Patent Application
20110195320
The present invention relates to an air secondary battery that can inhibit deterioration in charge-discharge properties caused by oxygen generated in an air cathode layer during charge.
An air secondary battery that uses a nonaqueous liquid electrolyte is a secondary battery that uses air (oxygen) as a cathode active material and has advantages in that an energy density is high and miniaturization and weight saving are readily achieved. Accordingly, an air secondary battery is gathering attention as a high capacity secondary battery superior to a lithium secondary battery that is at present in wide use.
Such an air secondary battery comprises, for example, an air cathode layer that has a conductive material (such as carbon black), a catalyst (such as manganese dioxide) and a binder (such as polyvinylidene fluoride); an air cathode current collector that collects a current of the air cathode layer; an anode layer that has an anode active material (such as metal Li); an anode current collector that collects a current of the anode layer; and a non-aqueous liquid electrolyte that bears conduction of metal ions (such as lithium ions).
An air secondary battery that makes use of oxygen in air as a supply source of oxygen used during discharge has been known. Such an air secondary battery usually has an opening in an exterior body (battery case), supplies oxygen from the opening during discharge, and exhausts oxygen from the opening during charge. On the other hand, an air secondary battery using a hermetically sealed exterior body that does not have an opening has been known. For example, in Patent Document 1, an air secondary battery that has an exterior body, inside of which a gas containing pressurized oxygen is encapsulated, has been disclosed. The technology, by use of a hermetically sealed exterior body, inhibits moisture in air from penetrating inside of a battery and thereby improves cycle characteristics of the battery. Furthermore, in the technology, a gas containing pressurized oxygen is encapsulated inside of an exterior body and thereby discharge properties are improved.
Patent Document 1: Japanese Patent Application Laid-Open (JP-A) No. 2001-273935
In a conventional air secondary battery, there is a problem in that when the charge-discharge is repeated, the charge-discharge properties (such as discharged capacitance maintenance) are deteriorated. The reason why for this is variously considered. As one of factors, it is considered that oxygen generated in an air cathode layer during charge causes the deterioration. The present invention was achieved considering the above-mentioned situations and mainly intends to provide an air secondary battery that can inhibit deterioration in the charge-discharge properties caused by oxygen generated in an air cathode layer during charge.
In order to solve the problem, the present inventors studied hard and came to a consideration that the reason why the charge-discharge properties are deteriorated exists in that bubbles of oxygen generated in an air cathode layer during charge stay in an interface between an air cathode layer and an electrolyte layer and thereby disturb ionic conduction in the interface. In this connection, the inventors lowered a pressure inside of an exterior body and found that oxygen generated in an air cathode layer during charge is readily diffused and thereby the charge-discharge properties are inhibited from deteriorating. The present invention is completed based on such findings.
That is, the invention provides an air secondary battery, comprising: a power generating element constituted of an air cathode layer containing a conductive material, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer; and an exterior body that houses the power generating element, wherein the exterior body is hermetically sealed with an oxygen-containing gas encapsulated therein; and at a charge start time, a pressure inside of the exterior body is lower than an atmospheric pressure.
According to the invention, since, at the charge start time, the inside of an exterior body is depressurized, oxygen generated in the air cathode layer during charge is prone to diffuse. Accordingly, bubbles of oxygen are inhibited from staying in an interface between the air cathode layer and the electrolyte layer and thereby it is possible to inhibit the ionic conduction in an interface from being disturbed. As the result, an air secondary battery in which the charge-discharge properties are inhibited from deteriorating can be obtained.
In the invention, at the charge start time, the power generating element is preferably in a state where SOC is 50% or less. This is because charge can be efficiently carried out.
In the invention, a pressure inside of the exterior body is preferably 0.9 atm or less. This is because, as long as the pressure is in the range, oxygen generated in the air cathode layer can be efficiently diffused.
Furthermore, the invention provide a method for producing an air secondary battery, comprising the steps of: hermetically sealing an exterior body in which a power generating element constituted of an air cathode layer containing a conductive material, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer is housed with an oxygen-containing gas encapsulated therein; discharging the power generating element; and depressurizing a pressure inside of the exterior body lower than an atmospheric pressure after the hermetically sealing step.
