Patent Grant
9865855
This application claims the benefit of Japanese patent application No. 2015-035172 filed on Feb. 25, 2015, which is incorporated by reference.
The present invention relates to an energy storage device.
Conventionally, an energy storage device is known which is equipped with a positive electrode and a negative electrode to have a structure in which the positive electrode includes a positive active material layer, the negative electrode includes a negative active material layer, and the positive active material layer and the negative active material layer are arranged to face each other.
As such an energy storage device, a nonaqueous electrolyte secondary battery is proposed which is further equipped with a porous layer for electrically insulating positive and negative electrodes from each other, the porous layer being arranged between the positive active material layer and the negative active material layer (WO 2010/050507).
In the energy storage device disclosed in WO 2010/050507, the positive and negative electrodes are electrically insulated from each other by the porous layer.
However, the nonaqueous electrolyte secondary battery disclosed in WO 2010/050507 merely includes the positive and negative electrodes, and the porous layer. Thus, immediately after charge-discharge cycles (for example, within 2 hours of the end of the cycles), the battery may be temporarily decreased in power (hereinafter, the power-decrease may be referred to temporary deterioration).
The following presents a simplified summary of the invention disclosed herein in order to provide a basic understanding of some aspects of the invention. This summary is not an extensive overview of the invention. It is intended to neither identify key or critical elements of the invention nor delineate the scope of the invention. Its sole purpose is to present some concepts of the invention in a simplified form as a prelude to the more detailed description that is presented later.
An object of the present invention is to provide an energy storage device in which temporary deterioration is suppressed.
An energy storage device according to an aspect of the present invention includes a positive electrode, a negative electrode, and an insulating layer arranged between the positive and negative electrodes to electrically insulate the positive and negative electrodes, the negative electrode includes a composite layer containing active material particles, the composite layer of the negative electrode, and the positive electrode are arranged to face each other across the insulating layer, the insulating layer contains electrically insulating particles, and is made porous by a gap between the electrically insulating particles, the composite layer of the negative electrode is made porous by a gap between the active material particles, and a following relational expression (1) is satisfied:
−0.8≦Log B−Log A≦1.0
in which in a distribution of pores in the composite layer, a pore peak diameter is represented by A (μm), and in a distribution of pores in the insulating layer, a pore peak diameter is represented by B (μm).
The foregoing and other features of the present invention will become apparent from the following description and drawings of an illustrative embodiment of the invention in which:
An energy storage device according to an aspect of the present invention includes a positive electrode, a negative electrode, and an insulating layer arranged between the positive and negative electrodes to electrically insulate the positive and negative electrodes from each other. The negative electrode includes a composite layer containing active material particles. The composite layer of the negative electrode, and the positive electrode are arranged to face each other across the insulating layer. The insulating layer contains electrically insulating particles, and is made porous by a gap between the electrically insulating particles. The composite layer of the negative electrode is made porous by a gap between the active material particles. A following relational expression (1) is satisfied:
−0.8≦Log B−Log A≦1.0
in which in a distribution of pores in the composite layer, a pore peak diameter is represented by A (μm), and in a distribution of pores in the insulating layer, a pore peak diameter is represented by B (μm).
According to the energy storage device having the above-mentioned configuration, the pore peak diameter A (μm) in the pore distribution of the composite layer of the negative electrode and the pore peak diameter B (μm) in the pore distribution of the insulating layer satisfy the relational expression (1). Thus, from the surface of the active material in the composite layer of the negative electrode to the insulating layer, paths for electrons are appropriately and sufficiently ensured. As a result, even immediately after charge-discharge cycles, reaction in the electrode plane direction does not turn into an ununiformed state. Accordingly, a temporary power-decrease (temporary deterioration) can be suppressed, which may be caused immediately after charge-discharge cycles.
In the energy storage device, the average primary particle diameter D90 of the active material particles in the composite layer may be 3 μm or more and 18 μm or less.
In the energy storage device, a following relational expression (2) may be satisfied: −3≦C−D≦6 in which an average primary particle diameter D90 of the active material particles in the composite layer is represented by C (μm), and an average primary particle diameter D90 of the electrically insulating particles in the insulating layer is represented by D (μm).
In the energy storage device, the active material particles in the negative electrode may include non-graphitizable carbon.
In the energy storage device, the composite layer of the negative electrode may further include carboxymethylcellulose.
With this configuration, temporary deterioration can be suppressed.
Hereinafter, with reference to the drawings, an embodiment of the energy storage device of the present invention will be described. The energy storage device may be primary battery, secondary battery, capacitor, and other. As an example of the energy storage device, a chargeable and dischargeable secondary battery will be explained. The name of each constituent member (each constituting element) of the present embodiment is a name exclusively for the embodiment. Thus, the name may be different from the name of each of the constituent members (each of the constituting elements) in the item “BACKGROUND”.
An energy storage device 1 according to the present embodiment includes a positive electrode 3, a negative electrode 5, and a sheet type insulating layer 7 arranged between the positive electrode 3 and the negative electrode 5 to electrically insulate the positive electrode 3 and the negative electrode 5 from each other. The negative electrode 5 includes a composite layer 5b containing active material particles. The composite layer 5b of the negative electrode and the positive electrode 3 are arranged to face each other across the insulating layer 7. The insulating layer 7 contains electrically insulating particles, and is made porous by a gap between the electrically insulating particles. The composite layer 5b of the negative electrode 5 is made porous by a gap between the active material particles. The energy storage device 1 satisfies the following relational expression (1):
−0.8≦Log B−Log A≦1.0
in which in the distribution of pores in the composite layer, the pore peak diameter is represented by A (μm), and in the distribution of pores in the insulating layer, the pore peak diameter is represented by B (μm).
The energy storage device 1 according to the present embodiment is a nonaqueous electrolyte secondary battery. More specifically, the energy storage device 1 is a lithium ion secondary battery 1, which makes use of electron transfer generated to the accompaniment of the transfer of lithium ions. This energy storage device 1 is used singly, or energy storage devices equivalent the energy storage device 1 are together used. Specifically, the energy storage device 1 is used singly when a power and a voltage required are small. In the meantime, when at least one of required power and voltage is large, the energy storage device 1 is used in an energy storage apparatus in the state of being combined with the other energy storage device(s). In this energy storage apparatus, the energy storage device 1 and the energy storage device(s) supply an electrical energy.
As illustrated in, for example,
As illustrated in
The positive electrode 3 is in a rectangular form, such as a band form. The thickness of the positive electrode 3 is usually from 35 to 250 μm.
As illustrated in each of
The material of the electrode substrate 3a of the positive electrode 3 is, for example, aluminum. The electrode substrate 3a may be in a film form. The thickness of the electrode substrate 3a may be from 5 to 50 μm.
The composite layer 3b of the positive electrode 3 extends, for example, along at least one of the two surfaces of the electrode substrate 3a of the positive electrode 3. The composite layer 3b of the positive electrode 3 contains positive active material particles, a conducting agent, and a binder. The composite layer 3b of the positive electrode 3 is made porous by at least a gap between the active material particles. The thickness of the composite layer 3b of the positive electrode 3 may be from 30 to 200 μm.
