WO2014034494A1 - Alloy particles, electrode, nonaqueous electrolyte secondary battery, and method for producing alloy particles - Google Patents

Alloy particles, electrode, nonaqueous electrolyte secondary battery, and method for producing alloy particles Download PDF

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WO2014034494A1
WO2014034494A1 PCT/JP2013/072301 JP2013072301W WO2014034494A1 WO 2014034494 A1 WO2014034494 A1 WO 2014034494A1 JP 2013072301 W JP2013072301 W JP 2013072301W WO 2014034494 A1 WO2014034494 A1 WO 2014034494A1
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alloy
silicon
mass
example
powder
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PCT/JP2013/072301
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French (fr)
Japanese (ja)
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永田 辰夫
禰宜 教之
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中央電気工業株式会社
新日鐵住金株式会社
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Publication of WO2014034494A1 publication Critical patent/WO2014034494A1/en

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/06Metal silicides
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of or comprising active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/362Composites
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of or comprising active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/38Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/386Silicon or alloys based on silicon
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators

Abstract

The objective of the present invention is to provide a negative electrode material for nonaqueous electrolyte secondary batteries, which has a charge/discharge cycle life equal to or longer than those of conventional negative electrode materials for nonaqueous electrolyte secondary batteries, and which has a charge/discharge capacity larger than those of conventional negative electrode materials for nonaqueous electrolyte secondary batteries. Each alloy particle of the present invention comprises a metal silicide phase and silicon phases. The metal silicide phase is formed of silicon atoms and at least two kinds of metal atoms. The silicon phases are mainly formed of silicon atoms. The silicon phases are dispersed in the metal silicide phase. The silicon phases account for 20% by mass or more of the total mass of each alloy particle. Meanwhile, silicon atoms account for 85% by mass or less of the total mass of each alloy particle.

Description

Alloy particle, electrode, non-aqueous electrolyte secondary battery, and alloy particle manufacturing method

The present invention relates to an alloy particle that can be used as a negative electrode active material for a non-aqueous electrolyte secondary battery. The present invention also relates to a method for producing the alloy particles. The present invention also relates to an electrode formed from the alloy particles. The present invention also relates to a nonaqueous electrolyte secondary battery including the electrode as a negative electrode.

In the past, "from one or more active material phases composed of one or more elements capable of reversibly reacting with lithium (Li), and long-period periodic table IIA group elements, transition elements, IIIB group elements and IVB group elements A negative electrode material for a non-aqueous electrolyte secondary battery that has been subjected to mechanical grinding and has one or more inert phases composed of one or more selected elements has been proposed (see JP-T-2007-502004). ).

Such negative electrode materials for non-aqueous electrolyte secondary batteries are “high charge / discharge capacity”, “excellent in charge / discharge cycle life”, “high charge / discharge efficiency”, “small variation in characteristics”. Therefore, it is attracting attention as a next-generation material.

JP 2004-095469 A

The problem of the present invention is that it has a charge / discharge cycle life equal to or higher than that of a conventional non-aqueous electrolyte secondary battery negative electrode material, and has a charge / discharge capacity higher than that of a conventional non-aqueous electrolyte secondary battery negative electrode material. The object is to provide a large negative electrode material for a non-aqueous electrolyte secondary battery.

The alloy particles according to one aspect of the present invention include a metal silicide phase and a silicon phase. The metal silicide phase is formed from silicon atoms and at least two metal atoms. The silicon phase is mainly formed from silicon atoms. The silicon phase is preferably formed only from silicon atoms. The silicon phase is dispersed in the metal silicide phase. In the alloy particles, the silicon phase accounts for 20% by mass or more with respect to the total amount of the alloy particles. The silicon phase preferably occupies a ratio of 22% by mass or more, more preferably occupies a ratio of 24% by mass or more, more preferably occupies a ratio of 26% by mass or more, based on the total amount of alloy particles. It is more preferable to occupy a ratio of not less than mass%, and it is particularly preferable to occupy a ratio of not less than 30 mass%. A silicon atom accounts for the ratio of 85 mass% or less with respect to the whole quantity. It is preferable that the silicon atom occupies a ratio of 70% by mass or less with respect to the total amount.

In this alloy particle, the silicon phase is dispersed in the metal silicide phase. For this reason, when this alloy particle is used as a negative electrode material for a non-aqueous electrolyte secondary battery, a metal silicide phase that is not substantially reactive with lithium (Li) is formed by occlusion / release of lithium (Li). The silicon phase that expands and contracts can be physically constrained. Therefore, the alloy particles can exhibit a charge / discharge cycle life equal to or higher than that of a conventional negative electrode material for a nonaqueous electrolyte secondary battery.

Further, in this alloy particle, the silicon phase occupies a ratio of 20% by mass or more with respect to the total amount of the alloy particle. For this reason, this alloy particle has a larger charge / discharge capacity than a conventional negative electrode material for a non-aqueous electrolyte secondary battery.

Therefore, the alloy particles have a charge / discharge cycle life equal to or higher than that of the conventional negative electrode material for nonaqueous electrolyte secondary batteries, and are more charged / discharged than the conventional negative electrode material for nonaqueous electrolyte secondary batteries. Large capacity.

It should be noted that metal silicides usually have good conductivity and are less susceptible to oxidation than silicon, so that there are few irreversible reactions caused by surface oxides. For this reason, when this alloy particle is used as a negative electrode material for a non-aqueous electrolyte secondary battery, electrons can be efficiently exchanged at the negative electrode of the non-aqueous electrolyte secondary battery. Can keep good.

When the alloy particles are used as a negative electrode material for a non-aqueous electrolyte secondary battery, the area of the silicon portion (silicon phase) that comes into contact with the electrolytic solution is reduced, so that decomposition of the electrolytic solution by silicon is suppressed.

Furthermore, in the alloy particles, silicon atoms have a chemical composition that occupies a ratio of 85% by mass or less, preferably 70% by mass or less, based on the total amount of the alloy particles. For this reason, this alloy particle is excellent in continuous castability at the time of manufacture.

In the above alloy particles, the silicon phase preferably has an average particle diameter of more than 0 nm and not more than 100 nm. This is because the charge / discharge cycle life is improved as the average particle size of the silicon phase is reduced.

In the above alloy particles, the metal silicide phase preferably has a composition of mainly MSix. Here, M is two or more metal elements, Si is silicon, and x is a value greater than 0 and less than 2.

M is preferably a metal element capable of forming a silicide. Note that M may be a metal element that does not form a silicide alone with silicon, or may be a metal element that forms a silicon compound when added together with other silicon compound-forming elements. Examples of such metal elements include aluminum (Al), iron (Fe), nickel (Ni), titanium (Ti), copper (Cu), cobalt (Co), and chromium (Cr).

Considering suppression of raw material costs, M includes at least one metal element selected from the group consisting of aluminum (Al), iron (Fe), nickel (Ni), titanium (Ti), and copper (Cu). Preferably.

In consideration of improvement in oxidation resistance, M preferably contains at least one metal element selected from the group consisting of cobalt (Co) and chromium (Cr).

In the alloy particles described above, the metal silicide phase preferably contains silicon (Si), nickel (Ni), and titanium (Ti). This is because in the alloy particles having such a composition, the silicon phase is more easily refined than before.

An electrode according to another aspect of the present invention includes the above-described alloy particles as an active material. In addition, it is preferable that this electrode is utilized as a negative electrode of a nonaqueous electrolyte secondary battery.

A nonaqueous electrolyte secondary battery according to another aspect of the present invention includes the above electrode as a negative electrode.