According to the invention, by performing a discharge step and a depressurizing step, an air secondary battery in which a power generating element is in a discharged state and the inside of an exterior body is in a depressurized state can be obtained. Thereby, oxygen generated in an air cathode layer during charge can be readily diffused. Accordingly, bubbles of oxygen can be inhibited from staying in an interface of an air cathode layer and an electrolyte layer and thereby it is possible to inhibit ionic conduction in an interface from being disturbed. As a result, an air secondary battery in which charge-discharge properties are inhibited from deteriorating can be obtained.
In the invention, during the discharging step, the power generating element is preferably discharged to a state where SOC is 50% or less. This is because as long as the SOC is in the above-mentioned range, time-lapse deterioration during initial storage can be efficiently inhibited.
In the invention, during the depressurizing step, a pressure inside of the exterior body is preferably depressurized to a pressure of 0.9 atm or less. This is because, as long as the pressure is in the range, oxygen generated in the air cathode layer can be efficiently diffused.
Furthermore, the invention provides a method for producing an air secondary battery, comprising the step of: hermetically sealing an exterior body in which a power generating element constituted of an air cathode layer containing a conductive material and a metal oxide that is a discharge product, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer is housed with an oxygen-containing gas encapsulated therein; and depressurizing a pressure inside of the exterior body lower than an atmospheric pressure after the hermetically sealing step.
According to the invention, by using an air cathode layer containing a metal oxide that is a discharge product, an air secondary battery in which a power generating element is in a discharged state and the inside of an exterior body is in a depressurized state can be obtained more conveniently.
In the invention, during the depressurizing step, a pressure inside of the exterior body is preferably depressurized to a pressure of 0.9 atm or less. This is because, as long as the pressure is in the range, oxygen generated in the air cathode layer can be efficiently diffused.
The present invention has an effect that it is possible to inhibit deterioration in the charge-discharge properties caused by oxygen generated in an air cathode layer during charge.
In what follows, an air secondary battery of the invention and a method for producing the same will be described.
A. Air Secondary Battery
In the beginning, an air secondary battery of the invention will be described. An air secondary battery of the invention comprises a power generating element constituted of an air cathode layer containing a conductive material, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer; and an exterior body that houses the power generating element, wherein the exterior body is hermetically sealed with an oxygen-containing gas encapsulated therein, and at a charge start time, a pressure inside of the exterior body is lower than atmospheric pressure.
According to the invention, at the charge start time, the inside of the exterior body is depressurized; as a result, oxygen generated in an air cathode layer during charge is easy to diffuse. Accordingly, bubbles of oxygen can be inhibited from staying in an interface of the air cathode layer and the electrolyte layer and thereby it is possible to inhibit ionic conduction in an interface from being disturbed. Thereby, an air secondary battery in which charge-discharge properties are inhibited from deteriorating can be obtained. Furthermore, in an air secondary battery of the invention, since the inside of the exterior body is depressurized at the charge start time, there is no need of connecting another device such as a vacuum pump. As a result, miniaturization of the air secondary battery and an improvement in energy efficiency accompanying the miniaturization can be attained. From these viewpoints, the exterior body is preferable not to have a gas flow portion (such as gas inlet and gas outlet described below) that flows a gas between the inside and the outside of the exterior body.
Here, an air secondary battery assembled under atmospheric pressure is shown in
In what follows, an air secondary battery of the invention will be described by dividing into members of the air secondary battery and a configuration of the air secondary battery.
1. Members of Air Secondary Battery
An air secondary battery of the invention comprises: a power generating element constituted of an air cathode layer containing a conductive material, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer; and an exterior body that houses the power generating element. Furthermore, an oxygen-containing gas is encapsulated inside of the exterior body.
(1) Power Generating Element
A power generating element in the invention contains at least an air cathode layer, an anode layer, and an electrolyte layer, and, as required, may contain an air cathode current collector and an anode current collector. In the invention, a member having an air cathode layer and an air cathode current collector is called an air cathode and a member having an anode layer and an anode current collector is called an anode.
