JP2014132556A - Negative electrode material, negative electrode active material, negative electrode, and alkaline metal ion battery - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a negative electrode material for an alkaline metal ion battery which has good storage characteristics and excellent capacity for charge and discharge while having average layer surface space of (002) plane being larger than that of a graphite material.SOLUTION: The negative electrode material is a carbonaceous negative electrode material that is used for an alkaline metal ion battery, its average layer surface space dof (002) plane determined by X-ray diffraction by using CuKα ray as a radiation source is 0.370 nm or more, and the negative electrode material contains nitrogen atoms of equal to or more than 10000 ppm and equal to or less than 20000 ppm.

Description

  The present invention relates to a negative electrode material, a negative electrode active material, a negative electrode, and an alkali metal ion battery.

  As a negative electrode material for an alkali metal ion battery, a graphite material is generally used. However, since the graphite material expands and contracts between the crystallite layers by doping and dedoping of alkali metal ions such as lithium, the crystallite is likely to be distorted. For this reason, the graphite material is likely to break the crystal structure due to repeated charge / discharge, and the alkali metal ion battery using the graphite material as the negative electrode material is inferior in charge / discharge cycle characteristics.

Patent Document 1 (Japanese Patent Laid-Open No. 8-115723) discloses that helium with respect to the density (ρ _B ) measured by using butanol as a substitution medium having an average layer spacing of (002) plane of 0.365 nm or more determined by X-ray diffraction method. A carbonaceous material for a secondary battery electrode is described in which the ratio (ρ _H / ρ _B ) of density (ρ _H ) measured using gas as a replacement medium is 1.15 or more.
Such a carbonaceous material is said to have excellent charge / discharge cycle characteristics because the crystallite layer is larger than the graphite material and the crystal structure is not easily destroyed by repeated charge / discharge compared to the graphite material. (See Patent Documents 1 and 2).

JP-A-8-115723 International Publication No. 2007/040007 Pamphlet

  However, as described in Patent Document 1, a carbonaceous material having a larger crystallite layer than a graphite material is more easily deteriorated in the atmosphere than a graphite material and has poor storage characteristics. For this reason, it has been necessary to store in an inert gas atmosphere immediately after production, and it has been difficult to handle compared to a graphite material.

In general, since a negative electrode material having a larger d ₀₀₂ than a graphite material has fine pores developed more than the graphite material, moisture is easily adsorbed inside the pores. When moisture is adsorbed, an irreversible reaction occurs between lithium doped in the negative electrode material and moisture, resulting in an increase in irreversible capacity during initial charging and a decrease in charge / discharge cycle characteristics. End up. For these reasons, it has been considered that a negative electrode material having a large d ₀₀₂ is inferior in storage characteristics to a graphite material (see, for example, Patent Document 2). Therefore, conventionally, attempts have been made to improve storage characteristics by closing the pores of the negative electrode material and reducing the equilibrium moisture adsorption amount (see, for example, Patent Document 2).

  However, when the present inventors regenerated the negative electrode material by heating and drying the deteriorated negative electrode material to remove the moisture adsorbed in the fine pores, the negative electrode material was completely regenerated. I couldn't. Further, as in Patent Document 2, when the pores of the negative electrode material are closed, there is a problem that the charge / discharge capacity decreases.

  Therefore, the present invention provides a negative electrode material for an alkali metal ion battery having excellent storage characteristics and charge / discharge capacity while having an average layer spacing of (002) planes larger than that of a graphite material.

  Such an object is achieved by the present inventions (1) to (12) below.

(1) A carbonaceous negative electrode material used for an alkali metal ion battery,
The average layer spacing d _{002 of the} (002) plane obtained by X-ray diffraction using CuKα rays as a radiation source is 0.370 nm or more,
Containing 10,000 ppm or more and 20000 ppm or less of nitrogen atoms,
Anode material for alkaline metal ion batteries.
(2) After holding the negative electrode material for 120 hours under conditions of a temperature of 40 ° C. and a relative humidity of 90% RH,
The negative electrode material is preliminarily dried by holding it at a temperature of 130 ° C. for 1 hour under a nitrogen atmosphere, and then the moisture generated by holding the negative electrode material after the preliminary drying at 200 ° C. for 30 minutes is Karl Fischer. When measured by coulometric titration,
The amount of water generated from the negative electrode material after the preliminary drying is 0.01% by weight or more and 0.20% by mass or less with respect to 100% by mass of the negative electrode material after the preliminary drying. (1) The negative electrode material described in 1.
(3) About a half cell produced using the negative electrode material formed as the negative electrode, metal lithium as the counter electrode, and LiPF ₆ dissolved in a carbonate-based solvent at a rate of 1M as the electrolytic solution,
Charge at 25 ° C under the conditions of a charging current of 25 mA / g, a charging voltage of 0 mV, and a charging end current of 2.5 mA / g by the constant current constant voltage method, and then a discharge current of 25 mA / g and a discharge end voltage of 2.5 V. The negative electrode material according to (1) or (2), wherein the discharge capacity when discharged by a constant current method is 360 mAh / g or more.
(4) After embedding the negative electrode material with an epoxy resin and curing the epoxy resin, the obtained cured product is cut and polished to expose a cross section of the negative electrode material, and then using an optical microscope When the cross section is observed in bright field at a magnification of 1000 times,
The negative electrode material according to any one of (1) to (3), wherein the cross section of the negative electrode material has a first region and a second region having different reflectivities.
(5) The negative electrode material according to any one of (1) to (4), wherein an adsorption amount of carbon dioxide gas is 0.05 ml / g or more and less than 10 ml / g.
(6) The negative electrode material according to any one of (1) to (5), wherein the pore diameter determined by mercury porosimetry is 0.003 μm or more and 5 μm or less and the pore volume is less than 0.55 ml / g.
(7) A negative electrode active material comprising the negative electrode material according to any one of (1) to (6).
(8) The negative electrode active material according to (7), further comprising a negative electrode material of a type different from the negative electrode material.
(9) The negative electrode active material according to (8), wherein the different types of the negative electrode materials are graphite materials.
(10) a negative electrode active material layer containing at least the negative electrode active material according to any one of (7) to (9);
A negative electrode current collector;
Are laminated in this order, and the negative electrode for alkaline metal ion batteries.
(11) An alkali metal ion battery comprising at least the negative electrode for an alkali metal ion battery according to (10), an electrolyte, and a positive electrode.
(12) The alkali metal ion battery according to (11), which is a lithium ion battery or a sodium ion battery.

  ADVANTAGE OF THE INVENTION According to this invention, the negative electrode material for alkaline metal ion batteries excellent in a storage characteristic and charging / discharging capacity can be provided, having a (002) plane average layer space | interval larger compared with a graphite material.

