U.S. patent application number 11/574423 was filed with the patent office on 2009-08-27 for negative electrode material for nonaqueous secondary cells, negative electrode for nonaqueous secondary cells, and nonaqueous secondary cell.
This patent application is currently assigned to MITSUBISHI CHEMICAL CORPORATION. Invention is credited to Nobuyuki Onishi, Hideharu Satoh, Keita Yamaguchi.
Application Number | 20090214954 11/574423 |
Document ID | / |
Family ID | 36000028 |
Filed Date | 2009-08-27 |
United States Patent
Application |
20090214954 |
Kind Code |
A1 |
Onishi; Nobuyuki ; et
al. |
August 27, 2009 |
NEGATIVE ELECTRODE MATERIAL FOR NONAQUEOUS SECONDARY CELLS,
NEGATIVE ELECTRODE FOR NONAQUEOUS SECONDARY CELLS, AND NONAQUEOUS
SECONDARY CELL
Abstract
A negative electrode material for a nonaqueous secondary battery
capable of realizing a nonaqueous secondary battery having a small
charging/discharging irreversible capacity at an initial cycle,
exhibiting an excellent high-rate charging/discharging
characteristics and an excellent cycle performances, and having no
electrodeposition problem is provided. The main component of the
material is graphite particles. The median diameter of the graphite
particles is 5 .mu.m or more, and 40 .mu.m or less in the
volume-basis particle size distribution based on the laser
diffraction/scattering particle size distribution measurement. The
tapping density of the negative electrode material is 0.7
g/cm.sup.3 or more. The specific surface area measured by a BET
method is 0.2 m.sup.2/g or more, and 8 m.sup.2/g or less. When an
electrode is produced from the negative electrode material by a
predetermined method for manufacturing an electrode, and the
surface of the resulting electrode is measured with a laser shape
measurement microscope, the skewness (Rsk) prescribed by JIS B 0601
of the surface roughness curve is -1.7 or more, and 0 or less.
Inventors: |
Onishi; Nobuyuki; (Kagawa,
JP) ; Satoh; Hideharu; (Ibaraki, JP) ;
Yamaguchi; Keita; (Mie, JP) |
Correspondence
Address: |
OBLON, SPIVAK, MCCLELLAND MAIER & NEUSTADT, P.C.
1940 DUKE STREET
ALEXANDRIA
VA
22314
US
|
Assignee: |
MITSUBISHI CHEMICAL
CORPORATION
Minato-ku ,Tokyo
JP
TOKAI CARBON CO., LTD
Minato-ku , Tokyo
JP
|
Family ID: |
36000028 |
Appl. No.: |
11/574423 |
Filed: |
August 30, 2005 |
PCT Filed: |
August 30, 2005 |
PCT NO: |
PCT/JP2005/015755 |
371 Date: |
December 24, 2008 |
Current U.S.
Class: |
429/231.8 |
Current CPC
Class: |
H01M 4/0435 20130101;
H01M 10/0525 20130101; H01M 2004/021 20130101; Y02E 60/10 20130101;
H01M 4/0409 20130101; H01M 4/0404 20130101; H01M 4/587 20130101;
H01M 4/1393 20130101 |
Class at
Publication: |
429/231.8 |
International
Class: |
H01M 4/58 20060101
H01M004/58 |
Foreign Application Data
Date |
Code |
Application Number |
Aug 30, 2004 |
JP |
2004-250415 |
Claims
1. A negative electrode material, which contains graphite particles
as a main component, for a nonaqueous secondary battery,
characterized in that: the median diameter of the graphite
particles is 5 .mu.m or more, and 40 .mu.m or less in the
volume-basis particle size distribution based on the laser
diffraction/scattering particle size distribution measurement; the
tapping density is 0.7 g/cm.sup.3 or more; the specific surface
area measured by a BET method is 0.2 m.sup.2/g or more, and 8
m.sup.2/g or less; and when an electrode is produced from the
negative electrode material by the following method for
manufacturing an electrode and the surface of the resulting
electrode is measured with a laser shape measurement microscope,
the skewness (Rsk), which is prescribed by JIS B 0601, of the
surface roughness curve is -1.7 or more, and 0 or less, [Method for
Manufacturing Electrode] a slurry is prepared by adding 1 part by
weight of aqueous dispersion of styrene-butadiene rubber in terms
of solid content and 1 part by weight of carboxymethyl cellulose
(molecular weight 250,000 to 300,000) aqueous solution in terms of
solid content to 100 parts by weight of the negative electrode
material, the resulting slurry is applied to a current collector
formed from copper foil having a thickness of 18 .mu.m by using a
doctor blade in such a way that 10.+-.0.1 mg/cm.sup.2 of the
negative electrode material in terms of weight after drying is
adhered, followed by drying, and consolidation is performed by
pressing once with a roll press (calender) while a press load is
adjusted in such a way that the electrode density (exclusive of the
copper foil) becomes 1.63.+-.0.03 g/cm.sup.3.
2. The negative electrode material for a nonaqueous secondary
battery according to claim 1, wherein the negative electrode
material comprises graphite granulated particles, in which a
plurality of carbonaceous particles are bonded to each other, as a
main component.
3. The negative electrode material for a nonaqueous secondary
battery according to claim 1, characterized in that when an
electrode is produced from the negative electrode material by the
following method for manufacturing an electrode, the press load is
350 kgf or more, and 1,800 kgf or less relative to the length of 5
cm, [Method for Manufacturing Electrode] a slurry is prepared by
adding 1 part by weight of aqueous dispersion of styrene-butadiene
rubber in terms of solid content and 1 part by weight of
carboxymethyl cellulose (molecular weight 250,000 to 300,000)
aqueous solution in terms of solid content to 100 parts by weight
of the negative electrode material, the resulting slurry is applied
to a current collector formed from copper foil having a thickness
of 18 .mu.m by using a doctor blade in such a way that 10.+-.0.1
mg/cm.sup.2 of the negative electrode material in terms of weight
after drying is adhered, followed by drying, and consolidation is
performed by pressing once with a roll press (calender) while a
press load is adjusted in such a way that the electrode density
(exclusive of the copper foil) becomes 1.63.+-.0.03 g/cm.sup.3.
4. The negative electrode material for a nonaqueous secondary
battery according to claim 1, characterized in that when an
electrode is produced from the negative electrode material by the
following method for manufacturing an electrode, the liquid
immersion speed, which is measured by the following method, of the
resulting electrode is 400 seconds/.mu.l or less, [Method for
Manufacturing Electrode] a slurry having a solid concentration of
50% is prepared by adding 1 part by weight of aqueous dispersion of
styrene-butadiene rubber in terms of solid content and 1 part by
weight of carboxymethyl cellulose (molecular weight 250,000 to
300,000) aqueous solution in terms of solid content to 100 parts by
weight of the negative electrode material, the resulting slurry is
applied to a current collector formed from copper foil having a
thickness of 18 .mu.m by using a doctor blade in such a way that
10.+-.0.1 mg/cm.sup.2 of the negative electrode material in terms
of weight after drying is adhered, followed by drying, and
consolidation is performed by pressing once with a roll press
(calender) while a press load is adjusted in such a way that the
electrode density (exclusive of the copper foil) becomes
1.63.+-.0.03 g/cm.sup.3, and [Method for Measuring Liquid Immersion
Speed] a microsyringe having a capacity of 5 .mu.l is used, the
following electrolytic solution A is dropped on the electrode from
the height of 5 mm, and the time elapsed from the dropping until
the electrolytic solution is eliminated is measured, where the
electrolytic solution elimination point is assumed to be the point
when visual identification of the boundary between a surface in
contact with the electrolytic solution and a surface not in contact
with the electrolytic solution becomes impossible, composition of
electrolytic solution A: 1.0 mol/l of LiPF.sub.6 is dissolved in a
mixed solvent of 30 percent by weight of ethylene carbonate and 70
percent by weight of ethyl methyl carbonate.
5. The negative electrode material for a nonaqueous secondary
battery according to claim 1, characterized in that when an
electrode is produced from the negative electrode material by the
following method for manufacturing an electrode, and a nonaqueous
secondary battery is prepared by the following method for
manufacturing a nonaqueous secondary battery through the use of the
resulting electrode as a negative electrode, the capacity
maintenance factor after 200 cycles of charging and discharging,
which is measured by the following measuring method, of the
resulting nonaqueous secondary battery is 70% or more, [Method for
Manufacturing Electrode] a slurry having a solid concentration of
50% is prepared by adding 1 part by weight of aqueous dispersion of
styrene-butadiene rubber in terms of solid content and 1 part by
weight of carboxymethyl cellulose (molecular weight 250,000 to
300,000) aqueous solution in terms of solid content to 100 parts by
weight of the negative electrode material, the resulting slurry is
applied to a current collector formed from copper foil having a
thickness of 18 .mu.m by using a doctor blade in such a way that
10.+-.0.1 mg/cm.sup.2 of the negative electrode material in terms
of weight after drying is adhered, followed by drying, and
consolidation is performed by pressing once with a roll press
(calender) while a press load is adjusted in such a way that the
electrode density (exclusive of the copper foil) becomes
1.63.+-.0.03 g/cm.sup.3, [Method for Manufacturing Nonaqueous
Secondary Battery] Aluminum foil of 40 mm length, 30 mm width, and
15 .mu.m thickness coated with LiCoO.sub.2 on both surfaces is used
as a positive electrode, an electrode for a negative electrode is
cut into a rectangle of 42 mm length and 32 mm width, an
electrolytic solution prepared by dissolving LiPF.sub.6 into a
mixed solvent of ethylene carbonate and ethyl methyl carbonate
(volume ratio=1:1) in such a way that the content becomes 1.0 mol/l
is used, the negative electrodes are disposed on both surfaces of
the positive electrode with polyethylene film separators
therebetween so as to prepare a laminate, and the resulting
laminate and the electrolytic solution are enclosed in a laminate
film so as to prepare a laminate film inclusion type nonaqueous
secondary battery, and [Method for Measuring Capacity Maintenance
Factor after 200 Cycles of Charging and Discharging] the resulting
laminate film inclusion type nonaqueous secondary battery is stood
for 24 hours, charging is performed at a current density of 49
mA/cm.sup.2 until the potential difference between the two
electrodes becomes 4.2 V, an operation, in which discharge is
performed at 70 mA/cm.sup.2 until the potential difference becomes
3.0 V as one cycle, is repeated, the discharge capacity at 206th
cycle is divided by the discharge capacity at 6th cycle, the
resulting value is expressed as a percentage (capacity maintenance
factor %), the capacity maintenance factor of each of three
laminate film inclusion type nonaqueous secondary batteries is
determined in the same manner, and the average value is taken as
the cycle capacity maintenance factor after 200 cycles of charging
and discharging.
