Electrochemical Devices

Abstract

Provided is an electrochemical device comprising a negative pole, a positive pole, and a separator disposed between the negative pole and the positive pole. In the electrochemical device according to the present invention, the negative pole is an electrode containing magnesium and is in contact with a fullerene-containing layer that contains fullerenes. An electrolytic solution of the electrochemical device contains a solvent and a magnesium salt contained in the solvent.

Description

[Technical field]

[0001] The present invention relates to electrochemical devices. [Background technology]

[0002] Electrochemical devices include capacitors, air batteries, fuel cells, secondary batteries, etc., and are used for various purposes. Electrochemical devices include a positive electrode and a negative electrode, and an electrolyte that transports ions between the positive electrode and the negative electrode.

[0003] For example, an electrode made of magnesium or an electrode containing at least magnesium is provided as an electrode for an electrochemical device, typified by a magnesium battery (hereinafter, such an electrode will be referred to as an "electrode containing magnesium" or simply as a "magnesium electrode", and an electrochemical device using an electrode containing magnesium will be referred to as a "magnesium electrode-based electrochemical device"). Magnesium is a more abundant resource than lithium, and is much cheaper. In addition, magnesium generally has a large amount of electricity per unit volume that can be extracted by an oxidation-reduction reaction, and is also highly safe when used in an electrochemical device. For this reason, magnesium batteries are attracting attention as a next-generation secondary battery to replace lithium-ion batteries. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] U.S. Patent Publication US2013 / 252112A1 Summary of the Invention [Problem to be solved by the invention]

[0005] The inventors of the present application have realized that there are still problems to be overcome in magnesium batteries and have found the need to take measures to address these problems. Specifically, the inventors of the present application have found the following problems:

[0006] Improving the cycle characteristics is one of the important issues for magnesium batteries that use magnesium in the negative electrode. Although this issue can be addressed by changing the type of Mg electrolyte and positive electrode material, there is still a need for further improvements to improve the cycle characteristics.

[0007] Although the cycle characteristics of lithium ion batteries, which are widely used as secondary batteries, can be improved by adding additives to the electrolyte, it is difficult to apply similar additives to magnesium batteries. This is because the Mg coordination structure in the electrolyte of magnesium batteries is very fragile, and additives for lithium ion batteries tend to impair the activity of Mg precipitation and dissolution. In other words, it is usually difficult to improve the cycle characteristics of the electrolyte of magnesium batteries.

[0008] Furthermore, improving the energy density of magnesium batteries is also an important issue. In particular, the discharge voltage during the first discharge can drop due to negative electrode overvoltage, and it is not possible to sufficiently suppress this voltage drop.

[0009] The present invention has been made in view of the above problems. That is, a main object of the present invention is to provide an electrochemical device including an electrode containing magnesium, which has superior cycle characteristics and a higher energy density. [Means for solving the problem]

[0010] The inventors of the present application attempted to solve the above problems by taking a new approach, rather than simply extending the conventional technology, and as a result, they have invented an electrolyte that achieves the above-mentioned main object.

[0011] In the present invention, An electrochemical device comprising a negative electrode, a positive electrode, and a separator disposed between the negative electrode and the positive electrode, the negative electrode is an electrode containing magnesium, the electrolyte of the electrochemical device comprises a solvent and a magnesium salt contained in the solvent; An electrochemical device is provided, wherein the negative electrode is in contact with a fullerenes-containing layer that includes fullerenes. Effect of the Invention

[0012] The electrochemical device of the present invention provides an electrochemical device with improved cycle characteristics and energy density. That is, the electrochemical device of the present invention is a so-called "magnesium electrode system" and yet has improved cycle characteristics and energy density. The improved cycle characteristics and energy density make the magnesium electrode system electrochemical device more suitable for use in a real environment.

[0013] It should be noted that the effects described in this specification are merely exemplary and are not limiting, and additional effects may also be provided. [Brief description of the drawings]

[0014] [Figure 1] FIG. 1 is a schematic diagram of a magnesium electrode-based electrochemical device (particularly a battery) according to one embodiment of the present invention. [Diagram 2] FIG. 2 is a schematic cross-sectional view of a magnesium secondary battery (cylindrical magnesium secondary battery) serving as one embodiment of the present invention. [Diagram 3] FIG. 3 is a schematic perspective view of a magnesium secondary battery (a flat laminate film type magnesium secondary battery) provided as one embodiment of the present invention. [Figure 4] FIG. 4 is a schematic cross-sectional view of an electrochemical device serving as a capacitor in one embodiment of the present invention. [Diagram 5] FIG. 5 is a schematic cross-sectional view of an electrochemical device serving as an air battery in one embodiment of the present invention. [Figure 6] FIG. 6 is a schematic cross-sectional view of an electrochemical device serving as a fuel cell in one embodiment of the present invention. [Figure 7] FIG. 7 is a block diagram showing an example of a circuit configuration when a magnesium secondary battery provided as one embodiment of the present invention is applied to a battery pack. [Figure 8] 8A, 8B, and 8C are block diagrams respectively showing the configurations of an electric vehicle, a power storage system, and an electric tool to which a magnesium secondary battery is applied as one embodiment of the present invention. [Figure 9] FIG. 9 is a development view that shows a schematic diagram of the battery produced in the Example of this specification. [Figure 10] FIG. 10 shows the charge / discharge curve results obtained in the Examples of this specification (Example 1). [Figure 11] FIG. 11 shows the charge / discharge curve results obtained in the Examples of this specification (Example 2). [Figure 12] FIG. 12 shows the charge / discharge curve results obtained in the Examples of the present specification (Comparative Example 1). [Figure 13] FIG. 13 shows the relationship between the specific capacity and the discharge voltage obtained in the Examples of this specification (Example 3 and Comparative Example 2). [Figure 14] FIG. 14 is a schematic cross-sectional view showing an embodiment in which a fullerene-containing layer partially covers a negative electrode. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] Hereinafter, an "electrochemical device" according to an embodiment of the present invention will be described in detail. Although the description will be made with reference to the drawings as necessary, the contents shown in the drawings are merely shown as schematic examples for understanding the present invention, and the appearance and dimensional ratios may differ from the actual product.

[0016] Various numerical ranges mentioned in this specification are intended to include the lower and upper limit numerical values ​​(i.e., the upper and lower limit values) themselves, unless otherwise specified terms such as "less than," "greater than," and "smaller." In other words, for example, in a numerical range such as 1 to 10, the numerical range 1 to 10 is interpreted as including the lower limit "1" and the upper limit "10."

[0017] In the present invention, the term "electrochemical device" broadly means a device capable of extracting energy by utilizing an electrochemical reaction. In the narrow sense, the term "electrochemical device" in the present invention means a device that includes a pair of electrodes and an electrolyte, and is charged and discharged in accordance with the movement of ions. As merely examples, examples of electrochemical devices include secondary batteries, capacitors, air batteries, and fuel cells.

[0018] [Electrochemical Devices] An electrochemical device according to an embodiment of the present invention (hereinafter also referred to as "the present embodiment") is a device that can extract energy by utilizing an electrochemical reaction.

[0019] The electrochemical device according to the present embodiment is an electrochemical device including a negative electrode, a positive electrode, and a separator disposed between the negative electrode and the positive electrode. As will be described in detail later, in the electrochemical device according to the present embodiment, the negative electrode is an electrode containing magnesium, while the positive electrode is preferably an electrode containing sulfur, i.e., a sulfur electrode. That is, in a preferred embodiment, the electrochemical device according to the present embodiment is a magnesium (Mg)-sulfur (S) electrode electrochemical device.

[0020] As used herein, the term "sulfur electrode" refers broadly to an electrode having sulfur (S) as an active component (i.e., active material). In the narrow sense, the term "sulfur electrode" refers to an electrode that at least comprises sulfur, for example, an electrode that comprises sulfur (S), such as S8 and / or polymeric sulfur, particularly such a positive electrode.

[0021] The sulfur electrode may contain components other than sulfur, such as a conductive assistant and / or a binder, etc. By way of example only, the sulfur content in the sulfur electrode is preferably 5% by mass or more and 95% by mass or less, for example, 70% by mass or more and 90% by mass or less, based on the entire electrode.

[0022] Examples of the conductive assistant include carbon materials such as graphite, carbon fiber, carbon black, and carbon nanotubes, and one or more of these materials can be used in combination. Examples of the carbon fiber include vapor growth carbon fiber (VGCF (registered trademark)). Examples of the carbon black include acetylene black and / or ketjen black. Examples of the carbon nanotubes include single-wall carbon nanotubes (SWCNT) and / or multi-wall carbon nanotubes (MWCNT) such as double-wall carbon nanotubes (DWCNT). Materials other than carbon materials can be used as long as they have good electrical conductivity, and for example, metal materials such as Ni powder and / or conductive polymer materials can be used.

[0023] Examples of the binder include fluorine-based resins such as polyvinylidene fluoride (PVdF) and / or polytetrafluoroethylene (PTFE), polyvinyl alcohol (PVA)-based resins, and / or styrene-butadiene copolymer rubber (SBR)-based resins. Conductive polymers may also be used as the binder. Examples of the conductive polymers that can be used include substituted or unsubstituted polyaniline, polypyrrole, polythiophene, and (co)polymers consisting of one or two types selected from these.

[0024] In addition, the term "electrode containing magnesium" as used herein refers, in a broad sense, to an electrode having magnesium (Mg) as an active component (i.e., active material). In a narrow sense, the term "electrode containing magnesium" refers to an electrode made of magnesium, for example, an electrode containing magnesium metal or a magnesium alloy, particularly such a negative electrode. Although such an electrode containing magnesium may contain components other than magnesium metal or a magnesium alloy, in a preferred embodiment, it is an electrode made of a magnesium metal body (for example, an electrode made of magnesium metal alone having a purity of 90% or more, preferably a purity of 95% or more, and more preferably a purity of 98% or more).

[0025] The material constituting the negative electrode (specifically, the negative electrode active material) is an "electrode containing magnesium" and is therefore preferably made of magnesium metal, a magnesium alloy, or a magnesium compound. When the negative electrode is made of a magnesium metal element (e.g., a magnesium plate, etc.), the Mg purity of the metal element is, for example, 90% or more, preferably 95% or more, and more preferably 98% or more. The negative electrode can be made, for example, from a plate-shaped material or a foil-shaped material, but is not limited thereto, and can also be formed (shaped) using a powder.

[0026] The negative electrode may have a structure in which a negative electrode active material layer is formed in the vicinity of its surface. For example, the negative electrode may have a layer having magnesium ion conductivity that contains magnesium (Mg) as the negative electrode active material layer and further contains at least any one of carbon (C), oxygen (O), sulfur (S) and halogen. Although this type of negative electrode active material layer is merely an example, it may have a single peak derived from magnesium in the range of 40 eV to 60 eV. As the halogen, for example, at least one type selected from the group consisting of fluorine (F), chlorine (Cl), bromine (Br) and iodine (I) may be mentioned. In this case, the negative electrode active material layer may have a peak of 2×10 in the direction perpendicular to the surface (depth direction) from the surface of the negative electrode active material layer. -7The negative electrode active material layer may have a single peak derived from magnesium in the range of 40 eV to 60 eV from the surface to the inside thereof. For the same reason, the oxidation state of magnesium may be 2×10 -7 m. Here, the surface of the negative electrode active material layer means the surface that constitutes the surface of the electrode among both sides of the negative electrode active material layer, and the back side means the surface opposite to the surface, that is, the surface that constitutes the interface between the current collector and the negative electrode active material layer. Whether the negative electrode active material layer contains the above elements can be confirmed based on the XPS (X-ray Photoelectron Spectroscopy) method. In addition, it can also be confirmed similarly based on the XPS method that the negative electrode active material layer has the above peak and has an oxidation state of magnesium.

