Lithium secondary battery

Abstract

The present invention provides a lithium secondary battery which has a high energy density and excellent cycle characteristics. The present invention pertains to a lithium secondary battery comprising a positive electrode, a negative electrode that does not include negative electrode active material, and an electrolyte, the negative electrode being coated, on at least a portion of the surface facing the positive electrode, with a compound that contains an aromatic ring in which two or more elements selected from the group consisting of N, S, and O are independently bonded, and the electrolyte comprising a lithium salt and a compound represented by formula (1) and / or a compound represented by formula (2).

Description

[Technical Field]

[0001] The present invention relates to a lithium secondary battery. [Background technology]

[0002] In recent years, technology for converting natural energy such as solar or wind power into electrical energy has been attracting attention. Accordingly, various secondary batteries have been developed as energy storage devices that are highly safe and can store large amounts of electrical energy.

[0003] Among these, lithium secondary batteries, which charge and discharge by transferring lithium ions between a positive electrode and a negative electrode, are known to exhibit high voltage and high energy density. A typical lithium secondary battery is the lithium-ion secondary battery (LIB), which has active materials capable of retaining lithium elements in the positive electrode and negative electrode, and charges and discharges by transferring lithium ions between the positive electrode active material and the negative electrode active material.

[0004] Furthermore, in order to achieve a high energy density, lithium secondary batteries (lithium metal batteries; LMBs) have been developed that use lithium metal as the negative electrode active material instead of materials that can insert lithium ions, such as carbon materials. For example, Patent Document 1 discloses a rechargeable battery that uses a lithium metal-based electrode as the negative electrode.

[0005] Furthermore, with the aim of achieving even higher energy density and improving productivity, lithium secondary batteries have been developed that use negative electrodes that do not have negative electrode active materials such as carbon materials or lithium metal. For example, Patent Document 2 discloses a lithium secondary battery that includes a positive electrode, a negative electrode, a separator membrane interposed between them, and an electrolyte, in which metal particles are formed on the negative electrode current collector of the negative electrode, and these particles are transferred from the positive electrode upon charging to form lithium metal on the negative electrode current collector within the negative electrode. Patent Document 2 discloses that such a lithium secondary battery can solve problems caused by the reactivity of lithium metal and problems that arise during the assembly process, thereby providing a lithium secondary battery with improved performance and lifespan. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] Special Publication No. 2006-500755 [Patent Document 2] Special Publication No. 2019-505971 Summary of the Invention [Problem to be solved by the invention]

[0007] However, the present inventors have conducted detailed studies of conventional batteries, including those described in the above patent documents, and have found that at least one of the energy density and cycle characteristics is insufficient.

[0008] For example, it is difficult to achieve a sufficiently high energy density in a lithium secondary battery equipped with a negative electrode having a negative electrode active material due to the volume and mass occupied by the negative electrode active material. Furthermore, in conventional anode-free lithium secondary batteries equipped with a negative electrode without a negative electrode active material, repeated charge and discharge easily causes dendritic lithium metal to form on the surface of the negative electrode, which easily leads to short circuits and / or capacity reduction, resulting in insufficient cycle characteristics.

[0009] The present invention has been made in view of the above problems, and has as its object to provide a lithium secondary battery having high energy density and excellent cycle characteristics. [Means for solving the problem]

[0010] A lithium secondary battery according to one embodiment of the present invention includes a positive electrode, a negative electrode having no negative electrode active material, and an electrolyte solution, wherein at least a portion of the surface of the negative electrode facing the positive electrode is coated with a compound including an aromatic ring to which two or more elements selected from the group consisting of N, S, and O are independently bonded, and the electrolyte solution includes a lithium salt and at least one of a compound represented by the following formula (1) and a compound represented by the following formula (2): [ka] (In formula (1), R 1 is an alkyl group which may contain an ether bond, and R 2 is a fluorine-substituted alkylene group, and R 3 is an alkyl group which may contain an ether bond. [ka] (In formula (2), R 4 is a fluorine-substituted alkyl group, and R 5 is an alkylene group which may contain an ether bond, and R 6 represents an alkyl group which may be substituted with fluorine.

[0011] The lithium secondary battery of the above embodiment uses a negative electrode that does not have a negative electrode active material, and therefore has a smaller overall volume and mass and, in principle, a higher energy density than a lithium secondary battery that has a negative electrode active material. The lithium secondary battery of the above embodiment is charged and discharged by depositing lithium metal on the surface of the negative electrode and electrolytically dissolving the deposited lithium metal.

[0012] Furthermore, by using a negative electrode in which at least a portion of the surface facing the positive electrode is coated with a compound containing an aromatic ring to which two or more elements selected from the group consisting of N, S, and O are independently bonded, deposition of lithium metal on the negative electrode surface and its dissolution are compensated for, and it is presumed that the lithium secondary battery of the above embodiment has excellent cycle characteristics.

[0013] Furthermore, the present inventors have discovered that, in addition to the above-described configuration, the above-described lithium secondary battery can achieve both high energy density and excellent cycle characteristics when the electrolyte solution contains at least one of the compound represented by the above formula (1) and the compound represented by the above formula (2). While the reason for this is unclear, it is presumed that the inclusion of a compound having two or more ether bonds in the electrolyte solution improves the solubility of the lithium salt, and that the presence of fluorinated sites in the compound makes it easier to form a solid electrolyte interface layer (hereinafter also referred to as "SEI layer") on the surface of the negative electrode, and / or that the SEI layer has better quality. However, the reasons for this are not limited to those described above.

[0014] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably further contains an ether compound having no fluorine atoms. According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0015] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably further contains a chain fluorine compound having at least one of the monovalent groups represented by the following formula (A) or formula (B): According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics. [ka] [ka] (In formulas (A) and (B), the wavy lines represent bonding sites in monovalent groups.)

[0016] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably contains both the compound represented by the formula (1) and the compound represented by the formula (2). According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0017] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably contains a compound represented by the formula (1) above, and 2 In the present invention, the ratio (F / (F+H)) of the number of fluorine atoms (F) to the total number of fluorine atoms and hydrogen atoms (F+H) is 0.30 or more and 0.80 or less. According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0018] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably contains a compound represented by the formula (1) above, and 2 In the formula (I), at least one of the carbon atoms bonded to the oxygen atoms at both ends does not have a fluorine atom. According to this embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0019] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably contains a compound represented by the formula (2), and the R 4 In the present invention, the ratio (F / (F+H)) of the number of fluorine atoms (F) to the total number of fluorine atoms and hydrogen atoms (F+H) is 0.40 or more and 0.90 or less. According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0020] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably contains a compound represented by the formula (2), and the R 5 The number of carbon atoms in the formula is from 1 to 4. According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0021] In the lithium secondary battery according to one embodiment of the present invention, the electrolyte preferably contains a compound represented by the formula (2), and the R 4 In this case, the carbon atom bonded to the oxygen atom does not have a fluorine atom. According to this embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0022] In the lithium secondary battery according to one embodiment of the present invention, the lithium salt preferably contains at least LiN(SO2F)2. According to such an embodiment, the lithium secondary battery tends to have even more excellent cycle characteristics.

[0023] In the lithium secondary battery according to one embodiment of the present invention, preferably, in the compound containing an aromatic ring, one or more nitrogen atoms are bonded to the aromatic ring. This configuration further enhances the strength of the interaction between the negative electrode coating agent and lithium ions, which tends to further improve the cycle characteristics of the lithium secondary battery.

[0024] In the lithium secondary battery according to one embodiment of the present invention, the aromatic ring-containing compound is preferably at least one selected from the group consisting of benzotriazole, benzimidazole, benzimidazole thiol, benzoxazole, benzoxazole thiol, benzothiazole, mercaptobenzothiazole, and derivatives thereof. According to such an embodiment, the electrical connection between the negative electrode and the lithium ions coordinated with the negative electrode coating agent is further improved, which tends to further improve the cycle characteristics of the lithium secondary battery. [Effects of the Invention]

[0025] According to the present invention, it is possible to provide a lithium secondary battery having high energy density and excellent cycle characteristics. [Brief explanation of the drawings]

[0026] [Figure 1] 1 is a schematic cross-sectional view of a lithium secondary battery according to an embodiment of the present invention. [Figure 2] 1 is a schematic cross-sectional view of a lithium secondary battery according to an embodiment of the present invention; DETAILED DESCRIPTION OF THE INVENTION

[0027] Hereinafter, an embodiment of the present invention (hereinafter referred to as "the present embodiment") will be described in detail with reference to the drawings as necessary. In the drawings, the same elements will be given the same reference numerals, and duplicate explanations will be omitted. Furthermore, unless otherwise specified, positional relationships such as up, down, left, and right will be based on the positional relationships shown in the drawings. Furthermore, the dimensional ratios of the drawings are not limited to those shown in the drawings.

[0028] [Present embodiment] (lithium secondary battery) Fig. 1 is a schematic cross-sectional view of a lithium secondary battery according to this embodiment. As shown in Fig. 1, the lithium secondary battery 100 of this embodiment includes a positive electrode 120, a negative electrode 140 that does not have a negative electrode active material, a separator 130 disposed between the positive electrode 120 and the negative electrode 140, and an electrolyte solution not shown in Fig. 1. The positive electrode 120 has a positive electrode current collector 110 on the surface opposite to the surface facing the separator 130. Each component of the lithium secondary battery 100 will be described below.