(i) Air Cathode Layer
An air cathode layer used in the invention contains at least a conductive material. As required, the air cathode layer may further contain at least one of a catalyst and a binder.
A conductive material used in the air cathode layer is not particularly restricted as long as it has conductivity. For example, a carbon material can be cited. This is because the carbon material is excellent in conductivity and corrosion resistance. Examples of the carbon material include graphite, acetylene black, carbon nanotube, carbon fiber, and mesoporous carbon. Content of the conductive material in the air cathode layer is preferably in the range of, for example, 10% by weight to 99% by weight.
Furthermore, the air cathode layer used in the invention may contain a catalyst that accelerates a reaction. This is because an electrode reaction is more smoothly carried out. In particular, it is preferable that a conductive material supports a catalyst. Examples of the catalyst include manganese dioxide (MnO2) and cobalt phthalocyanine. Content of the catalyst in the air cathode layer is in the range of, for example, 1% by weight to 30% by weight and preferably in the range of 5% by weight to 20% by weight.
The air cathode layer used in the invention may contain a binder that fixes the conductive material. Examples of the binder include fluorine-containing binders such as polyvinylidene fluoride (PVDF) and polytetrafluoroethylene (PTFE). Content of the binder in the air cathode layer is, for example, 40% by weight or less and preferably in the range of 1% by weight to 10% by weight.
A thickness of the air cathode layer is, though different depending on applications or the like of the air secondary battery, for example, in the range of 2 μm to 500 μm and preferably in the range of 5 μm to 300 μm.
The air cathode current collector used in the invention collects a current of the air cathode layer. Examples of a material of the air cathode current collector include a metal material and a carbon material, and the carbon material is preferred. This is because the carbon material is excellent in corrosion resistance. As a carbon material like this, for example, carbon fibers are preferred. This is because electrons can flow through fibers and thereby electroconductivity is high. Examples of the air cathode current collector that uses carbon fiber include carbon cloth and carbon paper. On the other hand, examples of metal material include stainless, nickel, aluminum, iron and titanium. Examples of the air cathode current collector that uses a metal material include a metal mesh.
A configuration of an air cathode current collector used in the invention is not particularly restricted as long as it can secure desired electron conductivity. The configuration thereof may be either a porous configuration having gas diffusivity or a dense configuration that does not have gas diffusivity. Above all, in the invention, it is preferable that the air current collector has a porous configuration having gas diffusivity. This is because oxygen can be rapidly diffused. The porosity of the porous configuration is not particularly restricted. However, the porosity is preferably in the range of, for example, 20% to 99%.
A thickness of the air cathode current collector is in the range of, for example, 10 μm to 1000 μm and preferably in the range of 20 μm to 400 μm.
A method for forming an air cathode is not particularly restricted as long as it can form the above-mentioned air cathode. As an example of a method for forming an air cathode, a method where firstly an air cathode layer forming composition containing a conductive material, a catalyst, a binder, and a solvent is prepared, then, the composition is coated on an air cathode current collector and dried can be cited. Examples of the solvent include acetone, N-methyl-2-pyrolidone (NMP), N,N-dimethylacetamide (DMA), N,N-dimethylformamide (DMF), methyl ethyl ketone (MEK), and tetrahydrofuran (THF).
(ii) Anode Layer
In the next place, an anode layer used in the invention will be described. An anode layer used in the invention contains at least an anode active material. The anode active material is not particularly restricted as long as it can store and release metal ions. Examples of the anode active material include metal alone, alloys, metal oxides, and metal nitrides. Examples of the metal ion include an alkali metal ion such as a Li ion, a Na ion, or a K ion; an alkaline earth metal ion such as a Mg ion or a Ca ion; an amphoteric metal ion such as an Al ion. Above all, an alkali metal ion is preferable and a Li ion is particularly preferable. This is because a battery having high energy density can be obtained.