It is a schematic diagram for demonstrating the example of the cross-section of the negative electrode material of embodiment which concerns on this invention. It is a schematic diagram which shows an example of the lithium ion battery of embodiment which concerns on this invention. 4 is a view showing an optical micrograph of a cross section of a negative electrode material obtained in Example 3. FIG. 6 is a view showing an optical micrograph of a cross section of a negative electrode material obtained in Comparative Example 1. FIG.

  Hereinafter, embodiments of the present invention will be described with reference to the drawings. In addition, the figure is a schematic diagram and does not necessarily match the actual dimensional ratio.

<Negative electrode material>
The negative electrode material according to the present embodiment is a carbonaceous negative electrode material used for alkali metal ion batteries such as lithium ion batteries and sodium ion batteries, and is obtained by an X-ray diffraction method using CuKα rays as a radiation source ( The average layer spacing d ₀₀₂ (hereinafter also referred to as “d ₀₀₂ ”) of the (002) plane is 0.370 nm or more, preferably 0.372 nm or more, more preferably 0.374 nm or more. When d ₀₀₂ is equal to or higher than the above lower limit, destruction of the crystal structure due to repeated doping and dedoping of alkali metal ions such as lithium is suppressed, and thus the charge / discharge cycle characteristics of the negative electrode material can be improved.
The upper limit of the average layer surface distance d ₀₀₂ is not particularly limited, but is usually 0.400 nm or less, preferably 0.395 nm or less, and more preferably 0.390 nm or less. When d ₀₀₂ is less than or equal to the above upper limit, the irreversible capacity of the negative electrode material can be suppressed.
Such a carbonaceous material having an average layer spacing d ₀₀₂ is generally called non-graphitizable carbon.

In the negative electrode material according to this embodiment, the lower limit of the nitrogen atom content is 10,000 ppm or more, preferably 11000 ppm or more, and more preferably 12000 ppm or more.
Moreover, the upper limit of content of a nitrogen atom is 20000 ppm or less, Preferably it is 19500 ppm or less, More preferably, it is 19000 ppm or less.

When content of the said nitrogen atom is more than the said lower limit, the charging / discharging capacity | capacitance of the alkali metal ion battery obtained using the said negative electrode material can be improved. Moreover, when content of the said nitrogen atom is below the said upper limit, the storage characteristic of the said negative electrode material can be improved.
Thus, when content of the said nitrogen atom is in the said range, the negative electrode material which concerns on this embodiment is excellent in the balance of a storage characteristic and charging / discharging capacity.

  The nitrogen atom content can be determined by elemental analysis.

Anode material according to the present embodiment as described above, even though d ₀₀₂ is equal to or greater than 0.370Nm, although the reason of excellent storage characteristics and charge-discharge capacity is not necessarily clear, the content of nitrogen atoms is above It is considered that the region contributing to the increase in capacity and the region contributing to the improvement of the storage characteristics are formed in an appropriate shape by being within the range.

  The negative electrode material according to the present embodiment is used as a negative electrode material for alkali metal ion batteries such as lithium ion batteries and sodium ion batteries. In particular, the negative electrode material according to this embodiment is suitably used as a negative electrode material for lithium ion batteries such as lithium ion secondary batteries.

Further, the negative electrode material according to the present embodiment exposes the cross section of the negative electrode material by embedding the negative electrode material with an epoxy resin and curing the epoxy resin, and then cutting and polishing the obtained cured product. Then, when the cross section is observed in a bright field with a magnification of 1000 times using an optical microscope, it is preferable that a first region and a second region having different reflectivities are observed in the cross section.
Thus, the negative electrode material according to the present embodiment in which the first region and the second region having different reflectivities are observed is more excellent in storage characteristics and charge / discharge capacity.

Hereinafter, the first region and the second region having different reflectivities will be described in more detail with reference to FIG.
FIG. 1 is a schematic diagram for explaining an example of a cross-sectional structure of a negative electrode material 100 according to an embodiment of the present invention.

  As shown in FIGS. 1A to 1C, for example, the negative electrode material 100 according to the present embodiment has a substantially constant reflectance in each of the first region 101 and the second region 103. It is preferable that the reflectance changes discontinuously at the interface with the two regions 103.

  Moreover, as shown to FIG.1 (a)-(c), the negative electrode material 100 which concerns on this embodiment has the 1st area | region 101, for example along the extension of the said cross section of the negative electrode material 100, and a 1st area | region. It is preferable that the second region 103 exists inside the 101.

  Furthermore, the negative electrode material 100 according to the present embodiment preferably has, for example, a reflectance (B) of the second region 103 larger than a reflectance (A) of the first region 101. That is, it is preferable that the second region 103 is observed whitish (brighter) than the first region 101 when observed with an optical microscope.

(Water content by Karl Fischer coulometric titration)
In the negative electrode material according to this embodiment, the negative electrode material is held for 120 hours under the conditions of a temperature of 40 ° C. and a relative humidity of 90% RH, and then the negative electrode material is held for 1 hour under the condition of a temperature of 130 ° C. and a nitrogen atmosphere. The moisture generated from the negative electrode material after the preliminary drying was measured by the Karl Fischer coulometric titration method. The amount is preferably 0.20% by mass or less, more preferably 0.15% by mass or less, particularly preferably 0.10% by mass or less, with respect to 100% by mass of the negative electrode material after the preliminary drying. is there.
Even when the negative electrode material according to the present embodiment is stored in the atmosphere for a long period of time when the water content is not more than the upper limit, deterioration of the negative electrode material can be further suppressed. The water content is an index of the amount of chemically adsorbed water that is desorbed by being held at 200 ° C. for 30 minutes.
Although the minimum of the said moisture content is not specifically limited, Usually, it is 0.01 mass% or more.

  The reason why the deterioration of the negative electrode material can be further suppressed when the water content by the Karl Fischer coulometric titration method is less than or equal to the above upper limit value is not necessarily clear, but the negative electrode material having a lower water content is more likely to adsorb moisture. This is thought to be because the structure is difficult to occur.

According to the study by the present inventors, the water adsorbed on the negative electrode material is roughly divided into physical adsorbed water and chemically adsorbed water, and the negative electrode material having a smaller amount of adsorbed chemical adsorbed water has better storage characteristics and higher charge. It became clear that the discharge capacity was better. That is, it has been found that the measure of the amount of chemically adsorbed water is effective as a design guideline for realizing a negative electrode material having excellent storage characteristics and charge / discharge capacity.
Here, the physically adsorbed water refers to adsorbed water physically present mainly as water molecules on the surface of the negative electrode material. On the other hand, chemically adsorbed water refers to adsorbed water that is present in a coordinated or chemically bonded state with the first layer on the surface of the negative electrode material.
A negative electrode material with a small amount of chemically adsorbed water has a structure in which the surface is difficult to coordinate or chemically bind moisture, or to a structure that does not easily change to such a structure when left in the atmosphere. It is thought that it has become. Therefore, if the amount of water is not more than the above upper limit value, even if stored for a long time in the atmosphere, moisture adsorption hardly occurs or the surface structure does not easily change, so it is considered that the storage characteristics are more excellent. .

