U.S. patent application number 13/067846 was filed with the patent office on 2011-11-17 for non-aqueous electrolyte secondary battery.
Invention is credited to Hiroyuki Fujimoto, Shin Fujitani, Kazuhiro Hasegawa, Akira Kinoshita, Tatsuyuki Kuwahara, Yasufumi Takahashi, Shingo Tode.
Application Number | 20110281181 13/067846 |
Document ID | / |
Family ID | 38444397 |
Filed Date | 2011-11-17 |
United States Patent
Application |
20110281181 |
Kind Code |
A1 |
Takahashi; Yasufumi ; et
al. |
November 17, 2011 |
Non-aqueous Electrolyte secondary battery
Abstract
The storage characteristics in a charged state are improved in a
non-aqueous electrolyte secondary battery containing a lithium
cobalt oxide as a positive electrode active material. The
non-aqueous electrolyte secondary battery includes a positive
electrode containing a positive electrode active material; a
negative electrode containing a negative electrode active material
other than metallic lithium; and a non-aqueous electrolyte. The
positive electrode active material contains a lithium cobalt oxide
as its main component. The non-aqueous electrolyte contains 0.1 to
10 volume % of a compound having an ether group. The positive
electrode active material and the negative electrode active
material are contained so that the charge capacity ratio of the
negative electrode to the positive electrode is from 1.0 to 1.2
when the battery is charged until the potential of the positive
electrode reaches 4.4 to 4.5 V (vs. Li/Li.sup.+).
Inventors: |
Takahashi; Yasufumi; (Osaka,
JP) ; Kinoshita; Akira; (Osaka, JP) ; Tode;
Shingo; (Osaka, JP) ; Kuwahara; Tatsuyuki;
(Osaka, JP) ; Hasegawa; Kazuhiro; (Osaka, JP)
; Fujimoto; Hiroyuki; (Osaka, JP) ; Fujitani;
Shin; (Osaka, JP) |
Family ID: |
38444397 |
Appl. No.: |
13/067846 |
Filed: |
June 29, 2011 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
11699000 |
Jan 29, 2007 |
7993783 |
|
|
13067846 |
|
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Current U.S.
Class: |
429/342 ;
429/188 |
Current CPC
Class: |
H01M 2004/028 20130101;
H01M 2300/0025 20130101; H01M 4/131 20130101; H01M 6/168 20130101;
H01M 2010/4292 20130101; H01M 4/1391 20130101; H01M 6/166 20130101;
H01M 10/0525 20130101; H01M 10/0566 20130101; H01M 6/162 20130101;
H01M 6/164 20130101; H01M 10/0567 20130101; H01M 10/0568 20130101;
H01M 10/0569 20130101; Y02E 60/10 20130101 |
Class at
Publication: |
429/342 ;
429/188 |
International
Class: |
H01M 4/131 20100101
H01M004/131; H01M 4/505 20100101 H01M004/505; H01M 4/525 20100101
H01M004/525; H01M 10/0564 20100101 H01M010/0564 |
Foreign Application Data
Date |
Code |
Application Number |
Jan 30, 2006 |
JP |
2006-020936 |
Claims
1. A non-aqueous electrolyte secondary battery comprising: a
positive electrode containing a positive electrode active material;
a negative electrode containing a negative electrode active
material other than metallic lithium; and a non-aqueous
electrolyte, wherein: the positive electrode active material
contains a lithium cobalt oxide as its main component and having a
potential of 4.4 to 4.5 V (vs. Li/Li.sup.+); the non-aqueous
electrolyte contains 0.1 to 10 volume % of a compound having an
ether group; and the battery is charged until the potential of the
positive electrode reaches 4.4 to 4.5 V (vs. Li/Li.sup.+).
2. The nonaqueous electrolyte secondary battery according to claim
1, wherein the lithium cobalt oxide is represented by the chemical
formula Li.sub.aCo.sub.1-x-y-zZr.sub.xMg.sub.yM.sub.zO.sub.2, where
M is at least one element selected from the group consisting of Al,
Ti, and Sn; 0.ltoreq.a.ltoreq.1.1; x>0; y>0; z.gtoreq.0; and
0<x+y+z.ltoreq.0.03.
3. The non-aqueous electrolyte secondary battery according to claim
2, wherein the lithium cobalt oxide has a zirconium-containing
compound in particulate form that has been sintered on a surface
thereof.
4. The non-aqueous electrolyte secondary battery according to claim
1, wherein the negative electrode active material is a graphite
material, and a battery voltage is 4.3 to 4.4 V when the potential
of the positive electrode reaches 4.4 to 4.5 V (vs.