The content of active material particles in the composite layer 3b of the positive electrode 3 is preferably 70% or more by mass, more preferably 85% or more by mass in order to make the energy density of the energy storage device 1 higher. Moreover, the content of the active material particles in the composite layer 3b of the positive electrode 3 is preferably 99% or less by mass, more preferably 96% or less by mass to make better the applicability of a positive composite (paste) that will be described later. In order to make the durability of the energy storage device 1 higher, the content of the active material particles in the composite layer 3b of the positive electrode 3 is preferably 98% or less by mass, more preferably 95% or less by mass.
The composite layer 3b of the positive electrode 3 may contain the conducting agent in a proportion of 2 to 10% by mass both inclusive. The composite layer 3b of the positive electrode 3 may contain the binder in a proportion of 2 to 10% by mass both inclusive.
The active material particles in the positive electrode 3 is made particulate, and contain an active material capable of occluding and releasing lithium ions in a proportion of 95% or more by mass. An average primary particle diameter D90 of the active material particles of the positive electrode 3 may be from 3 to 10 μm both inclusive.
The average primary particle diameter D90 is a particle diameter corresponding to the cumulative quantity of smaller 90%-particles out of the measured particles when the particle diameter of each of at least 500 primary particles is measured in accordance with a method described in the item “EXAMPLES”.
The active material of the active material particles in the positive electrode 3 is, for example, a material represented by the following composition formula:
LiaNibM1cM2dWxNbyZrzO2
wherein a, b, c, d, x, y and z satisfy the following: 0≦a≦1.2, 0≦b≦1, 0≦c≦0.5, 0≦d≦0.5, 0≦x≦0.1, 0≦y≦0.1, and 0≦z≦0.1, and b+c+d=1; and M1 and M2 are each at least one element selected from the group consisting of Mn, Ti, Cr, Fe, Co, Cu, Zn, Al, Ge, Sn, and Mg.
Examples of the active material include LipCoO2, LipNiO2, LipMn2O4, LipMnO3, LipNiqCo(1-q)O2, and LipNiqMnrCo(1-q-r)O2 in each of which 0<p≦1.3, 0<q<1, and 0<r<1, such as LiNi1/3Mn1/3CO1/3O2 and LipNiqMn(2-q)O4.
Other examples of the active material include polyanionic compounds such as LiFePO4, LiMnPO4, LiNiPO4, LiCoPO4, Li3V2(PO4)3, Li2MnSiO4, and Li2CoPO4F.
The elements or polyanions of each of these polyanion compounds may be partially substituted with one or more other elements or anionic species.
The surface of the active material particles in the positive electrode 3 may be covered with a metal oxide such as ZrO2, MgO or Al2O3, or carbon.
Additional examples of the active material include electroconductive polymeric compounds such as disulfide, polypyrrole, polyaniline, poly-para-styrene, polyacetylene, and polyacene materials; and pseudo-graphite-structural carbonaceous material. However, the active material is not limited to these examples.
About the active material in the positive electrode 3, one of these compounds may be used singly, or two or more thereof may be used in any combination.
The conducting agent in the composite layer 3b of the positive electrode 3 may be in a particulate form. The material that forms the conducting agent particles in the composite layer 3b of the positive electrode 3 may be, for example, a metallic material or nonmetallic material. The metallic material of the conducting agent may be, for example, Cu or Ni. The nonmetallic material may be, for example, a carbonaceous material such as graphite, carbon black, acetylene black, or ketchen black.
The binder in the composite layer 3b of the positive electrode 3 is not particularly limited as far as the binder is a material stable against a solvent to be blended into the positive composite or the electrolyte solution 9, and further stable against oxidizing or reducing reaction when the energy storage device is charged or discharged. Examples of the binder in the composite layer 3b of the positive electrode 3 include thermoplastic resins, such as polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), polyethylene, and polypropylene; and polymers having rubber elasticity, such as ethylene-propylene-diene terpolymer (EPDM), sulfonated EPDM, styrene-butadiene rubber (SBR), and fluorine-contained rubber. About the binder, one of such materials is used singly, or two or more thereof are used in any combination.
In the positive electrode 3, the composite layer 3b and another composite layer may be arranged to cover both surfaces of the electrode substrate 3a, respectively.
In the meantime, the negative electrode 5 is in a rectangular form such as a band form. The thickness of the negative electrode 5 may be from 35 to 250 μm. As illustrated in each of
The material of the electrode substrate 5a of the negative electrode 3 is, for example, copper. The electrode substrate 5a may be in a film form. The thickness of the electrode substrate 5a of the negative electrode 5 may be from 5 to 50 μm both inclusive.
The composite layer 5b of the negative electrode 5 extends, for example, along at least one of the two surfaces of the electrode substrate 5a of the negative electrode 5. The composite layer 5b of the negative electrode 5 contains active material particles and a binder, and may further contain a conducting agent. The composite layer 5b of the negative electrode 5 is made porous by at least a gap between the active material particles. The thickness of the composite layer 5b of the negative electrode 5 may be from 30 to 200 μm both inclusive.
The content of the active material particles in the composite layer 5b of the negative electrode 5 is preferably 80% or more by mass, more preferably 90% or more by mass in order to make the energy density of the energy storage device 1 higher. Moreover, the content of the active material particles composite layer 5b of the negative electrode 5 is preferably 99% or less by mass, more preferably 98% or less by mass to make the energy storage device 1 better in durability.
The composite layer 5b of the negative electrode 5 may contain the conducting agent in a proportion of 0 to 10% by mass both inclusive. The composite layer 5b of the negative electrode 5 may contain the binder in a proportion of 1 to 10% by mass both inclusive.
The active material particles in the negative electrode 5 is made particulate, and contain, in a proportion of 95% or more by mass, an active material capable of contributing to electrode reactions of charge reaction and discharge reaction in the negative electrode 5.
The average primary particle diameter D90 of the active material particles of the negative electrode 5 is preferably 3 μm or more, more preferably 4 μm or more. Moreover, the average primary particle diameter D90 of the active material particles in the negative electrode 5 is preferably 18 μm or less, more preferably 12 μm or less.
When the average primary particle diameter D90 of the active material particles in the negative electrode 5 is 3 μm or more, lowering of capacity retention ratio is suppressed. Moreover, when the average primary particle diameter D90 of the active material particles in the negative electrode 5 is 18 μm or less, the energy storage device can be further improved in power characteristics.
The average primary particle diameter D90 of the active material particles in the negative electrode 5 is determined in the same way as the average primary particle diameter D90 of the active material particles in the positive electrode 3.
The active material of the active material particles in the negative electrode 5 is, for example, a carbonaceous material, an element alloyable with lithium, an alloy, a metal oxide, a metal sulfide, or a metal nitride.
Examples of the carbonaceous material include amorphous carbons such as non-graphitizable carbon (hard carbon) and easily graphitizable carbon (soft carbon), and graphite.