  In this embodiment, the moisture desorbed from the negative electrode material in the preliminary drying held at a temperature of 130 ° C. for 1 hour under a nitrogen atmosphere is called physical adsorption water, and the negative electrode material after the preliminary drying is 200 ° C. The water desorbed from the negative electrode material in the above operation for 30 minutes is referred to as chemisorbed water.

(Crystallite size)
The negative electrode material according to the present embodiment preferably has a crystallite size in the c-axis direction obtained by X-ray diffraction (hereinafter sometimes abbreviated as “Lc ₍₀₀₂₎ ”) of 5 nm or less. More preferably, it is 3 nm or less, More preferably, it is 2 nm or less.

(Average particle size)
The negative electrode material according to this embodiment preferably has a 50% cumulative particle size (D ₅₀ , average particle size) in a volume-based cumulative distribution of 1 μm to 50 μm, and more preferably 2 μm to 30 μm. preferable. Thereby, a high-density negative electrode can be produced.

(Specific surface area)
In the negative electrode material of the present embodiment, the specific surface area according to the BET three-point method in nitrogen adsorption is preferably 1 m ² / g or more and 15 m ² / g or less, and more preferably 3 m ² / g or more and 8 m ² / g or less. .
When the specific surface area by the BET three-point method in nitrogen adsorption is not more than the above upper limit value, the irreversible reaction between the negative electrode material and the electrolytic solution can be further suppressed.
Moreover, appropriate permeability to the negative electrode material of electrolyte solution can be obtained because the specific surface area by the BET three point method in nitrogen adsorption is more than the said lower limit.

The calculation method of the specific surface area is as follows.
The monomolecular layer adsorption amount W _m is calculated from the following formula (1), the total surface area S _total is calculated from the following formula (2), and the specific surface area S is obtained from the following formula (3).
1 / [W · {(P _o / P) −1}] = {(C−1) / (W _m · C)} (P / P _o ) (1 / (W _m · C)) (1)

In the above formula (1), P: pressure of an adsorbate gas in adsorption equilibrium, P _o : saturated vapor pressure of the adsorbate at the adsorption temperature, W: adsorption amount at the adsorption equilibrium pressure P, W _m : monolayer adsorption Amount, C: constant related to the magnitude of the interaction between the solid surface and the adsorbate (C = exp {(E ₁ -E ₂ ) RT}) [E ₁ : heat of adsorption of the first layer (kJ / mol), E ₂ : Heat of liquefaction at measurement temperature of adsorbate (kJ / mol)]

S _total = (W _m NA _cs ) M (2)
In the above formula (2), N: Avogadro number, M: molecular weight, A _cs : adsorption cross section

S = S _total / w (3)
In formula (3), w: sample weight (g)

(Carbon dioxide adsorption amount)
In the negative electrode material according to the present embodiment, the upper limit value of the carbon dioxide adsorption amount is preferably less than 10 ml / g, more preferably less than 8.5 ml / g, and even more preferably less than 6.5 ml / g. is there. When the amount of carbon dioxide adsorption is less than the above upper limit, the storage characteristics of the negative electrode material can be further improved.
In the negative electrode material according to this embodiment, the lower limit value of the carbon dioxide adsorption amount is preferably 0.05 ml / g or more, more preferably 0.1 ml / g or more. When the lower limit of the carbon dioxide adsorption amount is equal to or higher than the lower limit, the charge capacity can be further improved.
The amount of carbon dioxide adsorbed is measured by using an ASAP-2000M manufactured by Micromeritics Instrument Corporation, which is obtained by vacuum drying a negative electrode material at 130 ° C. for 3 hours or more using a vacuum dryer. It can be carried out.

(Pore volume)
In the negative electrode material according to the present embodiment, from the viewpoint of improving the packing density, the pore volume obtained by mercury porosimetry is preferably 0.003 μm to 5 μm and the pore volume is preferably less than 0.55 ml / g, more preferably It is 0.53 ml / g or less, more preferably 0.50 ml / g or less.
In addition, the negative electrode material according to the present embodiment preferably has a pore volume of 0.003 μm to 5 μm, which is obtained by a mercury intrusion method, from the viewpoint of reducing irreversible capacity, and is preferably 0.10 ml / g or more. More preferably, it is 0.20 ml / g or more, More preferably, it is 0.30 ml / g or more.
Here, the pore volume by the mercury intrusion method can be measured by using Autopore III9420 manufactured by MICROMERITICS.

(Discharge capacity)
The negative electrode material of the present embodiment has a discharge capacity of 360 mAh / g or more, more preferably 380 mAh / g or more, when charging / discharging under the charge / discharge conditions described later for a half cell manufactured under the conditions described later. More preferably, it is 400 mAh / g or more, and particularly preferably 420 mAh / g or more. The upper limit of the discharge capacity is not particularly limited and is preferably as many as possible. However, in reality, it is 700 mAh / g or less, and usually 500 mAh / g or less. In the present specification, “mAh / g” indicates a capacity per 1 g of the negative electrode material.

(Half cell manufacturing conditions)
The conditions for producing the above-described half cell will be described.
The negative electrode used is formed of the negative electrode material. More specifically, an electrode is formed using a composition in which a negative electrode material, carboxymethyl cellulose, styrene-butadiene rubber, and acetylene black are mixed at a weight ratio of 100: 1.5: 3.0: 2.0. The formed one is used.
The counter electrode uses metallic lithium.
As the electrolytic solution, a solution obtained by dissolving LiPF ₆ in a carbonate solvent (a mixed solvent in which ethylene carbonate and diethyl carbonate are mixed at a volume ratio of 1: 1) at a ratio of 1 M is used.

The negative electrode can be produced, for example, as follows.
First, a predetermined amount of negative electrode material, carboxymethylcellulose, styrene-butadiene rubber, acetylene black, and water are mixed with stirring to prepare a slurry. The obtained slurry is applied onto a copper foil as a current collector, preliminarily dried at 60 ° C. for 2 hours, and then vacuum dried at 120 ° C. for 15 hours. Subsequently, the negative electrode comprised with the negative electrode material can be obtained by cutting out to a predetermined magnitude | size.

In addition, the negative electrode has a disk shape with a diameter of 13 mm, the negative electrode active material layer (a portion obtained by removing the current collector from the negative electrode) has a disk shape with a thickness of 50 μm, and the counter electrode (an electrode made of metallic lithium) It can be a disk with a diameter of 12 mm and a thickness of 1 mm.
Further, the shape of the half cell can be a 2032 type coin cell shape.

