Patent Application
20220045321
The present disclosure relates to a positive electrode active material for a secondary battery and a secondary battery.
Aqueous lithium secondary batteries using an aqueous solution as an electrolytic solution are known. Aqueous lithium secondary batteries need to be used in an electric potential range in which the electrolytic reaction of water does not occur. An active material needs to be used that is stable in an aqueous solution and can reversibly occlude and release a large amount of lithium in a potential range in which oxygen or hydrogen is not generated by water electrolysis, namely an active material that can exhibit large capacity in a specific potential range. It has been desired to use a neutral or alkaline electrolytic solution as an electrolytic solution. When a neutral electrolytic solution, namely an electrolytic solution of pH=7, is used, the hydrogen generating potential is 2.62 V and the oxygen generating potential is 3.85 V for the water decomposition voltage. When a strong alkaline electrolytic solution, namely an electrolytic solution of pH=14 is used, the hydrogen generating potential is 2.21 V and the oxygen generating potential is 3.44 V for the water decomposition voltage.
Therefore, a material from which more Li can be extracted before or when the potential reaches at least 3.85 V (pH=7) has been desired as a positive electrode active material. A material in which more Li can be inserted before or when the potential reaches 2.21 V (pH=14) has been desired as a negative electrode active material.
Patent Literature 1 discloses that a positive electrode active material for aqueous lithium secondary batteries has a compound having a layered structure and represented by the general formula LisNixCoyMnzMtO2 (0.9≤s≤1.2, 0.25≤x≤0.4, 0.25≤y≤0.4, 0.25≤z≤0.4, 0≤t≤0.25, and M is one or more selected from Mg, Al, Fe, Ti, Ga, Cu, V, and Nb) as the main ingredient.
In secondary batteries using aqueous solutions, technology has been required that enables expanding a potential region in which electrolysis does not occur and improving the durability thereof, namely suppressing battery deterioration at the time of charge and storage.
It is an advantage of the present disclosure to provide a positive electrode active material for a secondary battery and a secondary battery in which battery deterioration at the time of charge and storage is suppressed in the positive electrode active material for a secondary battery using an aqueous electrolytic solution and the secondary battery using an aqueous electrolytic solution.
The positive electrode active material for a secondary battery according to one aspect of the present disclosure is a positive electrode active material for a secondary battery having an electrolytic solution prepared by dissolving a lithium salt in water, wherein the positive electrode active material is represented by the general formula LiaNixCoyMnzMbO2, wherein
0.9<a<1.1,
0.4<x<1,
0≤y<0.4,
0≤z<0.4,
0≤b<0.2, and
0.9<(x+y+z+b)<1.1
are satisfied, and an element M includes at least one selected from the group consisting of Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, Al, Ga, and In.
According to the present disclosure, battery deterioration at the time of charge and storage may be suppressed.
The present inventors have earnestly examined and consequently found that the use of a specific material as a positive electrode active material in an electrolytic solution containing water as a solvent and a lithium salt as an electrolyte salt enables suppressing the deterioration of a battery at the time of charge and storage.
Embodiments of the positive electrode active material and the secondary battery according to one aspect of the present disclosure will be described hereinafter. However, the embodiments described below are examples, and the present disclosure is not limited to these.
[Aqueous Electrolytic Solution]
An aqueous electrolytic solution according to the present embodiment includes at least water and a lithium salt. When an electrolytic solution containing water as a solvent is used, water decomposes at a voltage of 1.23 V theoretically. Therefore, the development of a secondary battery in which even though higher voltage is impressed, water does not decompose and which operates steadily has also been desired.
(Solvent)
The aqueous electrolytic solution contains water as the main solvent. Here, containing water as the main solvent means that the volume ratio of the water content to the total volume of solvents included in the electrolytic solution is 50% or more. The content of water included in the electrolytic solution is preferably 90% or more based on the total amount of the solvents in terms of the volume ratio. The solvent included in the electrolytic solution may be a mixed solvent including water and a non-aqueous solvent. Examples of the non-aqueous solvent include alcohols such as methanol; carbonates such as dimethyl carbonate, ethyl methyl carbonate, diethyl carbonate, ethylene carbonate, and propylene carbonate; acetone; acetonitrile; and aprotic polar solvents such as dimethyl sulfoxide.
Since the aqueous electrolytic solution includes water, which does not have inflammability, as the main solvent, the safety of the secondary battery using the aqueous electrolytic solution can be enhanced. The content of water is preferably 8% by mass or more, and more preferably 10% by mass or more based on the total amount of the electrolytic solution from this viewpoint. The content of water is preferably 50% by mass or less, and more preferably 20% by mass or less based on the total amount of the electrolytic solution.
