JP5609300B2 - Active material, electrode including the same, lithium secondary battery including the electrode, and method for producing active material - Google Patents

Description

  The present invention relates to an active material, an electrode including the active material, a lithium secondary battery including the electrode, and an active material manufacturing method.

In the crystal represented by the structural formula LiVOPO ₄ , it is known that lithium ions are reversibly inserted and desorbed. Patent Document _1, using a V 2 _{O 5,} to prepare a LiVOPO ₄ of LiVOPO ₄ and α-type crystal structure of the solid-phase method by β-type crystal structure (orthorhombic) (triclinic), these non The use as an electrode active material of a water electrolyte secondary battery is disclosed. Then, the non-aqueous discharge capacity of electrolyte secondary battery, compared with the LiVOPO ₄ of α-type crystal structure (triclinic), towards the LiVOPO ₄ of β-type crystal structure is large is described.

Non-Patent Document 1 discloses a method for producing LiVOPO ₄ having a β-type crystal structure by heating VOPO ₄ and Li ₂ CO ₃ in the presence of carbon and reducing VOPO ₄ with carbon (a carbothermal reduction method). CTR method)) is disclosed. Non-Patent Document 2 discloses a method for producing LiVOPO ₄ having a β-type crystal structure by using tetravalent vanadium.

JP 2004-303527 A

J. et al. Baker et al. , J .; Electrochem. Soc. 151, A796 (2004) J. et al. Solid State Chem. , 95, 352 (1991)

However, the active material containing LiVOPO ₄ having a β-type crystal structure obtained by the methods described in Patent Document 1 and Non-Patent Documents 1 and 2 cannot obtain a sufficient discharge capacity.

  Then, an object of this invention is to provide the active material which can obtain sufficient discharge capacity, the electrode containing this, a lithium secondary battery provided with the said electrode, and the manufacturing method of an active material.

As a result of intensive studies to achieve the above object, the inventors of the present invention have developed a mixture containing a lithium source, a pentavalent vanadium source, a phosphoric acid source, water, and citric acid under pressure. It has been found that an active material in which the orientation of the LiVOPO ₄ crystal is highly controlled can be produced by heating to a temperature of not lower than 0 ° C., and according to this active material, a sufficient discharge capacity can be obtained.

Here, it is preferable that the method for producing an active material of the present invention further includes a step of heating LiVOPO ₄ having a β-type crystal structure obtained in the hydrothermal synthesis step.

  The mixture is preferably a suspension in which at least a part of the lithium source, the pentavalent vanadium source, and the phosphoric acid source is not dissolved in water. When such a mixture is used, the active material of the present invention can be reliably obtained.

In addition, the present invention contains LiVOPO ₄ having a β-type crystal structure as a main component, and the peak intensity attributed to the (102) plane relative to the peak intensity attributed to the (020) plane obtained by X-ray diffraction measurement. The ratio is 0.6 or more and 1.9 or less, and the ratio of the peak intensity attributed to the (201) plane to the peak intensity attributed to the (020) plane is 1.8 or more and 4.0 or less, Provided is an active material having a polyhedral particle shape.

  According to the active material of the present invention, a sufficient discharge capacity can be obtained. The reason is not clear, but it is presumed that lithium ions easily diffuse because the orientation to the (102) plane is low and the orientation to the (201) plane is high compared to the conventional active material. Is done.

  In the active material of the present invention, the ratio of the peak intensity attributed to the (102) plane to the peak intensity attributed to the (020) plane is 0.6 or more and 1.0 or less, and the (020) plane is The ratio of the peak intensity attributed to the (201) plane to the attributed peak intensity is preferably 1.8 or more and 3.0 or less. The ratio of the peak intensity attributed to the (102) plane to the peak intensity attributed to the (020) plane and the ratio of the peak intensity attributed to the (201) plane to the peak intensity attributed to the (020) plane are When the value is within the above specific range, a particularly large discharge capacity can be obtained.

  The present invention also provides an electrode comprising a current collector and an active material layer including the active material and provided on the current collector. Thereby, an electrode having a sufficient discharge capacity can be obtained.

  Moreover, this invention provides a lithium secondary battery provided with the said electrode. Thereby, a lithium secondary battery having a sufficient discharge capacity can be obtained.

  ADVANTAGE OF THE INVENTION According to this invention, the active material which can obtain sufficient discharge capacity, the electrode containing this, a lithium secondary battery provided with the said electrode, and the manufacturing method of an active material can be provided.

It is an electron micrograph which shows an example of the active material group formed by a plurality of active materials. It is a perspective view which shows typically the active material which concerns on this embodiment. 3 is an X-ray diffraction chart of an active material group according to the present embodiment. It is a schematic cross section of the lithium ion secondary battery according to the present embodiment.

  Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the drawings. In the following description, the same or corresponding parts are denoted by the same reference numerals, and redundant description is omitted. Further, the dimensional ratios in the drawings are not limited to the illustrated ratios.

<Active material>
First, the active material according to the present embodiment will be described. FIG. 1 is an electron micrograph showing an example of an active material group in which a plurality of active materials according to the present embodiment are assembled. FIG. 2 is a perspective view schematically showing one active material 1 constituting the active material group shown in FIG. The particle shape of the active material according to the present embodiment is a prismatic polyhedron that is mainly surrounded by a hexagonal surface and a pentagonal surface.
FIG. 3 is an X-ray diffraction chart of the active material group according to the present embodiment. The active material 1 contains LiVOPO ₄ having a β-type crystal structure as a main component, and the ratio of the peak intensity attributed to the (102) plane to the peak intensity attributed to the (020) plane obtained by X-ray diffraction measurement Active material in which the ratio of the peak intensity attributed to the (201) plane to the peak intensity attributed to the (020) plane is 1.8 to 4.0 It is.

Here, "mainly composed of LiVOPO ₄ of β-type crystal structure", the active material 1, the LiVOPO ₄ of β-type crystal structure, and LiVOPO ₄ of LiVOPO ₄ and α-type crystal structure of the β-type crystal structure It means that 80 mass% or more is included with respect to the sum total. Here, the amount of LiVOPO ₄ having a β-type crystal structure or LiVOPO _{4 having an} α-type crystal structure in the active material can be measured by, for example, an X-ray diffraction method. Usually, LiVOPO ₄ of β-type crystal structure peaks appear in 2 [Theta] = 27.0 degrees, LiVOPO ₄ of α-type crystal structure peaks appear in 2 [Theta] = 27.2 degrees. The active material 1 may contain a small amount of unreacted raw material components in addition to the β-type crystal structure LiVOPO ₄ and the α-type crystal structure LiVOPO ₄ .

  From the viewpoint of obtaining a larger discharge capacity, the active material 1 has a ratio of the peak intensity attributed to the (102) plane to the peak intensity attributed to the (020) plane is 0.6 or more and 1.0 or less. The ratio of the peak intensity attributed to the (201) plane to the peak intensity attributed to the (020) plane is preferably 1.8 or more and 3.0 or less.

The active material 1 is a polyhedron containing LiVOPO ₄ having a β-type crystal structure as a main component, and has lower orientation to the (102) plane and lower orientation to the (201) plane than the conventional active material. Since these ratios are values within the above specific range, a sufficient discharge capacity can be obtained even at a discharge of 0.1 C.

The particle shape of the active material 1 is a columnar polyhedron as shown in FIG. In the active material 1, the surfaces S1 and S2 along the polyhedron axis are presumed to be composed of {110} planes. Here, the {110} plane is a plane including planes represented by (110), (1-10), (−110), and (−1-10).
In the present embodiment, the diameter in the axial direction of the active material 1 that is a columnar polyhedron is expressed by the maximum axial movement distance, that is, the length between parallel tangents in a projection view (so-called Feret diameter). The length is preferably 1 μm to 10 μm. This diameter can be measured from an SEM image, for example. Moreover, it is preferable that the diameter orthogonal to this diameter is 0.3 micrometer-5 micrometers.

<Method for producing active material>
A method for producing an active material according to this embodiment will be described. The manufacturing method of the active material which concerns on this embodiment is equipped with the following hydrothermal synthesis process.
[Hydrothermal synthesis process]
The hydrothermal synthesis step is a step of heating a mixture containing a lithium source, a pentavalent vanadium source, a phosphoric acid source, water, and citric acid to 200 ° C. or higher under pressure.

(blend)
Examples of the lithium source include lithium compounds such as LiNO ₃ , Li ₂ CO ₃ , LiOH, LiCl, Li ₂ SO _4, and CH ₃ COOLi. Among these, LiNO ₃ and Li ₂ CO ₃ are preferable.
Examples of the pentavalent vanadium source include vanadium compounds such as V ₂ O ₅ and NH ₄ VO ₃ .
Examples of the phosphoric acid source include PO ₄ -containing compounds such as H ₃ PO ₄ , NH ₄ H ₂ PO ₄ , (NH ₄ ) ₂ HPO _4, and Li ₃ PO ₄ . Among these, H ₃ PO ₄ and (NH ₄ ) ₂ HPO ₄ are preferable.

  The lithium source is preferably blended so that the ratio of the number of moles of lithium atoms to the number of moles of pentavalent vanadium atoms is 0.95 to 1.2. Moreover, it is preferable to mix | blend a phosphoric acid source so that the ratio of the number of moles of a phosphorus atom with respect to the number of moles of a pentavalent vanadium atom may be 0.95-1.2. When the blending ratio of at least one of lithium atoms and phosphorus atoms is less than 0.95, the discharge capacity of the obtained active material tends to decrease, and the rate characteristics tend to decrease. When the blending ratio of at least one of lithium atoms and phosphorus atoms is more than 1.2, the discharge capacity of the obtained active material tends to decrease.