[0029] (Negative electrode) The negative electrode 140 does not have a negative electrode active material. In this specification, the term "negative electrode active material" refers to a material that causes an electrode reaction, i.e., an oxidation reaction and a reduction reaction, at the negative electrode. Specifically, the negative electrode active material of this embodiment includes lithium metal and a host material of lithium element (lithium ion or lithium metal). The host material of lithium element refers to a material provided to hold lithium ion or lithium metal in the negative electrode. The mechanism of such holding includes, but is not limited to, intercalation, alloying, and metal cluster occlusion, and is typically intercalation.

[0030] In the lithium secondary battery of this embodiment, the negative electrode does not have a negative electrode active material before the initial charge of the battery, so that lithium metal is deposited on the negative electrode and the deposited lithium metal is electrolytically dissolved, thereby performing charge and discharge. Therefore, compared with a lithium secondary battery having a negative electrode active material, the lithium secondary battery of this embodiment has a reduced volume occupied by the negative electrode active material and a reduced mass of the negative electrode active material, resulting in a smaller overall volume and mass of the battery, and therefore has a higher energy density in principle.

[0031] In the lithium secondary battery 100 of this embodiment, the negative electrode 140 does not contain a negative electrode active material before initial charging of the battery, and lithium metal is deposited on the negative electrode when the battery is charged, and the deposited lithium metal is electrolytically dissolved when the battery is discharged. Therefore, in the lithium secondary battery of this embodiment, the negative electrode functions as a negative electrode current collector.

[0032] In this specification, "lithium metal is deposited on the negative electrode" means that lithium metal is deposited on at least one of the surface of the negative electrode coated with the negative electrode coating agent and the surface of a solid electrolyte interface layer (SEI layer) (described later) formed on the surface of the negative electrode. Therefore, in the lithium secondary battery 100, lithium metal may be deposited on, for example, the surface of the negative electrode 140 coated with the negative electrode coating agent (the interface between the negative electrode 140 and the separator 130).

[0033] The lithium secondary battery 100 of this embodiment differs from a lithium ion battery (LIB) and a lithium metal battery (LMB) in the following respects. In a lithium ion battery (LIB), the negative electrode has a host material of lithium element (lithium ion or lithium metal), and when the battery is charged, the material is filled with lithium element, and when the host material releases the lithium element, the battery is discharged. LIBs differ from the lithium secondary battery 100 of this embodiment in that the negative electrode has a host material of lithium element. A lithium metal battery (LMB) is manufactured using an electrode having lithium metal on its surface or elemental lithium metal as the negative electrode. That is, an LMB differs from the lithium secondary battery 100 of this embodiment in that the negative electrode has lithium metal as the negative electrode active material immediately after the battery is assembled, i.e., before the initial charge of the battery. While an LMB uses an electrode containing highly flammable and reactive lithium metal in its manufacture, the lithium secondary battery 100 of this embodiment uses a negative electrode that does not contain lithium metal, and therefore is safer and more manufacturable.

[0034] In this specification, the anode "has no anode active material" means that the anode 140 has no or substantially no anode active material. The anode 140 has substantially no anode active material means that the content of the anode active material in the anode 140 is 10 mass% or less relative to the entire anode. The content of the anode active material in the anode is preferably 5.0 mass% or less relative to the entire anode 140, and may be 1.0 mass% or less, 0.1 mass% or less, or 0.0 mass% or less. When the anode 140 has no anode active material or the content of the anode active material in the anode 140 is within the above range, the energy density of the lithium secondary battery 100 becomes high.

[0035] In this specification, the term "before initial charging" refers to the state of the battery from assembly to the first charging, and the term "at the end of discharging" refers to the state of the battery when the voltage is between 1.0 V and 3.8 V, preferably between 1.0 V and 3.0 V.

[0036] As used herein, a "lithium secondary battery having a negative electrode that does not have a negative electrode active material" means that the negative electrode 140 does not have a negative electrode active material before the initial charge of the battery. Therefore, the phrase "negative electrode that does not have a negative electrode active material" may be rephrased as "a negative electrode that does not have a negative electrode active material before the initial charge of the battery," "a negative electrode that does not have a negative electrode active material other than lithium metal regardless of the state of charge of the battery and that does not have lithium metal before the initial charge," or "a negative electrode current collector that does not have lithium metal before the initial charge," etc. Furthermore, a "lithium secondary battery having a negative electrode that does not have a negative electrode active material" may be rephrased as an anode-free lithium battery, a zero-anode lithium battery, or an anode-less lithium battery.

[0037] In the negative electrode 140 of this embodiment, regardless of the state of charge of the battery, the content of negative electrode active materials other than lithium metal is 10% by mass or less relative to the entire negative electrode, and may preferably be 5.0% by mass or less, 1.0% by mass or less, 0.1% by mass or less, 0.0% by mass or less, or even 0% by mass. Furthermore, in the negative electrode 140 of this embodiment, before initial charging, the lithium metal content is 10% by mass or less relative to the entire negative electrode, and may preferably be 5.0% by mass or less, 1.0% by mass or less, 0.1% by mass or less, 0.0% by mass or less, or even 0% by mass.

[0038] In the lithium secondary battery 100 of this embodiment, when the battery voltage is 1.0 V or more and 3.5 V or less, the lithium metal content may be 10 mass % or less (preferably 5.0 mass % or less, and may be 1.0 mass % or less) with respect to the entire negative electrode 140; when the battery voltage is 1.0 V or more and 3.0 V or less, the lithium metal content may be 10 mass % or less (preferably 5.0 mass % or less, and may be 1.0 mass % or less) with respect to the entire negative electrode 140; or when the battery voltage is 1.0 V or more and 2.5 V or less, the lithium metal content may be 10 mass % or less (preferably 5.0 mass % or less, and may be 1.0 mass % or less) with respect to the entire negative electrode 140.

[0039] In the lithium secondary battery 100 of this embodiment, the mass M of lithium metal deposited on the negative electrode when the battery voltage is 4.2 V is 4.2 The mass M of lithium metal deposited on the negative electrode when the battery voltage is 3.0 V 3.0 Ratio of M 3.0 / M 4.2 is preferably 40% or less, more preferably 38% or less, and even more preferably 35% or less. 3.0 / M 4.2 may be 1.0% or more, 2.0% or more, 3.0% or more, or 4.0% or more.

[0040] Examples of the negative electrode active material of this embodiment include lithium metal and alloys containing lithium metal, carbon-based materials, metal oxides, and metals that alloy with lithium and alloys containing such metals. Examples of the carbon-based materials include, but are not limited to, graphene, graphite, hard carbon, mesoporous carbon, carbon nanotubes, and carbon nanohorns. Examples of the metal oxides include, but are not limited to, titanium oxide compounds, tin oxide compounds, and cobalt oxide compounds. Examples of the metals that alloy with lithium include silicon, germanium, tin, lead, aluminum, and gallium.

[0041] The negative electrode 140 of this embodiment is not particularly limited as long as it does not contain a negative electrode active material and can be used as a current collector. Examples include at least one selected from the group consisting of Cu, Ni, Ti, Fe, and other metals that do not react with Li, their alloys, and stainless steel (SUS). Preferably, the negative electrode is made of at least one selected from the group consisting of Cu, Ni, their alloys, and stainless steel (SUS). Use of such a negative electrode tends to improve the energy density and productivity of the battery. When SUS is used for the negative electrode, various types of SUS known in the art can be used. The above-mentioned negative electrode materials can be used alone or in combination. In this specification, the term "metal that does not react with Li" refers to a metal that does not react with lithium ions or lithium metal to form an alloy under the operating conditions of a lithium secondary battery.

[0042] The capacity of the negative electrode 140 is sufficiently smaller than the capacity of the positive electrode 120, and may be, for example, 20% or less, 15% or less, 10% or less, or 5% or less. The capacities of the positive electrode 120 and the negative electrode 140 can be measured by a conventionally known method.

[0043] The average thickness of the negative electrode 140 is preferably 4 μm or more and 20 μm or less, more preferably 5 μm or more and 18 μm or less, and even more preferably 6 μm or more and 15 μm or less. According to such an embodiment, the volume occupied by the negative electrode 140 in the lithium secondary battery 100 is reduced, and therefore the energy density of the lithium secondary battery 100 is further improved.

[0044] (negative electrode coating agent) The lithium secondary battery 100 has a high energy density because it includes a negative electrode 140 that does not include a negative electrode active material. However, the inventors have discovered that simply using a negative electrode that does not include a negative electrode active material can cause dendritic lithium metal to deposit on the negative electrode during battery charge and discharge, resulting in a short circuit of the battery, or when the dendritic lithium metal dissolves, the base of the dendritic lithium metal dissolves, causing some of the lithium metal to peel off from the negative electrode and become inactive, resulting in a decrease in battery capacity. In the lithium secondary battery 100, a specific compound is coated on the surface of the negative electrode 140, which prevents the lithium metal deposited on the negative electrode from growing into a dendritic shape.

[0045] In the lithium secondary battery 100, at least a portion of the surface of the negative electrode 140 facing the positive electrode 120 (and separator 130) is coated with a compound (negative electrode coating agent) containing an aromatic ring to which two or more elements selected from the group consisting of N, S, and O are independently bonded. The negative electrode coating agent is presumed to be held on the negative electrode 140 by at least one element selected from the group consisting of N, S, and O being coordinately bonded to a metal atom constituting the negative electrode 140. Therefore, it is presumed that the negative electrode coating agent will not be detached and / or decomposed even if the battery is repeatedly charged and discharged.