(Lithium Salt)
As long as a lithium salt included in the aqueous electrolytic solution is a compound which is dissolved in the solvent containing water, dissociates, and enables lithium ions to be present in the aqueous electrolytic solution, any lithium salt can be used. The lithium salt does not preferably deteriorate battery characteristics by reaction with materials constituting a positive electrode and a negative electrode. Examples of such a lithium salt include salts with inorganic acids such as perchloric acid, sulfuric acid, and nitric acid; salts with halide ions such as chloride ions and bromide ions; and salts with organic anions including carbon atoms in structure.
Examples of the organic anions constituting lithium salts include anions represented by the following general formulae (i) to (iii).
(R1SO2)(R2SO2)N− (i)
wherein R1 and R2 are each independently selected from halogen atoms, alkyl groups, or halogen-substituted alkyl groups, and R1 and R2 may be bonded to each other to form a ring.
R3SO3− (ii)
wherein R3 is selected from halogen atoms, alkyl groups, or halogen-substituted alkyl groups.
R4CO2− (iii)
wherein R4 is selected from alkyl groups or halogen-substituted alkyl groups.
In the above-mentioned general formulae (i) to (iii), the alkyl group or the halogen-substituted alkyl group has preferably 1 to 6 carbon atoms, more preferably 1 to 3 carbon atoms, and further preferably 1 to 2 carbon atoms. As the halogen of the halogen-substituted alkyl group is preferably fluorine. The number of halogen atoms substituted in the halogen-substituted alkyl group is not more than the number of the hydrogen atoms of the original alkyl group. As halogen atoms in the above-mentioned general formulae (i) to (ii), a fluorine atom is preferable.
When each of R1 to R4 is, for example, a saturated alkyl group or a saturated halogen-substituted alkyl group, and R1 to R2 are not bonded to each other not to form a ring, each of R1 to R4 may be a group represented by the following general formula (iv).
CnHaFbClcBrdIe (iv)
wherein n is an integer of 1 or more, and a, b, c, d, and e are integers of 0 or more, and satisfy 2n+1=a+b+c+d+e.
In the above-mentioned general formula (iv), a is preferably smaller, a=0 is more preferable, and 2n+1=b is the most preferable from the viewpoint of oxidation resistance.
Specific examples of the organic anion represented by the above-mentioned general formula (i) include bis(fluorosulfonyl)imide (FSI; [N(FSO2)2]−), bis(trifluoromethanesulfonyl)imide (TFSI; [N(CF3SO2)2]−), bis(perfluoroethanesulfonyl)imide (BETI; [N(C2F5SO2)2]−), and (perfluoroethanesulfonyl)(trifluoromethanesulfonyl)imide ([N(C2F2SO2)(CF3SO2)]−). Specific examples of the organic anion formed by binding R1 to R2 to each other to form a ring include cTFSI; ([N(CF2SO2)2]−). Specific examples of the organic anion represented by the above-mentioned general formula (ii) include FSO3−, CF3SO3−, and C2F5SO3−. Specific examples of the organic anion represented by the above-mentioned general formula (iii) include CF3CO2 and C2F5CO2−.
Examples of an organic anion other than the above-mentioned general formula (i) include anions such as bis(1,2-benzenediolate(2-)-O,O′)borate, bis(2,3-naphthalenediolate(2-)-O,O′)borate, bis(2,2′-biphenyldiolate(2-)-O,O′)borate, and bis(5-fluoro-2-olate-1-benzenesulfonate-O,O′)borate.
As an anion constituting a lithium salt, an imide anion is preferable. Suitable specific examples of the imide anion include (fluorosulfonyl)(trifluoromethanesulfonyl)imide (FTI; [N(FSO2)(CF3SO2)]−) besides an imide anion illustrated as the organic anion represented by the above-mentioned general formula (i).
Specific examples of the lithium salt having a lithium ion and an imide anion include lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), lithium bis(perfluoroethanesulfonyl)imide (LiBETI), lithium (perfluoroethanesulfonyl)(trifluoromethanesulfonyl)imide, lithium bis(fluorosulfonyl)imide (LiFSI), and lithium (fluorosulfonyl)(trifluoromethanesulfonyl)imide (LiFTI).
Specific examples of other lithium salts include CF3SO3Li, C2F5SO3Li, CF3CO2Li, C2F5CO2Li, lithium bis(1,2-benzenediolate(2-)-O,O′)borate, lithium bis(2,3-naphthalenediolate(2-)-O,O′)borate, lithium bis(2,2′-biphenyldiolate(2-)-O,O′)borate, lithium bis(5-fluoro-2-olate-1-benzenesulfonate-O,O′)borate, lithium perchlorate (LiClO4), lithium chloride (LiCl), lithium bromide (LiBr), lithium hydroxide (LiOH), lithium nitrate (LiNO3), lithium sulfate (Li2SO4), lithium sulfide (Li2S), and lithium hydroxide (LiOH).