As for the compounding quantity of a citric acid, it is preferable that the ratio of the number of moles of citric acid is 10-100 mol% with respect to the number of moles of pentavalent vanadium atoms. When citric acid is blended in the above ratio with respect to the number of moles of vanadium atoms, the active material according to the present embodiment can be obtained more reliably. Moreover, it is preferable that a citric acid is 0.1-1.0 mol / L on the basis of the mixture whole quantity.
By the way, when an active material-containing layer of an electrode is produced using the obtained active material, a conductive material such as a carbon material is usually brought into contact with the surface of the active material in order to increase conductivity. As this method, the active material and the conductive material may be mixed after the production of the active material to form the active material-containing layer. For example, the carbon material is used as the conductive material in the mixture as a raw material for hydrothermal synthesis. It can also be added to cause carbon to adhere to the active material.

  Examples of the conductive material in the case where a conductive material that is a carbon material is added to the mixture include activated carbon, graphite, soft carbon, and hard carbon. Among these, it is preferable to use activated carbon that can easily disperse carbon particles in a mixture during hydrothermal synthesis. However, the conductive material is not necessarily mixed in the mixture at the time of hydrothermal synthesis, and it is preferable that at least a part of the conductive material is mixed in the mixture at the time of hydrothermal synthesis. Thereby, the binder at the time of forming an active material content layer can be reduced, and a capacity density can be increased.

  The content of the conductive material such as carbon particles in the mixture in the hydrothermal synthesis step is as follows: the number of moles C of carbon atoms constituting the carbon particles and the number of moles M of vanadium atoms contained in a pentavalent vanadium compound, for example. It is preferable to prepare such that the ratio C / M satisfies 0.04 ≦ C / M ≦ 4. When there is too little content (mole number C) of an electrically conductive material, there exists a tendency for the electronic conductivity and capacity density of the electrode active material comprised with an active material and an electrically conductive material to fall. When there is too much content of a electrically conductive material, the weight of the active material which occupies for an electrode active material will reduce relatively, and there exists a tendency for the capacity density of an electrode active material to reduce. By setting the content of the conductive material within the above range, these tendencies can be suppressed.

  The amount of water in the mixture is not particularly limited as long as hydrothermal synthesis is possible, but the ratio of substances other than water in the mixture is preferably 35% by mass or less.

The order in which the raw materials are charged when adjusting the mixture is not particularly limited. For example, the raw materials of the above mixture may be mixed together, and first, a pentavalent vanadium compound is added to the mixture of water and PO ₄ -containing compound, then citric acid is added, and then A lithium compound may be added. It is preferable that the mixture is sufficiently mixed and the additional components are sufficiently dispersed. At least a part of the lithium compound, the pentavalent vanadium compound, and the PO ₄ -containing compound is not dissolved in water. A suspension is particularly preferred.

In the hydrothermal synthesis step, first, in a reaction vessel (for example, an autoclave) having a function of heating and pressurizing the inside, the above mixture (lithium compound, pentavalent vanadium compound, PO ₄ -containing compound, water, citric acid) Etc.). In addition, you may adjust a mixture within reaction container.

Next, the reaction vessel is sealed, and the mixture is heated to 200 ° C. or higher while being pressurized, thereby causing the hydrothermal reaction of the mixture to proceed. As a result, the hydrothermal synthesis of the substance having the β-type crystal structure of LiVOPO _{4 according} to the present embodiment as a main component and having a polyhedral particle shape is performed.

A substance containing, as a main component, LiVOPO ₄ having a β-type crystal structure obtained by hydrothermal synthesis and having a polyhedral particle shape usually precipitates as a solid in the liquid after hydrothermal synthesis. Then, the liquid after hydrothermal synthesis is filtered, for example, to collect solids, and the collected solids are washed with water, acetone, or the like, and then dried to obtain a high purity of LiVOPO ₄ having a β-type crystal structure. Can get to.

In the hydrothermal synthesis step, the pressure applied to the mixture is preferably 0.1 to 30 MPa. When the pressure applied to the mixture is too low, the crystallinity of the obtained LiVOPO ₄ having a β-type crystal structure is lowered, and the capacity density of the active material tends to be reduced. If the pressure applied to the mixture is too high, the reaction vessel is required to have high pressure resistance, and the active material production cost tends to increase. By setting the pressure applied to the mixture within the above range, these tendencies can be suppressed.

