Patent Application
20230070559
The present invention relates to an additive for a nonaqueous electrolyte, a nonaqueous electrolyte including the additive, and a nonaqueous electrolyte secondary battery.
A material containing a silicon element is promising as a high-capacity negative electrode material for a secondary battery. However, since the material containing a silicon element significantly expands and contracts with charge and discharge, it easily induces side reactions, and the capacity retention rate in charge/discharge cycles tends to be lowered.
Non-Patent Literature 1 reports that the capacity retention rate in charge/discharge cycles improves by adding a silane coupling agent containing a vinyl group to an electrolyte of a single electrode battery using a Si/C composite.
It is difficult to stably improve capacity retention rate in charge/discharge cycles with the proposal of Non-Patent Literature 1.
One aspect of the present disclosure relates to an additive for a nonaqueous electrolyte including an alkoxysilyl compound, wherein the alkoxysilyl compound has two or more silyl groups coupled with an alkylene group or an amino group, the two or more silyl groups each has at least one selected from the group consisting of an alkoxy group and an oxyalkyl group, and the oxyalkyl group is represented by —O—(CxH2+1Oy), where x is an integer of 1 or more, and y is an integer of 1 or more.
Another aspect of the present disclosure relates to a nonaqueous electrolyte including a nonaqueous solvent, a salt dissolved in the nonaqueous solvent, and the above-described additive for a nonaqueous electrolyte.
Yet another aspect of the present disclosure relates to a nonaqueous electrolyte secondary battery including a negative electrode including a negative electrode mixture layer, a positive electrode, and the above-described nonaqueous electrolyte, wherein the negative electrode mixture layer includes a negative electrode active material, and the negative electrode active material includes a material containing a silicon element.
According to the present disclosure, when the negative electrode active material contains the material containing a silicon element, capacity retention rate in charge/discharge cycles of a nonaqueous electrolyte secondary battery can be stably improved.
The additive for a nonaqueous electrolyte according to the embodiment of the present disclosure includes an alkoxysilyl compound. The alkoxysilyl compound has two or more silyl groups coupled with an alkylene group or an amino group. Each of the two or more silyl groups has at least one selected from the group consisting of an alkoxy group and an oxyalkyl group, the oxyalkyl group is represented by —O—(CxH2x+1Oy), where x is an integer of 1 or more, and y is an integer of 1 or more.
The alkoxysilyl compound may be a bis-alkoxysilyl compound or a tris-alkoxysilyl compound. In the bis-alkoxysilyl compound, the two silyl groups are coupled with an alkylene group or a secondary amino group. In the tris-alkoxysilyl compound, three alkoxysilyl groups are coupled with a tertiary amino group.
In the above-described configuration, the alkoxy group or oxyalkyl group of each silyl group is considered to form X—O—Si bonds with the surfaces of the material containing a silicon element. Here, X denotes the surface of the material containing a silicon element and O coupled with X denotes, for example, an O atom (or residue of OH group) that is present on the surface of the material containing a silicon element. By each of the alkoxy group or oxyalkyl group forming a bond with the surface of the material containing a silicon element, the surface of the material containing a silicon element is covered with a bis-silyl alkane or bis-silyl amine structure (including a tris-silyl amine structure) having stable siloxane bonds at both ends. That is, the surfaces of the material containing a silicon element are covered with a coating (hereinafter, also referred to as SRS coating) containing a bis-silyl alkane or bis-silyl amine structure. The SRS coating has a high elasticity, is stable against reversible elastic deformation, and is not easily damaged even when charge/discharge cycle is repeated. As a result, side reaction in the negative electrode is suppressed, and capacity retention rate in charge/discharge cycles is stably improved.
The alkoxysilyl compound may be at least one selected from the group consisting of bis(alkoxysilyl)alkane and bis(alkoxysilyl alkyl)amine represented by general formula (1) below:
The bis(alkoxysilyl alkyl)amine has an alkylene group between N and Si.