In the aqueous electrolytic solution according to the present embodiment, the content ratio of water to the lithium salt is preferably a molar ratio of 15:1 or less, and more preferably 4:1 or less. It is because when the content ratio of water to the lithium salt is in these ranges, the potential window of the aqueous electrolytic solution can be expanded, and voltage impressed on the secondary battery can be further increased. The content ratio of water to the lithium salt is preferably a molar ratio of 1.5:1 or more from the viewpoint of the safety of the secondary battery.
(Additive)
The aqueous electrolytic solution according to the present embodiment may further include additives and other electrolytes known in the art. As the other electrolytes, a lithium ion conductive solid electrolyte may further be included.
Examples of the additives include fluorophosphoates, carboxylic acid anhydrides, alkaline-earth metal salts, sulfur compounds, acids, and alkalis. The aqueous electrolytic solution preferably further include at least one of the group consisting of fluorophosphates, carboxylic acid anhydrides, alkaline-earth metal salts, and sulfur compounds. The content of these additives is, for example, 0.1% by mass or more and 5.0% by mass or less based on the total amount of the aqueous electrolytic solution.
Examples of the fluorophosphates which may be added to the aqueous electrolytic solution include lithium fluorophosphates represented by the general formula LixPFyOz (1≤x<3, 0<y≤2, 2≤z<4). When the aqueous electrolytic solution contains a fluorophosphate, the electrolysis of water can be suppressed. Specific examples of the lithium fluorophosphate include lithium difluorophosphates (LiPF2O2) and lithium monofluorophosphates (Li2PFO3), and LiPF2O2 is preferable. The fluorophosphate represented by the general formula LixPFyOz may be a mixture of two or more selected from LiPF2O2, Li2PFO3, and Li3PO4. In that case, x, y, and z may be numerical values other than integers. The content of the fluorophosphate may be, for example, 0.1% by mass or more, and is preferably 0.3% by mass or more based on the total amount of the aqueous electrolytic solution. The content of the lithium fluorophosphate may be, for example, 3.0% by mass or less, and is preferably 2.0% by mass or less based on the total amount of an aqueous electrolytic solution.
An alkaline-earth metal salt which may be added to the aqueous electrolytic solution is a salt having an ion of an alkaline-earth metal (Group 2 element) and an anion such as an organic anion. Examples of the alkaline-earth metal include beryllium (Be), magnesium (Mg), calcium (Ca), and strontium (Sr), and magnesium and calcium are preferable.
Examples of the organic anion constituting the alkaline-earth metal salt include organic anions described as the above-mentioned organic anions constituting lithium salts and represented by the general formulae (i) to (iii). However, the anion constituting the alkaline-earth metal salt may be an organic anion other than the organic anions represented by the general formulae (i) to (iii), or may be an inorganic anion.
The dissociation constant of the alkaline-earth metal salt in the aqueous electrolytic solution is preferably large. Suitable examples thereof include alkaline-earth-metal salts of perfluoroalkanesulfonic imides such as Ca[N(CF3SO3)2]2 (CaTFSI), Ca[N(CF3CF3SO2)2]2 (CaBETI), Mg[N(CF3SO3)2]2 (MgTFSI), and Mg[N(CF3CF3SO2)2]2 (MgBETI); alkaline-earth metal salts of trifluoromethanesulfonic acid such as Ca(CF3SO3)2 and Mg(CF3SO3)2; alkaline-earth metal perchlorates such as Ca[ClO4]2 and Mg[Clo4]2; and tetrafluoroborates such as Ca[BF4]2 and Mg[BF4]2. Among these, alkaline-earth metal salts of perfluoroalkanesulfonic imides are further preferable, and CaTFSI and CaBETI are particularly preferable from the viewpoint of plastic action. As the alkaline-earth metal salts, alkaline-earth metal salts having the same anion as the Li salts included in the electrolytic solution are also preferable. The alkaline-earth metal salts may be used alone, or may be used in combination of two or more. The content of the alkaline-earth metal salt may be, for example, 0.5% by mass or more and 3% by mass or less, and is preferably 1.0% by mass or more and 2% by mass or less based on the total amount of the aqueous electrolytic solution from the viewpoint of the expansion of the potential window to the base potential side.
