Lithium ion conductive solid electrolyte and method for manufacturing the same

Abstract

A solid electrolyte suitable for use in all solid type lithium ion secondary battery is made by sintering a form, particularly a greensheet, comprising at least lithium ion conductive inorganic substance powder. The solid electrolyte has porosity of 20 vol % or over.

Claims

1. A method for manufacturing a lithium ion conductive solid electrolyte comprising: preparing a slurry comprising lithium ion conductive glass or glass-ceramic powder as a main component and comprising also at least an organic binder and water used as a solvent, forming the slurry to a greensheet, isotropically pressing the greensheet so as to make the greensheet dense, and sintering the greensheet with variation in thickness of the greensheet being within a range from +10% to 10% relative to mean value of distribution of thickness of the greensheet, wherein the solid electrolyte has porosity of 10 vol % or less, and the solid electrolyte has thickness of 200 m or below wherein the glass or glass-ceramic powder comprises lithium, silicon, phosphorus and titanium, and average particle diameter of the glass or glass-ceramic powder is 20 m or below.

2. A method as defined in claim 1 further comprising a step of superposing a plurality of the greensheets and pressing the superposed greensheets before sintering.

3. A method as defined in claim 1 wherein the lithium ion conductive glass-ceramic powder comprises crystalline of
L.sub.1+x+y(Al,Ga).sub.x(Ti,Ge).sub.2-xSi.sub.yP.sub.3-yO.sub.12 where 0x1 and 0y1.

4. A method as defined in claim 3 wherein the crystalline is free of a pore or a crystal grain boundary which obstructs ion conduction.

Description

DESCRIPTION OF PREFERRED EMBODIMENTS

(1) Preferred embodiments of the invention will now be described.

(2) The solid electrolyte of the present invention is obtained by preparing a form comprising lithium ion conductive inorganic substance powder and sintering this form. The solid electrolyte of the invention has porosity of 20 vol % or below.

(3) If a pore exists in a solid electrolyte, there is no ion conduction path in this portion of the solid electrolyte and, as a result, ion conduction of the solid electrolyte is reduced. In case a solid electrolyte is used in a battery, the higher ion conductivity, the higher the moving speed of lithium ion and, therefore, a battery of a high output can be obtained. For this reason, porosity of a solid electrolyte should preferably be lower. In the present invention, the porosity of the solid electrolyte should preferably be 20 vol % or below, more preferably be 15 vol % or below and, most preferably, be 10 vol % or below. For making the porosity 20 vol % or below, the form to be sintered should preferably be a greensheet.

(4) The term porosity in the present specification means ratio of pores per unit volume and is expressed by the following formula:
Porosity (%)=(true densitybulk density)/true density100

(5) True density is density of substance per se which can be measured by a method such as Archimedes Method. In contrast, bulk density is density resulting from dividing weight of substance by apparent volume and includes pores.

(6) A greensheet comprising lithium ion conductive inorganic substance powder can be heated uniformly during sintering because the greensheet can be formed uniformly and, therefore, sintering progresses uniformly through the material and, as a result, a solid electrolyte in the form of a sheet having a very small porosity of 20 vol % or less can be produced. Therefore, variation in thickness of the greensheet before sintering should preferably be within a range from +10% to 10% relative to mean value of distribution of thickness of the greensheet before sintering. Further, by mixing materials of the greensheet sufficiently, the composition of the greensheet can be made uniform and, by making the composition of the greensheet dense before sintering by means of, e.g., roll pressing or uniaxial, isotropic pressing, a solid electrolyte which is dense and has a low porosity can be obtained after sintering whereby a solid electrolyte having high ion conductiviy and high output can be obtained. Thus, mixing of raw materials should preferably be made for at one hour or over by means of, e.g., a ball mill.

(7) When a solid electrolyte in the form of a sheet which is a preferred embodiment of the invention is used in a battery, the thinner the sheet is, the higher is the output of the battery because moving distance of lithium ion is shorter. Further, since a broader area of an electrode per unit volume can be secured, a battery of a higher capacity can be obtained. For these reasons, thickness of the solid electrolyte used as an electrolyte layer in a battery should preferably be 200 m or below, more preferably be 180 m or below and, most preferably, be 150 m or below.