In this non-aqueous electrolyte secondary battery, the capacity retention with respect to the initial cycle time is preferably 85% or more, more preferably 90% or more, and 95% or more at the time of 50 charge / discharge cycles. Is more preferable, and 98% or more is particularly preferable.

The alloy particle manufacturing method according to another aspect of the present invention includes a metal melting step, a rapid solidification step, a pulverization step, and a mechanical grinding step. In the metal melting step, at least silicon (Si) and at least two kinds of metals are melted to prepare a specific alloy molten metal. Note that nickel (Ni) and titanium (Ti) are preferably added to the specific alloy molten metal, and copper (Cu) is more preferably added. In the rapid solidification process, the specific alloy melt is rapidly solidified to produce a specific alloy solidified product. In the pulverization step, the specific alloy solidified product is pulverized to form a specific alloy powder. In the mechanical grinding step, the specific alloy powder is mechanically ground to produce the above-described alloy particles.

If this alloy particle manufacturing method is used, the silicon phase in the alloy particles can be refined as compared with the conventional negative electrode material for non-aqueous electrolyte secondary batteries. For this reason, if this alloy particle manufacturing method is utilized, the negative electrode material (namely, alloy particle) for nonaqueous electrolyte secondary batteries which is excellent in a charge / discharge cycle life can be obtained.

In the above alloy particle production method, silicon (Si) preferably occupies a ratio of 85% by mass or less, and preferably 70% by mass or less in the specific alloy molten metal. This is because continuous casting can be performed satisfactorily in the rapid solidification process, and the production efficiency of alloy particles can be increased.

In the above alloy particle production method, the specific alloy powder has a silicon phase content of 20% by mass or more, the specific gravity is y, and the silicon phase content (% by mass) is x, where y> It is preferable that the relationship of −0.02x + 3.8 is established. In the specific alloy powder, the silicon phase content preferably accounts for 30% by mass or more, more preferably 35% by mass or more, and more preferably 40% by mass or more. Preferably, it occupies a ratio of 45% by mass or more.

In the mechanical grinding process, the specific alloy powder is repeatedly crushed and granulated. And how often the specific alloy powder collides with the ball as the processing medium depends on the volume ratio. Therefore, when the specific alloy powder having the same mass is mechanically ground, the larger the specific gravity, the more efficiently it can be processed. That is, in this alloy particle manufacturing method, alloy particles can be efficiently processed while maintaining a high silicon phase content.

Also, when the volume ratio between the specific alloy powder and the ball is fixed to a certain value, the specific alloy powder having a larger specific gravity is processed in a larger amount in terms of mass. For this reason, if this alloy particle manufacturing method is utilized, the production amount of alloy particles per batch of the mechanical grinding apparatus can be increased.

It is a transmission electron micrograph of the alloy particle which concerns on Example 1 (a black part is a silicon phase). It is a graph which shows the relationship between the silicon phase content and specific gravity of the alloy particle which concerns on an Example and a comparative example.

<Composition of alloy particles>
The alloy particles according to an embodiment of the present invention include a metal silicide phase and a silicon phase. In the alloy particles according to the present embodiment, the silicon phase is dispersed in the metal silicide phase. Moreover, in this alloy particle, a silicon atom occupies the ratio of 85 mass% or less with respect to the whole quantity of an alloy particle. It is preferable that silicon atoms occupy a ratio of 70% by mass or less with respect to the total amount of alloy particles. In this alloy particle, the content of silicon atoms needs to be increased until the silicon phase is dispersed in the metal silicide phase as described above. Hereinafter, the metal silicide phase and the silicon phase will be described in detail.

(1) Metal silicide phase The metal silicide phase is formed from a silicon atom and at least two metal atoms. The metal silicide phase may be an intermetallic compound. In addition, strain (dislocation) is introduced into the metal silicide phase so as not to be completely crystalline. This metal silicide phase is required not to substantially react with lithium (Li), but may be reactive to lithium (Li) as long as the gist of the present invention is not impaired.

This metal silicide phase preferably has a composition of mainly MSix. Here, M is two or more metal elements, Si is silicon, and x is a value greater than 0 and less than 2. M is aluminum (Al), iron (Fe), nickel (Ni), titanium (Ti), copper (Cu), cobalt (Co), chromium (Cr), vanadium (V), manganese (Mn), Zinc (Zn), yttrium (Y), zirconium (Zr), niobium (Nb), molybdenum (Mo), ruthenium (Ru), rhodium (Rh), palladium (Pd), silver (Ag), hafnium (Hf), Two or more metal elements selected from the group consisting of tantalum (Ta), tungsten (W), platinum (Pt), lanthanum (La), cerium (Ce), praseodymium (Pr) and neodymium (Nd) Is preferred. The metal silicide phase preferably contains silicon (Si), nickel (Ni), and titanium (Ti), and more preferably contains copper (Cu).

The metal silicide phase may contain a structure other than MSix such as TiSi 2 , Ni 4 Ti 4 Si 7, and NiSi 2 as long as the gist of the present invention is not impaired. In such a case, the MSix content in the metal silicide phase is preferably 20% by volume or more, and more preferably 30% by volume or more.

(2) Silicon phase The silicon phase is mainly formed from silicon atoms. The silicon phase is preferably formed only from silicon atoms. As described above, this silicon phase is dispersed in the metal silicide phase. In this silicon phase, strain (dislocation) is introduced so as not to be completely crystalline.

This silicon phase occupies a ratio of 20% by mass or more with respect to the total mass of the alloy particles. More preferably, the silicon phase accounts for 30% by mass or more of the total mass of the alloy particles, more preferably 40% by mass or more, and 50% by mass or more of the total mass of the alloy particles. It is further preferable to occupy a ratio of 60% by mass or more with respect to the total mass of the alloy particles. The content of the silicon phase is increased as long as the state in which the silicon phase is dispersed in the metal silicide phase is maintained, that is, as long as the sea-island structure is maintained in which the silicon phase is an island and the metal silicide phase is the sea. be able to.

The average particle size of the silicon phase is preferably more than 0 nm and not more than 100 nm, more preferably more than 0 nm and not more than 90 nm, more preferably more than 0 nm and not more than 80 nm, and still more preferably more than 0 nm and not more than 70 nm. More preferably, more than 0 nm and less than 60 nm, more preferably more than 0 nm and less than 50 nm, further preferably more than 0 nm and less than 40 nm, more preferably more than 0 nm and less than 30 nm, more preferably more than 0 nm and less than 20 nm. More preferably, it is more than 0 nm and not more than 10 nm.

<Method for producing alloy particles>
The alloy particles having the above configuration are manufactured through a metal melting step, a rapid solidification step, a pulverization step, and a mechanical grinding step. Hereinafter, each process is explained in full detail.

(1) Metal melting step In the metal melting step, a plurality of metal raw materials containing silicon (Si) are melted to prepare a specific molten metal. In such a case, silicon (Si) is added to the metal raw material so that the silicon phase is 85 mass% or less with respect to the total mass of the metal raw material, and 20 mass% or more of the silicon phase is precipitated in the rapid solidification process in the subsequent step. Added. In such a case, the amount of silicon added can be easily determined using an equilibrium diagram. The metal raw material preferably contains nickel (Ni) and titanium (Ti) in addition to silicon (Si), and more preferably contains copper (Cu). Note that the metal raw materials are not necessarily melted at the same time, and may be melted in stages.

