JP2018190554A - Negative electrode active material for lithium ion secondary battery, negative electrode for lithium ion secondary battery, and lithium ion secondary battery - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a negative electrode active material for a lithium ion secondary battery having excellent initial charge/discharge efficiency, a negative electrode for a lithium ion secondary battery, and a lithium ion secondary battery. A negative electrode active material for a lithium ion secondary battery has active material particles capable of inserting and extracting lithium ions, and a coating film provided on at least a part of the surface of the active material particles, The coating includes a predetermined lithium-containing titanium oxide. The negative electrode for a lithium ion secondary battery has a negative electrode current collector and a negative electrode active material layer provided on at least one surface of the negative electrode current collector, and the negative electrode active material layer is the lithium ion secondary battery described above. Includes negative electrode active material for secondary batteries. The lithium-ion secondary battery includes a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and an electrolyte, and the negative electrode is the negative electrode for the lithium-ion secondary battery. [Selection diagram] Figure 1

Description

  The present invention relates to a negative electrode active material for a lithium ion secondary battery, a negative electrode for a lithium ion secondary battery, and a lithium ion secondary battery.

  Lithium ion secondary batteries have high energy density, and are therefore widely used as power sources for portable electronic devices such as notebook personal computers, communication devices such as mobile phones, and automobile power sources. This lithium ion secondary battery is generally composed of a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and an electrolyte for enabling ion movement between the positive electrode and the negative electrode. . In recent years, there has been a strong demand for lithium ion secondary batteries with higher energy density from the viewpoints of miniaturization and weight reduction of portable electronic devices and communication devices. Further, there is a strong demand for extending the life of automobile batteries.

By the way, negative electrode active material particles such as metal or metal oxide such as silicon (Si) and silicon oxide (SiO _x ) have a theoretical capacity much higher than the theoretical capacity of 372 mAh / g of graphite which is currently in practical use. As shown, it is the most promising material for increasing the energy density of batteries. However, since silicon and silicon oxide have a large theoretical capacity and large expansion and contraction upon insertion / extraction of lithium ions, fine powdering occurs. Since the active material that has been pulverized and dropped off cannot contribute to the charge / discharge reaction by being isolated, the charge / discharge efficiency is reduced. Furthermore, a sufficient charge / discharge cycle could not be obtained with a decrease in charge / discharge efficiency.

In order to solve such a problem, it has been studied to coat the surface of the negative electrode active material particles with a coating. In Patent Documents 1 and 2, the surface of the negative electrode active material particles is an oxide containing at least one element selected from the group consisting of silicon (Si), titanium (Ti), aluminum (Al) and zirconium (Zr). It has been proposed to coat with ceramics such as nitrides or carbides. Patent Document 3 proposes coating the surface of the negative electrode active material particles with a metal oxide such as TiO ₂ or ZrO ₂ .

JP 2004-335334 A JP 2004-335335 A JP 2007-141666 A

However, according to the study of the present inventor, when the surface of the negative electrode active material particles is coated with the coating described in Patent Documents 1 to 3, the initial charge / discharge efficiency may be lowered.
An object of the present invention is made in view of the above circumstances, and provides a negative electrode active material for a lithium ion secondary battery, a negative electrode for a lithium ion secondary battery, and a lithium ion secondary battery having excellent initial charge / discharge efficiency. It is in.

The present inventor has confirmed that the charge / discharge efficiency of the negative electrode active material particles is improved by coating at least a part of the negative electrode active material particles with a coating containing a specific lithium-containing titanium oxide containing titanium and lithium. I found it.
That is, this invention provides the following means in order to solve the said subject.

(1) A negative electrode active material for a lithium ion secondary battery according to a first aspect includes active material particles capable of occluding and releasing lithium ions, and a coating provided on at least a part of the surface of the active material particles The film contains a lithium-containing titanium oxide represented by the following formula (1).
Ti _{1-x / 4-a / 4-2b / 4-3c / 4-d} Li _x A _a B _b C _c D _d O ₂ (1)
However, in Formula (1), A is one or more monovalent metals selected from the group consisting of K and Na, and B is one or more divalents selected from the group consisting of Mg, Ca and Sr. C is one or more trivalent metals selected from the group consisting of Al, Y, La and Bi, and D is one selected from the group consisting of Zr, Si, Hf, Sn and Ge The above tetravalent metals, x is a number satisfying 0 <x ≦ 0.60, a is a number satisfying 0 ≦ a ≦ 0.27, and b is 0 ≦ b ≦ 0.27. C is a number that satisfies 0 ≦ c ≦ 0.27, and d is a number that satisfies 0 ≦ d ≦ 0.27.

(2) In the negative electrode active material for a lithium ion secondary battery according to the above aspect, the lithium-containing titanium oxide may contain at least one metal of Mg, Ca, Al, Zr, and Na.

(3) In the negative electrode active material for a lithium ion secondary battery according to the above aspect, the a in the formula (1) is a number satisfying 0 <a ≦ 0.27, and the ratio of x to the ratio x / a may be in the range of 0.07 to 60.

(3) The negative electrode active material for a lithium ion secondary battery according to the above aspect is such that b in the formula (1) satisfies 0 <b ≦ 0.27, and the ratio x / b of x / b b may be in the range of 0.07 to 60.

(4) In the negative electrode active material for a lithium ion secondary battery according to the above aspect, the c in the formula (1) is a number satisfying 0 <c ≦ 0.27, and the ratio x / c is x / c may be in the range of 0.07 to 60.

(5) The negative electrode active material for a lithium ion secondary battery according to the above aspect is such that the d in the formula (1) satisfies 0 <d ≦ 0.27, and the ratio of x to the ratio x / d may be in the range of 0.07 to 60.

(6) A negative electrode for a lithium ion secondary battery according to the second aspect includes a negative electrode current collector and a negative electrode active material layer provided on at least one surface of the negative electrode current collector. The negative electrode active material layer includes a negative electrode active material for a lithium ion secondary battery according to the first aspect.

(7) A lithium ion secondary battery according to a third aspect is a lithium ion secondary battery comprising a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and an electrolyte. The negative electrode is a negative electrode for a lithium ion secondary battery according to the second aspect.

  ADVANTAGE OF THE INVENTION According to this invention, the negative electrode active material for lithium ion secondary batteries which is excellent in initial stage charge / discharge efficiency, the negative electrode for lithium ion secondary batteries, and a lithium ion secondary battery can be provided.

It is a cross-sectional schematic diagram of the lithium ion secondary battery concerning this embodiment.