[0027] In the electrochemical device according to this embodiment, the positive electrode and the negative electrode are separated by a separator that allows magnesium ions to pass while preventing short circuits caused by contact between the two electrodes. Such a separator may be an inorganic separator and / or an organic separator. Examples of the inorganic separator include glass filters and glass fibers. Examples of the organic separator include porous membranes made of synthetic resins such as polytetrafluoroethylene, polypropylene, and / or polyethylene, and a structure in which two or more of these porous membranes are laminated can also be used. Among them, a porous membrane made of polyolefin is preferable because it has an excellent short circuit prevention effect and can improve the safety of the battery by its shutdown effect.

[0028] In the electrochemical device according to this embodiment, the negative electrode is in contact with the fullerene-containing layer. In this embodiment, the cycle characteristics and energy density of the electrochemical device can be improved due to the negative electrode being in contact with the fullerene.

[0029] The layer in the fullerene-containing layer may be a layer that continuously covers the object to be covered, or may be a layer that partially covers the object to be covered. The embodiment in which the fullerene-containing layer contacts the negative electrode is, for example, an embodiment in which the fullerene-containing layer is a coating layer that coats the negative electrode (first embodiment), and an embodiment in which the fullerene-containing layer is a separator (second embodiment). The first embodiment and the second embodiment may be combined. When the fullerene-containing layer is a separator and / or a coating layer that coats the negative electrode, the magnesium electrode-based electrochemical device according to this embodiment is more likely to exhibit higher cycle characteristics and energy density.

[0030] In the first embodiment, the fullerene-containing layer is a coating layer that coats the negative electrode. The fullerene-containing layer may contain fullerenes and may be made of fullerenes. The fullerene-containing layer may, for example, continuously coat the negative electrode surface, or may partially coat the negative electrode surface and expose a part of the negative electrode surface. The embodiment in which the negative electrode surface is continuously or partially coated can be confirmed, for example, by an electron microscope. The "fullerenes" can be identified by visible / ultraviolet absorption spectroscopy (UV), infrared absorption spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), and / or mass spectrometry (MS (including GC-MS and / or LS-MS, etc.)).

[0031] When the fullerene-containing layer contains fullerenes, the fullerenes may be contained in an amount of, for example, 90% by weight or more, 95% by weight or more, 97% by weight or more, 98% by weight or more, 99% by weight or more, 99.5% by weight or more, 99.9% by weight or more, or 99.95% by weight or more of the total mass of the fullerene-containing layer.

[0032] Referring to FIG. 14, the latter embodiment (i.e., the first embodiment) LaAn example of a fullerene-containing layer (an embodiment in which the fullerene-containing layer is a coating layer that partially coats the negative electrode) will be described. FIG. 14 is a schematic cross-sectional view showing an embodiment in which the fullerene-containing layer partially coats the negative electrode. When the fullerene-containing layer 2 is made of particles containing a plurality of fullerenes (hereinafter also referred to as "fullerene particles") 2a, the plurality of fullerene particles 2a are two-dimensionally connected on the surface of the negative electrode 1. Adjacent fullerene particles 2a are in contact with each other. Parts of the plurality of fullerene particles 2a are separated from each other, and at the separated portions, a part of the surface of the negative electrode 1 is exposed. The fullerene-containing layer 2 may also be configured by stacking the fullerene particles 2a in a direction perpendicular to the surface of the negative electrode. Such a fullerene-containing layer 2 can be formed, for example, by dropping a dispersion of fullerene particles 2a onto the surface of the negative electrode 1 to form a coating film, and drying the coating film. The fullerene particles 2a may be dispersed in the dispersion liquid in the form of primary particles, or in the form of secondary particles formed by aggregation of primary particles.

[0033] In the second embodiment, the fullerene-containing layer is a separator. In the electrochemical device according to the present embodiment, the negative electrode comes into contact with the fullerenes by having a structure in which the separator, at least a part of whose surface is covered with fullerenes, comes into contact with the negative electrode. For example, when the separator has a plurality of pores and the fullerene-containing layer is made of a plurality of fullerene particles, the surface of the separator is continuously or partially covered as in the first embodiment, and the fullerene particles may enter or become stuck in the pores.

[0034] In this embodiment, "improved cycle characteristics and energy density" means that in a magnesium electrode-based electrochemical device having a "negative electrode in contact with a fullerene-containing layer" and containing an electrolyte solution containing a "magnesium salt", the cycle characteristics are improved compared to the cycle characteristics and energy density of an electrochemical device having the same magnesium electrode system except that it does not have the "negative electrode in contact with a fullerene-containing layer". In terms of cycle characteristics, this means that the discharge capacity retention rate becomes relatively high when charge / discharge cycles are repeated (see FIG. 13). In terms of energy density, this means that the discharge voltage becomes relatively high (see FIGS. 10 to 11).

[0035] In this specification, the term "cycle characteristic" broadly means a characteristic in which the decrease in discharge capacity is more sufficiently suppressed even when charging and discharging are repeated. In the narrow sense, the term "cycle characteristic" refers to a characteristic based on the discharge capacity retention rate obtained by the following cycle test, and "improved cycle characteristic" means that the discharge capacity retention rate is relatively high. Cycle testing The cycle test is carried out in a thermostatic chamber at 25°C. Discharge is performed at a constant current of 0.1 mA until the end-of-charge voltage is 0.7 V. After one hour of rest, charging is started. Charge is performed at a constant current of 0.1 mA until the end-of-charge voltage is 2.2 V, and then one hour of rest is taken after charging. This charge / discharge cycle is repeated 20 times. In this case, the ratio of the cell discharge capacity after cycling to the initial discharge capacity is defined as the capacity retention rate after cycling.

[0036] In this specification, the term "energy density" broadly means a characteristic in which the decrease in discharge voltage (voltage drop) due to negative electrode overvoltage is more sufficiently suppressed. In the narrow sense, the term "energy density" refers to a characteristic based on the discharge voltage (particularly the discharge voltage in the first cycle) obtained by the cycle test, and "the energy density is improved" means that the discharge voltage is relatively high.

[0037] The cycle characteristics and energy density of a magnesium electrode-based electrochemical device having a negative electrode in contact with a fullerene-containing layer and charged with an electrolyte solution containing a "magnesium salt" can be improved. This is particularly true when the electrochemical device has a sulfur electrode as a positive electrode. In other words, the positive electrode of the electrochemical device according to this embodiment is preferably a sulfur electrode. In the case of an electrochemical device having such a magnesium electrode-sulfur electrode pair (hereinafter also referred to as a "magnesium-sulfur electrode-based electrochemical device" or "Mg-S battery"), the cycle characteristics and energy density of the electrochemical device according to this embodiment can be improved. When the cycle characteristics and energy density are increased in this way, the suitability of the magnesium-sulfur electrode-based electrochemical device in a practical environment is increased, and the device can be more easily realized as desired. Assuming that the magnesium-sulfur electrode-based electrochemical device is a secondary battery, this embodiment has found the possibility of a Mg-S battery that is more suitable for practical use.

[0038] The fullerenes are, for example, unsubstituted fullerenes or fullerene derivatives. Examples of unsubstituted fullerenes include C 60 (C1), C 70 , C 84 , C 90 and C 96 At least one fullerene selected from the group consisting of: 60 , C 70 , C 84 , C 90 and C 96When the fullerene is at least one type selected from the group consisting of, the magnesium electrode-based electrochemical device according to this embodiment is more likely to exhibit higher cycle characteristics and energy density. The fullerene derivative is a fullerene in which a functional group is added to or substituted on an unsubstituted fullerene. The number of functional groups added or substituted is, for example, an integer of 1 to 10. Such a functional group is, for example, at least one type of functional group selected from the group consisting of an alkyl group, an alkenyl group, a cycloalkyl group, an alkoxy group, an aryl group, an amino group, a hydroxyl group, a nitro group, an acyl group, and a halogen group. Of these, unsubstituted fullerene is preferable, and C 60 is more preferred. [ka]

[0039] The fullerenes may be one selected from the group consisting of the unsubstituted fullerenes and fullerene derivatives, or may be a combination of two or more. When the fullerenes are a combination of two or more, one of the two or more fullerenes may be included as a main component in the fullerenes. Here, the main component in this specification refers to a fullerene that is included in an amount of 90% by weight or more, 95% by weight or more, 97% by weight or more, 98% by weight or more, 99% by weight or more, 99.5% by weight or more, 99.9% by weight or more, or 99.95% by weight or more of the total content of fullerenes. For example, when the fullerene is C 60 And, C 60 When the fullerenes are composed of unsubstituted fullerenes other than C 60 Fullerenes Total The content may be 99.5% by weight or more.

[0040] In the electrochemical device according to this embodiment, the electrolyte contains at least a solvent and a magnesium salt contained in the solvent.

[0041] The solvent is, for example, at least one solvent selected from the group consisting of linear ethers, cyclic ethers, and dialkylsulfones. When the solvent is at least one solvent selected from the group consisting of linear ethers, cyclic ethers, and dialkylsulfones, the magnesium electrode-based electrochemical device according to this embodiment is more likely to exhibit higher cycle characteristics and energy density.

[0042] Linear ethers can be, for example, of the general formula: [ka] [In the general formula, R' and R'' each independently represent a hydrocarbon group having 1 to 10 carbon atoms and may be the same or different, and n represents an integer of 1 to 10.] When the linear ether is an ether having an ethyleneoxy structural unit represented by the above general formula, the magnesium electrode-based electrochemical device according to this embodiment is more likely to exhibit higher cycle characteristics and energy density.

[0043] The linear ether solvent used in the electrolyte of the magnesium electrode system according to this embodiment has one or more ethyleneoxy structural units. The term "ethyleneoxy structural unit" as used herein refers to a molecular structural unit (-O-C2H4-) in which an ethylene group is bonded to an oxygen atom, and one or more such molecular structural units are contained in the linear ether. For example, when one ethyleneoxy structural unit is contained, it may be a linear ether such as dimethoxyethane / DME (ethylene glycol dimethyl ether) and / or diethoxyethane / DEE (ethylene glycol diethyl ether).

[0044] In a preferred embodiment, the linear ether has one ethyleneoxy structure, that is, the linear ether is dimethoxyethane. In a preferred embodiment, the linear ether has two or more molecular structural units (-O-C2H4-). From another perspective, the linear ether in the electrolyte of the magnesium electrode system preferably has a structure in which two or more glycol molecules are dehydrated and condensed.

[0045] In the above general formula of the linear ether, R' and R'' each independently represent a hydrocarbon group. Therefore, R' and R'' each independently may be an aliphatic hydrocarbon group, an aromatic hydrocarbon group, and / or an araliphatic hydrocarbon group. Here, in this specification, "linear ether" means that at least the ethyleneoxy structural unit is not branched (i.e., does not have a branched structure). This means that R' and R'' in the above general formula of the linear ether do not necessarily have a linear structure, but may have a branched structure. In one preferred embodiment, the linear ether used in the electrolyte of the magnesium electrode system according to this embodiment is a glycol ether in which not only the ethyleneoxy structural unit is not branched, but also R' and R'' are not branched.