The temperature of the mixture in the hydrothermal synthesis step is preferably 200 to 300 ° C, and more preferably 220 to 280 ° C from the viewpoint of improving the discharge capacity of the obtained active material. When the temperature of the mixture is too low, the crystallinity of the obtained LiVOPO ₄ having a β-type crystal structure is lowered, and the capacity density of the active material tends to be reduced. When the temperature of the mixture is too high, the reaction vessel is required to have high heat resistance, and the production cost of the active material tends to increase. By setting the temperature of the mixture within the above range, these tendencies can be suppressed.

[Baking process]
The method for producing an active material according to the present embodiment further includes a step of heating a material obtained by hydrothermal synthesis, that is, a material containing β-type crystal structure LiVOPO ₄ as a main component and having a polyhedral shape. It may be provided (hereinafter may be referred to as “firing step”). In this step, it is considered that a phenomenon occurs in which impurities remaining in the active material obtained through the hydrothermal synthesis step are removed.

Here, in the firing step, LiVOPO ₄ having the above β-type crystal structure may be heated to 400 ° C. to 600 ° C. If the heating temperature is too high, grain growth of the active material proceeds and the particle size (primary particle size) increases, so that lithium diffusion in the active material is slowed and the capacity density of the active material tends to decrease. On the other hand, if the heating temperature is too low, the firing effect cannot be obtained. By setting the heating temperature within the above range, these tendencies can be suppressed. The heating time is not particularly limited, but is preferably 3 to 8 hours.

  The atmosphere of the firing step is not particularly limited, but is preferably an air atmosphere in order to facilitate the removal of citric acid. On the other hand, it can also be performed in an inert atmosphere such as argon gas or nitrogen gas.

According to the method for producing an active material according to the present embodiment, (102) with respect to the peak intensity attributed to the (020) plane, which is obtained by X-ray diffraction measurement, containing LiVOPO ₄ having a β-type crystal structure as a main component. The ratio of the peak intensity attributed to the plane is 0.6 or more and 1.9 or less, and the ratio of the peak intensity attributed to the (201) plane to the peak intensity attributed to the (020) plane is 1.8. An active material having a particle shape of 4.0 or less and a polyhedron shape can be obtained. And the electrode using such an active material and the lithium secondary battery using the said electrode can obtain big discharge capacity. Such knowledge has not been obtained so far, and such an effect is a remarkable effect as compared with the prior art.

<Electrode and lithium secondary battery using the electrode>
Next, an electrode using the active material according to the present embodiment and a lithium ion secondary battery using the electrode will be described. The electrode which concerns on this embodiment is an electrode provided with a collector and the active material layer provided on the said collector containing the said active material. FIG. 4 is a schematic cross-sectional view of a lithium ion secondary battery 100 according to this embodiment using the electrode.

  The lithium ion secondary battery 100 mainly includes a laminate 30, a case 50 that accommodates the laminate 30 in a sealed state, and a pair of leads 60 and 62 connected to the laminate 30.

  The laminated body 30 is configured such that a pair of the positive electrode 10 and the negative electrode 20 are opposed to each other with the separator 18 interposed therebetween. The positive electrode 10 is obtained by providing a positive electrode active material layer 14 on a plate-like (film-like) positive electrode current collector 12. The negative electrode 20 is obtained by providing a negative electrode active material layer 24 on a plate-like (film-like) negative electrode current collector 22. The positive electrode active material layer 14 and the negative electrode active material layer 24 are in contact with both sides of the separator 18. Leads 60 and 62 are connected to the end portions of the positive electrode current collector 12 and the negative electrode current collector 22, respectively, and the end portions of the leads 60 and 62 extend to the outside of the case 50.

  Hereinafter, the positive electrode 10 and the negative electrode 20 are collectively referred to as electrodes 10 and 20, and the positive electrode current collector 12 and the negative electrode current collector 22 are collectively referred to as current collectors 12 and 22, and the positive electrode active material layer 14 and the negative electrode The active material layers 24 are collectively referred to as active material layers 14 and 24.

First, the electrodes 10 and 20 will be specifically described.
(Positive electrode 10)
The positive electrode current collector 12 may be a conductive plate material, and for example, a thin metal plate of aluminum, copper, or nickel foil can be used.
The positive electrode active material layer 14 includes an active material according to the present embodiment, a binder, and a conductive material in an amount as necessary.

  The binder binds the active materials to each other and binds the active material to the positive electrode current collector 12.

  The binder may be made of any material as long as the above-described bonding is possible. For example, polyvinylidene fluoride (PVDF), polytetrafluoroethylene (PTFE), tetrafluoroethylene-hexafluoropropylene copolymer (FEP), tetrafluoro Ethylene-perfluoroalkyl vinyl ether copolymer (PFA), ethylene-tetrafluoroethylene copolymer (ETFE), polychlorotrifluoroethylene (PCTFE), ethylene-chlorotrifluoroethylene copolymer (ECTFE), polyvinyl fluoride A fluororesin such as (PVF) is used.