(Charge / discharge conditions)
The charging / discharging conditions of the half cell described above are as follows.
Measurement temperature: 25 ° C
Charging method: constant current constant voltage method, charging current: 25 mA / g, charging voltage: 0 mV, charging end current: 2.5 mA / g
Discharge method: constant current method, discharge current: 25 mA / g, final discharge voltage: 2.5 V

  Note that “charging” for a half cell refers to moving lithium ions from an electrode made of metallic lithium to an electrode made of a negative electrode material by applying a voltage. “Discharge” refers to a phenomenon in which lithium ions move from an electrode made of a negative electrode material to an electrode made of metallic lithium.

<Method for producing negative electrode material>
Next, the manufacturing method of the negative electrode material according to the present embodiment will be described.
The negative electrode material according to the present embodiment can be produced, for example, by carbonizing a specific resin composition as a raw material under appropriate conditions.
The production of the anode material using the resin composition as a raw material itself has been performed in the prior art. However, in the present embodiment, factors such as (1) the composition of the resin composition, (2) the conditions for the carbonization treatment, and (3) the ratio of the raw material to the space where the carbonization treatment is performed are highly controlled. In order to obtain the negative electrode material according to the present embodiment, it is important to highly control these factors.
In particular, in order to obtain the negative electrode material according to the present embodiment, the present inventors set the above conditions (1) and (2) appropriately, and (3) the raw material for the space to be carbonized. It was found that it is important to set the occupation ratio lower than the conventional standard.
Hereinafter, an example of the manufacturing method of the negative electrode material which concerns on this embodiment is shown. However, the manufacturing method of the negative electrode material according to the present embodiment is not limited to the following example.

(Resin composition)
First, (1) a resin composition to be carbonized is selected as a raw material for the negative electrode material.
Examples of the resin contained in the resin composition that is the raw material of the negative electrode material according to the present embodiment include a thermosetting resin; a thermoplastic resin; a petroleum-based tar and pitch that are by-produced during ethylene production, and a coal produced by dry distillation. Coal tar, heavy components or pitch obtained by distilling off low boiling components of coal tar, petroleum-based or coal-based tar or pitch such as tar or pitch obtained by coal liquefaction; Cross-linked ones; natural polymer substances such as coconut shells and wood; Among these, one kind or a combination of two or more kinds can be used. Among these, a thermosetting resin is preferable because it can be purified at the raw material stage, a negative electrode material with few impurities can be obtained, and the steps required for purification can be greatly shortened, leading to cost reduction.

Examples of the thermosetting resin include: phenol resins such as novolak type phenol resins and resol type phenol resins; epoxy resins such as bisphenol type epoxy resins and novolac type epoxy resins; melamine resins; urea resins; aniline resins; Examples include furan resins; ketone resins; unsaturated polyester resins; urethane resins. In addition, modified products obtained by modifying these with various components can also be used.
Among these, phenol resins such as novolac type phenol resin and resol type phenol resin; melamine resin; urea resin; aniline resin, which are resins using formaldehyde, are preferable because of the high residual carbon ratio.

Moreover, when using a thermosetting resin, the hardening | curing agent can be used together.
As the curing agent used, for example, hexamethylenetetramine, resol type phenol resin, polyacetal, paraformaldehyde and the like can be used in the case of a novolak type phenol resin. In the case of a resol type phenol resin, melamine resin, urea resin, aniline resin, hexamethylenetetramine or the like can be used.
The compounding quantity of a hardening | curing agent is 0.1 to 50 mass parts normally with respect to 100 mass parts of said thermosetting resins.

  Moreover, in the resin composition as a raw material of negative electrode material, an additive can be mix | blended other than the said thermosetting resin and a hardening | curing agent.

  Although it does not specifically limit as an additive used here, For example, the carbon material precursor carbonized at 200 to 800 degreeC, an organic acid, an inorganic acid, a nitrogen-containing compound, an oxygen-containing compound, an aromatic compound, nonferrous A metal element etc. can be mentioned. These additives can be used alone or in combination of two or more depending on the type and properties of the resin used.

  The method for preparing the resin composition is not particularly limited. For example, (1) a method in which the above resin and other components are melt-mixed, (2) the above resin and other components are dissolved in a solvent. (3) The resin and other components may be pulverized and mixed.

  The apparatus for preparing the resin composition is not particularly limited. For example, when melt mixing is performed, a kneading apparatus such as a kneading roll, a single screw or a twin screw kneader can be used. When performing dissolution and mixing, a mixing device such as a Henschel mixer or a disperser can be used. When performing pulverization and mixing, for example, an apparatus such as a hammer mill or a jet mill can be used.

  The resin composition thus obtained may be one obtained by physically mixing a plurality of types of components, or is applied during mixing (stirring, kneading, etc.) during preparation of the resin composition. A part of the material may be chemically reacted with mechanical energy and thermal energy converted from the mechanical energy. Specifically, a mechanochemical reaction using mechanical energy or a chemical reaction using thermal energy may be performed.

(Carbonization treatment)
Next, the obtained resin composition is carbonized.
Here, as the conditions for the carbonization treatment, for example, the temperature is raised from normal temperature to 1 ° C./hour to 200 ° C./hour, 800 ° C. to 3000 ° C., 0.01 Pa to 101 kPa (1 atm), The reaction can be performed for 1 hour to 50 hours, preferably 0.5 hours to 10 hours. The atmosphere during carbonization is preferably an inert atmosphere such as nitrogen or helium gas; a substantially inert atmosphere in which a trace amount of oxygen is present in the inert gas; a reducing gas atmosphere, or the like. . By doing in this way, thermal decomposition (oxidative decomposition) of resin can be suppressed and a desired negative electrode material can be obtained.

  Conditions such as temperature and time during the carbonization treatment can be appropriately adjusted in order to optimize the characteristics of the negative electrode material.

In addition, you may perform a pre carbonization process before performing the said carbonization process.
Here, the conditions for the pre-carbonization treatment are not particularly limited. Thus, even if the resin composition is infusibilized by performing pre-carbonization treatment before carbonization treatment and pulverization treatment of the resin composition or the like is performed before the carbonization treatment step, the resin composition after pulverization can be obtained. It is possible to prevent re-fusion during carbonization and to obtain a desired negative electrode material efficiently.

Moreover, you may perform the hardening process of a resin composition before this pre carbonization process.
Although it does not specifically limit as a hardening processing method, For example, it can carry out by the method of giving heat quantity which can perform hardening reaction to a resin composition, the method of thermosetting, or the method of using together a thermosetting resin and a hardening | curing agent. . As a result, the pre-carbonization treatment can be performed substantially in the solid phase, so that the carbonization treatment or the pre-carbonization treatment can be performed while maintaining the structure of the thermosetting resin to some extent, and the structure and characteristics of the negative electrode material are controlled. Will be able to.

  In addition, when performing the carbonization treatment or the pre-carbonization treatment, a metal, a pigment, a lubricant, an antistatic agent, an antioxidant, or the like is added to the resin composition to impart desired characteristics to the negative electrode material. You can also.

