and E2 on the two sides with respect to the table surface of the crystallite are generally darkened, and it is understood that the crystal is a crystal of a substance having a different edge from the table surface of the crystallite. .
- this final product has a three-dimensional network structure with crystallites connected to each other, and is composed of a material different from the crystal surface and edge.
- FIG. 9 shows a low-magnification restricted field ED diagram of the final product, with a low magnification of 5,000.
- FIG. 10 shows a high-magnification restricted field ED diagram of the final product, with a high magnification of 400,000.
- FIG. 11 is a graph showing the results of the transmission method using Ti K-edge EXAFS.
- Ti K-edge EXAFS determines the local structure around Ti.
- the transmission method there was little difference between the final product and the standard sample. That is, as for the entire crystallite, the Ti—O bond and the Ti—Ti bond are the same in the standard sample and the final product, and the entire crystallite of the final product is composed of Li 4 Ti 5 O 12. I understand that.
- FIG. 12 is a graph showing the result of the conversion electron yield method using Ti K-edge EXAFS.
- the standard sample and the final product were the same, but a change in the Ti—O bond was observed in the crystallites of the final product. That is, it can be seen that the Ti—O bond state changes on the surface of the crystallite of the final product.
- FIG. 13 is an enlarged view of FIG. As shown in FIG. 13, it can be seen that there are five peaks in the distance ( ⁇ ) between Ti and O. Peak A has a Ti-to-O distance of 1.713, Peak B has a Ti-to-O distance of 1.873, Peak C has a Ti-to-O distance of 1.991, and Peak D has a Ti-to-O distance of 2.993. 053, peak E had a distance between Ti and O of 2.317.
- FIG. 14 shows a comparison of the distance between Ti and O of each peak obtained by the conversion electron yield method using Ti K-edge EXAFS and Ti 4 O 7 .
- the spinel type Li 4 Ti 5 O 12 has a structure in which regular octahedrons overlap, the distance between Ti and O is only 1.995.
- Rutile or anatase TiO 2 approximates Li 4 Ti 5 O 12 .
- Ti 4 O 7 has a complicated structure, and the distance between Ti and O has peaks at 1.854, 1.934, 1.993, 2.024, 2.063, and 2.156. It has been known. Comparing the Ti and O distance with results and Ti 4 O 7 peaks A ⁇ E are the final surface of the resultant structure of the crystallites, Ti 4 O 7 and values together very well approximate the number and peak of You can see that
- the final crystallite is composed of Li 4 Ti 5 O 12 as a whole, but the surface of the crystallite is altered to Ti 4 O 7 .
- the final product has a card house structure in which the crystallites 2 of Li 4 Ti 5 O 12 are laminated as a whole, and the crystallites 2 of Li 4 Ti 5 O 12 It was confirmed that the edge surface was the titanium oxide particles 1 that had been altered to Ti 4 O 7 .
- this granule is carbon-free, there is no bond between carbon and lithium associated with heat treatment, and it is considered that there is no oxygen desorption associated with the gasification of carbon and lithium, and the magnetic phase 2a is formed. Not. In addition, since there is no carbon during the manufacturing process, there is no space from which the carbon has been removed.
- FIG. 15 shows a differential pore volume distribution in which the horizontal axis represents the pore diameter and the vertical axis represents the increase in pore volume between measurement points.
- Example 1 has a larger differential pore volume than Conventional Example 1. Since the differential pore volume is large in such a small pore diameter range (100 nm), it can be seen that the electrolyte enters the lithium titanate particles 1 and the area of the lithium titanate particles 1 in contact with the electrolyte is large. .
- the differential pore volume at a pore diameter in the range of 10 to 40 nm has a value of 0.01 cm 3 / g or more, and further a value of 0.02 cm 3 / g or more is obtained.
- the residual amount of carbon is preferably less than 5% by weight, and in particular, Example 1 in which the residual amount of carbon was 1% by weight or less gave good results.
- a slurry is formed by adding 5% by weight of polyvinylidene fluoride and an appropriate amount of N-methylpyrrolidone to the titanium oxide particles 1 of Example 1 and the lithium titanate granule of Conventional Example 1 and sufficiently kneading them. Then, it was coated on an aluminum foil and dried to obtain an electrode. Furthermore, using the obtained electrode, a 1M LiBF 4 propylene carbonate solution was used as an electrolyte, and a laminate-sealed capacitor using an activated carbon electrode as a counter electrode was prepared.
- FIG. 16 is a diagram showing the relationship between the rate and the capacity retention rate for the capacitors of Example 1 and Conventional Example 1 obtained.
- the capacitor of Example 1 can obtain good rate characteristics even at a high rate.
- good rate characteristics are obtained even when the electrode does not contain conductive carbon serving as a conductive additive.