Li/Li.sup.+).
5. The non-aqueous electrolyte secondary battery according to claim
1, wherein the non-aqueous electrolyte contains diethyl carbonate
as a solvent.
6. The non-aqueous electrolyte secondary battery according to claim
1, wherein the non-aqueous electrolyte contains 1 to 10 volume % of
diethyl ether as the compound having an ether group.
7. The non-aqueous electrolyte secondary battery according to claim
1, wherein the non-aqueous electrolyte contains 0.1 to 1 volume %
of tetrahydrofuran as the compound having an ether group.
8. The non-aqueous electrolyte secondary battery according to claim
1, wherein the non-aqueous electrolyte further contains 0.5 to 4
weight % of vinylene carbonate.
9. The non-aqueous electrolyte secondary battery according to claim
2, wherein the negative electrode active material is a graphite
material, and a battery voltage is 4.3 to 4.4 V when the potential
of the positive electrode reaches 4.4 to 4.5 V (vs.
Li/Li.sup.+).
10. The non-aqueous electrolyte secondary battery according to
claim 2, wherein the non-aqueous electrolyte contains diethyl
carbonate as a solvent.
11. The non-aqueous electrolyte secondary battery according to
claim 2, wherein the non-aqueous electrolyte further contains 0.5
to 4 weight % of vinylene carbonate.
12. The non-aqueous electrolyte secondary battery according to
claim 3, wherein the negative electrode active material is a
graphite material, and a battery voltage is 4.3 to 4.4 V when the
potential of the positive electrode reaches 4.4 to 4.5 V (vs.
Li/Li.sup.+).
13. The non-aqueous electrolyte secondary battery according to
claim 3, wherein the non-aqueous electrolyte contains diethyl
carbonate as a solvent.
14. The non-aqueous electrolyte secondary battery according to
claim 3, wherein the non-aqueous electrolyte further contains 0.5
to 4 weight % of vinylene carbonate.
15. The non-aqueous electrolyte secondary battery according to
claim 4, wherein the non-aqueous electrolyte further contains 0.5
to 4 weight % of vinylene carbonate.
Description
[0001] This application is a continuation of application Ser. No.
11/699,000, filed Jan. 29, 2007, which claims priority based on
Japanese Patent Application No. 2006-020936, filed Jan. 30, 2006,
which applications are incorporated herein by reference.
BACKGROUND OF THE INVENTION
[0002] 1. Field of the Invention
[0003] The present invention relates to non-aqueous electrolyte
secondary batteries that contain a lithium cobalt oxide as the
positive electrode active material.
[0004] 2. Description of Related Art
[0005] A high energy density battery that has drawn attention in
recent years is a non-aqueous electrolyte secondary battery that
employs a negative electrode active material composed of a carbon
material, metallic lithium, or an alloy capable of absorbing and
desorbing lithium ions, and a positive electrode active material
made of a lithium-transition metal composite oxide represented by
the chemical formula LiMO.sub.2 (where M is a transition
metal).
[0006] A representative example of the lithium-containing
transition metal complex oxide is lithium cobalt oxide
(LiCoO.sub.2), which has been already put to practical use as the
positive active material for non-aqueous electrolyte secondary
batteries. For non-aqueous electrolyte secondary batteries using a
lithium transition metal oxide, such as lithium cobalt oxide, as
the positive active material and a carbon material, such as
graphite, as the negative active material, an end-of-charge voltage
is generally prescribed at 4.1-4.2 V. In this case, the active
material of the positive electrode utilizes only 50-60% of its
theoretical capacity. Accordingly, if the end-of-charge voltage is
increased to a higher value, a capacity (utilization factor) of the
positive electrode can be improved to increase the battery capacity
and energy density.
[0007] However, when the end-of-charge voltage of the battery is
increased to a higher value, deterioration in the structure of
LiCoO2 and decomposition of the electrolyte solution at the
positive electrode surface tend to easily occur. In particular,
when the battery is stored in a charged state at high temperature,
a problem arises that the charge-discharge performance of the
battery degrades due to a battery thickness increase originating
from a gas generated by the reaction between the positive electrode
and the electrolyte solution, a resistance increase resulting from
reaction products, and disintegration of the positive electrode
material.
[0008] Japanese Published Unexamined Patent Application No.
7-272756 proposes that, in a non-aqueous electrolyte secondary
battery using a lithium cobalt oxide as a positive electrode active
material and a graphite material as a negative electrode active
material, the electrolyte solution contain a compound having an
ester group such as an alkyl ester therein, in order to improve the
high-temperature storage characteristics in a charged state.