  When the said hardening process or pre carbonization process is performed, you may grind | pulverize a processed material before the said carbonization process after that. In such a case, variation in the thermal history during carbonization can be reduced, and the uniformity of the surface state of the obtained negative electrode material can be increased. And the handleability of a processed material can be improved.

(Occupation ratio of raw materials in the space for carbonization)
Moreover, in order to obtain the negative electrode material according to the present embodiment, it is important to appropriately adjust the occupation ratio of the raw material in the space where the carbonization treatment is performed. Specifically, the occupation ratio of the raw material with respect to the space for carbonization is preferably set to 10.0 kg / m ³ or less, more preferably 5.0 kg / m ³ or less, and particularly preferably 1.0 kg / m ³ or less. . Here, the space for performing the carbonization treatment usually represents the furnace volume of the heat treatment furnace used for the carbonization treatment.
In addition, the conventional reference | standard of the occupation ratio of the raw material with respect to the space which carbonizes is about 100-500 kg / m < ³ >. Therefore, in order to obtain the negative electrode material according to the present embodiment, it is important to set the occupation ratio of the raw material with respect to the space to be carbonized lower than the conventional standard.
The reason why the negative electrode material according to the present embodiment can be obtained by setting the occupation ratio of the raw material in the space for performing the carbonization treatment to be equal to or less than the above upper limit value is not necessarily clear, but from the raw material (resin composition) during the carbonization treatment. It is considered that the generated gas is efficiently removed from the system.

The negative electrode material according to this embodiment can be obtained by the above procedure.

<Negative electrode active material>
Hereinafter, the negative electrode active material according to the present embodiment will be described.
The negative electrode active material refers to a substance capable of taking in and out alkali metal ions such as lithium ions in an alkali metal ion battery. The negative electrode active material according to the present embodiment includes the negative electrode material according to the present embodiment described above.

  The negative electrode active material according to the present embodiment may further include a type of negative electrode material different from the negative electrode material described above. Examples of such a negative electrode material include generally known negative electrode materials such as silicon, silicon monoxide, and graphite materials.

  Among these, the negative electrode active material according to the present embodiment preferably includes a graphite material in addition to the negative electrode material according to the present embodiment described above. Thereby, the charge / discharge capacity of the obtained alkali metal ion battery can be improved. Therefore, the obtained alkali metal ion battery can have a particularly excellent balance between charge / discharge capacity and charge / discharge efficiency.

  The particle size (average particle size) at the time of 50% accumulation in the volume-based cumulative distribution of the graphite material used is preferably 2 μm or more and 50 μm or less, and more preferably 5 μm or more and 30 μm or less. Thereby, a high-density negative electrode can be produced while maintaining high charge / discharge efficiency.

<Negative electrode for alkali metal ion battery, alkali metal ion battery>
Hereinafter, the negative electrode for an alkali metal ion battery and the alkali metal ion battery according to the present embodiment will be described.

The negative electrode for an alkali metal ion battery according to the present embodiment (hereinafter sometimes simply referred to as a negative electrode) is produced using the negative electrode active material according to the present embodiment described above. Thereby, the negative electrode excellent in storage characteristics and charge / discharge capacity can be provided.
In addition, the alkali metal ion battery according to the present embodiment is manufactured using the negative electrode according to the present embodiment. Thereby, the alkali metal ion battery excellent in storage characteristics and charge / discharge capacity can be provided.

  The alkali metal ion battery according to the present embodiment is, for example, a lithium ion battery or a sodium ion battery. Hereinafter, the case of a lithium ion battery will be described as an example.

FIG. 2 is a schematic diagram illustrating an example of a lithium ion battery according to the present embodiment.
As illustrated in FIG. 2, the lithium ion battery 10 includes a negative electrode 13, a positive electrode 21, an electrolytic solution 16, and a separator 18.

As shown in FIG. 2, the negative electrode 13 includes a negative electrode active material layer 12 and a negative electrode current collector 14.
The negative electrode current collector 14 is not particularly limited, and generally known negative electrode current collectors can be used. For example, copper foil or nickel foil can be used. Here, the negative electrode active material layer 12 and the negative electrode current collector 14 are preferably laminated in this order.

The negative electrode active material layer 12 is composed of the negative electrode active material according to the present embodiment described above.
The negative electrode 13 can be manufactured as follows, for example.

For 100 parts by weight of the negative electrode active material, generally known organic polymer binders (for example, fluorine-based polymers such as polyvinylidene fluoride and polytetrafluoroethylene; styrene / butadiene rubber, butyl rubber, butadiene rubber, etc.) 1 to 30 parts by weight and an appropriate amount of a viscosity adjusting solvent (N-methyl-2-pyrrolidone, dimethylformamide, etc.) or water is added and kneaded to prepare a negative electrode slurry. Prepare.
The negative electrode active material layer 12 can be obtained by molding the obtained slurry into a sheet shape, a pellet shape, or the like by compression molding, roll molding, or the like. And the negative electrode 13 can be obtained by laminating | stacking the negative electrode active material layer 12 and the negative electrode collector 14 which were obtained in this way.
Moreover, the negative electrode 13 can also be manufactured by apply | coating the obtained negative electrode slurry to the negative electrode collector 14, and drying.

  The electrolyte solution 16 fills the space between the positive electrode 21 and the negative electrode 13 and is a layer in which lithium ions move by charge / discharge.

  The electrolytic solution 16 is not particularly limited, and a generally known electrolytic solution can be used. For example, a solution obtained by dissolving a lithium salt serving as an electrolyte in a non-aqueous solvent is used.

  Examples of the non-aqueous solvent include cyclic esters such as propylene carbonate, ethylene carbonate, and γ-butyrolactone; chain esters such as dimethyl carbonate and diethyl carbonate; chain ethers such as dimethoxyethane; or a mixture thereof. Can be used.

Is not particularly limited as electrolytes generally be a known electrolyte, for example, it may be used lithium metal salt such as LiClO _4, LiPF _6. Further, the above salts can be mixed with polyethylene oxide, polyacrylonitrile, etc. and used as a solid electrolyte.

  It does not specifically limit as the separator 18, Generally a well-known separator can be used, For example, the porous film made from polyolefin, such as polyethylene and a polypropylene, a nonwoven fabric, etc. can be used.

As shown in FIG. 2, the positive electrode 21 includes a positive electrode active material layer 20 and a positive electrode current collector 22.
It does not specifically limit as the positive electrode active material layer 20, Generally, it can form with a well-known positive electrode active material. Is not particularly limited as the cathode active material include lithium cobalt oxide (LiCoO _2), lithium nickel oxide (LiNiO _2), composite oxides such as lithium manganese oxide (LiMn ₂ O _4); polyaniline, polypyrrole, etc. Or the like can be used.