Examples of the element alloyable with lithium include Al, Si, Zn, Ge, Cd, Sn, and Pb. These elements may be used singly, or in any combination of two or more thereof.
Examples of the alloy include Ni—Si alloy, Ti—Si alloy, and other alloys each containing a transition metal element.
Examples of the metal oxide include amorphous tin oxides such as SnB0.4P0.6O3.1, tin silicon oxides such as SnSiO3, silicon oxides such as SiO, and lithium titanates each having a spinel structure, such as Li4+xTi5O12.
Examples of the metal sulfide include lithium sulfides such as TiS2, molybdenum sulfides such as MoS2, and iron sulfides such as FeS, FeS2 and LixFeS2.
Out of these examples, the active material of the active material particles in the negative electrode 5 is preferably non-graphitizable carbon.
The binder in the composite layer 5b of the negative electrode 5 is not particularly limited as far as the binder is a material stable against a solvent to be blended into a positive composite or the electrolyte solution 9, and further stable against oxidizing or reducing reaction when the energy storage device is charged or discharged. Examples of the binder in the composite layer 5b of the negative electrode 5 include thermoplastic resins, such as carboxymethylcellulose, polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), polyethylene, and polypropylene; and polymers having rubber elasticity, such as ethylene-propylene-diene terpolymer (EPDM), sulfonated EPDM, styrene-butadiene rubber (SBR), and fluorine-contained rubber. One of such materials is used singly, or two or more thereof are used in any combination.
The binder in the composite layer 5b of the negative electrode 5 is preferably carboxymethylcellulose since a composite for producing the composite layer 5b, can be prepared in which the active material is stably dispersed in an aqueous solvent. Carboxymethylcellulose may be in the form of a salt thereof.
In the negative electrode 5, the composite layer 5b and another composite layer may be arranged to extend along both surfaces of the electrode substrate 5a, respectively.
The insulating layer 7 is a layer arranged between the positive electrode 3 and the negative electrode 5 to prevent a short circuit between the positive electrode 3 and the negative electrode 5. Specifically, the insulating layer 7 is arranged to contact the composite layer 5b of the negative electrode 5. The insulating layer 7 is arranged between the separator 4 and the composite layer 5b of the negative electrode 5. The insulating layer 7 contains at least electrically insulating particles, and further contains a binder.
The insulating layer 7 is made porous by a gap between the electrically insulating particles in such a manner that Li ions and others can transfer between the positive electrode 3 and the negative electrode 5.
The insulating layer 7 contains the electrically insulating particles in a proportion that is preferably 30% or more by mass, more preferably 50% or more by mass to make the electrically insulating property thereof better.
When the insulating layer 7 is formed by a coating method, the content of the electrically insulating particles in the insulating layer 7 is preferably 99% or less by mass, more preferably 98% or less by mass to make this layer better in bondability to the composite layer and in shape-keeping performance.
The insulating layer 7 may contain the binder in a proportion of 1 to 10% by mass both inclusive. The electrically insulating property of the insulating layer 7 is higher than that of each of the composite layer 3b of the positive electrode 3 and the composite layer 5b of the negative electrode 5. The electrical conductivity of the insulating layer 7 is less than 10−6 S/m.
The electrically insulating particles are particles containing an electrically insulating material having an electrical conductivity less than 10−6 S/m in a proportion of 95% or more by mass.
An average primary particle diameter D90 of the electrically insulating particles is preferably 0.5 μm or more, more preferably 1 μm or more. Moreover, the average primary particle diameter D90 of the electrically insulating particles is preferably 10 μm or less, more preferably 8 μm or less.
When the average primary particle diameter D90 of the electrically insulating particles is 0.5 μm or more, it can be suppressed that the pore diameter becomes too small. Moreover, when the average primary particle diameter D90 of the electrically insulating particles is 10 μm or less, the thickness of the insulating layer can be made small with a higher certainty.
The average primary particle diameter D90 of the electrically insulating particles is determined in the same way as the average primary particle diameter D90 of the active material particles in the positive electrode 3.
The electrically insulating particles are preferably inorganic particles since the particles are also excellent in heat resistance. The electrically insulating particles may be particles other than inorganic particles.
Examples of the inorganic particles include oxide particles, nitride particles, ion crystalline particles, covalently bonded crystalline particles, clay particles, and particles made of a mineral-resource-originating substance or an artificial substance corresponding thereto.
Examples of the oxide particles (metal oxide particles) include iron oxide, SiO2, Al2O3, TiO2, BaTiO2, ZrO, and alumina-silica complex oxide particles.
Examples of the nitride particles include aluminum nitride and silicon nitride particles.
Examples of the ion crystalline particles include calcium fluoride, barium fluoride, and barium sulfate particles.
Examples of the covalently bonded crystalline particles include silicon and diamond particles.
Examples of the clay particles include talc and montmorillonite particles.
Examples of the particles made of a mineral-resource-originating substance or an artificial substance corresponding thereto include boehmite (alumina hydrate), zeolite, apatite, kaolin, mullite, spinel, olivine, sericite, bentonite, and mica particles.
A fired body is usable which is obtained by firing a hydrate-containing natural mineral (such as any one of the above-mentioned clays and mineral-resource-originating substances).
The electrically insulating particles may be particles produced to have electrically insulating property by applying a surface treatment with an electrically insulating material (for example, a material constituting the above-mentioned electrically insulating inorganic particles) to the surface of electroconductive particles, such as metallic particles, oxide particles such as SnO2 and tin-indium oxide (ITO), or carbonaceous particles of carbon black, graphite or some other.
The inorganic particles may be particles of only one species of the above-mentioned particle species or particles of a mixture of two species thereof, or particles of a species obtained by compositing two or more of the above-mentioned material species.
The species of the inorganic particles is preferably at least one species selected from SiO2 particle, Al2O3 particle, and alumina-silica composite oxide particle species with each other.
Examples of the binder in the insulating layer 7 include polyacrylonitrile, polyvinylidene fluoride (PVDF), a copolymer made from vinylidene fluoride and hexafluoropropylene, polytetrafluoroethylene, polyhexafluoropropylene, polyethylene oxide, polypropylene oxide, polyphosphazene, polysiloxane, polyvinyl acetate, polyvinyl alcohol, polymethyl methacrylate, polyacrylic acid, polymethacrylic acid, styrene-butadiene rubber, nitrile-butadiene rubber, polystyrene, and polycarbonate.
The binder in the insulating layer 7 is preferably polyacrylonitrile, polyvinylidene fluoride, polyhexafluoropropylene, polyacrylic acid, polymethacrylic acid, styrene-butadiene rubber, or polyethylene oxide since the binder is more stable in electrochemical property.
The energy storage device 1 of the present embodiment satisfies the following relational expression (1): −0.8≦Log B−Log A≦1.0 in which in the distribution of pores in the composite layer 5b of the negative electrode 5, the pore peak diameter is represented by A (μm), and in the distribution of pores in the insulating layer 7, the pore peak diameter is represented by B (μm).