[0046] It is believed that the anode coating agent coordinated to the metal atoms constituting the anode interacts with lithium ions present on the surface of the anode at at least one element selected from the group consisting of N, S, and O. That is, since the anode coating agent can serve as a starting point or scaffold for the lithium metal deposition reaction on the surface of the anode, it is presumed that using an anode 140 coated with the anode coating agent can suppress the non-uniform deposition reaction of lithium metal on the surface, thereby suppressing the lithium metal deposited on the anode from growing into a dendritic shape.

[0047] Therefore, the negative electrode coating agent is not particularly limited as long as it is a compound containing an aromatic ring to which two or more elements selected from the group consisting of N, S, and O are independently bonded, i.e., a compound having a structure in which two or more N, S, or O are independently bonded to an aromatic ring. Examples of aromatic rings include aromatic hydrocarbons such as benzene, naphthalene, azulene, anthracene, and pyrene, and heteroaromatic compounds such as furan, thiophene, pyrrole, imidazole, pyrazole, pyridine, pyridazine, pyrimidine, and pyrazine. Among these, aromatic hydrocarbons are preferred, with benzene and naphthalene being more preferred, and benzene being even more preferred.

[0048] In the negative electrode coating agent, it is preferable that one or more nitrogen atoms are bonded to the aromatic ring. Furthermore, it is more preferable that the negative electrode coating agent is a compound having a structure in which a nitrogen atom is bonded to the aromatic ring and, in addition to the nitrogen atom, one or more elements selected from the group consisting of N, S, and O are each independently bonded. When such a compound in which a nitrogen atom is bonded to an aromatic ring is used as the negative electrode coating agent, the cycle characteristics of the battery tend to be further improved.

[0049] The negative electrode coating agent is preferably at least one selected from the group consisting of compounds represented by the following formula (C) and derivatives thereof. According to such an embodiment, the cycle characteristics of the battery tend to be further improved. [ka]

[0050] In the formula, X 1 is X 3 represents either C or N bonded to X 2 is X 4 represents any of N, S, and O to which X is bonded; 3 -R 1 , -NR 1 2, -OR 1 , or -SR 1 indicates an X 4 -R 2, -CO-X, -CS-NX2, -SO2-X, -SiX3, and -OX; R 1 represents a hydrogen atom, an unsubstituted monovalent hydrocarbon group, or a pyridyl group; R 2 represents a hydrogen atom or an optionally substituted monovalent hydrocarbon group; and X represents an arbitrary monovalent substituent.

[0051] In formula (C), X 1 is X 3 represents either C or N to which X is bonded. 3 The C to which is bonded is CR 1 , C-NR 1 2. C-OR 1 , or C-SR 1 In this case, the leftmost C is N and X 2 where R 1 is a hydrogen atom, an unsubstituted monovalent hydrocarbon group, or a pyridyl group. 1 In R, the unsubstituted monovalent hydrocarbon group is not particularly limited, but examples thereof include linear or branched, saturated or unsaturated hydrocarbon groups having 1 to 10 carbon atoms, and preferably a methyl group or an ethyl group. 1 In the formula, the pyridyl group is not particularly limited, but examples thereof include a 2-pyridyl group, a 3-pyridyl group, and a 4-pyridyl group, and preferably a 2-pyridyl group. 1 Preferred embodiments include N, CH, C—SH, C—C5H4N, and C—CH3.

[0052] In formula (C), X 2 is X 4 represents any of N, S, and O to which X is bonded. 4 The N bonded to NR 2 , N-CO-X, N-CS-NX2, N-SO2-X, N-SiX3, and N-OX, in which the leftmost N is the C and X of the benzene ring. 1 where R 2 is a hydrogen atom or an optionally substituted monovalent hydrocarbon group, and X is any monovalent substituent.

[0053] R 2 In the formula (I), the optionally substituted monovalent hydrocarbon group is not particularly limited, and examples thereof include linear or branched, saturated or unsaturated hydrocarbon groups having 1 to 10 carbon atoms which may be substituted. Here, the substituent on the optionally substituted monovalent hydrocarbon group is not particularly limited, and examples thereof include a nitrile group, a halogen group, a silyl group, a hydroxy group, an alkoxy group, an aryl group, and an aryloxy group. X is not particularly limited, and examples thereof include a hydrogen atom, an unsubstituted linear or branched, saturated or unsaturated hydrocarbon group having 1 to 10 carbon atoms, an optionally substituted amino group, an optionally substituted aryl group, an optionally substituted heteroaromatic group, an alkylcarbonyl group, and an arylcarbonyl group. X may also be a substituent that does not have an active hydrogen atom.

[0054] X 2 Preferred embodiments of the above include S, O, NH, N-CH2-C(CH), N-CH2-Cl, N-CH2-Si(CH3)3, N-CH2-O-CH3, N-CH2-C(=CH2)-CH3, N-CH3, N-CS-NH-C3HC5, N-CS-NH-C3H2NS, N-CS-NH-CH2-C6H5, N-CS-NC4H8, N-CO-CH3, N-CO-C6H5, N-CO-C5H4N, N-CO-NH2, N-CO-C6H4Cl, N-CO-C 10 H7, N—CO—NH—C6H5, N—SO2—CH3, N—SO2—C6H5, N—SO2—C3H2N2(CH3), N—SO2—C4H3S, N—SO2—C5H4N, and NO—CO—C6H5.

[0055] The compound represented by formula (C) may be a multimer such as a dimer or trimer, such as Tris-(1-benzotriazolyl)methane or 2,6-bis[(1H-benzotriazole-1-yl)methyl]-4-methylphenol, but it is preferable that the compound represented by formula (C) is a monomer.

[0056] Among these, the negative electrode coating agent is more preferably at least one selected from the group consisting of benzotriazole, benzimidazole, benzimidazole thiol, benzoxazole, benzoxazole thiol, benzothiazole, mercaptobenzothiazole, and derivatives thereof. According to such an embodiment, the cycle characteristics of the battery tend to be further improved.

[0057] From the same viewpoint, among these, the negative electrode coating agent is more preferably at least one selected from the group consisting of benzotriazole, benzimidazole, benzoxazole, mercaptobenzothiazole, and derivatives thereof.

[0058] The derivatives of the compound represented by the following formula (C), or derivatives of benzotriazole, benzimidazole, benzimidazole thiol, benzoxazole, benzoxazole thiol, benzothiazole, and mercaptobenzothiazole are not particularly limited as long as they are compounds derived from these compounds and have a substituent bonded to a part of these compounds. Examples of such derivatives include compounds in which one or more substituents selected from the group consisting of an optionally substituted hydrocarbon group, an optionally substituted amino group, a carboxy group, a sulfo group, a halogen group, and a silyl group are each independently bonded to an aromatic ring.

[0059] Specific examples of the negative electrode coating agent include, for example, 1H-benzotriazole, 5-methyl-1H-benzotriazole, 4-methyl-1H-benzotriazole, 1-benzoyl-1H-benzotriazole, 1-(2-pyridylcarbonyl)benzotriazole, 1-acetyl-1H-benzotriazole, 5-amino-1H-benzotriazole, 2-mercaptobenzothiazole, 6-amino-2-mercaptobenzothiazole, benzimidazole, 2-(2-pyridyl)benzimidazole, benzoxazole, 2-methylbenzoxazole, benzotriazole-5-carboxylic acid, benzotriazole-1-carboxamide, N-(2-propenyl)-1H-benzotriazole-1-carbothioamide, 1-(methoxymethyl)-1H-benzotriazole, 1-(2-thienylsulfonyl)-1H-benzotriazole, 1-(3-pyridinylsulfonyl)-1H-benzotriazole, 5-(trifluoromethyl)-1H-1,2,3-benzotriazole, bis(1-benzotriazolyl)methanethione, benzotriazol-1-ylpyrrolidin-1-ylmethanethione, 1-(1-naphthylcarbonyl)-1H-benzotriazole, 1-(2-methyl-allyl)-1H-benzotriazole, 1-(benzoyloxy)-1H-1,2,3-benzotriazole, N-phenyl-1H-1,2,3-benzotriazole-1-carboxamide, and 2,6-bis[(1H-benzotriazole-1-yl)methyl]-4-methylphenol, etc.

[0060] Among these, 1H-benzotriazole, 5-methyl-1H-benzotriazole, 4-methyl-1H-benzotriazole, 1-benzoyl-1H-benzotriazole, 1-(2-pyridylcarbonyl)benzotriazole, 2-mercaptobenzothiazole, 6-amino-2-mercaptobenzothiazole, benzimidazole, 2-(2-pyridyl)benzimidazole, 2-methylbenzoxazole, 1-(methoxymethyl)-1H-benzotriazole, 1-(1-naphthylcarbonyl)-1H-benzotriazole, 1-(2-methyl-allyl)-1H-benzotriazole, 1-(benzoyloxy)-1H-1,2,3-benzotriazole, and 2,6-bis[(1H-benzotriazole-1-yl)methyl]-4-methylphenol are preferred as the negative electrode coating agent, and 1H-benzotriazole is more preferred.

[0061] The anode coating agent is coated on at least a portion of the surface of the anode 140 facing the positive electrode 120. "Coated" on at least a portion of the surface of the anode with the anode coating agent means that 10% or more of the surface area of ​​the anode is covered with the anode coating agent. The anode 140 is preferably covered with the anode coating agent on an area ratio of 20% or more, 30% or more, 40% or more, or 50% or more, more preferably 70% or more, and even more preferably 80% or more.

