WO2024176531A1 - 亜鉛二次電池 - Google Patents

亜鉛二次電池 Download PDF

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Publication number
WO2024176531A1
WO2024176531A1 PCT/JP2023/040402 JP2023040402W WO2024176531A1 WO 2024176531 A1 WO2024176531 A1 WO 2024176531A1 JP 2023040402 W JP2023040402 W JP 2023040402W WO 2024176531 A1 WO2024176531 A1 WO 2024176531A1
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Prior art keywords
secondary battery
hydroxide
zinc
positive electrode
negative electrode
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PCT/JP2023/040402
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English (en)
French (fr)
Japanese (ja)
Inventor
淳宣 松矢
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NGK Insulators Ltd
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NGK Insulators Ltd
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Priority to CN202380090116.6A priority Critical patent/CN120391005A/zh
Priority to JP2025502109A priority patent/JPWO2024176531A1/ja
Priority to DE112023004935.1T priority patent/DE112023004935T5/de
Publication of WO2024176531A1 publication Critical patent/WO2024176531A1/ja
Priority to US19/306,184 priority patent/US20250372725A1/en
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/24—Electrodes for alkaline accumulators
    • H01M4/244—Zinc electrodes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/24—Alkaline accumulators
    • H01M10/26—Selection of materials as electrolytes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/24—Alkaline accumulators
    • H01M10/30—Nickel accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M12/00—Hybrid cells; Manufacture thereof
    • H01M12/02—Details
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M12/00—Hybrid cells; Manufacture thereof
    • H01M12/08—Hybrid cells; Manufacture thereof composed of a half-cell of a fuel-cell type and a half-cell of the secondary-cell type
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/411—Organic material
    • H01M50/414—Synthetic resins, e.g. thermoplastics or thermosetting resins
    • H01M50/417—Polyolefins
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/431—Inorganic material
    • H01M50/434—Ceramics
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/446—Composite material consisting of a mixture of organic and inorganic materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0002—Aqueous electrolytes
    • H01M2300/0014—Alkaline electrolytes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present invention relates to a zinc secondary battery.
  • Patent Document 1 JP Patent Publication No. 7-254396 discloses that in a button-type alkaline battery that uses mercury-free zinc as the negative electrode active material, the inner surface of the negative electrode terminal plate is coated with tin or a tin alloy to a thickness of 10 to 100 ⁇ m and the surface is polished to control the amount of tin oxide on the surface to a predetermined amount.
  • Patent Document 2 JP Patent Publication No. 6561915 discloses a nickel-metal hydride battery in which a non-conductive layer is formed on the surface of the electrode terminal and a metal layer containing nickel and/or a nickel-iron alloy is laminated on this non-conductive layer.
  • Patent Document 5 (WO 2019/069760) and Patent Document 6 (WO 2019/077953) propose a zinc secondary battery in which the entire negative electrode active material layer is covered or wrapped with a liquid-retaining member and an LDH separator, and the positive electrode active material layer is covered or wrapped with a liquid-retaining member.
  • a nonwoven fabric is used as the liquid-retaining member.
  • LDH-like compounds are known as hydroxides and/or oxides having a layered crystal structure similar to LDH, and exhibit hydroxide ion conductive properties similar enough to be collectively referred to as hydroxide ion conductive layered compounds together with LDH.
  • Patent Document 7 discloses a hydroxide ion conductive separator comprising a porous substrate and a layered double hydroxide (LDH)-like compound that blocks the pores of the porous substrate, in which the LDH-like compound is a hydroxide and/or oxide having a layered crystal structure containing Mg and one or more elements including at least Ti selected from the group consisting of Ti, Y, and Al.
  • LDH layered double hydroxide
  • Patent Document 8 discloses an LDH separator using an LDH-like compound containing (i) Ti, Y, and optionally Al and/or Mg, and (ii) an additive element M which is at least one selected from the group consisting of In, Bi, Ca, Sr and Ba.