In the energy storage device 1 of the embodiment, the ion conductivity of the outer surface of the negative electrode can be even, and the generation of any ununiformed reaction in the plane direction of the device 1 can be suppressed. In this way, a temporary power-decrease (temporary deterioration) can be suppressed which is generated immediately after charge-discharge cycles. The fact that A (μm) and B (μm) satisfy the relational expression (1) contributes largely to an improvement in the cycle performance of the energy storage device 1.
About the relational expression (1), A and B preferably satisfy “−0.6≦Log B−Log A”, and more preferably satisfy “−0.3≦Log B−Log A”. When A and B satisfy “−0.6≦Log B−Log A”, it can be suppressed that the ion conducting performance of the insulating layer becomes extremely shorter as compared with that of the composite layer.
About the relational expression (1), A and B preferably satisfy “Log B−Log A≦0.9”, and more preferably satisfy “Log B−Log A≦0.5”. When A and B satisfy “Log B−Log A≦0.9”, it can be suppressed that the ion conducting performance of the inside of the composite layer becomes extremely shorter as compared with that of the insulating layer.
The value A (the pore peak diameter in the pore distribution of the composite layer 5b of the negative electrode 5) is preferably from 0.5 to 1.5 μm both inclusive, more preferably from 0.9 to 1.2 μm both inclusive. The value B (the pore peak diameter in the pore distribution of the insulating layer 7) is preferably from 0.2 to 12.0 μm both inclusive, more preferably from 0.3 to 8.0 μm both inclusive, even more preferably from 0.5 to 3.5 μm both inclusive. When the values A and B are within the respective ranges while the relational expression (1) is satisfied, the temporary deterioration can be further suppressed.
The pore peak diameter is determined by a mercury intrusion method according to JIS R1655 at room temperature. Specifically, the pore peak diameter is determined by a method described in the item “EXAMPLES”.
The pore peak diameter is controllable by varying, for example, the pressing pressure when each of the negative electrode 5 and the insulating layer 7 is produced, the particle diameter of the active material particles or the inorganic particles, or the composition of any one of the composite layers or the insulating layer. Specifically, the pore peak diameter in the composite layer 5b can be made small by increasing the pressing pressure when the electrode substrate 5a and the composite layer 5b are pressed in the production of the negative electrode 5.
When the insulating layer 7 is formed on the composite layer 3b of the positive electrode 3 or the composite layer 5b of the negative electrode 5, the pore peak diameter in the insulating layer 7 can be made small by increasing the pressing pressure at the time of pressing a workpiece in which the positive electrode 3 or the negative electrode 5 is stacked onto the insulating layer 7.
Moreover, the pore peak diameter in the insulating layer 7 can be made small, for example, by increasing the pressing pressure at the time of pressing a workpiece in which the insulating layer 7 formed on a single surface of the separator 4 is stacked onto the separator 4.
The half band width of the pore peak diameter in the pore distribution of the insulating layer 7, this width being concerned with the value B, is usually from 0.3 to 0.8 both inclusive. The half band width is preferably from 0.4 to 0.7 both inclusive.
The energy storage device 1 of the present embodiment preferably satisfies the following relational expression (2): −3≦C−D≦6, and more preferably satisfies the following relational expression (2): 0≦C−D≦3 in which the average primary particle diameter D90 of the active material particles in the composite layer 5b of the negative electrode 5 is represented by C (μm), and the average primary particle diameter D90 of the electrically insulating particles in the insulating layer is represented by D (μm).
When the energy storage device 1 satisfies the relational expression (2) as described above while satisfying the relational expression (1), the temporary deterioration can be further suppressed. Specifically, when this device 1 satisfies the relational expression (2), the ion conductivity on the outer surface of the negative electrode is made even so that ununiformed reaction in the plane direction can be suppressed. Satisfying the relational expression (2) contributes largely to an improvement in the cycle performance of this device 1.
The value C (the average primary particle diameter D90 of the active material particles in the composite layer 5b of the negative electrode 5) is preferably from 3.0 to 18.0 μm both inclusive, more preferably from 4.0 to 12.0 μm both inclusive. The value D (the average primary particle diameter D90 of the electrically insulating particles in the insulating layer 7) is preferably from 0.5 to 14.0 μm both inclusive, more preferably from 1.0 to 10.0 μm both inclusive. When the values C and D are within the respective ranges while the relational expression (1) is satisfied, the temporary deterioration can be further suppressed.
As illustrated in, for example, each of
As illustrated in each of
As illustrated in, for example,
The intermediate layer 6 contains a conducting agent and a binder. Since the intermediate layer 6 contains the conducting agent, the intermediate layer 6 functions as a path for electrons between the electrode substrate 3a of the positive electrode 3 and the composite layer 3b of the positive electrode 3. Moreover, since the intermediate layer 6 contains the binder, separation between the electrode substrate 3a of the positive electrode 3 and the composite layer 3b of the positive electrode 3 can be prevented. The thickness of the intermediate layer 6 may be from 0.1 to 10 μm.
The intermediate layer 6 preferably has a sufficient adhesiveness onto the corresponding electrode substrate (for example, the electrode substrate 3a of the positive electrode). In other words, for example, the intermediate layer 6 preferably has a sufficient strength against separation from the electrode substrate. The intermediate layer 6 preferably has higher electron conductivity than the corresponding composite layer (for example, the composite layer 3b of the positive electrode).
The conducting agent in the intermediate layer 6 may be in a particulate form. Moreover, the conducting agent is usually formed by a material having an electrical conductivity of 10−6 S/m or more. Examples of the conducting agent in the intermediate layer 6 include carbonaceous materials such as carbon black, acetylene black and ketchen black, and metallic materials such as iron, nickel, copper and aluminum. The intermediate layer 6 contains the conducting agent in a proportion preferably from 5 to 99% by mass, more preferably from 10 to 98% by mass. When the intermediate layer 6 contains the conducting agent in a proportion within the range, the electroconductivity of the intermediate layer 6 can be kept with a higher certainty.
The binder in the intermediate layer 6 may be at least one selected from the group consisting of chitin-chitosan derivatives, cellulose derivatives, fluororesins, synthetic rubbers, polyamide resins, polyimide resins, polyolefin resins, and polyacrylic resins.
The chitin-chitosan derivatives may be at least one selected from the group consisting of hydroxyalkylchitosans such as hydroxyethylchitosan, hydroxypropylchitosan, hydroxybutylchitosan, and alkylated chitosans.
The hydroxyalkylchitosans are each preferably a chitosan crosslinked by mixing this chitosan with, for example, an organic acid such as salicylic acid, pyromellitic acid, citric acid or trimellitic acid.
Examples of the cellulose derivatives include a Na salt of carboxymethylcellulose (Na-CMC), an ammonium salt of carboxymethylcellulose (NH4-CMC), and carboxymethylcellulose (H-CMC).
Examples of the fluororesins include polyvinylidene fluoride and polytetrafluoroethylene.
Examples of the synthetic rubbers include styrene-butadiene rubber, acrylic rubber, and nitrile rubber.