  Hereinafter, the present embodiment will be described in detail with appropriate reference to the drawings. In the drawings used in the following description, in order to make the characteristics of the present invention easier to understand, there are cases where the characteristic parts are enlarged for the sake of convenience, and the dimensional ratios of the respective components are different from actual ones. is there. The materials, dimensions, and the like exemplified in the following description are examples, and the present invention is not limited to them, and can be appropriately modified and implemented without departing from the scope of the invention.

[Lithium ion secondary battery]
FIG. 1 is a schematic cross-sectional view of a lithium ion secondary battery according to this embodiment. A lithium ion secondary battery 100 shown in FIG. 1 mainly includes a laminated body 40, a case 50 that accommodates the laminated body 40 in a sealed state, and a pair of leads 60 and 62 connected to the laminated body 40. Although not shown, the electrolyte is housed in the case 50 together with the laminate 40.

  The stacked body 40 is configured such that the positive electrode 20 and the negative electrode 30 are disposed to face each other with the separator 10 interposed therebetween. The positive electrode 20 is obtained by providing a positive electrode active material layer 24 on a plate-like (film-like) positive electrode current collector 22. The negative electrode 30 is obtained by providing a negative electrode active material layer 34 on a plate-like (film-like) negative electrode current collector 32.

  The positive electrode active material layer 24 and the negative electrode active material layer 34 are in contact with both sides of the separator 10. Leads 62 and 60 are connected to the ends of the positive electrode current collector 22 and the negative electrode current collector 32, respectively, and the ends of the leads 60 and 62 extend to the outside of the case 50. In FIG. 1, the case 50 has one laminated body 40 in the case 50, but a plurality of laminated bodies 40 may be laminated.

"Negative electrode"
The negative electrode 30 includes a negative electrode current collector 32 and a negative electrode active material layer 34 provided on the negative electrode current collector 32.

(Negative electrode current collector)
The negative electrode current collector 32 may be a conductive plate material, and for example, a metal thin plate of aluminum foil, electrolytic copper foil, rolled copper foil, nickel foil, or SUS foil can be used.

(Negative electrode active material layer)
The negative electrode active material layer 34 includes a negative electrode active material and a negative electrode binder, and optionally includes a negative electrode conductive material.

(Negative electrode active material)
The negative electrode active material for a lithium ion secondary battery of the present embodiment has active material particles capable of occluding and releasing lithium ions, and a coating provided on at least a part of the surface of the active material particles. The coating is preferably provided on the entire surface of the active material particles. The presence and composition of the coating can be confirmed by XPS (X-ray photoelectron spectroscopy).

As materials for the negative electrode active material particles, various materials that are used as negative electrode active materials for known lithium ion secondary batteries can be used. Examples of the material of the negative electrode active material include, for example, carbon materials, silicon, silicon-containing compounds such as silicon oxide represented by SiO _x (0 <x <2), metal lithium, metal that forms an alloy with lithium, and Examples thereof include amorphous compounds mainly composed of oxides such as tin dioxide and lithium titanate (Li ₄ Ti ₅ O ₁₂ ). Examples of the carbon material include graphite (natural graphite, artificial graphite), carbon nanotube, non-graphitizable carbon, graphitizable carbon, low-temperature calcined carbon, and the like. Examples of the metal that forms an alloy with metallic lithium include aluminum, silicon, and tin. The negative electrode active material particles preferably have an average particle size in the range of 0.01 μm to 50 μm. More preferably, it exists in the range of 0.1 micrometer or more and 10 micrometers or less.

The coating provided on the surface of the active material particles contains a lithium-containing titanium oxide represented by the following formula (1).
Ti _{1-x / 4-a / 4-2b / 4-3c / 4-d} Li _x A _a B _b C _c D _d O ₂ (1)

  In formula (1), A is one or more monovalent metals selected from the group consisting of K and Na. B is one or more divalent metals selected from the group consisting of Mg, Ca and Sr. C is one or more trivalent metals selected from the group consisting of Al, Y, La and Bi. D is one or more tetravalent metals selected from the group consisting of Zr, Si, Hf, Sn and Ge.

x is a number satisfying 0 <x ≦ 0.60. Accordingly, the coating contains Li as an essential component.
a is a number satisfying 0 ≦ a ≦ 0.27, b is a number satisfying 0 ≦ b ≦ 0.27, c is a number satisfying 0 ≦ c ≦ 0.27, and d is , 0 ≦ d ≦ 0.27.

The reason why the initial charge / discharge efficiency is improved by using the negative electrode active material of the present embodiment having the lithium-containing titanium oxide on the surface thereof for a lithium ion secondary battery is considered as follows.
The lithium-containing titanium oxide has a Ti—O—Ti bond as a skeleton, and a part of Ti is substituted with Li to form a Ti—O—Li bond. Since O and Li in the Ti—O—Li bond have strong ionic bonds, the lithium-containing titanium oxide has higher conductivity than titanium oxide. Thus, since the negative electrode active material of this embodiment has high electroconductivity, initial stage charge / discharge efficiency improves.
In addition, Li in the Ti—O—Li bond of the lithium-containing titanium oxide is easily detached. When Li in the Ti—O—Li bond is desorbed, Li ions easily enter the lithium-containing titanium oxide, and the conductivity of Li ions between the negative electrode active material and the electrolyte is improved. Thus, since the negative electrode active material of this embodiment has high conductivity of Li ions, the initial charge / discharge efficiency is improved.

  If the Li content of the lithium-containing titanium oxide is too low, the above effects may not be easily achieved. On the other hand, when the Li content is excessively large, Li in the Ti—O—Li bond is difficult to desorb and Li ions may not easily enter the lithium-containing titanium oxide. For this reason, in this embodiment, the content of Li is set to a number where x in the formula (1) satisfies 0 <x ≦ 0.64.

  The lithium-containing titanium oxide of the present embodiment can contain a monovalent to tetravalent metal in addition to Li.

  When the lithium-containing titanium oxide contains a monovalent metal such as K or Na, the atomic ratio of lithium to the monovalent metal (lithium / monovalent metal) is preferably in the range of 0.07 to 60. That is, in the lithium-containing titanium oxide, when a in Formula (1) is a number satisfying 0 <a ≦ 0.50, the ratio x / a between x and a is in the range of 0.07 to 60. It is preferable. In this case, the initial charge / discharge efficiency of the negative electrode active material can be improved more reliably.

  When the lithium-containing titanium oxide contains a divalent metal such as Mg, Ca, or Sr, the atomic ratio of lithium to the divalent metal (lithium / divalent metal) may be in the range of 0.07 to 60. preferable. That is, when b in the formula (1) is a number satisfying 0 <b ≦ 0.27, the ratio x / b between x and b is preferably in the range of 0.07 to 60. In this case, the initial charge / discharge efficiency of the negative electrode active material can be improved more reliably.