[0046] In this embodiment, preferably, when the linear ether has an "ethyleneoxy structural unit" in this way, in combination with the "negative electrode in contact with the fullerene-containing layer", the cycle characteristics and energy density of the magnesium electrode-based electrochemical device are easily improved. In other words, the coexistence of the solvent of the linear ether having at least an "ethyleneoxy structural unit" and the "negative electrode in contact with the fullerene-containing layer" in the electrolyte can bring about a favorable effect on the cycle characteristics and energy density to a certain extent.

[0047] When the linear ether has "two or more ethyleneoxy structural units", the cycle characteristics and energy density of the magnesium electrode-based electrochemical device are more likely to be improved in combination with the presence of the "negative electrode in contact with the fullerene-containing layer". In other words, the coexistence of the linear ether solvent having at least "two or more ethyleneoxy structural units" and the "negative electrode in contact with the fullerene-containing layer" in the electrolyte can bring about a significant effect on the cycle characteristics and energy density. This is thought to be because the "negative electrode in contact with the fullerene-containing layer" effectively acts on the cycle characteristics and energy density of the magnesium electrode-based electrochemical device in combination with the linear ether solvent having "two or more ethyleneoxy structural units" containing magnesium salt.

[0048] The linear ether having two or more ethyleneoxy structural units is not particularly limited, but examples thereof include diethylene glycol-based ethers, triethylene glycol-based ethers, tetraethylene glycol-based ethers, pentaethylene glycol-based ethers, hexaethylene glycol-based ethers, etc. Similarly, the linear ether having two or more ethyleneoxy structural units may be heptaethylene glycol-based ethers, octaethylene glycol-based ethers, nonaethylene glycol-based ethers, decaethylene glycol-based ethers, etc., or even polyethylene glycol-based ethers having more ethyleneoxy structural units than the above.

[0049] In a preferred embodiment of the linear ether in this embodiment, the hydrocarbon group having 1 to 10 carbon atoms is an aliphatic hydrocarbon group. That is, for the linear ether contained in the magnesium electrode-based electrolyte according to this embodiment, R' and R'' in the general formula may each independently be an aliphatic hydrocarbon group having 1 to 10 carbon atoms. The linear ether in the preferred embodiment is not particularly limited, and examples thereof include ethylene glycol-based ether, diethylene glycol-based ether, triethylene glycol-based ether, tetraethylene glycol-based ether, pentaethylene glycol-based ether, and hexaethylene glycol-based ether, as listed below. Similarly, the linear ether in the preferred embodiment may be heptaethylene glycol-based ether, octaethylene glycol-based ether, nonaethylene glycol-based ether, and decaethylene glycol-based ether. Among these, R' and R'' in the general formula are each preferably independently an aliphatic hydrocarbon group having 1 to 4 carbon atoms (e.g., a lower alkyl group having 1 to 4 carbon atoms, such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, and an n-butyl group).

[0050] (Ethylene glycol ether) Examples of ethylene glycol ethers include ethylene glycol dimethyl ether, ethylene glycol ethyl methyl ether, ethylene glycol methyl propyl ether, ethylene glycol butyl methyl ether, ethylene glycol methyl pentyl ether, ethylene glycol methyl hexyl ether, ethylene glycol methyl heptyl ether, and ethylene glycol methyl octyl ether; ethylene glycol diethyl ether, ethylene glycol ethyl propyl ether, ethylene glycol butyl ethyl ether, ethylene glycol ethyl pentyl ether, ethylene glycol ethyl hexyl ether, ethylene glycol ethyl heptyl ether, and ethylene glycol ethyl octyl ether; ethylene glycol dipropyl ether, ethylene glycol butyl propyl ether, ethylene glycol propyl pentyl ether, ethylene glycol propyl hexyl ether, ethylene glycol propyl heptyl ether, and ethylene glycol propyl octyl ether; ethylene glycol dibutyl ether, ethylene glycol butyl pentyl ether, ethylene glycol butyl hexyl ether, ethylene glycol butyl heptyl ether, and ethylene glycol butyl octyl ether; ethylene glycol dipentyl ether, ethylene glycol hexyl pentyl ether, ethylene glycol heptyl pentyl ether, and ethylene glycol octyl pentyl ether; Ethylene glycol dihexyl ether, ethylene glycol heptyl hexyl ether, and ethylene glycol hexyl octyl ether; Ethylene glycol diheptyl ether, and ethylene glycol heptyl octyl ether; and Mention may be made of ethylene glycol dioctyl ether.

[0051] (Diethylene glycol ether) Examples of diethylene glycol ethers include diethylene glycol dimethyl ether, diethylene glycol ethyl methyl ether, diethylene glycol methyl propyl ether, diethylene glycol butyl methyl ether, diethylene glycol methyl pentyl ether, diethylene glycol methyl hexyl ether, diethylene glycol methyl heptyl ether, and diethylene glycol methyl octyl ether; diethylene glycol diethyl ether, diethylene glycol ethyl propyl ether, diethylene glycol butyl ethyl ether, diethylene glycol ethyl pentyl ether, diethylene glycol ethyl hexyl ether, diethylene glycol ethyl heptyl ether, and diethylene glycol ethyl octyl ether; diethylene glycol dipropyl ether, diethylene glycol butyl propyl ether, diethylene glycol propyl pentyl ether, diethylene glycol propyl hexyl ether, diethylene glycol propyl heptyl ether, and diethylene glycol propyl octyl ether; Diethylene glycol dibutyl ether, diethylene glycol butyl pentyl ether, diethylene glycol butyl hexyl ether, diethylene glycol butyl heptyl ether, diethylene glycol butyl octyl ether; diethylene glycol dipentyl ether, diethylene glycol hexyl pentyl ether, diethylene glycol heptyl pentyl ether, and diethylene glycol octyl pentyl ether; diethylene glycol dihexyl ether, diethylene glycol heptyl hexyl ether, and diethylene glycol hexyl octyl ether; Diethylene glycol diheptyl ether, diethylene glycol heptyl octyl ether; and Mention may be made of diethylene glycol dioctyl ether.

[0052] (Triethylene glycol ether) Examples of triethylene glycol ethers include triethylene glycol dimethyl ether, triethylene glycol ethyl methyl ether, triethylene glycol methyl propyl ether, triethylene glycol butyl methyl ether, triethylene glycol methyl pentyl ether, triethylene glycol methyl hexyl ether, triethylene glycol methyl heptyl ether, and triethylene glycol methyl octyl ether; Triethylene glycol diethyl ether, triethylene glycol ethyl propyl ether, triethylene glycol butyl ethyl ether, triethylene glycol ethyl pentyl ether, triethylene glycol ethyl hexyl ether, triethylene glycol ethyl heptyl ether, triethylene glycol ethyl octyl ether; triethylene glycol dipropyl ether, triethylene glycol butyl propyl ether, triethylene glycol propyl pentyl ether, triethylene glycol propyl hexyl ether, triethylene glycol propyl heptyl ether, and triethylene glycol propyl octyl ether; Triethylene glycol dibutyl ether, triethylene glycol butyl pentyl ether, triethylene glycol butyl hexyl ether, triethylene glycol butyl heptyl ether, triethylene glycol butyl octyl ether; triethylene glycol dipentyl ether, triethylene glycol hexyl pentyl ether, triethylene glycol heptyl pentyl ether, and triethylene glycol octyl pentyl ether; Triethylene glycol dihexyl ether, triethylene glycol heptyl hexyl ether, triethylene glycol hexyl octyl ether; triethylene glycol diheptyl ether, and triethylene glycol heptyl octyl ether; and Mention may be made of triethylene glycol dioctyl ether.

[0053] (Tetraethylene glycol ether) Examples of tetraethylene glycol ethers include tetraethylene glycol dimethyl ether, tetraethylene glycol ethyl methyl ether, tetraethylene glycol methyl propyl ether, tetraethylene glycol butyl methyl ether, tetraethylene glycol methyl pentyl ether, tetraethylene glycol methyl hexyl ether, tetraethylene glycol methyl heptyl ether, and tetraethylene glycol methyl octyl ether; tetraethylene glycol diethyl ether, tetraethylene glycol ethyl propyl ether, tetraethylene glycol butyl ethyl ether, tetraethylene glycol ethyl pentyl ether, tetraethylene glycol ethyl hexyl ether, tetraethylene glycol ethyl heptyl ether, and tetraethylene glycol ethyl octyl ether; tetraethylene glycol dipropyl ether, tetraethylene glycol butyl propyl ether, tetraethylene glycol propyl pentyl ether, tetraethylene glycol propyl hexyl ether, tetraethylene glycol propyl heptyl ether, and tetraethylene glycol propyl octyl ether; Tetraethylene glycol dibutyl ether, tetraethylene glycol butyl pentyl ether, tetraethylene glycol butyl hexyl ether, tetraethylene glycol butyl heptyl ether, tetraethylene glycol butyl octyl ether; tetraethylene glycol dipentyl ether, tetraethylene glycol hexyl pentyl ether, tetraethylene glycol heptyl pentyl ether, and tetraethylene glycol octyl pentyl ether; Tetraethylene glycol dihexyl ether, tetraethylene glycol heptyl hexyl ether, tetraethylene glycol hexyl octyl ether; Tetraethylene glycol diheptyl ether, and tetraethylene glycol heptyl octyl ether; and Mention may be made of tetraethylene glycol dioctyl ether.

[0054] (Pentaethylene glycol ether) Examples of pentaethylene glycol ethers include pentaethylene glycol dimethyl ether, pentaethylene glycol ethyl methyl ether, pentaethylene glycol methyl propyl ether, pentaethylene glycol butyl methyl ether, pentaethylene glycol methyl pentyl ether, pentaethylene glycol methyl hexyl ether, pentaethylene glycol methyl heptyl ether, and pentaethylene glycol methyl octyl ether; pentaethylene glycol diethyl ether, pentaethylene glycol ethyl propyl ether, pentaethylene glycol butyl ethyl ether, pentaethylene glycol ethyl pentyl ether, pentaethylene glycol ethyl hexyl ether, pentaethylene glycol ethyl heptyl ether, and pentaethylene glycol ethyl octyl ether; pentaethylene glycol dipropyl ether, pentaethylene glycol butyl propyl ether, pentaethylene glycol propyl pentyl ether, pentaethylene glycol propyl hexyl ether, pentaethylene glycol propyl heptyl ether, and pentaethylene glycol propyl octyl ether; Pentaethylene glycol dibutyl ether, pentaethylene glycol butyl pentyl ether, pentaethylene glycol butyl hexyl ether, pentaethylene glycol butyl heptyl ether, pentaethylene glycol butyl octyl ether; pentaethylene glycol dipentyl ether, pentaethylene glycol hexyl pentyl ether, pentaethylene glycol heptyl pentyl ether, and pentaethylene glycol octyl pentyl ether; Pentaethylene glycol dihexyl ether, pentaethylene glycol heptyl hexyl ether, pentaethylene glycol hexyl octyl ether; pentaethylene glycol diheptyl ether, and pentaethylene glycol heptyl octyl ether; and Mention may be made of pentaethylene glycol dioctyl ether.

