WO2005031773A1 - 有機電解質キャパシタ - Google Patents
有機電解質キャパシタ Download PDFInfo
- Publication number
- WO2005031773A1 WO2005031773A1 PCT/JP2004/014550 JP2004014550W WO2005031773A1 WO 2005031773 A1 WO2005031773 A1 WO 2005031773A1 JP 2004014550 W JP2004014550 W JP 2004014550W WO 2005031773 A1 WO2005031773 A1 WO 2005031773A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- negative electrode
- positive electrode
- active material
- electrode
- lithium
- Prior art date
Links
- 239000003990 capacitor Substances 0.000 title claims abstract description 43
- 229910001416 lithium ion Inorganic materials 0.000 claims abstract description 105
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims abstract description 104
- 239000007773 negative electrode material Substances 0.000 claims abstract description 85
- 239000007774 positive electrode material Substances 0.000 claims abstract description 55
- 239000003792 electrolyte Substances 0.000 claims abstract description 35
- 238000007600 charging Methods 0.000 claims abstract description 25
- 238000007599 discharging Methods 0.000 claims abstract description 19
- 239000005486 organic electrolyte Substances 0.000 claims description 66
- 150000001450 anions Chemical class 0.000 claims description 10
- 230000000149 penetrating effect Effects 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 230000005012 migration Effects 0.000 abstract 1
- 238000013508 migration Methods 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 description 128
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 84
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- 239000000956 alloy Substances 0.000 description 2
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- 229910003002 lithium salt Inorganic materials 0.000 description 2
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- 238000011068 loading method Methods 0.000 description 2
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- 150000004706 metal oxides Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
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- 238000000926 separation method Methods 0.000 description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 2
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- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
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- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
- H01G9/025—Solid electrolytes
- H01G9/028—Organic semiconducting electrolytes, e.g. TCNQ
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/04—Hybrid capacitors
- H01G11/06—Hybrid capacitors with one of the electrodes allowing ions to be reversibly doped thereinto, e.g. lithium ion capacitors [LIC]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/50—Electrodes characterised by their material specially adapted for lithium-ion capacitors, e.g. for lithium-doping or for intercalation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/66—Current collectors
- H01G11/70—Current collectors characterised by their structure
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M2010/4292—Aspects relating to capacity ratio of electrodes/electrolyte or anode/cathode
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
Definitions
- the present invention relates to an organic electrolyte capacity having a high energy density and a high power density.
- a battery using a carbon material such as graphite for the negative electrode and using a lithium-containing metal oxide such as iCo 2 for the positive electrode has been proposed.
- This battery is a so-called rocking chair type battery in which lithium ions are supplied from the lithium-containing metal oxide of the positive electrode to the negative electrode by charging after the battery is assembled, and lithium ions are returned from the negative electrode to the positive electrode during discharging.
- lithium ion since lithium ion only participates in charging and discharging without using metallic lithium for the negative electrode, it is called a lithium ion secondary battery and is distinguished from a lithium battery using metallic lithium.
- This battery is characterized by having a high voltage and a high capacity.
- lithium-ion secondary battery and electric double layer capacity have been attracting attention.
- lithium-ion batteries have high energy density, they still have problems with output characteristics, safety and cycle life.
- the electric double-layer capacity is an electronic component that is widely used as a backup power supply for memories of ICs and LSIs.
- the discharge capacity per charge is smaller than that of batteries, the instantaneous charge / discharge characteristics It has high output characteristics and maintenance-free properties that lithium-ion batteries and nickel-metal hydride batteries can withstand, even with tens of thousands of charge / discharge cycles.
- electric double-layer capacitors have these advantages
- general electric double-layer capacitors have an energy density of about 3 to 4 Wh1 and are about two orders of magnitude lower than lithium-ion batteries, making them ideal for electric vehicles.
- drive power supplies that require a high energy density such as these have not yet reached the level of practical use.
- an energy density of 6-1 O Wh Z 1 is required for practical use, and an energy density of 2 O Wh / 1 is required for widespread use.
- a power storage device called a hybrid capacity has attracted attention as a power storage device corresponding to an application requiring high energy density and high output characteristics.
- an electric double-layer capacitor has been proposed in which a carbon material capable of absorbing and desorbing lithium ions and a carbon material previously absorbing lithium ions by a chemical method or an electrochemical method is used as a negative electrode. (See, for example, page 2, column 2, line 38 to page 2, column 2, line 47 of JP-A-8-170488).
- the current collector of stainless steel fiber is mixed with the polarizable electrode material containing activated carbon powder.
- a positive or negative electrode, a carbon material capable of absorbing and desorbing lithium ions, a carbon material preliminarily absorbing lithium ions by a chemical or electrochemical method, and a collection of porous or fibrous metals There has been proposed an electric double layer capacity in which a combination of electric conductors is used as a negative electrode (for example, from page 4, column 6, line 1 to page 4, page 6 of JP-A-9-123210). See column 10 line 10).
- the positive electrode is a polarizable electrode made of a carbonaceous substance having a natural potential of 0.5 V to 2.6 V with Li / L i + as a counter electrode
- the negative electrode contains metallic lithium and lithium metal.
- an electric double layer capacitor composed of at least one material selected from a material in which lithium ions are stored and desorbed in a reversible manner in an alloy and a material capable of reversibly storing and releasing lithium ions (for example, (See, page 3, column 4, line 8 to page 3, column 4, line 16 of Kaihei 1 1—2 975 778).
- the negative electrode potential is lowered and the withstand voltage of the cell is increased by previously supporting lithium ions on the negative electrode.
- a cell configuration in which a pair of positive and negative electrodes face each other like a coin battery No specific examples are shown for large cells such as a cylindrical battery in which electrodes are wound or a rectangular battery in which a plurality of electrodes are stacked.
- the positive electrode current collector and the negative electrode current collector have holes penetrating on the front and back, respectively, the negative electrode active material can reversibly carry lithium ions, and lithium ions derived from the negative electrode face the negative electrode or the positive electrode.
- An organic electrolyte battery that is supported by electrochemical contact with a lithium electrode arranged at a distance has been proposed (for example, Japanese Patent Application No. 10-5311811, page 11, line 4 to line 4). (See page 12, line 27). '
- lithium ions can move between the front and back surfaces of the electrode without being blocked by the electrode current collector. Also in the power storage device, it is arranged near the lithium electrode through the through hole. Lithium ions can be electrochemically supported not only on the negative electrode but also on the negative electrode disposed apart from the lithium electrode.
- the negative electrode active material various materials can be used as long as they can support lithium ions reversibly, for example, graphite such as natural graphite and artificial graphite, coke, pitch, thermosetting resin, coconut shell and tree. It is known to use various carbon materials, carbon fibers, polyacenic materials, tin oxides, silicon oxides and the like starting from such materials.
- an insoluble infusible substrate having a polyacene skeleton structure which is a heat-treated aromatic condensation polymer and has an atomic ratio of hydrogen atoms to carbon atoms of 0.50 to 0.05, is preferably used. It can be used (for example, the scope of the claims in Japanese Patent Publication No. 1444242, the claims 1 to 222, or the claims in Japanese Patent Publication No. 3-240204). Scope, claims 1 to 8). Disclosure of the invention
- the negative electrode in which lithium ions have been occluded in advance in a carbon material that can occlude and desorb lithium ions has a lower potential than activated carbon used in electric double-layer capacities.
- the withstand voltage of the cell is improved, and the capacity of the negative electrode is much larger than that of activated carbon, resulting in a higher energy density.
- an object of the present invention is to provide an organic electrolyte capacity having a small change in internal resistance during charge and discharge, a high energy density, and a high output.
- the present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, the cell capacity when the organic electrolyte capacity was discharged from a charged state to a voltage of half the charging voltage over 1 ⁇ 0.25 hours was a (mA). h), the capacity when the charged negative electrode is discharged to 1.5 V (L i / L i +) is defined as the complete negative electrode capacity b (mAh).
- the ratio of the positive electrode active material and the negative electrode active material so as to achieve 3
- the internal resistance is low, the internal resistance change during charging and discharging is small, lithium ions can easily move, and high power density and high performance are achieved.
- the inventors have found that an organic electrolyte capacitor can be obtained, and have completed the present invention. That is, the present invention is as follows.
- An organic electrolyte capacity comprising a positive electrode, a negative electrode, and an electrolyte capable of transporting lithium ions, wherein the positive electrode can reversibly carry lithium ions and anions, and the negative electrode reversibly converts lithium ions.
- the organic electrolyte capacity is discharged from the charged state to half the charging voltage for 1 ⁇ 0.25 hours, the cell capacity is a (mAh), and the charged negative electrode is charged.
- the positive electrode active material is set so that when the capacity discharged to 1.5 V (L i / L i +) is defined as the complete negative electrode capacity b (mAh), it becomes 0.05 ⁇ a / b ⁇ 0.3.
- the organic electrolyte capacity is characterized in that the ratio of the negative electrode active material is controlled.
- the capacitance per unit weight of the negative electrode active material is at least three times the capacitance per unit weight of the positive electrode active material, and the weight of the positive electrode active material is larger than the weight of the negative electrode active material. 1] or the organic electrolyte capacitor according to [2].