The metal raw material is usually brought into a molten state by heating. The metal raw material is preferably heated and melted in an inert gas or vacuum atmosphere.

The heating method includes high frequency induction heating, arc discharge heating (arc melting), plasma discharge heating (plasma melting), resistance heating, and the like. In this step, it is important to form a compositionally uniform molten metal.

(2) Rapid solidification step In the rapid solidification step, the specific alloy melt is rapidly solidified to produce a specific alloy solidified product. In this rapid solidification step, the molten specific alloy is preferably rapidly solidified at a cooling rate of 100 K / second or more, and the molten specific alloy is preferably rapidly solidified at a cooling rate of 1,000 K / second or more.

Examples of the rapid solidification method (rapid casting method) include a gas atomizing method, a roll rapid cooling method, a plate casting method, a rotating electrode method, a liquid atomizing method, and a melt spinning method.

In the gas atomization method, the molten metal in the tundish is caused to flow out from the pores at the bottom of the tundish, and a high-pressure inert gas such as argon (Ar), nitrogen (N 2 ), and helium (He) is supplied to the fine stream of the molten metal. This is a method of solidifying in a powder form while spraying and pulverizing the molten metal, and spherical particles are obtained.

The roll rapid cooling method is a method in which a molten metal is dropped on a single roll or a double roll rotating at high speed, or a thin cast slab is obtained by pulling up the molten metal with a roll. In addition, the obtained thin cast slab is pulverized to an appropriate size in a pulverization process which is a subsequent process.

The flat plate casting method is a method of casting a molten metal into a flat plate mold so that the thickness of the ingot is thin, and the cooling rate is faster than that of the block shape ingot. In addition, the obtained flat plate-like ingot is pulverized to an appropriate size in a pulverization step which is a subsequent step.

(3) Pulverization step In the pulverization step, the specific alloy solidified product is pulverized to form a specific alloy powder.
The specific alloy powder satisfies the relationship of y> −0.02x + 3.8 (see FIG. 2), where y is the (bulk) specific gravity and x is the silicon phase content (mass%). preferable. The reason is as described in the section [Means for Solving the Problems].

In addition, this pulverization step is preferably performed in a non-oxidizing atmosphere. This is because, in the pulverization step, when the specific alloy solidified product is pulverized, a new surface is formed and the specific surface area is also increased. Note that an inert gas atmosphere is preferable as the non-oxidizing atmosphere, but there is no particular problem even if oxygen of about 2 to 5% by volume is contained.

(4) Mechanical Grinding Step In the mechanical grinding step, the specific alloy powder is subjected to mechanical grinding (hereinafter referred to as “MG treatment”) to produce the above-described alloy particles. The specific alloy powder subjected to the MG treatment preferably has an average particle size of 5 mm or less, more preferably 1 mm or less, and even more preferably 500 μm or less.

In the MG treatment, a compressive force and a shear force are applied to the powder as the material to be treated, and the powder is repeatedly disintegrated and granulated while being crushed. As a result, the original structure of the powder is collapsed, and particles having a structure in which the phase existing before the processing is ultrafinely dispersed on the nanometer order are formed. However, the type and content of the phase constituting the fine structure are substantially the same as before the treatment, and no new phase is formed by the treatment. Due to the characteristics of this MG treatment, when the alloy particles according to the present invention are used as a negative electrode material for a nonaqueous electrolyte secondary battery, the negative electrode exhibits a stable discharge capacity. This is different from the MA method (mechanical alloying method) in which an alloying reaction between elements occurs and the content of the phase is changed by the treatment. In the process of MG treatment, local mechanical alloying may occur in a very small part of the alloy powder.

On the other hand, since the structure (more specifically, the crystal structure) is not broken by simple pulverization, the particles after pulverization retain the structure before pulverization. That is, in the pulverization, only the particle diameter is reduced, and the structure is not refined. The MG process in which the structure is crushed and broken during processing and the structure becomes finer is different from pulverization in this respect.

MG treatment can be carried out by any pulverizer capable of grinding the material. Among such pulverizers, a pulverizer using a ball-shaped pulverizing medium, that is, a ball mill type pulverizer is preferable. The ball mill type grinder is simple in structure, the balls of the grinding media are easily available in various materials, and grinding / grinding occurs at the contact point between the balls, so it can be uniformly ground in many places. And the like (which is particularly important from the viewpoint of high uniformity of reaction, that is, product stability), and is particularly suitable for use in the present invention. Among ball mill-type pulverizers, not only simply rotating the pulverizing cylinder, but also a vibrating ball mill with increased pulverization energy by applying vibrations, and a rotating rod forcing the balls to be crushed and grinding media An attritor that stirs and a planetary ball mill in which grinding energy is increased by rotational force and centrifugal force are preferred.

MG treatment is preferably performed in an inert gas atmosphere such as argon in order to prevent oxidation of the material being treated. However, as in the rapid solidification process, when the material does not contain an easily oxidizable metal element, the material may be subjected to MG treatment in an air atmosphere. In the present embodiment, the metal particles after MG treatment preferably have an oxygen concentration of 2.5% by mass or less, and more preferably 2.0% by mass or less. When the oxygen concentration of the metal particles after MG treatment exceeds 2.5% by mass, when the metal particles are used as an electrode material for a non-aqueous electrolyte secondary battery, the irreversible capacity increases and the charge / discharge efficiency decreases remarkably. Because.

During the MG treatment, when the alloy temperature rises due to processing heat, the structure size inside the finally obtained alloy particles may be coarsened. For this reason, it is preferable that the pulverizer is provided with a cooling mechanism. In such a case, the MG process is performed while the system is cooled.

MG treatment is stearic acid, zinc stearate, lithium stearate, magnesium stearate, calcium stearate, barium stearate, calcium laurate, barium laurate, zinc laurate, polyvinylpyrrolidone, zinc octylate, calcium ricinoleate, ricinoleic acid Barium, zinc ricinoleate, or the like may be added to the material to be treated. Thereby, adhesion of the to-be-processed material to a container is reduced.

In addition, for one or more types of metal silicide phase and silicon phase, alloy powders are separately prepared by the steps (1) to (3) described above, and the mixed alloy powder mixed so as to satisfy the above relational expression is subjected to MG treatment. It doesn't matter. By producing alloy particles in this way, (i) a raw material alloy can be prepared with a chemical composition having good solubility and castability, and can be produced at a high yield. This is because, in the case of producing a plurality of different alloy powders, it is possible to enjoy the merits of being able to make them by simply changing the mixing ratio of the alloy powders prepared in advance.

<Production of electrode>
The electrode which concerns on embodiment of this invention can be formed from the above-mentioned alloy particle. For example, an electrode binder is prepared by mixing an appropriate binder with alloy particles and mixing an appropriate conductive powder as necessary to improve conductivity. Next, a solvent for dissolving the binder is added to the electrode mixture, and if necessary, the mixture is sufficiently stirred using a homogenizer and glass beads to form a slurry. At this time, a slurry kneader combining a rotation motion and a revolution motion may be used. When this slurry-like electrode mixture is applied to an electrode substrate (current collector) such as rolled copper foil or copper electrodeposited copper foil using a doctor blade or the like, dried, and then consolidated by roll rolling or the like, An electrode for a water electrolyte secondary battery is obtained. This electrode is usually used as a negative electrode.