[0055] (Hexaethylene glycol ether) Examples of hexaethylene glycol ethers include hexaethylene glycol dimethyl ether, hexaethylene glycol ethyl methyl ether, hexaethylene glycol methyl propyl ether, hexaethylene glycol butyl methyl ether, hexaethylene glycol methyl pentyl ether, hexaethylene glycol methyl hexyl ether, hexaethylene glycol methyl heptyl ether, and hexaethylene glycol methyl octyl ether; hexaethylene glycol diethyl ether, hexaethylene glycol ethyl propyl ether, hexaethylene glycol butyl ethyl ether, hexaethylene glycol ethyl pentyl ether, hexaethylene glycol ethyl hexyl ether, hexaethylene glycol ethyl heptyl ether, and hexaethylene glycol ethyl octyl ether; hexaethylene glycol dipropyl ether, hexaethylene glycol butyl propyl ether, hexaethylene glycol propyl pentyl ether, hexaethylene glycol propyl hexyl ether, hexaethylene glycol propyl heptyl ether, and hexaethylene glycol propyl octyl ether; Hexaethylene glycol dibutyl ether, hexaethylene glycol butyl pentyl ether, hexaethylene glycol butyl hexyl ether, hexaethylene glycol butyl heptyl ether, hexaethylene glycol butyl octyl ether; hexaethylene glycol dipentyl ether, hexaethylene glycol hexyl pentyl ether, hexaethylene glycol heptyl pentyl ether, and hexaethylene glycol octyl pentyl ether; Hexaethylene glycol dihexyl ether, hexaethylene glycol heptyl hexyl ether, hexaethylene glycol hexyl octyl ether; hexaethylene glycol diheptyl ether, and hexaethylene glycol heptyl octyl ether; and Mention may be made of hexaethylene glycol dioctyl ether.

[0056] In addition, the linear ether in the preferred embodiment may be a heptaethylene glycol ether, an octaethylene glycol ether, a nonaethylene glycol ether, a decaethylene glycol ether, or the like, or may be a polyethylene glycol ether.

[0057] Also, the cyclic ether is, for example, tetrahydrofuran. The dialkyl sulfone is, for example, a compound represented by the general formula: R'-SO2-R" [In the general formula, R' and R" are each independently a hydrocarbon group having 1 to 4 carbon atoms and may be the same or different.]

[0058] In a preferred embodiment of the dialkyl sulfone in this embodiment, the hydrocarbon group having 1 to 4 carbon atoms is an aliphatic hydrocarbon group. That is, for the dialkyl sulfone contained in the electrolyte solution of the electrochemical device according to this embodiment, R′ and R″ in the above general formula are each independently Number of carbon atomsIt may be an aliphatic hydrocarbon group having 1 to 4 carbon atoms (a lower alkyl group having 1 to 4 carbon atoms). The dialkyl sulfone is not particularly limited, but may be, for example, dimethyl sulfone, methyl ethyl sulfone, methyl-n-propyl sulfone, methyl-i-propyl sulfone, methyl-n-butyl sulfone, methyl-i-butyl sulfone, methyl-s-butyl sulfone, methyl-t-butyl sulfone, ethyl methyl sulfone, diethyl sulfone, ethyl-n-propyl sulfone, ethyl-i-propyl sulfone, ethyl-n-butyl sulfone, ethyl-i-butyl sulfone, ethyl-s-butyl sulfone, ethyl-t-butyl sulfone, di-n-propyl sulfone, di-i-propyl sulfone, n-propyl-n-butyl sulfone, n-butyl ethyl sulfone, i-butyl ethyl sulfone, s-butyl ethyl sulfone, and di-n-butyl sulfone.

[0059] The electrolyte of the magnesium electrode system in this embodiment comprises a magnesium salt. The magnesium salt may be one type or may be a magnesium salt consisting of more than one type. The magnesium salt is preferably at least one type of magnesium salt selected from the group consisting of magnesium halide, magnesium perfluoroalkylsulfonylimide, and magnesium bishexaalkyldisilazide. By using such a magnesium salt, the electrochemical device of the magnesium electrode system according to this embodiment is more likely to exhibit higher cycle characteristics and energy density.

[0060] Such magnesium salts have the general formula MgX n(wherein n is 1 or 2, and X is a monovalent or divalent anion). When X is a halogen (more specifically, F, Cl, Br, and I), the magnesium salt forms a halogen metal salt (magnesium halide). The halogen metal salt may be at least one selected from the group consisting of magnesium fluoride (MgF2), magnesium chloride (MgCl2), magnesium bromide (MgBr2), and magnesium iodide (MgI2). Among them, magnesium chloride is preferably used as the halogen metal salt. Magnesium chloride (MgCl2), in combination with the "negative electrode in contact with the fullerene-containing layer", can promote high cycle characteristics and energy density of the electrochemical device.

[0061] When X has a disilazide structure represented by the general formula (RSi)N (wherein R is a hydrocarbon group having 1 to 10 carbon atoms), the general formula MgX n (wherein n is 1 or 2, and X is a monovalent or divalent anion) forms a magnesium salt having a disilazide structure. In the general formula, R is preferably an aliphatic hydrocarbon group having 1 to 10 carbon atoms, more preferably a lower alkyl group having 1 to 4 carbon atoms. Such a magnesium salt is preferably a magnesium salt of hexaalkyldisilazide (magnesium bishexaalkyldisilazide (Mg(HRDS)2), where R is an alkyl group). Such a "magnesium salt" having a disilazide structure, in combination with a "negative electrode in contact with a fullerene-containing layer", can promote high cycle characteristics and energy density of a magnesium electrode-based electrochemical device.

[0062] When X has an imide (preferably a sulfonylimide) as a molecular structure, the general formula MgX n (wherein n is 1 or 2, and X is a monovalent or divalent anion) forms an imide metal salt. The imide metal salt is preferably a magnesium salt of a perfluoroalkylsulfonylimide (magnesium perfluoroalkylsulfonylimide: Mg((R f1SO2)2N)2). In the general formula, R f1 may be a perfluoroalkyl group having 1 to 10 carbon atoms, a perfluoroalkyl group having 1 to 8 carbon atoms, a perfluoroalkyl group having 1 to 6 carbon atoms, a perfluoroalkyl group having 1 to 4 carbon atoms, a perfluoroalkyl group having 1 to 3 carbon atoms, or a perfluoroalkyl group having 1 to 2 carbon atoms. Such an imide metal salt, in combination with the "negative electrode in contact with the fullerene-containing layer", may promote high cycle characteristics and energy density of the electrochemical device. As an example, the imide metal salt may be magnesium bis(trifluoromethanesulfonyl)imide, i.e., Mg(TFSI)2. Such Mg(TFSI)2 is likely to achieve high cycle characteristics and energy density in the electrochemical device according to this embodiment. In a preferred embodiment, Mg(TFSI)2, in combination with the above halogen metal salt (especially magnesium chloride (MgCl2)) and the "negative electrode in contact with the fullerene-containing layer", may promote high cycle characteristics and energy density of the magnesium electrode-based electrochemical device.

[0063] X may also be another anion, such as magnesium perchlorate (Mg(ClO)), magnesium nitrate (Mg(NO), magnesium sulfate (MgSO), magnesium acetate (Mg(CHCOO)), magnesium trifluoroacetate (Mg(CFCOO)), magnesium tetrafluoroborate (Mg(BF), magnesium tetraphenylborate (Mg(BH)), magnesium hexafluorophosphate (Mg(PF), magnesium hexafluoroarsenate (Mg(AsF), and magnesium salts of perfluoroalkylsulfonic acid (Mg(R). f2 SO3)2), except R f2 is a perfluoroalkyl group).

[0064] In another preferred embodiment, the magnesium salt is a combination of two salts, a halogen metal salt and an imide metal salt. The halogen metal salt may be, for example, magnesium chloride (MgCl2), and the imide salt may be a magnesium salt of perfluoroalkylsulfonylimide, for example, Mg(TFSI)2. MgCl2 and Mg(TFSI)2 are relatively stable Mg salts. Therefore, even if MgCl2 and Mg(TFSI)2 are contained at high concentrations in a straight-chain ether solvent, high safety can be obtained. This can be an advantage different from the conventional electrolyte using AlCl3 and Grignard. Moreover, since MgCl2 and Mg(TFSI)2 have low reactivity, no side reaction occurs other than the electrochemical reaction with sulfur, and a higher capacity can be expected. Furthermore, since the overvoltage of precipitation and dissolution of magnesium is low, the charge and discharge hysteresis can be narrower than that of conventional reports, and in this respect, a high energy density of the device can be expected. Furthermore, since the total Mg salt concentration can be made very high, high ionic conductivity and high rate characteristics can be expected, and the freezing point is lower and the boiling point is higher, which may result in an electrochemical device with a wide temperature range.

[0065] When two types of salts, such as a combination of a halogen metal salt and an imide metal salt, are used as the magnesium salt, the amounts of those substances may be approximately the same (in one specific example, they may be equimolar amounts to each other). Although not particularly limited, in the case of a combination of MgCl2 and Mg(TFSI)2, the molar ratio of MgCl2:Mg(TFSI)2 may be about 1:0.3 to 1.7, for example, about 1:0.4 to 1.6 or about 1:0.5 to 1.5, or, depending on the type of linear ether, it may be about 1:0.7 to 1.3, for example, about 1:0.85 to 1.25.

[0066] In the electrochemical device according to this embodiment, the electrolyte may further contain fullerenes as an additive. In this case, it is preferable to add a small amount of fullerenes to the electrolyte containing a solvent and a magnesium salt contained in the solvent. In this regard, the content of fullerenes in the electrolyte (based on the total amount of the electrolyte) may be less than the content of magnesium salt in the electrolyte (based on the total amount of the electrolyte). In a preferred embodiment, the content of fullerenes in the electrolyte (the amount of fullerenes relative to the total amount of the electrolyte) is 1 / 2 or less, 1 / 5 or less, or 1 / 10 or less, for example, of the content of magnesium salt in the electrolyte (the amount of magnesium salt relative to the total amount of the electrolyte).

[0067] In other words, the molar concentration of fullerenes based on the electrolyte may be less than the content of magnesium salt based on the electrolyte. By way of example only, the content of fullerenes in the electrolyte may be equivalent to a very small amount of addition, such as 0.5M or less (based on the total electrolyte), 0.1M or less (based on the total electrolyte), 0.05M or less (based on the total electrolyte), or 0.01M or less (based on the total electrolyte). Even with such a small content, the present embodiment can achieve the effect of further improving the cycle characteristics and energy density of the magnesium electrode-based electrochemical device.

[0068] The electrolyte according to this embodiment is a so-called "magnesium electrode-based" electrolyte. Even though it is a magnesium electrode-based electrolyte, the addition of "fullerenes" can further improve the cycle characteristics, which is an extremely useful effect. It was assumed that the Mg coordination structure was very fragile, and it was generally thought that it would be difficult to improve the cycle characteristics by using additives. In other words, even though the electrochemical device according to this embodiment is a "magnesium electrode-based" one, the improvement in cycle characteristics and energy density can provide a battery that is more suitable for use in a real environment.