- the organic electrolyte capacitor includes a positive electrode current collector and a negative electrode current collector, each current collector has a through hole on the front and back surfaces, and the negative electrode and the Z or lithium disposed opposite to the positive electrode. Lithium ions are supported on the negative electrode and the Z or positive electrode by electrochemical contact with the electrode,
- the ratio of the positive electrode active material to the negative electrode active material is controlled so that 0.05 ⁇ aZb ⁇ 0.3" is used to control the output characteristics of the cell. This is because it is indispensable to set the anode capacity (corresponding to the cell capacity a here) arbitrarily with respect to the lithium ion discharge capacity (here the complete anode capacity b).
- the ratio of the cell capacity a to the complete negative electrode capacity b (a / b) is determined by the ratio of the positive electrode active material to the negative electrode active material. If the ratio of the positive electrode active material increases, aZb increases. It has been found that the lower the ratio of the positive electrode active material, the smaller aZb becomes. Further, they found that the value of a / b affected the output characteristics of the cell, and found that high output characteristics were obtained at 0.05 ⁇ aZb ⁇ 0.3.
- the capacitance per unit weight of the negative electrode active material is at least three times the capacitance per unit weight of the positive electrode active material, and the weight of the positive electrode active material is larger than the weight of the negative electrode active material.
- the reason is that the energy density changes even when the discharge capacity of the cell is constant by changing the ratio of the weight of the positive electrode active material to the weight of the negative electrode active material.
- lowering the ratio of the weight of the negative electrode active material having a large electrostatic capacity per unit weight increases the energy density, and conversely, increasing the ratio of the weight of the negative electrode active material decreases the energy density. It is.
- the organic electrolyte capacitor of the present invention is an organic electrolyte capacitor including a positive electrode, a negative electrode, and an electrolyte capable of transporting lithium ions, wherein the positive electrode can reversibly carry lithium ions and anions.
- the negative electrode can reversibly carry lithium ions, and the cell capacity when the organic electrolyte capacitor is discharged from the charged state to half the voltage of the charging voltage over 0.25 hours per earth is a (mAh), the capacity when the charged negative electrode is discharged to 1.5 V (L i / L if) is defined as the complete negative electrode capacity b (mAh).
- the discharge is performed with a current that causes the discharge time to be 1 ⁇ 0.25 hours.
- the result obtained was that the cell capacity when discharged at a current 100 times that of the cell capacity at that time was maintained at 50% or more.
- the capacitance per unit weight of the negative electrode active material is at least three times the capacitance per unit weight of the positive electrode active material, and the weight of the positive electrode active material is the weight of the negative electrode active material. If it is larger, the energy density is particularly large, which is preferable.
- the organic electrolyte capacity of the present invention having such features is extremely effective as a driving storage power supply or an auxiliary storage power supply for electric vehicles, hybrid electric vehicles, fuel cell vehicles, and the like. Also, it is suitably used as a driving storage power supply or an auxiliary storage power supply for electric bicycles, electric scooters, electric wheelchairs and the like. Furthermore, these capacitors can be suitably used as a storage device for various types of energy such as a storage device for solar energy and a storage device for wind power generation, or as an uninterruptible power supply, and a storage power supply for household appliances. it can. Brief Description of Drawings
- FIG. 1 is a perspective view showing an internal structure of an organic electrolyte capacitor when a laminate film is used as an outer container.
- the internal structure of the organic electrolyte capacity is indicated by a solid line, and the outer container of the organic electrolyte capacity is indicated by a broken line.
- FIG. 2 is a plan view of FIG.
- FIG. 3 is a sectional view taken along the line II ′ of FIG.
- FIG. 4 is a cross-sectional view taken along the line II of FIG.
- FIG. 5 is an enlarged plan view of an electrode current collector (a positive electrode current collector 1a and a negative electrode current collector 2a) on which electrodes are formed.
- FIG. 5 shows an example in which expanded metal is used as an electrode current collector, and the portion surrounded by a dotted line is a through hole.
- FIG. 6 shows a cross-sectional view taken along the line II of FIG.
- the through holes of the expanded metal (positive electrode current collector 1a, negative electrode current collector 2a) are closed by conductive materials 1b and 2b, and positive electrode 1 and negative electrode 2 are closed. It is formed on the conductive layer on the expanded metal in which the through hole is closed.
- FIG. 7 shows an example of the electrode current collector.
- Figure 7 (a) is an example of expanded metal with a porosity of 38%
- Figure 7 (b) is an example of a metal mesh with a porosity of 37%
- Figure 7 (c) is an example of a punched metal with a porosity of 34%.
- the through-hole of the electrode current collector is round, but the shape of the through-hole is not limited to this.For example, the square (porous) shown in FIG. 7 (d) Porosity of 45%) and the cross shape (porosity of 35%) shown in Fig. 7 (e).
- FIG. 8 is a cross-sectional view showing a first example of a layer configuration of a three-electrode laminated unit.
- FIG. 9 is a cross-sectional view showing a second example of the layer configuration of the three-electrode laminated unit.
- FIG. 10 is a sectional view showing a third example of the layer configuration of the three-electrode laminated unit.
- FIG. 11 is a developed perspective view showing an example of the electrode stacking unit.
- FIG. 12 is a developed perspective view showing an example of the electrode stacking unit.
- 1 is the positive electrode
- la is the positive electrode current collector
- lc is the positive electrode terminal
- 2 is the negative electrode
- 2a is the negative electrode current collector
- 2c is the negative electrode terminal
- 3 is the separator
- 4 and 5 are laminating films
- 6 is Electrode laminated unit
- 7 is a lithium electrode
- 7a is a lithium electrode current collector
- 8 is a three-electrode laminated unit
- 9a and 9b are conductors A, B, and C heat fusion parts
- A is a terminal connection part
- the organic electrolyte capacity of the present invention is a positive electrode, a negative electrode, and an organic electrolyte capacity provided with an electrolyte capable of transporting lithium ions, wherein the positive electrode can reversibly carry lithium ions and anion,
- the negative electrode can carry lithium ions reversibly, and the cell capacity when the organic electrolyte capacity is discharged from the charged state to half the charge voltage for 1 ⁇ 0.25 hours is a (mA h), when the charged negative electrode is discharged to 1.5 V (L i / L i +), and the negative electrode capacity is b (mAh), then 0.55 ⁇ aZb ⁇ 0.30
- This is an organic electrolyte capacitor characterized in that the ratio of the positive electrode active material to the negative electrode active material is controlled so as to be as small as possible.
- the negative electrode and the Z or the positive electrode carry lithium ions in advance, and that the positive electrode and the negative electrode current collector have holes penetrating on the front and back surfaces thereof.
- a method for supporting lithium ions on the negative electrode and / or the positive electrode by electrochemical contact with a lithium electrode disposed opposite to the positive electrode is industrially optimal.
- FIG. 1 is a perspective view showing an internal structure of an organic electrolyte capacity according to the present invention as an example in which a laminate film is used as an outer container.
- the internal structure of the organic electrolyte capacity is indicated by a solid line
- the outer container of the organic electrolyte capacity is indicated by a broken line.
- 2 is a plan view of FIG. 1
- FIG. 3 is a cross-sectional view taken along the line I-I 'of FIG. 2
- FIG. 4 is a cross-sectional view of FIG.
- the organic electrolyte capacitor of the present invention shown in FIG. 1 a three-electrode laminated unit in which a positive electrode 1, a negative electrode 2, a lithium electrode 7 and the like are laminated inside a laminated film is installed, and an electrolyte capable of transporting lithium ions is injected. After that, the two laminated films 4 and 5 are sealed by heat fusion or the like.
- the “positive electrode” refers to a side on which current flows out during discharge, the side on which current flows during charging, and the “negative electrode” receives a current during discharge and a current during charging. Means the pole on the outflow side.
- the positive electrode 1 formed on the positive electrode current collector 1a and the negative electrode 2 formed on the negative electrode current collector 2a are laminated via a separator 3 so that they do not directly contact each other.
- the electrode stacking unit 6 is formed.
- a lithium electrode 7 is attached via a separator 3 by pressing and attaching lithium metal to one side of a lithium electrode current collector 7a.
- a three-electrode laminated unit is formed.
- an electrode current collector (a positive electrode current collector 1a, a negative electrode current collector 2a) and a lithium electrode current collector 7a each have a hole (see FIG. (Not shown). Even if the through-hole is closed by a conductive material, lithium ions can freely move between the electrodes through the through-hole closed by the conductive material.
- FIG. 5 shows an enlarged plan view of the electrode current collector (positive electrode current collector 1a, negative electrode current collector 2a) on which electrodes are formed.
- FIG. 5 shows an example in which expanded metal is used as an electrode current collector, and the portion surrounded by a dotted line is a through hole.
- FIG. 6 shows a cross-sectional view taken along the line II ′ of FIG. As shown in FIG. 6, the through holes of the expanded metal (positive electrode current collector 1a, negative electrode current collector 2a) are closed by conductive materials 1b and 2b, and positive electrode 1 and negative electrode 2 The through hole is formed on the conductive layer on the expanded metal which is closed.
- the electrode stack unit 6 has four layers each of the positive electrode 1 and the negative electrode 2, but the structure of the electrode stack unit is not particularly limited.
- the number of layers of the negative electrode is not particularly limited.