In the formula. R1 is an alkylene group, or a secondary or tertiary amino group. At least one of R2 to R4 is at least one selected from the group consisting of an alkoxy group having 1 to 6 carbon atoms, and an oxyalkyl group represented by —O—(CxH2x+1Oy), where x1 is an integer of 1 or more, and y1 is an integer of 1 or more. At least one of R5 to R7 is at least one selected from the group consisting of an alkoxy group having 1 to 6 carbon atoms, and an oxyalkyl group represented by —O—(Cx2H2x2+1Oy2), where x2 is an integer of 1 or more, and y2 is an integer of 1 or more. The remainder of R2 to R7 is each independently an alkyl group or oxyalkyl group represented by Cx3H2x3+1Oy3, where x3 is an integer of 1 or more, y3 is an integer of 0 or more. However, the oxyalkyl group is a group other than the alkoxy group.
The alkoxy group or oxyalkyl group included in R2 to R4 and R5 to R7 each forms a X—O—Si—R1 bond with the surface of the material containing a silicon element, and the surface of the material containing a silicon element is covered with a Si—R1—Si structure having stable siloxane bonds at both ends. That is, the surface of the material containing a silicon element is covered with an SRS coating containing a Si-R1-Si structure.
The alkylene group constituting R1 with a larger carbon number allows for better flexibility, which facilitates reversible deformation of the SRS coating. However, if the carbon number of R1 is excessively large, the alkylene chain becomes excessively long, the denseness of the SRS coating is reduced, and the effect of suppressing side reactions is reduced. Therefore, it is desirable that the carbon number of the alkylene group is 1 to 6, and the carbon number of 2 to 4 is more desirable. The bis(alkoxysilyl)alkane is desirably bis(alkoxysilyl)C1-6alkane, or may be bis(alkoxysilyl)C2-4alkane.
The amino group constituting R1 may have a structure represented by R11-N—R12. Here, R11 and R12 are each independently an alkylene group with 1 or more carbon atoms. It is considered that such R1 is excellent in flexibility, has significant electron-shielding properties, and is more effective in suppressing side reactions.
The amino group with a larger carbon number allows for better flexibility, which facilitates reversible deformation of the SRS coating. However, if the carbon number of the amino group is excessively large, R1 becomes excessively long, the denseness of the SRS coating is reduced, and the effect of suppressing side reactions is reduced. Therefore, it is desirable that the carbon number of the alkylene group is 1 to 6, and the carbon number of 2 to 4 is more desirable. For example, bis(alkoxysilyl alkyl)amine is desirably bis(alkoxysilyl C1-6alkyl)amine, or may be bis(alkoxysilyl C2-4alkyl)amine.
At least one of R2 to R4 may be at least one selected from the group consisting of an alkoxy group having 1 to 6 carbon atoms, and an oxyalkyl group represented by —O—(Cx1H2x+1Oy1), where x1 is an integer of 1 to 6, and y1 is 1 or 2; and at least one of R5 to R7 is at least one selected from the group consisting of an alkoxy group having 1 to 6 carbon atoms, and an oxyalkyl group represented by —O—(Cx2H2x2+1Oy2), where x2 is an integer of 1 to 6, and y2 is 1 or 2. The alkoxy group and oxyalkyl group may be smaller in view of increasing reactivity with the surfaces of the material containing a silicon element, and the carbon number of the alkoxy group and oxyalkyl group may be, for example, 1 to 3.
The remainder of R2 to R7 is each independently an alkyl group, or an oxyalkyl group other than the alkoxy group represented by Cx3H2x3+1Oy3, where x3 is an integer of 1 or more, and y3 is an integer of 0 or more (e.g., integer of 0 or more and 2 or less). In view of reducing steric hindrance at the time of reaction, the carbon number of the group represented by Cx3H2x3+1Oy3 may be 1 to 6, or may be 1 to 3. Each of R2 to R4 is independent, and R2 to R4 may each have the same or a different carbon number, or two of R2 to R4 may have the same carbon number. Similarly, each of R5 to R7 is independent, and R5 to R7 may each have the same or a different carbon number, or two of R5 to R7 may have the same carbon number.
In formula (1), two alkoxysilyl groups (R2R3R4Si—, or R5R6R7Si—) coupled with R1 may be the same or different from each other. However, to form a more symmetrical SRS coating structure for a more stable structure, the two alkoxysilyl groups coupled with R1 may be the same structure.
In formula (1), when R1 is an alkylene group, the alkoxysilyl compound is a type of bis(alkoxysilyl)alkane. The SRS coating formed when bis(alkoxysilyl)alkane) is used is composed of a stable siloxane structure and an alkylene structure. Such an SRS coating is not only easy to elastically deform but also chemically and structurally stable.