The carboxylic acid anhydrides which may be added to the aqueous electrolytic solution includes a cyclic carboxylic acid anhydride and a chain-like carboxylic acid anhydride. Examples of the cyclic carboxylic acid anhydride include succinic anhydride, glutaric anhydride, maleic anhydride, citraconic anhydride, glutaconic anhydride, itaconic anhydride, diglycollic anhydride, cyclohexanedicarboxylic acid anhydride, cyclopentanetetracarboxylic acid anhydride, and phenylsuccinic anhydride. The chain-like carboxylic acid anhydride is an anhydride of two carboxylic acids which are selected from carboxylic acids such as acetic acid, propionic acid, butyric acid, and isobutyric acid having 1 to 12 carbon atoms, and are the same or is different. Specific examples thereof include acetic anhydride and propionic anhydride. When the carboxylic acid anhydride is added to the aqueous electrolytic solution, the carboxylic acid anhydride may be used alone or in combination of two or more. The content of the carboxylic acid anhydride may be, for example, 0.1% by mass or more and 5.0% by mass or less, and is preferably 0.3% by mass or more and 2.0% by mass or less based on the total amount of the aqueous electrolytic solution.
Examples of a sulfur compound which may be added to the aqueous electrolytic solution include organic compounds containing a sulfur atom in a molecule and included in neither the above-mentioned lithium salts, carboxylic acids nor alkaline-earth metal salts. When the aqueous electrolytic solution contains the sulfur compound, components contained in a film derived from the reduction reaction of anions such as TFSI and BETI represented by the general formulae (i) to (iii) can be compensated, and hydrogen generation which proceeds parasitically on a negative electrode can be shut off effectively. Specific examples of the sulfur compound include cyclic sulfur compounds such as ethylene sulfite, 1,3-propanesultone, 1,4-butanesultone, sulfolane, and sulfolene; sulfonic esters such as methyl methanesulfonate and busulfan; sulfones such as dimethyl sulfone, diphenyl sulfone, and methyl phenyl sulfone; sulfides or disulfides such as dibutyl disulfide, dicyclohexyl disulfide, and tetramethyl thiuram monosulfide; and sulfonamides such as N,N-dimethylmethanesulfonamide and N,N-diethylmethanesulfonamide. Among these sulfur compounds, ethylene sulfite, 1,3-propanesultone, 1,4-butanesultone, sulfolane, sulfolene, and the like are preferable, and ethylene sulfite is particularly preferable. When the sulfur compound is added to the aqueous electrolytic solution, the sulfur compound may be used alone or in combination of two or more. The content of the sulfur compound may be, for example, 0.1% by mass or more and 5.0% by mass or less, and is preferably 0.3% by mass or more and 2.0% by mass or less based on the total amount of the aqueous electrolytic solution.
The method for preparing the aqueous electrolytic solution according to the present embodiment is not particularly limited, for example, water and the lithium salt as well as the above-mentioned additives, if the additives are added, may be suitably mixed to prepare the aqueous electrolytic solution.
Although the pH of the aqueous electrolytic solution is not particularly limited, the pH may be, for example, 3 or more and 14 or less, and is preferably more than 10. It is because when the pH of the aqueous electrolytic solution is in these ranges, the stability of the positive electrode active material in the positive electrode and the negative electrode active material in the negative electrode in the aqueous solution can be improved, and the occlusion and release reactions of lithium ions in the positive electrode active material and the negative electrode active material are performed more smoothly.
[Secondary Battery]
A secondary battery according to an example of embodiments of the present disclosure will be described hereinafter. The secondary battery which is an example of the embodiments comprises the above-mentioned aqueous electrolytic solution, a positive electrode, and a negative electrode. The secondary battery has, for example, a structure in which an electrode assembly having the positive electrode, the negative electrode, and a separator and the aqueous electrolytic solution are stored in a battery case. Although examples of the electrode assembly include a wound electrode assembly, which is formed by winding the positive electrode and the negative electrode through the separator and a laminated electrode assembly, which is formed by laminating the positive electrode and the negative electrode through the separator, the shape of the electrode assembly is not limited to these.
Examples of the battery case which stores the electrode assembly and the aqueous electrolytic solution include cases made of metals or resins in a cylindrical shape, a square shape, a coin shape, a button shape, and the like and cases made of resins and obtained by molding a sheet in which metal foil and a resin sheet are laminated (laminated battery).
The secondary battery according to the present embodiment may be manufactured by a well-known method, and can be manufactured, for example, by storing the wound or laminated electrode assembly in the battery case body, pouring the aqueous electrolytic solution and then sealing the opening of the battery case body with a gasket and a sealing assembly.
[Positive Electrode]
The positive electrode constituting the secondary battery according to the present embodiment comprises, for example, a positive electrode current collector and a positive electrode active material layer formed on the positive electrode current collector. The positive electrode active material layer may be formed on one side of the positive electrode current collector, or may be formed on both sides. The positive electrode active material layer includes, for example, the positive electrode active material, a binding agent, a conductive agent, and the like.
As the positive electrode current collector, foil of a metal which is stable in the potential range of the positive electrode, a film wherein the metal is disposed on the outer layer, or the like can be used. As the positive electrode current collector, a porous body such as a mesh body, a punching sheet, or an expanded metal of the metal may be used. As the material of the positive electrode current collector, stainless steel, aluminum, an aluminum alloy, titanium, or the like can be used. The thickness of the positive electrode current collector is, for example, preferably 3 μm or more and 50 μm or less in terms of a current collection property, mechanical strength, and the like.