- the lithium electrode 7 is arranged above the electrode stacking unit 6 to form a three-electrode stacking unit 8, but the position, the number of layers, and the shape of the lithium electrode 7 are not limited thereto. However, in order to carry lithium smoothly, it is preferable to arrange the lithium electrode 7 so as to face the negative electrode or the positive electrode. For example, the lithium electrode 7 may be directly attached on the negative electrode 2. When the lithium electrode 7 is directly adhered on the negative electrode 2, the adjacent negative electrode directly carries lithium ions, but the other non-adjacent negative electrodes penetrate at least one layer of the electrode current collector. As a result, lithium ions are carried.
- the lithium electrode 7 is provided for supplying lithium ions to the negative electrode 2. Therefore, it is sufficient that the amount is sufficient to obtain the desired negative electrode capacitance. Lithium ions can be supplied not only to the negative electrode but also to the positive electrode, or to both the positive and negative electrodes, although the effect can be obtained.However, the lithium ion storage capacity and stability of the positive and negative electrodes are taken into consideration. Appropriate amount Adjustment is preferred.
- the lithium electrode 7 emits lithium ions and gradually decreases. For this reason, it is preferable that a conductive porous body such as a stainless steel mesh is used as the lithium electrode current collector 7a, and at least a part of the lithium electrode 7 is filled in pores of the lithium electrode current collector and disposed. As a result, even if lithium ions are carried from the lithium electrode 7 to the electrode, a gap generated between the electrodes due to the disappearance of the lithium electrode is reduced, and lithium ion is smoothly carried by the electrode active material.
- a conductive porous body such as a stainless steel mesh
- a separator 3 is provided between each of the positive electrodes 1, the negative electrodes 2, and the lithium electrodes 7 so as not to make direct contact with each other.
- the inside of the cell is filled with an electrolyte capable of transporting lithium ions, and the electrolyte is also impregnated in Separe 3 that separates each electrode.
- the electrolyte is usually used in a liquid form by dissolving it in a solvent, and is also impregnated into Separator 3.In cases such as when Separation 3 is not used, the positive electrode 1 and the negative electrode 2 are not brought into direct contact with each other. In order to prevent electrolyte leakage, the electrolyte may be used in a gel or solid state.
- each positive electrode current collector 1a has a lead portion serving as a terminal connection portion A ', and a terminal welded portion A' (two pieces) of each positive electrode current collector 1a and a positive electrode current collector 1a are provided.
- the terminal 1c is welded.
- Each of the negative electrode current collectors 2a and the lithium electrode current collectors 7a has a lead-out portion serving as a terminal connection portion B ', and a terminal welding portion B' (3 pieces) of each negative electrode current collector 2a is provided.
- the terminal weld B '(one piece) of the lithium electrode current collector 7a are bundled and welded to the negative electrode terminal 2c.
- the sealing of the laminated films 4 and 5 is performed with the positive electrode terminal 1c and the negative electrode terminal 2c sandwiched, and the positive electrode terminal 1c and the negative electrode terminal 2c are laminated on the laminated films 4 and 5, respectively, as shown in FIG. It is heat-sealed at the heat-sealed parts A and B shown. That is, in the example of FIG. 2, the organic electrolyte capacitor is sealed at the heat-sealed portions A and B between the laminated films 4 and 5 and each terminal and at the heat-sealed portion C between the laminated films 4 and 5. Has been stopped.
- the positive electrode terminal 1c and the negative electrode terminal 2c extend out of the battery from between the laminated films 4 and 5, the positive electrode 1 passes through the positive electrode terminal 1c, and the negative electrode 2 and the lithium electrode 7 pass through the negative electrode terminal 2c.
- Each can be connected to an external circuit.
- the shape and size of the positive electrode terminal 1c and the negative electrode terminal 2c are not particularly limited. However, as long as the airtightness can be obtained within a limited cell volume, the thickest and widest terminal is. The resistance is small, which is preferable. It is preferable that the shape and size of each terminal be appropriately selected according to the characteristics of the target cell.
- the positive electrode current collector and the negative electrode current collector various materials generally proposed for applications such as organic electrolyte batteries can be used, and for the positive electrode current collector, aluminum and stainless steel are used.
- stainless steel, copper, nickel and the like can be suitably used, and foils, nets, and other shapes can be used.
- holes that penetrate the front and back surfaces for example, expanded metal, punched metal, metal net, foam, or through holes by etching. And the like.
- the thickness of the electrode current collector may be the same for the positive electrode and the negative electrode. However, if the materials are different, the thinner the specific gravity, the greater the effect in reducing the weight per cell volume. In the present invention, when aluminum is used as the positive electrode current collector and copper is used as the negative electrode current collector, it is more preferable to make the negative electrode current collector thinner than the positive electrode current collector.
- the shape and number of through-holes in the electrode current collector are adjusted so that lithium ions in the electrolyte solution described later can move between the front and back of the electrode without being blocked by the electrode current collector, and are closed by a conductive material. It can be set as appropriate to make it easier.
- the porosity of the electrode current collector is defined as a value obtained by converting a ratio of ⁇ 11 (current collector weight Z current collector specific gravity) / (current collector apparent volume) ⁇ into a percentage.
- the porosity of the electrode current collector used in the present invention is usually 10 to 79%, preferably 20 to 60%, more preferably 30 to 5%. 0%, most preferably 35-45%.
- the porosity of the electrode current collector is high, the time required for lithium ion to be supported on the negative electrode is short, and unevenness of lithium ion loading is unlikely to occur, but the strength of the current collector is reduced and wrinkles and cuts are generated. Likely to happen. In addition, it becomes difficult to hold the conductive material in the through-holes, and problems such as a drop in the electrode manufacturing yield due to the drop of the conductive material and the breakage of the electrode occur. On the other hand, when the porosity is low, the time required for lithium ion to be supported on the negative electrode becomes longer, causing problems such as a decrease in production efficiency and an increase in variation in cell characteristics, but the strength of the current collector increases.
- the porosity / pore diameter of the electrode current collector is desirably appropriately selected in the above range in consideration of the battery structure (laminated type, wound type, etc.) and productivity.
- FIG. 7 shows an example of the electrode current collector.
- Fig. 7 (a) shows an example of expanded metal having a porosity of 38%
- Fig. 7 (b) shows an example of a metal mesh having a porosity of 37%
- Fig. 7 (c) shows an example of a punched metal having a porosity of 34%.
- the through-hole of the electrode current collector is round, but the shape of the through-hole is not limited to this.
- the conductive material applied to the surface of the above-mentioned electrode current collector is a material which is hard to fall off from the through hole and allows lithium ions to permeate and move through the conductive material even when the through hole is closed. Others are not particularly limited.
- Such a conductive material mainly includes a conductive material and a binder resin.
- the type, composition, and the like of the conductive material and the binder resin can be set as appropriate.
- Examples of the conductive material used for such a conductive material include graphite, such as natural graphite or artificial graphite, which can be used as a negative electrode active material described later, coke-based, pitch-based, resin-based, and plant-based materials. And carbon materials such as acetylene black, Ketjen black, etc., carbon blacks, polyacene-based substances, tin oxide, silicon oxide and the like. Further, a metal powder such as nickel metal may be used. Of these, particularly preferred conductive materials include graphite-acetylene black, ketjen black and the like. Further, as the binder resin used for the conductive material, for example, any one may be used as long as it is insoluble in an organic electrolytic solution described later.
- a non-aqueous resin using an organic solvent such as alcohol or N-methylpyrrolidone as a dispersion medium or a solvent can be used.
- a rubber-based binder resin such as SBR, a carboxymethylcellulose-based resin, and the like are aqueous resins, and a phenol resin and a melamine resin can be used as an aqueous resin or a non-aqueous resin depending on the composition.
- Acrylic resin, polyamide resin, polyethylene resin and the like can be used as an aqueous resin by emulsifying the resin.
- fluorinated resins such as polytetrafluoroethylene and polyvinylidene fluoride, polyimide resins, and polyamide-imide copolymer resins are typical examples of non-aqueous resins.
- the use of a non-aqueous polyamide-imide resin is particularly preferable because the conductive material adheres tightly to the electrode current collector and does not easily fall off the through-hole.
- an electrode layer using an aqueous binder described below is formed on a conductive layer using a non-aqueous binder, the coatability and adhesiveness of the electrode layer are excellent, and the homogeneity and reliability are excellent. An electrode can be obtained.
- the negative electrode contains a negative electrode active material capable of reversibly supporting lithium ions.
- the negative electrode active material layer in the present invention is formed by adding a conductive material, a binder resin, and the like to the negative electrode active material as necessary.
- the negative electrode active material used in the present invention is not particularly limited as long as it can reversibly support lithium ions.
- Examples thereof include graphite such as natural graphite and artificial graphite, coke, pitch, and thermosetting resin.
- Various carbon materials, carbon fibers, polyacene-based substances, tin oxides, silicon oxides, and the like starting from palm shells and trees can be used.
- lithium ion has a small ion diameter
- a material whose structure is controlled so that the above-mentioned material is subjected to a treatment such as carbonization and processing under specific conditions to efficiently transfer lithium ions is particularly used. preferable.
- polyacene-based organic semiconductor has an amorphous structure, so there is no structural change such as swelling and shrinking upon insertion and desorption of lithium ions, so it has excellent cycle characteristics, and insertion and desorption of lithium ions. Since it has an isotropic molecular structure (higher-order structure), it has excellent characteristics in rapid charging and rapid discharging, and is particularly suitable as a negative electrode active material.