As the binder, water-insoluble resins such as polyvinylidene fluoride (PVDF), polymethyl methacrylate (PMMA), and polytetrafluoroethylene (PTFE) (however, those that are insoluble in the solvent used for the non-aqueous electrolyte of the battery) ), Water-soluble resins such as carboxymethyl cellulose (CMC) and polyvinyl alcohol (PVA), and aqueous dispersion type binders such as styrene-butadiene rubber (SBR). As a solvent for the binder, an organic solvent such as N-methylpyrrolidone (NMP) or dimethylformamide (DMF) or water can be used depending on the binder.

Examples of the conductive powder include carbon materials (eg, carbon black, graphite) and metals (eg, Ni). Among these, carbon materials are preferable. Since the carbon material can occlude Li ions between the layers, the carbon material can contribute to the capacity of the negative electrode in addition to the conductivity, and also has excellent liquid retention. Among these carbon materials, acetylene black is particularly preferable.

<Preparation of nonaqueous electrolyte secondary battery>
The nonaqueous electrolyte secondary battery according to the embodiment of the present invention is manufactured using the above-described negative electrode. The nonaqueous electrolyte secondary battery is, for example, a lithium ion secondary battery. And the above-mentioned alloy particle and electrode are suitable as a negative electrode material and a negative electrode of a lithium ion secondary battery. However, the alloy particles and electrodes according to the present embodiment can theoretically be applied to other nonaqueous electrolyte secondary batteries.

The nonaqueous electrolyte secondary battery includes a negative electrode, a positive electrode, a separator, and a nonaqueous electrolyte as a basic structure. As the negative electrode, the one manufactured according to the present invention as described above is used. As the positive electrode, the separator and the electrolyte, known materials or materials developed in the future may be appropriately used.

The nonaqueous electrolyte may be liquid, solid, or gel. Examples of the solid electrolyte include polymer electrolytes such as polyethylene oxide, polytetrafluoroethylene, fluorine-containing copolymers, and combinations thereof. Examples of the liquid electrolyte include ethylene carbonate, diethyl carbonate, propylene carbonate, and combinations thereof. The electrolyte is provided with a lithium electrolyte salt. Examples of suitable salts include lithium hexafluorophosphate (LiPF 6 ), lithium borofluoride (LiBF 4 ), and lithium perchlorate (LiClO 4 ). Further, suitable cathode compositions, for example, lithium cobalt oxide (LiCoO 2), lithium manganate (LiMn 2 O 4) and LiCo 0.2 Ni 0.8 O 2 and the like.

Hereinafter, the present invention will be described in more detail with reference to examples.
In addition, this invention is not limited by the Example shown below.

<Manufacture of alloy powder>
First, a pure crucible of nickel, titanium and silicon is melted into a crucible made of aluminum titanate so that the mass ratio of nickel (Ni), titanium (Ti) and silicon (Si) is 25.0: 17.0: 58.0. It was thrown into. Next, after the melting crucible was filled with an argon (Ar) atmosphere, the pure raw material (metal mixture) in the melting crucible was heated to 1500 ° C. by high frequency induction heating to be completely dissolved. Subsequently, the melt was rapidly solidified by bringing it into contact with a copper water-cooled roll rotating at a peripheral speed of 90 m / min to obtain a flaky slab (strip casting (SC) method). It is assumed that the cooling rate at this time is about 500 to 2,000 ° C./second. The cast slab thus obtained was pulverized and classified with a 63 μm sieve to produce a primary powder having an average particle size of 25 to 30 μm. The silicon phase content in the primary powder was calculated by a method based on the ternary equilibrium diagram, and the value was 38% by mass. The specific gravity of the primary powder particles was 4.34 (see Table 1). And substituting 38 for x in the formula: y> −0.02x + 3.8 (where x is the silicon phase content (% by mass) in the primary powder and y is the specific gravity of the primary powder). When 4.34 was substituted for y, it became 4.34> 3.04, and it became clear that the same formula was established for particles of the same primary powder. Further, this primary powder is put into a planetary ball mill (BX384E manufactured by Kurimoto Steel Co., Ltd.), and the primary powder is mechanically ground (hereinafter abbreviated as “MG treatment”) at a rotational speed of 500 rpm. A powder (hereinafter, one alloy powder may be referred to as “alloy particle”) was prepared. The MG treatment is performed in a glove box in a nitrogen atmosphere (less than 1% oxygen) in a primary powder and a ball (material: SUS304, ball diameter: 4 mm, ball ratio, primary powder: graphite (alloy powder fixed to the ball and outer wall). Prevention): Ball (mixed) = 34 g: 6 g: 600 g) is inserted into a pod (material: SUS304, inner diameter: 100 mm, depth: 67 mm, rotation speed: 500 rpm), and then the pod is covered for 10 hours. It was done over. After the MG treatment, the alloy powder was taken out and classified in a glove box in a nitrogen atmosphere (less than 1% oxygen) (63 μm).

The MG workability index value at the time of the MG treatment was 136 (see Table 1). This MG workability index value is obtained on the basis of the volume ratio of the ball to the alloy powder when the specific gravity of the particles of the alloy powder is 3.2. That is, for example, when the ball and the alloy powder are mixed at the volume ratio described above, if the specific gravity of the alloy particles is 1.2 times the specific gravity of the previous alloy particles, the batch processing mass becomes + 20%, and the MG The workability index value is 120%.

<Dimensions of silicon phase in alloy particles>
Using a transmission electron micrograph (bright field image) (see FIG. 1), the diameter of the silicon phase on the order of nm (less than 1 μm) was directly measured.

Moreover, the diameter of the silicon phase on the order of μm (1 μm or more) was directly measured using a scanning electron micrograph of the cross section of the sample piece cut so that the cross section of the alloy particles was exposed. The diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm (see Table 1).

<Negative electrode characteristics of alloy powder and silicon phase content in alloy particles>
(1) Production of negative electrode 5 parts by mass of styrene butadiene rubber (SBR) (binder), 5 parts by mass of carboxymethyl cellulose (CMC) (binder), 15 parts by mass of acetylene black with respect to 75 parts by mass of the above-described alloy powder Powder (conductive powder) was added, and distilled water was further added to the mixture, followed by kneading to prepare a uniform negative electrode mixture slurry.

This negative electrode mixture slurry was thinly applied onto a 30 μm thick electrolytic copper foil using a doctor blade and dried to form a coating film. This coating film was punched out using a punch having a diameter of 13 mm to obtain a negative electrode for a nonaqueous electrolyte secondary battery. The mixture coating amount on the copper foil was in the range of 2 to 3 mg / cm 2 .

(2) Method for evaluating negative electrode performance (2-1) Production of coin-type battery for negative electrode performance evaluation The performance of the negative electrode was evaluated by producing a coin-type battery (2016 type) using Li metal as a counter electrode. Specifically, a separator having a diameter of 19 mm is disposed on the negative electrode, and further, a metal Li punched to a diameter of 15 mm is disposed thereon, and the laminate is placed in the case, and then the outer periphery of the case is dedicated to A coin type battery (2016 type) was manufactured by pressing with a caulking machine. As the electrolyte, 1 of ethylene carbonate and ethyl methyl carbonate: 3 mixed solvent, LiPF 6 of the supporting electrolyte was used a solution obtained by dissolving LiPF 6 as a 1 Mol / L. Moreover, 8 mass% fluoroethylene carbonate was added to this electrolyte solution as an additive.