  In addition to the above, as the binder, for example, vinylidene fluoride-hexafluoropropylene fluorine rubber (VDF-HFP fluorine rubber), vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene fluorine rubber (VDF-HFP) -TFE fluorine rubber), vinylidene fluoride-pentafluoropropylene fluorine rubber (VDF-PFP fluorine rubber), vinylidene fluoride-pentafluoropropylene-tetrafluoroethylene fluorine rubber (VDF-PFP-TFE fluorine rubber) , Vinylidene fluoride-perfluoromethyl vinyl ether-tetrafluoroethylene fluorine rubber (VDF-PFMVE-TFE fluorine rubber), vinylidene fluoride-chlorotrifluoroethylene fluorine It may be used vinylidene fluoride-based fluorine rubbers such as beam (VDF-CTFE-based fluorine rubber).

  In addition to the above, for example, polyethylene, polypropylene, polyethylene terephthalate, aromatic polyamide, cellulose, styrene / butadiene rubber, isoprene rubber, butadiene rubber, ethylene / propylene rubber and the like may be used as the binder. Also, thermoplastic elastomeric polymers such as styrene / butadiene / styrene block copolymers, hydrogenated products thereof, styrene / ethylene / butadiene / styrene copolymers, styrene / isoprene / styrene block copolymers, and hydrogenated products thereof. May be used. Further, syndiotactic 1,2-polybutadiene, ethylene / vinyl acetate copolymer, propylene / α-olefin (carbon number 2 to 12) copolymer may be used.

  Alternatively, an electron conductive conductive polymer or an ion conductive conductive polymer may be used as the binder. Examples of the electron conductive conductive polymer include polyacetylene. In this case, since the binder exhibits the function of the conductive material, it is not necessary to add the conductive material.

As the ion-conductive conductive polymer, for example, those having ion conductivity such as lithium ion can be used. For example, polymer compounds (polyether-based polymer compounds such as polyethylene oxide and polypropylene oxide) A crosslinked polymer of a polyether compound, polyepichlorohydrin, polyphosphazene, polysiloxane, polyvinylpyrrolidone, polyvinylidene carbonate, polyacrylonitrile, etc.) monomers, and LiClO ₄ , LiBF ₄ , LiPF ₆ , LiAsF ₆ , LiCl, LiBr, Examples include Li (CF ₃ SO ₂ ) ₂ N, LiN (C ₂ F ₅ SO ₂ ) ₂ lithium salt, or a composite of alkali metal salt mainly composed of lithium. Examples of the polymerization initiator used for the combination include a photopolymerization initiator or a thermal polymerization initiator that is compatible with the above-described monomer.

  It is preferable that the content rate of the binder contained in the positive electrode active material layer 14 is 0.5-6 mass% on the basis of the mass of an active material layer. When the binder content is less than 0.5% by mass, the amount of the binder is too small and a tendency to fail to form a strong active material layer increases. Moreover, when the content rate of a binder exceeds 6 mass%, the quantity of the binder which does not contribute to an electric capacity will increase, and the tendency for it to become difficult to obtain sufficient volume energy density becomes large. In this case, particularly, when the electronic conductivity of the binder is low, the electric resistance of the active material layer is increased, and a tendency that a sufficient electric capacity cannot be obtained increases.

  Examples of the conductive material include carbon blacks, carbon materials, metal fine powders such as copper, nickel, stainless steel, and iron, a mixture of carbon materials and metal fine powders, and conductive oxides such as ITO.

(Negative electrode 20)
The negative electrode current collector 22 may be a conductive plate material, and for example, a thin metal plate of aluminum, copper, or nickel foil can be used.
The negative electrode active material is not particularly limited, and a known negative electrode active material for a battery can be used. Examples of the negative electrode active material include graphite, non-graphitizable carbon, graphitizable carbon, and low-temperature calcined carbon that can occlude / release (intercalate / deintercalate, or dope / dedope) lithium ions. Carbon materials, metals that can be combined with lithium such as Al, Si, and Sn, amorphous compounds mainly composed of oxides such as SiO ₂ and SnO ₂ , lithium titanate (Li ₄ Ti ₅ O ₁₂ ), etc. The particle | grains containing are mentioned.
As the binder and the conductive material, the same materials as those for the positive electrode can be used.

Next, a method for manufacturing the electrodes 10 and 20 according to this embodiment will be described.
(Method for manufacturing electrodes 10 and 20)
The manufacturing method of the electrodes 10 and 20 according to the present embodiment includes a step of applying a coating material, which is a raw material of the electrode active material layers 14 and 24, onto the aggregate (hereinafter, also referred to as “application step”), and a collector. And a step of removing the solvent in the paint applied on the electric body (hereinafter, also referred to as “solvent removal step”).

(Coating process)
An application process for applying the paint to the current collectors 12 and 22 will be described. The paint contains the active material, the binder, and the solvent. In addition to these components, the coating material may contain, for example, a conductive material for increasing the conductivity of the active material. As the solvent, for example, N-methyl-2-pyrrolidone, N, N-dimethylformamide and the like can be used.