6. A negative electrode for a nonaqueous secondary battery,
characterized in that a negative electrode active material layer,
which contains the negative electrode material according to claim 1
as an active material, is disposed on a current collector.
7. A nonaqueous secondary battery characterized by comprising a
positive electrode capable of absorbing and emitting lithium ions,
a negative electrode capable of absorbing and emitting lithium
ions, and an electrolyte, wherein the negative electrode for a
nonaqueous secondary battery according to claim 6 is used as the
negative electrode.
Description
TECHNICAL FIELD
[0001] The present invention relates to a negative electrode
material to be used for a nonaqueous secondary battery, a negative
electrode including this negative electrode material, and a
nonaqueous secondary battery including this negative electrode.
BACKGROUND ART
[0002] In recent years, as electronic apparatuses have been
miniaturized, demands for high-capacity secondary batteries have
been increased. In particular, nonaqueous secondary batteries
exhibiting a higher energy density as compared with those of
nickel-cadmium cells and nickel metal-hydride batteries have been
noted. Heretofore, metals, graphite, and the like have been studied
as negative electrode active materials of nonaqueous secondary
batteries. However, metal electrodes have problems in that when
charge and discharge are repeated, lithium is deposited on
electrodes dendritically and, finally, two electrodes are
short-circuited. Therefore, carbon materials, in particular,
graphite, have been noted because no lithium metal is deposited in
a charge and discharge process.
[0003] However, there are problems in that since graphite is a flat
crystal, graphite tends to be oriented parallel to the current
collector in the electrode and, thereby, a high-rate
charging/discharging characteristics tends to deteriorate; and
since the expansion of the electrode in the charging/discharging
cycle is significant, a cycle performances tends to
deteriorate.
[0004] According to the proposal in Japanese Unexamined Patent
Application Publication No. 10-188959, graphite granulated
particles, in which a plurality of graphite particles are bonded in
such a way that the oriented faces become not parallel to each
other, are used and, thereby, expansion in a thickness direction of
the electrode is suppressed and the high-rate charging/discharging
characteristics and the cycle performances are improved.
[0005] However, the graphite granulated particles described in this
patent document have problems in that the performance as a negative
electrode material for a lithium ion secondary battery, in
particular, a reduction of the irreversible capacity and an
improvement of the cycle performances are not always adequate. The
cause of these problems is not certain, but it is believed that in
the graphite granulated particles described in the above-described
patent document, amorphous portions are small, the binding force
between graphite particles are too weak, and the electrode surface
becomes in the state, in which no gap is present, when pressing is
performed in an electrode formation step. If graphitization of the
graphite granulated particles excessively proceeds, there is a
tendency of the characteristic, in particular the liquid immersion
property, in the preparation of secondary battery to become
inadequate.
[0006] If amorphous portions are large, there is a problem in that
it is hard to press. When the pressing is performed forcedly and
crushing occurs, the loss is increased, and it is difficult to
produce a high-capacity cell.
[0007] As described above, heretofore, a negative electrode
material composed of graphite granulated particles, which satisfy
all the low irreversible capacity, the high cycle performances, and
the high liquid immersion property, have not been realized.
DISCLOSURE OF INVENTION
[0008] It is an object of the present invention to provide a
negative electrode material formed from graphite particles having
these performances improved, a negative electrode formed from this
material, and a nonaqueous secondary battery including this
negative electrode.
[0009] A negative electrode material for a nonaqueous secondary
battery according to an aspect of the present invention contains
graphite particles, in which a plurality of graphite particles are
bonded to each other, as a main component.
[0010] The median diameter of the graphite particles is 5 .mu.m or
more, and 40 .mu.m or less in the volume-basis particle size
distribution based on the laser diffraction/scattering particle
size distribution measurement. The tapping density of the material
is 0.7 g/cm.sup.3 or more, and the specific surface area measured
by a BET method is 0.2 m.sup.2/g or more, and 8 m.sup.2/g or
less.
[0011] When an electrode is produced from the negative electrode
material by the following method for manufacturing an electrode and
the surface of the resulting electrode is measured with a laser
shape measurement microscope, the skewness (Rsk) prescribed by JIS
B 0601 of the surface roughness curve is -1.7 or more, and 0 or
less.
[Method for Manufacturing Electrode]
[0012] A slurry is prepared by adding 1 part by weight of aqueous
dispersion of styrene-butadiene rubber in terms of solid content
and 1 part by weight of carboxymethyl cellulose (molecular weight
250,000 to 300,000) aqueous solution in terms of solid content to
100 parts by weight of the above-described negative electrode
material, the resulting slurry is applied to a current collector
formed from copper foil having a thickness of 18 .mu.m by using a
doctor blade in such a way that 10.+-.0.1 mg/cm.sup.2 of the
negative electrode material in terms of weight after drying is
adhered, followed by drying, and consolidation is performed by
pressing once with a roll press (calender) while a press load is
adjusted in such a way that the electrode density (exclusive of the
copper foil) becomes 1.63.+-.0.03 g/cm.sup.3.
[0013] Hereafter, this method may be referred to as "a
predetermined method for manufacturing an electrode". An electrode
prepared by this predetermined method for manufacturing an
electrode may be referred to as "a predetermined electrode of the
present invention".
[0014] When a negative electrode material for a nonaqueous
secondary battery according to an aspect of the present invention
(hereafter may be referred to as "a negative electrode material of
the present invention") is used, a negative electrode for a
nonaqueous secondary battery having a small charging/discharging
irreversible capacity at an initial cycle and exhibiting an
excellent high-rate charging/discharging characteristics and an
excellent cycle performances is provided.
BRIEF DESCRIPTION OF THE DRAWINGS
[0015] FIG. 1 is an explanatory diagram of skewness, and is a
diagram showing the relationship between the surface roughness
curve and the probability density function, where A represents the
surface roughness curve in which valley portions are wider than
peak portions, and B represents the surface roughness curve in
which peak portions are wider than valley portions.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0016] The preferred embodiments of the present invention will be
described below in detail. However, the following description is an
example of the present invention, and the present invention is not
limited to the contents thereof.
[0017] [1] Negative Electrode Material for Nonaqueous Secondary
Battery
(1) Graphite Particles in Negative Electrode Material
[0018] The main component of the negative electrode material of the
present invention is graphite particles. In these graphite
particles, usually, it is preferable that carbonaceous particles
are bonded by and/or covered with a heat-treated binder which can
be graphitized.
[0019] Examples of carbonaceous particles constituting the graphite
particles include natural graphite, artificial graphite, a coke
powder, a needle coke powder, and a carbonaceous powder, e.g., a
powder of carbonized resin, which can be graphitized by firing.
Among them, it is particularly preferable that natural graphite or
a needle coke powder is used in the present invention.
[0020] It is essential only that the binder is carbonaceous and
graphitizable, and preferably, petroleum based and coal based
condensed polycyclic aromatics, from soft pitch to hard pitch, are
used.
[0021] Graphite granulated particles are characterized in that the
oriented faces are not parallel to each other, because carbonaceous
particles, which are primary particles, are bonded by a graphitized
carbonaceous material derived from a binder in such a way that the
crystalline directions are oriented at random in the
microstructure.
[0022] In the process in which the graphite particles are prepared
by a manufacturing method described below, usually, bonding of a
plurality of graphite particles by a binder, that is, granulation,
does not perfectly proceed. Therefore, particles, e.g., layered
structure particles, each of which is no more than a single
carbonaceous particle covered with the binder, and particles, which
are no more than produced by carbonization or graphitization of the
binder itself without containing a carbonaceous particle, are also
generated in addition to the graphite particles.
(2) Properties of Negative Electrode Material
[0023] Median Diameter
[0024] The median diameter of the graphite particles constituting
the negative electrode material of the present invention is 5 .mu.m
or more, preferably is 8 .mu.m or more, and further preferably is
10 .mu.m or more in the volume-basis particle size distribution
based on the laser diffraction/scattering particle size
distribution measurement. If the median diameter is too small, the
specific surface area is increased, and the strength of the
resulting electrode tends to become low. In pulverization to such a
diameter, the time required for the pulverization is increased and,
therefore, there is no economy.
[0025] The median diameter of the graphite particles is 40 .mu.m or
less, preferably is 35 .mu.m or less, and further preferably is 30
.mu.m or less. If the median diameter exceeds this upper limit,
when the graphite particles are used as the negative electrode
material, the unevenness occurs on the electrode surface, and a
separator used in the cell tends to be damaged.
[0026] In the present invention, the volume-basis particle size
distribution based on the laser diffraction/scattering particle
size distribution measurement is measured by the following
method.
[0027] <Method for Measuring Volume-Basis Particle Size
Distribution>
[0028] A negative electrode material is suspended in 10 ml of
0.2-percent by weight aqueous solution of surfactant
(polyoxyethylene sorbitan monolaurate, for example, Tween 20
(registered trade mark)). The suspension is introduced into a
commercially available laser diffraction/scattering particle size
distribution measurement apparatus. An ultrasonic wave of 28 kHz is
applied at an output of 60 W for 1 minute and, thereafter, a
measurement is performed.
[0029] Tapping Density
[0030] The tapping density of the negative electrode material of
the present invention is 0.7 g/cm.sup.3 or more. Preferably the
tapping density is 0.75 g/cm.sup.3 or more, furthermore 0.80
g/cm.sup.3 or more, and particularly 0.9 g/cm.sup.3 or more. The
tapping density is preferably 1.2 g/cm.sup.3 or less.
[0031] If the tapping density is too low, the slurry concentration
of the negative electrode material to be applied to a current
collector must be reduced in the preparation of the negative
electrode. Consequently, the density of a coating film is decreased
and graphite particles tend to be broken when being pressed, so
that the cell performance deteriorates. On the contrary, a high
tapping density is preferable for the cell performance. However,
further step is required for adjusting the shape and the particle
size distribution of the graphite particles, so that the yield is
decreased and the cost is increased.
[0032] In the present invention, the tapping density is measured by
the following method.