Among the bis(alkoxysilyl)alkane, readily available examples include at least one selected from the group consisting of 1,2-bis(trialkoxysilyl)ethane and 1,6-bis(trialkoxysilyl)hexane. Examples of the 1,2-bis(trialkoxysilyl)ethane include 1,2-bis(trimethoxysilyl)ethane, and 1,2-bis(triethoxysilyl)ethane. Examples of the 1,6-bis(trialkoxysilyl)hexane include 1,6-bis(trimethoxysilyl)hexane, and 1,6-bis(triethoxysilyl)hexane.
In formula (1), when R1 is an amino group, the alkoxysilyl compound is a type of alkoxysilyl alkylamine. More specifically, the alkoxysilyl alkylamine may be at least one selected from the group consisting of bis(alkoxysilyl alkyl)amine and tris(alkoxysilyl alkyl)amine.
Among bis or tris(alkoxysilyl alkyl)amine, readily available examples include at least one selected from the group consisting of bis[3-(trialkoxysilyl)propyl] amine and tris[3-(trialkoxysilyl)propyl] amine. Examples of the bis[3-(trialkoxysilyl)propyl] amine include bis[3-(trimethoxysilyl)propyl] amine, and bis[3-(triethoxy silyl)propyl] amine. Examples of the tris[3-(trialkoxysilyl)propyl] amine include tris[3-(trimethoxysilyl)propyl] amine, and tris[3-(triethoxy silyl)propyl] amine.
The nonaqueous electrolyte includes a nonaqueous solvent, a salt (solute) dissolved in the nonaqueous solvent, and the above-described additive for a nonaqueous electrolyte. The salt (solute) is an electrolyte salt whose ions dissociate in the nonaqueous solvent. When the nonaqueous electrolyte is used for a lithium ion secondary battery, the salt includes at least a lithium salt. The component of the nonaqueous electrolyte other than the nonaqueous solvent and salt is an additive, and at least a part of the additive is the above-described alkoxysilyl compound.
The concentration of the alkoxysilyl compound in the nonaqueous electrolyte may be, for example, 10 mass % or less, may be 8 mass % or less, or may be 5 mass % or less. The concentration in this range is sufficient for forming a good and suitable SRS coating, regardless of the amount of the material containing a silicon element contained in the negative electrode active material. With a concentration of the alkoxysilyl compound represented by the formula (1) in the nonaqueous electrolyte of, for example, 0.2 mass % or more, it is considered that a considerable SRS coating is formed, and a significant effect of improving capacity retention rate in charge/discharge cycles of a nonaqueous electrolyte secondary battery can be obtained.
However, since the alkoxysilyl compound reacts in the nonaqueous electrolyte secondary battery, the concentration in the nonaqueous electrolyte gradually decreases. Therefore, it is sufficient that the alkoxysilyl compound of the detection-limit or more remains in the nonaqueous electrolyte taken-out from disassembled batteries of those completed nonaqueous electrolyte secondary batteries or nonaqueous electrolyte secondary batteries distributed on the market.
For the nonaqueous solvent, for example, cyclic carbonate, chain carbonate, cyclic carboxylate, chain carboxylate, etc. are used. Examples of the cyclic carbonate include propylene carbonate (PC), ethylene carbonate (EC), and vinylene carbonate (VC). Examples of the chain carbonate include diethyl carbonate (DEC), ethyl methyl carbonate (EMC), and dimethyl carbonate (DMC). Examples of the cyclic carboxylate include γ-butyrolactone (GBL) and γ-valerolactone (GVL). Examples of the chain carboxylate include methyl acetate, ethyl acetate, propyl acetate, methyl propionate (MP), ethyl propionate (EP), and the like. A kind of nonaqueous solvent may be used singly, or two or more kinds thereof may be used in combination.
Of these examples, the chain carboxylate is suitable for preparation of a low viscosity nonaqueous electrolyte. Thus, the nonaqueous electrolyte may include 1 mass % or more and 90 mass % or less of the chain carboxylate. Among the chain carboxylate, methyl acetate has a particularly low viscosity. Therefore, 90 mass % or more of the chain carboxylate may be methyl acetate.
Examples of the nonaqueous solvent also include cyclic ethers, chain ethers, nitriles such as acetonitrile, and amides such as dimethylformamide.