Examples of the polyolefin resins include low-density polyethylene, high-density polyethylene, and polypropylene.
Examples of the polyacrylic resins include ethylene glycol dimethacrylate and propylene glycol dimethacrylate.
The intermediate layer 6 contains the binder in a proportion preferably from 1 to 95% by mass, more preferably from 2 to 90% by mass. When the intermediate layer 6 contains the binder in a proportion within the range, the intermediate layer 6 has an advantage of having both of electroconductivity and bonding performance with a higher certainty.
The separator 4 is a member of blocking electric connection between the positive electrode 3 and the negative electrode 5 and simultaneously allowing the electrolyte solution 9, which will be detailed later, to pass through this member. The separator 4 is made into, for example, a band form, and is arranged between the positive electrode 3 and the negative electrode 5 to block electric connection between the positive electrode 3 and the negative electrode 5. The separator 4 is larger in width than the composite layer 3b of the positive electrode 3 to prevent the short circuit with a higher certainty. The separator 4 is larger in width than the composite layer 5b of the negative electrode 5. The thickness of the separator 4 may be from 5 to 50 μm. In the present embodiment, the separator 4 contains no electrically insulating particles.
The separator 4 includes at least a sheet type separator substrate. The separator substrate may be porous. Examples of the material of the separator substrate include synthetic resin, natural resin, glass and ceramic materials. Specifically, the separator substrate is, for example, a woven fabric or nonwoven fabric made of synthetic fiber, natural fiber, glass fiber or ceramic fiber. More specifically, the separator substrate is, for example, a polyolefin finely porous membrane or a paper piece.
The separator substrate is preferably a woven fabric or nonwoven fabric made of synthetic fiber. Examples of the material of the synthetic fiber include polyacrylonitrile (PAN), polyamide (PA), polyester, polyethylene terephthalate (PET), and polyolefins (POs) such as polypropylene (PP) and polyethylene (PE). The synthetic fiber is preferably synthetic fiber made of a non-electroconductive resin and produced by combining respective fibers of two or more of these synthetic fiber materials.
The separator 4 may have a monolayered structure made of the separator substrate. The separator 4 may have a multilayered structure having the separator substrate and one or more layers other than the separator substrate.
As illustrated in
As described above, an example of the energy storage device 1 of the present embodiment may be the nonaqueous electrolyte secondary battery 1 illustrated in
As illustrated in
Specifically, the nonaqueous electrolyte secondary battery includes the case 8, the electrolyte solution 9 held in the case 8, two external electrically insulating members 12 fitted to an outside surface of the case 8, the electrode assembly 2 held in the case 8, two current collecting units 10 connecting electrically to the electrode assembly 2, and two external terminals 11 connected electrically to the two current collecting units 10, respectively.
As illustrated in
The lid plate 8b is, for example, rectangular when viewed from one of both the surface sides thereof. The lid plate 8b is formed to close the opening in the case body 8a airtightly. The lid plate 8b has therein two openings.
The two external electrically insulating members 12 are fitted to the outside surface of the lid plate 8b. An opening is made in each of the external electrically insulating members 12. The lid plate 8b and the external electrically insulating members 12 are arranged in such a manner that one of the two openings in the lid plate 8b is continuous to the opening in one of the two external electrically insulating members 12. The other opening in the lid plate 8b and the opening in the other external electrically insulating member 12 are in the same manner. One of the external terminals 11 is partially arranged inside each of two pairs of the continuous openings. Moreover, a non-illustrated electrically insulating member is further arranged between each of the external terminals 11 and the lid plate 8b, so that the electrically insulating member insulates each of the external terminals 11 and the lid plate 8b electrically from each other.
The external terminals 11 are connected, respectively, to the two current collecting units 10 connected to the electrode assembly 2. Additionally, each of the current collecting units 10 is electrically connected to the electrode assembly 2. Specifically, the two external terminals 11 are electrically connected through the two current collecting units 10, respectively, to the electrode assembly 2. The external terminals 11 are made of, for example, aluminum, or aluminum based metallic material such as any aluminum alloy.
The external electrically insulating members 12 are ones for the positive electrode and the negative electrode; the same matter is applied to the current collecting units 10 as well as the external terminals 11. The external electrically insulating member 12, the current collecting unit 10 and the external terminal 11 for the positive electrode are each arranged at one of both the end sides in the longitudinal direction of the lid plate 8b. In the meantime, the external electrically insulating member 12, the current collecting unit 10 and the external terminal 11 for the negative electrode are each arranged at the other end side in the longitudinal direction of the lid plate 8b.
As illustrated in
As illustrated in
Usually, the electrolyte solution 9 may be a nonaqueous electrolyte solution in which an electrolyte salt is dissolved in an organic solvent. In the case 8, the composite layer 3b of the positive electrode 3, the composite layer 5b of the negative electrode 5, the insulating layer 7 and the separator 4 are impregnated with the electrolyte solution 9. As illustrated in, for example,
The organic solvent may be a nonaqueous solvent, examples of which include cyclic carbonates such as propylene carbonate, ethylene carbonate, butylene carbonate, chloroethylene carbonate and vinylene carbonate; cyclic esters such as γ-butyrolactone and γ-valerolactone; linear carbonates such as dimethyl carbonate, diethyl carbonate and ethylmethyl carbonate; linear esters such as methyl formate, methyl acetate, and methyl butyrate; tetrahydrofuran and derivatives thereof, ethers such as 1,3-dioxane, 1,4-dioxane, 1,2-dimethoxyethane, 1,4-dibutoxyethane, and methyl diglyme; nitriles such as acetonitrile and benzonitrile; dioxolane and derivatives thereof, and ethylene sulfide, sulfolane and sultone, and respective derivatives thereof. As the organic solvent, one of such compounds may be used singly, or two or more thereof may be used in the form of, for example, a mixture. However, the organic solvent is not limited to these examples.
Examples of the electrolyte salt include inorganic ions each containing at least one of lithium (Li), sodium (Na) and potassium (K), such as LiClO4, LiBF4, LiAsF6, LiPF6, LiSCN, LiBr, LiI, Li2SO4, Li2B10Cl10, NaClO4, NaI, NaSCN, NaBr, KClO4, and KSCN; and LiCF3SO3, LiN(CF3SO2)2, LiN(C2F5SO2)2, LiN(CF3SO2)(C4F9SO2), LiC(CF3SO2)3, LiC(C2F5SO2)3, (CH3)4NBF4, (CH3)4NBr, (C2H5)4NClO4, (C2H5)4NI, (C3H7)4NBr, (n-C4H9)4NClO4, (n-C4H9)4NI, (C2H5)4N-maleate, (C2H5)4N-benzoate, (C2H5)4N-phtalate, lithium stearylsulfonate, lithium octylsulfonate, lithium dodecylbenzenesulfonate, and other organic ion salts. As the electrolyte salt, one of such ionic compounds is used singly, or two or more thereof are used in a mixture form.
The electrolyte solution 9 (nonaqueous electrolyte) may further contain known additives.