[0062] A method for coating the surface of the negative electrode 140 with the negative electrode coating agent will be described later in the method for manufacturing a lithium secondary battery. The above-mentioned negative electrode coating agents may be used alone or in combination of two or more.

[0063] (electrolyte) The electrolyte solution is an ionically conductive solution containing an electrolyte and a solvent, and acts as a conductive path for lithium ions. The electrolyte solution may be impregnated into the separator 130, or may be enclosed in a sealed container together with a laminate of the positive electrode 120, the separator 130, and the negative electrode 140.

[0064] The electrolyte solution of this embodiment contains a lithium salt and at least one of a compound represented by the following formula (1) and a compound represented by the following formula (2). The lithium secondary battery of this embodiment has such an electrolyte solution and therefore has excellent cycle characteristics. The reason for this is not necessarily clear, but the following factors are thought to be involved. In formula (1), R 1 is an alkyl group which may contain an ether bond, and R 2 is a fluorine-substituted alkylene group, and R 3 is an alkyl group which may contain an ether bond. 4 is a fluorine-substituted alkyl group, and R 5 is an alkylene group which may contain an ether bond, and R 6 represents an alkyl group which may be substituted with fluorine. [ka] [ka]

[0065] Generally, when an anode-free lithium secondary battery containing an electrolyte is charged and discharged, the solvent in the electrolyte decomposes, forming a solid electrolyte interfacial layer (SEI layer) on the surface of the negative electrode. The SEI layer prevents further decomposition of the electrolyte components and the resulting irreversible reduction of lithium ions and gas generation. Furthermore, because the SEI layer has ionic conductivity, the reactivity of the lithium deposition reaction is uniform across the surface of the negative electrode on which the SEI layer is formed. Therefore, promoting the formation of the SEI layer is crucial for improving the performance of anode-free lithium secondary batteries.

[0066] It is presumed that the reactivity of fluorine, particularly near the ether bond, is high in the compounds represented by the above formulas (1) and (2) due to the substitution of a part of the structure with fluorine. Therefore, it is presumed that in the lithium secondary battery of this embodiment, a part of the compounds represented by the formulas (1) and (2) is likely to react with the negative electrode during charging, and an SEI layer-forming reaction starting from this reaction is likely to occur, resulting in the favorable formation of an SEI layer with a high fluorine content. Furthermore, it is presumed that the compounds represented by the above formulas (1) and (2) contain two or more ether bonds, which further improves the solubility of the electrolyte in the electrolytic solution, thereby further reducing the internal resistance of the battery and further improving the properties of the SEI layer that is formed. It is presumed that the effects of the above-mentioned negative electrode coating agent and the above-mentioned electrolyte solution synergistically improve the capacity and cycle characteristics of the lithium secondary battery, although the factors are not limited to those mentioned above.

[0067] Hereinafter, in this specification, the compound represented by the above formula (1) is also referred to as a "first fluorine compound," and the compound represented by the above formula (2) is also referred to as a "second fluorine compound."

[0068] The electrolyte solution of the present embodiment preferably contains both the first fluorine compound and the second fluorine compound, which tends to improve the quality of the SEI layer and further improve the cycle characteristics of the lithium secondary battery.

[0069] In the above formula (1), R 2 In the above, the ratio (F / (F+H)) of the number of fluorine atoms (F) to the total number of fluorine atoms and hydrogen atoms (F+H) is preferably 0.30 or more and 0.80 or less. According to such an embodiment, the cycle characteristics of the battery tend to be further improved. From the same viewpoint, the ratio (F / (F+H)) is preferably 0.40 or more and 0.75 or less, more preferably 0.45 or more and 0.70 or less, and even more preferably 0.50 or more and 0.67 or less.

[0070] In the above formula (1), R 2 In the above formula, it is preferable that at least one of the carbon atoms bonded to the oxygen atoms at both ends does not have a fluorine atom. When the first fluorine compound of the present embodiment has such a structure, the properties of the SEI layer formed become more favorable, and the cycle characteristics of the lithium secondary battery tend to be further improved. From the same viewpoint, R 2 In the formula (I), it is more preferable that neither of the carbon atoms bonded to the oxygen atom has a fluorine atom.

[0071] The molecular weight of the first fluorine compound contained in the electrolytic solution of the present embodiment is not particularly limited and is, for example, from 100 to 500. From the viewpoint of further improving the cycle characteristics of the lithium secondary battery, the molecular weight of the first fluorine compound is preferably from 110 to 400, more preferably from 120 to 350, even more preferably from 130 to 300, and still more preferably from 140 to 250.

[0072] The molecular weight of the second fluorine compound contained in the electrolytic solution of the present embodiment is not particularly limited and is, for example, from 100 to 500. From the viewpoint of further improving the cycle characteristics of the lithium secondary battery, the molecular weight of the second fluorine compound is preferably from 110 to 450, more preferably from 120 to 400, even more preferably from 130 to 350, and still more preferably from 150 to 300.

[0073] The number of carbon atoms in the first fluorine compound is not particularly limited and is, for example, 3 or more and 30 or less. From the viewpoint of further improving the cycle characteristics of the battery, the number of carbon atoms in the first fluorine compound is preferably 4 or more, 5 or more, or 6 or more, and from the same viewpoint, it is preferably 25 or less, 20 or less, 15 or less, or 10 or less.

[0074] The first fluorine compound in this embodiment is not particularly limited as long as it is a compound represented by the above formula (1), and examples thereof include 2,2,3,3-tetrafluoro-1,4-dimethoxybutane (TFDMB), 2,2,3,3-tetrafluoro-1,4-diethoxybutane (TFDEB), 1,2,2,3-tetrafluoro-1,3-dimethoxypropane (TFDMP), 1,1,2,2-tetrafluoro-1,2-dimethoxyethane, 2- Examples of the first fluorine compound include methyl-2,3,3-trifluoro-1,4-dimethoxybutane, 2-methyl-2,3,3-trifluoro-1,4-methoxyethoxybutane, 2,3-methyl-2,3-difluoro-1,4-dimethoxybutane, 2,3-methyl-2,3-difluoro-1,4-methoxyethoxybutane, 2,2,3,3-tetrafluoromethoxyisopropioxybutane, 2,2,3,3-tetrafluorodiisopropioxybutane, etc. From the viewpoint of further improving the cycle characteristics of the lithium secondary battery, 2,2,3,3-tetrafluoro-1,4-dimethoxybutane, 2,2,3,3-tetrafluoro-1,4-diethoxybutane, and 1,2,2,3-tetrafluoro-1,3-dimethoxypropane are preferred, and 2,2,3,3-tetrafluoro-1,4-dimethoxybutane is more preferred.

[0075] In the above formula (2), R 4 In the above, the ratio (F / (F+H)) of the number of fluorine atoms (F) to the total number of fluorine atoms and hydrogen atoms (F+H) is preferably 0.40 or more and 0.90 or less. According to such an embodiment, the cycle characteristics of the battery tend to be further improved. From the same viewpoint, the ratio (F / (F+H)) is more preferably 0.50 or more and 0.88 or less, and even more preferably 0.60 or more and 0.85 or less.

[0076] In the above formula (2), R 4 In the above formula, it is preferable that the carbon atom bonded to the oxygen atom does not have a fluorine atom. When the second fluorine compound has such a structure, the properties of the SEI layer formed become more favorable, and the cycle characteristics of the lithium secondary battery tend to be further improved.

[0077] In the above formula (2), R 5 In the formula, the number of carbon atoms is preferably 1 or more and 4 or less. If the second fluorine compound has such a structure, the cycle characteristics of the battery tend to be more excellent. From the same viewpoint, R 5 The number of carbon atoms in is more preferably 1 or more and 3 or less, and further preferably 1 or more and 2 or less.

[0078] The number of carbon atoms in the second fluorine compound is not particularly limited and is, for example, 3 or more and 30 or less. From the viewpoint of further improving the cycle characteristics of the battery, the number of carbon atoms in the second fluorine compound is preferably 4 or more, 5 or more, or 6 or more, and from the same viewpoint, it is preferably 25 or less, 20 or less, 15 or less, or 10 or less.

[0079] The second fluorine compound in this embodiment is not particularly limited as long as it is a compound represented by the above formula (2), and examples thereof include 2,2,3,3-tetrafluoropropyl-2(2-methoxyethoxy)ethyl ether (TFPDGM), 1,2-bis(1,1,2,2-tetrafluoroethoxy)ethane (BisTFE), 2,2,3,3-tetrafluoropropyl-2-methoxyethyl ether (TFPME), and the like. From the viewpoint of further improving the cycle characteristics of the lithium secondary battery, the second fluorine compound is preferably 1,2-bis(1,1,2,2-tetrafluoroethoxy)ethane, 2,2,3,3-tetrafluoropropyl-2-methoxyethyl ether, or 2,2,3,3-tetrafluoropropyl-2(2-methoxyethoxy)ethyl ether, more preferably 1,2-bis(1,1,2,2-tetrafluoroethoxy)ethane or 2,2,3,3-tetrafluoropropyl-2(2-methoxyethoxy)ethyl ether, and even more preferably 1,2-bis(1,1,2,2-tetrafluoroethoxy)ethane.