  When the lithium-containing titanium oxide contains a trivalent metal such as Al, Y, La, Bi, the atomic ratio of lithium to the trivalent metal (lithium / trivalent metal) is in the range of 0.07 to 60. It is preferable. That is, when c in the formula (1) is a number satisfying 0 <c ≦ 0.27, the ratio x / c between x and c is preferably in the range of 0.07 to 60. In this case, the initial charge / discharge efficiency of the negative electrode active material can be improved more reliably.

  When the lithium-containing titanium oxide contains a tetravalent metal such as Zr, Si, Hf, Sn, or Ge, the atomic ratio of lithium to the tetravalent metal (lithium / 4-valent metal) is in the range of 0.07 to 60. It is preferable that it exists in. That is, when d in the formula (1) is a number satisfying 0 <d ≦ 0.27, the ratio x / d of x and d is preferably in the range of 0.07 to 60. In this case, the initial charge / discharge efficiency of the negative electrode active material can be improved more reliably.

  Among the above monovalent to tetravalent metals, at least one metal of Mg, Ca, Al, and Zr may be included. In this case, the initial charge / discharge efficiency of the negative electrode active material can be further reliably improved.

The lithium-containing titanium oxide is preferably a compound represented by the following formulas (2) to (6), for example.
(2) Ti _{1-x / 4} Li _x O ₂ (0 <x ≦ 0.60)
(3) Ti _{1-x / 4-2b / 4} Li _x Mg _b O ₂ (0 <x ≦ 0.60, 0 <b ≦ 0.27, 0.07 ≦ x / b ≦ 60)
(4) Ti _{1-x / 4-2b / 4} Li _x Ca _b O ₂ (0 <x ≦ 0.60, 0 <b ≦ 0.27, 0.07 ≦ x / b ≦ 60)
(5) Ti _{1-x / 4-3c / 4} Li _x Al _c O ₂ (0 <x ≦ 0.60, 0 <c ≦ 0.27, 0.07 ≦ x / c ≦ 60)
(6) Ti _{1-x / 4-d} Li _x Zr _d O ₂ (0 <x ≦ 0.60, 0 <d ≦ 0.27, 0.07 ≦ x / d ≦ 60)

(Negative electrode active material)
The negative electrode active material of this embodiment can be manufactured as follows, for example.
A film forming solution (solution A) is prepared by dissolving titanium alkoxide and monovalent to tetravalent metal alkoxide in a solvent. In addition, an active material particle dispersion (liquid B) is prepared in which a trace amount of moisture and active material particles capable of occluding and releasing lithium ions are dispersed in a solvent. Next, the liquid A is added to the liquid B while stirring the liquid B, and then the alkoxide of titanium and the alkoxide of the added metal are hydrolyzed and condensation-polymerized on the surface of the active material particles to obtain a monovalent to tetravalent valence. A titanium oxide sol film containing metal is formed. The active material particles on which the sol film is formed are collected, washed with pure water or alcohol, then dried under reduced pressure, and the film activated with a titanium oxide film containing a monovalent to tetravalent metal. Get material particles.

  Next, the coated active material particles are immersed in an aqueous hydrochloric acid solution to elute all or part of the monovalent to tetravalent metals (excluding titanium) in the coating as metal ions. The elution amount of metal ions can be adjusted by the concentration of the aqueous hydrochloric acid solution and the immersion time. Thereafter, the coated active material particles are recovered from the hydrochloric acid aqueous solution and sufficiently washed with pure water.

  Next, the coated active material particles are immersed in an aqueous lithium hydroxide solution, and lithium ions are inserted into defect sites generated by elution of metal ions. The aqueous lithium hydroxide solution preferably has a pH in the range of 9 to 14. The coated active material particles into which lithium ions are inserted are collected from the lithium hydroxide aqueous solution, washed with pure water or alcohol, and then dried under reduced pressure.

(Negative electrode conductive material)
Examples of the conductive material include carbon powder such as carbon black, carbon nanotube, carbon material, fine metal powder such as copper, nickel, stainless steel and iron, a mixture of carbon material and fine metal powder, and conductive oxide such as ITO. It is done. Among these, carbon powders such as acetylene black and ethylene black are particularly preferable. In the case where sufficient conductivity can be ensured with only the negative electrode active material 36, the lithium ion secondary battery 100 may not include a conductive material.

(Negative electrode binder)
The binder bonds the active materials to each other and bonds the active material to the negative electrode current collector 32. The binder is not particularly limited as long as the above-described bonding is possible. For example, polyvinylidene fluoride (PVDF), polytetrafluoroethylene (PTFE), tetrafluoroethylene-hexafluoropropylene copolymer (FEP), tetrafluoroethylene- Perfluoroalkyl vinyl ether copolymer (PFA), ethylene-tetrafluoroethylene copolymer (ETFE), polychlorotrifluoroethylene (PCTFE), ethylene-chlorotrifluoroethylene copolymer (ECTFE), polyvinyl fluoride (PVF) ) And the like.

  In addition to the above, as the binder, for example, vinylidene fluoride-hexafluoropropylene-based fluororubber (VDF-HFP-based fluororubber), vinylidene fluoride-hexafluoropropylene-tetrafluoroethylene-based fluororubber (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 fluoro rubber (VDF-PFMVE-TFE fluoro rubber), vinylidene fluoride-chlorotrifluoroethylene fluoro rubber The containing rubbers (VDF-CTFE-based fluorine rubber) vinylidene fluoride-based fluorine rubbers such as 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 also functions as a conductive material, it is not necessary to add a conductive material. Examples of the ion conductive conductive polymer include monomers of polymer compounds (polyether polymer compounds such as polyethylene oxide and polypropylene oxide, polyphosphazenes, etc.), LiClO ₄ , LiBF ₄ , LiPF _{6, and the} like. Examples include a composite of a lithium salt or an 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.

  In addition, as the binder, for example, cellulose, styrene / butadiene rubber, ethylene / propylene rubber, polyimide resin, polyamide resin, polyamideimide resin, polyacrylic resin, or the like may be used.

  The contents of the negative electrode active material 36, the conductive material, and the binder in the negative electrode active material layer 34 are not particularly limited. The constituent ratio of the negative electrode active material 36 in the negative electrode active material layer 34 is preferably 65% or more and 98% or less by mass ratio. The constituent ratio of the conductive material in the negative electrode active material layer 34 is preferably 0% or more and 20% or less by mass ratio, and the constituent ratio of the binder in the negative electrode active material layer 34 is 2.0% or more and 35% by mass ratio. % Or less is preferable.