[0069] The electrochemical device according to this embodiment can include an electrolyte layer made of the above-mentioned electrolyte solution and a polymer compound that is a support for holding the electrolyte solution. The polymer compound may be one that is swollen by the electrolytic solution. In this case, the polymer compound swollen by the electrolytic solution may be in a gel state. Examples of such polymer compounds include polyacrylonitrile, polyvinylidene fluoride, copolymers of 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 / or polycarbonate. In particular, if more importance is attached to the viewpoint of electrochemical stability, polyacrylonitrile, polyvinylidene fluoride, polyhexafluoropropylene or polyethylene oxide may be used. The electrolyte layer may be a solid electrolyte layer.

[0070] The magnesium electrode-based electrochemical device according to this embodiment can be configured as a secondary battery, and a conceptual diagram of this case is shown in FIG. 1. As shown in the figure, during charging, magnesium ions (Mg 2+ ) moves from the positive electrode 10 through the electrolyte layer 12 to the negative electrode 11, converting electrical energy into chemical energy and storing the electricity. During discharge, magnesium ions return from the negative electrode 11 through the electrolyte layer 12 to the positive electrode 10, generating electrical energy.

[0071] When the electrochemical device is a battery (primary battery or secondary battery) made of the above-mentioned electrolyte, such a battery can be used as a driving power source or auxiliary power source for, for example, notebook personal computers, PDAs (personal digital assistants), mobile phones, smartphones, parent and child units of cordless phones, video movies, digital still cameras, electronic books, electronic dictionaries, portable music players, radios, headphones, game consoles, navigation systems, memory cards, cardiac pacemakers, hearing aids, power tools, electric shavers, refrigerators, air conditioners, television receivers, stereos, hot water heaters, microwave ovens, dishwashers, washing machines, dryers, lighting equipment, toys, medical equipment, robots, road conditioners, traffic lights, railroad cars, golf carts, electric carts, and / or electric vehicles (including hybrid vehicles). It can also be installed as a power storage power source for buildings such as houses or power generation facilities, or can be used to supply power to these. In electric vehicles, the conversion device that converts power into driving force by supplying power is generally a motor. The control device (control unit) that processes information related to vehicle control includes a control device that displays the remaining battery capacity based on information about the remaining battery capacity. The battery can also be used in a power storage device in a so-called smart grid. Such a power storage device can store power by receiving power from other power sources, as well as supplying power. Examples of other power sources that can be used include thermal power generation, nuclear power generation, hydroelectric power generation, solar cells, wind power generation, geothermal power generation, and / or fuel cells (including biofuel cells).

[0072] The electrochemical device (i.e., secondary battery) according to the present embodiment can be applied to a battery pack having a secondary battery, a control means (or a control unit) for controlling the secondary battery, and an exterior that contains the secondary battery. In such a battery pack, the control means controls, for example, charging / discharging, over-discharging, or over-charging of the secondary battery.

[0073] The electrochemical device according to this embodiment (that is, the secondary battery) can also be applied to electronic devices that receive power from a secondary battery.

[0074] The electrochemical device according to the present embodiment can also be applied to a secondary battery in an electric vehicle having a conversion device that receives power from a secondary battery and converts it into driving force for the vehicle, and a control device (or a control unit) that processes information related to vehicle control based on information about the secondary battery. In such an electric vehicle, the conversion device typically receives power from the secondary battery to drive a motor to generate driving force. Regenerative energy can also be used to drive the motor. In addition, the control device (or the control unit) processes information related to vehicle control based on, for example, the remaining battery charge of the secondary battery. Such electric vehicles include, for example, electric cars, electric motorcycles, electric bicycles, and railroad cars, as well as so-called hybrid cars.

[0075] The electrochemical device (i.e., secondary battery) according to the present embodiment can be applied to a power system configured to receive power from a secondary battery and / or to supply power from a power source to the secondary battery. Such a power system may be any power system as long as it uses power, and includes simple power devices. Such a power system includes, for example, a smart grid, a home energy management system (HEMS), and / or a vehicle, and is also capable of storing power.

[0076] The electrochemical device (i.e., the secondary battery) according to the present embodiment can be applied to a power storage power source having a secondary battery and configured to be connected to an electronic device to which power is supplied. The power storage power source can be used for any purpose, and can basically be used in any power system or power device, for example, in a smart grid.

[0077] More detailed matters regarding the electrochemical device according to this embodiment, further specific aspects and other matters are described above in [Electrolyte solution for electrochemical device according to this embodiment], so description will be omitted to avoid duplication.

[0078] Here, a detailed description will be given of the case where the magnesium electrode-based electrochemical device according to this embodiment is used as a secondary battery. Hereinafter, such a secondary battery will also be referred to as a "magnesium secondary battery."

[0079] The magnesium secondary battery as an electrochemical device according to this embodiment can be applied to, without particular limitation, machines, devices, instruments, equipment, and systems (assembly of a plurality of devices, etc.) that can be used as a power source for driving and operating the battery or as a power storage source for storing power. The magnesium secondary battery (e.g., magnesium-sulfur secondary battery) used as a power source may be a main power source (power source used preferentially) or an auxiliary power source (power source used in place of the main power source or switched from the main power source). When the magnesium secondary battery is used as an auxiliary power source, the main power source is not limited to the magnesium secondary battery.

[0080] Specific applications of magnesium secondary batteries (particularly magnesium-sulfur secondary batteries) include various electronic devices and electrical appliances (including portable electronic devices), such as video cameras, camcorders, digital still cameras, mobile phones, personal computers, television receivers, various display devices, cordless telephones, headphone stereos, music players, portable radios, electronic books and / or electronic newspapers and other electronic paper, and personal digital assistants including PDAs; toys; portable lifestyle appliances such as electric shavers; lighting equipment such as indoor lights; medical electronic devices such as pacemakers and / or hearing aids; storage devices such as memory cards; Examples of applications include, but are not limited to, battery packs used in personal computers, etc. as removable power sources; power tools, such as electric drills and / or electric saws; power storage systems, such as home battery systems that store power in preparation for emergencies, and / or home energy servers (home power storage devices), power supply systems; power storage units and / or backup power sources; electric vehicles, such as electric cars, electric motorcycles, electric bicycles, and / or Segway (registered trademark); and driving power conversion devices (specifically, for example, power motors) for aircraft and / or ships.

[0081] Among them, magnesium secondary batteries (especially magnesium-sulfur secondary batteries) are effectively applied to battery packs, electric vehicles, power storage systems, power supply systems, power tools, electronic devices, and / or electric devices. The battery pack is a power source using a magnesium secondary battery, and is a so-called assembled battery. The electric vehicle is a vehicle that operates (for example, runs) using a magnesium secondary battery as a driving power source, and may be an automobile (for example, a hybrid automobile) that also includes a driving source other than a secondary battery. The power storage system (for example, a power supply system) is a system that uses a magnesium secondary battery as a power storage source. For example, in a home power storage system (power supply system), power is stored in a magnesium secondary battery that is a power storage source, and household electrical appliances can be used by utilizing the power. The power tool is a tool in which a movable part (for example, a drill) is operated using a magnesium secondary battery as a driving power source. The electronic device and the electric device are devices that perform various functions using a magnesium secondary battery as a power source for operation (i.e., a power supply source).

[0082] A cylindrical magnesium secondary battery and a flat laminate film type magnesium secondary battery will be described below.

[0083] FIG. 2 shows a schematic cross-sectional view of a cylindrical magnesium secondary battery 100. In the magnesium secondary battery 100, an electrode structure 121 and a pair of insulating plates 112, 113 are housed inside an electrode structure housing member 111 having a substantially hollow cylindrical shape. The electrode structure 121 can be produced, for example, by stacking a positive electrode 122 and a negative electrode 124 via a separator 126 to obtain an electrode structure, and then winding the electrode structure. The electrode structure housing member (for example, a battery can) 111 has a hollow structure with one end closed and the other end open, and is made of iron (Fe) and / or aluminum (Al) or the like. The pair of insulating plates 112, 113 are arranged to sandwich the electrode structure 121 and extend perpendicularly to the wound circumferential surface of the electrode structure 121. A battery cover 114, a safety valve mechanism 115, and a thermosensitive resistor element (e.g., a PTC element, a positive temperature coefficient element) 116 are crimped to the open end of the electrode structure housing member 111 via a gasket 117, thereby sealing the electrode structure housing member 111. The battery cover 114 is made of, for example, the same material as the electrode structure housing member 111. The safety valve mechanism 115 and the thermosensitive resistor element 116 are provided inside the battery cover 114, and the safety valve mechanism 115 is electrically connected to the battery cover 114 via the thermosensitive resistor element 116. In the safety valve mechanism 115, when the internal pressure exceeds a certain level due to an internal short circuit and / or external heating, the disk plate 115A is inverted. This cuts off the electrical connection between the battery cover 114 and the electrode structure 121. In order to prevent abnormal heat generation due to a large current, the resistance of the thermosensitive resistor element 116 increases with increasing temperature. The gasket 117 is made of, for example, an insulating material. The surface of the gasket 117 may be coated with asphalt or the like.

[0084] A center pin 118 is inserted into the winding center of the electrode structure 121. However, the center pin 118 does not have to be inserted into the winding center. A positive electrode lead portion 123 made of a conductive material such as aluminum is connected to the positive electrode 122. Specifically, the positive electrode lead portion 123 is attached to a positive electrode current collector. A negative electrode lead portion 125 made of a conductive material such as copper is connected to the negative electrode 124. Specifically, the negative electrode lead portion 125 is attached to a negative electrode current collector. The negative electrode lead portion 125 is welded to the electrode structure housing member 111 and is electrically connected to the electrode structure housing member 111. The positive electrode lead portion 123 is welded to the safety valve mechanism 115 and is electrically connected to the battery lid 114. In the example shown in FIG. 2, the negative electrode lead portion 125 is provided in one location (the outermost portion of the wound electrode structure), but it may be provided in two locations (the outermost and innermost portions of the wound electrode structure).

[0085] The electrode structure 121 is formed by stacking a positive electrode 122 in which a positive electrode active material layer is formed on a positive electrode current collector (more specifically, on both sides of the positive electrode current collector) and a negative electrode 124 in which a negative electrode active material layer is formed on a negative electrode current collector (more specifically, on both sides of the negative electrode current collector) via a separator 126. No positive electrode active material layer is formed in the region of the positive electrode current collector to which the positive electrode lead portion 123 is attached, and no negative electrode active material layer is formed in the region of the negative electrode current collector to which the negative electrode lead portion 125 is attached.

[0086] The magnesium secondary battery 100 can be manufactured, for example, according to the following procedure.

[0087] First, a positive electrode active material layer is formed on both sides of a positive electrode current collector, and a negative electrode active material layer is formed on both sides of a negative electrode current collector.

[0088] Next, the positive electrode lead portion 123 is attached to the positive electrode current collector by welding or the like. Also, the negative electrode lead portion 125 is attached to the negative electrode current collector by welding or the like. Next, the positive electrode 122 and the negative electrode 124 are laminated and wound via a separator 126 made of a microporous polyethylene film (more specifically, the electrode structure (i.e., the laminated structure) of the positive electrode 122 / separator 126 / negative electrode 124 / separator 126 is wound) to produce the electrode structure 121, and then a protective tape (not shown) is attached to the outermost periphery. Then, the center pin 118 is inserted into the center of the electrode structure 121. Next, the electrode structure 121 is stored inside the electrode structure storage member 111 while sandwiching the electrode structure 121 between a pair of insulating plates 112 and 113. In this case, the tip of the positive electrode lead portion 123 is attached to the safety valve mechanism 115 and the tip of the negative electrode lead portion 125 is attached to the electrode structure housing member 111 by using a welding method or the like. Then, the electrolyte is injected based on a reduced pressure method to impregnate the separator 126 with the electrolyte. Next, the battery lid 114, the safety valve mechanism 115, and the thermal resistor element 116 are crimped to the open end of the electrode structure housing member 111 via the gasket 117.