[0080] In addition to the first fluorine compound and the second fluorine compound, the electrolyte solution of this embodiment preferably further contains a chain fluorine compound having at least one of the monovalent groups represented by the following formula (A) or formula (B) (hereinafter also referred to as a "third fluorine compound"). When the electrolyte solution further contains a third fluorine compound, the cycle characteristics of the lithium secondary battery tend to be further improved. In addition, in formulas (A) and (B), the wavy lines represent bonding sites in the monovalent groups. [ka] [ka]

[0081] In this specification, among the first fluorine compounds and second fluorine compounds, those having at least one of the monovalent groups represented by the above formula (A) or formula (B) are treated as the first fluorine compound or the second fluorine compound, unless otherwise specified.

[0082] The third fluorine compound in this embodiment includes a compound containing both the structures represented by the formula (A) and the formula (B), a compound containing the structure represented by the formula (A) but not the structure represented by the formula (B), and a compound containing the structure represented by the formula (B) but not the structure represented by the formula (A).

[0083] The number of carbon atoms in the third fluorine compound is not particularly limited, but is, for example, 3 or more and 20 or less. From the viewpoint of further improving the solubility of the electrolyte in the electrolytic solution, the number of carbon atoms in the third fluorine compound is preferably 4 or more, 5 or more, 6 or more, 7 or more, 8 or more, or 10 or more. From the same viewpoint, the number of carbon atoms in the third fluorine compound is preferably 18 or less, 15 or less, or 12 or less.

[0084] In this embodiment, the third fluorine compound is not particularly limited as long as it is a compound having a monovalent group represented by the above formula (A) or formula (B), and examples thereof include compounds having an ether bond, compounds having an ester bond, and compounds having a carbonate bond, etc. From the viewpoint of further improving the solubility of the electrolyte in the electrolytic solution and further improving the cycle characteristics of the battery, the third fluorine compound is preferably an ether compound having an ether bond.

[0085] The tertiary fluorine compound which is an ether compound is not particularly limited, but examples thereof include the following: Examples of compounds containing both the structures represented by the above formula (A) and the above formula (B) include 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTFE) and 1,1,2,2-tetrafluoroethoxy-2,2,3,3-tetrafluoropropoxymethane. Furthermore, examples of compounds containing a structure represented by the above formula (A) but not containing a structure represented by the above formula (B) include 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether (TFEE), methyl-1,1,2,2-tetrafluoroethyl ether, ethyl-1,1,2,2-tetrafluoroethyl ether, and propyl-1,1,2,2-tetrafluoroethyl ether. Furthermore, examples of compounds that do not contain a structure represented by formula (A) above and contain a structure represented by formula (B) above include difluoromethyl-2,2,3,3-tetrafluoropropyl ether, trifluoromethyl-2,2,3,3-tetrafluoropropyl ether, and difluoromethyl-2,2,3,3-tetrafluoropropyl ether. From the viewpoint of improving the cycle characteristics and / or rate characteristics of the lithium secondary battery, the third fluorine compound is preferably selected from 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTFE) and 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether (TFEE).

[0086] The electrolytic solution of the present embodiment may also contain a fluorine compound other than the first, second, and third fluorine compounds described above, i.e., the electrolytic solution of the present embodiment may contain a fluorine compound that does not have the structure represented by the above formula (1), formula (2), formula (A), or formula (B).

[0087] The content of the first fluorine compound in the electrolytic solution is not particularly limited. The first fluorine compound may account for the entire solvent component of the electrolyte, i.e., 100% by volume of the total amount of the solvent component of the electrolyte. When the entire solvent is the first fluorine compound, phase separation of the electrolyte is less likely to occur even when the lithium secondary battery is repeatedly charged and discharged, and cycle stability tends to be further improved. The content of the first fluorine compound is preferably, for example, 10% by volume or more, 20% by volume or more, 30% by volume or more, or 40% by volume or more relative to the total amount of the solvent components of the electrolyte solution. The content of the first fluorine compound is preferably 90% by volume or less, 80% by volume or less, 75% by volume or less, or 70% by volume or less. When the content of the first fluorine compound is within the above range, the cycle characteristics of the lithium secondary battery tend to be further improved.

[0088] The content of the second fluorine compound in the electrolytic solution is not particularly limited. The content of the second fluorine compound may be 100% by volume based on the total amount of the solvent components of the electrolyte, which tends to make phase separation of the electrolyte less likely to occur and further improve cycle stability. The content of the second fluorine compound is preferably, for example, 10% by volume or more, 15% by volume or more, 20% by volume or more, or 25% by volume or more relative to the total amount of the solvent components of the electrolyte solution. The content of the second fluorine compound is preferably 70% by volume or less, 65% by volume or less, 60% by volume or less, or 55% by volume or less. By keeping the content of the second fluorine compound within the above range, the cycle characteristics of the lithium secondary battery tend to be further improved.

[0089] The content of the third fluorine compound in the electrolyte solution is not particularly limited, but is, for example, 0.0% by volume to 95% by volume, or 1.0% by volume to 90% by volume, relative to the total amount of the solvent components of the electrolyte solution. The content of the third fluorine compound is preferably 3.0% by volume or more, 5.0% by volume or more, 8.0% by volume or more, or 10% by volume or more. The content of the third fluorine compound is preferably 80% by volume or less, 70% by volume or less, 60% by volume or less, 50% by volume or less, 45% by volume or less, or 40% by volume or less. When the content of the third fluorine compound is within the above range, the cycle characteristics of the lithium secondary battery tend to be further improved.

[0090] The total content of the first fluorine compound and the second fluorine compound in the electrolyte solution is not particularly limited, but is, for example, 1% by volume or more and 100% by volume or less relative to the total amount of the solvent components of the electrolyte solution. The total content of the first fluorine compound and the second fluorine compound is preferably 40% by volume or more and 100% by volume or less, more preferably 50% by volume or more and 100% by volume or less, and even more preferably 60% by volume or more and 100% by volume or less. When the total content is within the above range, the cycle characteristics of the lithium secondary battery tend to be further improved.

[0091] The total content of the compounds having fluorine atoms in the electrolyte is not particularly limited, but is, for example, 10% by volume or more and 100% by volume or less relative to the total amount of the solvent components of the electrolyte. The total content of the compounds having fluorine atoms is preferably 20% by volume or more, 30% by volume or more, 40% by volume or more, 50% by volume or more, or 60% by volume or more. When the total content of the compounds having fluorine atoms is within the above range, the cycle characteristics of the lithium secondary battery tend to be further improved. In addition, the total content of the compounds having fluorine atoms may be 95% by volume or less, 90% by volume or less, or 85% by volume or less.

[0092] The electrolytic solution of the present embodiment preferably further contains an ether compound having no fluorine atoms (hereinafter also referred to as a "non-fluorine ether compound.") When the electrolytic solution contains an ether compound having no fluorine atoms, the solubility of the electrolyte in the electrolytic solution is further improved, which tends to reduce the internal resistance of the battery and further improve the cycle characteristics of the lithium secondary battery.

[0093] The number of carbon atoms in the non-fluorinated ether compound is not particularly limited and is, for example, 2 or more and 20 or less. From the viewpoint of further improving the solubility of the electrolyte in the electrolytic solution, the number of carbon atoms in the non-fluorinated ether compound is preferably 3 or more, 4 or more, 5 or more, or 6 or more. From the same viewpoint, the number of carbon atoms in the non-fluorinated ether compound is preferably 15 or less, 12 or less, 10 or less, 9 or less, or 7 or less.

[0094] The number of ether bonds in the non-fluorine ether compound is not particularly limited and is, for example, 1 or more and 10 or less. From the viewpoint of further improving the solubility of the electrolyte in the electrolytic solution, the number of ether bonds in the non-fluorine ether compound is preferably 2 or more, or 3 or more. Furthermore, the number of ether bonds in the non-fluorine ether compound is preferably 8 or less, or 5 or less.

[0095] The non-fluorinated ether compound may be linear or may have a branched chain. The electrolyte solution of the present embodiment preferably contains a non-fluorinated ether compound having a branched chain. By including a non-fluorinated ether compound having a branched chain, compatibility in the electrolyte solution tends to be improved and stability tends to be improved, thereby further improving the cycle characteristics of the lithium secondary battery.

[0096] The non-fluorinated ether compound may be a saturated ether compound or an unsaturated ether compound. From the viewpoint of further improving the cycle characteristics of the lithium secondary battery, the electrolyte preferably contains a saturated non-fluorinated ether compound.

[0097] The non-fluorine-containing ether compound is not particularly limited as long as it is an ether compound that does not have a fluorine atom, and examples thereof include 1,2-dimethoxyethane (DME), 1,2-dimethoxypropane (DMP), 2,3-dimethoxybutane (DMB), triethylene glycol dimethyl ether (TGM), diethylene glycol dimethyl ether (DGM), tetraethylene glycol dimethyl ether (TetGM), 1,3-dimethoxypropane, 1,4-dimethoxybutane, 1,1-dimethoxyethane, 2,2-dimethoxypropane, 1,3-dimethoxybutane, 1,2-dimethoxybutane, 2,2-dimethoxybutane, 1,2-diethoxypropane, 1,2-diethoxybutane, 2,3-diethoxybutane, and diethoxyethane. From the viewpoint of further improving the solubility of the electrolyte in the electrolytic solution, the non-fluorinated ether compound is preferably selected from 1,2-dimethoxyethane (DME), 1,2-dimethoxypropane (DMP), and 2,3-dimethoxybutane (DMB).