[0009] Even with the addition of the compound having an ester group
to the electrolyte solution, however, the battery swelling and
deterioration in battery performance that originate from
high-temperature storage in a charged state are considerable in the
case that the charge voltage of the battery is increased to a
higher value than conventionally used 4.2 V (that is, in the case
that the charge potential of the positive electrode is increased to
a higher value than 4.3 V versus a lithium reference [hereinafter
expressed as "4.3 V (vs. Li/Li.sup.+)"]). Thus, the foregoing
technique has been unable to achieve sufficient improvements.
BRIEF SUMMARY OF THE INVENTION
[0010] Accordingly, it is an object of the present invention to
provide a non-aqueous electrolyte secondary battery that exhibits
excellent storage characteristics in a charged state, with a
non-aqueous electrolyte secondary battery that contains a lithium
cobalt oxide as a positive electrode active material and that is
charged until the potential of the positive electrode reaches 4.4
to 4.5 V (vs. Li/Li.sup.+).
[0011] In order to accomplish the foregoing and other objects, the
present invention provides a non-aqueous electrolyte secondary
battery comprising a positive electrode containing a positive
electrode active material, a negative electrode containing a
negative electrode active material other than metallic lithium, and
a non-aqueous electrolyte, wherein the positive electrode active
material contains a lithium cobalt oxide as its main component, the
non-aqueous electrolyte contains 0.1 to 10 volume % of a compound
having an ether group, and the positive electrode active material
and the negative electrode active material are contained so that
the charge capacity ratio of the negative electrode to the positive
electrode (negative electrode charge capacity/positive electrode
charge capacity) is from 1.0 to 1.2 when the battery is charged
until the potential of the positive electrode reaches 4.4 to 4.5 V
(vs. Li/Li.sup.+).
[0012] According to the present invention, the storage
characteristics in a charged state are significantly improved in
the non-aqueous electrolyte secondary battery that contains a
lithium cobalt oxide as a positive electrode active material and
that is charged until the potential of the positive electrode
reaches 4.4 to 4.5 V (vs. Li/Li.sup.+).
DETAILED DESCRIPTION OF THE INVENTION
[0013] The non-aqueous electrolyte secondary battery according to
the present invention comprises a positive electrode containing a
positive electrode active material, a negative electrode containing
a negative electrode active material other than metallic lithium,
and a non-aqueous electrolyte. The positive electrode active
material contains a lithium cobalt oxide as its main component. The
non-aqueous electrolyte contains 0.1 to 10 volume % of a compound
having an ether group. The positive electrode active material and
the negative electrode active material are contained in the battery
so that the charge capacity ratio of the negative electrode to the
positive electrode (negative electrode charge capacity/positive
electrode charge capacity) is from 1.0 to 1.2 when the battery is
charged until the potential of the positive electrode reaches 4.4
to 4.5 V (vs. Li/Li.sup.+).
[0014] It is believed that when the non-aqueous electrolyte
secondary battery containing a lithium cobalt oxide as a positive
electrode active material is stored at high temperature in a
charged state, battery thickness increase and capacity degradation
take place because the oxidation state of the cobalt in the active
material is increased by charging, and the catalysis of the cobalt
with high oxidation state in the active material brings about
decomposition of the electrolyte solution, clogging of the
separator, deposition of a by-product on the negative electrode,
and so forth, leading to degradation in discharge performance.
[0015] By allowing the non-aqueous electrolyte to contain a
compound having an ether group in a predetermined amount according
to the present invention, the non-aqueous electrolyte secondary
battery that is charged until the potential of the positive
electrode reaches 4.4 to 4.5 V (vs. Li/Li.sup.+) is prevented from
the battery thickness increase and the capacity degradation as
described above that occur when stored at high temperature.
Although the details of why such an effect is obtained by allowing
the non-aqueous electrolyte to contain a compound having an ether
group according to the present invention are not clear, it is
believed that the compound having an ether group contained in the
non-aqueous electrolyte decomposes when the initial charging is
carried out at a charge voltage higher than that used
conventionally, forming a surface film containing carbon and oxygen
on the surface of the positive electrode active material and
preventing side reactions between the positive electrode and the
non-aqueous electrolyte. Such an effect cannot be obtained with a
compound having an ester group even if the compound similarly
contains carbon and oxygen.