[0033] <Method for Measuring Tapping Density>
[0034] A powder density measuring apparatus ("TAP DENSER KYT-4000"
produced by Seishin Enterprise Co., Ltd.) is used. The negative
electrode material is dropped into a 20-cm.sup.3 cylindrical tap
cell through a sieve with an opening of 300 .mu.m until the cell
becomes full of the negative electrode material. Thereafter,
tapping with a stroke length of 10 mm was performed 1,000 times,
and the tapping density at that time is measured.
[0035] Specific Surface Area Based on BET Method
[0036] The specific surface area, which is measured by a BET
method, of the negative electrode material of the present invention
is usually 0.2 m.sup.2/g or more, and preferably is 0.3 m.sup.2/g
or more. The upper limit thereof is usually 8 m.sup.2/g or less,
preferably 6 m.sup.2/g or less, and particularly preferably 4
m.sup.2/g or less. If the value of the specific surface area is
smaller than this range, the output characteristic tends to
deteriorate. If the value of the specific surface area exceeds this
range, the initial irreversible capacity is increased and the cycle
performances tends to deteriorate.
[0037] In the present invention, the specific surface area is
measured by the following method, for example.
[0038] <Method for Measuring Specific Surface Area>
[0039] A specific surface area measuring apparatus "AMS8000"
produced by OHKURA RIKEN CO., LTD., is used, and the measurement is
performed by a BET one point method based on a flow method through
the use of nitrogen gas absorption. Specifically, about 0.4 g of
sample (negative electrode material) is filled in a cell, and
pretreatment is performed by heating up to 350.degree. C.
Thereafter, cooling to a liquid nitrogen temperature is performed
so that a gas composed of 30% of nitrogen and 70% of He is adsorbed
to saturation. Subsequently, heating is performed up to room
temperature, the amount of desorbed gas is measured, and the
specific surface area is calculated from the obtained results by a
common BET method.
[0040] Skewness
[0041] When an electrode is prepared from the negative electrode
material of the present invention by the above-described
predetermined method for manufacturing an electrode and the surface
of the resulting electrode (hereafter may be referred to as "a
predetermined electrode of the present invention") is measured with
a laser shape measurement microscope, the skewness (Rsk), which is
prescribed by JIS B 0601, of the surface roughness curve is -1.7 or
more, preferably is -1.5 or more, particularly preferably is -1.3
or more, and 0 or less, preferably is -0.3 or less.
[0042] The skewness (Rsk) represents the asymmetry of the surface
roughness curve. An example thereof will be described below with
reference to FIG. 1.
[0043] With respect to the roughness curve in which valley portions
are wider than peak portions, as shown in FIG. 1 A, the
distribution form of the probability density function is leaning to
the valley side. As this tendency is significant, the skewness
takes on a large positive value. Conversely, with respect to the
roughness curve in which peak portions are wider than valley
portions, as shown in FIG. 1 B, the distribution form of the
probability density function is leaning to the peak side, and the
skewness takes on a large negative value.
[0044] With respect to the surface roughness curve of the
electrode, the value of skewness represents the resistance to
crushing of the negative electrode material of the electrode. That
is, a large positive skewness indicates that the surface shape of
the electrode is maintained after pressing, and represents that the
negative electrode material is resistant to crushing. On the
contrary, a large negative skewness represents that the negative
electrode material is vulnerable to crushing.
[0045] When the skewness is within the range specified by the
present invention, the negative electrode material of the electrode
tends to be crushed appropriately, and crushing of diffusion paths
of lithium ions and the like due to excessive crushing is avoided.
Therefore, excellent Rate performances and the like can be
exhibited.
[0046] Graphite Crystal Orientation Ratio on Electrode
[0047] With respect to the predetermined electrode of the present
invention prepared by the above-described predetermined method for
manufacturing an electrode by using the negative electrode material
of the present invention, it is preferable that the graphite
crystal orientation ratio I.sub.110/I.sub.004 on the electrode,
measured by the following method, is within the range of 0.02 or
more, most of all 0.03 or more, and furthermore 0.04 or more, and
0.20 or less, most of all 0.18 or less, and furthermore 0.16 or
less. If the orientation ratio I.sub.110/I.sub.004 is lower than
the above-described range, when a cell is prepared, the electrode
expansion during charging of the cell is increased, the cell
capacity per unit volume of the electrode is hard to be increased,
and furthermore, the cycle performances tends to deteriorate due
to, for example, falling out of active material resulting from
expansion and shrinkage during a cycle test. On the other hand, if
the orientation ratio I.sub.110/I.sub.004 exceeds the
above-described range, it becomes difficult to increase the filling
density of the electrode after pressing.
[0048] Here, the graphite crystal orientation ratio
I.sub.110/I.sub.004 on the electrode is an index representing the
degree of orientation of the graphite crystal hexagonal network in
the thickness direction of the electrode. As the orientation ratio
I.sub.110/I.sub.004 is increased, the state, in which the
directions of graphite crystal hexagonal networks of particles are
not aligned, is indicated.
[0049] <Method for Measuring Graphite Crystal Orientation Ratio
on the Electrode>
[0050] With respect to the predetermined electrode of the present
invention, a chart of the (110) face and the (004) face of graphite
on the electrode is obtained by X-ray diffraction. With respect to
the resulting chart, peak separation is performed by fitting
through the use of asymmetric Pearson VII as the profile function,
and the integrated intensities of the peaks of the (110) face and
the (004) face are calculated. A ratio represented by (110) face
integral intensity/(004) face integral intensity is calculated from
the resulting integrated intensities, and the ratio is defined as a
graphite crystal orientation ratio on the electrode.
[0051] Here, the X-ray diffraction measurement conditions are as
described below, where "2.theta." represents a diffraction
angle.
[0052] Target: Cu(K.alpha. ray) graphite monochromator
[0053] Slit: divergence slit=1 degree, light receiving slit=0.1 mm,
scattering slit=1 degree
[0054] Measurement range, and step angle/measurement time:
TABLE-US-00001 (110) face: 76.5 degrees .ltoreq. 2.theta. .ltoreq.
78.5 degrees 0.01 degrees/3 seconds (004) face: 53.5 degrees
.ltoreq. 2.theta. .ltoreq. 56.0 degrees 0.01 degrees/3 seconds
[0055] Sample preparation: a predetermined electrode is fixed to a
glass plate of 0.1 mm thickness with a double-faced tape
[0056] Press Load
[0057] When the predetermined electrode of the present invention is
prepared from the negative electrode material of the present
invention by the above-described predetermined method for
manufacturing an electrode, the press load is preferably 350 kgf or
more, particularly 400 kgf or more, and most of all 450 kgf or more
relative to the length of 5 cm, and preferably 1,800 kgf or less,
particularly 1,500 kgf or less, and most of all 1,200 kgf or
less.
[0058] If the press load is lower than this range, the negative
electrode material may be vulnerable to crushing, the electrode
density may be hard to control, the liquid immersion property may
deteriorate when an electrode is prepared, and the liquid immersion
speed may be decreased. Furthermore, paths of lithium ions may be
blocked due to crushing of the negative electrode material, and the
Rate performances may deteriorate. If the press load exceeds this
upper limit, peeling from the electrode tends to increase, and a
pressing apparatus having a higher performance is required, so that
it is not preferable from the view point of production.
[0059] Liquid Immersion Speed
[0060] When the predetermined electrode of the present invention is
prepared from the negative electrode material of the present
invention by the above-described predetermined method for
manufacturing an electrode, the liquid immersion speed measured by
the following method is preferably 10 seconds/.mu.l or more, and
preferably is 400 seconds/.mu.l or less, further preferably is 200
seconds/.mu.l or less.
[0061] If the liquid immersion speed exceeds this upper limit, the
productivity in the cell production tends to be decreased.
[0062] <Method for Measuring Liquid Immersion Speed>
[0063] A microsyringe having a capacity of 5 .mu.l is used, the
following electrolytic solution A is dropped on the electrode from
the height of 5 mm, and the time elapsed from the dropping until
the electrolytic solution is eliminated is measured. The
electrolytic solution elimination point is assumed to be the point
when visual identification of the boundary between a surface in
contact with the electrolytic solution and a surface not in contact
with the electrolytic solution becomes impossible.
[0064] Composition of electrolytic solution A: 1.0 mol/l of
LiPF.sub.6 is dissolved in a mixed solvent of 30 percent by weight
of ethylene carbonate and 70 percent by weight of ethyl methyl
carbonate.
[0065] Capacity Maintenance Factor after 200 Cycles of Charging and
Discharging
[0066] When the predetermined electrode of the present invention is
prepared from the negative electrode material of the present
invention by the above-described predetermined method for
manufacturing an electrode, and a nonaqueous secondary battery is
prepared by the following method for manufacturing a nonaqueous
secondary battery through the use of the resulting electrode as the
negative electrode, preferably, the capacity maintenance factor
after 200 cycles of charging and discharging, which is measured by
the following measuring method, of the resulting nonaqueous
secondary battery is 70% or more, most of all 80% or more,
furthermore 85% or more, and particularly 90% or more.
[0067] <Method for Manufacturing Nonaqueous Secondary
Battery>
[0068] Aluminum foil of 40 mm length, 30 mm width, and 15 .mu.m
thickness coated with LiCoO.sub.2 on both surfaces is used as a
positive electrode, a predetermined electrode of the present
invention is cut into a rectangle of 42 mm length and 32 mm width,
an electrolytic solution prepared by dissolving LiPF.sub.6 into a
mixed solvent of ethylene carbonate and ethyl methyl carbonate
(volume ratio=1:1) in such a way that the content becomes 1.0 mol/l
is used, and the negative electrodes are disposed on both surfaces
of the positive electrode with polyethylene film separators
therebetween so as to prepare a laminate. The resulting laminate
and the electrolytic solution are enclosed in a laminate film so as
to prepare a laminate film inclusion type nonaqueous secondary
battery
[0069] <Method for Measuring Capacity Maintenance Factor after
200 Cycles of Charging and Discharging>
[0070] The resulting laminate film inclusion type nonaqueous
secondary battery is stood for 24 hours, charging is performed at a
current density of 49 rmA/cm.sup.2 until the potential difference
between the two electrodes becomes 4.2 V, and an operation, in
which discharge is performed at 70 mA/cm.sup.2 until the potential
difference becomes 3.0 V as one cycle, is repeated. The discharge
capacity at 206th cycle is divided by the discharge capacity at 6th
cycle, and the resulting value is expressed as a percentage
(capacity maintenance factor %). The capacity maintenance factor of
each of three laminate film inclusion type nonaqueous secondary
batteries is determined in the same manner, and the average value
is taken as the cycle capacity maintenance factor after 200 cycles
of charging and discharging.