(2-2) Initial charge capacity, initial discharge capacity, initial efficiency In the above-described coin-type battery, first, constant current doping (lithium ion to the negative electrode) with a current value of 0.15 mA until the potential difference becomes 5 mV with respect to the counter electrode. Then, the doping was continued at a constant voltage until the current value reached 10 μA while maintaining 5 mV. After a 30-minute rest period, this coin-type battery is dedoped (corresponding to the detachment of lithium ions from the electrode and the discharge of the lithium ion secondary battery) with a constant current of 0.15 mA until the potential difference becomes 1.2 V. The initial charge capacity and the initial discharge capacity were determined. In this example, the initial charge capacity and the initial discharge capacity are calculated assuming that the lithium ion occlusion amount of graphite is 0 (zero), that is, calculated using the mass of only alloy particles as the denominator. That is, the initial charge capacity and the initial discharge capacity according to the present embodiment are values obtained by dividing the measured values of the initial charge capacity and the initial discharge capacity by 0.85 (= 34 / (34 + 6)). This coin-type battery had an initial charge capacity of 1051 mAh / g, an initial discharge capacity of 834 mAh / g, and an initial efficiency of 79%.

(2-3) Capacity Maintenance Rate In the above coin-type battery, first, constant current doping (with insertion of lithium ions into the negative electrode, lithium ion secondary, with a current value of 0.15 mA, until the potential difference becomes 5 mV with respect to the counter electrode) Then, doping was continued at a constant voltage until the current value reached 10 μA while maintaining 5 mV. After a 30-minute rest period, de-doping (corresponding to detachment of lithium ions from the electrode and discharging of the lithium ion secondary battery) was performed at a constant current of 0.15 mA until the potential difference became 1.2V.

After the second cycle, doping was performed at a constant current of 0.75 mA until the potential difference became 5 mV with respect to the counter electrode (corresponding to charging), and then the doping was continued at a constant voltage until 10 μA while maintaining 5 mV. Next, dedoping was performed at a constant current of 0.75 mA until the potential difference became 5 mV (corresponding to discharge), and the dedoping capacity was measured. The dedope capacity at this time was defined as the discharge capacity.

Doping and dedoping are repeated 51 times under the same conditions as described above, and the ratio of the “discharge capacity at the detachment at the 51st cycle” to the “discharge capacity at the detachment at the 2nd cycle” is defined as the capacity maintenance ratio (hereinafter referred to as “51C Called capacity retention rate). The ambient temperature was 25 ° C. If this 51C capacity maintenance rate is 85% or more, it can be regarded as a good practical battery. In addition, the 51C capacity maintenance rate of the coin-type battery according to this example was 89.8% (see Table 1).

(3) Silicon phase content in alloy particles The silicon phase content in the alloy particles is expressed as follows: "Discharge capacity at the first cycle of the coin-type battery" as described above "Electrode provided with active material layer using only silicon powder as active material" It was determined by dividing by 100 by dividing by “actual value 3200 mAh / g of discharge capacity in the first cycle of the coin-type battery in which is incorporated”. In addition, the silicon phase content rate in the alloy particle which concerns on a present Example was 26 mass% (refer Table 1).

The pure powder of nickel, titanium, and silicon was put into an aluminum titanate melting crucible so that the mass ratio of nickel, titanium, and silicon was 13.5: 21.5: 65.0, and the primary powder during MG treatment An alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of: graphite was 36 g: 4 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. In addition, as in Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was prepared, and the initial charge capacity, initial discharge capacity, and initial efficiency of the coin-type battery were determined. The silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.68, and the silicon phase content of the particles in the primary powder was 41% by mass. Then, substituting 41 for x in the formula: y> −0.02x + 3.8 and substituting 3.68 for y yields 3.68> 2.98, and this formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 115, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example was 958 mAh / g, the initial discharge capacity was 782 mAh / g, and the initial efficiency was 82%. The silicon phase content in the alloy particles according to this example was 24% by mass. (See Table 1)

The pure powder of nickel, titanium and silicon was put into a melting crucible made of aluminum titanate so that the mass ratio of nickel, titanium and silicon was 14.0: 19.0: 67.0, and the primary powder during MG treatment An alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of: graphite was 36 g: 4 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.66, and the silicon phase content of the particles in the primary powder was 46% by mass. Substituting 46 for x in the formula: y> −0.02x + 3.8 and substituting 3.66 for y yields 3.66> 2.88, and the same formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 115, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example is 979 mAh / g, the initial discharge capacity is 807 mAh / g, the initial efficiency is 82%, and the 51C capacity maintenance rate is 89.9%. It was. The silicon phase content in the alloy particles according to this example was 25% by mass. (See Table 1)

The pure powder of nickel, titanium, and silicon was put into a melting crucible made of aluminum titanate so that the mass ratio of nickel, titanium, and silicon was 12.0: 18.0: 70.0, and the primary powder during MG treatment An alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of: graphite was 36 g: 4 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. In addition, as in Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was prepared, and the initial charge capacity, initial discharge capacity, and initial efficiency of the coin-type battery were determined. The silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.51, and the silicon phase content of the particles in the primary powder was 50% by mass. Substituting 50 for x in the formula: y> −0.02x + 3.8 and substituting 3.51 for y yields 3.51> 2.80, and the same formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 110, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example was 1627 mAh / g, the initial discharge capacity was 1420 mAh / g, and the initial efficiency was 87%. The silicon phase content in the alloy particles according to this example was 44% by mass. (See Table 1)

Pure aluminum, nickel, and silicon raw materials are put into a melting crucible made of aluminum titanate so that the mass ratio of aluminum (Al), nickel (Ni), and silicon (Si) is 26.5: 28.9: 44.6. Except for the above, an alloy powder was prepared in the same manner as in Example 1, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.33, and the silicon phase content of the particles in the primary powder was 40% by mass. Then, when 40 is substituted for x in the formula: y> −0.02x + 3.8 and 4.33 is substituted for y, 4.33> 3.00 is obtained, and the same formula is established for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 135, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example is 1028 mAh / g, the initial discharge capacity is 833 mAh / g, the initial efficiency is 81%, and the 51C capacity maintenance rate is 85.8%. It was. The silicon phase content in the alloy particles according to this example was 26% by mass. (See Table 1)

A pure powder of aluminum, nickel and silicon was put into a melting crucible made of aluminum titanate so that the mass ratio of aluminum, nickel and silicon was 26.5: 28.9: 44.6, and the primary powder during MG treatment : The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of graphite was 36.8 g: 3.2 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. . Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.33, and the silicon phase content of the particles in the primary powder was 40% by mass. Then, when 40 is substituted for x in the formula: y> −0.02x + 3.8 and 4.33 is substituted for y, 4.33> 3.00 is obtained, and the same formula is established for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 135, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 1108 mAh / g, the initial discharge capacity is 960 mAh / g, the initial efficiency is 87%, and the 51C capacity maintenance rate is 85.2%. It was. The silicon phase content in the alloy particles according to this example was 30% by mass. (See Table 1)

Pure aluminum, nickel and silicon raw materials are put into an aluminum titanate melting crucible so that the mass ratio of aluminum (Al), nickel (Ni) and silicon (Si) is 30.1: 32.7: 37.2. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of primary powder: graphite during MG treatment was 36.8 g: 3.2 g. The dimensions of the silicon phase inside were measured. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.59, and the silicon phase content of the particles in the primary powder was 32% by mass. Then, substituting 32 for x in the formula: y> −0.02x + 3.8 and substituting 4.59 for y yields 4.59> 3.16, and the same formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 144, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example is 912 mAh / g, the initial discharge capacity is 772 mAh / g, the initial efficiency is 85%, and the 51C capacity maintenance rate is 89.7%. It was. The silicon phase content in the alloy particles according to this example was 24% by mass. (See Table 1)