  By making content of a negative electrode active material and a binder into the said range, it can prevent that the quantity of a binder is too small and it becomes impossible to form a strong negative electrode active material layer. In addition, the amount of the binder that does not contribute to the electric capacity increases, and the tendency that it is difficult to obtain a sufficient volume energy density can be suppressed.

"Positive electrode"
The positive electrode 20 includes a positive electrode current collector 22 and a positive electrode active material layer 24 provided on the positive electrode current collector 22.

(Positive electrode current collector)
The positive 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.

(Positive electrode active material layer)
The positive electrode active material used for the positive electrode active material layer 24 includes lithium ion occlusion and release, lithium ion desorption and insertion (intercalation), or counter ions (for example, PF ⁶⁻ ) of lithium ions and lithium ions. An electrode active material capable of reversibly proceeding doping and dedoping can be used.

For example, lithium cobalt oxide (LiCoO _2), lithium nickelate (LiNiO _2), lithium manganate (LiMnO _2), lithium manganese spinel (LiMn ₂ O _4), and the general _{formula: LiNi x Co y Mn z M} a O ₂ (x + y + z + a = 1, 0 ≦ x <1, 0 ≦ y <1, 0 ≦ z <1, 0 ≦ a <1, M is one type selected from Al, Mg, Nb, Ti, Cu, Zn, Cr Complex metal oxides represented by the above elements), lithium vanadium compounds (LiV ₂ O ₅ ), olivine-type LiMPO ₄ (where M is Co, Ni, Mn, Fe, Mg, Nb, Ti, Al, Zr) One or more elements or VO selected from the above, lithium titanate (Li ₄ Ti ₅ O ₁₂ ), LiNi _x Co _y Al _z O ₂ (0.9 <x + y + z < 1.1) and the like, and polyacetylene, polyaniline, polypyrrole, polythiophene, polyacene and the like.

(Conductive material)
Examples of the conductive material include carbon powder such as carbon black, carbon nanotube, carbon material, fine metal powder such as copper, nickel, stainless steel and iron, a mixture of carbon material and fine metal powder, and conductive oxide such as ITO. . In the case where sufficient conductivity can be ensured only by the positive electrode active material, the lithium ion secondary battery 100 may not include a conductive material.

(Positive electrode binder)
The binder used for the positive electrode can be the same as that for the negative electrode.

  The constituent ratio of the positive electrode active material in the positive electrode active material layer 24 is preferably 80% or more and 96% or less by mass ratio. The constituent ratio of the conductive material in the positive electrode active material layer 24 is preferably 2.0% or more and 10% or less by mass ratio, and the constituent ratio of the binder in the positive electrode active material layer 24 is 2.0% by mass ratio. It is preferable that it is 10% or less.

"Separator"
The separator 10 only needs to be formed of an electrically insulating porous structure, 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 cellulose, polyester, and Examples thereof include a fiber nonwoven fabric made of at least one constituent material selected from the group consisting of polypropylene.

"Electrolytes"
The electrolyte is contained in the positive electrode active material layer 24, the negative electrode active material layer 34, and the separator 10. The electrolyte is not particularly limited, and for example, in the present embodiment, an electrolytic 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, so that the withstand voltage during charging is limited to a low level. As the electrolytic solution, a lithium salt dissolved in a non-aqueous solvent (organic solvent) is preferably used. It does not specifically limit as lithium salt, The lithium salt used as an electrolyte of a lithium ion secondary battery can be used. For example, LiPF ₆ , LiClO ₄ , LiBF ₄ , LiCF ₃ SO ₃ , LiCF ₃ CF ₂ SO ₃ , LiC (CF ₃ SO ₂ ) ₃ , LiN (CF ₃ SO ₂ ) ₂ , LiN (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 , lithium salts such as LiBOB can be used. In addition, these lithium salts may be used individually by 1 type, and may use 2 or more types together. In particular, LiPF ₆ is preferably included from the viewpoint of the degree of ionization.

Examples of the organic solvent include aprotic high dielectric constant solvents such as ethylene carbonate, propylene carbonate, and fluoroethylene carbonate; aprotic acids such as dimethyl carbonate and ethyl methyl carbonate; and aprotic esters such as propionic acid esters. Low viscosity solvent. It is desirable to use these aprotic high dielectric constant solvents and aprotic low viscosity solvents in combination at an appropriate mixing ratio. Furthermore, ionic liquids using imidazolium, ammonium, and pyridinium type cations can be used. The counter anion is not particularly limited, and examples thereof include BF ₄ ⁻ , PF ₆ ⁻ , (CF ₃ SO ₂ ) ₂ N ^{− and the} like. The ionic liquid can be used by mixing with the organic solvent described above.
The concentration of the lithium salt in the electrolytic solution is preferably 0.5 to 2.0 M from the viewpoint of electrical conductivity. The conductivity of the electrolyte at 25 ° C. is preferably 0.01 S / m or more, and is adjusted by the type of electrolyte salt or its concentration.

When the electrolyte is a solid electrolyte or gel electrolyte, poly (vinylidene fluoride) or the like can be contained as a polymer material.
Furthermore, you may add various additives in the electrolyte solution of this embodiment as needed. Examples of additives include vinylene carbonate and methyl vinylene carbonate for the purpose of improving cycle life, biphenyl and alkyl biphenyl for the purpose of preventing overcharge, various carbonate compounds for the purpose of deoxidation and dehydration, Carboxylic anhydride, various nitrogen-containing and sulfur-containing compounds can be mentioned.

"Case"
The case 50 seals the laminated body 40 and the electrolytic solution therein. The case 50 is not particularly limited as long as it can suppress leakage of the electrolytic solution to the outside and entry of moisture and the like into the lithium ion secondary battery 100 from the outside.

  For example, as the case 50, as shown in FIG. 1, 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). Etc. are preferred.

"Lead"
The leads 60 and 62 are made of a conductive material such as aluminum. Then, the leads 60 and 62 are respectively welded to the positive electrode current collector 22 and the negative electrode current collector 32 by a known method, and a separator is provided between the positive electrode active material layer 24 of the positive electrode 20 and the negative electrode active material layer 34 of the negative electrode 30. 10 is inserted into the case 50 together with the electrolyte, and the entrance of the case 50 is sealed.

[Method for producing lithium ion secondary battery]
Next, a method for manufacturing the lithium ion secondary battery 100 will be specifically described.