[0071] Total Number
[0072] With respect to the negative electrode material of the
present invention, preferably, the total number of particles
determined in number-basis equivalent circle diameter distribution
measurement based on the above-described flow particle image
analysis is 30.times.10.sup.6/g or less, and 25.times.10.sup.6/g or
less is particularly preferable. In general, a large total number
of particles refers to that the amount of fine particles is large,
and the initial charging/discharging irreversible capacity, the
cycle performances of the cell, and the like tend to deteriorate.
It is favorable that the total number of particles is minimized.
However, 1.times.10.sup.6/g or more is preferable from the view
point of the cost and the operability.
[0073] d.sub.90/d.sub.10
[0074] With respect to the negative electrode material of the
present invention, preferably, the ratio (d.sub.90/d.sub.10) of the
particle size (d.sub.90) at the cumulative volume fraction of 90%
to the particle size (d.sub.10) at the cumulative volume fraction
of 10% is 5 or less in the particle size-basis volume distribution
based on the laser diffraction/scattering particle size
distribution measurement.
[0075] The d.sub.90/d.sub.10 represents the spreading of the
particle size distribution, and as this ratio is decreased, the
particle size distribution becomes narrow. In the present
invention, preferably, the d.sub.90/d.sub.10 is 4 or less. With
respect to the negative electrode material containing graphite
particles as a main component, a large d.sub.90/d.sub.10 indicates
that the particle size distribution is spread, and it is indicated
that many fine particles and coarse particles are present, in
particular, many fine particles are present. If many fine particles
are present, the following problems occur:
i) the specific surface area is increased and, thereby, the initial
charging/discharging irreversible capacity is increased, ii) fine
particles adsorbed by the binder for molding the electrode, the
binder being added in preparation of the negative electrode, are
filled in gaps between particles so as to block communicating holes
serving as diffusion paths of lithium ions and, thereby, a
high-rate charging/discharging characteristics deteriorates, and
iii) an increase of the specific surface area and blocking of the
communicating holes allow the cycle performances to further
deteriorate. Preferably, the d.sub.90/d.sub.10 is 2 or more from
the view point of the operation to adjust the particle size
distribution and the yield.
[0076] When the d.sub.90/d.sub.10 is within the above-described
range, there are advantages that the effect of the binder for
molding the electrode can be effectively exerted and the strength
of the negative electrode can be improved. When coarse particles
are reduced, it is possible to avoid the problem in that a
separator used in a cell tends to be damaged due to an occurrence
of unevenness on the electrode surface in the step of preparing the
negative electrode by application of a slurry of the negative
electrode material to the current collector.
[0077] A/B
[0078] With respect to the negative electrode material of the
present invention, in the equivalent circle diameter distribution
measurement based on the above-described flow particle image
analysis, preferably, the ratio (A/B) of an average frequency (A)
in the range from the smallest equivalent circle diameter up to
cumulative frequency of 20%+/-5% to an average frequency (B) in the
range from the smallest equivalent circle diameter up to cumulative
frequency of 80%+/-5% is 1.2 to 8.0.
[0079] According to the study of the inventors of the present
invention, with respect to the negative electrode material
containing graphite particles as a main component, it has been made
clear that particles in a small particle size portion, which have
exerted almost no influence on the above-described particle
size-basis cumulative volume distribution, have exerted influences
on the initial charging/discharging irreversible capacity, the
high-rate charging/discharging characteristics, the cycle
performances, and the like. The ratio (A/B) in the above-described
flow particle image analysis is an index representing the feature
of this small particle size portion, and is the index based on the
number of particles. Therefore, the ratio can appropriately
represent the feature of the small particle size portion. The A/B
is a ratio of the frequency at the cumulative frequency of 20% from
the smallest equivalent circle diameter to the frequency at the
cumulative frequency of 80%, and it is increased as the proportion
of fine particles having small diameters is increased.
[0080] The value of A/B is not specifically limited. However, a
smaller value is preferable from the view point of the cell
performance. It is preferably 1.2 or more, more preferably 1.3 or
more, more preferably 1.4 or more, further preferably 1.5 or more,
and particularly preferably 1.6 or more, and preferably 8.0 or
less, more preferably 7.0 or less, and further preferably 6.0 or
less from the view point of the cost of particle size adjustment
and the yield in preparation of graphite particles.
[0081] As the A/B is increased, the irreversible capacity is
increased, and the high-rate charging/discharging characteristics
and the cycle performances of the cell deteriorate. The reason the
high-rate charging/discharging characteristics and the cycle
performances of the cell become favorable when the A/B is within
the above-described range is not certain, but in consideration of
the fact that the A/B exceeds the above-described range, it is
estimated that the graphite particles contain large amounts of fine
particles or binding between graphite particles with each other is
weak and particles are broken by the ultrasonic irradiation in the
measurement. In the former case, it is believed that the presence
itself of the large amounts of fine particles increases the initial
irreversible capacity and causes deterioration of the high-rate
charging/discharging characteristics and the cycle performances of
the cell. In the latter case, it is estimated that in a pressing
step which is one of steps of working graphite particles into a
nonaqueous secondary battery negative electrode, graphite particles
present on the surface of the negative electrode are broken and
block communicating holes serving as diffusion paths of lithium
ions, so that the deterioration of the high-rate
charging/discharging characteristics and the deterioration of the
cycle performances are caused.
[0082] The number-basis equivalent circle diameter distribution for
obtaining the A/B is measured based on the above-described flow
particle image analysis.
[0083] Ra
[0084] When the predetermined electrode of the present invention is
prepared from the negative electrode material of the present
invention by the above-described predetermined method for
manufacturing an electrode, the surface roughness (Ra) is
preferably 0.1 or more, more preferably 0.2 or more, and preferably
1.2 or less, more preferably 1 or less.
[0085] If the surface roughness is less than this range, the
electrode is too flat and, thereby, the liquid immersion property
may deteriorate. If the surface roughness exceeds this range, the
cell capacity tends to be decreased because the active material
density in the cell cannot be increased.
[0086] The surface roughness can be measured in a manner similar to
that for the above-described skewness.
[0087] d(002) and Lc(002)
[0088] With respect to the negative electrode material of the
present invention, the value of d(002) based on the X-ray
diffraction analysis is 0.3359 nm or less, preferably is 0.3356 nm
or less, and 0.3354 nm, which is the value of highly crystalline
graphite, or more is desirable. If the d(002) is too large, the
crystallinity is inadequate to serve as graphite, and the
charging/discharging capacity for serving as the negative electrode
material is decreased. In addition, the strength of graphite
particle is too high and, therefore, a high pressure is required
when an active material layer applied to a current collector is
press-molded so as to have a predetermined bulk density.
Consequently, it may be difficult to increase the density.
[0089] With respect to the negative electrode material of the
present invention, it is desirable that the value of Lc(002), which
is the thickness of crystal, based on the X-ray diffraction
analysis is 80 nm or more, and preferably is 100 nm or more. In the
case where the Lc(002) is less than 80 nm as well, the
crystallinity is inadequate to serve as graphite, the
charging/discharging capacity for serving as the negative electrode
material is decreased. In addition, the strength of graphite
particle is too high and, therefore, a high pressure is required
when an active material layer applied to a current collector is
press-molded so as to have a predetermined bulk density, so that it
may be difficult to increase the density.
(3) Method for Manufacturing Negative Electrode Material
[0090] The negative electrode material containing graphite
particles as a main component is prepared by mixing raw materials,
e.g., carbonaceous particles and binder, and if necessary,
performing molding, firing for removing volatile matters,
graphitization, pulverization, and classification.
[0091] Preferably, needle coke or natural graphite is used as a
main component of the carbonaceous particle for preparing the
negative electrode material of the present invention satisfying the
above-described properties. In the step of kneading carbonaceous
particles and a binder, followed by graphitization, it is
preferable that an appropriate amount of amorphous is maintained by
such a method in which the type and the amount of the catalyst is
optimized in the graphitization (for example, in the case where the
graphitization catalyst is commonly used SiC, the amount of
addition is specified to be 30 parts or less relative to 100 parts
of base material.
[0092] Preferably, the type and the amount of pitch or the like
serving as a binder is optimized, and it is desirable that 20 to 50
parts of easily graphitizable material is used relative to 100
parts of base material.
[0093] Preferably, the graphitization temperature is optimized, and
2,800.degree. C. to 3,100.degree. C. is desirable.
[0094] Preferably, the kneading time is optimized, and 2 hours or
less is desirable.
[0095] A favorable method for manufacturing a negative electrode
material of the present invention will be described below in
detail.
[0096] Carbonaceous particles and a binder are mixed while being
heated. At this time, a graphitization catalyst may be added, if
desired. Favorable carbonaceous particles, binder, and
graphitization catalyst are as described below.
[0097] Carbonaceous Particles
[0098] Preferably, needle coke or green coke containing volatile
matters (hereafter may be referred to as "VM"), which volatilize
during a heat treatment, is used as the main component of the
carbonaceous particles, which are the raw material and which are
primary particles. Preferably, carbonaceous particles containing 2
to 10 percent by weight of volatile matters, which volatilize
during a heat treatment, is used as the green coke. Natural
graphite may be used together, or natural graphite may be used
alone.
[0099] The median diameter of the carbonaceous particles in the
volume-basis particle size distribution based on the laser
diffraction/scattering particle size distribution measurement is
not specifically limited. However, preferably, the median diameter
is 5 .mu.m or more, most of all 6 .mu.m or more, and particularly 8
.mu.m or more, and 40 .mu.m or less, most of all 35 .mu.m or less,
and particularly 30 .mu.m or less.
[0100] If the median diameter of the carbonaceous particles becomes
lower than this lower limit, the cost required for pulverizing the
carbonaceous particles is increased and there is no economy. If the
median diameter exceeds the upper limit, the initial irreversible
capacity of the graphite particles tends to be increased. The
median diameter of the carbonaceous particles can be measured in a
manner similar to that for the median diameter of the
above-described negative electrode material.