  The mixing method of the components constituting the paint such as the active material, the binder, the solvent, and the conductive material is not particularly limited, and the mixing order is not particularly limited. For example, first, an active material, a conductive material, and a binder are mixed, and N-methyl-2-pyrrolidone is added to the obtained mixture and mixed to prepare a paint.

  The paint is applied to the current collectors 12 and 22. There is no restriction | limiting in particular as an application | coating method, The method employ | adopted when producing an electrode normally can be used. Examples thereof include a slit die coating method and a doctor blade method.

(Solvent removal step)
Subsequently, the solvent in the paint applied on the current collectors 12 and 22 is removed. The removal method is not particularly limited, and the current collectors 12 and 22 to which the paint is applied may be dried, for example, in an atmosphere of 80 ° C. to 150 ° C.

  Then, the electrodes on which the active material layers 14 and 24 are formed in this way may then be pressed by a roll press device or the like as necessary. The linear pressure of the roll press can be, for example, 10 to 50 kgf / cm.

  The electrode according to this embodiment can be manufactured through the above steps.

  According to the electrode according to this embodiment, since the active material according to this embodiment is used as the positive electrode active material, an electrode having a sufficient discharge capacity can be obtained.

  Here, another component of the lithium ion secondary battery 100 using the electrode manufactured as described above will be described.

The electrolyte is contained in the positive electrode active material layer 14, the negative electrode active material layer 24, and the separator 18. The electrolyte is not particularly limited, and, for example, in the present embodiment, an electrolyte solution containing a lithium salt (electrolyte aqueous solution, electrolyte solution using an organic solvent) can be used. However, the electrolyte aqueous solution is preferably an electrolyte solution (non-aqueous electrolyte solution) using an organic solvent because the electrochemical decomposition voltage is low, and the withstand voltage during charging is limited to a low level. As the electrolyte solution, a lithium salt dissolved in a non-aqueous solvent (organic solvent) is preferably used. Examples of the lithium salt include LiPF ₆ , LiClO ₄ , LiBF ₄ , LiAsF ₆ , LiCF ₃ SO ₃ , LiCF ₃ CF ₂ SO ₃ , LiC (CF ₃ SO ₂ ) ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiN Salts such as (CF ₃ CF ₂ SO ₂ ) ₂ , LiN (CF ₃ SO ₂ ) (C ₄ F ₉ SO ₂ ), LiN (CF ₃ CF ₂ CO) ₂ , LiBOB can be used. In addition, these salts may be used individually by 1 type, and may use 2 or more types together.

  Moreover, as an organic solvent, propylene carbonate, ethylene carbonate, diethyl carbonate, etc. are mentioned preferably, for example. These may be used alone or in combination of two or more at any ratio.

  In the present embodiment, the electrolyte may be a gel electrolyte obtained by adding a gelling agent in addition to liquid. Further, instead of the electrolyte solution, a solid electrolyte (a solid polymer electrolyte or an electrolyte made of an ion conductive inorganic material) may be contained.

  The separator 18 is an electrically insulating porous body, for example, a single layer of a film made of polyethylene, polypropylene or polyolefin, a stretched film of a laminate or a mixture of the above resins, or a group consisting of cellulose, polyester and polypropylene. Examples thereof include a nonwoven fabric made of at least one selected constituent material.

  The case 50 seals the laminate 30 and the electrolyte solution therein. The case 50 is not particularly limited as long as it can prevent leakage of the electrolytic solution to the outside and entry of moisture and the like into the electrochemical device 100 from the outside. For example, as the case 50, as shown in FIG. 4, a metal laminate film in which a metal foil 52 is coated with a polymer film 54 from both sides can be used. For example, an aluminum foil can be used as the metal foil 52 and a film such as polypropylene can be used as the polymer film 54. For example, the material of the outer polymer film 54 is preferably a polymer having a high melting point such as polyethylene terephthalate (PET) or polyamide, and the material of the inner polymer film 54 is polyethylene (PE) or polypropylene (PP). preferable.

  The leads 60 and 62 are made of a conductive material such as aluminum.

  Then, the leads 60 and 62 are welded to the positive electrode current collector 12 and the negative electrode current collector 22 by a known method, respectively, and a separator is provided between the positive electrode active material layer 14 of the positive electrode 10 and the negative electrode active material layer 24 of the negative electrode 20. 18 may be inserted into the case 50 together with the electrolytic solution with the 18 interposed therebetween, and the entrance of the case 50 may be sealed.

  As described above, the preferred embodiment of the active material of the present invention, the electrode using the same, the lithium ion secondary battery including the electrode, and the manufacturing method thereof has been described in detail. It is not limited.