(8) Mobility of lithium ion during charging and discharging of a lithium ion secondary battery depends upon lithium ion conductivity and lithium ion transport number of the electrolyte. The solid electrolyte of the present invention, therefore, should preferably be made of a material having high lithium ion conductivity.

(9) Ion conductivity of the lithium ion conductive crystalline should preferably be 110.sup.4 Scm.sup.1 or over, more preferably be 510.sup.4 Scm.sup.1 or over and, most preferably be 110.sup.3 Scm.sup.1 or over.

(10) The lithium ion conductive inorganic substance powder used in the present invention is inorganic substance powder comprising either lithium ion conductive glass powder or lithium ion conductive crystalline powder (ceramics or glass-ceramics) or mixture thereof. For achieving high lithium ion conductivity, the lithium ion conductive inorganic substance powder should preferably comprise lithium, silicon, phosphorus and titanium as main components.

(11) By containing a large amount of lithium ion conductive crystalline in the solid electrolyte, higher conductivity can be obtained. Therefore, the solid electrolyte should preferably have lithium ion conductive crystalline in an amount of 50 wt % or over, more preferably 55 wt % and over and, most preferably, 60 wt % or over.

(12) By containing a large amount of lithium ion conductive crystalline also in lithium ion conductive inorganic substance powder contained in a form for producing a solid electrolyte, higher conductivity can be obtained. Therefore, the lithium ion conductive inorganic substance powder should preferably have lithium ion conductive crystalline in an amount of 50 wt % or over, more preferably 55 wt % or over and, most preferably 60 wt % or over.

(13) As lithium ion conductive crystalline used in the present invention, a crystalline which is free of crystal grain boundary which obstructs ion conduction can be advantageously used. For example, lithium ion conductive crystalline of perovskite structure such as LiN, LISICON, La.sub.0.55Li.sub.0.35TiO.sub.3, crystalline of NASICON structure such as LiTi.sub.2P.sub.3O.sub.12 and glass-ceramics which precipitate such crystalline can be used. A preferable lithium ion conductive crystalline is Li.sub.1+x+y(Al, Ga)(Ti,Ge).sub.2-xSi.sub.yP.sub.3-yO.sub.12 where 0x1 and 0y1. Since glass-ceramics which precipitate crystalline of NASICON structure have very few pores and crystal grain boundary which obstruct ion conduction, they have high ion conductivity and chemical stability and hence are preferable.

(14) Since a solid electrolyte containing a large amount of such glass-ceramics can achieve high ion conductivity, the solid electrolyte should preferably comprise lithium ion conductive glass-ceramics in an amount 80 wt % or over, more preferably 85 wt % or over and, most preferably 90 wt % or over.

(15) The term a pore or a crystal grain boundary which obstructs ion conduction in this specification means an ion conduction obstructing factor such as a pore and a crystal grain boundary which reduces conductivity of the entire inorganic substance including lithium ion conductive crystalline to one tenths or less of conductivity the lithium ion conductive crystalline per se included in the inorganic substance.

(16) In the present specification, glass-ceramics means a material which consists of an amorphous solid and crystalline and is obtained by heating a glass and thereby causing a crystal phase to precipitate in a glass phase of the glass. The glass-ceramics in the present invention includes a material in which a glass phase is completely shifted to a crystal phase on condition that the crystal phase is substantially free of pores in between crystal grains and in crystal grains, i.e., a material in which the amount of crystal (rate of crystallization) is 100 mass %. Ceramics and other sintered materials generally cannot avoid inclusion of pores and crystal grain boundary in between crystal grains and in crystal grains due to the manufacturing process of such ceramics and sintered materials and can be distinguished from glass-ceramics in this respect.

(17) As to ion conduction, in the case of ceramics, ion conductivity of the ceramics becomes lower than ion conductivity of crystal grains constituting the ceramics due to presence of pores and crystal grain boundary in the ceramics. In the case of glass-ceramics, reduction in ion conductivity between crystal grains can be prevented by controlling the crystallization process and same ion conductivity as its crystal grains themselves can be maintained.

(18) As a material other than glass-ceramics which is almost free of a pore or a crystal grain boundary which obstructs ion conduction, a single crystal of the above described crystalline can be cited. Since, however, such single crystal is hard to manufacture and requires a high manufacturing cost, lithium ion conductive glass-ceramics are the most preferable materials for the solid electrolyte of the present invention.