[0016] The compound having an ether group has been generally
considered inappropriate for use in a secondary battery that uses a
positive electrode material having a high battery reaction
potential, such as a lithium cobalt oxide, because it has a higher
vapor pressure and a lower oxidative decomposition potential and is
more susceptible to anodic oxidation than the carbonates that are
currently used as the solvents. However, with the non-aqueous
electrolyte secondary battery that is charged until the potential
of the positive electrode reaches 4.4 to 4.5 V (vs. Li/Li.sup.+) as
in the present invention, the storage characteristics in a charged
state can be improved by allowing the non-aqueous electrolyte to
contain a compound having an ether group in a predetermined amount
according to the present invention.
[0017] In the present invention, the lithium cobalt oxide is
contained in the positive electrode as the main component of the
positive electrode active material, and it is preferable that the
lithium cobalt oxide be contained as the positive electrode active
material in an amount of 60 weight % or greater. In addition, it is
preferable that in the present invention, the lithium cobalt oxide
contains zirconium and magnesium. It is preferable that the amount
of zirconium contained in the lithium cobalt oxide be within the
range of from 0.01 mole % to 2.0 mole % with respect to the
transition metals. The content of magnesium is preferably within
the range of from 0.1 mole % to 2.0 mole %. If the amounts of these
elements are too small, the effect of suppressing capacity
degradation may not be obtained sufficiently. On the other hand, if
the amounts of these elements are too large, they may cause adverse
effects on the discharge characteristics of the positive
electrode.
[0018] In addition, it is preferable that zirconium (Zr) in
particulate form be adhered on the surface of the lithium cobalt
oxide by sintering. When the zirconium-containing compound is
adhered on the surface of the lithium cobalt oxide, lithium ions
and electrons are transferred smoothly at the surface of the
lithium cobalt oxide during charge and discharge, and the oxidation
decomposition of the electrolyte solution can be suppressed.
[0019] Moreover, it has been confirmed that magnesium (Mg) is
present both in the lithium cobalt oxide and in the
zirconium-containing compound on the surface of the lithium cobalt
oxide. It has been confirmed that because Mg diffuses into both of
them, the zirconium-containing compound and the lithium cobalt
oxide are firmly sintered. Thus, the addition of Mg enhances the
adhesion between the zirconium-containing compound and the lithium
cobalt oxide, significantly enhancing the effect of suppressing the
decomposition of the electrolyte solution.
[0020] It is preferable that the lithium cobalt oxide usable in the
present invention be represented by the chemical formula
Li.sub.aCO.sub.1-x-y-zZr.sub.xMg.sub.yM.sub.zO.sub.2, where M is at
least one element selected from the group consisting of Al, Ti, and
Sn; 0.ltoreq.a.ltoreq.1.1; x>0; y>0; z.gtoreq.0; and
0<x+y+z.ltoreq.0.03.
[0021] Examples of the compound containing an ether group that is
contained in the non-aqueous electrolyte in the present invention
include diethyl ether and tetrahydrofuran. Although these compounds
that contain ether groups have low boiling points (the boiling
point of diethyl ether is 34.5.degree. C., and the boiling point of
tetrahydrofuran is 66.degree. C.), they are capable of suppressing
battery swelling during high-temperature storage, in comparison
with the batteries that do not contain the compound having an ether
group. Accordingly, it is believed that most of the compound
containing an ether group that has been added to the non-aqueous
electrolyte is decomposed before the storage, in other words, is
decomposed during the initial charging.
[0022] The content of the compound having an ether group in the
non-aqueous electrolyte is 0.1 to 10 volume %. More preferable
values of the content can vary depending on the type of the
compound having an ether group. For example, in the case of diethyl
ether, the content is preferably from 1 volume % to 10 volume %,
while in the case of tetrahydrofuran, the content is preferably
from 0.1 volume % to 1 volume %. If the content of the compound
having an ether group is too low, the effect of suppressing the
battery swelling and the capacity degradation cannot be
sufficiently obtained. On the other hand, if the content is too
high, the surface film formed on the positive electrode surface
becomes too great, which may cause adverse effects on the battery
performance.
[0023] The compound having an ether group that is used in the
present invention is preferably a compound having a hydrocarbon
chain. Examples thereof include diethyl ether, ethyl methyl ether,
dimethoxyethane, diethylene glycol dimethyl ether, triethylene
glycol dimethyl ether, tetraethylene glycol dimethyl ether,
ethylene glycol dimethyl ether, 1,3-dioxolane, tetrahydrofuran,
2-methyltetrahydrofuran, 12-crown-4-ether, and 15-crown-5-ether.