- the negative electrode active material is a heat-treated product of an aromatic condensation polymer, and has a polyacene-based skeleton structure in which the atomic ratio of hydrogen atoms / carbon atoms is 0.50 to 0.05. It is preferable to use an insoluble infusible substrate having a structure.
- the aromatic condensation polymer means a condensate of an aromatic hydrocarbon compound and an aldehyde.
- aromatic hydrocarbon compound so-called phenols such as phenol, cresol and xylenol can be suitably used.
- aromatic condensation polymer part of the aromatic hydrocarbon compound having a phenolic hydroxyl group is replaced with an aromatic hydrocarbon compound having no phenolic hydroxyl group, for example, xylene, toluene, aniline, or the like. It is also possible to use a modified aromatic condensation polymer such as a condensate of phenol, xylene and formaldehyde. Further, a modified aromatic polymer substituted with melamine or urea can be used, and a furan resin is also suitable.
- aldehydes such as formaldehyde, acetoaldehyde, and furfural can be used, and among these, formaldehyde is preferable.
- the phenol formaldehyde condensate may be a nopolak type, a resole type, or a mixture thereof.
- the insoluble infusible substrate is obtained by heat-treating the aromatic polymer, and the insoluble infusible substrate having the polyacene skeleton structure described above can be used.
- the position of the main 'peak is represented by 20 and exists at 24 ° or less, and the position of the main' peak is There are other broad peaks between 41 and 46 °. That is, it is suggested that the insoluble infusible substrate has a polyacene-based skeleton structure in which an aromatic polycyclic structure is appropriately developed and has an amorphous structure, and can stably dope lithium ions. It is useful as an active material for an organic electrolyte capacitor of the present invention.
- a conductive material such as a carbon-based material such as acetylene black, Ketjen black, or graphite, or a metal powder may be appropriately added to the negative electrode active material as needed.
- the negative electrode active material layer in the present invention contains the above-mentioned carbon material and the negative electrode active material such as PAS, and is formed by molding a negative electrode active material having a shape easy to be molded such as powder, granules, short fibers or the like with a binder resin.
- a binder resin for example, an aqueous resin that uses water as a dispersion medium or a solvent as long as it is insoluble in an organic electrolyte solution described later, or an organic solvent such as alcohol or N-methylpiperidone is dispersed.
- a medium or solvent The non-aqueous resin used can be used.
- a rubber-based binder resin such as SBR and a propyloxymethyl cellulose-based resin are water-based resins, and a phenol resin and a melamine resin can be used as an aqueous resin or a non-aqueous resin depending on the composition.
- Acrylic resin, polyamide resin, polyethylene resin and the like can be used as an aqueous resin by emulsifying the resin.
- fluorinated resins such as polytetrafluoroethylene and polyvinylidene fluoride, polyimide resins, and polyamide-imide copolymer resins are typical examples of non-aqueous resins.
- fluorine-based and water-based SBR resins are preferred.
- the thickness of the negative electrode active material layer is designed to balance the thickness with the positive electrode active material layer so as to secure the energy density of the cell.
- the thinner the negative electrode active material layer the more effective the active material This makes it possible to utilize them and improve the power density.
- the thickness of the negative electrode active material layer is usually one side, and is usually , 15 ⁇ 100 ⁇ m, preferably 20 ⁇ 80zm.
- the mixing ratio of the binder and the resin is 1 to 20%, preferably 2 to 10%, particularly preferably 2 to 5% by weight based on the active material.
- the positive electrode contains a positive electrode active material capable of reversibly supporting lithium ions and Z or an anion such as, for example, tetrafluoroporate.
- the positive electrode active material is not particularly limited as long as it can reversibly support lithium ions and Z or anion.
- starting materials include coke, pitch, resin, coconut shell, sawdust, and other plants.
- Various activated carbons, conductive polymers, polyacene-based substances activated with water vapor, carbon dioxide, potassium hydroxide, etc., mesopore carbon with mesopores with pore diameters of 2.0-5 O nm Can be used.
- the positive electrode active material layer in the present invention is formed by adding a conductive material, a binder resin, and the like as necessary to the positive electrode active material, and the type and composition of the conductive material and the binder resin are appropriately set. can do.
- a conductive material for example, activated carbon, carbon blacks such as acetylene black and Ketjen black, and carbon-based substances such as graphite can be suitably used.
- the mixing ratio of the conductive material varies depending on the electric conductivity of the active material, the shape of the electrode, and the like, but is preferably added at a ratio of 2 to 40% with respect to the active material.
- the binder resin may be, for example, one that is insoluble in an organic electrolyte solution described below, and may be an aqueous resin using water as a dispersion medium or a solvent, or an organic solvent such as alcohol or N-methylpyrrolidone as a dispersion medium.
- a non-aqueous resin used as a solvent can be used.
- rubber binder resins such as SBR and carboxymethyl cellulose resins are aqueous resins, and phenol resins and melamine resins can be used as aqueous resins or non-aqueous resins depending on the composition.
- Acrylic resin, polyamide resin, polyethylene resin and the like can be used as an aqueous resin by emulsifying the resin.
- fluorinated resins such as polytetrafluoroethylene and polyvinylidene fluoride, polyimide resins, and polyamide-imide copolymer resins are typical examples of non-aqueous resins.
- fluorine-based and water-based SBR resins are preferred.
- the mixing ratio of the binder and the resin is 1 to 20%, preferably 2 to 10%, particularly preferably 2 to 5% by weight based on the active material.
- the thickness of the positive electrode layer on one side is usually 30 to 150 / m, preferably 60 to: L00zm.
- the thickness of the positive electrode active material layer is designed to balance the thickness with the negative electrode active material layer so as to secure the energy density of the cell, but the thinner the positive electrode active material layer, the more effective the active material Although the active material layer can be used and the output density can be improved, if the active material layer is too thin, the energy density of the cell decreases, which is not preferable.In consideration of industrial productivity, the present invention considers The thickness of the positive electrode active material layer can be suitably used.
- a lithium electrode 7 is previously disposed inside an organic electrolyte capacitor as a lithium ion supply source.
- the lithium electrode contains at least lithium metal, such as lithium metal or lithium-aluminum alloy, A substance that can supply lithium ions is used.
- the amount of lithium electrodes (the weight of a substance capable of supplying lithium ions, such as lithium metal) to be disposed inside the organic electrolyte capacity is sufficient if it is sufficient to obtain a predetermined negative electrode capacitance.
- a predetermined amount may be supported from the lithium electrode 7 and then the lithium electrode 7 may be left inside the organic electrolyte capacitor (the definition of the electrostatic capacity will be described later).
- the lithium electrode is preferably formed on a lithium electrode current collector made of a conductive porous material, but the lithium electrode current collector may not be used.
- the conductive porous body serving as the lithium electrode current collector it is preferable to use a metal porous body that does not react with the lithium electrode, such as a stainless steel mesh.
- the lithium electrode current collector When a conductive porous body such as a stainless steel mesh is used as the lithium electrode current collector, it is preferable that at least a part of the lithium electrode is embedded in the pores of the lithium electrode current collector. Preferably, 80% or more of the lithium electrode is filled and arranged in the pores of the conductive porous body. As a result, even after the lithium ions are carried on the negative electrode, the gap generated between the electrodes due to the disappearance of the lithium electrode is reduced, and the reliability of the organic electrolyte capacity can be more reliably maintained.
- the lithium electrode current collector on which the lithium electrode is formed is disposed so as to face the negative electrode or the positive electrode.
- a lithium electrode 7 in which lithium metal is pressure-bonded to a lithium electrode current collector 7a is disposed below an electrode stack unit 6 in which a positive electrode 1, a separator 3 and a negative electrode 2 are sequentially stacked, and a three-electrode stack is formed. Unit 8 is formed.
- FIG. 9 shows another layer configuration of the three-electrode laminated unit 8.
- lithium electrodes 7 in which lithium metal is pressure-bonded to lithium electrode current collectors 7a are arranged above and below the electrode stack unit 6, respectively, to form a three-electrode stack unit 8. .
- FIG. 9 shows another example of the three-electrode laminated unit 8.
- a lithium electrode 7 is arranged in the middle of two electrode laminated units 6 to form a three-electrode laminated unit 8. With this arrangement, the lithium ions can be smoothly carried on the negative electrode.
- the lithium electrode current collector with the lithium electrode formed is placed in the cross-sectional direction of the electrode stack unit, and the negative electrode terminal and Z or the positive electrode terminal and the lithium electrode terminal are short-circuited to form the lithium active material and the Z or positive electrode active material with lithium. It is also possible to carry ions, but in this case, the negative electrode and If the width of the positive electrode is long, the unevenness of loading in the electrode may increase. Therefore, the position of the lithium electrode to be disposed must be appropriately selected in consideration of the cell configuration, the electrode size, and the like.
- the organic electrolyte capacitor of the present invention by locally disposing a lithium electrode carried on the negative electrode and Z or the positive electrode at a specific position, it is possible to improve the degree of freedom in cell design and improve mass productivity. Excellent charge / discharge characteristics can be provided.
- an electrolyte capable of transferring lithium ions is used.