For example, positive electrode mixture slurry including the positive electrode active material, the conductive agent, the binding agent, and the like is applied to the positive electrode current collector and dried to form the positive electrode active material layer on the positive electrode current collector, and the positive electrode active material layer is rolled to obtain the positive electrode. As dispersion medium used for the positive electrode mixture slurry, for example, water; an alcohol such as ethanol; an ether such as tetrahydrofuran; N-methyl-2-pyrrolidone (NMP); or the like is used. Although the thickness of the positive electrode active material layer is not particularly limited, the thickness is, for example, 10 μm or more and 100 μm or less.
The positive electrode active material is a lithium transition metal oxide containing lithium (Li) and transition metal elements such as cobalt (Co), manganese (Mn), and nickel (Ni). A specific example of the lithium transition metal oxide is a lithium transition metal oxide wherein the lithium transition metal oxide is represented by LiaNixCoyMnzMbO2, wherein
0.9<a<1.1,
0.4<x<1,
0≤y<0.4,
0≤z<0.4,
0≤b<0.2, and
0.9<(x+y+z+b)<1.1
are satisfied.
The element M preferably includes at least one selected from the group consisting of titanium (Ti), zirconium (Zr), hafnium (Hf), vanadium (V), niobium (Nb), tantalum (Ta), chromium (Cr), molybdenum (Mo), tungsten (W), aluminum (Al), gallium (Ga), and indium (In).
The lithium transition metal oxide contains preferably more than 40% by mol Ni, and further preferably more than 50% by mol Ni based on the total amount of transition metals other than lithium in view of increasing the capacity. Specifically, x satisfies 0.4<x<1.0, and it is further preferable that 0.5<x<1.0. It is preferable that 0≤y<0.4, 0≤z<0.4, 0≤b<0.2, and 0.9<(x+y+z+b)<1.1 in view of the stability of the crystal structure.
Here, a pattern in which the element M is present in a solid solution state in the positive electrode active material and a pattern in which the element M is present on the surface of the positive electrode active material as a compound are possible as forms in which the element M is present in the positive electrode active material. The element M of the present embodiment may be present in at least one pattern of the group consisting of these two patterns. It can be determined depending on the size of the element M and the firing temperature at the time of manufacturing the positive electrode whether the element M is dissolved in the positive electrode active material or unevenly distributed on the surface of the positive electrode active material. When the element M is present on the surface of the positive electrode active material as a compound, the element M is present as an oxide, a carbonate, and a polyanion such as a phosphate or a sulfate.
That is, the tendency of whether the element M is dissolved in the positive electrode active material (a different type of metal is incorporated into transition metal sites of the positive electrode active material) or unevenly distributed on the surface of the positive electrode active material is determined depending on the size of the element M to be added. Generally, Period 3 and 4 elements (small elements) tend to be dissolved, and Period 5 elements or subsequent elements (large elements) tend to be unevenly distributed on the surface. Examples of the Period 3 elements include Al. Examples of the Period 4 elements include Ti, V, Cr, and Ga. Examples of the Period 5 elements include Zr, Nb, Mo, and In. Examples of the Period 6 elements include Hf, Ta, and W.
It also changes depending on the firing temperature whether the element M to be added is dissolved or unevenly distributed on the surface. As the firing temperature becomes higher, the element M becomes dissolved more easily. However, another factor, for example, Li, volatilizes, the ratio of Li decreases, the resistance can increase, and the capacity can decrease. When the firing temperature is low, the active material is not crystallized, or does not function as an active material. Therefore, it can be said that a suitable firing temperature is 500° C. to 900° C.
More specifically, a comparatively small element which is a Period 3 or 4 element is used as the element M, and firing is performed at as high firing temperature as possible for a long period of time to dissolve the element M. When the firing temperature is too high, or the firing time is too long, sintering proceeds, the particle size is too large, Li volatilizes, the Li ratio decreases, and the resistance increases, which results in a battery capacity decrease. Therefore, firing is preferably performed, for example, at 900° C. or less for 24 hours or less. A comparatively large element which is a Period 5 element or a subsequent element is used as the element M, and firing is performed at as low firing temperature as possible for a short period of time to distribute the element M unevenly on the surface. When the firing temperature is too low, or the firing time is too short, the positive electrode active material is crystallized insufficiently, and the battery characteristic deteriorates. Therefore, firing is preferably performed, for example, at 700° C. or more for 6 hours or more.
