U.S. patent number RE35,818 [Application Number 08/539,825] was granted by the patent office on 1998-06-02 for non-aqueous electrolyte secondary battery and method of producing the same.
This patent grant is currently assigned to Seiko Instruments Inc.. Invention is credited to Hideki Ishikawa, Fumiharu Iwasaki, Tsugio Sakai, Akifumi Sakata, Kensuke Tahara, Seiji Yahagi.
United States Patent |
RE35,818 |
Tahara , et al. |
June 2, 1998 |
Non-aqueous electrolyte secondary battery and method of producing
the same
Abstract
A non-aqueous electrolyte secondary battery has a negative
electrode, a positive electrode and a non-aqueous electrolyte with
lithium ion conductivity. A composite oxide produced from a metal
or a metalloid and lithium represented by composition formula
Li.sub.x MO (where M represents metals or metalloids other than
alkali metals, and x satisifies 0.ltoreq.x) is used as an active
material of one or both of the negative electrode and the positive
electrode. The battery exhibits a large charging/discharging
capacity and a high energy density together with smaller
polarization (internal resistance) on charging and discharging
which facilitates a large current charging and discharging with a
long cycle life and reduces deterioration due to excess charging
and excess discharging.
Inventors: |
Tahara; Kensuke (Sendai,
JP), Ishikawa; Hideki (Sendai, JP), Sakai;
Tsugio (Sendai, JP), Sakata; Akifumi (Tokyo,
JP), Iwasaki; Fumiharu (Tokyo, JP), Yahagi;
Seiji (Tokyo, JP) |
Assignee: |
Seiko Instruments Inc.
(JP)
|
Family
ID: |
27564964 |
Appl.
No.: |
08/539,825 |
Filed: |
October 6, 1995 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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Reissue of: |
127960 |
Sep 28, 1993 |
05401599 |
Mar 28, 1995 |
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Foreign Application Priority Data
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Oct 1, 1992 [JP] |
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4-322028 |
Oct 2, 1992 [JP] |
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4-265179 |
Mar 18, 1993 [JP] |
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5-59165 |
Mar 22, 1993 [JP] |
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5-062264 |
Aug 17, 1993 [JP] |
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5-203479 |
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Current U.S.
Class: |
429/224; 204/219;
204/242; 204/292; 204/293; 204/291; 429/231; 429/231.1 |
Current CPC
Class: |
H01M
4/505 (20130101); H01M 4/485 (20130101); H01M
6/16 (20130101); Y02E 60/10 (20130101); H01M
6/164 (20130101); H01M 10/052 (20130101) |
Current International
Class: |
H01M
4/50 (20060101); H01M 4/48 (20060101); H01M
10/36 (20060101); H01M 10/40 (20060101); H01M
6/16 (20060101); H01M 004/02 () |
Field of
Search: |
;429/218,219,224
;204/242,291,292,293,219 |
References Cited
[Referenced By]
U.S. Patent Documents
|
|
|
4980251 |
December 1990 |
Thackeray et al. |
5011752 |
April 1991 |
Kordesch et al. |
|
Primary Examiner: Nuzzolillo; Maria
Attorney, Agent or Firm: Adams & Wilks
Claims
What is claimed is:
1. A non-aqueous electrolyte secondary battery comprising: a
negative electrode; a positive electrode; and a non-aqueous
electrolyte with lithium ion conductivity; wherein either one or
both of the negative and positive electrodes has an active material
comprised of a composite oxide represented by composition formula,
Li.sub.x MO, where M represents one or more elements selected from
metalloids and metals other than alkali metals, and x satisifies
0.ltoreq.x.
2. A non-aqueous electrolyte secondary battery according to claim
1; wherein the non-aqueous electrolyte comprises at least a
non-aqueous solvent containing ethylene carbonate and a supporting
electrolyte containing lithium ion.
3. A non-aqueous electrolyte secondary battery comprising: a
negative electrode; a positive electrode; and a non-aqueous
electrolyte with lithium ion conductivity; wherein the negative
electrode has an active material comprised of a composite oxide
represented by composition formula Li.sub.x MO, where M is one kind
or more kinds of elements selected from Mn, Ti, Zn and metals and
metalloids selected from Group 14 of the periodic table, and x
satisfies 0.ltoreq.x.
4. A non-aqueous electrolyte secondary battery according to claim
3; wherein the non-aqueous electrolyte comprises at least a
non-aqueous solvent containing ethylene carbonate and a supporting
electrolyte containing lithium ion.
5. A non-aqueous electrolyte secondary battery comprising: a
negative electrode; a positive electrode; and a non-aqueous
electrolyte with lithium ion conductivity; wherein the negative
electrode has an active material comprised of a composite oxide
represented by composition formula Li.sub.x MO, where M represents
one or more elements selected from metalloids and metals other than
alkali metals, and x satisfies 0.ltoreq.x; and wherein the positive
electrode has an active material comprised of a composite oxide
represented by composition formula Li.sub.a T.sub.b L.sub.c O.sub.2
and has a layer-like structure, where T is one or more transition
metal elements, L is one or more metalloid elements selected from
boron B and silicon Si, and a, b, and c satisfy 0<a.ltoreq.1.15,
0.85.ltoreq.b+c.ltoreq.1.3, and 0.ltoreq.c.
6. A non-aqueous electrolyte secondary battery according to claim
5; wherein the non-aqueous electrolyte comprises at least a
non-aqueous solvent containing ethylene carbonate and a supporting
electrolyte containing lithium ion.
7. A method for producing a non-aqueous electrolyte secondary
battery having a negative electrode, a positive electrode and a
non-aqueous electrolyte with lithium ion conductivity, the method
comprising: incorporating lithium ion into a monoxide MO or a metal
or a metalloid by electrochemical reaction; and producing a
composite oxide Li.sub.x MO of the metal or the metalloid and
lithium inside the battery after assembly of the battery, or inside
or outside the battery during production of the battery.
8. A non-aqueous electrolyte secondary battery comprising: positive
and negative electrodes separated by a non-aqueous electrolyte
capable of conducting lithium ions, at least one of the positive
and negative electrodes being comprised of an active material
composed of a composite oxide Li.sub.x MO, where M is one or more
elements selected from metalloids and metals other than alkali
metals, and x is 0.ltoreq.x.
9. A non-aqueous electrolyte secondary battery according to claim
8; wherein the negative electrode has an active material composed
of a composite oxide Li.sub.x MO, where M is one or more metalloids
and metals selected from Group 14 of the periodic table.
10. A non-aqueous electrolyte secondary battery according to claim
9; wherein the positive electrode has an active material composed
of a composite oxide Li.sub.a T.sub.b L.sub.c O.sub.2, where T is
one or more transition elements, L is one or more metalloid
elements selected from the group consisting of boron and silicon,
and a, b and c are 0<a.ltoreq.1.15, 0.85.ltoreq.b+c.ltoreq.1.3,
and 0.ltoreq.c.
11. A non-aqueous electrolyte secondary battery according to claim
10; wherein the positive electrode has a layered structure.
12. A non-aqueous electrolyte secondary battery according to claim
11; wherein the non-aqueous electrolyte includes a non-aqueous
solvent and an electrolyte containing lithium ions.
13. A non-aqueous electrolyte secondary battery according to claim
9; wherein the non-aqueous electrolyte includes a non-aqueous
solvent and an electrolyte containing lithium ions.
14. A non-aqueous electrolyte secondary battery according to claim
8; wherein the positive electrode has an active material composed
of a composite oxide Li.sub.a T.sub.b L.sub.c O.sub.2, where T is
one or more transition elements, L is one or more metalloid
elements selected from the group consisting of boron and silicon,
and a, b and c are 0<a.ltoreq.1.15, 0.85.ltoreq.b+c.ltoreq.1.3,
and 0.ltoreq.c.