Particularly preferred among these is at least one compound
selected from the group consisting of diethyl ether,
2-methyltetrahydrofuran, tetrahydrofuran, diethylene glycol
dimethyl ether, 1,4-dioxane, 12-crown-4-ether, and
15-crown-5-ether.
[0024] In the present invention, it is preferable that the
non-aqueous electrolyte further contain 0.5 to 4 weight % of
vinylene carbonate. The reason is that vinylene carbonate
decomposes and forms a surface film on the negative electrode
surface, suppressing the reaction between the negative electrode
and the electrolyte solution during high-temperature storage in a
charged state. For the same reason, it is preferable that the
solvent used for the non-aqueous electrolyte contain ethylene
carbonate.
[0025] In the present invention, a commonly used solvent in the
non-aqueous electrolyte is a mixed solvent of a cyclic carbonate,
such as ethylene carbonate and propylene carbonate, and a chain
carbonate, such as dimethyl carbonate, ethyl methyl carbonate, and
diethyl carbonate. In the present invention, it is particularly
preferable that the non-aqueous electrolyte contain diethyl
carbonate as the chain carbonate. Allowing the non-aqueous
electrolyte to contain diethyl carbonate can more effectively
prevent the oxidation decomposition of the electrolyte solution in
a highly charged state and at a high temperature. The content of
diethyl carbonate in the solvent is preferably within the range of
from 10 volume % to 70 volume %.
[0026] In the present invention, a preferable example of the
negative electrode active material is a graphite material. The
above-mentioned vinylene carbonate can form a desirable surface
film on the surface of the graphite material.
[0027] Examples of the solute in the non-aqueous electrolyte usable
in the present invention include LiPF.sub.6, LiBF.sub.4,
LiCF.sub.2SO.sub.3, LiN(CF.sub.3SO.sub.2).sub.2,
LiN(C.sub.2F.sub.5SO.sub.2).sub.2,
LiN(CF.sub.3SO.sub.2)(C.sub.4F.sub.9SO.sub.2),
LiC(CF.sub.3SO.sub.2).sub.3, LiC(C.sub.2F.sub.5SO.sub.2).sub.3,
LiAsF.sub.6, LiClO.sub.4, Li.sub.2B.sub.10Cl.sub.10,
Li.sub.2B.sub.12Cl.sub.12, and mixtures thereof. Among these,
LiPF.sub.6 (lithium hexafluorophosphate) is particularly
preferable.
[0028] In the present invention, the positive electrode active
material and the negative electrode active material are contained
in the battery so that the charge capacity ratio of the negative
electrode to the positive electrode (negative electrode charge
capacity/positive electrode charge capacity) is from 1.0 to 1.2
when the battery is charged until the potential of the positive
electrode reaches 4.4 to 4.5 V (vs. Li/Li.sup.+). The charge
capacity ratio is the charge capacity ratio of the portions where
the positive electrode and the negative electrode face each other.
Setting the charge capacity ratio of the negative electrode to the
positive electrode to be 1.0 or greater serves to prevent metallic
lithium from depositing on the negative electrode surface. Also,
setting the charge capacity ratio to be 1.2 or less serves to
prevent the energy density from lowering as a result of an
excessive amount of the negative electrode active material. When a
graphite material is used as a negative electrode active material,
the end-of-charge voltage is set at from 4.3 V to 4.4 V. If the
end-of-charge voltage is higher than 4.4 V, the effect of
suppressing decomposition of the electrolyte solution and
disintegration of the positive electrode becomes insufficient;
therefore, it is preferable that the end-of-charge voltage be 4.4 V
or lower.
EXAMPLES
[0029] Hereinbelow, the present invention is described in further
detail based on examples thereof. It should be construed, however,
that the present invention is not limited to the following examples
but various changes and modifications are possible without
departing from the scope of the invention.
Example 1
Preparation of Positive Electrode Active Material
[0030] Li.sub.2CO.sub.3, CO.sub.3O.sub.4, ZrO.sub.2, and MgO were
mixed in an Ishikawa-type automated mortar so that the mole ratio
of Li:Co:Zr:Mg became 1:0.993:0.002:0.005. Thereafter, the
resultant mixture was sintered in an air atmosphere at 850.degree.
C. for 20 hours, and then pulverized, whereby a lithium cobalt
oxide having an average particle size of about 6.4 .mu.m was
obtained. The resultant lithium cobalt oxide had a formula of
LiCo.sub.0.993Zr.sub.0.002Mg.sub.0.005O.sub.2 and a BET specific
surface area of 0.42 m.sup.2/g.
