Patent Application
20140242451
This application claims priority under 35 U.S.C. §119 to Japanese Patent Application No. 2013-035779 filed on Feb. 26, 2013, the entire content of which is hereby incorporated by reference.
1. Field of the Invention
The present invention relates to nonaqueous electrolytic secondary batteries.
2. Background Art
Nonaqueous electrolytic secondary batteries are used in applications such as the power supply of electronic devices, and a power storage for absorbing the output fluctuations of a power-generating unit. For example, coin-shaped, button-shaped, and other small nonaqueous electrolytic secondary batteries are widely used in portable devices or the like (see, for example, JP-A-10-162828).
The nonaqueous electrolytic secondary battery of JP-A-10-162828 is structured to include a positive electrode, a negative electrode, and an electrolyte stored inside a storage space surrounded by a positive electrode case and a negative electrode case. The positive electrode case and the negative electrode case are electrically connected to a positive electrode and a negative electrode, respectively. A terminal or the like is optionally welded to one of or both of the positive electrode case and the negative electrode case for easier electrical connection to outside.
The characteristics of a nonaqueous electrolytic secondary battery depend on such factors as the type of the electrode active material, and the type and the concentration of the electrolyte. For example, a sufficient discharge capacity can be obtained when SiOx (0≦x<2) is used as the negative electrode active material. Further, for example, when the electrolyte is an electrolytic solution prepared by dissolving a supporting electrolyte in a nonaqueous solvent, increasing the concentration of the supporting electrolyte lowers the internal resistance, and can improve battery characteristics.
As described above, the characteristics of a nonaqueous electrolytic secondary battery can improve with the use of the SiOx-containing negative electrode active material, and an electrolyte having a high supporting electrolyte concentration. However, such a nonaqueous electrolytic secondary battery is associated with problems, such as rupture and leakage, which may occur when the negative electrode case is subjected to a heat treatment such as welding. In view of preventing such problems, it may not be always possible to increase the concentration of the supporting electrolyte as much as it is needed for characteristics improvement.
Under these circumstances, there is a need for a nonaqueous electrolytic secondary battery of improved characteristics.
According to a first aspect of the present invention, there is provided a nonaqueous electrolytic secondary battery that includes:
a positive electrode case;
a negative electrode case fixed to the positive electrode case, and that forms a storage space with the positive electrode case in between the negative electrode case and the positive electrode case;
a positive electrode portion provided on the positive electrode case in the storage space, and that contains a lithium compound as positive electrode active material;
a negative electrode portion provided on the negative electrode case in the storage space, and that contains SiOx (0≦x<2) as negative electrode active material; and
a nonaqueous electrolyte stored inside the storage space,
the negative electrode case including:
a base layer; and
a nickel layer disposed opposite the storage space with respect to the base layer, and that has a higher thermal conductivity than the base layer, and a thickness of 2.6 μm or more.
In the nonaqueous electrolytic secondary battery, the nickel layer having a higher thermal conductivity than the base layer and a thickness of 2.6 μm or more is disposed opposite the storage space with respect to the base layer, and thus suppresses transfer of heat to the storage space via the base layer. It is therefore possible to suppress thermal expansion of an object stored inside the storage space, and gas generation from the object. Problems such as rupturing of the battery can thus be suppressed. This makes it possible to increase the concentration of the supporting electrolyte in the nonaqueous electrolyte while suppressing heat problems, and realize a nonaqueous electrolytic secondary battery of excellent characteristics.
The nonaqueous electrolytic secondary battery according to the first aspect of the present invention may include a terminal attached to the negative electrode case by heat treatment outside the storage space. In this way, the nonaqueous electrolytic secondary battery can charge and discharge via the terminal, and can have improved usability.
In the nonaqueous electrolytic secondary battery according to the first aspect of the present invention, the terminal may be welded to the negative electrode case at a peel strength of 2 kgf or more against the negative electrode case. In this way, detachment of the terminal from the negative electrode case can be suppressed in the nonaqueous electrolytic secondary battery.
In the nonaqueous electrolytic secondary battery according to the first aspect of the present invention, the negative electrode case may include a clad material that has a thickness of 130 μm or more, and the base layer may be a stainless steel layer contained in the clad material. This helps maintain the strength of the negative electrode case in the nonaqueous electrolytic secondary battery.