  • Patent Document 9 discloses an LDH separator containing a mixture of an LDH-like compound and In(OH) 3 , in which the LDH-like compound is a hydroxide and/or oxide having a layered crystal structure containing Mg, Ti, Y, and optionally Al and/or In. According to the separators disclosed in Patent Documents 7 to 9, it is said that the separators have excellent alkali resistance compared to conventional LDH separators, and can more effectively suppress short circuits caused by zinc dendrites.
  • Patent Documents 1 and 2 various attempts have been proposed to address the creep phenomenon in alkaline batteries, but there is a demand for a method that can more effectively suppress electrolyte leakage.
  • the inventors have now discovered that in a zinc secondary battery, by setting the total concentration of alkali metal hydroxides in the electrolyte to 5.0 to 6.0 mol/L and the concentration of sodium hydroxide to 0.5 to 6.0 mol/L, leakage of electrolyte caused by creep can be effectively suppressed while maintaining good battery resistance.
  • the object of the present invention is therefore to provide a zinc secondary battery that has good battery resistance while effectively suppressing electrolyte leakage caused by creep.
  • a positive electrode plate including a positive electrode active material layer and a positive electrode current collector; a negative electrode plate including a negative electrode active material layer including at least one selected from the group consisting of zinc, zinc oxide, a zinc alloy, and a zinc compound, and a negative electrode current collector; a hydroxide ion conductive separator that separates the positive electrode plate and the negative electrode plate so as to be capable of conducting hydroxide ions;
  • a zinc secondary battery comprising: the electrolyte is an aqueous solution containing an alkali metal hydroxide including at least sodium hydroxide, A zinc secondary battery, wherein the total concentration of the alkali metal hydroxides in the electrolytic solution is 5.0 to 6.0 mol/L, and the concentration of the sodium hydroxide in the electrolytic solution is 0.5 to 6.0 mol/L.
  • the porous substrate is made of a polymeric material.
  • the positive electrode active material layer contains nickel hydroxide and/or nickel oxyhydroxide, thereby forming the zinc secondary battery into a nickel-zinc secondary battery.
  • the positive electrode active material layer is an air electrode layer, thereby forming the zinc secondary battery into a zinc-air secondary battery.
  • FIG. 1 is a schematic cross-sectional view showing an example of a zinc secondary battery according to the present invention.
  • FIG. 2 is a schematic diagram showing a cross section of the zinc secondary battery shown in FIG. 1 taken along line A-A'.
  • FIG. 2 is a perspective view showing a schematic diagram of an electrode stack of the zinc secondary battery shown in FIG. 1.
  • FIG. 2 is a cross-sectional view showing a schematic diagram of an electrode laminate of the zinc secondary battery shown in FIG. 1.
  • FIG. 2 is a cross-sectional view showing an example of a mechanism for preventing creep in the zinc secondary battery of the present invention.
  • FIG. 2 is a conceptual diagram for explaining the mechanism of creep phenomenon when an aqueous potassium hydroxide solution is used as an electrolyte.
  • 7 is a cross-sectional view that illustrates a mechanism by which the electrolyte in FIG. 6 passes through a minute gap between a metal member and a sealing member.
  • the zinc secondary battery of the present invention is not particularly limited as long as it is a secondary battery using zinc as the negative electrode and an aqueous alkali metal hydroxide solution having the composition described below as the electrolyte. Therefore, it can be a nickel-zinc secondary battery, a silver oxide-zinc secondary battery, a manganese oxide-zinc secondary battery, an air-zinc secondary battery, or any other type of alkaline zinc secondary battery.
  • the positive electrode active material layer contains nickel hydroxide and/or nickel oxyhydroxide, thereby making the zinc secondary battery a nickel-zinc secondary battery.
  • the positive electrode active material layer may be an air electrode layer, thereby making the zinc secondary battery an air-zinc secondary battery.