Aluminum, nickel, cobalt, and silicon so that the mass ratio of aluminum (Al), nickel (Ni), cobalt (Co), and silicon (Si) is 26.5: 23.9: 5.0: 44.6. An alloy powder was prepared in the same manner as in Example 1 except that the pure raw material was put into a melting crucible made of aluminum titanate and the mass ratio of primary powder: graphite during MG treatment was 36.8 g: 3.2 g. In the same manner as in Example 1, the dimensions of the silicon phase in the alloy particles were measured. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.33, and the silicon phase content of the particles in the primary powder was 38% by mass. Then, substituting 38 for x in the formula: y> −0.02x + 3.8 and substituting 4.33 for y yields 4.33> 3.04, and the same formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 135, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example is 1076 mAh / g, the initial discharge capacity is 930 mAh / g, the initial efficiency is 86%, and the 51C capacity maintenance rate is 88.5%. It was. The silicon phase content in the alloy particles according to this example was 29% by mass. (See Table 1)

Pure aluminum, iron and silicon raw materials are put into an aluminum titanate melting crucible so that the mass ratio of aluminum (Al), iron (Fe) and silicon (Si) is 26.1: 21.6: 52.3. Except for the above, an alloy powder was prepared in the same manner as in Example 1, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.44, and the silicon phase content of the particles in the primary powder was 30% by mass. Substituting 30 for x and y for 3.44 in the formula: y> −0.02x + 3.8, and 3.44> 3.20, the same formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 107, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 946 mAh / g, the initial discharge capacity is 758 mAh / g, the initial efficiency is 80%, and the 51C capacity maintenance rate is 89.4%. It was. The silicon phase content in the alloy particles according to this example was 24% by mass. (See Table 2)

Aluminum, iron, cobalt, and silicon so that the mass ratio of aluminum (Al), iron (Fe), cobalt (Co), and silicon (Si) is 29.8: 12.7: 12.0: 45.5. An alloy powder was prepared in the same manner as in Example 1 except that the pure raw material was put into a melting crucible made of aluminum titanate, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.93, and the silicon phase content of the particles in the primary powder was 25% by mass. Then, substituting 25 for x in the formula: y> −0.02x + 3.8 and substituting 3.93 for y yields 3.93> 3.30, and the same formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 123, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example was 834 mAh / g, the initial discharge capacity was 651 mAh / g, the initial efficiency was 78%, and the 51C capacity maintenance rate was 95.2%. It was. The silicon phase content in the alloy particles according to this example was 20% by mass. (See Table 2)

Aluminum, iron, chromium and silicon so that the mass ratio of aluminum (Al), iron (Fe), chromium (Cr) and silicon element (Si) is 29.8: 14.7: 10.0: 45.5. An alloy powder was prepared in the same manner as in Example 1 except that the pure raw material was put into a melting crucible made of aluminum titanate, and the dimensions of the silicon phase in the alloy particles were measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.74, and the silicon phase content of the particles in the primary powder was 25% by mass. Then, substituting 25 for x in the formula: y> −0.02x + 3.8 and substituting 3.74 for y yields 3.74> 3.30, and the same formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value during the MG treatment according to this example was 117, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 849 mAh / g, the initial discharge capacity is 672 mAh / g, the initial efficiency is 79%, and the 51C capacity maintenance rate is 91.2%. It was. The silicon phase content in the alloy particles was 21% by mass. (See Table 2)

Copper, nickel, titanium, and silicon so that the mass ratio of copper (Cu), nickel (Ni), titanium (Ti), and silicon (Si) is 7.5: 23.8: 18.4: 50.3. An alloy powder was prepared in the same manner as in Example 1, except that the pure raw material was put into a melting crucible made of aluminum titanate, and the mass ratio of primary powder: graphite during MG treatment was 36 g: 4 g. In the same manner as in Example 1, the dimensions of the silicon phase in the alloy particles were measured. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.79, and the silicon phase content of the particles in the primary powder was 30% by mass. Then, when 30 is substituted for x in the formula: y> −0.02x + 3.8 and 4.79 is substituted for y, 4.79> 3.20 is obtained, and this formula is established for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 150, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example is 948 mAh / g, the initial discharge capacity is 780 mAh / g, the initial efficiency is 82%, and the 51C capacity maintenance rate is 93.7%. It was. The silicon phase content in the alloy particles according to this example was 24% by mass. (See Table 2)

Copper, nickel, titanium, and silicon so that the mass ratio of copper (Cu), nickel (Ni), titanium (Ti), and silicon (Si) is 15.0: 21.1: 15.4: 48.5. An alloy powder was prepared in the same manner as in Example 1, except that the pure raw material was put into a melting crucible made of aluminum titanate, and the mass ratio of primary powder: graphite during MG treatment was 36 g: 4 g. In the same manner as in Example 1, the dimensions of the silicon phase in the alloy particles were measured. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 5.04, and the silicon phase content of the particles in the primary powder was 35% by mass. Then, when 35 is substituted for x in the formula: y> −0.02x + 3.8 and 5.04 is substituted for y, 5.04> 3.10 is obtained, and this formula is established for particles of the same primary powder. It became clear to do. Further, the MG workability index value during MG treatment according to this example was 158, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 1109 mAh / g, the initial discharge capacity is 926 mAh / g, the initial efficiency is 83%, and the 51C capacity maintenance rate is 92.6%. It was. The silicon phase content in the alloy particles according to this example was 29% by mass. (See Table 2)

Copper, nickel, titanium, and silicon so that the mass ratio of copper (Cu), nickel (Ni), titanium (Ti), and silicon (Si) is 15.0: 19.2: 13.8: 52.0. An alloy powder was prepared in the same manner as in Example 1, except that the pure raw material was put into a melting crucible made of aluminum titanate, and the mass ratio of primary powder: graphite during MG treatment was 36 g: 4 g. In the same manner as in Example 1, the dimensions of the silicon phase in the alloy particles were measured. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.88, and the silicon phase content of the particles in the primary powder was 38% by mass. Substituting 38 for x in the formula: y> −0.02x + 3.8 and substituting 4.88 for y yields 4.88> 3.04, and this formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 153, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 1266 mAh / g, the initial discharge capacity is 1111 mAh / g, the initial efficiency is 88%, and the 51C capacity maintenance rate is 85.2%. It was. The silicon phase content in the alloy particles according to this example was 35% by mass. (See Table 2)

The mass ratio of copper (Cu), nickel (Ni), titanium (Ti), cobalt (Co), and silicon (Si) is 11.2: 15.6: 15.4: 5.0: 52.8. In Example 1, except that pure raw materials of copper, nickel, titanium, cobalt and silicon were put into a melting crucible made of aluminum titanate, and the primary powder: graphite mass ratio during MG treatment was 36 g: 4 g. Similarly, an alloy powder was prepared, and the dimensions of the silicon phase in the alloy particles were measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.76, and the silicon phase content of the particles in the primary powder was 36% by mass. Substituting 36 for x in the formula: y> −0.02x + 3.8 and substituting 4.76 for y yields 4.76> 3.08, and the same formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value during MG treatment according to this example was 149, and the diameter of the silicon phase in the alloy particles according to this example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this example is 1227 mAh / g, the initial discharge capacity is 1064 mAh / g, the initial efficiency is 87%, and the 51C capacity maintenance rate is 87.2%. It was. The silicon phase content in the alloy particles according to this example was 33% by mass. (See Table 2)