Examples of the cyclic ether include 1,3-dioxolane, 4-methyl-1,3-dioxolane, tetrahydrofuran, 2-methyl tetrahydrofiunn, propylene oxide, 1,2-butylene oxide, 1,3-dioxane, 1,4-dioxane, 1,3,5-trioxane, furan, 2-methyl-fiuran, 1,8-cineol, and crown ether.
Examples of the chain ether include 1,2-dimethoxyethane, dimethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, dihexyl ether, ethyl vinyl ether, butyl vinyl ether, methyl phenyl ether, ethyl phenyl ether, butyl phenyl ether, pentyl phenyl ether, methoxy toluene, benzyl ethyl ether, diphenyl ether, dibenzyl ether, o-dimethoxy benzene, 1,2-diethoxyethane, 1,2-dibutoxy ethane, diethylene glycol dimethylether, diethylene glycol diethyl ether, diethylene glycol dibutyl ether, 1,1-dimethoxy methane, 1,1-diethoxy ethane, triethylene glycol dimethylether, tetraethylene glycol dimethyl ether, and the like.
These solvents may be a fluorinated solvent in which part of the hydrogen atoms is substituted with a fluorine atom. Fluoro ethylene carbonate (FEC) may be used as the fluorinated solvent.
Examples of the lithium salt include, a lithium salt of chlorine containing acid (LiClO4, LiAlCl4, LiB10Cl10, etc.), a lithium salt of fluorine containing acid (LiPF6, LiPF2O2, LiBF4, LiSbF6, LiAsF6, LiCF3SO3, LiCF3CO2, etc.), a lithium salt of fluorine containing acid imide (LiN(FSO2)2, LiN(CF3SO2)2, LiN(CF3SO2)(C4F9SO2), LiN (C2F5SO2)2, etc.), a lithium halide (LiCl, LiBr, LiI etc.) and the like. A kind of lithium salt may be used singly, or two or more kinds thereof may be used in combination.
The concentration of the lithium salt in the nonaqueous electrolyte may be 0.5 mol/liter or more and 2 mol/liter or less, or may be 1 mol/liter or more and 1.5 mol/liter or less. By controlling the concentration of lithium salt to be in the above-described range, a nonaqueous electrolyte having excellent ion conductivity and low viscosity can be obtained.
Examples of the additive other than the alkoxysilyl compound include 1,3-propanesultone, methylbenzenesulfonate, cyclohexylbenzene, biphenyl, diphenyl ether, and fluorobenzene.
A nonaqueous electrolyte secondary battery according to the present disclosure includes a positive electrode, a negative electrode, and the nonaqueous electrolyte described above.
The negative electrode includes, for example, a negative electrode current collector, and a negative electrode mixture layer formed on the surface of the negative electrode current collector. The negative electrode mixture layer contains a negative electrode active material as an essential component, and may contain a binder, a conductive agent, a thickener, and the like as an optional component. Known materials can be used for the optional component such as the binder, the conductive material, and the thickener.
The negative electrode mixture layer can be formed, for example, by applying a negative electrode slurry, in which a negative electrode mixture containing a negative electrode active material and a predetermined optional component are dispersed in a dispersion medium, on a surface of the negative electrode current collector and drying. The dried coating film may be rolled, if necessary. The negative electrode mixture layer may be formed on one surface of the negative electrode current collector, or on both surfaces thereof.
The negative electrode active material includes a material containing a silicon element. The material containing a silicon element may be treated as a type of alloy based materials. Here, the alloy based material refers to a material containing an element capable of forming an alloy with lithium. Silicon and tin are examples of the element that can form an alloy with lithium, and silicon (Si) is particularly promising.
As the material containing silicon, a silicon alloy, a silicon compound, or the like may be used, and a composite material may also be used. Among them, a composite material containing a lithium ion conductive phase and silicon particles dispersed in the lithium ion conductive phase is promising. As the lithium ion conductive phase, for example, a silicon oxide phase, silicate phase, carbon phase, or the like can be used. The silicon oxide phase has a relatively large irreversible capacity. On the other hand, the silicate phase is preferable in that its irreversible capacity is small.
The main component (e.g., 95 to 100 mass %) of the silicon oxide phase may be silicon dioxide. The composition of the composite material including the silicon oxide phase and silicon particles dispersed therein, as a whole, can be expressed as SiOx. SiOx has a structure in which fine particles of silicon are dispersed in SiO2 in an amorphous form. The content ratio x of oxygen to silicon is, for example, 0.5≤x≤2.0, more preferably 0.8≤x≤1.5.