The positive electrode current collector 22 is not particularly limited, and generally known positive electrode current collectors can be used. For example, an aluminum foil can be used.
And the positive electrode 21 in this embodiment can be manufactured with the manufacturing method of a well-known positive electrode generally.

As mentioned above, although embodiment of this invention was described, these are illustrations of this invention and various structures other than the above are also employable.
Further, the present invention is not limited to the above-described embodiment, and modifications, improvements, and the like within the scope that can achieve the object of the present invention are included in the present invention.

  Hereinafter, although an example and a comparative example explain the present invention, the present invention is not limited to these. In the examples, “part” means “part by weight”.

[1] Evaluation method of negative electrode material First, the evaluation method of the negative electrode material obtained by the Example and comparative example which are mentioned later is demonstrated.

1. Particle size distribution The particle size distribution of the negative electrode material was measured by a laser diffraction method using a laser diffraction particle size distribution measuring apparatus LA-920 manufactured by Horiba. From the measurement results, the particle size (D ₅₀ , average particle size) at 50% accumulation in the volume-based cumulative distribution was determined for the negative electrode material.

2. Specific surface area It measured by the BET 3 point | piece method in nitrogen adsorption | suction using the Nova-1200 apparatus made from Yuasa. The specific calculation method is as described above.

3. Negative electrode material d ₀₀₂ and Lc ₍₀₀₂₎
Using an X-ray diffractometer “XRD-7000” manufactured by Shimadzu Corporation, the average layer spacing d ₀₀₂ of the (002) plane was measured.
From the spectrum obtained from the X-ray diffraction measurement of the negative electrode material, the average layer spacing d ₀₀₂ of the (002) plane was calculated from the following Bragg equation.
λ = 2d _hkl sinθ Bragg equation (d _hkl = d ₀₀₂ )
λ: wavelength of characteristic X-ray K _α1 output from the cathode θ: reflection angle of spectrum Lc ₍₀₀₂₎ was measured as follows.
It was determined from the half width of the 002 plane peak and the diffraction angle in the spectrum obtained from the X-ray diffraction measurement using the following Scherrer equation.
Lc ₍₀₀₂₎ = 0.94 λ / (βcos θ) (Scherrer equation)
Lc ₍₀₀₂₎ : Crystallite size λ: Wavelength of characteristic X-ray K _α1 output from the cathode β: Half width of peak (radian)
θ: Spectral reflection angle

4). Carbon dioxide gas adsorption amount Carbon dioxide gas adsorption amount was measured using a vacuum drier with a negative electrode material vacuum-dried at 130 ° C. for 3 hours or more as a measurement sample, using ASAP-2000M manufactured by Micromeritics Instrument Corporation. Done using.
A measurement sample tube (0.5 g) was placed in a measurement sample tube and dried under reduced pressure at 300 ° C. for 3 hours or more under a reduced pressure of 0.2 Pa or less. Thereafter, the amount of carbon dioxide adsorbed was measured.
The adsorption temperature is 0 ° C., the pressure is reduced until the pressure of the sample tube containing the measurement sample becomes 0.6 Pa or less, carbon dioxide gas is introduced into the sample tube, and the equilibrium pressure in the sample tube is 0.11 MPa (relative pressure). The amount of carbon dioxide adsorbed until it reached (corresponding to 0.032) was determined by the constant volume method and expressed in ml / g. The adsorption amount is a value converted to a standard state (STP).

5. Measurement of water content by Karl Fischer coulometric titration The water content by Karl Fischer coulometric titration was measured by the following procedure.
(Procedure 1) In an apparatus of a small environmental tester (SH-241 manufactured by ESPEC), 1 g of a negative electrode material was held for 120 hours under the conditions of a temperature of 40 ° C. and a relative humidity of 90% RH. The negative electrode material was spread in a container having a length of 5 cm, a width of 8 cm, and a height of 1.5 cm so as to be as thin as possible, and then left in the apparatus.
(Procedure 2) The negative electrode material was preliminarily dried by holding it for 1 hour under conditions of a temperature of 130 ° C. and a nitrogen atmosphere. The water generated by holding at 30 ° C. for 30 minutes was measured by the Karl Fischer coulometric titration method.

6). Measurement of total water absorption After 1 g of the negative electrode material was vacuum dried at 200 ° C. for 24 hours, the weight of the negative electrode material was measured. Subsequently, it hold | maintained for 120 hours on the conditions of the temperature of 40 degreeC, and relative humidity 90% RH in the apparatus of a small environment tester (SH-241 by ESPEC). The negative electrode material was spread in a container having a length of 5 cm, a width of 8 cm, and a height of 1.5 cm so as to be as thin as possible, and then left in the apparatus. Thereafter, the weight of the negative electrode material was measured, and the total water absorption was measured from the following formula.
Total water absorption [%] = 100 × (weight after holding for 120 hours−weight after vacuum drying) / (weight after vacuum drying)

7). Storage characteristics The initial efficiency of each of the negative electrode material immediately after production and the negative electrode material after the following storage test was measured according to the following method. Next, the change rate of the initial efficiency was calculated.

(Preservation test)
1 g of the negative electrode material was held for 7 days under conditions of a temperature of 40 ° C. and a relative humidity of 90% RH in a small environmental tester (SH-241 manufactured by ESPEC). The negative electrode material was spread in a container having a length of 5 cm, a width of 8 cm, and a height of 1.5 cm so as to be as thin as possible, and then left in the apparatus. Thereafter, the negative electrode material was dried by holding at a temperature of 130 ° C. for 1 hour under a nitrogen atmosphere.

(1) Production of half cell With respect to 100 parts of the negative electrode material obtained in Examples and Comparative Examples described later, 1.5 parts of carboxymethyl cellulose (manufactured by Daicel Finechem, CMC Daicel 2200), styrene
Add 3.0 parts of butadiene rubber (manufactured by JSR, TRD-2001), 2.0 parts of acetylene black (manufactured by Denki Kagaku Kogyo, Denka Black), and 100 parts of distilled water, and stir and mix with a rotating / revolving mixer. A negative electrode slurry was prepared.

  The prepared negative electrode slurry was applied to one side of a 14 μm-thick copper foil (Furukawa Electric, NC-WS), then pre-dried in air at 60 ° C. for 2 hours, and then vacuumed at 120 ° C. for 15 hours. Dried. After vacuum drying, the electrode was pressure-formed by a roll press. This was cut into a disk shape having a diameter of 13 mm to produce a negative electrode. The thickness of the negative electrode active material layer was 50 μm.

  Metallic lithium was formed in a disk shape with a diameter of 12 mm and a thickness of 1 mm to produce a counter electrode. In addition, a polyolefin porous film (manufactured by Celgard, trade name: Celgard 2400) was used as a separator.