15. A non-aqueous electrolyte secondary battery according to claim
14; wherein the positive electrode has a layered structure.
16. A non-aqueous electrolyte secondary battery according to claim
14; wherein the non-aqueous electrolyte includes a non-aqueous
solvent and an electrolyte containing lithium ions.
17. A non-aqueous electrolyte secondary battery according to claim
8; wherein the non-aqueous electrolyte includes a non aqueous
solvent and an electrolyte containing lithium ions.
18. A non-aqueous electrolyte secondary battery according to claim
8; wherein M is one or more elements selected from Mn, Ti, Zn,
metalloids and metals selected from Group 14 of the periodic
table.
19. A non-aqueous electrolyte secondary battery according to claim
18; wherein the non-aqueous electrolyte includes a non-aqueous
solvent and an electrolyte containing lithium ions.
Description
BACKGROUND OF THE INVENTION
The present invention relates to non-aqueous electrolyte secondary
batteries using non-aqueous electrolyte with lithium ion
conductivity where material capable of occluding and emitting
lithium is used as the negative active material and/or positive
active material. In particular, it relates to novel negative active
material and positive active material which provide novel secondary
batteries of high voltage and high energy density having a long
cycle service life with a graded charge/discharge
characteristic.
A non-aqueous electrolyte battery, which uses lithium as a negative
active material, has advantages such as lower self-discharge, high
reliability for a long time, high voltage and high energy density,
and so forth, and is widely utilized in power sources for a memory
backup, camera and the like as a primary battery. However in the
recent years, with the remarkable development of portable type
electronic devices and communication equipment and the like, there
have been proposed various kinds and types of equipments which
require large current output to the batteries as a power supply,
thus secondary batteries of high energy densities capable of
recharging and re-discharging are now in strong demand from the
view point of economical efficiency, and compact size and light
weight of the devices. For this reason, research and development
for increasing the secondary batteries from among the non-aqueous
electrolyte batteries having a high energy density are actively
performed and a part thereof is now in practical use. However, the
energy density, charge and discharge cycle life time, and
reliability are still unsatisfactory.
Conventionally, the positive active material constituting the
positive electrode of a secondary battery of such kind includes
three kinds of types due to charge and discharge reaction profiles
as undermentioned. The first type is one in which lithium ion
(cation) only moves in or out of spaces between layer-to-layer,
lattice positions, or gaps among lattices of the crystal depending
on intercalation and deintercalation reactions and the like as seen
in metal chalcogenides such as TiS.sub.2, MoS.sub.2, and
NbSe.sub.3, and in metal oxides such as MnO.sub.2, MoO.sub.3,
V.sub.2 O.sub.5, Li.sub.x CoO.sub.2, Li.sub.x NiO.sub.2, and
Li.sub.x Mn.sub.2 O.sub.4, and in like cases. The second-type is
one in which mainly anion only stably moves in and out by means of
doping and undoping reactions as seen in conductive polymers such
as polyaniline, polypyrrole, polyparaphenylene. The third type is
one in which, lithium cation and anion can together move in or out
as seen in graphite intercalation compounds and conductive polymers
such as polyacene and the like (intercalation, deintercalation or
doping, undoping and the like).
On the other hand, for the negative active material constituting
the negative electrode of the battery of this kind, the basest
electrode potential is provided in case of using metal lithium
independently, and correspondingly the battery combined with the
positive electrode using the positive active material as described
above advantageously has the highest output voltage with a high
energy density. However in this case, the problem arises because
dendrite or passive compounds are generated on the negative
electrode depending on charge or discharge to produce considerable
deterioration due to charge and discharge and to shorten the cycle
service life time. To solve this problem there are proposed various
utilizations of materials as a negative active material; namely,
(1) alloys obtained by combining lithium with other metals such as
Al, Zn, Sn, Pb, Bi, and Cd; (2) intercalation compounds or
insertion compounds where lithium ion is incorporated into the
crystal structure of inorganic compounds such as WO.sub.2,
MoO.sub.2, Fe.sub.2 O.sub.3, TiS.sub.2, and the like, graphite and
carbonaceous materials obtained by baking organic material; and (3)
conductive polymers such as polyacene, polyacetylene and the like
in which lithium ion is doped.
However in general, in case where the negative electrode using
material capable of occlusion and emission of lithium ion (other
than metal lithium described above as the negative active material)
is combined with the positive electrode using the positive active
material described above to produce the battery, then the electrode
potential of these negative active materials is nobler than the
electrode potential of metal lithium, and a drawback therefore
arises in considerably lowering an operating voltage of the battery
compared to the case of independently using the metal lithium as a
negative active material. For example, the operating voltage is
lowered by 0.2 to 0.8 V in case of using an alloy of lithium and
metals such as Al, Zn, Pb, Sn, Bi, and Cd, by 0 to 1 V for
carbon-lithium intercalation compounds, and by 0.5 to 1.5 V for
lithium ion insertion compounds such as MoO.sub.2, WO.sub.2 and the
like.
Since elements other than lithium are involved as negative
electrode constituent elements, the capacity and energy density per
unit volume and unit weight are considerably lowered
correspondingly.
In addition, when using an alloy of lithium and other metals in (1)
described above, there are such problems that the utilization
efficiency of lithium is low during charge and discharge, and the
cycle life is short due to occurrence of cracks in the electrode to
generate splits on account of repeated charge and discharge and the
like. In the lithium intercalation compound or insertion compound
in case (2), deteriorations such as decay of the crystal structure
and generation of irreversible material are generated by excess
charge and excess discharge, and the electrode potential is high
(noble) in many cases, which results in a drawback of reducing an
output voltage of the battery. In the conductive polymer in case
(3), there is such a problem that the charge and discharge
capacity, in particular, the charge and discharge capacity per unit
volume, is small.
For these reasons, to obtain a long cycle life secondary battery
having a graded charge and discharge characteristic with high
voltage and high energy density, there is required a negative
active material having a larger effective charge and discharge
capacity, i.e., the amount capable of reversible occlusion and
emission of lithium ion simultaneously with a lower (baser)
electrode potential with respect to lithium without deterioration
of crystal structure decay and irreversible substance generation
due to the occlusion and emission of lithium ion at charge and
discharge.
On the other hand, in the positive active material, the first type
has a drawback in that a considerable deterioration arises due to
crystal deintegration and irreversible substance generation on
excess charging and excess discharging although its energy density
is larger. To the contrary, in the second and third types, the
charge and discharge capability, in particular, disadvantageously
the charge and discharge capacity, and energy density per unit
volume are significantly smaller.
Therefore, to obtain a high capacity and high energy density of a
secondary battery having an upgraded excess charging characteristic
and excess discharging characteristic, there is required a positive
active material in which a larger amount of lithium ion can
reversibly be occluded and emitted without crystal deintegration
and irreversible substance generation due to the excess charge and
excess discharge.
SUMMARY OF THE INVENTION
An object of the present is to provide a non-aqueous electrolyte
secondary battery using a material capable of absorbing and
releasing lithium as a negative electrode active material.
Another object of the present is to provide a novel secondary
battery having a high voltage and a high energy density in which
charge and discharge characteristics are excellent, the cycle life
is long, and reliability is high.
Still another object of the present invention is to provide a
non-aqueous electrolyte secondary battery using a composite oxide
containing lithium as a negative electrode active material.
A further object of the present invention is to provide a method
for producing a non-aqueous electrolyte secondary battery in which
inside the battery after assembly thereof or inside or outside the
battery depending on the way of producing the battery, monoxide MO
of metal or metalloid M and lithium or material containing lithium
are electrochemically reacted to incorporate lithium ion into the
monoxide MO of the metal or the metalloid and to produce composite
oxide Li.sub.x MO of the metal or the metalloid and lithium.