- Such an electrolyte is usually in a liquid state and is impregnated over the separator.
- the separator for example, a porous material having continuous air holes that is durable with respect to an electrolytic solution or an electrode active material and has no electron conductivity can be used.
- a gel or solid electrolyte can be used, but in this case, separation may not be used, which is also effective in preventing liquid leakage.
- the electrolyte can be transferred lithium ions, without causing electrolysis even at a high voltage, from the viewpoint of lithium Umuion can stably be present, for example, L i C 10 4, L i As F 6, L i BF 4, L i Lithium salts such as PF 6 and Li (C 2 F 5 S ⁇ 2 ) 2 N can be suitably used. In that case, it is preferable to use an aprotic organic solvent as the solvent for dissolving the lithium salt.
- aprotic organic solvent examples include ethylene carbonate, propylene carbonate, dimethyl carbonate, getyl carbonate, carboxylactone, acetonitrile, dimethoxyethane, tetrahydrofuran, dioxolan, methylene chloride, sulfolane, and the like.
- a mixed solution in which two or more of these aprotic organic solvents are mixed can also be used.
- the above electrolyte and solvent are mixed in a sufficiently dehydrated state to form an electrolyte.
- concentration of the electrolyte in the electrolyte is at least 0.1 mol Z 1 or more in order to reduce the internal resistance due to the electrolyte. And more preferably in the range of 0.5 to 1.5 mol / 1.
- the material of the outer container of the organic electrolyte capacity of the present invention is not particularly limited, and various materials generally used for batteries or capacitors can be used. Metallic materials, plastic materials, or composite materials obtained by laminating them can be used. Also, the shape of the outer container is not particularly limited, and can be appropriately selected depending on the application, such as a cylindrical shape or a square shape. From the viewpoint of reducing the size and weight of the organic electrolyte capacity, it is preferable to use a film type outer container using a laminate film of aluminum and a polymer material such as nylon or polypropylene.
- a three-layer laminate film in which a nylon film is adhered to the outside of an aluminum foil and a layer of modified polypropylene or the like is adhered to the inside is used as an exterior material.
- the laminated film is usually deep drawn to a predetermined size, and a unit in which a positive electrode, a negative electrode, and a separator are laminated or wound is inserted, an electrolyte is injected, and the laminated film is heat-sealed or the like.
- the positive electrode terminal for example, an aluminum foil with a thickness of about 100 m
- the negative electrode terminal for example, a nickel foil with a thickness of 100 m
- the sealing of the laminate film is performed by a simple method of fusing while sandwiching the positive electrode terminal and the negative electrode terminal.
- laminated films 4 and 5 are used as the outer containers, and deep drawing is performed on laminated film 5 by the thickness of the three-electrode laminated unit, but deep drawing is performed on either laminated film 4 or 5 or on both. May be applied.
- a set of two laminated films is used, they are stacked so as to cover the contents, and the contents are sealed by heat sealing the overlapped outer peripheral portion.
- the film member is not limited to the sheet-like film used in FIG. 1, but may be a film member that has been formed into a tubular shape or a bag shape in advance.
- the contents are sealed by heat-sealing the two opposite sides, and when using a bag-shaped film member, one open side is heat-sealed. The contents are sealed.
- Conventional electric double layer capacitors usually use the same active material (mainly activated carbon) for the positive and negative electrodes. Almost the same amount is used.
- the active materials used for the positive and negative electrodes have a potential of about 3 V based on the Li ZL i + potential at the time of cell assembly, and when charged, anions form an electric double layer on the positive electrode surface.
- the potential of the positive electrode rises, while a force layer forms an electric double layer on the surface of the negative electrode, and the potential drops.
- an active material capable of reversibly carrying lithium ions and Z or zion for the positive electrode.
- the negative electrode is made of an active material capable of reversibly supporting lithium ions, and includes a carbon material such as graphite generally used in lithium ion secondary batteries.
- the organic electrolyte capacity of the present invention has a cell capacity of a (mAh) when discharged from a charged state to a voltage of half the charging voltage over 1 ⁇ 0.25 hours, and a charged negative electrode of 1.5 V (
- the ratio of the positive electrode active material to the negative electrode active material is controlled so that 0.05 ⁇ aZb ⁇ 0.3, where b (mAh) is the negative electrode capacity when discharging to Li / Li +). It is designed.
- the capacitance and the capacitance are defined as follows.
- the cell capacitance indicates the slope of the cell's discharge curve.
- the unit is F (farad).
- the capacitance per unit weight of the cell is the weight of the positive electrode active material filling the cell with the cell capacitance.
- the capacitance of the positive electrode is the slope of the discharge curve of the positive electrode
- the unit is F
- the capacitance per unit weight of the positive electrode is Is the value obtained by dividing the capacitance of the positive electrode by the weight of the positive electrode active material filled in the cell, the unit is FZ g
- the capacitance of the negative electrode is the slope of the discharge curve of the negative electrode, and the unit is F
- the capacitance per unit weight of the negative electrode is a value obtained by dividing the capacitance of the negative electrode by the weight of the negative electrode active material filled in the cell, and the unit is F / g.
- the cell capacity is the difference between the discharge start voltage and the discharge end voltage of the cell, that is, the product of the amount of voltage change and the cell capacitance.
- the unit is C (coulomb). 1 C is 1 A per second. The current of In this patent, it is expressed as mAh because it is the amount of charge when flowing.
- Positive electrode capacity is the product of the difference between the positive electrode potential at the start of discharge and the positive electrode potential at the end of discharge (positive electrode potential change) and the positive electrode capacitance.
- the unit is C or mAh. It is the product of the difference between the negative electrode potential and the negative electrode potential at the end of discharge (negative electrode potential change) and the negative electrode capacitance, in C or mAh.
- the discharge capacity of the cell changes depending on the current density flowing. Generally, the capacity decreases when the battery is discharged at a large current density, and the capacity increases when the battery is discharged at a small current density. Therefore, in the present application, the cell capacity a (mAh) is defined as the capacity at the time of discharging from the charged state to half the charging voltage with a current that can be discharged over 1 ⁇ 0.25 hours.
- the charging voltage is a voltage set to obtain a discharge capacity.
- lithium-ion secondary batteries are designed to charge to 4.2 V and discharge to about 3 V. At this time, the negative electrode is discharged to about 0.5 to 1.0 V.
- the negative electrode used in a lithium ion secondary battery does not have a capacity of 1.5 V or more.In this application, the negative electrode taken out of a charged cell is 1.5 V (L The capacity when discharged to L i +) was defined as the complete negative electrode capacity b (mAh).
- the cell capacity a (mAh) and the complete negative electrode capacity b (mAh) described above are obtained by adding the positive electrode active material and the negative electrode active material so that 0.05 ⁇ a / b ⁇ 0.3.
- the ratio is designed to be controlled. Thereby, high output characteristics can be obtained.
- the ratio of the positive electrode active material to the negative electrode active material is a value obtained by dividing the weight of the positive electrode active material by the weight of the negative electrode active material.
- the cell capacity a (mAh) is defined as the capacity when the battery is discharged from the charged state to a voltage half of the charging voltage with a current that can be discharged in 1 ⁇ 0.25 hours.
- the range of the ratio between the positive electrode active material and the negative electrode active material to achieve 0.05 ⁇ aZb ⁇ 0.3 is expanded. It is suitable.
- the capacitance per unit weight of the negative electrode active material is at least three times the capacitance per unit weight of the positive electrode active material and the weight of the positive electrode active material is larger than the weight of the negative electrode active material, the value is high. It is preferable because an energy density can be obtained.
- the negative electrode potential when a predetermined amount of lithium ions is preliminarily supported on the negative electrode in order to obtain the required capacity as the negative electrode capacity, the negative electrode potential is about 3 V while the positive electrode potential is about 3 V. Is lower than 3 V.
- the extent to which the charging voltage in the capacity can be increased is substantially determined by the positive electrode potential. In other words, if the positive electrode potential increases, the oxidative decomposition of the electrolytic solution occurs, and this becomes the limit potential.
- the difference between the positive potential and the negative potential can be increased because the negative potential is low.
- the withstand voltage of the electric double layer capacitor is about 2.3 to 2.7 V, whereas the structure of the present invention can be set to about 3.6 to 4. IV, which is as high as 3 V or more, thereby improving the energy density. be able to.
- the capacity of the positive electrode can be increased due to the low potential of the negative electrode. That is, since the negative electrode potential is low, it is possible to increase the amount of potential change in discharging the positive electrode. Specifically, it is possible to lower the positive electrode potential at the end of discharge to a value lower than 3 V, for example, 2 V. This is because at the positive electrode, the release of anion occurs mainly up to 3 V discharge, and at 3 V or lower, the potential drops due to doping of lithium ions.
- the potential of the positive electrode drops only to about 3 V at the time of discharging, because the negative electrode potential also becomes 3 V at that point and the cell voltage becomes 0 V. That is, the configuration of the present invention in which the positive electrode potential can be reduced to 2 V can have a higher capacity than the conventional configuration of the electric double layer capacity that can be reduced to only 3 V.
- the through holes of the electrode current collector are closed with a conductive material.
- the method of closing the through-hole of the electrode current collector with a conductive material is not particularly limited, and is a known method such as a coating method such as a die method, a dipping method, or a spray method, or a printing method such as gravure, screen, or transfer. Can be used.