  First, a negative electrode active material, a binder, and a solvent are mixed to prepare a paint. A conductive material may be further added as necessary. As the solvent, for example, water, N-methyl-2-pyrrolidone or the like can be used. The constituent ratio of the negative electrode active material, the conductive material, and the binder is preferably 65 wt% to 98 wt%: 0 wt% to 20 wt%: 2.0 wt% to 35 wt% in mass ratio. These mass ratios are adjusted so as to be 100 wt% as a whole.

  The mixing method of these components constituting the paint is not particularly limited, and the mixing order is not particularly limited. The paint is applied to the negative electrode current collector 32. 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. Similarly, the positive electrode paint is applied on the positive electrode current collector 22 for the positive electrode.

  Subsequently, the solvent in the paint applied on the positive electrode current collector 22 and the negative electrode current collector 32 is removed. The removal method is not particularly limited. For example, the positive electrode current collector 22 and the negative electrode current collector 32 to which the paint is applied may be dried in an atmosphere of 80 ° C. to 150 ° C.

  Then, the electrode on which the positive electrode active material layer 24 and the negative electrode active material layer 34 are formed in this way is subjected to a press treatment by a roll press device or the like as necessary.

  Next, the positive electrode 20 having the positive electrode active material layer 24, the negative electrode 30 having the negative electrode active material layer 34, the separator 10 interposed between the positive electrode and the negative electrode, and the electrolytic solution are sealed in a case 50.

  For example, the positive electrode 20, the negative electrode 30, and the separator 10 are stacked, and the positive electrode 20 and the negative electrode 30 are heated and pressed with a press tool from a direction perpendicular to the stacking direction, and the positive electrode 20, the separator 10, and the negative electrode 30. Adhere. For example, the laminated body 40 is put into a bag-like case 50 prepared in advance.

  Finally, the lithium ion secondary battery is manufactured by injecting the electrolytic solution into the case 50. Instead of injecting the electrolytic solution into the case, the laminate 40 may be impregnated with the electrolytic solution.

  As described above, the negative electrode active material according to the present embodiment is conductive because at least a part of the negative electrode active material particles is coated with a film containing a specific lithium-containing titanium oxide containing titanium and lithium. It is thought that the conductivity of Li ions increases. For this reason, the lithium ion secondary battery 100 using the negative electrode 30 including the negative electrode active material according to the present embodiment is excellent in the initial charge / discharge efficiency.

  Although the embodiments of the present invention have been described in detail with reference to the drawings, the configurations and combinations of the embodiments in the embodiments are examples, and the addition and omission of configurations are within the scope not departing from the gist of the present invention. , Substitutions, and other changes are possible.

[Example 1]
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 0.015 g of magnesium ethoxide [Mg (OC ₂ H ₅ ) ₂ ] was added, followed by stirring with a magnetic stirrer. After magnesium ethoxide is dissolved, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] are added and stirred for 1 hour to mix magnesium ethoxide and titanium (IV) tetrabutoxide. A solution was prepared. This solution was designated as solution A.
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 100 g of Si powder (average particle size 1 μm) was added and stirred for 1 hour. Next, 7 mL of 28% strength aqueous ammonia was added and stirred for 5 minutes to prepare a dispersion of Si powder. This dispersion was designated as B liquid.

  Next, while stirring the liquid B, the liquid A is added to the liquid B, and then the stirring is continued for another hour to hydrolyze and polycondensate magnesium ethoxide and titanium (IV) tetrabutoxide with water in the ammonia water. Thus, a titanium oxide sol film containing magnesium was formed on the surface of the Si powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was recovered, washed with pure water and ethanol, and then dried in a vacuum drying oven at 150 ° C., with a film having a titanium oxide film containing magnesium. Si powder was obtained.

  Next, the obtained coated Si powder was put into 100 mL of a 0.1 mol / L hydrochloric acid aqueous solution and immersed for 15 minutes to elute all the magnesium in the coating as magnesium ions. Thereafter, the Si powder was recovered by filtration and washed with pure water for 5 minutes. Next, the washed coated Si powder was put into 100 mL of a lithium hydroxide aqueous solution having a pH adjusted to 10 and having a concentration of 0.04 mol / L, immersed for 15 minutes, and lithium ions were dissolved at the defect sites generated by elution of magnesium ions. Ions were inserted. Thereafter, the coated Si powder was recovered by filtration. The recovered coated Si powder was washed with pure water for 2 minutes and then dried in a vacuum drying oven at 150 ° C., and this was used as the negative electrode active material of Example 1. The work so far was performed in a dry room.

[Comparative Example 1]
The Si powder (average particle size 1 μm) used in Example 1 was used as the negative electrode active material of Comparative Example 1.

[Comparative Example 2]
30 mL of acetonitrile is added to 100 mL of 2-ethoxyethanol, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] are added, and the mixture is stirred for 1 hour, and titanium (IV) tetrabutoxide is added. A solution was prepared. This solution was designated as solution A.
A Si powder dispersion was prepared in the same manner as in Example 1, and this dispersion was designated as Liquid B.
Next, while the liquid B is being stirred, the liquid A is added to the liquid B, and then the stirring is continued for another hour to hydrolyze and polycondense titanium (IV) tetrabutoxide with water in the ammonia water. A titanium oxide sol film was formed on the surface of the powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was collected, washed with pure water and ethanol, and then dried in a vacuum drying oven at 150 ° C. to obtain a coated Si powder having a titanium oxide film. The negative electrode active material of Comparative Example 2 was prepared.

[Examples 2 to 8, Comparative Example 3]
By changing the amount of magnesium ethoxide input, the coated Si powder having a titanium oxide film containing magnesium obtained in Example 1 was obtained to obtain a coated Si powder having a different magnesium content. A coated Si powder was prepared in the same manner as in Example 1 except that it was immersed in an aqueous hydrochloric acid solution and an aqueous lithium hydroxide solution, and used as negative electrode active materials in Examples 2 to 8 and Comparative Example 3.

[Evaluation]
About the negative electrode active material obtained in Examples 1-8 and Comparative Examples 1-3, the composition of the film and the charge / discharge characteristics were measured. The results are shown in Table 1 below. However, the composition of the film of the negative electrode active material of Comparative Example 1 was not measured.
The composition of the coating film was measured by the following method. For the charge / discharge characteristics, a negative electrode was produced using a negative electrode active material by the following method, and the charge / discharge characteristics of a half cell produced using this negative electrode were measured.

(1) Composition of coating The content of Ti, Li, Mg and O in the coating was measured using XPS, and the content (atomic%) relative to the total amount of each element was calculated. And the composition formula of the film formed in the surface of Si powder was calculated | required from content (atom%) of each obtained element.