To solve the problem hereinbefore described, the present invention
uses a novel lithium ion occlusion/emission material composed of
composite oxide which is composed of metal or metalloid M and
lithium Li according to composition formula Li.sub.x MO (where M
represents a metal or a metalloid other than alkali metals, and
0.ltoreq.x is satisfied) as an active material of at least one of
the negative electrode or positive electrode of the battery of this
kind. The composite oxide capable of lithium ion occlusion/emission
in a non-aqueous electrolyte by electrochemical reaction is used
wherein lithium is contained in crystal structure or amorphous
structure of the oxide having a composition ratio of 1:1 composed
of metal or metalloid M other than alkali metals and oxygen O. For
the metal or the metalloid M forming the composite oxide, any
suitable material that can produce monoxide is used; namely,
transition metals such as Fe, Mn, Ti, V, Nb, Co, and Ni; metals
other than alkali metals such as Zn, Cd, Mg, Ba, Pb, and Sn; and
metalloids such as Si, B, Ge, and Sb; and the like. Such metals or
metalloids M and oxygen O provide a composition ratio of 1:1 as a
standard as described above, however on synthesizing, a
non-stoichiometric compound generates due to deficiency or excess
of the metal or the metalloid M and oxygen O, and the range of such
deficiency and excess depends on the kinds of M, and reaches as
high as .+-.25%. One possessing such non-stoichiometric composition
is also included in the present invention. In particular, when the
transition metal is used as a metal M, deficiency of the metal M or
oxygen O tends to produce a compound having a high
non-stoichiometric degree, thus such produced compound provides a
good amount of sites capable of occlusion of lithium ion into the
crystal structure or amorphous structure of that product material.
This provides an advantage that lithium ion has a high mobility and
a high electron conductivity to easily produce a larger
charge/discharge capacity and a lower polarization. Lithium content
x may preferably be within a range where the composite oxide can
stably be present, and in particular within a scope of
0.ltoreq.x.ltoreq.2.
Two methods are proposed for a preferable method of producing the
composite oxide composed of the metal or the metalloid M and
lithium which are used for negative and/or positive active
materials of the battery according to the present invention,
however such methods are not limited to these examples.
The first method is that each element of the metal or the metalloid
and lithium, or the compound of these but including oxygen, are
mixed at a predetermined mol ratio, thermal treated, and
synthesized in a non-oxidation atmosphere such as an inert
atmosphere or vacuum and the like or in a weak reduction atmosphere
or in an atmosphere where the oxygen amount is controlled. The
metal or the metalloid and lithium to be starting materials may
preferably be their oxide or hydroxide, or salt such as carbonate
or nitrate, or organic compound or compounds producing oxide by
heating in an inert atmosphere or in vacuum. A temperature for
heating depends on the starting materials and the heating
atmospheres, where the composition is available at a temperature
equal to or more than 400.degree. C., preferably equal to or more
than 600.degree. C., and more preferably at equal to or more than
700.degree. C.
The composite oxide of the metal or the metalloid and lithium thus
obtained is used as it is, or used after crushing and granulating
depending on the requirement, as a negative and/or positive active
material. As in the second method mentioned below, there can be
used, as an active material, one in which the composite oxide
containing the lithium and metal lithium or material including
lithium are electrochemically reacted with each other, whereby the
composite oxide is allowed to occlude therein with lithium ion, or
reversely to emit lithium ion, and to enable an increase or
decrease of the lithium content.
The second method is that the metal such as FeO, MnO, TiO, VO, NbO,
Nio, CoO, ZnO, SnO, MgO, BaO, SiO or GeO or monoxide MO of the
metal or the metalloid M is electrochemically reacted with lithium
or material containing lithium so that the lithium ion is occluded
in the monoxide MO to produce the composite oxide composed of the
metal or the metalloid and the lithium.
For the material containing the lithium used for such
electrochemical reaction, there can be used, for example, the
material capable of occluding or emitting lithium ion as used in
the positive active material or the negative active material
described hereinabove with respect to the prior art.
The occlusion of lithium ion into the monoxide MO of the metal or
the metalloid by the electrochemical reaction can be achieved in
the battery after assembling the battery, or inside or outside the
battery depending on the battery producing process, which is
described below.
More specifically, (1) the method is that monoxide composed of the
metal or the metalloid or mixed composite agent composed of those
described above and a conductive agent and a bonding agent are
formed in a predetermined shape to produce one-side electrode
(working electrode), while metal lithium or a material containing
lithium is made the other-side electrode (counter electrode). These
electrodes are opposingly arranged in contact with the non-aqueous
electrolyte with lithium ion conductivity to produce an
electrochemical cell, and hence the working electrode conducts or
discharges a suitable current in the direction of cathode reaction
to occlude the lithium ion electrochemically into the monoxide. The
working electrode thus obtained is used as a negative electrode
and/or positive electrode as it is or as an active material
constituting the negative electrode and/or positive electrode to
constitute the non-aqueous electrolyte secondary battery. (2)
Monoxide composed of the metal or the metalloid, or composite agent
composed of those described above, and a conductive agent and a
bonding agent are formed into a predetermined shape, and lithium or
alloy of lithium or the like is press fit or contact bonded to
produce a laminated electrode, which is assembled into the
non-aqueous electrolyte secondary battery as a negative electrode
or as a positive electrode. The laminated electrode contacts with
the electrolyte in the battery to form a kind of local battery and
to produce self discharge, thus a method of electrochemically
occluding lithium into the monoxide is provided. (3) Monoxide of
the metal or the metalloid is made an active material of one-side
electrode, and the other-side electrode is allowed to contain
lithium to produce material capable of occluding and emitting
lithium ion as an active material, thus such active materials
constitute the non-aqueous electrolyte secondary battery. This is a
method of occluding lithium ion into the monoxide by electrical
charging or discharging while being used as a battery.
The materials thus obtained, the composite oxide Li.sub.x MO
composed of the metals or the metalloids M other than alkali metals
and lithium, are used as a negative and/or positive active
material.
The electrodes using the composite oxide Li.sub.x MO can be used as
an active material for the positive/negative electrodes to form the
secondary battery, and moreover this can be used as either of a
positive electrode or a negative electrode, and an electrode using
various kinds of other negative active materials or positive active
materials capable of occlusion and emission of the lithium or
lithium ion can therefore be used as another electrode in
combination therewith. In particular, the electrode using the
composite oxide Li.sub.x MO as an active material according to the
present invention has less deterioration due to excess charging and
discharging in addition to a larger charge/discharge capacity of
baser region where an electrode potential is equal to or less than
1.9 V relative to that of metal lithium. This therefore is used as
a negative electrode to combine with the positive electrode using a
high potential active material with an electrode potential equal to
or more than 3 V or 4 V relative to the metal lithium such as metal
oxides, V.sub.2 O.sub.5, Li.sub.x CoO.sub.2, Li.sub.x NiO.sub.2,
and Li.sub.x Mn.sub.2 O.sub.4, and to more preferably obtain the
secondary battery of a large current charging and discharging
characteristic having a high voltage and a high energy density with
less deterioration due to the excess charge and excess discharge.
Among these, in the case where M forming the composite oxide
Li.sub.x MO is Mn, Ti, Zn or metal or metalloid (Sn, Pb, Si, Ge) in
Group 14 of the periodic table, this is considered superior as a
negative active material because tile charging/discharging capacity
of baser region with an electrode potential equal to or less than
1.5 V relative to metal lithium is greatly larger with less
deterioration due to the excess charging/discharging.