Furthermore, an anode layer used in the invention may contain either an anode active material alone or at least one of a conductive material and a binder in addition to the anode active material. For example, when an anode active material is flaky, an anode layer may contain an anode active material alone. On the other hand, when an anode active material is powdery, an anode layer can contain, for example, an anode active material, a conductive material and a binder. The conductive material and the binder are the same as that described in the “(i) Air cathode layer”; accordingly descriptions thereof are omitted here. Furthermore, a thickness of an anode layer is preferably appropriately selected in accordance with a configuration of an aimed air secondary battery.
An anode current collector used in the invention collects a current of an anode layer. A material of the anode current collector is not particularly restricted as long as it has conductivity. Examples of the material of the anode current collector include copper, stainless and nickel. Examples of a shape of the anode current collector include a flaky shape, a planar shape and a meshed (grid) shape. A thickness of the anode current collector is preferably appropriately selected in accordance with a configuration of an aimed air secondary battery.
A method for forming an anode is not particularly restricted as long as it can form the above-mentioned anode. As an example of a method for forming an anode, a method where a flaky anode active material is disposed on an anode current collector, followed by pressurizing can be cited. Furthermore, as another example of a method for forming an anode, a method where an anode layer-forming composition containing an anode active material, a binder and a solvent is prepared, then, the composition is coated on an anode current collector, followed by drying can be cited.
(iii) Electrolyte Layer
In the next place, an electrolyte layer used in the invention will be described. An electrolyte layer used in the invention is a layer that is formed between the air cathode layer and the anode layer and performs conduction of metal ions. Examples of an electrolyte that constitutes an electrolyte layer include a liquid form electrolyte (liquid electrolyte), a gel electrolyte, and a solid electrolyte. Above all, a liquid electrolyte and a gel electrolyte are preferred and a liquid electrolyte is particularly preferred. This is because high ion conductivity is obtained. Furthermore, when an electrolyte used in the invention is a liquid electrolyte or a gel electrolyte, a solvent that is used may be either a nonaqueous solvent or water. Above all, a nonaqueous solvent is preferred.
It is preferable that a kind of a nonaqueous liquid electrolyte is appropriately selected in accordance with a kind of conducting metal ions. For example, a nonaqueous liquid electrolyte of a lithium air secondary battery usually contains a lithium salt and a nonaqueous solvent. Examples of the lithium salt include an inorganic lithium salt such as LiPF6, LiBF4, LiClO4, or LiAsF6; and an organic lithium salt such as LiCF3SO3, LiN(CF3SO2)2, LiN(O2F5SO2)2 or LiC(CF3SO2)3. Examples of the nonaqueous solvent include ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), butylene carbonate, γ-butylolactone, sulfolane, acetonitrile, 1,2-dimethoxymethane, 1,3-dimethoxypropane, diethyl ether, tetrahydrofuran, 2-methyl tetrahydrofuran and mixtures thereof. The nonaqueous solvent is preferred to be a solvent high in oxygen solubility. This is because dissolved oxygen can be efficiently used in a reaction. A concentration of a lithium salt in the nonaqueous electrolyte is, for example, in the range of 0.5 mol/L to 3 mol/L. In the invention, as the nonaqueous liquid electrolyte, a liquid having low volatility such as an ionic liquid may be used.
Furthermore, a nonaqueous gel electrolyte used in the invention is usually obtained by gelling a nonaqueous liquid electrolyte by adding a polymer thereto. For example, a nonaqueous gel electrolyte of a lithium air secondary battery can be obtained by gelling the nonaqueous liquid electrolyte by adding a polymer such as polyethylene oxide (PEO), polyacrylnitrile (PAN), or polymethyl methacrylate (PMMA) thereto. In the invention, a LiTFSI(LiN(CF3SO2)2)-PEO based nonaqueous gel electrolyte is preferable.
An air secondary battery of the invention preferably has a separator between an air cathode layer and an anode layer. This is because a battery high in safety can be obtained. Examples of the separator include a porous film made of polyethylene or polypropylene; and a nonwoven fabric such as a resin nonwoven fabric or a glass fiber nonwoven fabric.