In the pattern in which the element M is unevenly distributed on the surface, a pattern in which the element M is unevenly distributed only on the surfaces of secondary particles constituted by aggregation of primary particles and a pattern in which the element M is unevenly distributed both on the surfaces of primary particles (inside a secondary particle) and on the surfaces of secondary particles are possible. In the pattern in which the element M is unevenly distributed only on the surfaces of secondary particles, for example, a precursor and a Li raw material are mixed and fired without adding a metal compound to produce an active material having secondary particles, a metal compound (material for adding the element M) is then mixed, the mixture is heat-treated at a lower temperature (around 700° C.) for a short period of time, thus the element M can be unevenly distributed only on the surfaces of secondary particles. Here, note that if the element M is a comparatively large element which is a Period 5 element or a subsequent element, the element M is hardly dissolved, and is easily and unevenly distributed on the surface. Meanwhile, in the pattern in which the element M is unevenly distributed on the surfaces of primary particles (inside a secondary particle) and on the surfaces of secondary particles, a precursor (transition metal hydroxide), a metal compound (material for adding the element M), and a Li raw material (LiOH or Li2CO3) are mixed, the mixture is then fired at a lower temperature (around 700° C.) for a short period of time, thus the element M can be unevenly distributed on the surfaces of primary particles (inside a secondary particle) and on the surfaces of secondary particles.
The element M dissolved in the lithium transition metal oxide and the element M present on the surfaces of the active material particles may be the same type, or may be different elements. Even though the dissolved element M and the element M present on the surface are the same type of element, these are different in crystal structure and the like, and are therefore distinguished clearly. The element M unevenly distributed on the surface of the active material mainly constitutes an oxide having a different crystal structure from the lithium transition metal oxide. The dissolved element M and the element M unevenly distributed on the surface can be distinguished by various analytical methods including element mapping using EPMA (electron probe micro-analysis), the analysis of the chemical bond state using XPS (X-ray photoelectron spectroscopy), and SIMS (secondary ionization mass spectroscopy).
The average particle size (D50) of the lithium transition metal oxide particles is preferably, for example, 2 μm or more and 20 μm or less. When the average particle size (D50) is less than 2 μm and more than 20 μm, the packing density in the positive electrode active material layer may decrease, and the capacity may decrease as compared with when the above-mentioned range is satisfied. The average particle size (D50) of the positive electrode active material can be measured by laser diffractometry, for example, using MT3000II manufactured by MicrotracBEL Corp.
Examples of the conductive agent included in the positive electrode active material layer include carbon powders such as carbon black, acetylene black, ketjen black and graphite. These may be used singly or in combinations of two or more.
Examples of the binding agent included in the positive electrode active material layer include fluorine-containing polymers and rubber-based polymers. Examples of the fluorine-containing polymers include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), or modified product thereof. Examples of the rubber-based polymers include an ethylene-propylene-isoprene copolymer and an ethylene-propylene-butadiene copolymer. These may be used singly or in combinations of two or more.
The positive electrode of the present embodiment is obtained, for example, by forming a positive electrode active material layer on a positive electrode current collector by applying positive electrode mixture slurry including the positive electrode active material, the conductive agent, the binding agent and the like and drying the slurry, and rolling the positive electrode mixture layer.
[Negative Electrode]
The negative electrode constituting the secondary battery according to the present embodiment comprises, for example, a negative electrode current collector and a negative electrode active material layer formed on the negative electrode current collector. The negative electrode active material layer may be formed on one side of the negative electrode current collector, or may be formed on both sides. The negative electrode active material layer includes, for example, the negative electrode active material, a binding agent, and the like.
As the negative electrode current collector, foil of a metal which is stable in the potential range of the negative electrode, a film wherein the metal is disposed on the outer layer, or the like can be used. As the negative electrode current collector, a porous body such as a mesh body, a punching sheet, or an expanded metal of the metal may be used. As the material of the negative electrode current collector, copper, a copper alloy, aluminum, an aluminum alloy, stainless steel, nickel, or the like can be used. The thickness of the negative electrode current collector is, for example, preferably 3 μm or more and 50 μm or less in terms of a current collection property, mechanical strength, and the like.
For example, negative electrode mixture slurry including the negative electrode active material, the binding agent, and the dispersion medium is applied to the negative electrode current collector, the coating film is dried and then rolled, the negative electrode active material layer is formed on one side or both sides of the negative electrode current collector, and the negative electrode can be manufactured. The negative electrode active material layer may include optional components such as a conductive agent if required. Although the thickness of the negative electrode active material layer is not particularly limited, the thickness is, for example, 10 μm or more and 100 μm or less.