(19) As the inorganic substance powder having a high ion conductivity contained in the solid electrolyte, powder obtained by crushing the lithium ion conductive inorganic substance comprising a lithium ion conductive crystalline or the lithium ion conductive glass-ceramics may preferably be used. Such powder should preferably be dispersed uniformly in the solid electrolyte from the standpoints of ion conductivity of the solid electrolyte and mechanical strength. For enhancing dispersion of such powder and achieving a desired thickness of the solid electrolyte, average particle diameter of the powder should preferably be 20 m or below, more preferably 15 m or below and, most preferably 10 m or below.

(20) The lithium ion conductive glass-ceramics are made by heat treating a Li.sub.2OAl.sub.2O.sub.3TiO.sub.2SiO.sub.2P.sub.2O.sub.5 mother glass for crystallization and has a predominant crystal phase of Li.sub.1+x+yAl.sub.xTi.sub.2-xSi.sub.yP.sub.3-yO.sub.12 (0x1, 0y1). From the standpoint of achieving excellent ion conductivity, x and y should preferably be 0x0.4, 0<y0.6, and most preferably 0.1x0.3, 0.1<y0.4.

(21) Composition ratios expressed in mol % and results thereof of respective components constituting the lithium ion conductive glass-ceramics will now be specifically described.

(22) Li.sub.2O is an indispensable component for providing Li.sup.+ ion carrier and thereby imparting the glass-ceramics with lithium ion conductivity. For achieving an excellent ion conductivity, the lower limit of the amount of this component should preferably be 12%, more preferably be 13% and, most preferably be 14%. The upper limit of the amount of this component should preferably be 18%, more preferably be 17% and, most preferably be 16%.

(23) Al.sub.2O.sub.3 is effective for improving thermal stability of the mother glass and also for providing Al.sup.3+ ion as a solid solution in the above described crystal phase and thereby improving lithium ion conductivity. For achieving these effects, the lower limit of the amount of this component should preferably be 5%, more preferably be 5.5% and, most preferably be 6%. If, however, the amount of this component exceeds 10%, thermal stability of the glass is deteriorated rather than is improved and ion conductivity of the glass-ceramics is reduced. Therefore, the upper limit of the amount of this component should preferably be 10%, more preferably be 9.5% and, most preferably be 9%.

(24) TiO.sub.2 contributes to forming of the glass and also constitutes the above described crystal phase. For causing the above described crystal phase to precipitate as a predominant crystal phase and thereby improving ion conductivity, the lower limit of the total amount of this component should preferably be 35%, more preferably be 36% and, most preferably be 37%. The upper limit of this component should preferably be 45%, more preferably be 43% and, most preferably be 42%.

(25) SiO.sub.2 is effective for improving thermal stability of the mother glass and also for providing Si.sup.4+ ion as a solid solution in the above described crystal phase and thereby improving lithium ion conductivity. For achieving these effects sufficiently, the lower limit of the amount of this component should preferably be 1%, more preferably be 2% and, most preferably be 3%. If, however, the amount of this component exceeds 10%, ion conductivity of the glass-ceramics is reduced rather than is improved. Therefore, the upper limit of the amount of this component should preferably be 10%, more preferably be 8% and, most preferably be 7%.

(26) P.sub.2O.sub.5 is an indispensable component as a glass former and also is a component which constitutes the above described crystal phase. If the amount of this component is less than 30%, difficulty arises in vitrification. Therefore, the lower limit of the amount of this component should preferably be 30%, more preferably be 32% and, most preferably be 33%. If the amount of this component exceeds 40%, difficulty arises in the precipitation of the above described crystal phase in the glass. Therefore, the upper limit of the amount of this component should preferably be 40%, more preferably be 39% and, most preferably be 38%.

(27) In the above described composition, a glass can be easily obtained by casting molten glass and glass-ceramics obtained by heat treating this glass have the above described crystal phase and exhibit an excellent lithium ion conductivity.

(28) Aside from the above described composition, in glass-ceramics having a crystal structure similar to the one described above, Al.sub.2O.sub.3 can be replaced by Ga.sub.2O.sub.3 partly or in whole and TiO.sub.2 can be replaced by GeO.sub.2 partly or in whole. In the manufacture of the glass-ceramics, other materials may be added in small amounts for lowering the melting point or improving stability of the glass within a range not to deteriorate ion conductivity.