(2) Exterior Body
Then, an exterior body used in the invention will be described. An exterior body used in the invention houses the power generating element. Furthermore, the exterior body is hermetically sealed with an oxygen-containing gas encapsulated. Examples of a material of the exterior body include a metal such as iron, nickel, stainless, or aluminum; glass; and a polymer material. It is usually necessary for the exterior body to have a structure stable to pressure variation. In the invention in particular, the inside of the exterior body is depressurized; accordingly, the exterior body preferably has a structure stable to depressurization. A thickness of the exterior body is preferable to be, for example, 0.05 mm or more. A shape of the exterior body is not particularly restricted. Examples of the shape of the exterior body include a coin shape, a plain plate shape, a cylindrical shape, and a rectangular shape. Furthermore, an internal volume of the exterior body is preferably appropriately selected by considering factors such as a magnitude of a power generating element and an oxygen concentration in a depressurized state.
(3) Oxygen-Containing Gas
In the next place, an oxygen-containing gas used in the invention will be described. In the invention, an oxygen-containing gas is encapsulated inside of the exterior body. The oxygen-containing gas used in the invention is not particularly restricted as long as it is a gas containing at least oxygen. As a component other than oxygen gas, at least one kind selected from a group consisting of, for example, nitrogen, hydrogen, methane, and ethylene can be cited. Above all, the oxygen-containing gas in the invention is preferable to be high in oxygen concentration and particularly preferable to be a pure oxygen gas. This is because a discharge reaction can be efficiently carried out. In the invention, air may be used as an oxygen-containing gas. Furthermore, in the case where, for example, a nonaqueous air secondary battery is formed, content of moisture contained in the oxygen-containing gas is preferable to be as small as possible. This is because a nonaqueous liquid electrolyte can be inhibited from deteriorating. A moisture content contained in the oxygen-containing gas is preferable to be, for example, 1000 ppm or less and more preferable to be 500 ppm or less.
2. Configuration of Air Secondary Battery
Then, a configuration of an air secondary battery of the invention will be described. The air secondary battery of the invention is hermetically sealed with an oxygen-containing gas encapsulated in an exterior body and a pressure inside of the exterior body is lower than atmospheric pressure at the charge start time.
In the invention, at the charge start time, a power generating element is preferably in a state where SOC is 50% or less, more preferably in a state where the SOC is 20% or less, and particularly preferably in a state where the SOC is 5% or less. On the other hand, in the invention, at the charge start time, the power generating element is preferably in a state where the SOC is 0% or more. Furthermore, in the invention, at the charge start time in the first charge, the SOC of the power generating element is preferably in the above-mentioned range.
In the invention, at the charge start time, a pressure inside of the exterior body is lower than atmospheric pressure. Above all, in the invention, a pressure inside of the exterior body is preferable to be 0.9 atm or less and more preferable to be 0.5 atm or less. This is because when the pressure is in the range, oxygen generated in an air cathode layer can be efficiently diffused. On the other hand, in the invention, the pressure inside of the exterior body is preferable to be 0.01 atm or more. This is because when the pressure inside of the exterior body is excessively reduced, an oxygen concentration becomes relatively low and thereby sufficient discharge property may not be exerted.
Furthermore, a kind of an air secondary battery of the invention varies depending on a kind of a metal ion that is a conductive ion. Examples of the metal ion include an alkali metal ion such as a Li ion, a Na ion, or a K ion; an alkaline earth metal ion such as a Mg ion or a Ca ion; and an amphoteric metal ion such as an Al ion, among these, an alkali metal ion being preferable and a Li ion being particularly preferable. This is because a battery high in energy density can be obtained. Examples of application of the air secondary battery of the invention include an in-car battery, a stationary power supply battery, and a home power supply battery.
B. Method for Producing Air Secondary Battery
In the next place, methods of the invention for producing an air secondary battery will be described. The methods of the invention for producing an air secondary battery can be roughly divided into two embodiments. In what follows, descriptions for every embodiment will be given.