Put pure raw materials of nickel, titanium and silicon into melting crucible made of aluminum titanate so that mass ratio of nickel (Ni), titanium (Ti) and silicon (Si) is 20.9: 17.1: 62.0. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.08, and the silicon phase content of the particles in the primary powder was 44% by mass. Substituting 44 for x in the formula: y> −0.02x + 3.8 and substituting 4.08 for y yields 4.08> 2.92, which holds for the same powder particles. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 127, and the diameter of the silicon phase in the alloy particles according to this example was 10 to 40 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 1573 mAh / g, the initial discharge capacity is 1352 mAh / g, the initial efficiency is 86%, and the 51C capacity maintenance rate is 91.5%. It was. The silicon phase content in the alloy particles according to this example was 42% by mass. (See Table 2)

Put pure raw materials of nickel, titanium and silicon into a melting crucible made of aluminum titanate so that the mass ratio of nickel (Ni), titanium (Ti) and silicon (Si) is 16.8: 13.6: 69.6. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.73, and the silicon phase content of the particles in the primary powder was 56% by mass. Substituting 56 for x in the formula: y> −0.02x + 3.8 and substituting 3.73 for y yields 3.73> 2.68, and the same formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value during the MG treatment according to this example was 117, and the diameter of the silicon phase in the alloy particles according to this example was 10 to 40 nm. The initial charge capacity of the coin-type battery according to this example is 1688 mAh / g, the initial discharge capacity is 1482 mAh / g, the initial efficiency is 88%, and the 51C capacity maintenance rate is 90.1%. It was. The silicon phase content in the alloy particles according to this example was 46% by mass. (See Table 3)

Put pure raw materials of nickel, titanium and silicon into melting crucible made of aluminum titanate so that mass ratio of nickel (Ni), titanium (Ti) and silicon (Si) is 12.6: 10.2: 77.2. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.38, and the silicon phase content of the particles in the primary powder was 67% by mass. Then, when 67 is substituted for x in the formula: y> −0.02x + 3.8 and 3.38 is substituted for y, 3.38> 2.46 is obtained, and this formula is established for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 106, and the diameter of the silicon phase in the alloy particles according to this example was 10 to 40 nm. The initial charge capacity of the coin-type battery according to this example is 2074 mAh / g, the initial discharge capacity is 1824 mAh / g, the initial efficiency is 88%, and the 51C capacity maintenance rate is 88.5%. It was. The silicon phase content in the alloy particles according to this example was 57% by mass. (See Table 3)

Put pure raw materials of nickel, titanium and silicon into melting crucible made of aluminum titanate so that mass ratio of nickel (Ni), titanium (Ti) and silicon (Si) is 8.4: 6.8: 84.8. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.03, and the silicon phase content of the particles in the primary powder was 78% by mass. Substituting 78 for x in the formula: y> −0.02x + 3.8 and substituting 3.03 for y yields 3.03> 2.24, and the same formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 95, and the diameter of the silicon phase in the alloy particles according to this example was 20 to 50 nm. In addition, the initial charge capacity of the coin-type battery according to this example is 2460 mAh / g, the initial discharge capacity is 2045 mAh / g, the initial efficiency is 83%, and the 51C capacity maintenance rate is 83.4%. It was. The silicon phase content in the alloy particles according to this example was 64% by mass. (See Table 3)

Put nickel, iron and silicon pure materials into aluminum aluminum titanate melting crucible so that the mass ratio of nickel (Ni), iron (Fe) and silicon (Si) is 21.3: 8.7: 70.0. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.21, and the silicon phase content of the particles in the primary powder was 56% by mass. Substituting 56 for x in the formula: y> −0.02x + 3.8 and substituting 4.21 for y yields 4.21> 2.68, and the same formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 132, and the diameter of the silicon phase in the alloy particles according to this example was 10 to 40 nm. The initial charge capacity of the coin-type battery according to this example is 1750 mAh / g, the initial discharge capacity is 1540 mAh / g, the initial efficiency is 88%, and the 51C capacity maintenance rate is 89.3%. It was. The silicon phase content in the alloy particles according to this example was 48% by mass. (See Table 3)

Put pure raw materials of nickel, chromium and silicon into melting crucible made of aluminum titanate so that mass ratio of nickel (Ni), chromium (Cr) and silicon (Si) is 21.6: 8.2: 70.2. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.15, and the silicon phase content of the particles in the primary powder was 56% by mass. Substituting 56 for x in the formula: y> −0.02x + 3.8 and substituting 4.15 for y yields 4.15> 2.68, and this formula holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this example was 130, and the diameter of the silicon phase in the alloy particles according to this example was 10 to 40 nm. The initial charge capacity of the coin-type battery according to this example is 1882 mAh / g, the initial discharge capacity is 1664 mAh / g, the initial efficiency is 88%, and the 51C capacity maintenance rate is 88.8%. It was. The silicon phase content in the alloy particles according to this example was 52% by mass. (See Table 3)

(Comparative Example 1)
Except that the pure raw materials of titanium and silicon were put into an aluminum titanate melting crucible such that the mass ratio of titanium (Ti) and silicon (Si) was 46.0: 54.0, the same as in Example 1 An alloy powder was prepared, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. In addition, as in Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was prepared, and the initial charge capacity, initial discharge capacity, and initial efficiency of the coin-type battery were determined. The silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.33, and the silicon phase content of the particles in the primary powder was 0% by mass. Then, when 0 is substituted for x in the formula: y> −0.02x + 3.8 and 3.33 is substituted for y, 3.33 <3.80 is obtained, and the same formula is established for particles of the same primary powder. It became clear not to. The MG workability index value during MG processing according to this comparative example was 104. The initial charge capacity of the coin-type battery according to this comparative example was 26 mAh / g, the initial discharge capacity was 6 mAh / g, and the initial efficiency was 23%. The silicon phase content in the alloy particles according to this comparative example was 0% by mass. (See Table 4)

(Comparative Example 2)
An alloy powder was prepared in the same manner as in Example 1 except that a pure raw material of titanium and silicon was put into an aluminum titanate melting crucible so that the mass ratio of titanium and silicon was 36.8: 63.2. In the same manner as in Example 1, the dimensions of the silicon phase in the alloy particles were measured. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.13, and the silicon phase content of the particles in the primary powder was 20% by mass. Substituting 20 for x in the formula: y> −0.02x + 3.8 and substituting 3.13 for y yields 3.13 <3.40, and this formula holds for particles of the same powder. It became clear not to. The MG workability index value during MG treatment according to this comparative example was 98, and the diameter of the silicon phase in the alloy particles according to this comparative example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this comparative example is 851 mAh / g, the initial discharge capacity is 681 mAh / g, the initial efficiency is 80%, and the 51C capacity maintenance rate is 88.0%. It was. The silicon phase content in the alloy particles according to this comparative example was 21% by mass. (See Table 4)

(Comparative Example 3)
Titanium and silicon pure raw materials were put into a melting crucible made of aluminum titanate so that the mass ratio of titanium and silicon was 34.5: 65.5, and the primary powder: graphite mass ratio during the MG treatment was 36 g: An alloy powder was prepared in the same manner as in Example 1 except that the amount was 4 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. Similarly to Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was produced. The initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity of the coin-type battery were maintained. While calculating | requiring the rate, the silicon phase content rate in an alloy particle was calculated | required.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.08, and the silicon phase content of the particles in the primary powder was 25% by mass. Then, substituting 25 for x in the formula: y> −0.02x + 3.8 and substituting 3.08 for y yields 3.08 <3.30, and the same formula holds for particles of the same powder. It became clear not to. Further, the MG workability index value at the time of MG treatment according to this comparative example was 96, and the diameter of the silicon phase in the alloy particles according to this comparative example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this comparative example is 891 mAh / g, the initial discharge capacity is 738 mAh / g, the initial efficiency is 83%, and the 51C capacity maintenance rate is 81.0%. It was. The silicon phase content in the alloy particles according to this comparative example was 23% by mass. (See Table 4)