[0089] Next, a flat laminate film type secondary battery will be described. A schematic exploded perspective view of such a secondary battery is shown in FIG. 3. In this secondary battery, an electrode structure 221 similar to that described above is basically housed inside an exterior member 200 made of a laminate film. The electrode structure 221 can be produced by laminating a positive electrode and a negative electrode with a separator and an electrolyte layer interposed therebetween, and then winding the laminated structure. A positive electrode lead portion 223 is attached to the positive electrode, and a negative electrode lead portion 225 is attached to the negative electrode. The outermost periphery of the electrode structure 221 is protected by a protective tape. The positive electrode lead portion 223 and the negative electrode lead portion 225 protrude in the same direction from the inside to the outside of the exterior member 200. The positive electrode lead portion 223 is formed of a conductive material such as aluminum. The negative electrode lead portion 225 is formed of a conductive material such as copper, nickel, and / or stainless steel.

[0090] The exterior member 200 is a single film that can be folded in the direction of the arrow R shown in FIG. 3, and a recess (e.g., embossment) for accommodating the electrode structure 221 is provided in a part of the exterior member 200. The exterior member 200 is, for example, a laminate film in which a fusion layer, a metal layer, and a surface protection layer are laminated in this order. In the manufacturing process of the secondary battery, the exterior member 200 is folded so that the fusion layers face each other via the electrode structure 221, and then the outer peripheral edges of the fusion layers are fused together. However, the exterior member 200 may be one in which two separate laminate films are bonded together via an adhesive or the like. The fusion layer is made of, for example, a film of polyethylene and / or polypropylene. The metal layer is made of, for example, an aluminum foil. The surface protection layer is made of, for example, nylon and / or polyethylene terephthalate. Among them, the exterior member 200 is preferably an aluminum laminate film in which a polyethylene film, an aluminum foil, and a nylon film are laminated in this order. However, the exterior member 200 may be a laminate film having another laminated structure, a polymer film such as polypropylene, or a metal film. Specifically, the exterior member 200 may be made of a moisture-resistant aluminum laminate film in which a nylon film, an aluminum foil, and a non-oriented polypropylene film are laminated in this order from the outside.

[0091] In order to prevent the intrusion of outside air, an adhesive film 201 is inserted between the exterior member 200 and the positive electrode lead portion 223, and between the exterior member 200 and the negative electrode lead portion 225. The adhesive film 201 may be made of a material having adhesion to the positive electrode lead portion 223 and the negative electrode lead portion 225, such as a polyolefin resin, and more specifically, may be made of a polyolefin resin such as polyethylene, polypropylene, modified polyethylene, or modified polypropylene.

[0092] Although the above description has been given mainly with secondary batteries in mind, the present disclosure also applies to other electrochemical devices, such as capacitors, air batteries, and fuel cells, which will be described below.

[0093] The electrochemical device according to this embodiment can be used as a capacitor, as shown in a schematic cross-sectional view in Fig. 4. In the capacitor, a positive electrode 31 and a negative electrode 32 are arranged to face each other with a separator 33 impregnated with an electrolytic solution interposed therebetween. A gel electrolyte membrane impregnated with the electrolytic solution according to this embodiment may be arranged on the surface of at least one of the separator 33, the positive electrode 31, and the negative electrode 32. Reference numerals 35 and 36 denote current collectors, and reference numeral 37 denotes a gasket.

[0094] Alternatively, the electrochemical device according to this embodiment can be used as an air battery, as shown in the conceptual diagram of Fig. 5. Such an air battery is composed of, for example, an oxygen selectively permeable membrane 47 that is impermeable to water vapor and selectively permeable to oxygen, an air electrode side current collector 44 made of a conductive porous material, a porous diffusion layer 46 made of a conductive material and disposed between the air electrode side current collector 44 and a porous positive electrode 41, a porous positive electrode 41 containing a conductive material and a catalyst material, a separator and an electrolyte solution (or a solid electrolyte containing an electrolyte solution) 43 that is impermeable to water vapor, a negative electrode 42 that releases magnesium ions, a negative electrode side current collector 45, and an exterior body 48 that houses each of these layers.

[0095] Oxygen 52 in air (e.g., atmospheric air) 51 is selectively permeated by the oxygen selective permeable membrane 47, passes through the air electrode side current collector 44 made of a porous material, is diffused by the diffusion layer 46, and is supplied to the porous positive electrode 41. The progress of oxygen that has permeated the oxygen selective permeable membrane 47 is partially blocked by the air electrode side current collector 44, but oxygen that has passed through the air electrode side current collector 44 is diffused and spreads by the diffusion layer 46, so that it efficiently spreads over the entire porous positive electrode 41, and the supply of oxygen to the entire surface of the porous positive electrode 41 is not hindered by the air electrode side current collector 44. In addition, since the permeation of water vapor is suppressed by the oxygen selective permeable membrane 47, deterioration due to the influence of moisture in the air is reduced, and oxygen is efficiently supplied to the entire porous positive electrode 41, making it possible to increase the battery output and ensure stable long-term use.

[0096] Alternatively, the electrochemical device according to this embodiment can be used as a fuel cell, as shown in the conceptual diagram of Fig. 6. The fuel cell is composed of, for example, a positive electrode 61, a positive electrode electrolyte 62, a positive electrode electrolyte transport pump 63, a fuel flow path 64, a positive electrode electrolyte storage container 65, a negative electrode 71, a negative electrode electrolyte 72, a negative electrode electrolyte transport pump 73, a fuel flow path 74, a negative electrode electrolyte storage container 75, and an ion exchange membrane 66. The positive electrode electrolyte 62 flows (circulates) continuously or intermittently through the fuel flow path 64 via the positive electrode electrolyte storage container 65 and the positive electrode electrolyte transport pump 63, and the negative electrode electrolyte 72 flows or circulates continuously or intermittently through the fuel flow path 74 via the negative electrode electrolyte storage container 75 and the negative electrode electrolyte transport pump 73, and power is generated between the positive electrode 61 and the negative electrode 71. As the positive electrode electrolyte 62, an electrolyte according to this embodiment to which a positive electrode active material has been added can be used, and as the negative electrode electrolyte 72, an electrolyte according to this embodiment to which a negative electrode active material has been added can be used.

[0097] As for the negative electrode in the electrochemical device, a Mg metal plate can be used, and it can also be manufactured by the following method. For example, a Mg electrolytic solution (Mg-EnPS) containing MgCl2 and EnPS (ethyl-n-propyl sulfone) can be prepared, and this Mg electrolytic solution can be used to deposit Mg metal on a Cu foil based on an electrolytic plating method to form a Mg plating layer on the Cu foil as a negative electrode active material layer. Incidentally, the surface of the Mg plating layer obtained by such a method was analyzed based on the XPS method, and it was revealed that Mg, C, O, S, and Cl were present on the surface of the Mg plating layer, and the Mg-derived peak observed in the surface analysis was not split, and a single Mg-derived peak was observed in the range of 40 eV to 60 eV. Furthermore, the surface of the Mg plating layer was dug in the depth direction by about 200 nm based on the Ar sputtering method, and the surface was analyzed based on the XPS method, and it was found that the position and shape of the Mg-derived peak after Ar sputtering were unchanged compared to the position and shape of the peak before Ar sputtering.

[0098] The electrochemical device according to this embodiment can be particularly used as a magnesium secondary battery as described with reference to Figures 1 to 3, and several application examples of such magnesium secondary batteries will be described in more detail below. Note that the configurations of the application examples described below are merely examples, and the configurations can be changed as appropriate.

[0099] The magnesium secondary battery can be used in the form of a battery pack. Such a battery pack is a simplified battery pack (so-called soft pack) using a magnesium secondary battery, and is mounted, for example, in electronic devices such as smartphones. Instead of or in addition to this, a battery pack made up of six magnesium secondary batteries connected in two parallel and three series may be provided. The connection form of the magnesium secondary batteries may be in series, in parallel, or a mixture of both.

[0100] FIG. 7 shows a block diagram showing an example of a circuit configuration when the magnesium secondary battery according to this embodiment is applied to a battery pack. The battery pack includes a cell (for example, a battery pack) 1001, an exterior member, a switch unit 1021, a current detection resistor 1014, a temperature detection element 1016, and a control unit 1010. The switch unit 1021 includes a charge control switch 1022 and a discharge control switch 1024. The battery pack also includes a positive terminal 1031 and a negative terminal 1032, and during charging, the positive terminal 1031 and the negative terminal 1032 are connected to the positive terminal and the negative terminal of a charger, respectively, for charging. During use of an electronic device, the positive terminal 1031 and the negative terminal 1032 are connected to the positive terminal and the negative terminal of the electronic device, respectively, for discharging.

[0101] The cell 1001 is configured by connecting a plurality of magnesium secondary batteries 1002 according to the present disclosure in series and / or parallel. Note that, although Fig. 7 shows a case where six magnesium secondary batteries 1002 are connected in 2 parallel 3 series (2P3S), any other connection method such as p parallel q series (where p and q are integers) may be used.

[0102] The switch unit 1021 includes a charge control switch 1022 and a diode 1023, as well as a discharge control switch 1024 and a diode 1025, and is controlled by the control unit 1010. The diode 1023 has a reverse polarity with respect to the charge current flowing from the positive terminal 1031 to the cell 1001, and a forward polarity with respect to the discharge current flowing from the negative terminal 1032 to the cell 1001. The diode 1025 has a forward polarity with respect to the charge current, and a reverse polarity with respect to the discharge current. In this example, the switch unit is provided on the positive (+) side, but it may be provided on the negative (-) side. The charge control switch 1022 is closed when the battery voltage reaches the overcharge detection voltage, and is controlled by the control unit 1010 so that the charge current does not flow in the current path of the cell 1001. After the charge control switch 1022 is closed, only discharge is possible through the diode 1023. Also, when a large current flows during charging, the switch is controlled by the control unit 1010 to be closed, thereby cutting off the charging current flowing through the current path of the cell 1001. The discharge control switch 1024 is controlled by the control unit 1010 to be closed when the battery voltage reaches the over-discharge detection voltage, thereby preventing the discharge current from flowing through the current path of the cell 1001. After the discharge control switch 1024 is closed, only charging is possible via the diode 1025. Also, when a large current flows during discharging, the switch is controlled by the control unit 1010 to be closed, thereby cutting off the discharge current flowing through the current path of the cell 1001.

[0103] Temperature detection element 1016 is, for example, a thermistor and is provided near cell 1001. Temperature measurement unit 1015 measures the temperature of cell 1001 using temperature detection element 1016 and sends the measurement result to control unit 1010. Voltage measurement unit 1012 measures the voltage of cell 1001 and the voltage of each magnesium secondary battery 1002 that constitutes cell 1001, A / D converts the measurement result, and sends it to control unit 1010. Current measurement unit 1013 measures the current using current detection resistor 1014 and sends the measurement result to control unit 1010.