[0101] Preferably, the average particle size of the carbonaceous
particles to be used is smaller than the average particle size of
the aimed graphite particles. The average particle size of the
carbonaceous particles is preferably less than or equal to twice,
more preferably less than or equal to the average particle size of
the aimed graphite particles, and preferably more than or equal to
one-tenth the average particle size of the aimed graphite
particles, and more preferably more than or equal to one-fifth.
[0102] The average circularity of the carbonaceous particles is
preferably 0.82 or more, more preferably 0.90 or more, and
preferably 1.00 or less, more preferably 0.96 or less.
[0103] If the average circularity of the carbonaceous particles
becomes lower than this range, the degree of orientation tends to
be decreased. If the average circularity exceeds the range, the
cost tends to be increased. The average circularity of the
carbonaceous particles can be measured in a manner similar to that
for the average circularity of the above-described negative
electrode material.
[0104] Binder
[0105] Specific examples of binders include coal based heavy oils,
e.g., impregnation pitch, coal tar pitch, and coal liquid; and
petroleum based heavy oils, for example, straight heavy oils, e.g.,
asphaltene, and cracking heavy oils, e.g., ethylene heavy end
tar.
[0106] In general, a quinoline-insoluble component contained in a
binder is 0 to 10 percent by weight, and a smaller content is
preferable from the view point of the hardness of the graphite
particle and the capacity when a cell is prepared. If the content
of quinoline-insoluble component in the binder is too large, the
resulting graphite particles become hard, and even when an active
material layer applied to the current collector is pressed,
deformation of particles is hard to occur. Therefore, an increase
of density tends to become difficult. In addition, the capacity
also tends to decrease.
[0107] The binder is used in such a way that the proportion of
those derived from the binder becomes preferably 5 percent by
weight or more, more preferably 10 percent by weight or more, and
preferably 60 percent by weight or less, more preferably 40 percent
by weight or less, further preferably 30 percent by weight or less
in the graphite particle having been subjected to a graphitization
treatment, produced by carbonization and graphitization. If the
amount of binder is too large, since an amorphous portion derived
from the binder is increased in a final product, the cell capacity
may be decreased when a cell is prepared. Furthermore, the
resulting graphite particles become hard and, therefore, when an
active material layer applied to the current collector is pressed,
aggregate particles themselves rather than the binder portion tend
to be broken.
[0108] On the other hand, the cell characteristics become favorable
when the amount of binder becomes small. However, if the amount is
too small, molding after kneading becomes difficult and, thereby,
the manufacturing cost is increased. With respect to the graphite
granulated particles, binding between graphite particles, which
constitute the graphite granulated particles, with each other is
weak, and in a pressing step which is one of steps of working the
negative electrode material containing graphite particles as a main
component into a plate for a negative electrode, since graphite
granulated particles present on the surface of the electrode tend
to break, communicating holes serving as diffusion paths of lithium
ions are blocked, and the high-rate charging/discharging
characteristics deteriorates. For these reasons, the quick charging
characteristic and, by extension, the cycle performances tend to
become inadequate. Furthermore, fine-powdering of graphite
granulated particles tends to occur during handling, e.g.,
preparation of a coating solution.
[0109] The amount of binder in the negative electrode material is
controlled by the amount of binder added in the stage before
kneading. For example, in the case where the carbon residue of the
binder determined by the method described in, for example, JIS K
2270 is X %, the binder in an amount 100/X times the desired amount
is added.
[0110] Preferably, the addition of the binder, e.g., pitch or tar,
is designed to be performed while the binder is dispersed uniformly
at a low temperature for a short time as much as possible in order
to reduce the initial irreversible capacity and reduce the press
load. In order to ensure the dispersion at a low temperature for a
short time, it is favorable to intensify agitation within the
bounds of not breaking the carbonaceous particles.
[0111] Graphitization Catalyst
[0112] In order to increase the charging/discharging capacity and
improve the pressing performance, preferably, a graphitization
catalyst is added in the mixing of the carbonaceous particles and
the binder. Examples of graphitization catalysts include metals,
e.g., iron, nickel, titanium, silicon, and boron, and compounds,
e.g., carbides, oxides, and nitrides, thereof. Most of all,
silicon, silicon compounds, iron, and iron compounds are
preferable. Among the silicon compounds, silicon carbide is
particularly preferable, and among the iron compounds, iron oxides
are particularly preferable.
[0113] In the case where silicon or a silicon compound is used as
the graphitization catalyst, silicon carbide generated by heating
is entirely heat-decomposed at a temperature of 2,800.degree. C. or
more, graphite having very good crystallinity is grown, and when
silicon volatilizes, pores are formed between graphite crystals.
Consequently, a charge transfer reaction and diffusion of lithium
ions in the particles are facilitated, and the cell performance can
be improved. In the case where iron or a compound thereof is used
as the graphitization catalyst, graphite having good crystallinity
is grown due to a mechanism of dissolution of carbon into the
catalyst and deposition and, therefore, an effect similar to that
of silicon can be exerted.
[0114] The amounts of addition of these graphitization catalysts
are preferably 30 percent by weight or less, more preferably 20
percent by weight or less, further preferably 10 percent by weight
or less, and particularly preferably 5 percent by weight or less
relative to carbonaceous primary particles as the raw material. If
the graphitization catalyst is excessive, graphitization proceeds
to an excessive degree, problems occurs in that when a lithium ion
secondary battery is prepared, the characteristics, in particular,
a liquid immersion property, are inadequate. In addition, the
strength of particles are decreased, although this may be due to
formation of pores in the graphite particles. As a result, the
surface is smoothed in the pressing step of preparation of the
electrode and, thereby, movement of ions may be inhibited.
[0115] On the other hand, if the graphitization catalyst is short,
graphitization becomes inadequate, and a problem occurs in that the
charging/discharging capacity is decreased when a nonaqueous
secondary battery is prepared. Furthermore, a high pressure is
required in the pressing step of preparation of the electrode, it
may be difficult to increase the density.
[0116] Kneading (Mixing)
[0117] Raw materials, e.g., carbonaceous particles, a binder, and a
graphitization catalyst added as desired, are kneaded while being
heated. In this manner, a state, in which the liquid binder is
adhered to the carbonaceous particles and raw materials not melted
at a kneading temperature, is brought about.
[0118] In this case, all raw materials may be charged into a
kneader and kneading and temperature raising may be performed
simultaneously. Alternatively, the components other than the binder
may be charged into the kneader, and heated while being agitated.
After the temperature is raised to the kneading temperature, the
binder at ambient temperature or in the heated-molten state may be
charged.
[0119] The heating temperature is higher than or equal to the
softening point of the binder. If the heating temperature is too
low, the viscosity of the binder is increased and uniform kneading
becomes difficult. Therefore, usually, the heating temperature is
specified to be at least 10.degree. C. higher than the softening
point, preferably at least 20.degree. C. higher than the softening
point. If the heating temperature is too high, the viscosity of the
mixture system becomes too high due to volatilization and
polycondensation of the binder. Therefore, the temperature is
usually 300.degree. C. or lower, and preferably 250.degree. C. or
lower.
[0120] Preferably, the kneader is a model having agitating blades,
and common agitating blades of Z type or masticator type can be
used. The amount of the raw material put into the kneader is
usually 10 percent by volume or more of the kneader volume,
preferably 15 percent by volume or more, and 50 percent by volume
or less, preferably 30 percent by volume or less. The kneading time
must be 5 minutes or more, and until the time, at which the
viscosity begins changing significantly due to volatilization of
the volatile matter, at the longest. The kneading time is usually
30 to 120 minutes. It is preferable that the kneader is preheated
up to the kneading temperature prior to the kneading.
[0121] Molding
[0122] The resulting kneaded product, as it is, may be subjected to
a firing step for removing VM for the purposes of removal of the
volatile matter (VM) and carbonization. However, it is preferable
that the kneaded product is subjected to a firing step for removing
VM after molding is performed in order to facilitate the
handling.
[0123] The molding method is not specifically limited insofar as
the shape can be maintained, and extrusion, die molding, isostatic
molding, or the like can be adopted. Among them, the die molding,
in which the operation is relatively easy and a molded product can
be obtained without breaking a structure allowed to exhibit a
random orientation by the kneading, is preferable rather than
extrusion in which particles tend to orient in the molded product
and the isostatic molding, in which the random orientation of
particles is maintained but the productivity is hard to
increase.
[0124] With respect to the molding temperature, either room
temperature (cold) or under heating (hot, a temperature higher than
or equal to the softening point of the binder) is adopted. In the
case where cold molding is performed, in order to improve the
moldability and the uniformity of the molded product, it is
desirable that the kneaded product cooled after the kneading is
coarsely crushed to a size of 1 mm or less at the maximum in
advance. The shape and the size of molded product is not
specifically limited. However, in the hot molding, if the molded
product is too large, there is a problem in that it takes much time
to preheat uniformly prior to the molding. Therefore, the size is
usually specified to be about 150 cm or less at the maximum
size.
[0125] With respect to the molding pressure, if the pressure is too
high, there are problems in that removal of volatilized matters (VM
removal) through pores of the molded product becomes difficult and,
in addition, carbonaceous particles, which are not perfect circles,
are oriented so as to make pulverization in a downstream step
difficult. Therefore, the molding pressure is preferably 3
tf/cm.sup.2 (294 Pa) or less, more preferably 500 kgf/cm.sup.2 (49
MPa) or less, and further preferably 10 kgf/cm.sup.2 (0.98 MPa) or
less. The lower limit of the pressure is not specifically limited,
but it is preferable that the pressure is set at a level at which
the shape of the molded product can be maintained during the step
of VM removal.
[0126] Firing for VM Removal
[0127] The resulting molded product is subjected to firing for VM
removal in order to remove volatile matters (VM) in the
carbonaceous particles and the binder and prevent contamination of
a filler and adhesion of the filler to the molded product during
graphitization. The firing for VM removal is performed at a
temperature of usually 500.degree. C. or higher, preferably
600.degree. C. or higher, and preferably 1,700.degree. C. or lower,
more preferably 1,400.degree. C. or lower for preferably 0.1 to 10
hours. In general, heating is performed while flowing an inert gas,
e.g., nitrogen or argon, or in a non-oxidizing atmosphere in which
granular carbon materials, e.g., breeze and packing coke, are
filled in gaps in order to prevent oxidation.