  For example, the electrode using the active material of the present invention can be used for an electrochemical element other than a lithium ion secondary battery. Electrochemical elements include secondary batteries other than lithium ion secondary batteries such as metal lithium secondary batteries (those using the active material of the present invention as the cathode and metal lithium as the anode), and electric batteries such as lithium capacitors. Examples include chemical capacitors. These electrochemical elements can be used for power sources such as self-propelled micromachines and IC cards, and distributed power sources arranged on or in a printed circuit board.

  EXAMPLES Hereinafter, although this invention is demonstrated more concretely based on an Example and a comparative example, this invention is not limited to a following example.

Example 1
[Hydrothermal synthesis process]
A 500 ml Meyer flask was charged with 23.06 g (0.20 mol) of H ₃ PO ₄ (Nacalai Tesque, purity 85%) and 180 g of distilled water (Nacalai Tesque, HPLC). Stir with a stirrer. Subsequently, 18.37 g (0.10 mol) of V ₂ O ₅ (manufactured by Nacalai Tesque, 99% purity) was added and stirred for about 2.5 hours to obtain a yellow-orange suspension. After increasing the number of rotations of stirring, 10.56 g (0.05 mol) of citric acid monohydrate was added to the mixture while stirring was continued. When citric acid was added and stirring was continued for about 60 minutes, a fluid pasty substance was obtained.
After adding 8.48 g (0.20 mol) of LiOH.H ₂ O (manufactured by Nacalai Tesque, purity 99%) and 20 g of distilled water in this order to the obtained paste-like substance, the substance 258 in the flask was added. .70 g was transferred into a 0.5 L autoclave glass cylinder. The raw material mixture before hydrothermal synthesis was a suspension. The container was sealed and held at 250 ° C. for 12 hours to perform hydrothermal synthesis.

After the heater was turned off, the container was allowed to cool until the temperature in the container reached 23 ° C. to obtain a brown solution containing a brown precipitate. The pH of this substance was measured and found to be 3. After removing the supernatant, about 300 ml of distilled water was added, and the precipitate in the container was washed while stirring. Thereafter, suction filtration was performed (washing with water). After repeating this operation twice, about 800 ml of acetone was added, and the precipitate was washed in the same manner as the above water washing. The material after filtration was passed through a sieve (pore diameter constituting the mesh: 52 μm). This material was transferred to a petri dish and dried in air to give 30.83 g of a brown solid. The yield was 91.9% in terms of LiVOPO ₄ .

[Baking process]
1. 3.0 g of the substance after washing with acetone is put in an alumina crucible, heated from room temperature to 450 ° C. over 45 minutes in an air atmosphere, and heat treated at 450 ° C. for 4 hours. 97 g of powder was obtained.

[Confirmation of crystal structure]
X-ray diffraction measurement was performed on the active material of Example 1. Among the plurality of peaks, relatively high peaks are obtained at 2θ = 26.966 °, 27.582 °, and 28.309 °, and the active material is mainly composed of LiVOPO ₄ having a β-type crystal structure. It was confirmed that

[Calculation of peak intensity ratio of active material (I _{(102) / (020)} and I _{(201) / (020)} ) by X-ray diffraction measurement]
The peak at 2θ = 26.966 ° was assigned to (201), the peak at 2θ = 27.582 ° was assigned to (102), and the peak at 2θ = 28.309 ° was assigned to (020). The peak intensity ratio (I _{(102) / (020)} ) between the peak at 2θ = 27.582 ° and the peak at 2θ = 28.309 °, the peak at 2θ = 26.966 °, and 2θ = 28.309 Table 1 shows the peak intensity ratio (I _{(201) / (020)} ) with the peak at °.

[Observation of active material shape]
The shape of the active material of Example 1 was observed using a scanning electron microscope. An electron micrograph of the active material of Example 1 is shown in FIG. The particle shape of the active material was a columnar polyhedron. The crystal plane along the polyhedron axis was measured by electron diffraction. The crystal plane was assigned to the {110} plane.

[Measurement of discharge capacity]
A mixture of the active material of Example 1, polyvinylidene fluoride (PVDF) as a binder, and acetylene black as a conductive material is dispersed in N-methyl-2-pyrrolidone (NMP) as a solvent. To prepare a slurry. The slurry was prepared so that the weight ratio of the active material, acetylene black, and PVDF was 84: 8: 8 in the slurry. This slurry was applied onto an aluminum foil as a current collector, dried, and then rolled to obtain an electrode (positive electrode) on which an active material layer containing the active material of Example 1 was formed.

Next, the obtained electrode and the Li foil as the counter electrode were laminated with a separator made of a polyethylene microporous film interposed therebetween to obtain a laminate (element body). This laminate was put in an aluminum laminate pack, and 1M LiPF ₆ solution was injected as an electrolyte into the aluminum laminate pack, followed by vacuum sealing to produce an evaluation cell of Example 1.