[0098] The content of the non-fluorinated ether compound in the electrolytic solution of this embodiment is not particularly limited, but is, for example, 0.0 vol% or more and 80 vol% or less relative to the total amount of the solvent components of the electrolytic solution. From the viewpoint of further improving the solubility of the electrolyte in the electrolytic solution, the content of the non-fluorinated ether compound is preferably 5.0 vol% or more, 10 vol% or more, 15 vol% or more, or 20 vol% or more relative to the total amount of the solvent components of the electrolytic solution. From the same viewpoint, the content of the non-fluorinated ether compound is preferably 75 vol% or less, 70 vol% or less, 65 vol% or less, 60 vol% or less, or 55 vol% or less relative to the total amount of the solvent components of the electrolytic solution.

[0099] The electrolyte solution may further contain a fluorine-free compound other than the above-mentioned non-fluorine-containing ether compounds as a solvent. Such compounds are not particularly limited and may have at least one group selected from the group consisting of a carbonate group, a carbonyl group, a ketone group, and an ester group. Examples of such compounds include acetonitrile, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, ethylene carbonate, propylene carbonate, chloroethylene carbonate, methyl acetate, ethyl acetate, propyl acetate, methyl propionate, ethyl propionate, trimethyl phosphate, and triethyl phosphate.

[0100] As long as the solvent of the electrolytic solution contains at least one of the first fluorine compound or the second fluorine compound, the first fluorine compound, the second fluorine compound, the third fluorine compound, the non-fluorinated ether compound, etc. can be freely and arbitrarily combined and used. Furthermore, each solvent may be used alone or in combination of two or more.

[0101] The structural formulas of compounds that may be contained as solvents in this embodiment are shown in the tables below. Tables 1, 2, and 3 respectively list examples of the first fluorine compound, second fluorine compound, and third fluorine compound. Table 4 lists examples of the non-fluorine ether compound. However, the types of compounds that can be used as solvents are not limited to these.

[0102] [Table 1]

[0103] [Table 2]

[0104] [Table 3]

[0105] [Table 4]

[0106] The lithium salt contained in the electrolyte solution is not particularly limited, and examples thereof include inorganic and organic salts of lithium, such as LiI, LiCl, LiBr, LiF, LiBF, LiPF, LiPFO, LiPF(C0), LiPF(C0), LiAsF, LiSOCF, LiN(SOF), LiN(SOCF), LiN(SOCFCF), LiBF(C0), LiB(C0), LiB(C0), LiB(OC0), LiB(OC0), LiB(OCH), LiB(OCH)F, LiB(OCOCF), LiNO, and LiSO. From the viewpoint of further improving the energy density and cycle characteristics of the lithium secondary battery 100, it is preferable that the lithium salt contains at least one selected from the group consisting of LiN(SO2F)2, LiPF2O2, and LiPF2(C2O4)2, and it is more preferable that the lithium salt contains at least LiN(SO2F)2. Note that the above lithium salts may be used alone or in combination of two or more. The electrolytic solution may further contain a salt other than a lithium salt as an electrolyte, such as salts of Na, K, Ca, and Mg.

[0107] The structural formulae of compounds that can be included as electrolytes in this embodiment are shown below. Formulae (D), (E), and (F) represent the above-mentioned LiN(SO2F)2, LiPF2O2, and LiPF2(C2O4)2, respectively. However, the types of compounds that can be used as electrolytes are not limited to these. [ka] [ka] [ka]

[0108] The total concentration of lithium salts in the electrolyte is not particularly limited, but is preferably 0.30M or more, more preferably 0.40M or more, even more preferably 0.50M or more, and even more preferably 0.80M or more. When the lithium salt concentration is within the above range, the SEI layer tends to be formed more easily and the internal resistance tends to be lower. In particular, a lithium secondary battery 100 containing a fluorine compound as a solvent can have a high concentration of lithium salt in the electrolyte, thereby further improving cycle characteristics and rate performance. The upper limit of the lithium salt concentration is not particularly limited, and the lithium salt concentration may be 10.0M or less, 5.0M or less, or 2.0M or less.

[0109] The lithium secondary battery of this embodiment may contain an electrolytic solution or components of an electrolytic solution in a state other than a liquid. For example, by adding an electrolytic solution when preparing a separator, which will be described later, a battery containing the electrolytic solution in a solid or semi-solid (gel) material can be obtained. The electrolytic solution can also be referred to as an electrolyte.

[0110] The presence of a cyclic fluorine compound and an ether co-solvent in the electrolyte solution can be confirmed by various conventionally known methods, such as NMR measurement, mass spectrometry such as HPLC-MS, and IR measurement.

[0111] The molecular structure of the solvent contained in the electrolyte solution can be estimated by measurement or analysis using known methods. Examples of such methods include NMR, mass spectrometry, elemental analysis, and infrared spectroscopy. The molecular structure of the solvent can also be estimated by theoretical calculations using molecular dynamics, molecular orbital methods, etc.

[0112] (separator) The separator 130 is a component that prevents the battery from short-circuiting by isolating the positive electrode 120 and the negative electrode 140, while ensuring ionic conductivity of lithium ions, which serve as charge carriers between the positive electrode 120 and the negative electrode 140. That is, the separator 130 has the function of physically and / or electrically isolating the positive electrode 120 and the negative electrode 140, and the function of ensuring ionic conductivity of lithium ions. Therefore, the separator 130 is not electronically conductive and is made of a material that does not react with lithium ions. The separator 130 may also serve to retain the electrolyte. As such a separator, one kind of material having the above two functions may be used alone, or two or more kinds of materials having one of the above functions may be used in combination. The separator is not particularly limited as long as it has the above function, but examples thereof include insulating porous materials, polymer electrolytes, gel electrolytes, and inorganic solid electrolytes, and is typically at least one selected from the group consisting of insulating porous materials, polymer electrolytes, and gel electrolytes.

[0113] When the separator includes an insulating porous member, the pores of the member are filled with an ion-conductive substance, such as the above-mentioned electrolytic solution, polymer electrolyte, or gel electrolyte, to thereby provide the member with ion conductivity. An insulating porous material, a polymer electrolyte, or a gel electrolyte can be used singly or in combination as the separator 130. When an insulating porous material is used alone as the separator, the lithium secondary battery must further include an electrolyte solution.

[0114] The material constituting the insulating porous member is not particularly limited, but examples thereof include insulating polymer materials, specifically polyethylene (PE) and polypropylene (PP). That is, the separator 130 may be a porous polyethylene (PE) film, a porous polypropylene (PP) film, or a laminated structure thereof.

[0115] The separator 130 may be coated with a separator coating layer. The separator coating layer may cover both sides of the separator 130 or only one side. The material of the separator coating layer is not particularly limited, but preferably contains, for example, a binder that is non-reactive with lithium ions and can firmly bond the separator to adjacent layers. The use of such a material tends to suppress side reactions other than lithium ion deposition and electrolytic elution near the electrodes, further improving the cycle characteristics of the battery. Examples of such materials include at least one selected from the group consisting of polyvinylidene fluoride (PVDF), a composite of styrene butadiene rubber and carboxymethyl cellulose (SBR-CMC), polyacrylic acid (PAA), lithium polyacrylate (Li-PAA), polyimide (PI), polyamideimide (PAI), and aramid. Alternatively, polyvinylidene fluoride (PVDF) may be used. The separator coating layer may contain inorganic particles such as silica, alumina, titania, zirconia, magnesium oxide, magnesium hydroxide, and lithium nitrate added to the binder.

[0116] The average thickness of the separator 130, including the separator coating layer, is preferably 30 μm or less, more preferably 25 μm or less, and even more preferably 20 μm or less. According to such an embodiment, the volume occupied by the separator 130 in the lithium secondary battery 100 is reduced, thereby further improving the energy density of the lithium secondary battery 100. In addition, the average thickness of the separator 130 is preferably 5.0 μm or more, more preferably 7.0 μm or more, and even more preferably 10 μm or more. According to such an embodiment, the positive electrode 120 and the negative electrode 140 can be reliably isolated from each other, and short-circuiting of the battery can be further prevented.

[0117] (positive electrode) The positive electrode 120 is not particularly limited as long as it is a material generally used in lithium secondary batteries, and known materials can be appropriately selected depending on the application of the lithium secondary battery. From the viewpoint of improving the stability and output voltage of the battery, the positive electrode 120 preferably contains a positive electrode active material. When the positive electrode has a positive electrode active material, lithium ions are typically charged into and desorbed from the positive electrode active material by charging and discharging the battery.

[0118] In this specification, the term "positive electrode active material" refers to a material that causes an electrode reaction, i.e., an oxidation reaction and a reduction reaction, at the positive electrode. Specifically, the positive electrode active material may be a host material for lithium element (typically, lithium ion).

[0119] Such positive electrode active materials are not particularly limited, but include, for example, metal oxides and metal phosphates. Examples of the metal oxides include, but are not particularly limited, cobalt oxide-based compounds, manganese oxide-based compounds, and nickel oxide-based compounds. Examples of the metal phosphates include, but are not particularly limited, iron phosphate-based compounds and cobalt phosphate-based compounds. Typical positive electrode active materials include LiCoO2, LiNi x Co y Mn z O(x+y+z=1), LiNi x Co y Al z O(x+y+z=1), LiNi x Mn y O(x+y=1), LiNiO2, LiMn2O4, LiFePO4, LiCoPO4, LiFeOF, LiNiOF, and LiTiS2. The above-mentioned positive electrode active materials may be used singly or in combination of two or more.