[0031] Preparation of Positive Electrode
[0032] Carbon (acetylene black) as a conductive agent,
polyvinylidene fluoride as a binder agent, and
N-methyl-2-pyrrolidone as a dispersion medium were added to the
positive electrode active material thus obtained so that the active
material, the conductive agent, and the binder agent were mixed in
a weight ratio f 90:5:5, and thereafter the mixture was kneaded to
prepare a positive electrode slurry. The prepared slurry was
applied onto an aluminum foil serving as a current collector, and
then dried. Thereafter, the resultant material was pressure-rolled
using pressure rollers, and a current collector tab was attached
thereto. Thus, a positive electrode was prepared.
[0033] Preparation of Negative Electrode
[0034] Artificial graphite (average particle size of 21 .mu.m and
BET specific surface area of 4.0 m.sup.2/g) as a negative electrode
active material and styrene-butadiene rubber as a binder were added
to an aqueous solution of carboxymethylcellulose, serving as a
thickening agent, so that the active material, the binder, and the
thickening agent were mixed in a weight ratio of 95:3:2.
Thereafter, the mixture was kneaded to prepare a negative electrode
slurry. The slurry thus prepared was applied onto a copper foil
serving as a current collector, and then dried. Thereafter, the
resultant material was pressure-rolled using pressure rollers, and
a current collector tab was attached thereto. Thus, a negative
electrode was prepared.
[0035] Preparation of Electrolyte Solution
[0036] Lithium hexafluorophosphate (LiPF0 was dissolved at a
concentration of 1 mole/liter into a mixed solvent of 0.3:7 volume
ratio of ethylene carbonate (EC) and diethyl carbonate (DEC).
Further, 2.0 weight % of vinylene carbonate (VC) and 1.0 volume %
of diethyl ether with respect to the electrolyte solution were
added to the mixture. Thus, an electrolyte solution was
prepared.
[0037] Preparation of Battery
[0038] The positive electrode and the negative electrode prepared
in the above-described manner were wound together in such a manner
that they oppose each other across a separator interposed
therebetween so that the ratio of negative electrode charge
capacity/positive electrode charge capacity became 1.0 when the
charge voltage was set at 4.4 V (when the potential of the positive
electrode was set at 4.5 V (vs. Li/Li.sup.+)), to prepare a wound
assembly. Then, in a glove box under an Ar (argon) atmosphere, the
wound assembly and the electrolyte solution were sealed into an
aluminum laminate whereby a non-aqueous electrolyte secondary
battery Al in a battery standard size of 3.6 mm thickness.times.3.5
cm width.times.6.2 cm length was obtained.
[0039] Evaluation of Storage Characteristics in Charged State
[0040] The non-aqueous electrolyte secondary battery thus prepared
was charged at a constant current of 650 mA until the battery
voltage reached 4.4 V, then further charged at a constant voltage
of 4.4 V until the current became 32 mA. Thereafter, the battery
was discharged at a constant current of 650 mA until the battery
voltage reached 2.75 V, in order that the discharge capacity (mAh)
of the battery before storage was measured.
[0041] Furthermore, the battery was charged to 4.4 V in the
foregoing manner, and the thickness of the battery before storage
was measured.
[0042] The battery was stored for 5 days in a thermostatic chamber
at an elevated temperature of 60.degree. C. and was thereafter
taken out. After the battery was sufficiently cooled, the battery
thickness was measured. The battery swelling rate thereof was
obtained by dividing the difference between the battery thickness
after storage in a charged state and the battery thickness before
storage in a charged state by the battery thickness before storage
in a charged state.
[0043] The battery that had been cooled was discharged at a
constant current of 650 mA until the battery voltage lowered to
2.75 V, to determine the discharge capacity (mAh) of the battery
after storage. The discharge capacity obtained after storage in a
charged state was defined as the remaining capacity, and the
capacity retention rate was obtained by dividing the remaining
capacity by the discharge capacity before storage.
[0044] Table 1 below shows the battery swelling rate and the
capacity retention rate.
Example 2
[0045] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 2.0 volume % of diethyl ether
was added to the electrolyte solution in the preparation of the
electrolyte solution.
[0046] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A2 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 3
[0047] An electrolyte solution was prepared in the same manner as
described in Example 1, except that the amount of the additive
compound diethyl ether was 5.0 volume % in the preparation of the
electrolyte solution.
[0048] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A3 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 4
[0049] An electrolyte solution was prepared in the same manner as
described in Example 1, except that the amount of the additive
compound diethyl ether was 10.0 volume % in the preparation of the
electrolyte solution.