Using the negative electrode, the counter electrode, and the separator described above, a mixed solvent obtained by mixing ethylene carbonate and diethyl carbonate at a volume ratio of 1: 1 as an electrolytic solution and adding LiPF ₆ at a ratio of 1 M was used in an argon atmosphere. A 2032 type coin cell-shaped bipolar half cell was manufactured in the glove box, and the evaluation described below was performed on the half cell.

(2) Charging / discharging of a half cell Charging / discharging was performed on the following conditions.
Measurement temperature: 25 ° C
Charging method: constant current constant voltage method, charging current: 25 mA / g, charging voltage: 0 mV, charging end current: 2.5 mA / g
Discharge method: constant current method, discharge current: 25 mA / g, final discharge voltage: 2.5 V

Further, the charge capacity and discharge capacity [mAh / g] per gram of the negative electrode material were determined based on the charge capacity and discharge capacity values obtained under the above conditions. Further, the initial efficiency and the rate of change of the initial efficiency were obtained from the following formula.
Initial efficiency [%] = 100 x (Discharge capacity) / (Charge capacity)
Rate of change in initial efficiency [%] = 100 x (initial efficiency after storage test) / (initial efficiency immediately after production)

8). Pore volume The pore volume by the mercury intrusion method was measured using Autopore III9420 manufactured by MICROMERITICS.
The negative electrode material is put in a sample container and deaerated at a pressure of 2.67 Pa or less for 30 minutes. Next, mercury is introduced into the sample container and gradually pressurized to press the mercury into the pores of the negative electrode material (maximum pressure 414 MPa). From the relationship between the pressure at this time and the amount of mercury injected, the pore volume distribution of the negative electrode material is measured using the following equation. The volume of mercury that was pressed into the negative electrode material from a pressure corresponding to a pore diameter of 5 μm (0.25 MPa) to a maximum pressure (414 MPa: equivalent to a pore diameter of 3 nm) was defined as a pore volume having a pore diameter of 5 μm or less. The calculation of the pore diameter is based on the assumption that when mercury is pressed into a cylindrical pore having a diameter D at a pressure P, the surface tension of the surface tension and the pore are given by the surface tension γ of mercury and the contact angle between mercury and the pore wall as θ. From the balance of pressure acting on the cross section, the following equation holds.
−πDγcos θ = π (D / 2) ² · P
D = (− 4γcos θ) / P
Here, the surface tension of mercury is 484 dyne / cm, the contact angle between mercury and carbon is 130 degrees, the pressure P is expressed in MPa, and the pore diameter D is expressed in μm. Sought a relationship.
D = 1.27 / P

9. Measurement of density ρ ^B : Measured by the butanol method according to the method defined in JIS R7212.
ρ ^H : Using a dry density meter Accupic 1330 manufactured by Micromeritics, the sample was measured after drying at 120 ° C. for 2 hours. The measurement was performed at 23 ° C. All pressures are gauge pressures, and are the pressures obtained by subtracting the ambient pressure from the absolute pressure.

The measuring device has a sample chamber and an expansion chamber, and the sample chamber has a pressure gauge for measuring the pressure in the chamber. The sample chamber and the expansion chamber are connected by a connecting pipe having a valve. A helium gas introduction pipe having a stop valve is connected to the sample chamber, and a helium gas distribution pipe having a stop valve is connected to the expansion chamber.
The measurement was performed as follows. Using a standard sphere, the volume of the sample chamber (V _CELL ) and the volume of the expansion chamber (V _EXP ) are measured in advance.

A sample is put into the sample chamber, and helium gas is allowed to flow for 2 hours through the helium gas inlet tube, the connecting tube in the sample chamber, and the helium gas discharge tube in the expansion chamber, and the inside of the apparatus is replaced with helium gas. Next, the valve between the sample chamber and the expansion chamber and the valve of the helium gas discharge pipe from the expansion chamber are closed, and helium gas is introduced from the helium gas introduction tube of the sample chamber to 134 kPa. Thereafter, the stop valve of the helium gas introduction pipe is closed. Measure the pressure (P ₁ ) in the sample chamber 5 minutes after closing the stop valve. Next, the valve between the sample chamber and the expansion chamber is opened to transfer helium gas to the expansion chamber, and the pressure (P ₂ ) at that time is measured.
The volume of the sample (V _SAMP ) was calculated by the following formula.
V _SAMP = V _CELL −V _EXP / [(P ₁ / P ₂ ) −1]
Therefore, if the weight of the sample is W _SAMP , the density is ρ ^H = W _SAMP / V _SAMP .

10. Cross-sectional observation of negative electrode material with optical microscope After adding about 10% by weight of negative electrode material to liquid epoxy resin and mixing well, the mold was filled and the negative electrode material was embedded with epoxy resin. Next, the epoxy resin was cured by holding at 120 ° C. for 24 hours. Thereafter, the epoxy resin cured at an appropriate position was cut so that the negative electrode material appeared on the surface, and the cut surface was polished to give a mirror surface. Next, bright field observation and photography were performed on the cross section of the negative electrode material at a magnification of 1000 times using an optical microscope (Axioskop2 MAT manufactured by Carl Zeiss).

11. Content of Nitrogen A nitrogen content was measured by a combustion method using a Sumika graph manufactured by Sumika Chemical Analysis.

[2] Manufacture of negative electrode material

Example 1
Using the phenol resin PR-55321B (manufactured by Sumitomo Bakelite Co., Ltd.), which is a thermosetting resin, as a raw material, the treatment was performed in the order of the following steps (a) to (f) to obtain a negative electrode material 1.

(A) 510 g of thermosetting resin was spread and allowed to stand as thin as possible in a heat treatment furnace having a furnace internal volume of 60 L (length 50 cm, width 40 cm, height 30 cm). Thereafter, the temperature was raised from room temperature to 500 ° C. at 100 ° C./hour without any of reducing gas replacement, inert gas replacement, reducing gas flow, and inert gas flow.

(B) Next, degreasing treatment was performed at 500 ° C. for 2 hours without cooling gas replacement, inert gas replacement, reducing gas flow, and inert gas flow, and then cooled.

(C) The obtained powder was finely pulverized with a vibration ball mill.
(D) Thereafter, 204 g of the obtained powder was spread and allowed to stand as thin as possible in a heat treatment furnace having a furnace volume of 24 L (length 40 cm, width 30 cm, height 20 cm). Subsequently, the temperature was raised from room temperature to 1200 ° C. at 100 ° C./hour under inert gas (nitrogen) substitution and circulation.

(E) Under an inert gas (nitrogen) flow, it was kept at 1200 ° C. for 8 hours and carbonized.
(F) Under natural gas (nitrogen) circulation, the mixture was naturally cooled to 600 ° C., and then cooled from 600 ° C. to 100 ° C. at 100 ° C./hour.

In addition, the occupation ratio of the raw material with respect to the space which carbonizes was 3.5 kg / m < ³ >.