[0120] The positive electrode 120 may contain components other than the above-mentioned positive electrode active material. Such components are not particularly limited, but include, for example, a conductive additive, a binder, a gel electrolyte, and a polymer electrolyte.

[0121] The positive electrode 120 may be a gel electrolyte. In such an embodiment, the gel electrolyte functions to improve the adhesive strength between the positive electrode and the positive electrode current collector, making it possible to attach a thinner positive electrode current collector, thereby further improving the energy density of the battery. When attaching the positive electrode current collector to the surface of the positive electrode, a positive electrode current collector formed on release paper may be used.

[0122] The conductive additive in the positive electrode 120 is not particularly limited, but examples thereof include carbon black, single-walled carbon nanotubes (SWCNT), multi-walled carbon nanotubes (MWCNT), carbon nanofibers (CF), and acetylene black. The binder is not particularly limited, but examples thereof include polyvinylidene fluoride, polytetrafluoroethylene, styrene butadiene rubber, acrylic resin, and polyimide resin.

[0123] The content of the positive electrode active material in the positive electrode 120 may be, for example, 50% by mass or more and 100% by mass or less, based on the entire positive electrode 120. The content of the conductive additive may be, for example, 0.50% by mass or more and 30% by mass or less, based on the entire positive electrode 120. The content of the binder may be, for example, 0.50% by mass or more and 30% by mass or less, based on the entire positive electrode 120. The content of the gel electrolyte or polymer electrolyte may be, for example, 0.50% by mass or more and 30% by mass or less, preferably 5.0% by mass or more and 20% by mass or less, and more preferably 8.0% by mass or more and 15% by mass or less, based on the entire positive electrode 120.

[0124] The average thickness of the positive electrode 120 is preferably 20 μm or more and 100 μm or less, more preferably 30 μm or more and 80 μm or less, and even more preferably 40 μm or more and 70 μm or less, although the average thickness of the positive electrode can be adjusted appropriately depending on the desired battery capacity.

[0125] (Positive electrode current collector) A positive electrode current collector 110 is disposed on one side of the positive electrode 120. The positive electrode current collector is not particularly limited as long as it is a conductor that does not react with lithium ions in the battery. An example of such a positive electrode current collector is aluminum. The positive electrode current collector 110 may not be provided, in which case the positive electrode itself functions as a current collector. The positive electrode current collector functions to donate and receive electrons to the positive electrode (particularly the positive electrode active material). The positive electrode current collector 110 is in physical and / or electrical contact with the positive electrode 120.

[0126] In this embodiment, the average thickness of the positive electrode current collector is preferably 1.0 μm or more and 15 μm or less, more preferably 2.0 μm or more and 10 μm or less, and even more preferably 3.0 μm or more and 6.0 μm or less. According to such an embodiment, the volume occupied by the positive electrode current collector in the lithium secondary battery 100 is reduced, and therefore the energy density of the lithium secondary battery 100 is further improved.

[0127] (Use of lithium secondary batteries) 2 shows one usage mode of the lithium secondary battery of this embodiment. In the lithium secondary battery 200, a positive electrode terminal 210 and a negative electrode terminal 220 for connecting the lithium secondary battery 200 to an external circuit are joined to a positive electrode current collector 110 and a negative electrode 140, respectively. The lithium secondary battery 200 is charged and discharged by connecting the negative electrode terminal 220 to one end of the external circuit and the positive electrode terminal 210 to the other end of the external circuit.

[0128] The lithium secondary battery 200 is charged by applying a voltage between the positive electrode terminal 210 and the negative electrode terminal 220 such that a current flows from the negative electrode terminal 220 (negative electrode 140) through an external circuit to the positive electrode terminal 210 (positive electrode 120). The lithium secondary battery 200 may have a solid electrolyte interface layer (SEI layer) formed on the surface of the negative electrode 140 (the interface between the negative electrode 140 and the separator 130) coated with the negative electrode coating agent by the first charge (initial charge) after assembly of the battery. The SEI layer to be formed is not particularly limited, and may include, for example, an inorganic compound containing lithium, an organic compound containing lithium, or the like. The SEI layer typically has an average thickness of 1.0 nm or more and 10 μm or less.

[0129] When the positive electrode terminal 210 and the negative electrode terminal 220 of the charged lithium secondary battery 200 are connected, the lithium secondary battery 200 is discharged. As a result, the lithium metal deposited on the negative electrode is electrolytically dissolved.

[0130] (Lithium secondary battery manufacturing method) The method for manufacturing the lithium secondary battery 100 as shown in FIG. 1 is not particularly limited as long as it is a method that can manufacture a lithium secondary battery having the above-described configuration, and examples thereof include the following methods.

[0131] The positive electrode current collector 110 and the positive electrode 120 are manufactured, for example, as follows. The above-described positive electrode active material, conductive additive, and binder are mixed to obtain a positive electrode mixture. The compounding ratios may be, for example, 50% by mass to 99% by mass of the positive electrode active material, 0.5% by mass to 30% by mass of the conductive additive, and 0.5% by mass to 30% by mass of the binder, relative to the total positive electrode mixture. The obtained positive electrode mixture is applied to one side of a metal foil (e.g., Al foil) having a predetermined thickness (e.g., 5.0 μm to 1.0 mm) as a positive electrode current collector, and press-molded. The obtained molded body is punched to a predetermined size by a punching process to obtain the positive electrode current collector 110 and the positive electrode 120.

[0132] Next, a negative electrode 140 is manufactured in which at least a portion of one or both sides is coated with the negative electrode coating agent. First, the above-mentioned negative electrode material, for example, a metal foil (e.g., electrolytic Cu foil) having a thickness of 1.0 μm to 1.0 mm, is washed with a solvent containing sulfamic acid. Next, the negative electrode material is washed with water, and then immersed in a solution containing the above-mentioned negative electrode coating agent (e.g., a solution containing 0.010 vol % to 10 vol % of the negative electrode coating agent), and further dried in the atmosphere to coat the negative electrode coating agent. At this time, one side of the negative electrode material may be masked so that the negative electrode coating agent is coated on only one side. The negative electrode material coated with the negative electrode coating agent in this manner is punched to a predetermined size to obtain the negative electrode 140.

[0133] In the manufacturing process of the anode 140, the order of coating the anode coating agent and punching the anode material may be reversed. That is, the anode 140 may be manufactured by punching a cleaned anode material to a predetermined size and then coating the anode coating agent on its surface using the method described above. However, a manufacturing method of an anode in which the anode material is punched after coating with the anode coating agent is preferred because it allows the anode material coated with the anode coating agent to be easily manufactured using a roll-to-roll method.

[0134] Next, the separator 130 having the above-described structure is prepared. The separator 130 may be manufactured by a conventionally known method, or a commercially available separator may be used.

[0135] Next, at least one of the first fluorine compound and the second fluorine compound, and optionally other compounds, is mixed to obtain a solution, which is then used as a solvent, and a lithium salt is dissolved in the solution to prepare an electrolyte solution. The mixing ratio of the solvent and the lithium salt may be appropriately adjusted so that the contents or concentrations of the solvent and the lithium salt in the electrolyte solution fall within the above-mentioned ranges.

[0136] Next, the positive electrode current collector 110 on which the positive electrode 120 is formed, the separator 130, and the negative electrode 140 coated with the negative electrode coating agent obtained as described above are stacked in this order to obtain a laminate as shown in FIG. 1. If only one side of the negative electrode 140 is coated with the negative electrode coating agent, the negative electrode 140 is stacked so that this surface faces the positive electrode 120 (and the separator 130). The laminate obtained as described above is enclosed in a sealed container together with an electrolyte solution to obtain a lithium secondary battery 100. The sealed container is not particularly limited, but examples thereof include laminate films.

[0137] [Variations] The above-described embodiment is an example for explaining the present invention, and is not intended to limit the present invention to only this embodiment. The present invention can be modified in various ways without departing from the gist of the invention.

[0138] For example, the separator 130 may be omitted from the lithium secondary battery 100. In that case, it is preferable to fix the positive electrode 120 and the negative electrode 140 in a state where they are sufficiently separated so that they do not come into physical or electrical contact with each other.

[0139] The lithium secondary battery of this embodiment may also have a current collector disposed on the surface of the negative electrode so as to be in contact with the negative electrode. Such a current collector is not particularly limited, but examples thereof include those that can be used as negative electrode materials. When the lithium secondary battery does not have a positive electrode current collector or a negative electrode current collector, the positive electrode or the negative electrode itself functions as a current collector, respectively.

[0140] In the lithium secondary battery of this embodiment, terminals for connecting to an external circuit may be attached to the positive electrode current collector and / or the negative electrode. For example, metal terminals (e.g., Al, Ni, etc.) having a thickness of 10 μm to 1.0 mm may be bonded to one or both of the positive electrode current collector and the negative electrode. A conventionally known method may be used as the bonding method, and ultrasonic welding may be used, for example.

[0141] In this specification, "high energy density" or "having a high energy density" means that the capacity per total volume or mass of the battery is high, and is preferably 700 Wh / L or more or 300 Wh / kg or more, more preferably 800 Wh / L or more or 350 Wh / kg or more, and even more preferably 900 Wh / L or more or 400 Wh / kg or more.