(29) The glass-ceramics composition should preferably not contain Na.sub.2O or K.sub.2O, i.e., alkali metal oxides other than Li.sub.2O. When these alkali metal oxides are present in the glass-ceramics, conduction of Li ion is obstructed due to an effect caused by mixing of alkali ions whereby ion conductivity is reduced.

(30) Addition of sulfur to the glass-ceramics composition improves lithium ion conductivity to a small degree but it deteriorates chemical durability and chemical stability and, therefore sulfur should preferably not be contained.

(31) The glass-ceramics composition should preferably not contain Pb, As, Cd or Hg which tends to cause adverse effects to the environment and human body.

(32) For preparing a greensheet, lithium ion conductive inorganic substance powder, i.e., powder of glass or crystalline (ceramics or glass-ceramics) having high lithium ion conductivity and chemical stability, or mixture thereof is mixed with an organic binder and, if necessary, a dispersant etc. by using a solvent. The mixture is then formed to a greensheet by a simple method such as a method using a doctor blade. The greensheet thus prepared is processed to a desired shape and then preferably is pressed by roll pressing or uniaxial, isotropic pressing and thereafter is sintered to remove an organic component of the organic binder. Thus, an all solid electrolyte in the form of a thin sheet or any other desired shape can be produced.

(33) As the organic binder used for preparing a greensheet, a commercially available binder used as an additive in using a doctor blade can be used. Additives used in other processes than a doctor blade, e.g., rubber press and extruding, can also be used as the binder. More specifically, acrylic resin, ethyl cellulose, polyvinyl butyral, methacrylate resin, urethane resin, butyl methacrylate and vinyl copolymers, for example, may be used. In addition to such binder, other additives such as a dispersant for improving dispersion of particles of the materials and surfactants for improving defoaming during a drying process may be added in a proper amounts.

(34) For improving electron conductivity without deteriorating lithium ion conductivity, other inorganic substance powder or organic substance may also be added. As such inorganic substance powder, a small amount of insulating crystalline or glass having high dielectric capacity may be added. These insulating crystalline or glass includes, for example, BaTiO.sub.3, SrTiO.sub.3, Nb.sub.2O.sub.5 and LaTiO.sub.3.

(35) Since organic substance is removed during sintering, such organic substance may be used for, for example, for adjusting viscosity of the slurry during forming.

(36) For forming the greensheet, simple conventional means such as doctor blade, roll coater and die coater may be used. If viscosity of the greensheet is adjusted, conventional machines used for kneading and extruding may also be used. Thus, solid electrolytes of various shapes can be manufactured efficiently and cheaply.

(37) By coating a positive electrode and a negative electrode on either side of the sheet obtained in the above described manner, and drying or sintering the sheet, a lithium ion secondary battery can be provided.

(38) The solid electrolyte in the form of a sheet obtained by sintering has the same shape as the shape of the greensheet formed and, therefore, processing to any desired shape is easy and manufacture of a solid electrolyte having the shape of a thin film or any other desired shape and a lithium ion secondary battery using this solid electrolyte can be easily realized.

(39) Since the solid electrolyte after sintering does not contain an organic substance, it has excellent heat resisting property and chemical durability and, moreover, is not likely to cause an adverse effect to the environment and human body.

(40) As the active material used for a positive electrode material of the lithium ion secondary battery and a lithium primary battery of the invention, a transition metal compound which can store and discharge lithium may be used. For example, at least one transition metal compound selected from the group consisting of manganese, cobalt, nickel, vanadium, niobium, molybdenum, titanium, iron and phosphorus may be used. Since most active materials scarcely have electron conductivity and ion conductivity, an electron conduction additive and an ion conduction additive should preferably be used. Such electron conduction additives include, for example, conductive carbon, graphite, carbon fiber, metal powder, metal fiber and electron conductive polymer. Such ion conduction additives include, for example, an ion conductive glass-ceramics and an ion conductive polymer. These electron and ion conduction additives should preferably be added in an amount within a range from 3-35 mass %, more preferably 4-30 mass % and, most preferably, 5-25 mass %, to the positive electrode active material.