Hereinafter, a method for producing the nonaqueous electrolyte secondary battery 1, as one example of the energy storage device of the present embodiment, will be described.
In the method for producing the nonaqueous electrolyte secondary battery 1, for example, a sheet type positive electrode 3, a sheet type negative electrode 5 and a separator 4 are stacked onto each other. For example, an insulating layer 7 is arranged to be put onto a single surface of any one of the positive electrode 3, the negative electrode 5 and the separator 4. The stacked body is wound up to produce an electrode assembly 2. Furthermore, the produced electrode assembly 2 and an electrolyte solution 9 are held in the case 8.
Specifically, the method for producing the nonaqueous electrolyte secondary battery 1 includes, for example, the following: producing a negative electrode 5 (step 1); producing a positive electrode 3 (step 2); forming an insulating layer 7 onto at least one surface of the negative electrode 5, the positive electrode 3, or a separator 4 (step 3); stacking the negative electrode 5, the positive electrode 3, the separator 4, and the insulating layer 7 onto each other, and then winding up the stacked body to produce an electrode assembly 2 (step 4); and holding the electrode assembly 2 and an electrolyte solution 9 into the case to fabricate the battery (step 3).
In the production of the negative electrode (step 1), for example, active material particles and a binder for the negative electrode 5 are mixed with each other, and this mixture is added to a solvent. The resultant is then kneaded to prepare a negative composite. This negative composite is applied onto a single surface of a band-form electrode substrate 5a. The application of the negative composite is attained to make the width of the applied composite larger than that of a composite layer 3b of the positive electrode 3 in the width direction of the electrode substrate 5a of the negative electrode 5. The solvent is then evaporated from the applied negative composite. As required, the resultant composite layer 5b of the negative electrode 5 is pressed. In this way, the negative electrode 5 is produced, in which the composite layer 5b is formed on the electrode substrate 5a.
In the production of the positive electrode (step 2), at least a composite layer is formed and, if necessary, an intermediate layer is further formed. Specifically, the positive electrode production (step 2) includes: applying an intermediate-layer-forming composition containing a conducting agent (carbonaceous material), a binder and a solvent onto one of the two surfaces of an electrode substrate 3a to form an intermediate layer 6 (step 21), and applying a positive composite containing a positive active material, a conducing aid, a binder and a solvent onto the applied intermediate-layer-forming composition to form a composite layer 3b of the positive electrode 3 (step 22).
In order to form the composite layer of the positive electrode, for example, the positive active material, the conducting agent, and the binder are mixed with each other, and this mixture is added to the solvent. The resultant is kneaded to prepare the positive composite. This positive composite is applied onto the electrode substrate 3a of the positive electrode 3 or the intermediate layer 6. The solvent is then evaporated from the applied positive composite. When the intermediate layer 6 is formed in the positive electrode production (step 2), the positive composite is applied onto the intermediate layer 6 to form the composite layer 3b of the positive electrode 3.
In order to form the intermediate layer, for example, the conducting agent (carbonaceous material) and the binder are mixed with each other, and this mixture is added to the solvent. The resultant is kneaded to prepare the intermediate-layer-forming composition. This intermediate-layer-forming composition is applied onto one of the two surfaces of the electrode substrate 3a of the positive electrode 3. Furthermore, the solvent is evaporated from the applied intermediate-layer-forming composition. As required, the composite layer 3b of the positive electrode 3 and the intermediate layer 6 are pressed.
In the formation of the insulating layer (step 3), for example, electrically insulating particles are mixed with a binder, and this mixture is added to a solvent. The resultant is then kneaded to prepare an insulating-layer-forming composition. This insulating-layer-forming composition is applied to, for example, the composite layer 3b of the positive electrode 3, the composite layer 5b of the negative electrode 5, or a single surface of the separator 4. The solvent is then evaporated from the applied insulating-layer-forming composition. As required, the insulating layer 7 is pressed together with the negative electrode 5 or the separator 4.
In each of the positive electrode production (step 2), the negative electrode production (step 1) and the insulating layer formation (step 3), the method for the application may be an ordinary method.
In the production of the electrode assembly (step 4), the positive electrode 3 and the negative electrode 5 are stacked onto each other in such a way that the formed composite layer 5b of the negative electrode 5 faces the formed composite layer 3b of the negative electrode 3. Additionally, the positive electrode 3 and the negative electrode 5 are stacked onto each other to locate the separator 4 and the insulating layer 7 between the positive electrode 3 and the negative electrode 5. At this time, it is preferred the insulating layer 7 is located nearer to the negative electrode 5 than the separator 4. Specifically, in order to produce the electrode assembly, the positive electrode 3, the negative electrode 5, the separator 4 and the insulating layer 7 are stacked onto each other in the state of making the respective longitudinal directions thereof consistent with each other. Specifically, the positive electrode 3 and the negative electrode 5 are arranged in such a way that the composite layer 3b of the positive electrode 3 faces the composite layer 5b of the negative electrode 5. The separator 4 is arranged between the positive electrode 3 and the negative electrode 5. The stacked positive electrode 3, negative electrode 5, separator 4 and insulating layer 7 are wound up into the longitudinal direction to produce the electrode assembly 2.
In the fabrication of the battery (step 5), a current collecting units 10 are connected to each of the positive electrode 3 and the negative electrode 5 in the produced electrode assembly 2. Next, the electrode assembly 2 and the current collecting units 10 connected to the electrode assembly 2 are arranged in the case body 8a of the case 8. When plural electrode assembles are used, for example, current collecting units 10 of the electrode assembles are electrically connected to each other in parallel and then the resultant is arranged in the case body 8a. Next, external terminals 11 in external electrically insulating members 12 fitted to a lid plate 8b are connected to the current collecting units 10 by fastening rivets or welding. Thereafter, the lid plate 8b is connected to the case body 8a.
Subsequently, in order to fabricate the battery, the electrolyte solution 9 is filled into the case 8 through solution-filling holes in the case 8. The solution-filling holes are sealed. The electrolyte solution 9 may be a solution prepared by blending LiPF6 into a mixed solvent of ethylene carbonate (EC), dimethyl carbonate (DMC) and ethylmethyl carbonate (EMC) (the ratio by volume of EC/DMC/EMC=3/2/5). Furthermore, known additives may be added to the electrolyte solution 9.
Through this process, the nonaqueous electrolyte secondary battery 1 can be produced.
In the embodiment, the nonaqueous electrolyte secondary battery 1 as an energy storage device is described as an example. However, the energy storage device is not limited to the nonaqueous electrolyte secondary battery 1, and may be, for example, a capacitor. The energy storage device is preferably a nonaqueous electrolyte secondary battery, more preferably a lithium ion secondary battery. The energy storage device may be a capacitor, and may be specifically a lithium ion capacitor or ultra-capacitor.
The energy storage device of the present embodiment is as demonstrated above. However, the present invention is not limited to the demonstrated energy storage device. In other words, various forms equivalent to forms usable for ordinary energy storage devices may be used as far as the forms do not damage the advantageous effects of the invention.