  • FIGs 1 to 4 show an embodiment of a zinc secondary battery and its internal structure according to the present invention.
  • the zinc secondary battery 10 shown in these figures comprises a positive electrode plate 12, a negative electrode plate 14, a hydroxide ion conductive separator 16, and an electrolyte 18. Note that the electrolyte 18 is only shown locally in Figure 4, because it is distributed throughout the positive electrode plate 12 and the negative electrode plate 14.
  • the positive electrode plate 12 includes a positive electrode active material layer 12a and a positive electrode current collector (not shown).
  • the negative electrode plate 14 includes a negative electrode active material layer 14a and a negative electrode current collector 14b.
  • the negative electrode active material layer 14a includes at least one selected from the group consisting of zinc, zinc oxide, zinc alloy, and zinc compound.
  • the hydroxide ion conductive separator 16 isolates the positive electrode plate 12 and the negative electrode plate 14 so that hydroxide ions can be conducted.
  • the electrolyte 18 is an aqueous solution containing an alkali metal hydroxide. This alkali metal hydroxide includes at least sodium hydroxide. The total concentration of alkali metal hydroxides in the electrolyte 18 is 5.0 to 6.0 mol/L. The concentration of sodium hydroxide in the electrolyte 18 is 0.5 to 6.0 mol/L.
  • electrolyte 18 in which the total concentration of alkali metal hydroxides and the concentration of sodium hydroxide are each within a predetermined range in a zinc secondary battery, leakage of the electrolyte due to creeping can be effectively suppressed while maintaining good battery resistance.
  • the creep phenomenon is a phenomenon in which the electrolyte creeps up the surface of the electrode terminal and leaks out of the battery container.
  • FIG. 6 conceptually shows the mechanism of the creep phenomenon when a part of the metal member 30 (assuming an electrode terminal or a current collecting member) is immersed in the electrolyte 118 (assuming an aqueous potassium hydroxide solution). As shown in FIG. 6, the creep phenomenon progresses as follows: 1) H 2 O molecules derived from the surrounding environment combine with electrons e ⁇ present in the metal member 30 to generate OH ⁇ , and 2) K + in the electrolyte 118 is attracted to this OH ⁇ .
  • the terminal inside the container and the terminal outside the container are connected via a sealing member such as an O-ring or a gasket.
  • a sealing member such as an O-ring or a gasket.
  • the electrolyte 18 containing sodium hydroxide at a predetermined concentration, leakage of the electrolyte caused by the creep phenomenon is effectively suppressed.
  • alkali metal hydroxides such as potassium hydroxide and sodium hydroxide exist in the electrolyte in a state in which cations such as K + and Na + are hydrated.
  • the hydrated ionic radius of Na + (about 1.8 ⁇ ) is larger than the hydrated ionic radius of K + (about 1.3 ⁇ ). 5
  • the electrolyte solution 18 containing sodium hydroxide is less likely to pass through the minute gap between the metal member 30 and the sealing member 32 than the potassium hydroxide aqueous solution that has been commonly used as an electrolyte.
  • the electrolyte solution 18 containing a predetermined concentration of sodium hydroxide has a higher viscosity than the potassium hydroxide aqueous solution.
  • the speed at which the electrolyte solution 18 creeps up the metal member 30 becomes slower, which is also considered to be one of the factors that can suppress leakage of the electrolyte due to the creep phenomenon.
  • the electrolyte 18 is an aqueous solution containing an alkali metal hydroxide.
  • the total concentration C A of the alkali metal hydroxide in the electrolyte 18 is 5.0 to 6.0 mol/L, preferably 5.0 to 5.8 mol/L, more preferably 5.0 to 5.6 mol/L, and particularly preferably 5.2 to 5.6 mol/L.
  • the resistance of the electrolyte can be desirably reduced, and the performance of the zinc secondary battery can be improved.