(41) As the active material used for a negative electrode material of the lithium ion secondary battery and the lithium primary battery of the invention, metal lithium, alloys which can store and discharge lithium such as a lithium-aluminum alloy, and a lithium-indium alloy, transition metal compounds such as titanium and vanadium, and carbon type materials such as graphite may preferably be used. As an electron conduction additive used when the active material has not sufficient electron conductivity, for example, conductive carbon, graphite, carbon fiber, metal powder, metal fiber and electron conductive polymer may be preferably used. As an ion conduction additive, for example, an ion conductive glass-ceramics, and an ion conductive polymer may preferably be used. These electron and ion conduction additives should preferably be added in an amount within a range from 3-35 mass %, more preferably 4-30 mass % and, most preferably, 5-25 mass %, to the negative electrode active material.

(42) It is preferable that ion conductive glass-ceramics added to the positive and negative electrodes are the same glass-ceramics that are contained in the solid electrolyte. When these glass-ceramics are the same, the ion moving mechanism of the electrolyte becomes the same as the ion moving mechanism of the electrodes and moving of ion between the electrolyte and the electrodes thereby becomes smooth with the result that a battery of higher output and capacity can be provided.

EXAMPLES

(43) Description will now be made about specific examples of the solid electrolyte of the present invention and the lithium ion secondary battery and lithium primary battery using this solid electrolyte.

(44) The present invention, however, is not limited to these examples but modifications may be made within the spirit and scope of the present invention.

Example 1

(45) Raw materials of H.sub.3PO.sub.4, Al(PO.sub.3).sub.3, Li.sub.2CO.sub.3, SiO.sub.2 and TiO.sub.2 were weighed and mixed uniformly to make a composition of 35.0% P.sub.2O.sub.5, 7.5% Al.sub.2O.sub.3, 15.0% Li.sub.2O, 38.0% TiO.sub.2 and 4.5% SiO.sub.2 expressed in mol % on oxide basis. The mixture was put in a platinum pot and heated and melted in an electric furnace at 1500 C. for three hours, while the glass melt was stirred. Then, the glass melt was dropped into flowing water to produce glass in the form of flakes. This glass was subjected to crystallization by heat treatment at 950 C. for twelve hours to produce target glass-ceramics. The predominant crystal phase precipitating in the glass-ceramics was confirmed to be L.sub.1+x+yAl.sub.xTi.sub.2-xSi.sub.yP.sub.3-yO.sub.12 where 0x0.4 and 0<y0.6 by the powder X-ray diffraction. The flakes of the glass-ceramics were milled by a jet mill and glass-ceramics powder having an average particle diameter of 5 m and a maximum particle diameter of 20 m was obtained.

(46) To this lithium ion conductive glass-ceramics powder and water were added and dispersed urethane resin by adding also a dispersant and these components were mixed to prepare a slurry. The slurry was formed by using a doctor blade to a sheet having thickness of 200 m and this sheet was dried at 90 C. to provide a greensheet. This greensheet was cut into cubes having length of 50 mm and sintered at 1000 C. to produce a solid electrolyte in the form of a sheet having thickness of 120 m. The solid electrolyte had ion conductivity of 1.510.sup.4 Scm.sup.1. The porosity of the solid electrolyte measured on the basis of true density and bulk density was 16 vol %.

Comparative Example 1

(47) Glass-ceramics which are the same as those of Example 1 were put in a mold for uniaxial press molding having a diameter of 40 mm and was formed to a pellet having thickness of 5 mm by pressing the glass-ceramics at 2t. This form was sintered at 1000 C. for five hours. Ion conductivity of this pellet was 3.110.sup.5 Scm.sup.1 and porosity thereof was 21 vol %.

Example 2

(48) Glass-ceramics which were the same as those of Example 1 were milled by using a ball mill to particles each having an average particle diameter of 1 m and a maximum particle diameter of 8 m. The glass-ceramics were mixed and dispersed with acrylic resin and a dispersant by using water as a solvent to prepare a slurry. The mixture was formed by a roll coater and then dried to form a greensheet having thickness of 100 m. This greensheet was pressed by a roll press to make it fine and was sintered at 1050 C. to provide a solid electrolyte having thickness of 75 m. This solid electrolyte had ion conductivity of 310.sup.4 Scm.sup.1 and porosity of 7 vol %. By making the texture of the solid electrolyte fine by pressing the greensheet by the roll press, porosity was reduced to less than half of the solid electrolyte of Example 1 and a solid electrolyte having high conductivity was obtained.