[0104] The switch control unit 1020 controls the charge control switch 1022 and the discharge control switch 1024 of the switch unit 1021 based on the voltage and current sent from the voltage measurement unit 1012 and the current measurement unit 1013. When the voltage of any one of the magnesium secondary batteries 1002 becomes equal to or lower than the overcharge detection voltage or the overdischarge detection voltage, and / or when a large current flows suddenly, the switch control unit 1020 sends a control signal to the switch unit 1021 to prevent overcharging, overdischarging, and overcurrent charging and discharging. The charge control switch 1022 and the discharge control switch 1024 can be composed of semiconductor switches such as MOSFETs. In this case, the diodes 1023 and 1025 are composed of the parasitic diodes of the MOSFETs. When a p-channel FET is used as the MOSFET, the switch control unit 1020 supplies a control signal DO and a control signal CO to the gates of the charge control switch 1022 and the discharge control switch 1024, respectively. The charge control switch 1022 and the discharge control switch 1024 are made conductive by a gate potential that is lower than the source potential by a predetermined value or more. That is, in normal charging and discharging operations, the control signals CO and DO are set to low level, and the charge control switch 1022 and the discharge control switch 1024 are made conductive. Then, for example, in the event of overcharging or overdischarging, the control signals CO and DO are set to high level, and the charge control switch 1022 and the discharge control switch 1024 are made closed.

[0105] The memory 1011 is composed of, for example, an EPROM (Erasable Programmable Read Only Memory), which is a non-volatile memory. The memory 1011 stores in advance values ​​calculated by the control unit 1010 and / or the internal resistance value of each magnesium secondary battery 1002 in its initial state measured during the manufacturing process, and can be rewritten as necessary. Also, by storing the full charge capacity of the magnesium secondary battery 1002, Memory 1011 Together with the control unit 1010, for example, the remaining capacity can be calculated.

[0106] The temperature measurement unit 1015 measures the temperature using a temperature detection element 1016, and performs charge / discharge control in the event of abnormal heat generation, and also performs correction in the calculation of remaining capacity.

[0107] Next, application of magnesium secondary batteries to electric vehicles will be described. FIG. 8A shows a block diagram showing the configuration of an electric vehicle such as a hybrid car, which is an example of an electric vehicle. The electric vehicle includes, for example, a control unit 2001, various sensors 2002, a power source 2003, an engine 2010, a generator 2011, inverters 2012 and 2013, a driving motor 2014, a differential gear 2015, a transmission 2016, and a clutch 2017 inside a metal housing 2000. In addition, the electric vehicle includes, for example, a front wheel drive shaft 2021, front wheels 2022, a rear wheel drive shaft 2023, and a rear wheel 2024 connected to the differential gear 2015 and / or the transmission 2016.

[0108] The electric vehicle can run using, for example, either the engine 2010 or the motor 2014 as a drive source. The engine 2010 is a main power source, and is, for example, a gasoline engine or the like. When the engine 2010 is used as a power source, the drive force (for example, rotational force) of the engine 2010 is transmitted to the front wheels 2022 or the rear wheels 2024 via, for example, a differential device 2015, a transmission 2016, and a clutch 2017, which are drive units. The rotational force of the engine 2010 is also transmitted to the generator 2011, which generates AC power using the rotational force, and the AC power is converted into DC power via the inverter 2013 and stored in the power source 2003. On the other hand, when the motor 2014, which is a conversion unit, is used as a power source, the power (for example, DC power) supplied from the power source 2003 is converted into AC power via the inverter 2012, and the AC power is used to drive the motor 2014. The driving force (eg, rotational force) converted from electric power by the motor 2014 is transmitted to the front wheels 2022 or the rear wheels 2024 via, for example, a differential gear 2015, a transmission 2016, and a clutch 2017, which are the driving parts.

[0109] When the electric vehicle decelerates via a braking mechanism (not shown), the resistance force generated during deceleration is transmitted to the motor 2014 as a rotational force, and the motor 2014 may generate AC power by utilizing the rotational force. The AC power is converted into DC power via the inverter 2012, and the regenerative DC power is stored in the power source 2003.

[0110] The control unit 2001 controls the operation of the entire electric vehicle, and includes, for example, a CPU. The power source 2003 can include one or more magnesium secondary batteries (not shown) according to the present invention. The power source 2003 can also be configured to be connected to an external power source and accumulate power by receiving power from the external power source. The various sensors 2002 are used, for example, to control the number of revolutions of the engine 2010 and to control the opening degree (throttle opening degree) of a throttle valve (not shown). The various sensors 2002 include, for example, a speed sensor, an acceleration sensor, and / or an engine revolution sensor.

[0111] Although the electric vehicle has been described as a hybrid car, the electric vehicle may be a vehicle (eg, an electric car) that operates using only the power source 2003 and the motor 2014 without using the engine 2010.

[0112] Next, application of the magnesium secondary battery to a power storage system (for example, a power supply system) will be described. A block diagram showing the configuration of a power storage system (for example, a power supply system) is shown in Fig. 8B. The power storage system includes a control unit 3001, a power source 3002, a smart meter 3003, and a power hub 3004 inside a house 3000 such as a general residence or a commercial building.

[0113] The power source 3002 is connected to an electric device (e.g., electronic device) 3010 installed inside the house 3000, and can be connected to an electric vehicle 3011 parked outside the house 3000. The power source 3002 is also connected to a private generator 3021 installed in the house 3000 via a power hub 3004, and can be connected to an external centralized power system 3022 via a smart meter 3003 and the power hub 3004. The electric device (e.g., electronic device) 3010 includes, for example, one or more home appliances. Examples of the home appliances include a refrigerator, an air conditioner, a television receiver, and / or a water heater. The private generator 3021 is composed of, for example, a solar power generator and / or a wind power generator. Examples of the electric vehicle 3011 include an electric car, a hybrid car, an electric motorcycle, an electric bicycle, and / or a Segway (registered trademark). Examples of the centralized power system 3022 include commercial power sources, power generation equipment, power transmission networks, and / or smart grids (e.g., next-generation power transmission networks), and also include, for example, thermal power plants, nuclear power plants, hydroelectric power plants, and / or wind power plants, and examples of power generation equipment provided in the centralized power system 3022 include, but are not limited to, various solar cells, fuel cells, wind power generation equipment, micro-hydroelectric power generation equipment, and / or geothermal power generation equipment.

[0114] The control unit 3001 controls the operation of the entire power storage system (including the usage state of the power source 3002) and includes, for example, a CPU. The power source 3002 can include one or more magnesium secondary batteries (not shown) according to the present invention. The smart meter 3003 is, for example, a network-compatible power meter installed in a house 3000 on the power demand side, and is capable of communicating with the power supply side. The smart meter 3003 can control the balance between supply and demand in the house 3000 while communicating with the outside, thereby enabling an efficient and stable energy supply.

[0115] In such a power storage system, for example, power is stored in a power source 3002 from a centralized power system 3022, which is an external power source, via a smart meter 3003 and a power hub 3004, and power is also stored in the power source 3002 from a private power generator 3021, which is an independent power source, via the power hub 3004. The power stored in the power source 3002 is supplied to an electric device (e.g., an electronic device) 3010 and an electric vehicle 3011 in response to an instruction from a control unit 3001, thereby enabling the electric device (e.g., an electronic device) 3010 to operate and enabling the electric vehicle 3011 to be charged. In other words, the power storage system is a system that enables the storage and supply of power in the house 3000 using the power source 3002.

[0116] The power stored in the power source 3002 can be used as desired. Therefore, for example, power can be stored in the power source 3002 from the centralized power grid 3022 late at night when electricity rates are low, and the power stored in the power source 3002 can be used during the day when electricity rates are high.

[0117] The power storage system described above may be installed for each house (for example, one household) or for multiple houses (for example, multiple households).

[0118] Next, application of magnesium secondary batteries to power tools will be described. A block diagram showing the configuration of a power tool is shown in FIG. 8C. The power tool is, for example, an electric drill, and includes a control unit 4001 and a power source 4002 inside a tool body 4000 made of a plastic material or the like. A drill part 4003, which is a movable part, is rotatably attached to the tool body 4000. The control unit 4001 controls the operation of the entire power tool (including the use state of the power source 4002), and includes, for example, a CPU or the like. The power source 4002 can include one or more magnesium secondary batteries (not shown) according to the present invention. The control unit 4001 supplies power from the power source 4002 to the drill part 4003 in response to the operation of an operation switch (not shown).

[0119] Although the embodiments of the present invention have been described above, they are merely typical examples. Therefore, the present invention is not limited to these, and those skilled in the art will easily understand that various aspects are possible without departing from the spirit of the present invention. For example, the present invention can be modified in design without departing from the spirit of the present invention, and the features described in each embodiment can be combined.

[0120] For example, the composition of the electrolyte solution, the raw materials used in the production, the production method, the production conditions, the properties of the electrolyte solution, and the configuration or structure of the electrochemical device or battery described above are merely examples and are not limited thereto, and may be appropriately changed. The electrolyte solution according to this embodiment may also be mixed with an organic polymer (e.g., polyethylene oxide, polyacrylonitrile, and / or polyvinylidene fluoride (PVdF)) to be used as a gel electrolyte.

[0121] The effects described in this specification are merely examples, and are not necessarily limited to these effects, and there may be additional effects.

[0122] In the electrochemical device according to this embodiment, the electrolyte solution comprises a solvent and a magnesium salt contained in the solvent, and the presence of components that may be unavoidably or accidentally mixed in during preparation, storage and / or use of the electrolyte solution (for example, components present in trace or extremely trace amounts, components that a person skilled in the art would recognize as being in trace or extremely trace amounts) is acceptable. EXAMPLES

[0123] The present invention will be described in more detail below using examples, but the present invention is not limited to these examples.

[0124] In order to confirm the effects of the present invention, the following verification test was carried out. Specifically, the verification test was carried out to determine whether the contact of a magnesium-containing electrode with a fullerene-containing layer contributes to improving the energy density and cycle characteristics of an electrochemical device.

[0125] [Energy density] Example 1 As an electrochemical device, a magnesium-sulfur secondary battery having the following specifications was fabricated. (Specifications of Magnesium-Sulfur Secondary Battery) Negative electrode: Electrode containing magnesium (Mg plate with a diameter of 15 mm and a thickness of 200 μm (purity 99.9%, magnesium plate manufactured by Rikazai Co., Ltd.), the Mg plate is coated with fullerene) ● Positive electrode: Sulfur electrode (an electrode containing 10% by mass of S8 sulfur, product number 197-17892, manufactured by Wako Pure Chemical Industries, Ltd.; a conductive additive, Ketjen Black (KB), manufactured by Lion Corporation, containing 65% by mass of product number ECP600JD; a binder, polytetrafluoroethylene (PTFE), manufactured by Asahi Glass Co., Ltd., containing 25% by weight of product number CD-1E; and a current collector, containing nickel (φ15 mm)) ●Separator: Glass fiber (Advantec glass fiber, part number GC50) ●Electrolyte Magnesium salts: halogen metal salts (MgCl2 (anhydrous): Sigma-Aldrich, product number 449172, 0.8M) and imide metal salts (Mg(TFSI)2: Toyama Pharmaceutical Co., Ltd., product number MGTFSI, 0.8M) · Linear ether solvent: Diethylene glycol dimethyl ether (dimethoxyethane) (super dehydrated product), (Toyama Pharmaceutical Co., Ltd., product number G2) "Fullerenes": C 60 Fullerene 0.01M (Sigma-Aldrich, product number 379646) ● Secondary battery type: Coin battery CR2016 type

[0126] FIG. 9 shows a schematic development of the battery produced. The positive electrode 23 was made by mixing 10% by mass of sulfur (S8), 60% by mass of Ketjen Black as a conductive assistant, and 30% by mass of polytetrafluoroethylene (PTFE) as a binder in an agate mortar. The mixture was then rolled and molded about 10 times using a roller compactor while being mixed with acetone. The mixture was then dried in a vacuum at 70° C. for 12 hours. Thus, the positive electrode 23 was obtained. A nickel mesh was used as a current collector and attached to the positive electrode.