- a positive electrode and a negative electrode are formed on the electrode current collector in which the through holes are closed with a conductive material.
- the positive electrode is formed by mixing a positive electrode active material with a binder resin to form a slurry, coating the slurry on a positive electrode current collector, and drying.
- a negative electrode is formed by mixing a negative electrode active material with a binder resin to form a slurry, coating the slurry on a negative current collector, and drying.
- the lithium electrode is formed by pressing lithium metal on a lithium electrode current collector made of a conductive porous material.
- the thickness of the lithium current collector is about 10 to 20 O ⁇ m, and the thickness of lithium metal is generally about 50 to 300 m, depending on the amount of the negative electrode active material used.
- the electrodes are dried, they are cut to the width appropriate for the size of the outer container of the organic electrolyte capacity. In the case of forming an electrode stack unit having a wrap-around structure, cut in a ripon shape. At this time, it may be cut into a shape having a lead portion as a terminal welding portion.
- FIGS. 11 and 12 are exploded views of the electrode stacking unit, showing the shape of the terminal welding portion and the stacking direction.
- Fig. 11 shows an example in which the positive electrode terminal weld and the negative electrode terminal weld protrude from opposite sides, respectively
- Fig. 12 shows the positive electrode terminal weld and the negative electrode terminal weld protrude from the same side. This is an example.
- the directions of the terminals of the positive electrode and the negative electrode are not limited to these two types.
- the terminal weld of the positive electrode current collector and the positive electrode terminal of the assembled three-electrode laminated unit, and the terminal weld of the negative electrode current collector and the negative electrode terminal of the lithium electrode current collector are each welded by ultrasonic welding or the like.
- the triode laminated unit which is welded to the external terminal, is placed inside the outer container, and the outer container is closed by heat fusion, etc., leaving the electrolyte injection port. At this time, at least a part of the external terminal is exposed to the outside of the outer container so that it can be connected to an external circuit.
- the electrolyte injection port is closed by heat fusion or the like, and the outer container is completely sealed, whereby the organic electrolyte capacity of the present invention is obtained. Evening can get.
- the contact pressure from the outer container is weaker than batteries using metal cases such as cylindrical or square batteries, so the external pressure is applied to make the positive and negative electrodes flat. Thereby, the distortion of the cell itself is eliminated, and the cell performance is improved, which is preferable.
- a 5 mm thick phenolic resin molded plate is placed in a siliconite electric furnace, heated to 500 ° C in a nitrogen atmosphere at a speed of 50 ° CZ for 50 ° CZ, and further heated to 650 ° C at a speed of 10 ° CZ for heat treatment.
- PAS were synthesized.
- the PAS plate thus obtained was pulverized with a pole mill to obtain a PAS powder having an average particle diameter of 7 m.
- the HZC ratio of this PAS powder was 0.22.
- the slurry was sufficiently mixed with a composition of 92 parts by weight of the PAS powder, 4 parts by weight of acetylene black powder, 4 parts by weight of SBR, 3.2 parts by weight of carboxymethyl cellulose, and 120 parts by weight of ion-exchanged water. Obtained.
- the slurry was applied to one surface of a copper foil having a thickness of 18 m so as to have a solid content of about 7 mg / cm 2 , dried and pressed to obtain a PAS negative electrode.
- the above negative electrode was cut out to a size of 1.5 ⁇ 2.0 cm 2 and used as a negative electrode for evaluation.
- Metallic lithium was used as a reference electrode.
- propylene force one Poneto using a solution of L i PF 6 to a concentration of 1 mole Z 1.
- One cell was charged with 40 OmAhZg of lithium ion with respect to the weight of the negative electrode active material at a charging current of 1 mA, and then discharged to 1.5 V at 1 mA.
- the electrostatic capacity per unit weight of the negative electrode was found to be 652 FZg from the discharge time during which the potential of the negative electrode changed by 0.2 V from the potential of the negative electrode one minute after the start of discharge.
- the remaining one cell was charged with lithium ion corresponding to 50 OmAhZg with respect to the weight of the negative electrode active material at a charging current of 1 mA, and then discharged to 1.5 V at 1 mA.
- the capacitance per unit weight of the negative electrode was found to be 748 FZg from the discharge time during which the potential of the negative electrode changed by 0.2 V from the potential of the negative electrode one minute after the start of discharge.
- coconut shell as a raw material, put it in an electric furnace, heat it up to 950 ° C at a rate of 50 ° C in a nitrogen stream for 950 ° C, and then activate it for 2 hours with a 1: 1 mixture of nitrogen and Z steam to obtain a specific surface area of 186.
- Om 2 Zg activated carbon was produced.
- the activated carbon was pulverized with a pole mill to obtain an activated carbon powder having an average particle diameter of 5 m.
- a slurry was obtained by sufficiently mixing with a composition consisting of 92 parts by weight of the activated carbon powder, 4 parts by weight of acetylene black powder, 4 parts by weight of SBR, 1 part by weight of propyloxymethyl cellulose, and 150 parts by weight of ion-exchanged water.
- the slurry was applied to one surface of a 20-m-thick aluminum foil coated with a carbon-based conductive paint to a solid content of about 7 mg / cm 2 , dried and pressed to obtain a positive electrode.
- the above positive electrode was cut into three pieces of 1.5 ⁇ 2.0 cm 2 size, one of which was a positive electrode, and the other was a negative electrode and a reference electrode.
- a simulated capacity cell was assembled with a 50 im thick paper non-woven fabric as the separator and the anode as the positive and negative electrodes.
- As the positive electrode electrolyte a solution in which triethylmethylammonium'tetrafluoroborate (TEM A.BF4) was dissolved in propylene carbonate at a concentration of 1 mol Z1 was used.
- TEM A.BF4 triethylmethylammonium'tetrafluoroborate
- the battery was charged to 2.5 V at a charging current of 10 mA, and then charged at a constant voltage. After a total charging time of 1 hour, the battery was discharged to 0 V at 1 mA.
- the capacitance per unit weight of the cell was calculated from the discharge time between 2.0 V and 1.5 V and found to be 22 F / g.
- the capacitance per unit weight of the positive electrode was determined from the potential difference between the reference electrode and the positive electrode to be 88 F / g. I got it.
- Non-aqueous carbon conductive paint (Nippon Acheson Co., Ltd .: EB-815) is spray coated on both sides. Then, the resultant was dried and dried to obtain a negative electrode current collector having a conductive layer formed thereon. The total thickness (the sum of the thickness of the current collector and the thickness of the conductive layer) was 49, and the through-hole was almost completely closed by the conductive paint.
- the negative electrode slurry is formed on both surfaces of the negative electrode current collector by a roll roller, and after pressing, the entire thickness of the negative electrode (the thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) The negative electrode 1 with a total of 155 was obtained.
- Non-aqueous carbon-based conductive paint (Nippon Acheson Co., Ltd .: EB-815) is coated on both sides of aluminum expanded metal (Nippon Metal Industry Co., Ltd.) with a thickness of 35 m (porosity: 50%) by spraying. Then, by drying, a current collector for a positive electrode having a conductive layer formed thereon was obtained. The total thickness (the total of the thickness of the current collector and the thickness of the conductive layer) was 52 / m, and the through holes were almost completely closed by the conductive paint.
- the slurry of the positive electrode is formed on both surfaces of the positive electrode current collector with a roll roller, and after pressing, the entire thickness of the positive electrode (the thickness of the positive electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the positive current collector)
- the positive electrode 1 has a total length of 214 m.
- Negative 1 electrode area of the positive electrode 1 in the shape shown in Figure 11 having a thickness of 214 111, respectively, was cut so as to 5.
- 0 X 8. 0 cm 2 thickness as evening separator of thickness 155 m
- connection terminal welds the welds of the positive and negative electrode current collectors to the connection terminals
- the terminals were overlapped and ultrasonically welded.
- a nickel-made negative electrode terminal with a width of 10 mm, a length of 30 mm, and a thickness of 0.2 mm, in which a sealant film was heat-sealed in advance, was placed on the terminal welds (eight sheets) of the negative electrode current collector.
- the capacitance ratio per unit weight of the negative electrode active material and the positive electrode active material is 7.41.
- the remaining two cells were charged with a constant current of 1000 mA until the cell voltage reached 3.6 V, and then a constant-current constant-voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Next, discharging was performed at a constant current of 100 mA until the cell voltage reached 1.8 V. This 3.6 V-1.8 V cycle was repeated, and the third discharge capacity was 105 mAh on average for two cells (the discharge time was 1.05 hours). The energy density was 14. OWh / 1 when the cell was 100 mm long and 50 mm wide.
- one cell After evaluating the cell capacity, one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour.
- the positive and negative electrodes were disassembled in an argon box so as not to be short-circuited, and eight negative electrodes were taken out.
- a prototype of a three-electrode cell was fabricated using lithium metal for each negative electrode as the working electrode and the counter and reference electrodes, and was discharged at a constant current of 100 mA until the negative electrode potential reached 1.5 V. Was 497 mAh in total of the eight discharge capacities.
- the remaining one cell is charged with a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, followed by a constant current of 10 A. Discharge was performed until the cell voltage reached 1.8V. The discharge capacity at this time was 57 mAh. Table 1 shows the results.