A first embodiment of a method of the invention for producing an air secondary battery comprises the steps of: hermetically sealing an exterior body in which a power generating element that is constituted of an air cathode layer containing a conductive material, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer is housed with an oxygen-containing gas encapsulated therein; discharging the power generating element; and depressurizing a pressure inside of the exterior body to a pressure lower than the atmospheric pressure after the hermetically sealing step.
According to the first embodiment, when a discharging step and a depressurizing step are performed, an air secondary battery where a power generating element is discharged and the inside of an exterior body is depressurized can be obtained. Thereby, oxygen generated in an air cathode layer during charge can be easily diffused. Accordingly, bubbles of oxygen can be inhibited from staying in an interface of an air cathode layer and an electrolyte layer and thereby it is possible to inhibit ionic conduction in an interface from being disturbed. As a result, an air secondary battery in which charge-discharge properties are inhibited from deteriorating can be obtained. Furthermore, in the air secondary battery obtained according to the first embodiment, the inside of the exterior body is depressurized at the charge start time; accordingly, there is no need of connecting another device such as a vacuum pump. As a result, miniaturization of the air secondary battery and an improvement in energy efficiency accompanying the miniaturization can be attained. Furthermore, according to the first embodiment, an air secondary battery in which a power generating element is in a discharged state can be obtained. Accordingly, a metal ion (such as Li ion) that is a conducting ion is rendered a chemically stable metal oxide (such as Li2O, or Li2O2) in an air cathode layer. As a result, there is an advantage that time-lapse deterioration during initial storage can be efficiently suppressed.
In what follows, a first embodiment in a method of the invention for producing an air secondary battery will be described step by step.
(1) Hermetically Sealing Step
Firstly, a hermetically sealing step in the first embodiment will be described. A hermetically sealing step in the first embodiment is a step for hermetically sealing an exterior body in which a power generating element that is constituted of an air cathode layer containing a conductive material, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer is housed with an oxygen-containing gas encapsulated therein.
A method for forming the power generating element in the first embodiment is not particularly restricted as long as it can form the predetermined power generating element. For example, when an electrolyte contained in an electrolyte layer of the power generating element is a liquid form electrolyte or a gel electrolyte, usually, a power generating element is formed inside of an exterior body. In the
Furthermore, an atmosphere when a power generating element is formed is preferably appropriately selected depending on factors such as kinds of constituent members of the power generating element. For example, when an anode layer and an electrolyte used tend to react with atmospheric components, it is preferable to form a power generating element in an inert gas atmosphere. Examples of the inert gas include nitrogen and argon. On the other hand, when an anode layer and an electrolyte used are difficult to react with atmospheric components, a power generating element can be formed in the atmosphere.
In the first embodiment, a method for hermetically sealing an exterior body in which a power generating element is housed with an oxygen-containing gas encapsulated in the exterior body is preferably appropriately selected depending on factors such as kinds of constituent members of the power generating element. For example, when an anode layer and an electrolyte used are prone to react with atmospheric components, as is shown in the
(2) Discharging Step
In the next place, a discharging step in the first embodiment will be described. A discharging step in the first embodiment is a step for discharging the power generating element.
In the first embodiment, the power generating element is discharged preferably to a state where the SOC is 50% or less, more preferably to a state where the SOC is 20% or less, and particularly preferably to a state where the SOC is 5% or less. On the other hand, in the first embodiment, it is preferable to discharge the power generating element to a state where the SOC is 0% or more. This is because when the SOC of the power generating element is within the range, the time-lapse deterioration during an initial storage time can be efficiently suppressed.
Discharge conditions in the discharging step are not particularly restricted as long as a desired discharge can be performed. A constant current discharge in the range of, for example, 0.01 mA/cm2 to 1 mA/cm2 can be cited.
Furthermore, the discharging step in the first embodiment can be applied at an arbitrary timing. That is, the discharging step may be applied before the hermetically sealing step, may be applied between the hermetically sealing step and the depressurizing step, or may be applied after the depressurizing step. Among these, in the first embodiment, the discharging step is preferably applied before the depressurizing step. This is because with an oxygen concentration maintained high, the discharging step can be efficiently performed.