The present invention will be described in more detail by way of working examples thereof. However, the invention is not limited to these examples.
In each of the working examples and the comparative examples, a lithium ion secondary battery was produced as described below. Tables 1 to 3 described below show the average primary particle diameter D90 of active material particles in a negative electrode in each of the examples and the comparative examples, the average primary particle diameter D90 of electrically insulating particles therein, the pore peak diameter in a composite layer of the negative electrode therein, the pore peak diameter in an insulating layer therein, and others.
[Production of Positive Electrode]
Active material: LiNi1/3Mn1/3CO1/3O2, or LiFePo4 particles
Conducting agent: acetylene black
Binder: polyvinylidene fluoride (PVDF)
Blend ratio (by mass): active material/acetylene black/PVDF=90/5/5
Electrode substrate of a positive electrode: aluminum film (thickness: 20 μm)
The active material, the conducting agent, the binder, and an organic solvent (NMP) were mixed with each other to prepare a positive composite. A predetermined amount of the positive composite (the mass per area of this composite after the composite was dried: 0.01 g/cm2) was applied onto the aluminum film, and the resultant was dried to volatilize the organic solvent. In this way, a composite layer of the positive electrode was produced. Furthermore, the composite layer of the positive electrode and the aluminum film were pressed to produce the positive electrode.
[Production of Negative Electrode]
Active material: non-graphitizable carbon (hard carbon: HC) particles, artificial graphite, or spherical natural graphite
Binder: styrene-butadiene rubber (SBR), and
Blend ratio (by mass): active material/SBR/CMC=96/2.5/1.5
Electrode substrate of the negative electrode: copper film (thickness: 10 μm)
The active material, the binder, and an organic solvent (NMP) were mixed with each other, and the mixture was kneaded. A predetermined amount of the kneaded product (the mass per area of this product after the product was dried: 0.05 g/cm2) was applied onto a copper film, and the resultant was dried to volatilize the organic solvent. The resultant was further pressed to produce the negative electrode. After the pressing, this electrode had a porosity of 38%.
[Formation of Insulating Layer]
Inorganic particles (alumina particles), a binder (PVDF), a surfactant, and an organic solvent (NMP) were mixed with each other to prepare a slurry-form insulating-layer-forming composition.
The ratio by mass of the alumina particles to the binder was as follows: alumina particles/binder=97/3.
The insulating-layer-forming composition was applied onto the composite layer of the negative electrode, or onto (only a single surface of) a separator by a gravure printing method. After the application, the workpiece was dried. In this way, the insulating layer was produced, which in principle had a thickness of 5 μm.
In order to adjust the wettability of the outer surface of the composite layer of the negative electrode before the application of the insulating-layer-forming composition, the composite layer outer surface of the negative electrode was appropriately subjected to surface modifying treatment.
[Separator]
As the separator (separator substrate), the following was prepared: a polyolefin finely porous film having a Gurley air permeability of 280 s/100 cc and a thickness of 20 μm (trade name: “HIPORE ND420”, manufactured by Asahi Kasei Corp.).
[Production of Electrode Assembly]
The positive electrode, the negative electrode, the separator and the insulating layer were staked onto each other to arrange, between the composite layer of the negative electrode and the separator, the insulating layer on one of the two surface sides of the composite layer of the negative electrode or on one of the two surface sides of the separator. The stacked body was wound up to produce an electrode assembly.
[Fabrication of Battery]
LiPF6 was dissolved into a mixed solvent of propylene carbonate (PC), dimethyl carbonate (DMC) and ethylmethyl carbonate (EMC) (ratio by volume of PC/DMC/EMC=3/2/5) to give a concentration of 1 mol/L to prepare an electrolyte solution. Any additive was able to be further added to this electrolyte solution; however, no additive was added to this electrolyte solution. Thereafter, the electrode assembly and the electrolyte solution were enclosed in a rectangular case.
About each of the batteries produced once, the following were measured as described below: the average primary particle diameter D90 of active material particles in the negative electrode, the average primary particle diameter D90 of the electrically insulating particles, the pore peak diameter in the composite layer of the negative electrode, the pore peak diameter in the insulating layer, the thickness of the insulating layer, and others. The measured value of the thickness was the average of measured values obtained by measuring five points of the layer.
In order to measure the physical properties of the battery produced in each of the examples and the comparative examples, the battery was disassembled in the state of being discharged (2 V). The negative electrode and the insulating layer were taken out therefrom, sufficiently washed with dimethyl carbonate (DMC), and then subjected to vacuum drying at 25° C. All of the physical property measurements described below were conducted using samples of the negative electrode and samples of the insulating layer after the washing and drying.
<Average Primary Particle Diameter D90 of the Active Material Particles of the Negative Electrode>
A cross section of the negative electrode obtained by cutting the electrode in the thickness direction was processed using a cross section polisher (CP), and the processed cross section was observed through an SEM.
A measurement was conducted about the diameter of each of at least 500 active material particles picked up at random from particles observed in the SEM observed image. In the measurement of the diameter, the diameter of a minimum circumscribing circle of the particle was regarded as the diameter of the particles. In this way, the particle was regarded as a spherical particle. From particles smaller in particle diameter, out of the entire particles, the spherical volumes thereof were then cumulated to gain the cumulative volume. The particle diameter when the cumulative volume exceeded 90% was defined as the average primary particle diameter D90.
<Average Primary Particle Diameter D90 of the Electrically Insulating Particles>
The average primary particle diameter D90 of the electrically insulating particles contained in the insulating layer was also obtained in the same way as described above.
<Pore Peak Diameter Measurements>
The pore peak diameter in the composite layer of the negative electrode and that in the insulating layer were each obtained by measuring the pore distribution of the composite layer of the negative electrode and that of the insulating layer by a mercury intrusion method. A measuring device used was a device, in WIN 9400 series, manufactured by Micrometritics Instrument Corp. The measurement was according to JIS R1655.
Specifically, each of the pore peak diameters was obtained as follows:
1) The washed and dried negative electrode was used as it was, and the mercury intrusion porosity thereof was measured to obtain pore peak diameters X and Y in the pore distribution of the composite layer (when the negative electrode had only one peak, the diameters X and Y were regarded to be equal to each other).
2) The insulating layer was peeled off by polishing peeling with a tape, a cutter or some other. After the peeling, the mercury intrusion porosity of the sample was measured to obtain the pore peak diameter Z in the pore distribution of the insulating layer.
3) The pore diameter Z was defined as the pore peak diameter in the composite layer. Out of the natural logarithm of the pore peak diameter X and that of the pore peak diameter Y, a natural logarithm that is farther from the natural logarithm of Z was defined as the pore peak diameter. When X was equal to Y, Z was defined as the pore peak diameter in the insulating layer.
The pore peak diameter in the distribution of pores is obtained as follows: the diameter (μm) of the pores is represented by U, and the cumulative pore volume (mL/g) is represented by V; at this time, the differential value of a change in the cumulative pore volume to a change in the pore diameter (dV/d log U) is calculated out; a graph is drawn in which X axis represents log U, and Y axis represents dV/d log U; and at this time, the value of U that is a maximum value is defined as the pore peak diameter.