- the negative electrode 2 coated so that the total thickness of the negative electrode after pressing (the total thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) is 188 m;
- a film was prepared in the same manner as in Example 1 except that the positive electrode 2 coated so that the thickness (the total thickness of the positive electrode layer on both sides, the thickness of the conductive layer on both sides, and the thickness of the positive electrode current collector) was 209 m was used. Three-cell capacitors were assembled.
- the number of positive and negative electrodes was eight each, and the cell thickness was 4.3 mm.
- the lithium metal of 40 OmAh / g with respect to the weight of the negative electrode active material a lithium metal foil having a thickness of 180 mm pressed to a stainless steel net having a thickness of 80 m was used, and was set so as to face the negative electrode. One sheet was placed at the outermost part of the electrode stacking unit.
- the weight of the positive electrode active material was 0.72 times the weight of the negative electrode active material.
- each cell After standing at room temperature for 14 days, each cell was disassembled.Since lithium metal had completely disappeared, lithium ions for obtaining a capacitance of 65 OFZg or more per unit weight of the negative electrode active material were generated. It was determined that the battery was precharged. The capacitance ratio per unit weight between the negative electrode active material and the positive electrode active material is 7.41.
- the remaining two cells were charged with a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Then, discharging was performed at a constant current of 10 OmA until the cell voltage reached 1.8 V. This 3.6V—1.8V The cycle was repeated, and the third discharge capacity was 104 mAh on average for the two cells (discharge time was 1.04 hours).
- the energy density when the cell was 100 mm long and 50 mm wide was 13. lWhZl.
- one cell After evaluating the cell capacity, one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour. Then, the anode and cathode were disassembled in an argon box so as not to be short-circuited, and eight anodes were taken out. Next, a three-electrode cell was prototyped using lithium metal as the working electrode and the counter and reference electrodes for each negative electrode, and discharged at a constant current of 100 mA until the negative electrode potential reached 1.5 V. Was 706 mA in total for eight discharge capacities.
- the remaining one cell is charged with a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, followed by a constant current of 10 A
- the battery was discharged until the cell voltage reached 1.8V.
- the discharge capacity at this time was 59 mAh. Table 2 shows the results.
- the negative electrode 3 coated so that the total thickness of the negative electrode after pressing (the total thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the negative electrode current collector) is 137 m; Except for using the positive electrode 3 coated so that the thickness (the sum of the thickness of the positive electrode layer on both sides, the thickness of the conductive layer on both sides, and the thickness of the positive electrode current collector) is 219, a film mold was used in the same manner as in Example 1. Assembled 3 cells of Capsi Yu.
- the number of positive and negative electrodes was eight each, and the cell thickness was 3.9 mm.
- As the lithium metal equivalent to 40 OmAhZg with respect to the weight of the negative electrode active material a lithium metal foil having a thickness of 110 im pressed on a stainless steel net having a thickness of 80 m was used, and the electrode was placed so as to face the negative electrode. One sheet was placed on the outermost part of the laminated unit.
- the weight of the positive electrode active material is the weight of the negative electrode active material. 1.21 times that of
- each cell was disassembled.Since lithium metal had completely disappeared, lithium to obtain a capacitance of 65 OF / g or more per unit weight of the negative electrode active material was used. It was determined that the ions were precharged. The capacitance ratio per unit weight between the negative electrode active material and the positive electrode active material is 7.41.
- the remaining two cells were charged with a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Next, discharging was performed at a constant current of 100 mA until the cell voltage reached 1.8 V.
- This 3.6 V-1.8 V cycle was repeated, and the third discharge capacity was 105 mAh on average for two cells (the discharge time was 1.05 hours).
- the energy density was 15.7 WhZl when the vertical length of the cell was 100 mm and the horizontal length was 50 mm.
- one cell After evaluating the cell capacity, one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour. Then, the anode and cathode were disassembled in an argon box so as not to be short-circuited, and eight anodes were taken out. Next, a three-electrode cell was prototyped using lithium metal as the working electrode and the counter and reference electrodes for each negative electrode, and discharged at a constant current of 100 mA until the negative electrode potential reached 1.5 V. Was 40 ImAh in total of the discharge capacity of 8 sheets.
- the remaining one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, and then the cell is charged at a constant current of 10 A. Discharged until the voltage reached 1.8V. The discharge capacity at this time was 55 mAh. Table 3 shows the results.
- the negative electrode 4 coated so that the total thickness of the negative electrode after pressing (the sum of the thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) is 116 m; Except for using the positive electrode 4 coated so that the thickness (the sum of the thickness of the positive electrode layer on both sides, the thickness of the conductive layer on both sides, and the thickness of the positive electrode current collector) is 227 im, the film type is the same as in Example 1 Three capacitors were assembled. The number of positive and negative electrodes was eight each, and the cell thickness was 3.8 mm.
- the lithium metal equivalent to 40 OmAh / g with respect to the weight of the negative electrode active material was obtained by pressing a 90-m-thick lithium metal foil on a 80-xm-thick stainless steel mesh so as to face the negative electrode. One sheet was placed at the outermost part of the electrode stacking unit.
- the weight of the positive electrode active material is 1.66 times the weight of the negative electrode active material.
- each cell was disassembled.Since lithium metal had completely disappeared, lithium to obtain a capacitance of 65 OF / g or more per unit weight of the negative electrode active material was used. It was determined that the ions were precharged. The capacitance ratio per unit weight between the negative electrode active material and the positive electrode active material is 7.41.
- the remaining two cells were charged with a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Then, discharging was performed at a constant current of 10 OmA until the cell voltage reached 1.8 V. This 3.6 V-1.8 V cycle was repeated, and the third discharge capacity was 106 mA on average for two cells (discharge time was 1.06 hours).
- one cell After evaluating the cell capacity, one cell is charged at a constant current of 100 OmA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour. Then, the anode and cathode were disassembled in an argon box so as not to be short-circuited, and eight anodes were taken out. Next, a prototype of a three-electrode cell was fabricated using lithium metal as the working electrode and the counter and reference electrodes for each negative electrode, and discharged at a constant current of 10 OmA until the negative electrode potential reached 1.5 V. Was 298 mAh in total of the eight discharge capacities.
- the remaining one cell is charged with a constant current of 100 OmA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, followed by a constant current of 10 A
- the battery was discharged until the cell voltage reached 1.8 V.
- the discharge capacity at this time is 49 mAh. It was. Table 4 shows the results.
- the negative electrode 5 coated so that the total thickness of the negative electrode after pressing (the sum of the thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) is 101 m;
- the lithium metal equivalent to 40 OmAhZg with respect to the weight of the negative electrode active material a 70-meter-thick lithium metal foil bonded to an 80-m-thick stainless steel net was used, and the electrode was laminated so as to face the negative electrode. One was placed on the outermost part of the unit.
- the weight of the positive electrode active material is 2.33 times the weight of the negative electrode active material.
- each cell was disassembled.Since lithium metal had completely disappeared, lithium to obtain a capacitance of 65 OF / g or more per unit weight of the negative electrode active material was used. It was determined that the ions were precharged. The capacitance ratio per unit weight between the negative electrode active material and the positive electrode active material is 7.41.
- the remaining two cells were charged with a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Next, discharging was performed at a constant current of 10 OmA until the cell voltage reached 1.8 V.
- This 3.6 V-1.8 V cycle was repeated, and the third discharge capacity was 105 mAh on average for two cells (the discharge time was 1.05 hours).
- the energy density was 16.5 Wh / 1 when the vertical length of the cell was 10 Omm and the horizontal length was 5 Omm.
- one cell After evaluating the cell capacity, one cell has a constant current of 100 OmA until the cell voltage reaches 3.6 V. After charging for 1 hour at constant current and constant voltage, applying a constant voltage of 3.6 V, the cathode and anode were disassembled in an argon box so that they did not short-circuit, and eight anodes were taken out . Next, a prototype of a three-electrode cell using lithium metal as the working electrode and the counter electrode and the reference electrode for each negative electrode was discharged at a constant current of 100 mA until the negative electrode potential reached 1.5 V. b was 222 mAh in total of the eight discharge capacities.
- the remaining one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, and then the cell is charged at a constant current of 10 A. Discharged until the voltage reached 1.8V. The discharge capacity at this time was 4 ImAh. Table 5 shows the results.
- the negative electrode 6 coated so that the total thickness of the negative electrode after pressing (the sum of the thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) is 233 m;
- a film type was prepared in the same manner as in Example 1 except that the positive electrode 6 coated so that the thickness (the total thickness of the positive electrode layer on both sides, the thickness of the conductive layer on both sides, and the thickness of the positive electrode current collector) was 205 was used.
- the lithium metal equivalent to 50 OmAh / g with respect to the weight of the negative electrode active material a metal foil of 150 zm in thickness pressed with a stainless steel net of 80 m in thickness was used. Two sheets were arranged above and below the electrode stacking unit. The weight of the positive electrode active material is 0.53 times the weight of the negative electrode active material.
- each cell was disassembled.Since lithium metal had completely disappeared, lithium to obtain a capacitance of 748 F / g or more per unit weight of the negative electrode active material was used. It was determined that the ions were precharged. Negative active material and positive active material The capacitance ratio per unit weight is 8.50.