While on the other hand, a negative electrode using the composite
oxide Li.sub.x MO as a negative active material according to the
invention is combined with a positive electrode using the composite
oxide represented by composition formula of Li.sub.a T.sub.b
L.sub.c O.sub.2 containing lithium with a layered structure as a
positive active material, thus it is particularly preferable to
obtain a long cycle life secondary battery of particularly high
energy density having an upgraded charging/discharging
characteristic with less deterioration due to the excess charge and
excess discharge, where T represents transition metal element, L
represents one or more metalloid element(s) selected from among
boron B and silicon Si, a, b, and c satisfy 0<a<1.15,
0.85<b+c<1,3, and 0.ltoreq.c.
The composite oxide Li.sub.a, T.sub.b L.sub.c O.sub.2 used as a
positive active material of the battery according to the invention
can be composed in an arrangement that each element, or each oxide
or hydroxide, or salts such as carbonate or nitrate with respect to
lithium Li, transition metal T and element L are mixed it a
predetermined ratio, heated, and baked in the air or atmosphere
containing oxygen at equal to or more than 600.degree. C.,
preferably at 700.degree. to 900.degree. C. When, for a supply
source of Li, T, and L, the oxide thereof or the compound thereof
having oxygen is used, it is possible to heat and compose in an
inert atmosphere. The amount of time for heating is ordinarily 4 to
50 hours which is enough to complete the treatment, however in
order to promote the composition reaction axed to raise a
uniformity, it is effective to repeat the processes of baking,
cooling, and crushing and mixing several times.
In the composition formula Li.sub.a T.sub.b L.sub.c O.sub.2, the
amount "a" of Li is standardized at a fixed composition ratio of
a=1 in the heating and composing described above, however, a
non-stoichiometric composition of an extent of .+-.15% is
available, also 0<a<1.15 is satisfied by electrochemical
intercalation, deintercalation and the like.
For transition metal T, the Co, Ni, Fe, Mn, Cr, and V and the like
are preferable, and in particular Co and Ni are more superior and
preferable for the charging/discharging characteristic. For an
amount "c" of boron and/or silicon and an amount "b" of transition
metal T, a remarkable effect is preferably exhibited for
polarization (internal resistance) reduction on charging and
discharging and improvement of a cycle characteristic and the like
under the condition of 0<c and 0.85<b+c<1.3. On the other
hand, the charge/discharge capacity at every cycle is lowered with
an excess amount "c" of boron and/or silicon, and comes to maximum
at 0<c<0.5, whose ravage is particularly suitable.
The electrolyte may preferably be a non-aqueous electrolyte of
lithium ion conductivity such as; organic electrolyte solution
where a lithium ion dissociation salt such as LiClO.sub.4,
LiPF.sub.6, LiBF.sub.4, LiCF.sub.3 SO.sub.3 as a supporting
electrolyte are dissolved in single or mixed solvent of organic
solvent such as .gamma.-butyrolactone, propylene carbonate,
ethylene carbonate, butylene carbonate, dimethyl carbonate, dicthyl
carbonate, methylformate, 1, 2-dimethoxyethane, tetrahydrofuran,
dioxolane, and dimethlylformamide; polymer solid electrolyte where
the lithium salt is a solid soluted into polymer such as
polyethylene oxide, polyphosphasen cross-linked substance or
inorganic solid electrolyte such as Li.sub.3 N and LiI etc.
Particularly, the use of the nonaqueous electrolyte solution
(organic electrolyte solution) containing ethylene carbonate as an
organic solvent is preferred and provides a long cycle life
secondary battery having a higher charge/discharge
characteristic.
The electrodes using composite oxide Li.sub.x MO as an active
material composed of metal or metalloid M other than alkali metals
and lithium according to the present invention, can stably
repeatedly occlude or emit lithium ion for an electrode potential
at least ranging from 0 to 3 V relative to metal lithium in the
non-aqueous electrolyte, and can be used, by such electrode
reaction, as the negative electrode and/or positive electrode of
the secondary battery capable of repeatedly charging and
discharging. Since a high capacity region capable of stably
occluding and emitting lithium ion and repeatedly charging and
discharging is provided in a baser potential region of 0 to 1.9 V
relative to a lithium reference electrode, then a higher
performance can be realized in case of using as a negative
electrode than in case of using as a positive electrode. In
particular, when M is Mn, Ti, and Zn or metals or metalloids in
Group 14 of the periodic table, a baser region with an electrode
potential equal to or less than 1.5 V relative to metal lithium has
a particularly larger charging/discharging capacity together with
less deterioration due to excess charging and excess discharging,
thereby providing a high grade of negative active material.
Compared to the conventional carbonaceous material such as graphite
and the like which has been used for the electrodes of the battery
of this kind, the amount of reversible occlusion and emission of
lithium ion, that is, the charge and discharge capacity is
considerably larger with less polarization of charging/discharging,
therefore charging and discharging at a larger current is
available, deterioration such as decomposition or crystal
deintegration and the like due to the excess charging and excess
discharging is hardly found, and thus an extremely stable battery
with a long cycle life time can be obtained.
The reason why such a satisfactory charge/discharge characteristic
can be obtained is not always clear, which however is estimated as
mentioned below. The composite oxide Li.sub.x MO composed of the
metals or the metalloid M other than alkali metals and lithium, has
a higher mobility of lithium ion in such structure, and in
addition, it is estimated that a considerably good amount of sites
capable of occluding lithium ion are provided to facilitate
occlusion and emission of the lithium ion.
On the other hand, the composite oxide Li.sub.a T.sub.b K.sub.c
O.sub.2 used as a positive active material has an electrode
potential equal to or more than about as high as 4 V relative to
metal lithium, moreover reversible charging and discharging by
intercalation and deintercalation of Li ion are available at least
between 0.ltoreq.a<1.15, and thus an upgraded cycle
characteristic can be obtained with less deterioration due to the
excess charge and excess discharge. Particularly, a polarization is
reduced in 0.05.ltoreq.c<0.5 for B and/or Si content "c" and
resulting in a higher cycle characteristic. In this way, the reason
why such a satisfactory charge/discharge characteristic can be
obtained is not always clear, which however is estimated as
mentioned below. The positive active material Li.sub.a T.sub.b
L.sub.c O.sub.2 according to the present invention has a skeletal
structure similar to a-NaCrO.sub.2 type where a part of the
transition metal element T of oxide Li.sub.a T.sub.b L.sub.c
O.sub.2 with a layered structure of the a-NaCrO.sub.2 type without
containing B and Si is replaced by B or Si. However, B atoms and Si
atoms are possible to reside in the interstices among lattices of
the crystal or at Li sites (replaced by Li). In either of these
cases, it is estimated that crystal structure and electron state
are changed depending on the presence of B or Si, and Li ion comes
to increase its conductivity and to facilitate occlusion and
emission of the lithium ion.
For this reason, the battery, which is used by combining the
negative active material with the positive active material
according to the present invention, has a particularly upgraded
performance in that, with a higher operating voltage of 4 to 2 V,
the amount of reversible occlusion and emission of the lithium ion,
i.e., the charging/discharging capacity, is considerably larger
with less polarization on the charge and discharge, and thus larger
current charging/discharging is available, moreover decomposition
or crystal deintegration of the active material due to the excess
charging and excess discharging are hardly found and an extremely
stable long cycle service life is provided.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a view showing one example of a battery for comparison
evaluation of an electrode active material in the present
invention.
FIG. 2 is a graphical representation of a charging characteristic
of active materials at the third cycle for comparison of a battery
according to the present invention with the conventional
battery.
FIG. 3 is a graphical representation of a discharging
characteristic of active materials at the third cycle for
comparison of a battery according to the present invention with the
conventional battery.