[0127] Fullerenes were dispersed in toluene to prepare a fullerene suspension. The fullerene suspension was dropped onto an Mg plate to form a coating film. The coating film was dried to form a fullerene-containing layer on the Mg plate. In this way, a negative electrode coated with a fullerene-containing layer was produced. When the surface of the Mg plate was observed with an optical microscope, it was confirmed that the surface of the Mg plate was discontinuously coated with a fullerene-containing layer.

[0128] A gasket 22 was placed on a coin battery can 21, and a positive electrode 23 made of sulfur, a glass fiber separator 24, a negative electrode 25 made of a Mg plate with a diameter of 15 mm and a thickness of 200 μm, a spacer 26 made of a stainless steel plate with a thickness of 0.5 mm, and a coin battery lid 27 were laminated in this order, and then the coin battery can 21 was crimped and sealed. The spacer 26 was spot welded to the coin battery lid 27 in advance. The electrolyte was used in a form that was impregnated in the separator 24 of the coin battery 20.

[0129] The prepared battery was charged and discharged under the following conditions: (Charge / discharge conditions) Discharge conditions: CC discharge 0.1mA / 0.7V cutoff Charging conditions: CC charging 0.1mA / 2.2V cutoff Temperature: 25℃

[0130] Example 2 A magnesium-sulfur secondary battery was produced in the same manner as in Example 1, except that a Mg plate (a Mg plate not coated with a fullerene-containing layer) was used instead of the "Mg plate coated with a fullerene-containing layer" in Example 1, and a "separator containing fullerene" was used instead of the "separator" in Example 1, and the battery was charged and discharged in the same manner as in Example 1. The separator containing fullerene was prepared by dropping the fullerene suspension prepared in Example 1 onto a separator (one surface of a flat separator) and drying it. When the prepared separator was observed with an optical microscope, it was confirmed that the surface of the separator was discontinuously covered with a fullerene-containing layer. In preparing the coin battery, the separator was laminated on the negative electrode so that the surface on which the fullerene-containing layer was formed was in contact with the negative electrode.

[0131] Comparative Example 1 A magnesium-sulfur secondary battery was prepared in the same manner as in Example 1, except that a Mg plate (a Mg plate not coated with a fullerene-containing layer) was used instead of the "Mg plate coated with a fullerene-containing layer" in Example 1, and a sulfur electrode coated with a fullerene-containing layer was used instead of the sulfur electrode (a sulfur electrode not coated with a fullerene-containing layer). The battery was then charged and discharged in the same manner as in Example 1. 。

[0132] (result) The results are shown in Figures 10 to 12. Figures 10 to 12 show charge / discharge curves in Example 1, Example 2, and Comparative Example 1, respectively. The numbers attached to the charge / discharge curves indicate the cycle numbers. It was found that the initial (first cycle) discharge curves of Examples 1 and 2 were larger than the discharge curve of Comparative Example 1. In other words, it was found that the discharge voltages of Examples 1 and 2 were higher than the discharge voltage of Comparative Example 1.

[0133] From the above results, it was revealed that when the fullerene-containing layer is a separator or a coating layer that covers the negative electrode, the negative electrode is in contact with the fullerene-containing layer, and thus the voltage drop due to the negative electrode overvoltage during the initial discharge of the magnesium-sulfur secondary battery (electrochemical device) is suppressed, and the energy density is improved. This contributes to an electrochemical device having a high energy density.

[0134] [Cycle characteristics] Example 3 From the charge / discharge curves obtained in Example 1, the relationship between the specific capacity and the number of cycles (the decay curve shown by the solid line in FIG. 13) was obtained.

[0135] Comparative Example 2 A magnesium-sulfur secondary battery was produced in the same manner as in Example 3, except that a Mg plate (a Mg plate not coated with a fullerene-containing layer) was used instead of the "Mg plate coated with a fullerene-containing layer" in Example 3, and the battery was charged and discharged in the same manner as in Example 3. From the resulting charge and discharge curves, the relationship between the specific capacity and the number of cycles (the decay curve shown by the dashed line in FIG. 13) was obtained. A fullerene suspension was prepared in the same manner as in Example 1. The fullerene suspension was dropped onto a sulfur electrode to form a coating film. The coating film was dried to form a fullerene-containing layer on the sulfur electrode (positive electrode). In this way, a positive electrode covered with a fullerene-containing layer was produced. When the surface of the sulfur electrode was observed with an optical microscope, it was confirmed that the surface of the sulfur electrode was discontinuously covered with a fullerene-containing layer.

[0136] (result) The results are shown in FIG. 13. The decay curves indicated by the solid line and the dashed line in FIG. 13 are the decay curves in Example 3 and Comparative Example 2, respectively. It was found that the decay curve in Example 3 decayed more gently with an increase in the number of cycles compared to the decay curve in Comparative Example 2. The ratio of the specific capacity at the 10th cycle discharge to the specific capacity at the initial (1st cycle) discharge (discharge capacity retention rate) was 65% in Example 3 and 50% in Comparative Example 2. It was found that the discharge capacity retention rate in Example 3 was 15% higher than that in Comparative Example 2.

[0137] From the above results, it is clear that when the fullerene-containing layer is a separator or a coating layer that covers the negative electrode, the negative electrode is in contact with the fullerene-containing layer, and thus the decrease in discharge capacity due to cycles of the magnesium-sulfur secondary battery (electrochemical device) is suppressed, and the cycle characteristics are improved, which contributes to the extension of the life of the electrochemical device. [Industrial Applicability]

[0138] The electrochemical device of the present invention can be used in various fields where energy is extracted by utilizing electrochemical reactions. By way of example only, the electrochemical device of the present invention can be used as a secondary battery, but is not limited to this, and can be used as various electrochemical devices such as a capacitor, an air battery, and a fuel cell. [Explanation of symbols]

[0139] 1 negative electrode, 2 fullerene-containing layer, 2a fullerene particle, 10 positive electrode, 11 negative electrode, 12 electrolyte layer, 20 coin battery, 21 coin battery can, 22 gasket, 23 positive electrode, 24 separator, 25 negative electrode, 26 spacer, 27 coin battery cover, 31 positive electrode, 32 negative electrode, 33 separator, 35, 36 current collector, 37 gasket, 41 porous positive electrode, 42 negative electrode, 43 separator and electrolyte, 44 ·Air electrode side current collector, 45···Anode side current collector, 46···Diffusion layer, 47···Oxygen selective permeable membrane, 48···Exterior body, 51···Air (atmosphere), 52···Oxygen, 61···Positive electrode, 62···Positive electrode electrolyte, 63···Positive electrode electrolyte transport pump, 64···Fuel flow path, 65···Positive electrode electrolyte storage container, 71···Anode, 72···Anode electrolyte, 73···Anode electrolyte transport pump, 74···Fuel flow path, 75···Anode electrolyte storage container, 66···Ion exchange membrane, 100···Magnesium secondary battery, 111··· Electrode structure housing member (battery can), 112, 113...insulating plate, 114...battery lid, 115...safety valve mechanism, 115A...disk plate, 116...thermal resistance element (PTC element), 117...gasket, 118...center pin, 121...electrode structure, 122...positive electrode, 123...positive electrode lead portion, 124...negative electrode, 125...negative electrode lead portion, 126...separator, 200...outer packaging member, 201...adhesive film, 221...electrode structure, 223...positive electrode lead portion, 225...negative Electrode lead section, 1001...cell (battery assembly), 1002...magnesium secondary battery, 1010...control section, 1011...memory, 1012...voltage measurement section, 1013...current measurement section, 1014...current detection resistor, 1015...temperature measurement section, 1016...temperature detection element, 1020...switch control section, 1021...switch section, 1022...charge control switch, 1024...discharge control switch, 1023, 1025...diode, 1031...positive terminal, 1032...negative terminal, CO,DO···Control signal, 2000···Housing, 2001···Control unit, 2002···Various sensors, 2003···Power supply, 2010···Engine, 2011···Generator, 2012,2013···Inverter, 2014···Drive motor, 2015···Differential device, 2016···Transmission, 2017···Clutch, 2021···Front drive shaft, 2022···Front wheels, 2023· ··Rear wheel drive shaft, 2024···Rear wheel, 3000···House, 3001···Control unit, 3002···Power source, 3003···Smart meter, 3004···Power hub, 3010···Electric equipment (electronic equipment), 3011···Electric vehicle, 3021···Private generator, 3022···Centralized power system, 4000···Tool body, 4001···Control unit, 4002···Power source, 4003···Drill unit,

Claims

1. An electrochemical device comprising: a negative electrode, a positive electrode, a separator disposed between the negative electrode and the positive electrode, and an electrolyte solution filling a space between the negative electrode, the positive electrode, and the separator, the negative electrode is an electrode containing magnesium, the electrolytic solution comprises a solvent and a magnesium salt contained in the solvent, the negative electrode is in contact with a fullerene-containing layer containing fullerenes, The electrochemical device, wherein the fullerene-containing layer continuously or partially covers the separator surface or the negative electrode surface.

2. 10. The electrochemical device of claim 1, wherein the fullerene-containing layer is a solid.

3. 3. The electrochemical device according to claim 1, wherein the fullerene-containing layer covers the surface of the separator.

4. 4. The electrochemical device according to claim 1, wherein the fullerene-containing layer is a coating layer that coats the negative electrode.

5. the fullerene-containing layer contains particles containing the fullerenes, 5. The electrochemical device according to claim 1, wherein at least a portion of the particles containing fullerenes are layered on a surface of the negative electrode.

6. The fullerenes are C ６０ , C ７０ , C ８４ , C ９０ and C ９６ 6. The electrochemical device according to claim 1, wherein the fullerene is at least one kind selected from the group consisting of:

7. 7. The electrochemical device according to claim 1, wherein the magnesium salt is at least one magnesium salt selected from the group consisting of magnesium halide, magnesium perfluoroalkylsulfonylimide, and magnesium bishexaalkyldisilazide.

8. 8. The electrochemical device according to claim 1, wherein the solvent is at least one solvent selected from the group consisting of linear ethers, cyclic ethers, and dialkyl sulfones.

9. The linear ether has the general formula: 【Chemical 1】 [In the above general formula, R′ and R″ each independently represent a hydrocarbon group having from 1 to 10 carbon atoms, and may be the same or different, and n represents an integer of from 1 to 10.] 9. The electrochemical device according to claim 8, wherein the ethyleneoxy group is an ether having an ethyleneoxy structural unit represented by the formula:

10. 10. The electrochemical device according to claim 1, wherein the positive electrode is a sulfur electrode containing sulfur.

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