<Half Band Width of the Pore Peak Diameter in Each of the Pore Distributions>
At the pore peak diameter, the value of the half of dV/d log U was used as a y intercept to draw a line parallel in the X axis. At this time, out of the respective diameters of two points crossing the pore distribution, a smaller diameter and a larger diameter were represented by Dmin and Dmax, respectively. At this time, the value of “log(Dmax)−log(Dmin)” was defined as the half band width of the peak.
<Evaluation of Battery Performances>
About the battery of each of examples and comparative examples, battery performances were evaluated as described below. The result of each of the evaluations is represented as the average value of plural (n=3) results.
[Test for Checking Battery Capacity]
A test for checking the battery capacity was conducted in a thermostat of 25° C. Specifically, the test was as follows:
1) At a lower limit voltage of 2.4 V, a 4-ampere constant current discharge test was conducted.
2) At an upper limit voltage of 4.1 V, the battery was subjected to 4-ampere constant current and constant voltage charge for 3 hours. Thereafter, at a lower limit voltage of 2.4 V, the battery was subjected to 4-ampere constant current discharge in a discharge test.
3) The current capacity at the discharge item in the item 2) was defined as the battery capacity.
[Power Test at 25° C.]
The battery was adjusted to an SOC of 50%. Specifically, the value 1 C(A) of the battery was decided according to the capacity checking test just before the present test. The battery was then adjusted to an SOC of 50%, from the discharged state by charging at 25° C. and 0.5 C(A) for 1 hour.
The value 1 C(A) means a current value capable of attaining an electricity amount of Q1 (Ah) in an current application period of 1 hour when Q1 (Ah) is electricity amount discharged in the 4-ampere discharge test (the upper limit: 4.1 V; and the upper limit: 2.1 V) at 25° C. just before the present test. After the adjustment, a current application test was conducted under the following conditions:
Current application period: 10 seconds
Temperature: 25° C.
Current: 40 C in the discharge direction
The resistance value, the power value and the power density of the battery were calculated in accordance with the following calculating expressions:
Resistance D1: (difference between 1-second voltage at discharge and voltage before current application)/current
Power W1: (“voltage before current application”−“lower limit voltage”)/D1*(lower limit voltage)
Resistance D2: (difference between 10-second voltage at discharge and voltage before current application)/current
Power W2: (“voltage before current application”−“lower limit voltage”)/D2*(lower limit voltage)
Weight power density: W1/(battery weight)
Voltage power density: W1/(battery volume)
After the current application test, the battery was again adjusted to an SOC of 50% by charging a quantity corresponding to the electric quantity discharged when the power of the battery was measured, at a current value of 6 A.
[Power Temporary Deterioration Test]
The resistance of the battery before the cycles was gained in the same way as in the above-mentioned power test at 25° C. The battery was subjected to continuous 1000 cycles each including continuous discharge for 30 seconds and continuous charge for 30 seconds within 2 minutes at a current of 10 C in the state of the SOC of 50%. Within 2 hours of the end of the cycles, the battery was subjected to the same power test as described above, so that the resistance value D3 at the 10-second discharge was calculated out. The temporary deterioration ratio R3 was calculated according to D3/D2.
In Tables 1 to 3 are shown details of the batteries of the examples and the comparative examples, and evaluated results of the temporary deterioration ratio of the batteries. In Tables 1 to 3, A to I each represent a value described below. The result of the temporary deterioration of Example 1 is regarded as 100, and the value of the temporary deterioration ratio of each of the other examples is relative to the value 100 of Example 1. The value is smaller, the temporary deterioration is further suppressed.
A: the pore peak diameter (μm) in the composite layer of the negative electrode
B: the pore peak diameter (μm) in the insulating layer
C: the average primary particle diameter D90 (μm) of the active material particles in the negative electrode
D: the average primary particle diameter D90 (μm) of the electrically insulating particles
E: the value relative (to the value of Example 1) of the mass of the applied positive composite
F: the value relative (to the value of Example 1) of the mass of the applied negative composite
G: the value relative (to the value of Example 1) of the thickness of the insulating layer
H: the value of “Log B−Log A”
I: the half band width of the pore peak diameter in the insulating layer
The results of the temporary deterioration ratio of the examples and the comparative examples are shown as a graph in
The reason why temporary deterioration is suppressed when the relational expression (1) is satisfied by the pore peak diameter A in the pore distribution of a composite layer of the negative electrode and the pore peak diameter B in the pore distribution of the insulating layer is not completely clarified. However, a reason would be assumed that the ion conductivity of the insulating layer is made even in the plane direction thereof, whereby the ununiformed reaction thereof in the electrode plane direction can be suppressed, and, as a result, temporary deterioration of the battery can be suppressed.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2015-035172 | Feb 2015 | JP | national |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20040033421 | Shibuya | Feb 2004 | A1 |
| 20060188785 | Inoue | Aug 2006 | A1 |
| 20060199294 | Nishino | Sep 2006 | A1 |
| 20070202404 | Suzuki | Aug 2007 | A1 |
| 20080166637 | Inagaki | Jul 2008 | A1 |
| 20090253033 | Hirose | Oct 2009 | A1 |
| 20090325074 | Hayashi | Dec 2009 | A1 |
| 20110159370 | Sakurai | Jun 2011 | A1 |
| 20120251878 | Ueki | Oct 2012 | A1 |
| 20140154557 | Kako | Jun 2014 | A1 |
| 20140295263 | Abe | Oct 2014 | A1 |
| Number | Date | Country |
|---|---|---|
| 2654107 | Oct 2013 | EP |
| 10241656 | Sep 1998 | JP |
| 3765396 | Apr 2006 | JP |
| 2008186803 | Aug 2008 | JP |
| 2009252580 | Oct 2009 | JP |
| 4476254 | Jun 2010 | JP |
| 2010192365 | Sep 2010 | JP |
| 2010244818 | Oct 2010 | JP |
| 4667242 | Apr 2011 | JP |
| 4763253 | Aug 2011 | JP |
| 4847861 | Dec 2011 | JP |
| 2011249207 | Dec 2011 | JP |
| 2012064544 | Mar 2012 | JP |
| 5055865 | Oct 2012 | JP |
| 5112853 | Jan 2013 | JP |
| 5164413 | Mar 2013 | JP |
| 2014063753 | Apr 2014 | JP |
| 2014089887 | May 2014 | JP |
| 2014132563 | Jul 2014 | JP |
| 2014191912 | Oct 2014 | JP |
| 2010050507 | May 2010 | WO |
| 2011036797 | Mar 2011 | WO |
| 2013073011 | May 2013 | WO |
| Entry |
|---|
| Extended European Search Report dated Jun. 13, 2016 issued in the corresponding European patent application No. 16157176.5. |
| Number | Date | Country | |
|---|---|---|---|
| 20160248065 A1 | Aug 2016 | US |