[0128] The equipment, e.g., an electric furnace, a gas furnace, or
a lead hammer furnace for an electrode material, to be used for the
firing for VM removal is not specifically limited insofar as firing
can be performed in a non-oxidizing atmosphere. It is desirable
that the temperature raising rate during heating is low in order to
remove the volatile matters. In general, the temperature is raised
at a rate of 3.degree. C. to 100.degree. C./hr from the
neighborhood of 200.degree. C., at which volatilization of the low
boiling point component is started, to the neighborhood of
700.degree. C., at which merely hydrogen is generated.
[0129] Graphitization
[0130] The carbonized molded product resulting from the firing for
VM removal is graphitized by being hearted at a high temperature.
As the heating temperature during graphitization becomes lower,
graphitization does not proceed. Consequently, the A/B of the
resulting negative electrode material is decreased, whereas the
graphite particles become hard, and there is a tendency that a high
pressure is required when the active material layer applied to the
current collector is press-molded so as to have a predetermined
bulk density and an increase of density becomes difficult.
Therefore, the heating is performed preferably at 2,900.degree. C.
or higher, and more preferably at 3,000.degree. C. or higher. If
the heating temperature is too high, sublimation of graphite
becomes significant. Therefore, 3,300.degree. C. or lower is
preferable. The heating is necessary until the binder and the
carbonaceous particles are converted to graphite and, therefore,
the heating time is preferably 1 to 24 hours.
[0131] With respect to an atmosphere during the graphitization, for
the purpose of preventing oxidation, the graphitization is
performed while flowing an inert gas, e.g., nitrogen or argon, or
in a non-oxidizing atmosphere in which granular carbon materials,
e.g., breeze and packing coke, are filled in gaps.
[0132] The equipment, e.g., an electric furnace, a gas furnace, or
an Acheson furnace for an electrode material, to be used for the
graphitization is not specifically limited insofar as the equipment
serves the above-described purpose. The temperature raising rate,
the cooling rate, the heat treatment time, and the like can be set
arbitrarily within the allowable range of the equipment to be
used.
[0133] Pulverization
[0134] In general, the thus prepared graphitization treatment
product, which has been subjected to no further treatment, does not
have a particle size distribution specified in the present
invention. Therefore, an adjustment is performed to have a
predetermined particle size distribution by pulverization, sieving,
or the like.
[0135] The method for pulverizing the graphitization treatment
product is not specifically limited. Examples of pulverization
devices include mechanical trituration devices, e.g., a ball mill,
a hammer mill, a CF mill, an atomizer mill, and a pulverizer; and
pulverization devices through the use of wind force, e.g., a jet
mill. With respect to coarse crushing and medium crushing, crushing
systems, e.g., a jaw crusher, a hammer mill, and a roller mill,
through the use of an impact force may be used.
[0136] Here, the timing of pulverization is either before the
graphitization or after the graphitization. The latter is more
preferable because operations, e.g., packing into a crucible, are
unnecessary and, therefore, the production can be performed
inexpensively.
[0137] Classification
[0138] Large diameter particles and small diameter particles (fine
powder) are removed from the resulting pulverized product in such a
way that the d.sub.90/d.sub.10 and the A/B become within the
above-described range. An occurrence of short circuit can be
prevented and variations during coating can be eliminated by
removing large diameter particles. It is desirable that grading is
performed in such a way that particles having a particle size of
100 .mu.m or more becomes 3% or less relative to the entirety and
particles having a particle size of 1 .mu.m or less becomes 1% or
less relative to the entirety in the volume-basis particle size
distribution based on the laser diffraction/scattering particle
size measurement by removing large diameter particles and fine
powders.
[0139] There are various methods for removing large diameter
particles and small diameter particles. However, it is preferable
that the removal is performed by sieving or classification from the
view point of the simplicity of apparatuses, the operability, and
the cost. Furthermore, the sieving or the classification have
advantages that the particle size distribution and the average
particle size, which are varied by the following graphitization and
removal of the above-described particles, of the granulated product
can be readjusted, if necessary.
[0140] Examples of the sieving for removing large diameter
particles include fixed net face type, in-plane movement type, and
rotary sieve type. However, the fixed net face type blow through
sieve is particularly preferable from the view point of the
handling capacity. The size of opening of the sieve to be used is
80 .mu.m or less, and 30.mu. or more, and is appropriately selected
for the use in accordance with the generation status (in
particular, the amount and the particle size) of particles to be
removed and the requirements for adjusting the particle size
distribution and the average particle size of the granulated
product. If the size of opening exceeds 80 .mu.m, the removal of
the particles becomes inadequate. If the size is less than 30
.mu.m, the granulated product may be removed excessively, so that,
unfavorably, a large product loss occurs and, in addition, the
adjustment of the particle size distribution becomes difficult.
Commercially available common size sieves having openings of 45
.mu.m and 38 .mu.m can be used favorably.
[0141] Classification can be performed by a method based on wind
force classification, wet classification, specific gravity
classification, or the like. When particles of 100 .mu.m or more
are removed, although not specifically limited, it is preferable to
use the wind force classifier, e.g., a swirling flow classifier, in
consideration of the influence on the properties of granulated
product and adjustment of the particle size distribution and the
average particle size of granulated product. In this case, when the
amount of wind and the speed of wind are controlled, the removal of
the particles and the adjustment of the particle size distribution
and the average particle size of granulated product can be
performed in a manner similar to that in the above-described
adjustment of the size of opening of the sieve.
[0142] [2] Negative Electrode for Nonaqueous Secondary Battery
[0143] The negative electrode material of the present invention is
suitable for the use as a negative electrode active material of a
nonaqueous secondary battery, in particular, a lithium secondary
battery.
[0144] A negative electrode constituting a nonaqueous secondary
battery is produced by forming an active material layer containing
a negative electrode active material, a binder for forming an
electrode, a thickener, and if necessary, an electrically
conductive material on a current collector. In general, the active
material layer is produced by preparing a slurry containing a
negative electrode active material, a binder for forming an
electrode, a thickener, if necessary an electrically conductive
material, and a solvent, and applying the slurry to the current
collector, followed by drying and pressing.
[0145] With respect to the negative electrode active material, a
material usually used as a negative electrode active material may
also be used in addition to the negative electrode materials of the
present invention.
[0146] With respect to the binder for forming an electrode, an
arbitrary material can be used insofar as the material is stable
against a solvent and an electrolytic solution to be used in
preparation of the electrode. Examples thereof include
polyvinylidene fluoride, polytetrafluoroethylene, polyethylene,
polypropylene, styrene-butadiene rubber, isoprene rubber, butadiene
rubber, ethylene-acrylic acid copolymer, and ethylene-methacrylic
acid copolymer. The weight ratio of active material/binder for
forming electrode in the binder for forming an electrode is within
the range of preferably 90/10 or more, more preferably 95/5 or
more, and preferably 99.9/0.1 or less, preferably 99.5/0.5 or
less.
[0147] Examples of thickeners include carboxymethyl cellulose,
methyl cellulose, hydroxymethyl cellulose, ethyl cellulose,
polyvinyl alcohol, oxidized starch, phosphorylated starch, and
casein.
[0148] Examples of electrically conductive materials include carbon
materials, e.g., graphite and carbon black; and metal materials,
e.g., copper and nickel.
[0149] Examples of materials for the current collector include
copper, nickel, and stainless steel. Among them, copper foil is
preferable from the view point of the workability into a thin film
and the cost.
[0150] The gravity of the active material layer is varied depending
on the use. In the use in which the capacity is important, the
density is preferably 1.55 g/cm.sup.3 or more, most of all 1.60
g/cm.sup.3 or more, furthermore 1.65 g/cm.sup.3 or more, and
particularly preferably 1.70 g/cm.sup.3 or more. If the density is
too low, the capacity of the cell per unit volume is not always
adequate. If the density is too high, the Rate performances
deteriorates. Therefore, 1.9 g/cm.sup.3 or less is preferable.
[0151] Here, the active material layer refers to a mixture layer
composed of an active material, a binder for forming an electrode,
a thickener, an electrically conductive material, and the like on
the current collector, and the density thereof refers to a bulk
density at the time of assembling into a cell.
[0152] [3] Nonaqueous Secondary Battery
[0153] The negative electrode for a nonaqueous secondary battery of
the present invention prepared by using the negative electrode
material of the present invention is very useful as a negative
electrode for a nonaqueous secondary battery, in particular, a
lithium secondary battery.
[0154] Selection of a positive electrode, an electrolytic solution,
and the like, which are components necessary for constituting a
cell, constituting the above-described nonaqueous secondary battery
is not specifically limited. Examples of materials and the like for
the components constituting the nonaqueous secondary battery will
be described below. However, usable materials are not limited to
these specific examples.
[0155] The nonaqueous secondary battery of the present invention is
usually composed of the above-described negative electrode of the
present invention, a positive electrode, and an electrolyte.
[0156] The positive electrode is produced by forming an active
material layer containing a positive electrode active material, an
electrically conductive material, and a binder for forming an
electrode on a positive electrode current collector. In general,
the active material layer is produced by preparing a slurry
containing the positive electrode active material, the electrically
conductive material, and the binder for forming an electrode, and
applying the slurry to the current collector, followed by
drying.
[0157] Examples of materials usable as the positive electrode
active material include materials capable of absorbing and
releasing lithium, such as lithium transition metal compound oxide
materials, e.g., lithium cobalt oxide, lithium nickel oxide, and
lithium manganese oxide; transition metal oxide materials, e.g.,
manganese dioxide; and carbonaceous materials, e.g., graphite
fluoride. Specifically, LiFeO.sub.2, LiCoO.sub.2, LiNiO.sub.2,
LiMn.sub.2O.sub.4, non-stoichiometric compounds thereof, MnO.sub.2,
TiS.sub.2, FeS.sub.2, Nb.sub.3S.sub.4, Mo.sub.3S.sub.4, CoS.sub.2,
V.sub.2O.sub.5, P.sub.2O.sub.5, CrO.sub.3, V.sub.3O.sub.3,
TeO.sub.2, GeO.sub.2, and the like can be used.
[0158] With respect to the positive electrode current collector,
preferably, a metal, which forms a passive film on a surface due to
anodization in the electrolytic solution, or an alloy thereof is
used. Examples thereof can include groups IIIa, IVa, and Va (groups
3B, 4B, and 5B) metals and alloys thereof. Specific examples can
include Al, Ti, Zr, Hf, Nb, Ta, and alloys containing these metals.
Preferably, Al, Ti, Ta, and alloys containing these metals can be
used. In particular, Al and alloys thereof are desirable because
they are lightweight and, therefore, the energy density is
high.