In the nonaqueous electrolytic secondary battery according to the first aspect of the present invention, the proportion of the thickness of the nickel layer in the thickness of the clad material may be 2% or more. In this way, transfer of heat to the storage space via the base layer can be greatly suppressed in the nonaqueous electrolytic secondary battery.
In the nonaqueous electrolytic secondary battery according to the first aspect of the present invention, the thickness of the clad material may be 200 μm or less, and the thickness of the nickel layer may be 16 μm or more. In this way, transfer of heat to the storage space via the base layer can be greatly suppressed in the nonaqueous electrolytic secondary battery.
The present invention can provide a nonaqueous electrolytic secondary battery of excellent characteristics.
An embodiment of the present invention is described below.
The nonaqueous electrolytic secondary battery 1 (hereinafter, simply “battery 1”) shown in
The battery case 2 is substantially disc-like in shape, and has a pair of circular surfaces, and a cylindrical side surface. For convenience of explanation, one of the circular surfaces will be referred to as bottom surface 2a, and the other top surface 2b. The battery case 2 includes a positive electrode case 6 that includes the bottom surface 2a, a negative electrode case 7 that includes the top surface 2b, and a gasket 8.
The positive electrode case 6 and the negative electrode case 7 each have a form of a closed-end cylinder. The maximum inner diameter of the positive electrode case 6 is larger than the maximum outer diameter of the negative electrode case 7. The negative electrode case 7 is inserted into the positive electrode case 6 from the opposite side of the top surface 2b (from the opening side). The positive electrode case 6 is swaged inward at the circumference portion of its opening, preventing the negative electrode case 7 from coming off the opening of the positive electrode case 6. The negative electrode case 7 is a lid-like member for closing the opening of the positive electrode case 6. A storage space 10 is formed between the negative electrode case 7 and the positive electrode case 6.
The positive electrode case 6 has a bottom portion 6a that includes the bottom surface 2a, and a side wall portion 6c that includes an inner circumferential surface 6b (side surface). The positive electrode case 6 is conductive at at least the bottom portion 6a. The positive electrode case 6 is made of metallic material such as stainless steel, and includes the bottom portion 6a and the side wall portion 6c as an integral unit.
The negative electrode case 7 has a lid portion 7a that includes the top surface 2b, and a side wall portion 7c that includes an outer circumferential surface 7b (side surface). The negative electrode case 7 is conductive at at least the lid portion 7a. The negative electrode case 7 is structured as a laminate of a plurality of metal layers layered in thickness direction, and the metal layers have different thermal conductivities. The structure of the negative electrode case 7 will be described later in greater detail with reference to
The gasket 8 is provided between the inner circumferential surface 6b of the positive electrode case 6 and the outer circumferential surface 7b of the negative electrode case 7. The gasket 8 is a so-called sealing member, fixing the positive electrode case 6 and the negative electrode case 7 to each other, and sealing the storage space 10 airtight. The gasket 8 is made of insulating material, and prevents shorting of the positive electrode case 6 and the negative electrode case 7.
Examples of the material of the gasket 8 include polypropylene (PP), polyphenylsulfide (PPS), polyethylene terephthalate (PET), polyamide (PA), liquid crystal polymer (LCP), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer resin (PFA), polyetheretherketone resin (PEEK), polyethernitrile resin (PEN), polyetherketone resin (PEK), polyallylate resin, polybutylene terephthalate resin (PBT), polycyclohexane dimethylene terephthalate resin, polyethersulfone resin (PES), polyaminobismaleimide resin, polyetherimide resin, and fluororesin. When subjected to a heat treatment such as a reflow process, the material of the gasket 8 is selected by taking into consideration the processing temperature of the heat treatment (heat resistance in the heat treatment).
The battery element 3 is contained (sealed) inside the storage space 10 between the negative electrode case 7 and the positive electrode case 6. The battery element 3 includes a positive electrode portion 11, a negative electrode portion 12, a separator 13, and a nonaqueous electrolyte 14. The battery element 3 can accumulate charges (charging) and release charges (discharge) by allowing lithium ions to move between the positive electrode portion 11 and the negative electrode portion 12.