(Comparative Example 4)
The pure powder of nickel, titanium, and silicon was put into a melting crucible made of aluminum titanate so that the mass ratio of nickel, titanium, and silicon was 18.0: 26.0: 56.0, and the primary powder during MG treatment An alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of: graphite was 36 g: 4 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. In addition, as in Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was prepared, and the initial charge capacity, initial discharge capacity, and initial efficiency of the coin-type battery were determined. The silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 4.08, and the silicon phase content of the particles in the primary powder was 15% by mass. Substituting 15 for x in the formula: y> −0.02x + 3.8 and substituting 4.08 for y yields 4.08> 3.50, and the same formula holds for particles of the same powder. It became clear to do. Further, the MG workability index value during MG treatment according to this comparative example was 128, and the diameter of the silicon phase in the alloy particles according to this comparative example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this comparative example was 570 mAh / g, the initial discharge capacity was 422 mAh / g, and the initial efficiency was 74%. The silicon phase content in the alloy particles according to this comparative example was 13% by mass. (See Table 4)

(Comparative Example 5)
The pure powder of aluminum, iron and silicon was put into a melting crucible made of aluminum titanate so that the mass ratio of aluminum, iron and silicon was 33.5: 27.8: 38.7, and the primary powder during MG treatment An alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of: graphite was 36 g: 4 g, and the size of the silicon phase in the alloy particles was measured in the same manner as in Example 1. In addition, as in Example 1, a negative electrode was produced from this alloy powder and a coin-type battery incorporating the negative electrode was prepared, and the initial charge capacity, initial discharge capacity, and initial efficiency of the coin-type battery were determined. The silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 3.99, and the silicon phase content of the particles in the primary powder was 10% by mass. Substituting 10 for x and y for 3.99 and 3.99 for x: y> −0.02x + 3.8, 3.99> 3.60, and the same equation holds for particles of the same primary powder. It became clear to do. Further, the MG workability index value during the MG treatment according to this comparative example was 125, and the diameter of the silicon phase in the alloy particles according to this comparative example was 5 to 20 nm. The initial charge capacity of the coin-type battery according to this comparative example was 254 mAh / g, the initial discharge capacity was 133 mAh / g, and the initial efficiency was 52%. The silicon phase content in the alloy particles according to this comparative example was 4% by mass. (See Table 4)

(Comparative Example 6)
Put pure raw materials of nickel, titanium and silicon into melting crucible made of aluminum titanate so that mass ratio of nickel (Ni), titanium (Ti) and silicon (Si) is 4.2: 3.4: 92.4. The alloy powder was prepared in the same manner as in Example 1 except that the mass ratio of the primary powder to graphite during the MG treatment was 94 g: 6 g. The silicon phase in the alloy particles was prepared in the same manner as in Example 1. The dimensions of were measured. The negative electrode mixture slurry was prepared by adding 52.5 parts by mass of graphite powder, 5.0 parts by mass of SBR, 5.0 parts by mass of CMC, 15.0 parts per 22.5 parts by mass of the above-described alloy powder. A coin in which a negative electrode was produced from this alloy powder and the negative electrode was incorporated in the same manner as in Example 1, except that mass parts of acetylene black powder was added and distilled water was further added to the mixture followed by kneading. A type battery was produced. Then, in the same manner as in Example 1, the initial charge capacity, initial discharge capacity, initial efficiency and 51C capacity maintenance rate of the coin-type battery were determined, and the silicon phase content in the alloy particles was determined.

The specific gravity of the particles of the primary powder during the production of the alloy powder was 2.68, and the silicon phase content of the particles in the primary powder was 89% by mass. Then, when 89 is substituted for x in the formula: y> −0.02x + 3.8 and 2.68 is substituted for y, 2.68> 2.02, and the same formula is established for particles of the same primary powder. It became clear to do. Further, the MG workability index value at the time of MG treatment according to this comparative example was 84, and the diameter of the silicon phase in the alloy particles according to this comparative example was 20 to 50 nm. The initial charge capacity of the coin-type battery according to this comparative example is 2956 mAh / g, the initial discharge capacity is 2409 mAh / g, the initial efficiency is 81%, and the 51C capacity maintenance rate is 77.4%. It was. The silicon phase content in the alloy particles according to this comparative example was 75% by mass. (See Table 4)

Figure JPOXMLDOC01-appb-T000001

Figure JPOXMLDOC01-appb-T000002

Figure JPOXMLDOC01-appb-T000003

Figure JPOXMLDOC01-appb-T000004

The alloy particles according to the present invention can be used as a negative electrode active material for a non-aqueous electrolyte secondary battery.

Claims (13)

  1. A metal silicide phase formed from a silicon atom and at least two metal atoms;
    A silicon phase formed mainly from silicon atoms and dispersed in the metal silicide phase;
    The silicon phase accounts for 20% by mass or more based on the total amount,
    The said silicon atom is an alloy particle which occupies the ratio of 85 mass% or less with respect to the whole quantity.
  2. The alloy particles according to claim 1, wherein the silicon atoms occupy a ratio of 70% by mass or less based on the total amount.
  3. The alloy particles according to claim 1, wherein the silicon phase has an average particle size of 100 nm or less.
  4. The metal silicide phase mainly has a composition of MSix (where M is two or more metal elements, Si is silicon, and x is a value greater than 0 and less than 2). 4. Alloy particles according to any one of 3
  5. 5. The M according to claim 4, wherein the M includes at least one metal element selected from the group consisting of aluminum (Al), iron (Fe), nickel (Ni), titanium (Ti), and copper (Cu). Alloy particles.
  6. The alloy particle according to claim 4 or 5, wherein the M includes at least one metal element selected from the group consisting of cobalt (Co) and chromium (Cr).
  7. 4. The alloy particle according to claim 1, wherein the metal silicide phase contains silicon (Si), nickel (Ni), and titanium (Ti).
  8. An electrode comprising the alloy particles according to any one of claims 1 to 7 as an active material.
  9. A nonaqueous electrolyte secondary battery comprising the electrode according to claim 8 as a negative electrode.
  10. The non-aqueous electrolyte secondary battery according to claim 9, wherein the capacity retention rate relative to the initial cycle time is 85% or more at 50 charge / discharge cycle times.
  11. A metal melting step of preparing a specific alloy molten metal by melting at least silicon (Si) and at least two kinds of metals;
    A rapid solidification step in which the specific alloy melt is rapidly solidified to produce a specific alloy solidified product;
    Crushing step of crushing the specific alloy solidified product to form a specific alloy powder;
    An alloy particle manufacturing method comprising: a mechanical grinding process for manufacturing the alloy particles according to claim 1 or 2 by subjecting the specific alloy powder to mechanical grinding.
  12. The alloy particle manufacturing method according to claim 11, wherein the silicon (Si) occupies a ratio of 85% by mass or less in the specific alloy molten metal.
  13. The specific alloy powder has a silicon phase content of 20% by mass or more, a specific gravity of y, and a silicon phase content (% by mass) of x, where y> −0.02x + 3. The method for producing alloy particles according to claim 11 or 12, wherein a relationship of .8 is established.
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