[0159] Examples of electrolytes can include an electrolytic
solution, a solid electrolyte, and a gel electrolyte. Most of all,
the electrolytic solution, in particular, a nonaqueous electrolytic
solution is preferable. For the nonaqueous electrolytic solution, a
solution, in which a solute is dissolved into a nonaqueous solvent,
can be used.
[0160] For the solute, alkali metal salts, quaternary ammonium
salts, and the like can be used. Specifically, it is preferable
that at least one compound selected from the group consisting of
LiClO.sub.4, LiPF.sub.6, LiBF.sub.4, LiCF.sub.3SO.sub.3,
LiN(CF.sub.3SO.sub.2).sub.2, LiN(CF.sub.3CF.sub.2SO.sub.2).sub.2,
LiN(CF.sub.3SO.sub.2) (C.sub.4F.sub.9SO.sub.2), and
LiC(CF.sub.3SO.sub.2).sub.3 is used.
[0161] Examples of solvents usable as the nonaqueous solvent
include cyclic carbonates, e.g., ethylene carbonate, butylene
carbonate, and vinylene carbonate; cyclic ester compounds, e.g.,
.gamma.-butyrolactone; chain ethers, e.g., 1,2-dimethoxyethane;
cyclic ethers, e.g., crown ether, 2-methyltetrahydrofuran,
1,2-dimethyltetrahydrofuran, 1,3-dioxolane, and tetrahydrofuran;
and chain carbonates, e.g., diethyl carbonate, ethyl methyl
carbonate, and dimethyl carbonate. With respect to each of the
solute and the solvent, one type may be selected and used, or at
least two types may be mixed and used. Among them, it is preferable
that the nonaqueous solvent contains the cyclic carbonate and the
chain carbonate.
[0162] preferably, the content of these solutes in the electrolytic
solution is 0.2 mol/l or more, particularly 0.5 mol/l or more, and
2 mol/l or less, particularly 1.5 mol/l or less.
[0163] Among them, a nonaqueous secondary battery formed by
combining the negative electrode according to the present
invention, a metal chalcogenide based positive electrode commonly
used for a lithium ion cell, and an organic electrolytic solution
mainly containing a carbonate based solvent has a large capacity, a
small irreversible capacity observed in an initial cycle, a high
quick charging/discharging capacity (good Rate performances), an
excellent cycle performances, high storage stability and
reliability of a cell stood at high temperatures, a high-efficiency
discharge characteristic, and very excellent discharge
characteristic at low temperatures.
[0164] The nonaqueous electrolytic solution may contain a
film-former. Examples of film-formers include carbonate compounds,
e.g., vinylene carbonate, vinyl ethyl carbonate, and methyl phenyl
carbonate; alkene sulfides, e.g., ethylene sulfide and propylene
sulfide; sulton compounds, e.g., 1,3-propane sulton and 1,4-butane
sulton; and acid anhydrides, e.g., maleic anhydride and succinic
anhydride. The content of the film-former is usually 10 percent by
weight or less, preferably 8 percent by weight or less, further
preferably 5 percent by weight or less, and most preferably 2
percent by weight or less. If the content of the film-former is too
large, adverse effects, e.g., an increase of the initial
irreversible capacity, deterioration of the low temperature
characteristic, and deterioration of the Rate performances, may be
exerted with respect to the other characteristics.
[0165] In general, a separator is disposed between the positive
electrode and the negative electrode in order to avoid physical
contact between the positive electrode and the negative electrode.
Preferably, the separator has high ion permeability and a low
electric resistance. The material and the shape of the separator
are not specifically limited, but it is preferable that high
stability is exerted against the electrolytic solution, and
excellent solution preserving property is exhibited. Specific
Examples thereof include porous sheets and nonwoven fabrics derived
from a polyolefin, e.g., polyethylene or polypropylene.
[0166] The shape of the nonaqueous secondary battery of the present
invention is not specifically limited. Examples thereof include a
cylinder type in which sheet electrodes and a separator are made
into a spiral shape, a cylinder type having an inside out structure
in which pellet electrodes and a separator are combined, and a coin
type in which pellet electrodes and a separator are laminated.
EXAMPLES
[0167] The specific aspects of the present invention will be
described below in further detail with reference to the examples.
However, the present invention is not limited to these
examples.
Example 1
[0168] An amorphous carbon material (needle coke) was subjected to
coarse crushing, and was further pulverized with a fine grinding
mill ("Sample Mill" produced by Hosokawa Micron Corporation).
Coarse particles were removed with a sieve having an opening of 45
.mu.m, so that carbonaceous particles having a median diameter of
12.2 .mu.m, a minimum particle size of 1.5 .mu.m, a maximum
particle size of 68 .mu.m, and an average circularity of 0.80 were
produced.
[0169] The resulting carbonaceous particles and a binder pitch
having a softening point of 88.degree. C. were mixed in a weight
ratio of 100:34. The resulting mixture was put into a kneader
having a masticator type agitating blade heated to 128.degree. C.
in advance and kneading was performed for 20 minutes.
[0170] The kneaded product, which had been kneaded adequately, was
filled in a mold of a mold pressing machine preheated to
108.degree. C. in advance, and was stood for 5 minutes. After the
temperature of the kneaded product was stabilized, a plunger was
pushed, and molding was performed by applying a pressure of 2
kgf/cm.sup.2 (0.20 MPa). This pressure was maintained for 1 minute,
and the movement was stopped. After the pressure reduction was
completed, a molded product having a diameter of 6 cm and a length
of 9 cm was taken out.
[0171] The resulting molded product was put into a metal saggar,
which was a heat-resistant container, and gaps were filled with
graphite breeze. The temperature was raised from room temperature
to 1,000.degree. C. over 48 hours in an electric furnace, and was
kept at 1,000.degree. C. for 3 hours, so that the firing for
removing VM was performed. Subsequently, the molded product was put
into a graphite crucible, and gaps were filled with graphite
breeze. Graphitization was performed by heating in an Acheson
furnace at 3,000.degree. C. for 4 hours.
[0172] The resulting graphite molded product was coarsely crushed
with a jaw crusher, and was pulverized with Sample Mill. Coarse
particles were removed with a sieve having an opening of 45 .mu.m
and, furthermore, grading was performed by removing 5% of fine
particles through wind force classification ("NPK-MC-MDS-2"
produced by Nippon Pneumatic Mfg. Co., Ltd., was used, a spacer
thickness was 4 mm, the number of revolutions of a feeder was 500
rpm, and evacuation was performed at a reduced pressure of 540
mmH.sub.2O while an appropriate amount of air was fed), so that
graphite particles having a median diameter of 21.1 .mu.m were
produced.
[0173] The resulting graphite particles had a tapping density of
0.79 g/cm.sup.3, a BET specific surface area of 2.3 m.sup.2/g, the
total number of particles of 23.3.times.10.sup.6/g, the
d.sub.90/d.sub.10 of 3.8, the A/B of 1.6, the d(002) of 0.3359 nm,
and Lc(002) of 132 nm.
[0174] These graphite particles were used as the negative electrode
material, and a coin type cell was prepared by the following
method. The initial charging/discharging capacity, the initial
charge irreversible capacity, and the Rate performances were
determined. The predetermined electrode of the present invention
was prepared by the above-described predetermined method for
manufacturing an electrode, and the skewness (Rsk), the surface
roughness Ra, the graphite crystal orientation ratio
(I.sub.110/I.sub.004) on the electrode, the press load, and the
liquid immersion speed were measured. Furthermore, the resulting
predetermined electrode was used, and a laminate film inclusion
type cell was prepared by the above-described method for
manufacturing a nonaqueous secondary battery. Subsequently, the
capacity maintenance factor after 200 cycles of charging and
discharging was measured by the above-described method.
[0175] In the measurement of the skewness, a color laser microscope
("Model VK-9500" produced by KEYENCE CORPORATION) was used, and a
form in the depth direction in the vicinity of the electrode sample
surface was observed. The skewness (Rsk) was calculated from the
resulting information. There was no cutoff, and the observation
field of view was specified to be 280 .mu.m in length, 210 .mu.m in
width, and 17 .mu.m in depth. Here, the depth was assumed to be a
distance from the electrode surface layer.
[0176] The results thereof are shown in Table 1.
[0177] <Preparation of Coin Type Cell>
[0178] A slurry was produced by agitating 10 g of the negative
electrode material, 0.1 g of carboxymethyl cellulose aqueous
solution in terms of solid content, and 0.1 g of styrene-butadiene
rubber aqueous dispersion in terms of solid content for 3 minutes
with a hybrid mixer produced by KEYENCE CORPORATION. The resulting
slurry was applied to the copper foil serving as a current
collector by a doctor blade method in such a way that 10.+-.0.1
mg/cm.sup.2 of negative electrode material is adhered, and air
drying was performed at room temperature. Furthermore, drying was
performed at 110.degree. C. for 12 minutes and, thereafter, the
electrode density was adjusted at 1.6.+-.0.03 g/cm.sup.3 by
pressing, so that a negative electrode sheet was produced.
[0179] The resulting negative electrode sheet was stamped into the
shape of a disk having a diameter of 12.5 mm so as to produce a
negative electrode, and lithium metal foil was stamped into the
shape of a disk having a diameter of 12.5 mm so as to produce a
positive electrode. A separator (formed from a porous polyethylene
film) impregnated with an electrolytic solution, in which
LiPF.sub.6 was dissolved in a mixed solvent of ethylene carbonate
and ethyl methyl carbonate (volume ratio=1:1) in such a way that
the concentration became 1 mol/l, was disposed between the negative
electrode and the positive electrode so as to prepare a 2016 coin
type cell.
[0180] <Initial Charging/Discharging Capacity, Initial Charge
Irreversible Capacity>
[0181] The resulting 2016 coin type cell was stood for 24 hours,
charging was performed at a current density of 0.16 mA/cm.sup.2
until the potential difference between the two electrodes became 0
V and, thereafter, discharging was performed at 0.33 mA/cm.sup.2
until 1.5V was reached. A reference charging/discharging test was
carried out, and an average value of discharge capacities at the
first cycle was taken as the initial charging/discharging capacity.
The irreversible capacity (initial charge capacity-initial
discharge capacity) occurred at the first cycle was taken as the
initial charge irreversible capacity. The initial discharge
capacity and the initial charge irreversible capacity of each of
three coin type cells were measured and the average values were
determined.