As long as the negative electrode active material is a material which enables occluding and emitting lithium ions, the negative electrode active material is not particularly limited. The material constituting the negative electrode active material may be a non-carbon-based material, may be a carbon material, or may be a combination thereof. Examples of the non-carbon-based material include a lithium metal and alloys including a lithium element as well as metallic compounds such as metal oxides, metal sulfides, and metal nitrides containing lithium. Examples of the alloys containing a lithium element include lithium-aluminum alloys, lithium-tin alloys, lithium-lead alloys, and lithium-silicon alloys. Examples of the metal oxides containing lithium include a metal oxide containing lithium and titanium, tantalum or niobium, and lithium titanate (Li4Ti5O12 and the like) is preferable.
Examples of the carbon materials used as the negative electrode active material include graphite and hard carbon. Among others, graphite is preferable due to high capacity and small irreversible capacity. Graphite is a general term for a carbon material having graphite structure, and include natural graphite, artificial graphite, expanded graphite, and graphitized mesophase carbon particles. When graphite is used as the negative electrode active material, the surface of the negative electrode active material layer is preferably covered with a film to decrease the activity of the reductive decomposition of the aqueous electrolytic solution. These negative electrode active materials may be used alone or in combination of two or more.
As the binding agent included in the negative electrode active material layer, for example, a fluorine-containing polymer, a rubber-based polymer, or the like may be used in the same way as the positive electrode, and a styrene-butadiene copolymer (SBR) or a modified product thereof may be used. The content of the binding agent included in the negative electrode active material layer is preferably 0.1% by mass or more and 20% by mass or less, and more preferably 1% by mass or more and 5% by mass or less based on the total amount of the negative electrode active material. Examples of the thickener included in the negative electrode active material layer include carboxymethylcellulose (CMC) and polyethylene oxide (PEO). These may be used alone or in combination of two or more.
[Separator]
As long as the separator has functions of allowing lithium ions to permeate and electrically separating the positive electrode and the negative electrode, the separator is not particularly limited. As the separator, for example, a porous sheet or the like comprising a resin, an inorganic material, and the like is used. Specific examples of the porous sheet include fine porous thin films, woven fabrics and nonwoven fabrics. Examples of the resin material constituting the separator include olefin-based resins such as polyethylene and polypropylene; polyamides; polyamide-imides; and cellulose. Examples of the inorganic material constituting a separator include glass and ceramics such as borosilicate glass, silica, alumina, and titania. The separator may be a layered body having a cellulose fiber layer and a thermoplastic resin fiber layer of an olefin-based resin or the like. The separator may be a multilayer separator including a polyethylene layer and a polypropylene layer, and a separator wherein a material such as an aramid-based resin or a ceramic is applied to the surface of the separator may be used.
Although the secondary battery comprising the aqueous electrolytic solution was described in the above-mentioned embodiments, the aqueous electrolytic solution according to one example of the present embodiment may be used for a power storage device other than the secondary battery, and may be used, for example, for a capacitor. In this case, the capacitor comprises, for example, the aqueous electrolytic solution according to one example of the present embodiment and the two electrodes. The electrode materials constituting the electrodes can be used for the capacitor, and may be a material which enables occluding and emitting lithium ions. Examples thereof include materials such as a graphite-containing material such as natural graphite or artificial graphite and lithium titanate.
Although Examples and Comparative Examples of the present disclosure will be described specifically hereinafter, the present disclosure is not limited to the following Examples.
A secondary battery was manufactured in the following procedure.
[Manufacturing of Positive Electrode]
A precursor [(Ni0.55Co0.30Mn0.15)(OH)2], LiOH, and Al2O3 were mixed at a predetermined ratio and fired in the air atmosphere at 850° C. for 7 hours to produce a lithium transition metal oxide (LiNi0.55Co0.30Mn0.15Al0.0015O2) as a positive electrode active material. This lithium transition metal oxide, acetylene black (AB) as a conductive agent, and polyvinylidene fluoride (PVdF) as a binder were mixed at a mass ratio of NCA:AB:PVdF=100:1:0.9, N-methyl-2-pyrrolidone (NMP) was further added in a suitable amount, and the mixture was stirred to prepare positive electrode slurry. Subsequently, the obtained positive electrode slurry was applied to both sides of aluminum foil (positive electrode current collector) and then dried, and the coating film of the positive electrode mixture was rolled using a roller to manufacture the positive electrode of Example 1.
[Manufacturing of Negative Electrode]
Graphite as a negative electrode active material, a styrene-butadiene copolymer (SBR) as a binding agent, and carboxymethyl cellulose (CMC) as a thickening agent were mixed so that the mass ratio was 100:1:1, water was added to prepare negative electrode slurry. Subsequently, the negative electrode slurry was applied to both sides of a negative electrode current collector comprising copper foil, and this was dried and then rolled with the rolling roller to manufacture a negative electrode in which negative electrode active material layers were formed on both sides of the negative electrode current collector.
[Production of Aqueous Electrolytic Solution]
LiN(SO2CF3)2, LiN(SO2C2F5)2, LiOH.H2O, and water (ultrapure water) were mixed at a molar ratio of 0.7:0.3:0.034:1.923.