(2) Production of negative electrode A negative electrode active material and acetylene black (AB) as a conductive additive were mixed to obtain a mixed powder. Further, a polyamideimide resin [manufactured by Hitachi Chemical Co., Ltd., HPC-1000] as a binder was dissolved in N-methylpyrrolidone (NMP) to prepare a binder solution. A mixed powder of the negative electrode active material and AB, and a binder solution were mixed to prepare a slurry. The compounding ratio of the negative electrode active material, AB, and binder (solid content) was 80: 5: 15 by mass ratio. The prepared slurry was applied to the surface of a rolled copper foil (current collector) having a thickness of 10 μm using a doctor blade, and a negative electrode active material layer was formed on the rolled copper foil. Then, it dried at 110 degreeC for 1 hour and volatilized and removed NMP from the negative electrode active material layer. After drying, the current collector and the negative electrode active material layer were firmly and closely joined with a roll press. This was heated and cured at 300 ° C. for 1 hour to obtain an electrode having an active material layer thickness of about 10 μm.

(3) Production of half cell A lithium ion secondary battery (half cell) was produced using the negative electrode produced in (2) above as an evaluation electrode. The counter electrode was a metal lithium foil. Thereafter, a separator (material: polypropylene) was sandwiched between the evaluation electrode and the counter electrode to obtain a laminate. This laminated body was accommodated in the battery case. In addition, a non-aqueous electrolyte in which LiPF ₆ was dissolved at a concentration of 1 M was injected into the battery case in a mixed solvent in which fluoroethylene carbonate and dimethyl carbonate were mixed at a volume ratio of 4: 6. The battery case was sealed to obtain a half cell.

(4) Charge / Discharge Evaluation of Negative Electrode Active Material The half cell produced in (3) above was subjected to a charge / discharge test [TOSCAT-3000, manufactured by Toyo System Co., Ltd.] to evaluate the initial charge / discharge capacity. First, under a temperature environment of 25 ° C., the battery was charged with a constant current of 0.05 C to a final charge voltage of 0.01 V on the basis of metallic Li, and then discharged with a constant current of 0.05 C to a final discharge voltage of 2.0 V. The operation to be performed was defined as one cycle, and this cycle was performed twice.
Then, charge / discharge evaluation was performed at a constant current of 0.2C. In the charge / discharge test, after charging at a constant current of 0.2 C to a charge end voltage of 0.01 V, an operation of discharging at a constant current of 0.2 C to a discharge end voltage of 2.0 V was defined as one cycle. Table 1 shows the charge capacity, discharge capacity, and initial efficiency (= discharge capacity / charge capacity × 100) in the first cycle. “Charge” is the direction in which the active material of the evaluation electrode occludes Li, and “discharge” is the direction in which the active material of the evaluation electrode releases Li. Further, the charge capacity and the discharge capacity are the capacity per unit mass of the negative electrode active material, respectively.

  As is apparent from Table 1, Examples 1 to 8 using Si powder coated with lithium titanium oxide containing Li within the scope of the present invention as the negative electrode active material were obtained by using Si powder without a coating as the negative electrode active material. As compared with Comparative Example 1 used as Comparative Example 2 and Comparative Example 2 using Si powder coated with titanium oxide as a negative electrode active material, the initial charge / discharge efficiency was improved and the discharge capacity per unit mass was improved. On the other hand, Comparative Example 3 using Si powder coated with lithium titanium oxide containing more Li ions than the range of the present invention as the negative electrode active material was compared with Examples 1-8 in the initial stage. The charge / discharge efficiency, the charge capacity per unit mass, and the discharge capacity decreased.

[Example 9]
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 0.5 g of magnesium ethoxide [Mg (OC ₂ H ₅ ) ₂ ] was added, followed by stirring with a magnetic stirrer. After magnesium ethoxide is dissolved, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] are added and stirred for 1 hour to mix magnesium ethoxide and titanium (IV) tetrabutoxide. A solution was prepared. This solution was designated as solution A.
A Si powder dispersion was prepared in the same manner as in Example 1, and this dispersion was designated as Liquid B.

  Next, while stirring the liquid B, the liquid A is added to the liquid B, and then the stirring is continued for another hour to hydrolyze and polycondensate magnesium ethoxide and titanium (IV) tetrabutoxide with water in the ammonia water. Thus, a titanium oxide sol film containing magnesium was formed on the surface of the Si powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was recovered, washed with pure water and ethanol, and then dried in a vacuum drying oven at 30 ° C., with a film having a titanium oxide film containing magnesium. Si powder was obtained.

  Next, the obtained coated Si powder was put in 100 mL of a hydrochloric acid aqueous solution having a concentration of 0.01 mol / L and immersed for 15 minutes to elute a part of magnesium in the coating as magnesium ions. Thereafter, the Si powder was recovered by filtration and washed with pure water for 5 minutes. Next, the washed coated Si powder was put into 100 mL of a lithium hydroxide aqueous solution having a pH adjusted to 10 and having a concentration of 0.04 mol / L, immersed for 15 minutes, and lithium ions were dissolved at the defect sites generated by elution of magnesium ions. Ions were inserted. Thereafter, the coated Si powder was recovered by filtration. The recovered coated Si powder was washed with pure water for 2 minutes and then dried in a vacuum drying oven at 150 ° C., and this was used as the negative electrode active material of Example 9. The work so far was performed in a dry room.

[Examples 10 to 16]
Coating was carried out in the same manner as in Example 9 except that the immersion time in an aqueous hydrochloric acid solution having a concentration of 0.01 mol / L was changed so that the Li / Mg molar ratio was adjusted to the value shown in Table 2 below. Attached Si powder was prepared and used as the negative electrode active material of Example 10.
[Evaluation]
About the negative electrode active material obtained in Examples 9-16, the composition and charging / discharging characteristic of the film were measured by the above method. The results are shown in Table 2 below.

  As is apparent from Table 2, Examples 9 to 16 using Si powder coated with lithium titanium oxide containing lithium and magnesium within the scope of the present invention as the negative electrode active material have improved initial charge / discharge efficiency. It was confirmed that the discharge capacity per unit mass was improved.

[Example 17]
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 1.15 g of aluminum sec-butoxide [Al (OCHCH ₃ CH ₂ CH ₃ ) ₃ ] was added, followed by stirring with a magnetic stirrer. After aluminum sec-butoxide is dissolved, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] are added and stirred for 1 hour, and then aluminum sec-butoxide and titanium (IV) tetrabutoxide are added. A mixed solution was prepared. This solution was designated as solution A.
A Si powder dispersion was prepared in the same manner as in Example 1, and this dispersion was designated as Liquid B.