Example 3

(49) The glass before being subjected to crystallization which was obtained in the processing of Example 1 was milled by a ball mill to glass particles having an average diameter of 2 m and a maximum particle diameter of 10 m. The glass particles were mixed and dispersed with urethane resin and a dispersant by using water as a solvent to prepare a slurry. The mixture was formed by a roll coater and then dried to form a greensheet having thickness of 100 m. This greensheet was made fine by using CIP and sintered at 1050 C. to provide a solid electrolyte having thickness of 80 m. This solid electrolyte had ion conductivity of 410.sup.4 Scm.sup.1 and porosity of 5 vol %.

Example 4

(50) The lithium ion conductive glass-ceramics powder having an average particle diameter of 1 m obtained by Example 2 and the glass before crystallization obtained by Example 1 which was milled to glass particles each having an average particle diameter of 0.5 m were mixed at a ratio of 9:1 (=glass-ceramics:glass) and dispersed with acrylic resin and a dispersant by using water as a solvent to prepare a slurry. The mixture was formed by a roll coater and then dried to form a greensheet having thickness of 120 m. This greensheet was pressed by a roll press to make it fine and was sintered at 1050 C. to provide a solid electrolyte having thickness of 90 m. This solid electrolyte had ion conductivity of 410.sup.4 Scm.sup.1 and porosity of 8.5 vol %.

Example 5

(51) On one side of the solid electrolyte obtained by Example 1 was coated a slurry comprising Li.sub.4Ti.sub.5O.sub.12 as an active material and lithium ion conductive glass-ceramics having an average particle diameter of 0.3 m as an ion conduction additive. This slurry was dried and sintered to constitute a positive electrode. This positive electrode had thickness of 13 m. Al was sputtered on this positive electrode to constitute a positive electrode collector.

(52) On the other side of the solid electrolyte was thinly coated a slurry in which a copolymer of polyethylene oxide added with LiTFSI as a lithium salt and polypropylene oxide was solved in THF solution. This slurry was dried. Then, Li metal foil having thickness of 0.1 mm was attached onto the dried copolymer to constitute a negative electrode. The coated copolymer had thickness of 4 m. Lead wires were attached to the positive electrode and the negative electrode to assemble a lithium ion secondary battery.

(53) The assembled lithium ion secondary battery could be driven at an average discharging voltage of 1.5 V.

Example 6

(54) By using the solid electrolyte of Example 2, a lithium ion secondary battery was assembled in the same manner as in Example 5. This secondary battery could be driven at an average discharging voltage of 1.5 V.

Example 7

(55) By using the solid electrolyte of Example 3, a lithium ion secondary battery was assembled in the same manner as in Example 5. This secondary battery could be driven at an average discharging voltage of 1.5 V.

Example 8

(56) By using the solid electrolyte of Example 4, a lithium ion secondary battery was assembled in the same manner as in Example 5. This secondary battery could be driven at an average discharging voltage of 1.5 V.

Example 9

(57) The lithium ion conductive glass-ceramics powder obtained by Example 1 was wet-milled by using ethanol as a solvent to provide a fine powder slurry of lithium ion conductive glass-ceramics having an average particle diameter of 0.2 m and a maximum particle diameter of 0.3 m. The slurry was mixed and dispersed with a vinyl copolymer and urethane resin by using water as a solvent and the mixture was formed by a roll coater and then dried to provide a greensheet having thickness of 90 m. This greensheet was stamped out in the form of a disk having a diameter of 20 mm and the stamped out disk was pressed by a hand press and then sintered at 1000 C. to provide a disk-form solid electrolyte having thickness of 50 m. On one side of the solid electrolyte was coated a slurry comprising LiCoO.sub.2 as an active material and fine powder slurry of lithium ion conductive glass-ceramics which was the same as the glass-ceramics used for the solid electrolyte as an ion conduction additive and this slurry was dried and sintered to constitute a positive electrode. Al was sputtered on this positive electrode to constitute a positive electrode collector.