  • the alkali metal hydroxide include potassium hydroxide, lithium hydroxide, and the like, in addition to sodium hydroxide.
  • the alkali metal hydroxide contained in the electrolyte 18 includes sodium hydroxide.
  • the concentration C B of sodium hydroxide in the electrolyte 18 is 0.5 to 6.0 mol/L, preferably 2.5 to 6.0 mol/L, more preferably 3.0 to 6.0 mol/L, even more preferably 4.0 to 6.0 mol/L, even more preferably 5.0 to 6.0 mol/L, particularly preferably 5.0 to 5.8 mol/L, and most preferably 5.2 to 5.6 mol/L.
  • the concentration C B of sodium hydroxide is equal to or less than the total concentration C A of the alkali metal hydroxides (i.e., C B ⁇ C A ).
  • the ratio of the concentration of sodium hydroxide C B to the total concentration of alkali metal hydroxides C A is preferably 0.4 to 1.0, more preferably 0.6 to 1.0, even more preferably 0.8 to 1.0, and particularly preferably 0.9 to 1.0.
  • the electrolytic solution 18 may contain an alkali metal hydroxide other than sodium hydroxide as an inevitable impurity (for example, a concentration of less than 0.1 mol/L).
  • an alkali metal hydroxide other than sodium hydroxide may be intentionally added to the electrolyte 18.
  • the electrolyte 18 may further contain potassium hydroxide and/or lithium hydroxide as the alkali metal hydroxide described above.
  • the battery resistance can be further reduced.
  • the concentration C C of potassium hydroxide in the electrolyte 18 is preferably 4.0 mol/L or less, more preferably 3.0 mol/L or less, even more preferably 2.0 mol/L or less, particularly preferably 1.5 mol/L or less, and most preferably 1.0 mol/L or less.
  • the ratio of the concentration C C of potassium hydroxide to the total concentration C A of the alkali metal hydroxides is preferably 0.8 or less, more preferably 0.6 or less, even more preferably 0.4 or less, and particularly preferably 0.3 or less.
  • lithium hydroxide in the alkali metal hydroxide in the electrolyte By further containing lithium hydroxide in the alkali metal hydroxide in the electrolyte 18, leakage of the electrolyte can be further suppressed. That is, Li + has a larger hydrated ion radius (about 2.4 ⁇ ) than K + and Na + .
  • the lithium hydroxide aqueous solution has a higher viscosity than the sodium hydroxide aqueous solution of the same concentration. Therefore, by adding lithium hydroxide to the electrolyte 18, the creep phenomenon can be more effectively prevented.
  • the concentration C D of lithium hydroxide in the electrolyte 18 is preferably 1.5 mol/L or less, more preferably 1.0 mol/L or less, even more preferably 0.1 to 0.8 mol/L or less, and particularly preferably 0.2 to 0.5 mol/L or less.
  • lithium hydroxide When lithium hydroxide is added to the electrolyte 18, it is desirable to also add potassium hydroxide to the electrolyte 18 from the viewpoint of achieving a good balance between reducing the battery resistance and suppressing leakage of the electrolyte.
  • the alkali metal hydroxide contains sodium hydroxide and lithium hydroxide, it is desirable to further contain potassium hydroxide.
  • a zinc compound such as zinc oxide or zinc hydroxide may be added to the electrolyte.
  • the electrolyte 18 may be gelled.
  • the gelling agent it is preferable to use a polymer that absorbs the solvent in the electrolyte and swells, and examples of such polymers include polyethylene oxide, polyvinyl alcohol, polyacrylamide, and starch.
  • the zinc secondary battery 10 preferably includes an electrode laminate 11 and an electrolyte 18 in a battery container 20.
  • the electrode laminate 11 includes a plurality of positive electrode plates 12, a plurality of negative electrode plates 14, and a plurality of hydroxide ion conductive separators 16, and is in the form of a positive and negative electrode laminate in which the unit of positive electrode plate 12/hydroxide ion conductive separator 16/negative electrode plate 14 is repeated.