(Example 2)
A negative electrode material 2 was produced in the same manner as in Example 1 except that the occupation ratio of the raw material with respect to the space to be carbonized was changed to 0.9 kg / m ³ .

(Example 3)
A negative electrode material 3 was produced in the same manner as in Example 1 except that the occupation ratio of the raw material to the space for carbonization was changed to 0.5 kg / m ³ .

(Example 4)
A negative electrode material 4 was produced in the same manner as in Example 1 except that the occupation ratio of the raw material to the space for carbonization was changed to 0.3 kg / m ³ .

(Example 5)
A negative electrode material 5 was produced in the same manner as in Example 1 except that the occupation ratio of the raw material with respect to the space to be carbonized was changed to 9.0 kg / m ³ .

(Comparative Example 1)
In accordance with the method described in paragraph 0051 of JP-A-8-279358, an oxidized pitch was produced from petroleum pitch. Next, using this oxidized pitch as a raw material, processing was performed in the order of the following steps (a) to (f) to obtain a negative electrode material 6.

(A) In a heat treatment furnace having a furnace internal volume of 60 L (length 50 cm, width 40 cm, height 30 cm), 510 g of oxidation pitch was spread and allowed to stand as thin as possible. Thereafter, the temperature was raised from room temperature to 500 ° C. at 100 ° C./hour without any of reducing gas replacement, inert gas replacement, reducing gas flow, and inert gas flow.

(B) Next, degreasing treatment was performed at 500 ° C. for 2 hours without cooling gas replacement, inert gas replacement, reducing gas flow, and inert gas flow, and then cooled.

(C) The obtained powder was finely pulverized with a vibration ball mill.
(D) Thereafter, 204 g of the obtained powder was spread and allowed to stand as thin as possible in a heat treatment furnace having a furnace volume of 24 L (length 40 cm, width 30 cm, height 20 cm). Subsequently, the temperature was raised from room temperature to 1200 ° C. at 100 ° C./hour under inert gas (nitrogen) substitution and circulation.

(E) Under an inert gas (nitrogen) flow, it was kept at 1200 ° C. for 8 hours and carbonized.
(F) Under natural gas (nitrogen) circulation, the mixture was naturally cooled to 600 ° C., and then cooled from 600 ° C. to 100 ° C. at 100 ° C./hour.

In addition, the occupation ratio of the raw material with respect to the space which carbonizes was 16.0 kg / m < ³ >.

(Comparative Example 2)
A negative electrode material 7 was produced in the same manner as in Example 1 except that the occupation ratio of the raw material with respect to the space to be carbonized was changed to 16.0 kg / m ³ .

  The various evaluations described above were performed for each negative electrode material obtained in the above Examples and Comparative Examples. The results are shown in Table 1. 3 and 4 show optical micrographs of cross sections of the negative electrode materials obtained in Example 3 and Comparative Example 1, respectively.

In the negative electrode material obtained in each example, the first region and the second region having different reflectivities were observed, and the reflectivity changed discontinuously at the interface between the first region and the second region. Furthermore, the negative electrode material obtained in each example has a first region along the outer periphery of the cross section of the negative electrode material, and a second region having a higher reflectance than the first region exists inside the first region. Was.
The lithium ion battery using the negative electrode material having such a structure was excellent in storage characteristics and charge / discharge capacity.

  On the other hand, in the negative electrode materials obtained in the respective comparative examples, the first region and the second region having different reflectivities were not observed. The lithium ion battery using the negative electrode material having such a structure was inferior in storage characteristics and charge / discharge capacity than the negative electrode material obtained in each example.

DESCRIPTION OF SYMBOLS 10 Lithium ion battery 12 Negative electrode active material layer 13 Negative electrode 14 Negative electrode collector 16 Electrolyte 18 Separator 20 Positive electrode active material layer 21 Positive electrode 22 Positive electrode collector 100 Negative electrode material 101 1st area | region 103 2nd area | region

Claims (12)

A carbonaceous negative electrode material used in an alkali metal ion battery,
The average layer spacing d _{002 of the} (002) plane obtained by X-ray diffraction using CuKα rays as a radiation source is 0.370 nm or more,
Containing 10,000 ppm or more and 20000 ppm or less of nitrogen atoms,
Anode material for alkaline metal ion batteries. After holding the negative electrode material for 120 hours under conditions of a temperature of 40 ° C. and a relative humidity of 90% RH,
The negative electrode material is preliminarily dried by holding it at a temperature of 130 ° C. for 1 hour under a nitrogen atmosphere, and then the moisture generated by holding the negative electrode material after the preliminary drying at 200 ° C. for 30 minutes is Karl Fischer. When measured by coulometric titration,
The amount of water generated from the negative electrode material after the preliminary drying is 0.01 wt% or more and 0.20 mass% or less with respect to 100 mass% of the negative electrode material after the preliminary drying. The negative electrode material described in 1. About a half cell produced using a negative electrode material formed as the negative electrode, metallic lithium as the counter electrode, and LiPF ₆ dissolved in a carbonate solvent at a rate of 1 M as the electrolyte,
Charge at 25 ° C under the conditions of a charging current of 25 mA / g, a charging voltage of 0 mV, and a charging end current of 2.5 mA / g by the constant current constant voltage method, and then a discharge current of 25 mA / g and a discharge end voltage of 2.5 V. The negative electrode material according to claim 1, wherein a discharge capacity when discharged by a constant current method is 360 mAh / g or more. After embedding the negative electrode material with an epoxy resin and curing the epoxy resin, the obtained cured product is cut and polished to expose a cross section of the negative electrode material, and then the cross section using an optical microscope Is observed in bright field at a magnification of 1000 times,
The negative electrode material according to claim 1, wherein the cross section of the negative electrode material has a first region and a second region having different reflectivities.   The negative electrode material according to any one of claims 1 to 4, wherein an adsorption amount of carbon dioxide gas is 0.05 ml / g or more and less than 10 ml / g.   The negative electrode material according to any one of claims 1 to 5, wherein the pore diameter determined by mercury porosimetry is 0.003 µm or more and 5 µm or less and the pore volume is less than 0.55 ml / g.   A negative electrode active material comprising the negative electrode material according to claim 1.   The negative electrode active material according to claim 7, further comprising a negative electrode material of a type different from the negative electrode material.   The negative electrode active material according to claim 8, wherein the different types of the negative electrode materials are graphite materials. A negative electrode active material layer comprising at least the negative electrode active material according to any one of claims 7 to 9,
A negative electrode current collector;
Are laminated in this order, and the negative electrode for alkaline metal ion batteries.   An alkali metal ion battery comprising at least the negative electrode for an alkali metal ion battery according to claim 10, an electrolyte, and a positive electrode. The alkali metal ion battery according to claim 11, which is a lithium ion battery or a sodium ion battery.