[0050] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A4 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 5
[0051] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 0.1 volume % of
2-methyl-tetrahydrofuran (2Me-THF) was used as the additive
compound in place of diethyl ether in the preparation of the
electrolyte solution.
[0052] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A5 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 6
[0053] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 0.5 volume % of
2-methyl-tetrahydrofuran (2Me-THF) was used as the additive
compound in place of diethyl ether in the preparation of the
electrolyte solution.
[0054] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A6 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 7
[0055] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 1.0 volume % of
2-methyl-tetrahydrofuran (2Me-THF) was used as the additive
compound in place of diethyl ether in the preparation of the
electrolyte solution.
[0056] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A7 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 8
[0057] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 0.1 volume % of tetrahydrofuran
(THF) was used as the additive compound in place of diethyl ether
in the preparation of the electrolyte solution.
[0058] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A8 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 9
[0059] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 0.5 volume % of tetrahydrofuran
(THF) was used as the additive compound in place of diethyl ether
in the preparation of the electrolyte solution.
[0060] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A9 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 10
[0061] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 1.0 volume % of tetrahydrofuran
(THF) was used as the additive compound in place of diethyl ether
in the preparation of the electrolyte solution.
[0062] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A10 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 11
[0063] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 1.0 volume % of 1,4-dioxane
(1,4-DO) was used as the additive compound in place of diethyl
ether in the preparation of the electrolyte solution.
[0064] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery All was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 12
[0065] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 1.0 volume % of diethylene
glycol dimethyl ether (DDE) was used as the additive compound in
place of diethyl ether in the preparation of the electrolyte
solution.
[0066] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A12 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 13
[0067] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 1.0 volume % of
12-crown-4-ether was used as the additive compound in place of
diethyl ether in the preparation of the electrolyte solution.
[0068] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A13 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Example 14
[0069] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 1.0 volume % of
15-crown-5-ether was used as the additive compound in place of
diethyl ether in the preparation of the electrolyte solution.
[0070] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery A14 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Comparative Example 1
[0071] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 2 weight % of vinylene
carbonate (VC) alone was used as the additive compound in the
preparation of the electrolyte solution.
[0072] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery X1 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Comparative Example 2
[0073] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 2 weight % of vinylene
carbonate (VC) and 1 volume % of methyl acetate were used as the
additive compounds in the preparation of the electrolyte
solution.
[0074] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery X2 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
Comparative Example 3
[0075] An electrolyte solution was prepared in the same manner as
described in Example 1, except that 2 weight % of vinylene
carbonate (VC) and 1 volume % of ethyl propionate were used as the
additive compounds in the preparation of the electrolyte
solution.
[0076] Using the electrolyte solution thus prepared, a non-aqueous
electrolyte secondary battery X3 was fabricated in the same manner
as described in Example 1, and the storage characteristics in a
charged state were evaluated.
[0077] Table 1 below shows the evaluation results of the storage
characteristics in a charged state for the non-aqueous electrolyte
secondary batteries A1 to A14 of Examples 1 to 14 as well as the
non-aqueous electrolyte secondary batteries X1 to X3 of Comparative
Examples 1 to 3, prepared in the above-described manners.
[0078] The values of battery swelling rate and capacity retention
rate in the table are expressed in percentages.
TABLE-US-00001 TABLE 1 Additive to Battery swelling Capacity
retention electrolyte rate after rate after 5-day solution 5-day
storage storage at Battery (Amount added) at 60.degree. C. (%)
60.degree. C. (%) Ex. 1 A1 VC (2.0 wt. %), 28.4 67.7 diethyl ether
(1.0 vol. %) Ex. 2 A2 VC (2.0 wt. %), 11.0 68.5 diethyl ether (2.0
vol. %) Ex. 3 A3 VC (2.0 wt. %), 5.2 68.0 diethyl ether (5.0 vol.
%) Ex. 4 A4 VC (2.0 wt. %), 9.3 60.2 diethyl ether (10 vol. %) Ex.
5 A5 VC (2.0 wt. %), 34.6 65.9 2Me-THF (0.1 vol. %) Ex. 6 A6 VC
(2.0 wt. %), 24.4 69.4 2Me-THF (0.5 vol. %) Ex. 7 A7 VC (2.0 wt.
%), 25.1 70.2 2Me-THF (1.0 vol. %) Ex. 8 A8 VC (2.0 wt. %), 39.9
71.7 THF (0.1 vol. %) Ex. 9 A9 VC (2.0 wt. %), 23.4 73.3 THF (0.5
vol. %) Ex. 10 A10 VC (2.0 wt. %), 13.7 71.6 THF (1.0 vol. %) Ex.