- the capacitor of Conventional Example 1 had a capacity retention rate of less than 10%, whereas the capacitor of Example 1 reached a capacity retention rate of slightly less than 70%.
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Abstract
Description
図1に示すように、本発明に係る新規のチタン酸化物粒子1は、複数の結晶子2が連続的に結合して三次元ネットワーク構造を成し、結晶子2の表面の一部にマグネリ相2aを有する造粒体である。結晶子2は、ランダムに配向して互いに卓面や端面などの表面で結合している。結晶子2が平板形状の場合、三次元ネットワーク構造はカードハウス構造である。チタン酸化物粒子1の内部にはナノサイズの空間部3を多数存在させている。結晶子2の接合界面に粒界を無くし、一方で結晶子2間には微小の細孔4を多数存在させている。
このチタン酸化物粒子1は、チタン酸化物の結晶子2とカーボンの複合体を酸素雰囲気下で熱処理することで得られる。図2に示すように、酸素雰囲気下で複合体を熱処理することによって、複合体からカーボンが焼失し、結晶子2同士が焼結する。更に、酸素雰囲気下で複合体を熱処理することによって、結晶子2の表面がマグネリ相2aへ変質し、以ってチタン酸化物粒子1が生成される。
以下、本発明の実施例1を示すが、本発明は実施例1に限定されるものではない。まず、実施例1として、最初に混合工程を実行した。カーボンナノファイバ20gとテトライソプロポキシチタン245gとをイソプロピルアルコール1300gに添加して、テトライソプロポキシチタンをイソプロピルアルコールに溶解させた。チタンアルコキシドとカーボンナノファイバの重量比は、第1熱処理工程後のチタン酸リチウムとカーボンナノファイバの重量比が約8:2となるように選択した。得られた液を、外筒と内筒の同心円筒からなり、内筒の側面に貫通孔が設けられ、外筒の開口部にせき板が配置されている反応器の内筒内に導入し、35000kgms-2の遠心力が液に印加されるように内筒を300秒間旋回させて、カーボンナノファイバを液に高分散させた。
(従来例1)
従来例1として、水酸化リチウム38g、水800gの水溶液に、ナノサイズ(200nm程度)となるように粉砕した酸化チタン(TiO2)87gを添加して攪拌して溶液を得る。この溶液をスプレードライ装置に導入し噴霧乾燥して乾燥物を得た。得られた乾燥造粒物を大気中で700℃の温度で3時間熱処理を行いチタン酸リチウムの造粒体を得た。この造粒体は、カーボン未使用であるため、熱処理に伴うカーボンとリチウムの結びつきがなく、カーボンとリチウムのそれぞれのガス化に伴う酸素脱離はないものと思われ、マグネリ相2aは形成されていない。また、製造工程中にカーボンが存在しないために、カーボンが除去された空間そのものが存在しない。
実施例1のチタン酸化物粒子1及び従来例1のチタン酸リチウムの細孔分布を測定した。測定方法としては、窒素ガス吸着測定法を用いる。具体的には、粒子表面及び、粒子表面と連通した内部に形成された細孔に窒素ガスを導入し、窒素ガスの吸着量を求める。次いで、導入する窒素ガスの圧力を徐々に増加させ、各平衡圧に対する窒素ガスの吸着量をプロットし、吸着等温曲線を得る。高精度ガス/蒸気吸着量測定装置BELSORP-max-N(日本ベル株式会社製)を用いて測定した。図15は、横軸に細孔径を取り、測定ポイント間の細孔容積の増加分を縦軸に取った差分細孔容積分布を示す。
第2熱処理工程において、実施例1では500℃で6時間の熱処理を施したのに対し、実施例2では収集物100gを350℃で3時間の熱処理を施し、実施例3では収集物100gを300℃で1時間の熱処理を施した。それ以外は、実施例1乃至3は全て同じである。
実施例1のチタン酸化物粒子1及び従来例1のチタン酸リチウムの造粒体に対して5重量%のポリフッ化ビニリデンと適量のN-メチルピロリドンを加えて十分に混練してスラリーを形成し、アルミニウム箔上に塗布し、乾燥して、電極を得た。さらに、得られた電極を用いて、1MのLiBF4のプロピレンカーボネート溶液を電解液とし、対極に活性炭電極を用いたラミネート封止のキャパシタを作成した。
2 結晶子
2a マグネリ相
3 空間部
4 細孔
Claims (21)
- チタン酸化物の結晶子が連なった三次元ネットワーク構造を有し、
前記結晶子の表面にマグネリ相が形成されていること、
を特徴とするチタン酸化物粒子。 - 前記チタン酸化物は、一般式LiαTiβOγで表されるチタン酸リチウムであること、
を特徴とする請求項1記載のチタン酸化物粒子。 - 前記チタン酸化物は、Li4Ti5O12で表されるスピネル型のチタン酸リチウムであること、
を特徴とする請求項2記載のチタン酸化物粒子。 - 前記マグネリ相は、一般式TinO2n-1(3≦n≦10)で表されるチタン酸化物であること、
を特徴とする請求項1乃至3の何れかに記載のチタン酸化物粒子。 - 前記マグネリ相は、Ti4O7であること、
を特徴とする請求項4記載のチタン酸化物粒子。 - 前記結晶子の連なりにより前記マグネリ相を含む電子パスが形成されていること、
を特徴とする請求項1乃至5の何れかに記載のチタン酸化物粒子。 - 前記三次元ネットワーク構造内に複数の空間部を有すること、
を特徴とする請求項1乃至6の何れかに記載のチタン酸化物粒子。 - 前記結晶子間に前記三次元ネットワーク構造内部に繋がる複数の細孔を有すること、