  Next, while stirring the B liquid, the A liquid is added to the B liquid, and then the stirring is continued for another hour to hydrolyze and shrink aluminum sec-butoxide and titanium (IV) tetrabutoxide with water in the ammonia water. Polymerization was performed to form a titanium oxide sol film containing aluminum on the surface of the Si powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was recovered, washed with pure water and ethanol, and then dried in a vacuum drying oven at 30 ° C., with a film having a titanium oxide film containing aluminum. Si powder was obtained.

  Next, the obtained coated Si powder was put in 100 mL of a hydrochloric acid aqueous solution having a concentration of 0.01 mol / L and immersed for 15 minutes to elute a part of aluminum in the coating as aluminum ions. Thereafter, the coated Si powder was collected by filtration and washed with pure water for 5 minutes. Next, the washed coated Si powder is put into 100 mL of a lithium hydroxide aqueous solution having a pH adjusted to 10 and having a concentration of 0.04 mol / L, immersed for 15 minutes, and lithium ions are dissolved into the defect sites generated by elution of aluminum ions. Ions were inserted. Thereafter, the coated Si powder was recovered by filtration. The recovered coated Si powder was washed with pure water for 2 minutes and then dried in a vacuum drying oven at 150 ° C., and this was used as the negative electrode active material of Example 17. The work so far was performed in a dry room.

[Examples 18 to 24]
Coating was carried out in the same manner as in Example 17 except that the immersion time in an aqueous hydrochloric acid solution having a concentration of 0.01 mol / L was changed so that the Li / Al molar ratio was adjusted to the value shown in Table 3 below. Attached Si powder was prepared and used as negative electrode active materials of Examples 18 to 24.
[Evaluation]
About the negative electrode active material obtained in Examples 17-24, the composition and charge / discharge characteristic of the film were measured by the above method. The results are shown in Table 3 below.

  As is apparent from Table 3, Examples 17 to 24 using Si powder coated with lithium titanium oxide containing lithium and aluminum within the scope of the present invention as the negative electrode active material have improved initial charge / discharge efficiency. It was confirmed that the discharge capacity per unit mass was improved.

[Example 25]
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 0.44 g of calcium methoxide [Ca (OCH ₃ ) ₂ ] was added, followed by stirring with a magnetic stirrer. After calcium methoxide is dissolved, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] is added and stirred for 1 hour to mix calcium methoxide and titanium (IV) tetrabutoxide. A solution was prepared. This solution was designated as solution A.
A Si powder dispersion was prepared in the same manner as in Example 1, and this dispersion was designated as Liquid B.

  Next, while stirring the B liquid, the A liquid is added to the B liquid, and then the stirring is continued for another hour to hydrolyze and polycondensate calcium methoxide and titanium (IV) tetrabutoxide with water in the ammonia water. Thus, a titanium oxide sol film containing calcium was formed on the surface of the Si powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was collected, washed with pure water and ethanol, and then dried in a vacuum drying oven at 30 ° C., with a film having a titanium oxide film containing calcium. Si powder was obtained.

  Next, the obtained coated Si powder was put into 100 mL of an aqueous hydrochloric acid solution having a concentration of 0.01 mol / L and immersed for 15 minutes to elute a part of calcium in the coating as calcium ions. Thereafter, the coated Si powder was collected by filtration and washed with pure water for 5 minutes. Next, the cleaned Si powder is put into 100 mL of a lithium hydroxide aqueous solution having a pH adjusted to 10 and having a concentration of 0.04 mol / L, immersed for 15 minutes, and calcium ions are eluted to generate lithium ions at the defect sites. Inserted. Thereafter, the coated Si powder was recovered by filtration. The recovered coated Si powder was washed with pure water for 2 minutes and then dried in a vacuum drying oven at 150 ° C., and this was used as the negative electrode active material of Example 25. The work so far was performed in a dry room.

[Examples 26 to 32]
Coating was carried out in the same manner as in Example 25 except that the immersion time in an aqueous hydrochloric acid solution having a concentration of 0.01 mol / L was changed so that the Li / Ca molar ratio was adjusted to the value described in Table 4 below. Attached Si powder was prepared and used as negative electrode active materials of Examples 26 to 32.
[Evaluation]
About the negative electrode active material obtained in Examples 25-32, the composition of the film and the charge / discharge characteristics were measured by the above method. The results are shown in Table 4 below.

  As is apparent from Table 4, Examples 25 to 32 using Si powder coated with lithium titanium oxide containing lithium and calcium within the scope of the present invention as the negative electrode active material have improved initial charge / discharge efficiency. It was confirmed that the discharge capacity per unit mass was improved.

[Example 33]
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 1.98 g of zirconium (IV) tetrabutoxide [Zr (C ₄ H ₉ O) ₄ ] was added, followed by stirring with a magnetic stirrer. After the dissolution of zirconium (IV) tetrabutoxide, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] are added, and the mixture is stirred for 1 hour, and zirconium (IV) tetrabutoxide and titanium ( IV) A mixed solution of tetrabutoxide was prepared. This solution was designated as solution A.
A Si powder dispersion was prepared in the same manner as in Example 1, and this dispersion was designated as Liquid B.

  Next, while stirring the B liquid, the A liquid is added to the B liquid, and then the stirring is further continued for 1 hour to hydrolyze zirconium (IV) tetrabutoxide and titanium (IV) tetrabutoxide with water in the ammonia water. Then, a polycondensation was performed to form a titanium oxide sol film containing zirconium on the surface of the Si powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was collected, washed with pure water and ethanol, and then dried in a vacuum drying oven at 30 ° C., with a film having a titanium oxide film containing zirconium. Si powder was obtained.

  Next, the obtained coated Si powder was put into 100 mL of a 0.01 mol / L hydrochloric acid aqueous solution and immersed for 15 minutes to elute a part of zirconium in the coating as zirconium ions. Thereafter, the coated Si powder was collected by filtration and washed with pure water for 5 minutes. Next, the washed coated Si powder was put into 100 mL of a lithium hydroxide aqueous solution having a pH adjusted to 10 and having a concentration of 0.04 mol / L, immersed for 15 minutes, and lithium ions were dissolved into the defect sites generated by elution of zirconium ions. Ions were inserted. Thereafter, the coated Si powder was recovered by filtration. The recovered coated Si powder was washed with pure water for 2 minutes and then dried in a vacuum drying oven at 150 ° C., and this was used as the negative electrode active material of Example 33. The work so far was performed in a dry room.