The positive electrode portion 11 is provided on the positive electrode case 6, inside the storage space 10 (inside the battery case 2), and is in contact with the positive electrode case 6. The terminal 4 (positive electrode-side terminal) shown in
The positive electrode portion 11 contains a lithium compound as positive electrode active material. The lithium compound is a multiple oxide containing lithium and a transition metal, for example, such as lithium titanate, and lithium manganate. The positive electrode portion 11 of the present embodiment is a lithium titanate-containing pellet (positive electrode pellet), and is press bonded to the bottom portion 6a of the positive electrode case 6.
The positive electrode pellet (positive electrode portion 11) is produced, for example, by molding a positive electrode mixture into the desired shape under pressure. The positive electrode mixture contains, for example, a granular positive electrode active material, and may contain a conductive auxiliary agent and/or a positive electrode binder. The molding pressure under pressure is decided, for example, according to such factors as the type of the conductive auxiliary agent, and may be 0.2 to 5 ton/cm2.
The proportion (content) of the positive electrode active material in the positive electrode pellet (positive electrode mixture) is decided according to such factors as the discharge capacity required of the battery 1, and may be 50 to 95 mass %, and 70 to 88 mass %. It becomes easier to maintain discharge capacity at or above these lower limits, whereas molding of the positive electrode portion 11 becomes easier at or below the foregoing upper limits.
The conductive auxiliary agent may contain one or more carbon materials such as furnace black, Ketjen black, acetylene black, and graphite. The content of the conductive auxiliary agent in the positive electrode pellet (positive electrode mixture) may be 4 to 40 mass %, and 10 to 20 mass %. It becomes easier to maintain the conductivity of the positive electrode portion 11 and mold the positive electrode portion 11 into a form of a pellet at or above these lower limits, whereas the discharge capacity of the positive electrode portion 11 can more easily be maintained at or below the foregoing upper limits.
The positive electrode binder may contain at least one selected from polymers (such as polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), styrene-butadiene rubber (SBR), and polyacrylic acid (PA)), carboxymethylcellulose (CMC), and polyvinyl alcohol (PVA).
For example, the positive electrode binder may contain polyacrylic acid, particularly crosslinked polyacrylic acid. When using polyacrylic acid, the polyacrylic acid may be brought to pH 3 to 10 in advance. The pH may be adjusted with alkali metal hydroxides such as lithium hydroxide, and alkali earth metal hydroxides such as magnesium hydroxide. The content of the positive electrode binder in the positive electrode pellet (positive electrode mixture) may be 1 to 20 mass %.
The positive electrode portion 11 may be configured to include a layer of a positive electrode mixture formed on a collector made of conductive materials such as a conductive resin adhesive (containing carbon as a conductive filler), aluminum, and copper. The collector may be a separate member from the positive electrode case 6, or may be at least a part of the positive electrode case 6. For example, the positive electrode portion 11 may be configured by layering a positive electrode mixture on the positive electrode case 6, using the surface layer of the positive electrode case 6 as a collector.
The negative electrode portion 12 is provided on the negative electrode case 7, inside the storage space 10, and is in contact with the negative electrode case 7. The terminal 5 (negative electrode-side terminal) shown in
The negative electrode portion 12 contains a SiOx (0≦x<2)-containing negative electrode active material. The negative electrode portion 12 of the present embodiment is a SiOx-containing pellet (negative electrode pellet), and is press bonded to the lid portion 7a of the negative electrode case 7.
The negative electrode pellet is produced, for example, by molding a negative electrode mixture into the desired shape under pressure. The negative electrode mixture contains, for example, a granular negative electrode active material, and may contain a conductive auxiliary agent and/or a negative electrode binder. The proportion (content) of the negative electrode active material in the negative electrode pellet (negative electrode mixture) may be, for example, 40 to 85 mass %. The content of the negative electrode active material in the negative electrode pellet is determined, for example, according to such factors as the conductivity of the negative electrode active material. When the negative electrode active material used has low conductivity, the content may be increased, for example, when the material is surface coated with carbon to increase the actual conductivity.
The conductive auxiliary agent may contain one or more carbon materials such as furnace black, Ketjen black, acetylene black, and graphite.
The negative electrode binder may contain at least one of polyvinylidene fluoride (PVDF), styrene-butadiene rubber (SBR), polyacrylic acid (PA), carboxymethylcellulose (CMC), polyimide (PI), and polyamideimide (PAI).