を特徴とする請求項7記載のチタン酸化物粒子。 - 前記細孔から前記空間部に繋がるイオンパスが形成されていること、
を特徴とする請求項8記載のチタン酸化物粒子。 - 前記結晶子は、互いに粒界なく結合していること、
を特徴とする請求項1乃至9の何れかに記載のチタン酸化物粒子。 - 粒子全体に対してカーボンがゼロを含む5重量%未満であること、
を特徴とする請求項1乃至10の何れかに記載のチタン酸化物粒子。 - 前記結晶子は、平板形状を有し、
前記三次元ネットワーク構造はカードハウス構造であること、
を特徴とする請求項1乃至11の何れかに記載のチタン酸化物粒子。 - 前記結晶子の縁表面にマグネリ相が形成されていること、
を特徴とする請求項1乃至12の何れかに記載のチタン酸化物粒子。 - 請求項1乃至13の何れかに記載のチタン酸化物粒子を含み構成されること、
を特徴とする蓄電デバイス用電極。 - 請求項1乃至13の何れかに記載のチタン酸化物粒子を含み構成される電極を備えた蓄電デバイス。
- チタン酸化物の結晶子とカーボンとの複合体を酸素雰囲気下で熱処理することで、前記カーボンを焼失させ、且つ前記チタン酸化物の結晶子同士を連ならせて三次元ネットワーク構造の粒子を形成するとともに、前記結晶子の表面にマグネリ相を形成すること、
を特徴とするチタン酸化物粒子の製造方法。 - 前記熱処理の温度は400~600℃であること、
を特徴とする請求項16記載のチタン酸化物粒子の製造方法。 - 前記熱処理の時間は、0.5以上10時間以下であること、
を特徴とする請求項16又は17記載のチタン酸化物粒子の製造方法。 - 前記複合体は、
前記チタン酸化物源とカーボン源の混合工程と、
前記混合工程を経た混合物を不活性雰囲気下で熱処理する工程と、
により生成されること、
を特徴とする請求項16乃至18の何れかに記載のチタン酸化物粒子の製造方法。 - 前記不活性雰囲気下での熱処理の温度は、600~950℃であること、
を特徴とする請求項19記載のチタン酸化物粒子の製造方法。 - 前記混合工程は、溶液中の前記チタン酸化物源とカーボン源に対するメカノケミカル処理を含むこと、
を特徴とする請求項16乃至20の何れかに記載のチタン酸化物粒子の製造方法。
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005332684A (ja) * | 2004-05-20 | 2005-12-02 | Toshiba Corp | 非水電解質二次電池 |
JP2009043679A (ja) * | 2007-08-10 | 2009-02-26 | Toshiba Corp | 電池用活物質、電池用活物質の製造方法、非水電解質電池および電池パック |
JP2011236061A (ja) * | 2010-05-04 | 2011-11-24 | Nippon Chemicon Corp | チタン酸リチウム結晶構造体、チタン酸リチウム結晶構造体とカーボンの複合体、その製造方法、その複合体を用いた電極及び電気化学素子 |
CN102496704A (zh) * | 2011-12-08 | 2012-06-13 | 中信国安盟固利电源技术有限公司 | 一种钛酸锂/亚氧化钛负极材料及其制备方法 |
WO2014034933A1 (ja) * | 2012-09-03 | 2014-03-06 | 日本ケミコン株式会社 | リチウムイオン二次電池用電極材料、この電極材料の製造方法、及びリチウムイオン二次電池 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5173215A (en) * | 1991-02-21 | 1992-12-22 | Atraverda Limited | Conductive titanium suboxide particulates |
JP3894615B2 (ja) * | 1996-03-18 | 2007-03-22 | 石原産業株式会社 | チタン酸リチウムおよびその製造方法ならびにそれを用いてなるリチウム電池 |
DK1516376T3 (da) | 2002-06-25 | 2009-11-16 | Applied Intellectual Capital L | Zink-luft-batteri med syreelektrolyt |
GB0518139D0 (en) | 2005-09-06 | 2005-10-12 | Univ Cambridge Tech | Synthesis of rutile structure titanium oxide nanostructures |
US8118035B2 (en) * | 2005-12-13 | 2012-02-21 | Philip Morris Usa Inc. | Supports catalyst for the combustion of carbon monoxide formed during smoking |
GB0716441D0 (en) * | 2007-08-23 | 2007-10-03 | Atraverda Ltd | Powders |
CN101465213B (zh) * | 2007-12-17 | 2011-03-16 | 复旦大学 | 复合材料及其制备方法,包括该复合材料的电极材料及电容器 |
WO2009154274A1 (ja) * | 2008-06-20 | 2009-12-23 | 大阪瓦斯株式会社 | 酸化チタン構造体及び多孔質酸化チタン組成物 |