(58) On the other side of the solid electrolyte was coated a slurry comprising Li.sub.4Ti.sub.5O.sub.12 as an active material and fine powder slurry of lithium ion conductive glass-ceramics which was the same as the glass-ceramics used for the solid electrolyte as an ion conduction additive and this slurry was dried and sintered to constitute a negative electrode. Paste comprising cupper fine powder was coated on this negative electrode and dried and sintered to constitute a negative electrode collector. The laminate was then sealed in a coin cell and a lithium ion secondary battery thereby was assembled. It was confirmed that this battery could be performed at an average discharging voltage of 3 v.

Example 10

(59) A lithium primary battery was prepared in the following manner.

(60) The glass-ceramics obtained in Example 1 were milled by a ball mill and milled particles were classified to provide glass-ceramics powder having an average particle diameter of 1 m and a maximum particle diameter of 5 m. The glass-ceramics powder was mixed and dispersed with acrylic resin and a dispersant by using water as a solvent and the mixture was formed by a roll coater and dried to provide a greensheet having thickness of 140 m. This greensheet was pressed to make it fine and was sintered at 1075 C. to provide a solid electrolyte having thickness of 100 m. This solid electrolyte had ion conductivity of 310.sup.4 Scm.sup.1.

(61) A positive electrode compound was prepared by using commercially available MnO.sub.2 as a positive electrode active material, acetylene black as an electron conduction additive, and PVdF (polyvinylidene fluoride) as a binder. These materials were mixed and formed by a roll press to a sheet having thickness of 0.3 mm. The sheet was stamped out to a disk having a diameter of 18 mm to constitute a positive electrode.

(62) The solid electrolyte was stamped out to a disk having a diameter of 20 mm. On one side of the solid electrolyte was sputtered Al and on this Al was attached a LiAl alloy negative electrode material having a diameter of 18 mm to constitute a negative electrode. On the other side of the solid electrolyte was attached the positive electrode compound to constitute a positive electrode. The cell thus produced was put in a coin cell made of stainless steel and a mixed solvent of propylene carbonate added with 1 mol % of LiClO.sub.4 as a lithium salt and 1,2-dimethoxiethane was also put in the coin cell. The coin cell was sealed to provide a lithium primary cell. In this coin cell, the solid electrolyte was fixed to the coin cell and no flexion due to change in the volume caused by discharging takes place as in the conventional separator made of resin and, as a result, very stable discharging voltage could be maintained during use of this battery.

INDUSTRIAL APPLICABILITY

(63) The electrolyte of the present invention comprising lithium ion conductive glass-ceramics has high lithium ion conductivity and is electrochemically very stable and, therefore, it can be used not only for a lithium ion secondary battery but for a lithium primary battery, an electrochemical capacitor called a hybrid capacitor, a dye sensitized solar cell, and other electrochemical elements using lithium ion as a charge transfer carrier. Some examples of such electrochemical elements will be described below.

(64) By attaching a desired sensitive electrode to the electrolyte, the electrolyte can be used for various gas sensors and other detectors. For example, by using carbonate as an electrode, it can be used as a carbon dioxide gas sensor. By using nitrate as an electrode, it can be used as a NO.sub.x sensor. By using sulfate as an electrode, it can be used as a SO.sub.x sensor. By assembling the electrolyte in an electrolytic cell, it can be used as an electrolyte for decomposing and catching NO.sub.x and SO.sub.x in exhaust gas.

(65) By attaching an inorganic or organic compound which is colored or changes its color by insertion or removal of lithium ion to the electrolyte, and attaching a transparent electrode such as ITO thereto, an electrochromic device can be composed whereby an electrochromic display of a small power consumption having a memory function can be provided.

(66) Since the ion conduction path of the electrolyte of the present invention has an optimum size for passing lithium ion, it can pass lithium ion selectively when alkali ion other than lithium ion also exists. The electrolyte therefore can be used as a partition of a lithium ion selective collection device or a partition of a lithium ion selection electrode. Since the speed of passing of lithium ion is higher as the mass of the ion is smaller, the electrolyte can be used for separating isotope of lithium ion. This enables concentration and separation of 6Li concentrate (7.42% in the ratio existing in nature) which is necessary for a blanket material for producing tritium which is a fuel of a fusion reactor.