The silicate phase may include, for example, at least one selected from the group consisting of Group 1 element and Group 2 element of the long-form periodic table. Examples of the Group 1 element and Group 2 element of the long-form periodic table include lithium (Li), potassium (K), sodium (Na), magnesium (Mg), calcium (Ca), strontium (Sr), barium (Ba), and the like. Other elements that can be included are aluminum (Al), boron (B), lanthanum (La), phosphorus (P), zirconium (Zr), titanium (Ti), and the like. In particular, the silicate phase containing lithium (hereinafter also referred to as lithium silicate phase) is preferable because of its small irreversible capacity and high initial charge/discharge efficiency.
The lithium silicate phase may be any oxide phase containing lithium(Li), silicon (Si), and oxygen (O), and may include other element. The atomic ratio of O to Si in the lithium silicate phase: O/Si is, for example, larger than 2 and less than 4. Preferably, O/Si is larger than 2 and less than 3. The atomic ratio of Li to Si in the silicate phase: Li/Si is, for example, larger than 0 and less than 4. The lithium silicate phase may have a composition represented by the formula: Li2zSiO2+z(0<z<2). Preferably, the relation 0<z<1 is satisfied, and z=½ is more preferable. Examples of the elements other than Li, Si, and O included in the lithium silicate phase include iron (Fe), chromium(Cr), nickel (Ni), manganese (Mn), copper (Cu), molybdenum (Mo), zinc (Zn), aluminum (Al), etc.
The carbon phase may be composed of, for example, an amorphous carbon with less crystallinity. The amorphous carbon may be, for example, hard carbon, soft carbon, or something else.
In addition to the material containing a silicon element, the negative electrode active material may include a material that electrochemically stores and releases lithium ions, lithium metal, lithium alloy, and the like. As the material that electrochemically stores and releases lithium ions, a carbon material is preferable.
Examples of the carbon material include graphite, soft carbon, hard carbon, and the like. Particularly, graphite with excellent charge/discharge stability and low irreversible capacity is preferable.
For the negative electrode current collector, for example, a metal sheet or metal foil is used. As the material of the negative electrode current collector, stainless steel, nickel, nickel alloy, copper, copper alloy, and the like can be exemplified.
The positive electrode includes, for example, a positive electrode current collector, and a positive electrode mixture layer formed on the surface of the positive electrode current collector. The positive electrode mixture layer contains a positive electrode active material as an essential component, and may contain a binder, a conductive agent, a thickener, and the like as an optional component. Known materials can be used for the optional component such as the binder, the conductive material, and the thickener.
The positive electrode mixture layer can be formed, for example, by applying a positive electrode slurry, in which a positive electrode mixture containing a positive electrode active material and a predetermined optional component are dispersed in a dispersion medium on a surface of the positive electrode current collector and drying. The dried coating film may be rolled, if necessary. The positive electrode mixture layer may be formed on one surface of the positive electrode current collector, or may be formed on both surfaces thereof.
The positive electrode active material includes, for example, a lithium-containing composite oxide. The lithium-containing composite oxide is not particularly limited, but one having a layered rock salt type crystal structure containing lithium and transition metal is promising. Specifically, the lithium-containing composite oxide may be, for example, LiaNi1−x−yCoxMyO2(where 0<a≤1.2, 0≤x≤0.1, 0≤y≤0.1, 0<x+y≤0.1, and M is at least one selected from the group consisting of Na, Mg, Sc, Y, Mn, Fe, Cu, Zn, Al, Cr, Pb, Sb, and B). From the viewpoint of stabilities of the crystal structure, Al may be contained as M. Note that the value “a” indicating the molar ratio of lithium is increased or decreased by charging and discharging. Specific examples include LiNi0.9Co0.05Al0.05O2, LiNi0.91Co0.06Al0.03O2, and the like.
The positive electrode active material (particularly lithium-containing composite oxide) usually is in the form of secondary particles of coagulated primary particles. The avenge particle size of the positive electrode active material may be, for example, 2 μm or more, and 20 μm or less. Here, the average particle size refers to a median diameter in which the cumulative volume in volume-based particle size distribution is 50%. The volume-based particle size distribution can be measured by laser diffraction particle size distribution analyzer.