For example, the binder may contain polyacrylic acid, particularly crosslinked polyacrylic acid. When using polyacrylic acid, the polyacrylic acid may be brought to pH 3 to 10 in advance. The pH may be adjusted with alkali metal hydroxides such as lithium hydroxide, and alkali earth metal hydroxides such as magnesium hydroxide.
The separator 13 is provided between the positive electrode portion 11 and the negative electrode portion 12, and has the property to allow lithium ions to pass therethrough. The separator 13 may contain a glass nonwoven fabric and/or a resin nonwoven fabric. Because of the excellent mechanical strength and the large ion permeation rate, the glass nonwoven fabric can reduce internal resistance and improve discharge capacity. The thickness of the separator 13 is decided by taking into consideration such factors as the size of the battery 1, and the material of the separator 13, and is, for example, 5 to 300 μm.
The material of the glass nonwoven fabric used for the separator 13 may contain at least one of borosilicate glass, alkali glass, fused quartz, and lead glass. The material of the resin nonwoven fabric used for the separator 13 may contain at least one of polypropylene (PP), polyphenylene sulfide (PPS), polyetheretherketone (PEEK), polyethylene terephthalate (PET), polyamideimide (PAI), and polyimide (PI).
The nonaqueous electrolyte 14 of the present embodiment is an electrolytic solution prepared by dissolving a supporting electrolyte in a nonaqueous solvent. The positive electrode portion 11, the negative electrode portion 12, and the separator 13 are at least partially immersed in the nonaqueous electrolyte 14. The lithium ions responsible for the charge movement in the battery 1 move between the positive electrode portion 11 and the negative electrode portion 12 via the nonaqueous electrolyte 14.
The nonaqueous solvent used for the nonaqueous electrolyte 14 may contain at least one of carbonates (such as ethylene carbonate (EC), propylene carbonate (PC), 1,2-butylene carbonate (BC), vinylene carbonate (VC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and ethylmethyl carbonate(EMC)), γ-butyrolactone (GBL), sulfolane (SL), 1,2-dimethoxyethane (DME), 1,2-diethoxyethane (DEE), 1,2-ethoxymethoxyethane (EME), tetrahydrofuran (THF), and 1,3-dioxolan (DOL).
The supporting electrolyte used for the nonaqueous electrolyte 14 may contain an organic acid lithium salt and/or an inorganic acid lithium salt. The organic acid lithium salt may include at least one of LiCH3SO3, LiCF3SO3, LiN(CF3SO2)2, LiN(C2F5SO2)2, LiC(CF3SO2)3, LiN(CF3SO3)2, and LiN(FSO2)2. The inorganic acid lithium salt may include at least one of LiPF6, LiBF4, LiB(C6H5)4, LiCl, and LiBr. The nonaqueous electrolyte 14 can have improved lithium ion conductivity when at least one of LiN(CF3SO2)2, LiN(FSO2)2, and LiBF4 is used. When LiN(CF3SO2)2 is used, the nonaqueous electrolyte 14 can have improved heat resistance and low moisture reactivity, and can thus improve the storage characteristic.
The content (concentration) of the supporting electrolyte in the nonaqueous electrolyte 14 is decided, for example, by taking into consideration such factors as the type of the supporting electrolyte, and the conductivity required of the nonaqueous electrolyte 14. When a lithium salt is used as the supporting electrolyte, the concentration of the supporting electrolyte in the nonaqueous electrolyte 14 may be, for example, 0.5 to 3.5 mol/L, 0.5 to 3.0 mol/L, or 1 to 2.5 mol/L.
The battery case 2, the terminal 4, and the terminal 5 shown in
Referring to
The terminal 5 on the negative electrode side is attached to the negative electrode case 7 by being welded. Here, the terminal 5 is welded to the top surface 2b of the negative electrode case 7 by laser spot welding. Welding is made at a plurality of welding points 15 along the direction from the base end toward the tip of the terminal 5 (longitudinal direction, X axis direction in the figure). The welding points 15 are disposed substantially at the center with respect to the shorter side as opposed to the longer side of the terminal 5. Similarly, the terminal 4 on the positive electrode side is welded to the bottom surface 2a of the positive electrode case 6 by laser spot welding.