CN101794876B (zh) * | 2010-03-19 | 2012-10-03 | 苏州能斯特新能源有限公司 | 高倍率性能电池负极材料及其制备方法 |
JP5672859B2 (ja) * | 2010-08-26 | 2015-02-18 | 宇部興産株式会社 | 微細な炭素繊維と複合化されたリチウムチタン複合酸化物電極材料 |
JP2012169217A (ja) | 2011-02-16 | 2012-09-06 | Asahi Glass Co Ltd | リチウムイオン二次電池用の正極活物質およびその製造方法 |
US20120251887A1 (en) * | 2011-04-04 | 2012-10-04 | Brookhaven Science Associates, Llc | Carbon-Coated Magneli-Phase TinO2n-1 Nanomaterials and a Method of Synthesis Thereof |
JP5916007B2 (ja) * | 2011-09-28 | 2016-05-11 | 日本ケミコン株式会社 | チタン酸リチウムとカーボンナノファイバーとの複合体の製造方法 |
WO2013062129A1 (ja) * | 2011-10-29 | 2013-05-02 | 日本ケミコン株式会社 | 電極材料の製造方法 |
JP6363550B2 (ja) | 2014-12-16 | 2018-07-25 | 日本ケミコン株式会社 | 金属化合物粒子群の製造方法、金属化合物粒子群及び金属化合物粒子群を含む蓄電デバイス用電極 |
CN107428553B (zh) * | 2015-03-31 | 2020-09-29 | 日本贵弥功株式会社 | 钛氧化物粒子、钛氧化物粒子的制造方法、蓄电元件用电极、及蓄电元件 |
-
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- 2015-05-27 CN CN201580078101.3A patent/CN107428553B/zh active Active
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- 2016-03-31 JP JP2016073302A patent/JP6375331B2/ja active Active
-
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- 2018-07-13 JP JP2018133195A patent/JP6830928B2/ja active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005332684A (ja) * | 2004-05-20 | 2005-12-02 | Toshiba Corp | 非水電解質二次電池 |
JP2009043679A (ja) * | 2007-08-10 | 2009-02-26 | Toshiba Corp | 電池用活物質、電池用活物質の製造方法、非水電解質電池および電池パック |
JP2011236061A (ja) * | 2010-05-04 | 2011-11-24 | Nippon Chemicon Corp | チタン酸リチウム結晶構造体、チタン酸リチウム結晶構造体とカーボンの複合体、その製造方法、その複合体を用いた電極及び電気化学素子 |
CN102496704A (zh) * | 2011-12-08 | 2012-06-13 | 中信国安盟固利电源技术有限公司 | 一种钛酸锂/亚氧化钛负极材料及其制备方法 |
WO2014034933A1 (ja) * | 2012-09-03 | 2014-03-06 | 日本ケミコン株式会社 | リチウムイオン二次電池用電極材料、この電極材料の製造方法、及びリチウムイオン二次電池 |
Non-Patent Citations (1)
Title |
---|
KATSUHIKO NAOI ET AL.: "New hybrid supercapacitors and their prospect", CARBONS, vol. 256, 15 January 2013 (2013-01-15), pages 22 - 32, XP009504532 * |
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KR102394216B1 (ko) | 2022-05-09 |
EP3279143A1 (en) | 2018-02-07 |
US20180072584A1 (en) | 2018-03-15 |
US10490316B2 (en) | 2019-11-26 |
CN107428553A (zh) | 2017-12-01 |
JP2016193816A (ja) | 2016-11-17 |
CN107428553B (zh) | 2020-09-29 |
JP6375331B2 (ja) | 2018-08-15 |
JP6830928B2 (ja) | 2021-02-17 |
KR20170133323A (ko) | 2017-12-05 |
JP2018203615A (ja) | 2018-12-27 |
EP3279143A4 (en) | 2018-10-31 |
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