[Manufacturing of Secondary Battery]
The above-mentioned positive electrode and negative electrode were wound through a separator to manufacture an electrode assembly, the electrode assembly was stored with the above-mentioned aqueous electrolyte in a bottomed cylindrical battery case, and the opening of the battery case was sealed with a gasket and a sealing assembly. This was used as the secondary battery of Example 1. As to the secondary battery of Example 1, the stability at the time of charge and storage was evaluated. Table 1 described the amount of change in open circuit voltage as an evaluation result of the stability at the time of charge and storage. In Table 1, the amount of change in open circuit voltage was called the amount of change in voltage.
[Evaluation of Stability at Time of Charge and Storage]
The battery was charged at a constant current of 0.1 C until the closed circuit voltage of the battery reached 2.75 V. The battery was then stored at 25° C. for 72 hours. After storage, the amount of change in the open circuit voltage of the battery (V) was determined. The charge and storage test was performed under the condition of 25° C. The amount of change in open circuit voltage (V) was considered as the evaluation of the stability at the time of charge and storage.
A positive electrode was manufactured by the same method as in Example 1 except that Al2O3 was not added at the time of the manufacturing of a positive electrode active material. A secondary battery was manufactured using the manufactured positive electrode and evaluated in the same way as in Example 1. That is, the secondary battery of Comparative Example 1 uses LiNi0.55Co0.30Mn0.15O2 as a positive electrode active material.
A precursor [(Ni0.55Co0.30Mn0.15)(OH)2], LiOH, and TiO2 were mixed at a predetermined ratio and fired in the air atmosphere at 850° C. for 7 hours to produce a lithium transition metal oxide (LiNi0.55Co0.30Mn0.15Ti0.0015O2) as a positive electrode active material. The secondary battery of Example 2 was manufactured in the same method as in Example 1 except that LiNi0.55Co0.30Mn0.15Ti0.0015O2 was used as a positive electrode active material, and the battery was evaluated in the same way as in Example 1.
A precursor [(Ni0.55Co0.30Mn0.15)(OH)2], LiOH, and ZrO2 were mixed at a predetermined ratio and fired in the air atmosphere at 850° C. for 7 hours to produce a lithium transition metal oxide (LiNi0.55Co0.30Mn0.15Zr0.0005O2) as a positive electrode active material. The secondary battery of Example 3 was manufactured in the same method as in Example 1 except that LiNi0.55Co0.30Mn0.15Zr0.0005O2 was used as a positive electrode active material, and the battery was evaluated in the same way as in Example 1.
Table 1 shows the evaluation results collectively.
As shown in Table 1, the secondary batteries of Examples 1 to 3 enabled suppressing voltage decreases at the time of charge and storage by adding Al, Ti, and Zr to the positive electrode active material, respectively, as compared with the secondary battery of Comparative Example 1. That is, the charge and storage stabilities of the secondary batteries of Examples 1 to 3 were improved as compared with the secondary battery of Comparative Example 1. It is presumed that the reason why the charge and storage stability of the secondary battery of Example 1 was improved is that since Al was dissolved, the distance between layers in the layered structure of the positive electrode active material narrowed, and proton insertion was suppressed. It is presumed that the reason why the charge and storage stability of the secondary battery of Example 2 was improved is that since Ti was dissolved, the distance between layers in the layered structure of the positive electrode active material narrowed, and proton insertion was suppressed. It is presumed that the reasons why the charge and storage stability of the secondary battery of Example 3 was improved are that since Zr was dissolved, the distance between layers in the layered structure of the positive electrode active material narrowed, and proton insertion was suppressed and that since a part of Zr was unevenly distributed on the surface, the insertion of protons between positive electrode active material layers was blocked in the interface between positive electrode active material and the aqueous electrolytic solution in addition.
The negative electrodes of the manufactured batteries are lithium titanate, and are a material wherein the potentials of the negative electrodes hardly fluctuate. The suppression of a decrease in open circuit voltage means the suppression of a decrease in the potential of a positive electrode from this. Therefore, it is found that since the different types of elements was added to the positive electrode active material and dissolved therein, the potential decreases of the positive electrodes were suppressed, and the charge and storage stabilities of the batteries could be improved.
The effect of the addition of the element M is exhibited to suppress proton insertion thus. When the additive element M is dissolved in the crystal of the active material, proton insertion is suppressed due to the shrinkage of the crystal lattice. Even when the additive element M is not dissolved in the crystal, and is unevenly distributed on the surface of the active material, the different type of element covers the surface of the active material, and suppresses proton insertion. As mentioned above, the additive element M may be dissolved and unevenly distributed on the surface simultaneously.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2018-181201 | Sep 2018 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2019/030122 | 8/1/2019 | WO | 00 |