(3) Depressurizing Step
In the next place, a depressurizing step in the first embodiment will be described. A depressurizing step in the first embodiment is a step for reducing a pressure inside of the exterior body to a pressure lower than atmospheric pressure after the hermetically sealing step.
A pressure inside of the exterior body after depressurization is not particularly restricted as long as it is a pressure lower than the atmospheric pressure. However, the pressure is preferably 0.9 atm or less and more preferably 0.5 atm or less. This is because when the pressure is within the range, oxygen generated in an air cathode layer can be efficiently diffused. On the other hand, in the first embodiment, a pressure inside of the exterior body after depressurization is preferable to be 0.01 atm or more. This is because when the inside of the exterior body is excessively depressurized, an oxygen concentration becomes relatively low and thereby discharge properties may not be sufficiently exerted.
As a method for depressurizing the inside of the exterior body, a method where, for example, a vacuum (depressurizing) pump is used can be cited. As is shown in, for example, the
In the next place, a second embodiment in a method of the invention for producing an air secondary battery will be described. A second embodiment in a method of the invention for producing an air secondary battery comprises the steps of: hermetically sealing an exterior body in which a power generating element that is constituted of an air cathode layer containing a conductive material and a metal oxide that is a discharge product, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer is housed with an oxygen-containing gas encapsulated therein; and depressurizing a pressure inside of the exterior body to a pressure lower than the atmospheric pressure after the hermetically sealing step.
According to the second embodiment, when an air cathode layer containing a metal oxide that is a discharge product is used, an air secondary battery where a power generating element is in a discharged state and the inside of an exterior body is in a depressurized state can be obtained more conveniently. Thereby, oxygen generated in an air cathode layer during charge can be easily diffused. Accordingly, bubbles of oxygen can be inhibited from staying in an interface of an air cathode layer and an electrolyte layer and thereby it is possible to inhibit ionic conduction in an interface from being disturbed. As a result, an air secondary battery in which charge-discharge properties are inhibited from deteriorating can be obtained. Furthermore, in the air secondary battery obtained according to the second embodiment, the inside of the exterior body is depressurized at the charge start time; accordingly, there is no need of connecting another device such as a vacuum pump. As a result, miniaturization of the air secondary battery and an improvement in energy efficiency accompanying the miniaturization can be attained. Furthermore, according to the second embodiment, an air secondary battery in which a power generating element is in a discharged state can be obtained. Accordingly, a metal ion (such as Li ion) that is a conducting ion is rendered a chemically stable metal oxide (such as Li2O or Li2O2) in an air cathode layer. As a result thereof, there is an advantage that time-lapse deterioration during initial storage can be efficiently inhibited.
(1) Hermetically Sealing Step
A hermetically sealing step in the second embodiment is a step for hermetically sealing an exterior body in which a power generating element that is constituted of an air cathode layer containing a conductive material and a metal oxide that is a discharge product, an anode layer containing an anode active material, and an electrolyte layer formed between the air cathode layer and the anode layer is housed with an oxygen-containing gas encapsulated therein.
The air cathode layer used in the second embodiment contains a conductive material and a metal oxide that is a discharge product. Usually, a metal oxide that is a discharge product is supported on a surface of the conductive material. Furthermore, a kind of the metal oxide that is a discharge product is different depending on a kind of an aimed air secondary battery. In the case of a lithium air secondary battery, the metal oxide is usually at least one of Li2O and Li2O2.
As a method for forming an air cathode layer like this, for example, a method where an air cathode layer is discharged to pre-treat can be cited. Specifically, a method where from an air cathode layer before discharge and an anode layer and an electrolyte layer for pre-treatment, a power generating element for pre-treatment is formed and the power generating element is discharged can be cited. Thus, in the second embodiment, a power generating element can be formed from an air cathode layer pretreated in advance. Discharge conditions and others in the pre-treatment are the same as that described in “(2) Discharging step” in the first embodiment. Furthermore, other issues concerning hermetically sealing step are the same as that described in “(1) Hermetically sealing step” in the first embodiment.