[0182] <Rate Performances>
[0183] The resulting 2016 coin type cell was charged at a current
density of 0.16 mA/cm.sup.2 until the potential difference between
the two electrodes became 0 V and, thereafter, discharging was
performed at 7.0 mA/cm.sup.2 until 1.5 V was reached. The discharge
capacity at this time was divided by the discharge capacity when
discharge was performed at 0.7 mA/cm.sup.2, and the resulting value
was expressed as a percentage (Rate performances). The Rate
performances of each of three coin type cells was determined and
the average value was obtained.
Example 2
[0184] An amorphous carbon material containing less than 0.1
percent by weight of volatile matter was subjected to coarse
crushing, and was further pulverized with a fine grinding mill
("Sample Mill" produced by Hosokawa Micron Corporation). Coarse
particles were removed with a sieve having an opening of 45 .mu.m,
so that carbonaceous particles having a median diameter of 9.0
.mu.m, a minimum particle size of 0.6 .mu.m, a maximum particle
size of 51.5 .mu.m, and an average circularity of 0.80 were
produced.
[0185] The resulting carbonaceous particles and a binder pitch
having a softening point of 88.degree. C. were mixed in a weight
ratio of 100:34, and 30 parts by weight of graphitization catalyst
(Fe.sub.2O.sub.3) was added relative to 100 parts by weight of the
mixture. The resulting mixture was put into a kneader having a
masticator type agitating blade heated to 128.degree. C. in advance
and kneading was performed for 20 minutes. In a manner similar to
that in Example 1, molding, removal of VM, graphitization,
pulverization, and grading were performed, so that graphite
particles having a median diameter of 20.5 .mu.m were produced.
[0186] The resulting graphite particles had a tapping density of
0.79 g/cm.sup.3, a BET specific surface area of 2.9 m.sup.2/g, the
total number of particles of 21.0.times.10.sup.6/g, the
d.sub.90/d.sub.10 of 4.0, the A/B of 0.8, the d(002) of 0.3357 nm,
and Lc(002) of 187 nm.
[0187] These graphite particles were used as the negative electrode
material, and a coin type cell was prepared as in Example 1. The
initial charging/discharging capacity, the initial charge
irreversible capacity, and the Rate performances were determined.
The predetermined electrode of the present invention was prepared
similarly. The skewness (Rsk), the surface roughness Ra, the
graphite crystal orientation ratio (I.sub.110/I.sub.004) on the
electrode, the press load, the liquid immersion speed, and the
capacity maintenance factor after 200 cycles of charging and
discharging were measured. The results thereof are shown in Tables
1 and 2.
Example 3
[0188] Natural graphite having a median diameter of 13.7 .mu.m, a
minimum particle size of 5.1 .mu.m, and a maximum particle size of
51.5 .mu.m and a binder pitch having a softening point of
88.degree. C. were mixed in a weight ratio of 100:30. The resulting
mixture was put into a kneader having a masticator type agitating
blade heated to 128.degree. C. in advance and kneading was
performed for 20 minutes.
[0189] The kneaded product, which had been kneaded adequately, was
filled in a mold of a mold pressing machine preheated to
108.degree. C. in advance, and was stood for 5 minutes. After the
temperature of the kneaded product was stabilized, a plunger was
pushed, and molding was performed by applying a pressure of 5
kgf/cm.sup.2 (0.20 MPa). This pressure was maintained for 1 minute,
and the movement was stopped. After the pressure reduction was
completed, a molded product was taken out.
[0190] The resulting molded product was put into a metal saggar,
which was a heat-resistant container, and gaps were filled with
graphite breeze. The temperature was raised from room temperature
to 1,300.degree. C. over 48 hours in an electric furnace, and was
kept at 1,300.degree. C. for 3 hours, so that the firing for
removing VM was performed. Subsequently, the molded product was put
into a graphite crucible, and gaps were filled with graphite
breeze. Graphitization was performed by heating in an Acheson
furnace at 3,000.degree. C. for 4 hours.
[0191] The resulting graphite molded product was coarsely crushed
with a jaw crusher, and was pulverized with a high speed rotation
mill. Coarse particles were removed with a sieve having an opening
of 45 .mu.m, so that graphite particles having a median diameter of
15.8 .mu.m were produced.
[0192] The resulting graphite particles had a tapping density of
1.16 g/cm.sup.3, a BET specific surface area of 1.9 m.sup.2/g, the
total number of particles of 3.6.times.10.sup.6/g, the
d.sub.90/d.sub.10 of 2.5, the A/B of 0.7, the d(002) of 0.3354 nm,
and Lc(002) of more than 1,000 nm.
[0193] These graphite particles were used as the negative electrode
material, and a coin type cell was prepared as in Example 1. The
initial charging/discharging capacity, the initial charge
irreversible capacity, and the Rate performances were determined.
The predetermined electrode of the present invention was prepared
similarly. The skewness (Rsk), the surface roughness Ra, the
graphite crystal orientation ratio (I.sub.110/I.sub.004) on the
electrode, the press load, the liquid immersion speed, and the
capacity maintenance factor after 200 cycles of charging and
discharging were measured. The results thereof are shown in Tables
1 and 2.
Example 4
[0194] Graphite particles having a median diameter of 22.0 .mu.m
were produced by performing mixing with the binder, molding,
removal of VM, graphitization, pulverization, and grading as in
Example 3 except that natural graphite having a median diameter of
21.7 .mu.m, a minimum particle size of 7.7 .mu.m, and a maximum
particle size of 77.3 .mu.m was used as the raw material, and
weight ratio of the natural graphite to the binder pitch having a
softening point of 88.degree. C. was specified to be 100:40.
[0195] The resulting graphite particles had a tapping density of
1.05 g/cm.sup.3, a BET specific surface area of 3.7 m.sup.2/g, the
total number of particles of 26.7.times.10.sup.6/g, the
d.sub.90/d.sub.10 of 3.0, the A/B of 1.1, the d(002) of 0.3354 nm,
and Lc(002) of more than 1,000 nm.
[0196] These graphite particles were used as the negative electrode
material, and a coin type cell was prepared as in Example 1. The
initial charging/discharging capacity, the initial charge
irreversible capacity, and the Rate performances were determined.
The predetermined electrode of the present invention was prepared
similarly. The skewness (Rsk), the surface roughness Ra, the
graphite crystal orientation ratio (I.sub.110/I.sub.004) on the
electrode, the press load, the liquid immersion speed, and the
capacity maintenance factor after 200 cycles of charging and
discharging were measured. The results thereof are shown in Tables
1 and 2.
Comparative Example 1
[0197] Graphite particles having a median diameter of 16.7 .mu.m
were produced as in Example 2 except that the graphitization
catalyst to be added was silicon carbide and the amount of addition
was 50 parts relative to 100 parts by weight of carbonaceous
particles. The resulting graphite particles had a tapping density
of 0.77 g/cm.sup.3, a BET specific surface area of 4.7 m.sup.2/g,
the total number of particles of 18.5.times.10.sup.6/g, the
d.sub.90/d.sub.10 of 3.0, the A/B of 1.2, the d(002) of 0.3356 nm,
and Lc(002) of 217 nm.
[0198] These graphite particles were used as the negative electrode
material, and a coin type cell was prepared as in Example 1. The
initial charging/discharging capacity, the initial charge
irreversible capacity, and the Rate performances were determined.
The predetermined electrode of the present invention was prepared
similarly. The skewness (Rsk), the surface roughness Ra, the
graphite crystal orientation ratio (I.sub.110/I.sub.004) on the
electrode, the press load, the liquid immersion speed, and the
capacity maintenance factor after 200 cycles of charging and
discharging were measured. The results thereof are shown in Tables
1 and 2.
TABLE-US-00002 TABLE 1 Amount of catalyst Negative electrode
material Percent by The total weight relative Median Tappig BET
specific number of to carbonaceous diameter density surface area
particles d (002) Lc (002) particles (.mu.m) (g/cm.sup.3)
(m.sup.2/g) (.times.10.sup.6/g) d.sub.90/d.sub.10 A/B (nm) (nm)
Example 1 0 21.1 0.79 2.3 23.3 3.8 1.6 0.3359 132 Example 2 30 20.5
0.79 2.9 21.0 4.0 0.8 0.3357 187 Example 3 0 15.8 1.16 1.9 3.6 2.5
0.7 0.3354 >1000 Example 4 0 22.0 1.05 3.7 26.7 3.0 1.1 0.3354
>1000 Comparative 50 16.7 0.77 4.7 18.5 3.0 1.2 0.3356 217
example 1
TABLE-US-00003 TABLE 2 Electrode evaluation Laminate film Surface
Crystal Liquid Coin type cell inclusion type cell roughness
orientation immersion Discharge Irreversible Rate 200-cycle
capacity Skewness Ra ratio Press load speed capacity capacity
perfomances maintenance factor Rsk (.mu.m) (I.sub.110/I.sub.004)
(kgf/5 cm) (sec/.mu.l) (mAh/g) (mAh/g) (%) (%) Example 1 -0.46 0.77
0.02 1170 37 345 34 82 81 Example 2 -0.93 0.92 0.02 450 282 348 33
80 75 Example 3 -1.18 0.70 0.07 790 115 359 32 82 83 Example 4
-1.45 0.65 0.06 540 142 358 32 85 81 Comparative -1.82 0.46 0.06
300 565 350 32 78 69 example 1
[0199] As is clear from Tables 1 and 2, the cell including the
negative electrode material of the present invention has a small
charging/discharging irreversible capacity at an initial cycle and
exhibits excellent high-rate charging/discharging characteristics
and excellent cycle performances.
INDUSTRIAL APPLICABILITY
[0200] By using the negative electrode material of the present
invention, a negative electrode for a nonaqueous secondary battery
having a small charging/discharging irreversible capacity at an
initial cycle and exhibiting excellent high-rate
charging/discharging characteristics and excellent cycle
performances when a nonaqueous secondary battery is produced and a
nonaqueous secondary battery can be prepared stably and
efficiently. Therefore, the present invention is industrially very
useful in the field of various nonaqueous secondary batteries.
[0201] The present invention has been described in detail with
reference to specific aspects. However, it is clear for those
skilled in the art that various modifications can be made within
the spirit and scope of the present invention.
[0202] This application is based on Japanese patent application
(Japanese Patent Application No. 2004-250415) filed on Aug. 30,
2004, the entire contents of which are incorporated herein by
reference.
* * * * *