FIG. 4 is a graphical representation of a cycle characteristic of
active materials for comparison of a battery according to the
present invention with the conventional battery.
FIG. 5 is a graphical representation of a charging characteristic
of active materials at the third cycle for comparison of a battery
according to the present invention with the conventional
battery.
FIG. 6 is a graphical representation of a discharging
characteristic of active materials at the third cycle for
comparison of a battery according to the present invention with the
conventional battery.
FIG. 7 is a graphical representation of a cycle characteristic of
active materials for comparison of a battery according to the
present invention with the conventional battery.
FIG. 8 is a graphical representation of a discharging
characteristic of active materials at the third cycle for
comparison of a battery according to the present invention with the
conventional battery.
FIG. 9 is a graphical representation of a charging characteristic
of active materials at the third cycle for comparison of a battery
according to the present invention with the conventional
battery.
FIG. 10 is a graphical representation of a cycle characteristic of
active materials for comparison of a battery according to the
present invention with the conventional battery.
FIG. 11 is a graphical representation of a discharging
characteristic of active materials at the third cycle for
comparison of a battery according to the present invention with the
conventional battery.
FIG. 12 is a graphical representation of a charging characteristic
of active materials at the third cycle for comparison of a battery
according to the present invention with the conventional
battery.
FIG. 13 is a graphical representation of a cycle characteristic of
active materials for comparison of a battery according to the
present invention with the conventional battery.
FIG. 14 is a graphical representation of a discharging
characteristic of active materials at the first cycle for
comparison of a battery according to the present invention with the
conventional battery.
FIG. 15 is a graphical representation of a charging characteristic
of active materials at the first cycle for comparison of a battery
according to the present invention with the conventional
battery.
FIG. 16 is a graphical representation of a discharging
characteristic of active materials at the third cycle for
comparison of a battery according to the present invention with the
conventional battery.
FIG. 17 is a graphical representation of a charging characteristic
of active materials at the third cycle for comparison of a battery
according to the present invention with the conventional
battery.
FIG. 18 is a graphical representation of a cycle characteristic of
active materials for comparison of a battery according to the
present invention with the conventional battery.
FIG. 19 is a view showing one example of a battery of an embodiment
in the present invention.
FIG. 20 is a graphical representation showing a charging and
discharging characteristic at the first cycle and the second cycle
of a battery according to the present invention.
FIG. 21 is a graphical representation showing a cycle
characteristic of a battery according to the present invention.
FIG. 22 is a graphical representation showing a charging and
discharging characteristic at the first cycle and the second cycle
of a battery according to the present invention.
FIG. 23 is a graphical representation showing a cycle
characteristic of a battery according to the present invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
The present invention is described in more detail with reference to
the following embodiments.
In the embodiments hereinafter described, FIG. 1 is a sectional
view of a coin type battery showing one example of a test cell used
for performance evaluation of an electrode active material of a
non-aqueous electrolyte secondary battery according to the present
invention. In the drawing, numeral 1 depicts a counter electrode
casing simultaneously used as a counter electrode terminal and
comprised at a stainless steel plate with Ni plating on its
external side surface. Numeral 2 depicts a counter electrode
collector composed of stainless steel net and spot welded to the
counter electrode casing 1. A counter electrode 3 is formed at
lithium foil having a predetermined thickness, which is punched at
a diameter of 14 mm, and press fit on an aluminum plate with a
predetermined thickness that is punched at a diameter of 15 mm and
fixed on the counter electrode collector 2. 7 depicts a working
electrode casing of stainless steel with its side surface Ni plated
and which is simultaneously used as a working electrode terminal. 5
depicts a working electrode formed using an active material
according to the invention described later or the comparison active
material by the conventional method, 6 depicts a working electrode
collector composed of a stainless steel net or a conductive bonding
agent using carbon as a conductive filler, where the working
electrode 5 and the working electrode casing 7 are electrically
connected to each other. 4 depicts a separator formed of a porous
film of polypropylene and which electrolyte solution is
impregnated. 8 depicts a gasket mainly formed of polypropylene,
which is arranged between the counter electrode casing 1 and the
working electrode casing 7 to maintain electrical insulation
between the counter electrode and the working electrode. An opening
edge of the working electrode casing 7 is bent and caulked inside
to tightly seal the contents of the battery. The battery has an
outside diameter of 20 mm with a thickness of 1.6 mm.
(Embodiment 1)
The working electrode 5 of this embodiment is produced as described
below. Iron monoxide FeO obtained in the market is crushed and
granulated equal to or less than a particle diameter 53 .mu.m by an
automatic mortar to produce an active material "a" according to the
invention, the resultant product is mixed with graphite as a
conductive agent and a cross-linked type acrylic acid resin and the
like as a binding agent in a weight ratio of 30:65:5 to obtain a
working electrode composite agent. Next, the working electrode
composite agent is press molded at 2 ton/cm.sup.2 to a pellet
having a diameter of 15 mm with a thickness of 0.5 mm together with
the working electrode collector 6 formed of stainless steel net,
thereafter depressured, heated, and dried during 10 hours at
200.degree. C. thereby to produce a working electrode.
For comparison, the same electrodes (comparison working electrodes)
are produced as in the case of the working electrode of the present
invention described above with exception that the same graphite as
used in the conductive agent described above is used as an active
material (referred to as an active material "r1" for
simplification) instead of the active material "a" according to the
present invention.
Lithium perchlorate LiClO.sub.4 is dissolved by 1 mol/l into a
mixed solvent composed of propylene carbonate and 1,
2-dimethoxyethane with a volume ratio of 1:1 to produce electrolyte
solution to be used.
The battery thus produced is aged at room temperature for a week,
and then performed charging and discharging which are described
later. This aging permits lithium-aluminum laminated electrodes of
counter electrodes to contact with non-aqueous electrolyte solution
within the battery to satisfactorily enable alloying, whereby the
lithium foil is substantially all converted into li-Al alloy, and
thus the battery voltage is reduced by about 0.4 V compared to the
independent use of metal lithium as a counter electrode to become
stable accordingly.
The batteries thus obtained are hereinafter referred to, for
simplification, as "battery A" and "battery R1" in a corresponding
manner to the active materials "a" and "r1" of the working
electrodes respectively used therein.
A charging characteristic and a discharging characteristic each for
the third cycle are shown in FIG. 2 and FIG. 3 respectively under
the condition when the batteries A and R1 are cycle charged and
discharged at a constant current 0.4 mA with a final voltage -0.4 V
of charging (in the current direction of battery reaction where
lithium ion is occluded into the working electrode from inside the
electrolyte) and a final voltage 2.5 V of discharging (in the
current direction of battery reaction where lithium ion is emitted
to the electrolyte from the working electrode). A cycle
characteristic is shown in FIG. 4. The charging/discharging cycle
starts from charging. As is apparent from FIGS. 2 to 4, the battery
A of the invention has a considerably larger charge/discharge
capacity compared to the comparison battery R1 to remarkably
enlarge the reversible region of charge/discharge. The discharge
capacity reduction (cycle deterioration) due to repeated charge and
discharge is almost prevented together with an extremely reduced
difference of operational voltage between the charge and the
discharge over the entire charge/discharge region, thus the battery
polarization (internal resistance) is considerably small to
facilitate the large current charging and discharging.
(Embodiment 2)
Instead of the active material "a" in the embodiment 1, silicon
monoxide SiO with a purity degree of 99.9% obtained in the market
is crushed and granulated at a particle size equal to or less than
53 .mu.m to produce an active material of the working electrode (an
active material "b" according to the present invention)to be used.
A battery B is produced in the same manner as in the battery A of
the embodiment 1 other than the working electrode active material
described above.