For the positive electrode current collector, for example, a metal sheet or metal foil is used. As the material of the positive electrode current collector, stainless steel, aluminum, aluminum alloy, titanium, and the like can be exemplified.
Examples of the conductive material used for the positive electrode mixture layer and negative electrode mixture layer include carbon materials such as carbon black (CB), acetylene black (AB), Ketjen Black (KB), carbon nanotube (CNT), and graphite. A kind of the conductive material may be used singly, or two or more kinds may be used in combination.
Examples of the binder for the positive electrode mixture layer and negative electrode mixture layer include fluororesin (polytetrafluoroethylene, polyvinylidene fluoride, etc., polyacrylonitrile (PAN), polyimide resin, acrylic resin, polyolefin resin, and the like. A kind of the binder may be used singly, or two or more kinds may be used in combination.
Usually, a separator is interposed between the positive electrode and the negative electrode. The separator has excellent ion permeability and suitable mechanical strength and electrically insulating properties. The separator may be, for example, a microporous thin film, a woven fabric, or a nonwoven fabric. The separator is preferably made of, for example, polyolefin, such as polypropylene and polyethylene.
In an example structure of a secondary battery, an electrode group and a nonaqueous electrolyte are accommodated in an outer package, the electrode group having a positive electrode and a negative electrode wound with a separator. Alternatively, instead of the wound electrode group, other forms of electrode group may be applied, such as a laminated electrode group in which a positive electrode and negative electrode are laminated with a separator interposed. The nonaqueous electrolyte secondary battery may be in any form, e.g., cylindrical, prismatic, coin-shaped, button shaped, sheet (laminate) shaped, etc.
Referring to
As shown in
The electrode group 4 has a structure in which a positive electrode 10, a separator 30, and a negative electrode 20 are stacked in this order, and the positive electrode 10 and the negative electrode 20 face each other with the separator 30 interposed therebetween. The electrode group 4 is formed in this manner. The electrode group 4 is impregnated with a nonaqueous electrolyte.
The positive electrode 10 includes a positive electrode active material layer 1a and a positive electrode current collector 1b. The positive electrode active material layer 1a is formed on the surface of the positive electrode current collector 1b.
The negative electrode 20 includes a negative electrode mixture layer 2a and a negative electrode current collector 2b. The negative electrode mixture layer 2a is formed on the surface of the negative electrode current collector 2b.
A negative electrode tab lead 1c is connected to the negative electrode current collector 1b, and a negative electrode tab lead 2c is connected to the negative electrode current collector 2b. The positive electrode tab lead 1c and negative electrode tab lead 2c each extends out of the outer case 5.
An insulating tab film 6 insulates the positive electrode tab lead 1c from the outer case 5, and the negative electrode tab lead 2c from the outer case 5.
In the following, the present disclosure will be specifically described based on Examples and Comparative Examples, but the present disclosure is not limited to Examples below.
A negative electrode slurry was made by mixing SiOx(x=1) (Shin-Etsu Chemical Co., KSC1064), carbon black (Denka Company Limited, HS-100), and an aqueous solution of polyacrylamide (binder) so that mass ratio of SiOx: carbon black: polyacrylamide was 75:15:10; further adding water to the mixture; and agitating the mixture. Next, a coating film was formed by applying the negative electrode slurry on one side of a negative electrode current collector (electrolytic copper foil). After the coating film was dried, the coating film was rolled together with the negative electrode current collector by a roller to obtain a negative electrode including a negative electrode mixture layer.
A negative electrode was cut into the form shown in
A counter electrode was produced by attaching a lithium metal foil to one surface of an electrolytic copper foil (current collector).
The counter electrode was cut out into the same shape as the negative electrode, and the lithium metal foil formed on the connecting region formed in the same manner as the negative electrode was peeled off to expose the current collector. The exposed part of the current collector was connected to the tab lead in the same manner as the negative electrode, and afterwards, a predetermined region of the outer periphery of the tab lead was covered with an insulating tab film.
A nonaqueous electrolyte was prepared by dissolving LiPF6 in a solvent mixture of fluoroethylene carbonate (FEC) and dimethyl carbonate (DMC) (volume ratio 20:80) at a concentration of 1 moL/L. To the nonaqueous electrolyte, 0.25 mass % of 1,2-bis(trimethoxysilyl)ethane (EBTMOS) represented by the following formula (1-1) was added.