The terminal 5 is welded to the negative electrode case 7 at a peel strength of, for example, 2 to 4 kgf against the negative electrode case 7. In this embodiment, the peel strength against the negative electrode case 7 is about 3 kgf. With a peel strength of 2 kgf or more against the negative electrode case 7, detachment of the terminal 5 from the negative electrode case 7 can be suppressed. The heat input to the negative electrode case 7 by the welding can be reduced when the peel strength is 4 kgf or less.
Generally, the conductivity of the electrolyte becomes a maximum with the supporting electrolyte concentration as determined by such factors as the type of the supporting electrolyte. Accordingly, from the standpoint of lowering the resistance of the electrolyte, the supporting electrolyte concentration has an optimum value. However, in view of preventing problems, it may not be always possible to increase the supporting electrolyte concentration as much as it is needed (optimum value) for characteristics improvement.
With the structure of the negative electrode case 7 described below with reference to
The base layer 20 is made of conductive material, for example, the same material (stainless steel) used for the terminal 5. In the following, the base layer 20 is also referred to as stainless steel layer. The base layer 20 of the present embodiment represents the thickest layer among the metal layers contained in the negative electrode case 7. The thickness of the base layer 20 is determined, for example, by taking into consideration such factors as the size and the strength of the negative electrode case 7, and may be 70% to 98% of the thickness of the negative electrode case 7.
The nickel layer 21 is made of nickel having higher thermal conductivity than the base layer 20 (stainless steel layer), and has a thickness of 2.6 μm or more. Among the metal layers contained in the negative electrode case 7, the nickel layer 21 of the present embodiment is closest in position to the boundary of the negative electrode case 7 and the terminal 5. One surface of the nickel layer 21 is adjacent to the base layer 20, whereas the other surface is adjacent to the terminal 5 in thickness direction. That is, the nickel layer 21 includes the surface welded to the terminal 5.
The proportion of the thickness of the nickel layer 21 with respect to the thickness of the negative electrode case 7 may be 2% or more. For example, when the negative electrode case 7 has a thickness of 130 μm, and the thickness proportion of the nickel layer 21 is 2%, the nickel layer 21 has a thickness of 2.6 μm. It follows from this that the thickness of the nickel layer 21 exceeds 2.6 μm when the thickness of the negative electrode case 7 and/or the thickness proportion of the nickel layer 21 are/is increased.
The thickness proportion of the nickel layer 21 with respect to the thickness of the negative electrode case 7 may be 8% or more. For example, when the negative electrode case 7 has a thickness of 200 μm, and the thickness of the nickel layer 21 is 16 μm, the thickness proportion of the nickel layer 21 is 8%. It follows from this that the thickness proportion of the nickel layer 21 exceeds 8% when the thickness of the negative electrode case 7 is decreased, or when the thickness of the nickel layer 21 is increased.
The negative electrode case 7 of the present embodiment includes a copper layer 22 disposed on the same side as the storage space 10 with respect to the base layer 20. Specifically, the negative electrode case 7 has a three-layer structure of the base layer 20, the nickel layer 21, and the copper layer 22.
One surface of the copper layer 22 is adjacent to the base layer 20, whereas the other surface is adjacent to the negative electrode portion 12 in thickness direction. In the present embodiment, the copper layer 22 has the highest conductivity among the metal layers contained in the negative electrode case 7. For example, the copper layer 22 may serve to lower the resistance of the negative electrode case 7 in thickness direction, or may serve as at least a part of the collector of the negative electrode portion 12. The copper layer 22 may be omitted.
The negative electrode case 7 of the present embodiment is formed, for example, by bending a clad material. The clad material is a composite material of bonded different metals. For example, the clad material is produced by press bonding laminated metal layers (metal plates or metal foils) after a surface activation treatment. The clad material may include an alloy layer where the metal atoms of the overlying and underlying different metal layers are diffused. For this reason, the thickness of the metal layer in the clad material is given as the product of the thickness proportion of the metal layer in the total metal layer thickness before press bonding and the total thickness of the clad material after press bonding.
For example, the clad material as the base material of the negative electrode case 7 of the present embodiment is produced by press bonding a stainless steel material (base layer 20) with a copper material (copper layer 22) and a nickel material (nickel layer 21) after laminating these metal materials on the both surfaces of the stainless steel material. Assume here that the thickness ratio of the nickel material, the stainless steel material, and the copper material before press bonding is 16:76:8, and that the thickness of the resulting clad material is 200 μm. In this case, the proportion of the nickel material in the total thickness of the metal materials before press bonding is 8/100, and accordingly the thickness of the nickel layer in the clad material translates into 16 μm (200 μm×8/100).