A charging/discharging cycle test is performed for the battery B
thus obtained and the comparison battery R1 described above under
the condition of a constant current of 0.4 mA with a final charging
voltage of -0.8 V and a final charging voltage of 2.5 V. The
charging characteristic and discharging characteristic each for the
third cycle at that time are shown in FIGS. 5 and 6 respectively. A
cycle characteristic is shown in FIG. 7.
As is apparent from the drawings, the battery B of this embodiment
is found to have a high grade of charging/discharging
characteristic as in the battery A of the embodiment 1 according to
the invention.
(Embodiment 3)
This embodiment uses LixMnO as an active material. The same battery
as in the embodiment 1 is produced with exception that a working
electrode and electrolyte solution as described below are used
instead of the working electrode and electrolyte solution in the
embodiment 1, and 1.6 times of the lithium amount is used for a
counter electrode 3.
A working electrode 5 is produced as follows. Manganese monoxide
MnO obtained in the market is crushed and granulated at a particle
size of equal to or less than 53 .mu.m by the automatic mortar to
produce an active material "c" of the invention, which is mixed of
the same graphite as used in the embodiment 1 as a conductive agent
and of cross-linked type acrylic acid resin and the like as a
binding agent at a weight ratio of 65:20:15 to produce a working
electrode composite agent. Next, this working electrode composite
agent is pressed and molded at 2 ton/cm.sup.2 on a pellet having a
diameter 15 mm with a thickness of 0.3 mm to produce the working
electrode 5. The working electrode 5 thus obtained is then contact
fit into a unitary shape with a working casing 7 by a working
electrode collector 6 composed of a conductive resin bonding agent
using carbon as a conductive filler, and thereafter the resultant
product is depressured, heated, and dried for 10 hours at
200.degree. C. and used to produce a coin shaped battery as
formerly described.
For comparison, the same electrode (comparison working electrode)
is produced as in the case of the working electrode of the
invention described above with exception that the same graphite
used for the conductive agent as described is used as an active
material (referred to as an "active material r2" for
simplification) instead of the active material "c" of the invention
described above.
Lithium perchlorate LiClO.sub.4 is dissolved by 1 mol/l into mixed
solvent of propylene carbonate and ethylene carbonate and 1,
2-dimethoxyethane at a volume ratio of 1:1:2 to produce electrolyte
to be used.
The battery thus produced is placed and aged for a week at room
temperature, and then the charge/discharge test is performed, which
is described later. This aging enables lithium-aluminum laminated
electrodes of counter electrodes to contact with non-aqueous
electrolyte solution within the battery to satisfactorily achieve
alloying, and thus the lithium foil is all substantially changed
into Li-Al alloy, and a battery voltage is decreased by about 0.4
V, which is stable, compared to the independent use of metal
lithium as a counter electrode.
The batteries thus made up are hereinafter referred to as batteries
C and R2 for simplification in a corresponding manner to the
respectively used active materials "c" and "r2" of the working
electrodes.
FIGS. 8 and 9 show a discharging characteristic and charging
characteristic each of the third cycle when the these batteries C
and R2 are cycle charged and discharged at a constant current of 1
mA with a final voltage -0.4 V of charging (in the current
direction of battery reaction where lithium ion is occluded into
the working electrode from the electrolyte solution) and a final
voltage 2.5 V of discharging (in the current direction of battery
reaction where lithium ion is emitted to the electrolyte solution
from the working electrode). The cycle characteristic is shown in
FIG. 10. The charging and discharging cycle starts from the
charging. As is apparent from FIG. 8 to 10, the battery C according
to the present invention has a relatively larger charge/discharge
capacity compared to the comparison battery R2 to considerably
enlarge the reversible region of charge/discharge. The discharge
capacity reduction (cycle deterioration) due to repeated charge and
discharge is almost prevented together with an extremely reduced
difference of operational voltage between the charge and the
discharge over the entire charge/discharge region, and thus the
battery polarization (internal resistance) is considerably small
and this facilitates the large current charging and
discharging.
(Embodiment 4)
Instead of the active material "c" in the embodiment 3, titanium
monoxide TiO obtained in the market is crushed and granulated at a
particle size equal to or less than 53 .mu.m to produce an active
material for the working electrode (an active material "d"
according to the present invention) to be used. A battery D is
produced in the same manner is in the battery C of the embodiment 3
other than this working electrode active material described
above.
A charging/discharging cycle test is performed as in the embodiment
3 for the battery D thus obtained and the comparison battery R2
described above under the condition of a constant current of 1 mA
with a final charging voltage of -0.4 V and a final discharging
voltage of 2.5 V. The discharging characteristic and charging
characteristic each for the third cycle at that time are shown in
FIGS. 11 and 12 respectively. A cycle characteristic is shown in
FIG. 13.
As is apparent from the drawings, the battery D of this embodiment
is found to have a high grade of charging/discharging
characteristic as in the batteries A, B, C of the embodiments 1, 2,
3 according to the invention.
(Embodiment 5)
Zinc monoxide ZnO obtained in the market is crushed and granulated
at a particle size equal to or less than 53 .mu.m to produce an
active material of the working electrode (an active material "e"
according to the invention) to be used.
A battery E is produced in the same manner as in the battery C of
the embodiment 3 other than this working electrode active material
described above. A charging/discharging cycle test is performed as
in the embodiment 3 for the battery E thus obtained and the
comparison battery R2 described above under the condition of a
constant current of 1 mA with a final charging voltage of -0.4 V
and a final discharging voltage of 2.5 V. The discharging
characteristic and charging characteristic each for the first cycle
at that Lime are shown respectively in FIGS. 14 and 15.
As is apparent from the drawings, the battery E of this embodiment
is found to have a high grade of charging/discharging
characteristic as in the batteries A to D of the embodiments 1 to 4
according to the invention. The battery E according to the present
invention is found to have a considerably larger charge/discharge
capacity compared the comparison battery R2 to greatly enlarge the
reversible region of charge/discharge. A difference of operational
voltage between the charge and the discharge is remarkably reduced
over the entire charge/discharge region, and thus the battery
polarization (internal resistance) is considerably small, and this
facilitates the large current charging and discharging.
(Embodiment 6)
Tin monoxide SnO obtained in the market is crushed and granulated
at a particle size equal to or less than 53 .mu.m to produce an
active material of the working electrode (an active material "f"
according to the invention) to be used.
A battery F is produced in the same manner as in the battery C of
the embodiment 3 other than this working electrode active material
described above. A charging/discharging cycle test is performed as
in the embodiment 3 for the thus obtained battery F under the
condition of a constant current of 1 mA with a final charging
voltage of -0.4 V and a final discharging voltage of 2.5 V. The
discharging characteristic and charging characteristic each for the
third cycle at that time are shown respectively in FIGS. 16 and 17.
The cycle characteristic is shown in FIG. 18.
As is apparent from FIGS. 16 to 18, the battery F according to the
present invention is found to have a considerably larger
charging/discharging capacity compared to the comparison battery R2
as in the battery C of the embodiment 3 to greatly enlarge the
reversible region of charge/discharge. A difference of operational
voltage between the charge and the discharge is considerably
reduced over the entire charge/discharge region, and thus the
battery polarization (internal resistance) is remarkably reduced,
which facilitates the large current charging and discharging.