Using the negative electrode for evaluation as described above and a counter electrode, a cell with a designed capacity of 114 mAh, which is regulated by the negative electrode, was produced. First, the negative electrode and counter electrode were allowed to face each other with two sheets of a polyethylene made separator (thickness 15 μm) having an aramid coating so that the negative electrode mixture layer overlaps with the lithium metal foil, thereby producing an electrode group. Next, an Al laminate film (thickness 100 μm) cut into a rectangular shape was folded in half, and longitudinal ends were heat-sealed at 230° C. to form an envelope. Afterwards, the fabricated electrode group was put into the envelope from one of short sides, and heat-sealing at 230° C. was performed, aligning the position of the thermal welding resin of respective tab leads with the end face of the Al laminate film. Next, 1.2 cm3 of the nonaqueous electrolyte was injected from the not heat-sealed portion of the short side of the envelope, and after the injection, the operation of allowing it to stand for 3 minutes under a reduced pressure of 0.02 MPa, and to return to an atmospheric pressure environment was carried out twice to impregnate the negative electrode mixture layer with the nonaqueous electrolyte. Finally, the end face of the liquid-injected side of the Al laminate film was heat-sealed at 230° C. to obtain a cell A1 for evaluation. The evaluation cell was prepared in a dry air atmosphere having a dew point of −60° C. or less.
The evaluation cell was sandwiched with a clamp between a pair of 10×5 cm stainless steel (thickness 6 mm) plates and fixed under pressure with 3.2 MPa.
In a thermostatic chamber at 25° C., the negative electrode was charged with lithium over 2 hours at a constant current of 0.05 C (1 C is a current value at which designed capacity is discharged by an hour), and the negative electrode was allowed to stand for 12 hours. The negative electrode was then charged further to a cell voltage of 0.01 V with a constant current of 0.05 C, and allowed to stand for 20 minutes. Lithium was then discharged from the negative electrode to a cell voltage of 1.5 V at a constant current of 0.05 C, and the cell was allowed to stand for 20 minutes.
The negative electrode was then charged with lithium to a cell voltage of 0.01 V with a constant current of 0.05 C, and allowed to stand for 20 minutes. Lithium was then discharged from the negative electrode to a cell voltage of 1.5 V at a constant current of 0.05 C and the cell was allowed to stand for 20 minutes.
The negative electrode was charged with lithium at a constant current of 0.3 C to a cell voltage of 0.01 V, and allowed to stand for 20 minutes, and thereafter, lithium was discharged from the negative electrode to a cell voltage of 1.5 V at a constant current of 0.3 C, and the cell was allowed to stand for 20 minutes: this cycle was repeated.
The ratio of the capacity obtained by the lithium discharge of the 50th cycle to the capacity obtained by the lithium discharge of 1st cycle was determined as 50th cycle capacity retention rate. Table 1 shows the results.
Evaluation cells A2 to A7 were prepared and evaluated in the same manner as in Example 1, except that in preparation of the nonaqueous electrolyte, the content of EBTMOS to be added to the nonaqueous electrolyte was changed as shown in Table 1.
Evaluation cells A8 to A10 were prepared and evaluated in the same manner as in Example 1, except that 1,6-bis(trimethoxysilyl)hexane (HBTMOS) represented by the formula (1-2) below was added in an amount shown in Table 1 to the nonaqueous electrolyte instead of EBTMOS in preparation of the nonaqueous electrolyte.
[Chemical Formula 3]
Evaluation cells B1 and B2 were prepared and evaluated in the same manner as in Example 1, except that vinyltris(2-methoxyethoxy)silane (VTMS) represented by the formula (2) below was added in an amount shown in Table 1 to the nonaqueous electrolyte instead of EBTMOS in preparation of the nonaqueous electrolyte. VTMS is the additive used in Non-Patent Literature 1.
An evaluation cell B3 was prepared and evaluated in the same manner as in Example 1, except that in preparation of the nonaqueous electrolyte, EBTMOS was not added.
Table 1 and
On the other hand, as shown in
The additive for a nonaqueous electrolyte according to the present disclosure is suitably used for a nonaqueous electrolyte secondary battery in which a negative electrode active material contains a material containing a silicon element.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-014238 | Jan 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/001956 | 1/21/2021 | WO |