- the remaining two cells were charged with a constant current of 1000 mA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Next, discharging was performed at a constant current of 100 mA until the cell voltage reached 1.8 V.
- one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V. Charge the battery, and then apply a constant voltage of 3.6 V and perform constant-current constant-voltage charging for 1 hour.
- the positive and negative electrodes were disassembled in an argon box so as not to be short-circuited, and eight negative electrodes were taken out.
- a prototype of a three-electrode cell was fabricated using lithium metal for each negative electrode as the working electrode and the counter and reference electrodes, and discharged at a constant current of 100 mA until the negative electrode potential reached 1.5 V.
- the total discharge capacity of the eight sheets was 1098 mAh.
- the remaining one cell is charged at a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, and then the cell is charged at a constant current of 10 A. Discharged until the voltage reached 1.
- the discharge capacity at this time was 6 ImAh. Table 6 shows the results.
- a granular phenol resin having an average particle size of 20 (Kanebo Co., Ltd .: Bellpearl R800) is heated in an electric furnace to 600 ° C in a nitrogen gas atmosphere at a heating rate of 50 tZ hours, and maintained at the temperature for 5 hours. After that, the temperature was further increased to 1200 ° C at a rate of 80 ° C / hour, After holding at the temperature for 10 hours, it was cooled to prepare a non-graphitizable carbon sample.
- the sample thus obtained was pulverized with a pole mill to adjust the particle size to obtain a non-graphitizable carbon powder having an average particle size of 15 m.
- the specific surface area of the powder measured by the BET method was 8 m 2 / g.
- a slurry was obtained by sufficiently mixing with a composition consisting of 92 parts by weight of the non-graphitizable carbon powder, 4 parts by weight of acetylene black powder, 4 parts by weight of SBR, 1.2 parts by weight of carboxymethyl cellulose, and 120 parts by weight of ion-exchanged water.
- a composition consisting of 92 parts by weight of the non-graphitizable carbon powder, 4 parts by weight of acetylene black powder, 4 parts by weight of SBR, 1.2 parts by weight of carboxymethyl cellulose, and 120 parts by weight of ion-exchanged water.
- the negatively graphitizable carbon slurry was applied to one surface of a copper foil having a thickness of 18 so as to have a solid content of about 7 mgZcm 2 , dried and pressed to obtain a non-graphitizable carbon negative electrode.
- Four pieces of the above negative electrode were cut into 1.5 ⁇ 2.0 cm 2 sizes to obtain a negative electrode for evaluation.
- lithium ion corresponding to 40 OmAhZg with respect to the weight of the negative electrode active material was charged, and then discharged to 1.5 V at 1 mA.
- the capacitance per unit weight of the negative electrode was found to be 8426 F / g from the discharge time during which the potential of the negative electrode changed by 0.2 V from the potential of the negative electrode one minute after the start of discharge.
- Copper expanded metal with a thickness of 32 m (porosity: 50%) (manufactured by Nippon Metal Industry Co., Ltd.)
- Non-aqueous carbon-based conductive paint (manufactured by Nippon Acheson Co., Ltd .: EB_8 15) is spray-coated on both sides. Then, the resultant was dried to obtain a current collector for a negative electrode on which a conductive layer was formed.
- the total thickness (total of the thickness of the current collector and the thickness of the conductive layer) was 49 m, and the through-hole was almost completely closed by the conductive paint.
- the above non-graphitizable carbon slurry is formed on both surfaces of the negative electrode current collector with a roll roller, and after pressing, the entire thickness of the negative electrode (the thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) Negative electrode 7 having a total of 168 xm.
- the negative electrode 7 having a thickness of 168 / im and the total thickness of the positive electrode after pressing (the sum of the thickness of the positive electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the positive electrode current collector) as in Example 1 were 197 Except for using the positive electrode 7 coated so as to have a thickness of m, three cells of a film-type capacity were assembled in the same manner as in Example 1. The number of the positive electrode and the negative electrode was eight each, and the thickness of the cell was 4.0 mm.
- the lithium metal of 40 OmAh / g with respect to the weight of the negative electrode active material a material obtained by pressing a 150-m-thick lithium metal foil to a 80-m-thick stainless steel net so that it faces the negative electrode is used. One sheet was placed at the outermost part of the electrode stacking unit. The weight of the positive electrode active material is 0.78 times the weight of the negative electrode active material.
- the remaining two cells were charged with a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Then, discharging was performed at a constant current of 10 OmA until the cell voltage reached 1.8 V.
- one cell was charged at a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current-constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Then, the anode and cathode were disassembled in an argon box so as not to short-circuit, and eight anodes were taken out. Next, a prototype of a three-electrode cell was fabricated using lithium metal as the working electrode and the counter and reference electrodes for each negative electrode, and discharged at a constant current of 10 OmA until the negative electrode potential reached 1.5 V. Was 927 mAh in total with eight discharge capacities.
- the negative electrode 8 coated so that the total thickness of the negative electrode after pressing (the sum of the thickness of the negative electrode layer on both surfaces, the thickness of the conductive layer on both surfaces, and the thickness of the negative electrode current collector) is 453 m;
- a film type was formed in the same manner as in Example 1 except that the positive electrode 8 coated so that the thickness (the total thickness of the positive electrode layer on both sides, the thickness of the conductive layer on both sides, and the thickness of the positive electrode current collector) was 200 was used. Assembled 3 cells of Capsi Yu.
- the number of positive and negative electrodes was eight each, and the cell thickness was 6.7 mm.
- the lithium metal corresponding to 50 OmAh / g with respect to the weight of the negative electrode active material a lithium metal foil having a thickness of 255 m pressed against a stainless steel net having a thickness of 80 was used, and was made to face the negative electrode. Two sheets were arranged above and below the electrode stacking unit. The weight of the positive electrode active material was 0.23 times the weight of the negative electrode active material.
- each cell was disassembled.Since lithium metal had completely disappeared, lithium to obtain a capacitance of 748 F / g or more per unit weight of the negative electrode active material was used. It was determined that the ions were precharged. The capacitance ratio per unit weight between the negative electrode active material and the positive electrode active material is 8.50.
- the remaining two cells were charged with a constant current of 100 OmA until the cell voltage reached 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V was performed for 1 hour. Next, discharging was performed at a constant current of 10 OmA until the cell voltage reached 1.8 V. This 3.6V-1.8V cycle was repeated, and the third discharge capacity was 103 mAh on average for two cells (discharge time was 1.03 hours).
- the energy density when the vertical length of the cell was 10 Omm and the horizontal length was 5 Omm was 8.30 WhZl.
- one cell After evaluating the cell capacity, one cell has a constant current of 100 OmA until the cell voltage reaches 3.6 V. After charging for 1 hour at constant current and constant voltage to apply a constant voltage of 3.6 V,
- the positive electrode and the negative electrode were disassembled so as not to be short-circuited, and eight negative electrodes were taken out.
- a three-electrode cell was prototyped using lithium metal as the working electrode and the counter and reference electrodes for each negative electrode, and discharged at a constant current of 100 mA until the negative electrode potential reached 1.5 V.
- b was 2625 mAh in total of the eight discharge capacities.
- the remaining one cell is charged with a constant current of 1000 mA until the cell voltage reaches 3.6 V, and then a constant current constant voltage charge of applying a constant voltage of 3.6 V is performed for 1 hour, followed by a constant current of 10 A. Discharge was performed until the cell voltage reached 1.8V. The discharge capacity at this time was 56 mAh. Table 8 shows the results.
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CN2004800283857A CN1860568B (zh) | 2003-09-30 | 2004-09-27 | 有机电解质电容器 |
US10/573,943 US7443651B2 (en) | 2003-09-30 | 2004-09-27 | Organic electrolyte capacitor |
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JP2007173615A (ja) * | 2005-12-22 | 2007-07-05 | Fuji Heavy Ind Ltd | 電池又はキャパシタ用リチウム金属箔 |
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WO2012117794A1 (ja) | 2011-02-28 | 2012-09-07 | Jmエナジー株式会社 | リチウムイオンキャパシタ |
US9208958B2 (en) | 2011-02-28 | 2015-12-08 | Jm Energy Corporation | Lithium ion capacitor |
WO2019163896A1 (ja) | 2018-02-22 | 2019-08-29 | Jsr株式会社 | 蓄電デバイス、蓄電デバイス用負極、及びそれらの製造方法 |
KR20200124253A (ko) | 2018-02-22 | 2020-11-02 | 제이에무에나지 가부시키가이샤 | 축전 디바이스, 축전 디바이스용 부극, 및 그들의 제조 방법 |
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Publication number | Publication date |
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JP4751199B2 (ja) | 2011-08-17 |
US7443651B2 (en) | 2008-10-28 |
JPWO2005031773A1 (ja) | 2006-12-07 |
CN1860568A (zh) | 2006-11-08 |
KR100863562B1 (ko) | 2008-10-15 |
CN1860568B (zh) | 2010-10-13 |
EP1670008A4 (en) | 2010-01-06 |
EP1670008B1 (en) | 2012-09-12 |
JP2011146734A (ja) | 2011-07-28 |
US20070002524A1 (en) | 2007-01-04 |
KR20060097007A (ko) | 2006-09-13 |
JP5236765B2 (ja) | 2013-07-17 |
EP1670008A1 (en) | 2006-06-14 |
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