(2) Depressurizing Step
A depressurizing step in the second embodiment is the same as that described in “(3) Depressurizing step” in the first embodiment. Accordingly, a description thereof is omitted here.
The present invention is not restricted to the above-mentioned embodiments. The embodiments are shown only for illustration and whatever that has a substantially same configuration with a technical idea described in claims of the invention and exerts an effect the same as that described above is included in a technical range of the invention.
In what follows, the invention will be more specifically described with reference to Examples.
(Preparation of Air Cathode)
In the beginning, 1 g of Ketjen Black (manufactured by Ketjen Black International Company), 1.9 g of electrolytic manganese dioxide (manufactured by Kojundo Chemical Laboratory Co., Ltd.), and 1.5 g of PVDF polymer (manufactured by Kureha Corporation) were mixed, NMP (N-methyl pyrrolidone, manufactured by Kanto Kagaku) was added thereto, followed by stirring with a kneader under conditions of 2000 rpm for 30 min, and thereby an air cathode layer-forming composition was obtained. Thereafter, the air cathode layer-forming composition was coated on a carbon paper (air cathode current collector, trade name: TGP-H-090®, manufactured by Toray Industries, Inc., thickness: 0.28 mm) by a doctor blade method so as to have a thickness of 100 μm. In the next place, the coated carbon paper was dried at 80° C. for 1 hour and vacuum dried at 60° C. for 1 day to remove NMP. Finally, a dried coated carbon paper was punched into a φ of 18 mm and thereby an air cathode having an air cathode current collector and an air cathode layer was obtained.
(Assembly of Air Secondary Battery Element)
In the next place, an air secondary battery element with the resulted air cathode was prepared (see
(Preparation of Cell for Evaluation)
Then, an air cathode lead 23 was connected to a SUS current output portion 13, an anode lead 25 was connected to the SUS case 11c and the air secondary battery element 20 was housed in a glass container 21 having a volume of 1000 cc. Thereafter, the glass container 21 was hermetically sealed, and the hermetically sealed glass container 21 was taken out of the inside of the argon box. In the next place, oxygen was introduced from an oxygen gas bomb through a gas inlet 22, simultaneously therewith the inside of the glass container was exhausted from a gas outlet 24 and thereby the inside of the glass container was changed from an argon atmosphere to an oxygen atmosphere at atmospheric pressure. Thereafter, discharge was performed under a constant current condition of 0.01 mA/cm2. Thereby, a state where the SOC is 10% was attained. After the discharge, a vacuum pump (not shown in the drawing) was connected to the gas outlet 24 and a pressure inside of the glass container was reduced to 0.5 atm. A pressure inside of the glass container was measured by use of a commercially available manometer. Thereby, a cell for evaluation was obtained.
A cell for evaluation was obtained in a manner similar to that of Example 1 except that depressurization was not applied.
[Evaluation]
A charge-discharge test was performed with each of the cells for evaluation obtained in Example 1 and Comparative Example 1. Charge-discharge conditions are shown below. The charge-discharge was started from charge and performed in a thermostat bath at 25° C.
Here, “g-carbon” represents a weight of a conductive material.
When discharged capacitance maintenances of Example 1 and Comparative Example 1 are compared, in Comparative Example 1, it is found that the discharged capacitance maintenance was remarkably deteriorated. This is considered that, since bubbles of oxygen generated in the air cathode layer during charge stayed in an interface between the air cathode layer and an electrolyte layer, ionic conduction in the interface was disturbed. On the other hand, in Example 1, the discharged capacitance maintenance was excellent. This is considered that since the inside of the exterior body is depressurized at the charge start time, oxygen generated during charge is readily diffused, and thereby bubbles of oxygen are inhibited from staying in an interface between an air cathode layer and an electrolyte layer. Thus, it is confirmed that an air secondary battery of the invention can inhibit deterioration in the charge-discharge properties caused by oxygen generated in an air cathode layer during charge.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2009/050546 | 1/16/2009 | WO | 00 | 5/25/2010 |