[0142] In addition, in this specification, "excellent cycle characteristics" means that the rate of decrease in battery capacity is low before and after a number of charge-discharge cycles that can be expected in normal use. That is, when comparing the first discharge capacity after initial charge-discharge with the capacity after a number of charge-discharge cycles that can be expected in normal use, the capacity after charge-discharge cycles is almost no decrease compared to the first discharge capacity after initial charge-discharge. Here, "the number of cycles that can be expected in normal use" refers to, for example, 30, 50, 70, 100, 300, or 500 cycles, depending on the application of the lithium secondary battery. Furthermore, "the capacity after charge-discharge cycles is almost no decrease compared to the first discharge capacity after initial charge-discharge" refers to, for example, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, or 85% or more of the first discharge capacity after initial charge-discharge, depending on the application of the lithium secondary battery.

[0143] In this specification, numerical ranges described as preferred ranges, etc. may be replaced with numerical ranges obtained by arbitrarily combining the described upper and lower limits. For example, if a certain parameter is preferably 50 or more, more preferably 60 or more, and preferably 100 or less, more preferably 90 or less, the parameter may be any of 50 or more and 100 or less, 50 or more and 90 or less, 60 or more and 100 or less, or 60 or more and 90 or less. [Example]

[0144] The present invention will be explained in more detail below using examples and comparative examples, but the present invention is not limited to the following test examples.

[0145] [Example 1] The lithium secondary battery of Example 1 was fabricated as follows.

[0146] (Preparing the negative electrode) First, an 8.0 μm thick electrolytic Cu foil was washed with a solvent containing sulfamic acid and then rinsed with water. The electrolytic Cu foil was then immersed in a solution containing 1H-benzotriazole as an anode coating agent, dried, and then rinsed with water to obtain a Cu foil coated with the anode coating agent. The resulting Cu foil was punched to a specified size (45 mm × 45 mm) to obtain an anode.

[0147] (Preparation of positive electrode) Next, a positive electrode was fabricated. LiNi was used as the positive electrode active material. 0.85 Co 0.12 Al 0.03 A mixture of 96 parts by mass of O2, 2.0 parts by mass of carbon black as a conductive additive, and 2.0 parts by mass of polyvinylidene fluoride (PVDF) as a binder was applied to one side of a 12 μm Al foil and press-molded. The resulting molded body was punched out to a specified size (40 mm × 40 mm) to obtain a positive electrode with a positive electrode current collector on one side.

[0148] (Preparing the separator) A separator of a predetermined size (50 mm x 50 mm) was prepared, in which both sides of a 12 μm polyethylene microporous membrane were coated with 2.0 μm polyvinylidene fluoride (PVDF).

[0149] (Preparation of Electrolyte) The electrolyte solution was prepared as follows: LiN(SO2F)2 was dissolved in 2,2,3,3-tetrafluoro-1,4-dimethoxybutane to a molar concentration of 0.50 M to obtain an electrolyte solution.

[0150] (Battery assembly) The positive electrode current collector with the positive electrode formed thereon, the separator, and the negative electrode were stacked in this order, with the positive electrode facing the separator, to obtain a laminate. Furthermore, a 100 μm Al terminal and a 100 μm Ni terminal were joined to the positive electrode current collector and the negative electrode, respectively, by ultrasonic welding, and then inserted into a laminate outer casing. The electrolyte solution obtained as described above was then poured into the outer casing. The outer casing was sealed to obtain a lithium secondary battery.

[0151] [Examples 2 to 24] A lithium secondary battery was obtained in the same manner as in Example 1, except that the electrolyte solution was prepared using the electrolyte type, electrolyte concentration, and solvent composition shown in Table 5.

[0152] [Comparative Example 1] A lithium secondary battery was obtained in the same manner as in Example 8, except that the electrolyte solution was prepared using the solvents listed in Table 5. That is, the battery of Comparative Example 1 was prepared using an electrolyte solution that had been subjected to a negative electrode coating and did not contain either the compound represented by formula (1) or the compound represented by formula (2). [Comparative Examples 2 to 3] A lithium secondary battery was obtained in the same manner as in Example 1, except that an 8.0 μm thick electrolytic Cu foil was washed with a solvent containing sulfamic acid, dried, and then punched to a predetermined size (45 mm × 45 mm) to obtain a negative electrode without immersing it in a negative electrode coating agent, and that an electrolyte solution was prepared using the solvent listed in Table 5. Thus, the battery of Comparative Example 2 was not subjected to negative electrode coating and was produced using an electrolyte solution that did not contain both the compound represented by formula (1) and the compound represented by formula (2), and the battery of Comparative Example 3 was not subjected to negative electrode coating and was produced using an electrolyte solution that contained the compound represented by formula (1).

[0153] In Table 5, "TFDMB" is 2,2,3,3-tetrafluoro-1,4-dimethoxybutane, "TFDEB" is 2,2,3,3-tetrafluoro-1,4-diethoxybutane, "TFDMP" is 1,2,2,3-tetrafluoro-1,3-dimethoxypropane, "TFPDGM" is 2,2,3,3-tetrafluoropropyl-2(2-methoxyethoxy)ethyl ether, and "BisTFE" is 1,2-bis(1,1,2,2-tetrafluoroethoxy)ethyl ether. "TFPME" stands for 2,2,3,3-tetrafluoropropyl-2-methoxyethyl ether, "TFEE" stands for 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether, "TTFE" stands for 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether, "DMP" stands for 1,2-dimethoxypropane, "DME" stands for 1,2-dimethoxyethane, and "DMB" stands for 2,3-dimethoxybutane. For lithium salts, "LiFSI" stands for LiN(SO2F)2.

[0154] In Table 5, each solvent is classified as a first fluorine compound, a second fluorine compound, a third fluorine compound, or a non-fluorine ether compound, as defined above. Furthermore, in Table 5, the value to the right of each solvent indicates the content in volume percent relative to the total amount of solvent. For example, Example 1 listed in Table 5 contains 100 volume percent TFDMB as the solvent in the electrolyte solution, and 0.50 M LiN(SO2F)2 as the lithium salt.

[0155] [Evaluation of cycle characteristics] The cycle characteristics of the lithium secondary batteries prepared in each of the Examples and Comparative Examples were evaluated as follows.

[0156] The fabricated lithium secondary batteries were CC charged at 3.2 mA until the voltage reached 4.2 V (initial charge), and then CC discharged at 3.2 mA until the voltage reached 3.0 V (hereinafter referred to as "initial discharge"). The batteries were then CC charged at 13.6 mA until the voltage reached 4.2 V, and then CC discharged at 13.6 mA until the voltage reached 3.0 V. This cycle was repeated in an environment at a temperature of 25°C. For each example, the capacity determined from the initial discharge (hereinafter referred to as "initial capacity" and referred to as "capacity" in the table) is shown in Table 5. For each example, the number of cycles at which the discharge capacity reached 80% of the initial capacity (referred to as "cycle number" in the table) is also shown in Table 5.

[0157] [Table 5]

[0158] In Table 5, "-" indicates that the corresponding component was not present. Comparative examples marked with [ ] indicate that no coating agent was used on the negative electrode.

[0159] From Table 5, it can be seen that Examples 1 to 24, which use a negative electrode coated with a compound containing an aromatic ring to which at least two elements selected from the group consisting of N, S, and O are independently bonded, and an electrolyte solution containing at least one of the compound represented by formula (1) and the compound represented by formula (2), have a significantly higher number of cycles and excellent cycle characteristics than the comparative example, which does not use such an electrolyte solution.

[0160] The lithium secondary battery of the present invention has high energy density and excellent cycle characteristics, and therefore has industrial applicability as an electricity storage device for a variety of uses. [Explanation of symbols]

[0161] 100, 200... Lithium secondary battery, 110... positive electrode current collector, 120... positive electrode, 130... separator, 140... negative electrode, 210... positive electrode terminal, 220... negative electrode terminal.

Claims

1. A battery comprising a positive electrode, a negative electrode having no negative electrode active material, and an electrolyte solution, The negative electrode has at least a portion of its surface facing the positive electrode coated with 1H-benzotriazole, The electrolyte solution contains at least LiN(SO 2 F) 2 and at least one of a first fluorine compound containing one or more compounds selected from the group consisting of 2,2,3,3-tetrafluoro-1,4-dimethoxybutane, 2,2,3,3-tetrafluoro-1,4-diethoxybutane, and 1,2,2,3-tetrafluoro-1,3-dimethoxypropane, and a second fluorine compound containing one or more compounds selected from the group consisting of 1,2-bis(1,1,2,2-tetrafluoroethoxy)ethane, 2,2,3,3-tetrafluoropropyl-2-methoxyethyl ether, and 2,2,3,3-tetrafluoropropyl-2(2-methoxyethoxy)ethyl ether, Lithium secondary battery.

2. 2. The lithium secondary battery according to claim 1, wherein the electrolyte solution further contains an ether compound having no fluorine atoms.

3. 3. The lithium secondary battery according to claim 1, wherein the electrolyte solution further contains a chain fluorine compound having at least one of monovalent groups represented by the following formula (A) or (B): 【Chemistry 1】 【Chemistry 2】 (In formulas (A) and (B), the wavy lines represent bonding sites in monovalent groups.)

4. 4. The lithium secondary battery according to claim 1, wherein the electrolyte solution contains both the first fluorine compound and the second fluorine compound.

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