In the embodiments as hereinbefore described, the batteries A to F
according to the present invention have active materials "a" to "f"
of the working electrodes to produce composite oxide Li.sub.x MO (M
represents Fe, Si, Mn, Ti, Zn and Sn) containing lithium by the
first charging. Due to such charging, lithium ion, which is emitted
into the electrolyte from the Li-Al alloy of the counter electrode,
moves through the electrolyte to electrode-react with the active
material MO of the working electrode, and thus the lithium ion is
electrochemically occluded into the active material MO to produce
the composite oxide Li.sub.x MO containing lithium. Next, on
discharging, the lithium ion is emitted into the electrolyte from
the composite oxide to move through the electrolyte and to be
occluded into the Li-Al alloy of the counter electrode, whereby
stably repeated charging/discharging are available. The active
materials "a" to "f" (MO) produce the composite oxide Li.sub.x MO
containing lithium by the first charging, and thereafter in
charging-discharging cycles also form the composite oxide Li.sub.x
MO containing lithium other than at the time of bring completely
discharged.
It is found that the active materials "a" to "f" of the batteries A
to F according to the present invention are not only used as a
positive active material of the nonaqueous electrolyte secondary
battery but also exhibit a high grade property as a negative active
material because a charge/discharge capacity of a baser potential
region of -0.4 to +1.5 V (corresponding to about 0 to 1.9 V for
metal lithium) is equal to or more than that of a nobler potential
region of 1.5 to 2.5 V (corresponding to about 1.9 to 2.9 V for
metal lithium) with respect to the Li-Al alloy electrode.
Particularly, the active material Li.sub.x MO of the embodiments 2
to 6 (where M represents Mn, Ti, Zn, or metal Sn or metalloid Si in
periodic table 14 group) has a larger charge/discharge capacity in
the baser potential region of -0.4 to +1.1 V (corresponding to
about 0 to 1.5 V for metal lithium) with respect to the Li-Al alloy
electrode, and in addition, has a more baser potential, and is
superior as a negative active material.
(Embodiment 7)
FIG. 19 is a sectional view of a coin type battery showing one
example of a non-aqueous electrolyte secondary battery according to
the present invention. In the drawing, 11 depicts a negative
electrode casing simultaneously used is a negative electrode
terminal, and which comprises a stainless steel plate with its
outer side surface Ni plated. 13 depicts a negative electrode
formed using a negative active material according to the present
invention which is described later, the negative electrode being
fixed on a negative electrode casing at by a negative electrode
collector 12 composed of a conductive bonding agent using carbon as
a conductive filler. Numeral 17 is a positive electrode casing made
of stainless steel with its outer side surface Ni plated, and is
simultaneously used as a positive electrode terminal. 15 is a
positive electrode composed of the positive active material of the
invention described later, and is fixed on the positive electrode
casing 17 by a positive electrode collector 16 formed of the
conductive bonding agent using carbon as a conductive filler. 14 is
a separator formed of a porous film of polypropylene, and is
impregnated with electrolyte solution. 18 is a gasket mainly made
of polylpropylene, which is disposed between the negative electrode
casing 11 and the positive electrode casing 17 to maintain an
electrical insulation between the negative electrode and the
positive electrode, and in which the positive electrode casing has
an opening with an edge that is bent and caulked inside to tightly
seal the contents of the battery. For the electrolyte solution,
lithium perchlorate LiClO.sub.4 is dissolved by 1 mol/l into mixed
solvent at a volume ratio of 1:1:2 of propylene carbonate, ethylene
carbonate and 1, 2-dimethoxyethane to produce the electrolyte
solution to be used. The battery has a size of outside diameter at
20 mm with a thickness of 1.6 mm.
The negative electrode 13 is produced as follows. Manganese
monoxide MnO with a purity degree of 99.9% obtained in the market
is crushed and granulated at a particle size equal to or less than
53 .mu.m by the automatic mortar to produce a negative electrode
active material according to the invention, which is mixed with
graphite as a conductive agent and a cross-linked type acrylic acid
resin and the like as a binding agent at a weight ratio of 65:20:15
to produce a negative electrode composite agent, which is next
press molded at a weight of 2 ton/cm.sup.2 to a pellet having a
diameter of 15 mm with a thickness of 0.23 mm, thereafter is
depressured, heated, and dried at 200 .degree. C. for 10 hours to
produce a negative electrode.
The positive electrode 15 is produced as follows. Lithium hydroxide
LiOH.H.sub.2 O and cobalt carbonate CoCO.sub.3 are weighed to
obtain a mol ratio of Li:Co of 1:1 and sufficiently mixed using a
mortar, the resultant mixture is heated and baked at a temperature
of 850 .degree. C. in the atmosphere for 12 hours, and after
cooling, crushed and granulated at a particle size equal to or less
than 53 .mu.m. The baking, crushing, and granulating are repeated
two times to compose the positive active material LiCoO.sub.2
according to the present invention.
This product material is made as a positive active material, which
is mixed with graphite as a conductive agent and fluorine resin and
the like as a binding agent at a weight ratio of 80:15:5 to produce
a positive electrode composite agent, which next is pressed and
molded at 2 ton/cm.sup.2 on a pellet having a diameter of 16.2 mm
with a thickness of 0.67 mm, thereafter is depressured, heated, and
dried at 100.degree. C. for 10 hours to produce a positive
electrode.
The battery (referred to as a battery G) thus made-up is aged at
room temperature for a week, and then the charge/discharge test is
performed, which is described later.
FIG. 20 shows a charge/discharge characteristic of the first cycle
and second cycle when the battery G is cycle charged and discharged
at a constant current 1 mA under the condition of a final charging
voltage of 4.4 V and final discharging voltage of 2.0 V, and FIG.
21 shows a cycle characteristic. The charge and discharge cycle
starts from charging.
The battery G, which emits lithium ion into the electrolyte
solution from the positive active material LiCoO.sub.2 by charging,
causes the lithium ion to move through the electrolyte solution and
to electrode-react with the negative active material, and thus the
lithium ion is electrochemically occluded into the negative active
material to produce lithium manganese composite oxide Li.sub.x MnO
containing lithium. Next, on discharging, lithium ion is emitted
into the electrolyte solution from the lithium manganese composite
oxide of negative electrode to move through the electrolyte
solution and to be occluded into the positive active material, thus
stable repeated charging and discharging becomes possible. Here,
the negative active material produces the composite oxide Li.sub.x
1 MnO containing lithium by the first charging, thereafter in the
charging/discharging cycle, the composite oxide Li.sub.x MnO
containing lithium is formed other than at the time of being
completely discharged.
As is apparent from FIGS. 20 and 21, the battery G according to the
present invention has a considerably larger charge/discharge
capacity. The discharging capacity relative to the charging
capacity (charging/discharging efficiency) is hardly decreased
other than at the first cycle together with the small decrease of
the discharging capacity (cycle deterioration) due to repeated
charging/discharging. In addition, it is found that a difference of
operational voltage between the charging and the discharging over
the entire charge/discharge region is considerably small with an
extremely reduced polarization (internal resistance) of the battery
to facilitate a larger current charging/discharging.
The reason why there arises considerable decrease of the
discharging capacity (initial loss) at the first cycle relative to
the charging capacity at the first cycle resides in a side reaction
as a main cause generated between the graphite as a conductive
agent or a binding agent added to the negative composite agent and
Li when lithium ion is electrochemically occluded into the negative
active material at the first cycle charging, and such reason is
also considered due to the presence of remaining Li which is
occluded into MnO of the negative active material but is not
emitted at the time of discharging.
(Embodiment 8)
A battery H is produced in the same manner as in the embodiment 7
with exception that a negative electrode 23 and a positive
electrode 25 produced as described below are used instead of the
negative electrode 13 and the positive electrode 15 of the
embodiment 7.
The negative electrode 23 is produced as the following. A negative
active material and a negative composite agent as in the embodiment
7 are used to press and mold at 2 ton/cm.sup.2 on a pellet having a
diameter of 15 mm with a thickness of 0.33 mm to produce a negative
electrode pellet. The negative electrode pellet, which is fixed on
a negative electrode casing 11 by a negative electrode collector 12
composed of the conductive bonding agent using carbon as a
conductive filler, is depressured, heated, and dried at 200.degree.