[Examples 34 to 40]
Coating was carried out in the same manner as in Example 33 except that the immersion time in an aqueous hydrochloric acid solution having a concentration of 0.01 mol / L was changed so that the Li / Zr molar ratio was adjusted to the value shown in Table 5 below. Attached Si powder was prepared and used as the negative electrode active material of Examples 31-36.
[Evaluation]
About the negative electrode active material obtained in Examples 34-40, the composition and charge / discharge characteristic of the film were measured by the above method. The results are shown in Table 5 below.

  As is apparent from Table 5, Examples 33 to 40 using Si powder coated with lithium titanium oxide containing lithium and zirconium within the scope of the present invention as the negative electrode active material have improved initial charge / discharge efficiency. It was confirmed that the discharge capacity per unit mass was improved.

[Example 41]
30 mL of acetonitrile was added to 100 mL of 2-ethoxyethanol, and then 0.27 g of sodium ethoxide (NaOC ₂ H ₅ ) was added, followed by stirring with a magnetic stirrer. After sodium ethoxide is dissolved, 5.0 g of titanium (IV) tetrabutoxide and monomer [Ti (OC ₄ H ₉ ) ₄ ] are added and stirred for 1 hour to mix sodium ethoxide and titanium (IV) tetrabutoxide. A solution was prepared. This solution was designated as solution A.
A Si powder dispersion was prepared in the same manner as in Example 1, and this dispersion was designated as Liquid B.

  Next, while stirring the B liquid, the A liquid is added to the B liquid, and then the stirring is continued for another hour to hydrolyze and polycondensate sodium ethoxide and titanium (IV) tetrabutoxide with water in the ammonia water. Thus, a titanium oxide sol film containing sodium was formed on the surface of the Si powder. After stirring, the mixture was allowed to stand at 25 ° C. for 30 minutes. Next, the Si powder on which the sol film was formed by filtration was collected, washed with pure water and ethanol, and then dried in a vacuum drying oven at 30 ° C., with a film having a titanium oxide film containing sodium. Si powder was obtained.

  Next, the obtained coated Si powder was put into 100 mL of a hydrochloric acid aqueous solution having a concentration of 0.01 mol / L and immersed for 15 minutes to elute a part of sodium in the coating as sodium ions. Thereafter, the coated Si powder was collected by filtration and washed with pure water for 5 minutes. Next, the washed coated Si powder was put into 100 mL of a lithium hydroxide aqueous solution with a pH adjusted to 10 and having a concentration of 0.04 mol / L, immersed for 15 minutes, and lithium ions were dissolved into the generated defect sites. Ions were inserted. Thereafter, the coated Si powder was recovered by filtration. The recovered coated Si powder was washed with pure water for 2 minutes and then dried in a vacuum drying oven at 150 ° C., and this was used as the negative electrode active material of Example 41. The work so far was performed in a dry room.

[Examples 42 to 48]
Coating was carried out in the same manner as in Example 33 except that the immersion time in an aqueous hydrochloric acid solution having a concentration of 0.01 mol / L was changed so that the Li / Zr molar ratio was adjusted to the value shown in Table 6 below. Attached Si powder was produced and used as negative electrode active materials of Examples 42 to 48.
[Evaluation]
About the negative electrode active material obtained in Examples 41-48, the composition of the film and the charge / discharge characteristics were measured by the above method. The results are shown in Table 6 below.

  As is clear from Table 6, Examples 41 to 48 using Si powder coated with lithium titanium oxide containing lithium and sodium within the scope of the present invention as the negative electrode active material have improved initial charge / discharge efficiency. It was confirmed that the discharge capacity per unit mass was improved.

  DESCRIPTION OF SYMBOLS 10 ... Separator, 20 ... Positive electrode, 22 ... Positive electrode collector, 24 ... Positive electrode active material layer, 30 ... Negative electrode, 32 ... Negative electrode collector, 34 ... Negative electrode active material layer, 40 ... Laminate, 50 ... Case, 52 ... Metal foil, 54 ... Polymer film, 60, 62 ... Lead, 100 ... Lithium ion secondary battery

Claims (8)

Active material particles capable of occluding and releasing lithium ions, and a coating provided on at least a part of the surface of the active material particles,
The negative electrode active material for a lithium ion secondary battery, wherein the coating film includes a lithium-containing titanium oxide represented by the following formula (1):
Ti _{1-x / 4-a / 4-2b / 4-3c / 4-d} Li _x A _a B _b C _c D _d O ₂ (1)
However, in Formula (1), A is one or more monovalent metals selected from the group consisting of K and Na, and B is one or more divalents selected from the group consisting of Mg, Ca and Sr. C is one or more trivalent metals selected from the group consisting of Al, Y, La and Bi, and D is one selected from the group consisting of Zr, Si, Hf, Sn and Ge The above tetravalent metals, x is a number satisfying 0 <x ≦ 0.60, a is a number satisfying 0 ≦ a ≦ 0.27, and b is 0 ≦ b ≦ 0.27. C is a number that satisfies 0 ≦ c ≦ 0.27, and d is a number that satisfies 0 ≦ d ≦ 0.27.   The negative electrode active material for a lithium ion secondary battery according to claim 1, wherein the lithium-containing titanium oxide contains at least one metal of Mg, Ca, Al, and Zr.   The a in the formula (1) is a number satisfying 0 <a ≦ 0.27, and the ratio x / a between the x and the a is in a range of 0.07 or more and 60 or less. Negative electrode active material for lithium ion secondary battery.   The b in the formula (1) is a number satisfying 0 <b ≦ 0.27, and a ratio x / b between the x and the b is in a range of 0.07 or more and 60 or less. Negative electrode active material for lithium ion secondary battery.   The c in the formula (1) is a number satisfying 0 <c ≦ 0.27, and a ratio x / c between the x and the c is in a range of 0.07 or more and 60 or less. Negative electrode active material for lithium ion secondary battery.   The d in the formula (1) is a number satisfying 0 <d ≦ 0.27, and a ratio x / d between the x and the d is in a range of 0.07 or more and 60 or less. Negative electrode active material for lithium ion secondary battery. A negative electrode having a negative electrode current collector and a negative electrode active material layer provided on at least one surface of the negative electrode current collector,
The negative electrode for lithium ion secondary batteries in which the said negative electrode active material layer contains the negative electrode active material for lithium ion secondary batteries as described in any one of Claims 1-6. A lithium ion secondary battery comprising a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and an electrolyte,
The lithium ion secondary battery whose said negative electrode is a negative electrode for lithium ion secondary batteries of Claim 7.

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