Examples of the present invention are described below.
In the Example represented in
In the Comparative Example in which the nickel layer was formed as a 1 μm-thick layer, the battery case ruptured when the welding heat quantity became 1.6 J or more. Linear interpolation suggests that a battery case rupture occurs when the heat quantity exceeds about 1.5 J. The welding heat quantity that can maintain the peel strength between the negative electrode case and the terminal is, for example, 1.65 J. In Comparative Example, the expected percentage rupture is about 50% when the welding heat quantity is 1.65 J to maintain the peel strength between the battery case and the terminal.
In the Example according to the present embodiment, there was hardly any rupture in the battery case 2 until at least 2.0 J after the welding heat quantity exceeded 1.5 J. It is thus expected that there will be essentially no rupture in the battery case 2 even when the welding heat quantity is set to 1.65 J to maintain the peel strength between the battery case 2 and the terminal 5. As demonstrated above, the present embodiment can suppress a battery case rupture due to the heat of welding.
Each plot in the graph of
Negative electrode case: stainless steel layer and nickel layer
Stainless steel layer thickness: 200 μm
Nickel layer thickness: 1 μm
Negative electrode case: clad material (thickness 130 μm) of copper layer, stainless steel layer, and nickel layer
Copper layer thickness: 9.1 μm
Stainless steel layer thickness: 118.3 μm
Nickel layer thickness: 2.6 μm (thickness proportion is 2%)
Negative electrode case: clad material (thickness 230 μm) of copper layer, stainless steel layer, and nickel layer
Copper layer thickness: 9.1 μm
Stainless steel layer thickness: 209.3 μm
Nickel layer thickness: 4.6 μm (thickness proportion is 2%)
Negative electrode case: Clad material (thickness 200 μm) of copper layer, stainless steel layer, and nickel layer
Copper layer thickness: 32 μm
Stainless steel layer thickness: 152 μm
Nickel layer thickness: 16 μm (thickness proportion is 8%)
As shown in
It should be noted that the technical scope of the present invention is not limited to the embodiment described above. For example, one or more elements described in the foregoing embodiment may be omitted. Further, the various elements described in the foregoing embodiment may be appropriately combined.
The nonaqueous electrolytic secondary battery 1, described as having the terminals 4 and 5, may include either one of or neither of the terminals 4 and 5. For example, the nonaqueous electrolytic secondary battery 1 may be adapted so that it is shipped without terminals, and terminals may be, for example, welded by a user, as required. The nonaqueous electrolytic secondary battery 1 can suppress not only the problems caused by the welding of terminals, but problems caused by a heat treatment such as a reflow process.
In the nonaqueous electrolytic secondary battery 1, the negative electrode case 7 is formed of clad material, and the nickel layer 21 represents one of the metal layers contained in the clad material. However, the nickel layer 21 may be formed by a method such as plating. Further, the nickel layer 21 contained in the negative electrode case 7 may be a single layer or multiple layers. When more than one nickel layer is disposed opposite the storage space 10 with respect to the base layer 20, the thickness of the nickel layer 21 may be defined as the total thickness of these nickel layers.
In the foregoing embodiment, the thickness of the metal layer in the clad material is calculated from the thickness ratio before press bonding and the thickness of the clad material. However, the metal layer thickness may be measured by using devices such as an X-ray fluorescence thickness meter, an X-ray diffraction device (XRD), and an X-ray photoelectron spectrometer (XPS). When the adjacent two metal layers are alloyed in the vicinity of the metal layer boundary, the position of the alloy layer where the composition ratio (the ratio of the number of atoms) of the two metals reverses may be defined as the boundary, and the thickness of each metal layer may be defined by using this boundary as a reference.
The nonaqueous electrolytic secondary battery 1 is described as having a coin structure. However, the invention is not limited to this particular embodiment. For example, the nonaqueous electrolytic secondary battery 1 may be a chip-shaped electric double-layer capacitor, or some other electrochemical cell subjected to heat treatment. Such small nonaqueous electrolytic secondary batteries are often installed by using a method such as laser welding, and the problems caused by the heat of such processes can be suppressed.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013-035779 | Feb 2013 | JP | national |