C. for 10 hours, thereafter a lithium foil with a predetermined
thickness, which is punched at a diameter of 14 mm, is press fit on
the negative electrode pellet. The lithium-negative electrode
pellet laminated electrode thus obtained is used as a negative
electrode.
The positive electrode 25 is produced as described below. Lithium
hydroxide LiOH.H.sub.2 O, cobalt carbonate CoCO.sub.3 and boron
oxide B.sub.2 O.sub.3, are weighed for a ratio of Li:Co:B of
1:0.9:0.1 to be mixed sufficiently by the mortar, thereafter the
mixture is heated and baked at the atmosphere of 850.degree. C. for
12 hours, and after cooling, crushed and granulated into particles
with a diameter equal to or less than 53 82 m. The two times of
baking, crushing, and granulating provide positive active material
LiCo.sub.0.9 B.sub.0.1 O.sub.2 according to the present
invention.
The product material described above as a positive active material
is mixed with graphite as a conductive agent and fluorine resin and
the like as a binding agent at a weight ratio of 80:15:5 to produce
a positive electrode composite agent, which is press molded at 2
ton/cm.sup.2 on a pellet having a diameter of 16.2 mm with a
thickness of 0.47 mm, and then the resultant product is
depressured, heated, and dried at 100.degree. C. for 10 hours to
obtain a positive electrode.
The battery thus obtained (hereinafter referred to as a battery H
for simplification) is aged at room temperature for a week and then
the charging/discharging test is performed, which is described
later. The aging causes lithium-negative electrode pellet laminated
electrode of the negative electrode 23 to contact with the
nonaqueous electrolyte solution within the battery and to
spontaneously electrochemically react, whereby lithium foil is
electrochemically occluded substantially completely into the
negative electrode composite agent.
The battery H thus obtained is performed of the
charging/discharging cycle test at a constant current 1 mA as in
the embodiment 7 under the condition of a final charging voltage of
4.4 V and a final discharging voltage of 2.0 V. The
charging/discharging characteristics at the first cycle and second
cycle are shown in FIG. 22, and the cycle characteristic is shown
in FIG. 23.
As is apparent from the drawing, the battery H of this embodiment
is found to have a considerably superior charging/discharging
characteristic compared to that of the battery G of the embodiment
7. In particular, a notable improvement compared to the battery G
of the embodiment 7 is found in almost eliminating the decrease of
discharge capacity at the first cycle (initial loss) relative to
that of the charging capacity at the first cycle. This is because
the lithium, whose amount corresponds to the side reaction with the
conductive agent or the binding agent with respect to lithium ion
generated by charging/discharging or corresponds to the remaining
lithium occluded in MnO on charging without emitting on
discharging, is spontaneously occluded by reacting with the
negative electrode composite agent since the battery is made up on
the negative electrode composite agent by layer-building to produce
such a laminated electrode in contact with the electrolyte solution
in the battery. Therefore, thereafter loss occurrence relating to
the lithium in the negative electrode on charging and discharging
is prevented.
Furthermore, composite oxide containing boron as a positive active
material is used to increase the charging/discharging capacity, and
thus it is found to improve the cycle deterioration
considerably.
(Embodiment 9)
This embodiment uses a positive active material described below
instead of the positive active material in the embodiment 8. A
battery is produced in the same manner as in the embodiment 8 other
than the positive active material.
The positive active material of this embodiment is produced as
explained below. Lithium hydroxide LiOH.H.sub.2 O, cobalt carbonate
CoCO.sub.3 and silicon dioxide SiO.sub.2 are weighed at a mol ratio
of Li:Co:Si of 1:0.9:0.1 to be mixed sufficiently by the mortar,
thereafter the mixture is heated, and baked at atmosphere of a
temperature 850.degree. C. for 12 hours, and after cooling, crushed
and granulated into a particle with a diameter equal to or less
than 53 .mu.m. Two times of baking, crushing and granulating
produce the composite oxide in a layer-like structure having
approximate composition of LiCo.sub.0. 9 Si.sub.0. 1 O.sub.2, which
is used as a positive active material according to the present
invention.
The battery thus obtained (hereinafter referred to as a "battery 1"
for simplification) is performed of the charging/discharging cycle
test as in the embodiment 8 to exhibit a high grade of
charging/discharging characteristic and cycle characteristic each
substantially similar to the battery H.
(Embodiment 10)
In this embodiment, LiPF.sub.6 is dissolved at 1 mol/l into a mixed
solvent of ethylene carbonate and diethyl carbonate at a volume
ratio of 1:1 to produce an electrolyte solution and to be used
instead of the electrolyte solution of the embodiment 8. The
battery J is produced in the same manner as in the embodiment 8
with exception of the electrolyte solution.
The battery J is performed of the charging/discharging cycle test
as in the embodiment 8, where the charging/discharging capacity at
the first to fourth cycles is smaller by 20 to 3% compared to the
battery H, but the thereafter repeated charging/discharging cycle
provides minimized reduction of the discharge capacity (cycle
deterioration) together with a high grade cycle characteristic.
In the embodiments, the counter electrodes have been shown and
described only for cases of lithium-aluminum alloy. LiCoO.sub.2 and
Li.sub.a T.sub.b L.sub.c O.sub.2. However, the present invention is
not limited to such examples. As hereinbefore described, it is
understood that the electrode according to the present invention
can be used combined with tire negative or positive electrodes as a
counter electrode: first, the negative electrode using as an active
material the materials capable of occluding and emitting lithium
including; namely, metal lithium or alloys of lithium with the
other metals such as Zn, Sn, Pb, Bi; lithium insertion compound
such as carbon or MoO.sub.2, WO.sub.2, Fe.sub.2 O.sub.3 ;
conductive polymer capable of doping lithium ion such as
polyacetylene, polypyrrole, polyacene, and the like: and secondly,
the positive electrode as a counter electrode including as an
active material the materials capable of occluding and emitting
lithium cation and/or anion; namely, metal chalcogenide such as
TiS.sub.2, MoS.sub.2, NbSe.sub.3 ; metal oxide such as MnO.sub.2,
MoO.sub.3, V.sub.2 O.sub.5, LixCoO.sub.2, LixNiO.sub.2, LixMn.sub.2
O.sub.4 ; conductive polymer such as polyaniline, polypyrrole,
polyparaplienylene, polyacene; graphite intercalation compound; and
the like.
As hereinbefore fully described, the present invention uses novel
active materials composed of composite oxide Li.sub.x MO produced
from metals or metalloid M other than alkali metals and lithium as
an active material of at least either a negative electrode or a
positive electrode of the non-aqueous electrolyte secondary
battery, to produce a considerably larger charging/discharging
capacity that is an amount capable of reversibly occluding and
emitting lithium ion by charging and discharging, and to reduce
polarization of charging and discharging, so that there can thus be
obtained a considerably stable and long cycle life battery capable
of charging and discharging at a larger current without
deterioration such as decomposition and crystal disintegration due
to excess charging and excess discharging. In particular, the
active materials according to the present invention are used as a
negative active material, which are combined with a positive
electrode using the (nobler) active materials having an electrode
potential equal to or more than as high as 3 V or 4 V for metal
lithium such as metal oxide such as V.sub.2 O.sub.5, MnO.sub.2,
LiCoO.sub.2, Li.sub.x NiO.sub.2, LiMn.sub.2 O.sub.4, and so forth,
particularly like Li.sub.a T.sub.b L.sub.c O.sub.2, thereby a
higher effect can be obtained in producing a long cycle life
secondary battery having a high grade of charging/discharging
characteristic with high voltage and high energy density.
* * * * *