11 A11 VC (2.0 wt. %), 24.3 62.7 1,4 DO (1.0 vol. %) Ex. 12 A12 VC
(2.0 wt. %), 32.0 72.2 DDE (1.0 vol. %) Ex. 13 A13 VC (2.0 wt. %)
25.2 72.5 12-crown-4-ether (1.0 vol. %) Ex. 14 A14 VC (2.0 wt. %),
8.4 60.6 15-crown-5-ether (1.0 vol. %) Comp. X1 VC (2.0 wt. %) 43.4
59.5 Ex. 1 Comp. X2 VC (2.0 wt. %), 52.3 58.5 Ex. 2 methyl acetate
(1.0 vol. %) Comp. X3 VC (2.0 wt. %), 54.9 58.7 Ex. 3 ethyl
propionate (1.0 vol. %)
[0079] The results shown in Table 1 clearly demonstrate that the
batteries A1 to A14 of Examples 1 to 14 according to the present
invention exhibited smaller battery swelling rates and better
capacity retention rates than those of the batteries X1 to X3 of
Comparative Examples 1 to 3. Although a compound having an ester
group was added in Comparative Examples 2 and 3, the advantageous
effects of the present invention were not obtained even with the
addition of the compound having an ester group.
[0080] In addition, in Examples 1 to 14 according to the present
invention, the battery swelling rates were smaller than those in
Comparative Examples 1 to 3. It is believed that, in each battery
according to the present invention, the compound having an ether
group, which is a low-boiling point component, was decomposed
during the initial charging.
REFERENCE EXPERIMENT
Reference Example 1
[0081] A non-aqueous electrolyte secondary battery B1 was
fabricated in the same manner as described in Example 4, except
that the positive electrode and the negative electrode were
prepared so that the ratio of negative electrode charge
capacity/positive electrode charge capacity became 1.1 when the
charge voltage was set at 4.2 V.
Reference Example 2
[0082] A non-aqueous electrolyte secondary battery Y1 was
fabricated in the same manner as described in Comparative Example
1, except that the positive electrode and the negative electrode
were prepared so that the ratio of negative electrode charge
capacity/positive electrode charge capacity became 1.1 when the
charge voltage was set at 4.2 V.
[0083] Table 2 below shows the evaluation results of the storage
characteristics in a charged state for the non-aqueous electrolyte
secondary batteries B1 and Y1 of Reference Examples 1 and 2,
respectively, prepared in the above-described manners.
[0084] The values of battery swelling rate and capacity retention
rate in the table are expressed in percentage.
TABLE-US-00002 TABLE 2 Additive to Battery swelling Capacity
retention electrolyte rate after rate after 5-day solution 5-day
storage storage at Battery (Amount added) at 60.degree. C. (%)
60.degree. C. (%) Ref. B1 VC (2.0 wt. %), 27.8 78.2 Ex. 1 diethyl
ether (10.0 vol. %) Ref. Y2 VC (2.0 wt. %) 2.8 91.8 Ex. 2
[0085] As clearly seen from the results shown in Table 2, even the
addition of the compound having an ether group to the non-aqueous
electrolyte cannot prevent the swelling of the battery, causes the
degradation of the capacity retention rate, and cannot obtain the
advantageous effect of the present invention, when the battery is
charged according to the conventionally common charge condition of
a charge voltage of 4.2 V, in other words, when the battery is
charged so that the potential of the positive electrode becomes 4.3
V (vs. Li/Li.sup.+). It is believed that when the battery is
charged at a charge voltage of 4.2 V, the added compound having an
ether group does not sufficiently decompose during the initial
charging and remains in the electrolyte solution, and this remnant
of the added compound vaporizes or reacts with the positive
electrode during the high-temperature storage, causing gas
generation and exacerbating battery deterioration.
[0086] For the reason described above, it will be appreciated that
the effect of adding a compound having an ether group to the
electrolyte solution according to the present invention is
exhibited in the battery systems in which the charge voltage is
higher than conventionally used 4.2 V.
[0087] Only selected embodiments have been chosen to illustrate the
present invention. To those skilled in the art, however, it will be
apparent from the foregoing disclosure that various changes and
modifications can be made herein without departing from the scope
of the invention as defined in the appended claims.
[0088] Furthermore, the foregoing description of the embodiments
according to the present invention is provided for illustration
only, and not for limiting the invention as defined by the appended
claims and their equivalents.
[0089] This application claims priority of Japanese Patent
Application No. 2006-020936 filed Jan. 30, 2006, which is
incorporated herein by reference.
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