  Using the evaluation cell of Example 1, the discharge capacity (unit: mAh / unit) when the discharge rate is 0.1 C (current value at which discharge is completed in 10 hours when constant current discharge is performed at 25 ° C.) g) was measured. The results are shown in Table 1.

(Example 2)
After the hydrothermal synthesis step, an active material was prepared in the same manner as in Example 1 except that the firing step was not performed. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Example 2, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 3)
In the hydrothermal synthesis step, an active material was produced in the same manner as in Example 2 except that the hydrothermal synthesis time was 15 hours. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Example 3, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

Example 4
In the hydrothermal synthesis step, an active material was produced in the same manner as in Example 1 except that the hydrothermal synthesis temperature was 220 ° C. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Example 4, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 5)
In the hydrothermal synthesis step, an active material was produced in the same manner as in Example 1 except that the hydrothermal synthesis temperature was 280 ° C. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Example 5, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 6)
An active material was produced in the same manner as in Example 1 except that the firing time was 430 ° C. in the firing step. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Example 6, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 7)
In the firing step, an active material was produced in the same manner as in Example 1 except that the firing time was 7 hours. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Example 7, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

(Comparative Example 1)
In the hydrothermal synthesis step, an active material was prepared in the same manner as in Example 1 except that hydrazine was used as a reducing agent for hydrothermal synthesis. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Comparative Example 1, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

(Comparative Example 2)
In the hydrothermal synthesis step, an active material was prepared in the same manner as in Example 1 except that the hydrothermal synthesis temperature was 190 ° C. In the same manner as in Example 1, X-ray diffraction measurement was performed on the active material, and I _{(102) / (020)} and I _{(201) / (020)} were calculated.
Using the obtained active material, an electrode and an evaluation cell were produced in the same manner as in Example 1. Using the evaluation cell of Comparative Example 2, the discharge capacity (unit: mAh / g) was measured in the same manner as in Example 1. The results are shown in Table 1.

In the hydrothermal synthesis process, in Comparative Example 1 using hydrazine as a reducing agent, the particle shape of the active material is indefinite, the orientation to the (201) plane is low, and the discharge capacity is compared to Examples 1-7. It was low. In Comparative Example 2 in which the hydrothermal synthesis temperature was 190 ° C. in the hydrothermal synthesis process, the particle shape of the active material was indefinite, and the discharge capacity was lower than in Examples 1-7.
In Examples 3 and 4 where I _{(102) / (020)} is larger than 1.0 and I _{(201) / (020)} is larger than 3.0, the discharge capacity is larger than that in Examples 1, 2, and 5. Was inferior. In Example 6 where I _{(201) / (020)} is greater than 3.0, the discharge capacity was also inferior to Examples 1, 2, and 5. In Example 7 where I _{(102) / (020)} is larger than 1.0, the discharge capacity was inferior to Examples 1, 2, and 5.

  DESCRIPTION OF SYMBOLS 1 ... Active material, S1, S2 ... The surface containing the longest edge, L1 ... The longest edge.

Claims (7)

Hydrothermal heat to obtain LiVOPO ₄ having a β-type crystal structure by heating a mixture containing a lithium source, a pentavalent vanadium source, a phosphoric acid source, water, and citric acid to 200 ° C. or higher under pressure. The manufacturing method of the active material for lithium secondary batteries provided with a synthetic | combination process. The method for producing an active material for a lithium secondary battery according to claim 1, further comprising a step of heating LiVOPO ₄ having a β-type crystal structure obtained in the hydrothermal synthesis step.   The lithium secondary battery according to claim 1 or 2, wherein the mixture is a suspension in which at least a part of the lithium source, the pentavalent vanadium source, and the phosphoric acid source is not dissolved in the water. For producing an active material. It contains LiVOPO ₄ having a β-type crystal structure as a main component,
The ratio of the peak intensity attributed to the (102) plane to the peak intensity attributed to the (020) plane obtained by X-ray diffraction measurement is 0.6 or more and 1.9 or less, and on the (020) plane The ratio of the peak intensity attributed to the (201) plane to the attributed peak intensity is 1.8 or more and 4.0 or less,
An active material for a lithium secondary battery having a polyhedron particle shape.   The ratio of the peak intensity attributed to the (102) plane to the peak intensity attributed to the (020) plane is 0.6 or more and 1.0 or less, and the peak intensity attributed to the (020) plane is 5. The active material for a lithium secondary battery according to claim 4, wherein the ratio of the peak intensity attributed to the (201) plane is 1.8 or more and 3.0 or less. An electrode for a lithium secondary battery, comprising: a current collector; and an active material layer including the active material for a lithium secondary battery according to claim 4 or 5 and provided on the current collector. A lithium secondary battery comprising the electrode for a lithium secondary battery according to claim 6 .