  • the zinc secondary battery 10 preferably includes a plurality of unit cells 10a including a positive electrode plate 12, a positive electrode current collector 13, a negative electrode plate 14, a negative electrode current collector 15, a hydroxide ion conductive separator 16, and an electrolyte 18, and the plurality of unit cells 10a form a multi-layer cell as a whole.
  • This is the configuration of a so-called assembled battery or stacked battery, and is advantageous in that a high voltage and a large current can be obtained.
  • the positive electrode plate 12 includes a positive electrode active material layer 12a.
  • the positive electrode active material constituting the positive electrode active material layer 12a may be appropriately selected from known positive electrode materials according to the type of zinc secondary battery, and is not particularly limited.
  • a positive electrode containing nickel hydroxide and/or nickel oxyhydroxide may be used.
  • an air electrode may be used as the positive electrode.
  • the positive electrode plate 12 further includes a positive electrode collector (not shown), and it is preferable that a metallic positive electrode collector member 13 extending (e.g., upward) from or connected to the positive electrode collector is further provided.
  • a preferred example of a positive electrode collector is a nickel porous substrate such as a foamed nickel plate.
  • a paste containing an electrode active material such as nickel hydroxide is uniformly applied to a nickel porous substrate and dried to preferably produce a positive electrode plate consisting of a positive electrode/positive electrode collector.
  • the positive electrode plate 12 shown in FIG. 4 includes a positive electrode current collector (e.g., nickel foam), but is not shown.
  • the positive electrode current collector 13 may be made of the same material as the positive electrode current collector, or may be made of a different material.
  • the positive electrode current collector is a nickel porous substrate such as a nickel foam plate, it can be processed into a tab shape by pressing it.
  • the positive electrode current collector 13 may be extended by adding another current collector such as a tab lead to such a tab.
  • the positive electrode terminal 26 is typically connected to the positive electrode current collecting member 13 and protrudes from the battery container 20.
  • the positive electrode plate 12 may contain at least one additive selected from the group consisting of silver compounds, manganese compounds, and titanium compounds, which can promote the positive electrode reaction that absorbs hydrogen gas generated by the self-discharge reaction.
  • the positive electrode plate 12 may further contain cobalt. Cobalt is preferably contained in the positive electrode plate 12 in the form of cobalt oxyhydroxide. In the positive electrode plate 12, cobalt functions as a conductive additive, thereby contributing to improving the charge/discharge capacity.
  • the negative electrode plate 14 includes a negative electrode active material layer 14a.
  • the negative electrode active material constituting the negative electrode active material layer 14a includes at least one selected from the group consisting of zinc, zinc oxide, zinc alloys, and zinc compounds. Zinc may be included in any form of zinc metal, zinc compound, or zinc alloy, so long as it has electrochemical activity suitable for a negative electrode. Preferred examples of negative electrode materials include zinc oxide, zinc metal, calcium zincate, etc., and a mixture of zinc metal and zinc oxide is more preferred.
  • the negative electrode active material may be configured in a gel form, or may be mixed with the electrolyte 18 to form a negative electrode composite. For example, a gelled negative electrode can be easily obtained by adding an electrolyte and a thickener to the negative electrode active material. Examples of thickeners include polyvinyl alcohol, polyacrylate, CMC, alginic acid, etc., and polyacrylic acid is preferred because of its excellent chemical resistance to strong alkali.
  • a mercury- and lead-free zinc alloy known as a mercury-free zinc alloy can be used.
  • a zinc alloy containing 0.01 to 0.1 mass% indium, 0.005 to 0.02 mass% bismuth, and 0.0035 to 0.015 mass% aluminum is preferable because it has the effect of suppressing hydrogen gas generation.
  • indium and bismuth are advantageous in terms of improving discharge performance.
  • the use of a zinc alloy for the negative electrode can improve safety by suppressing hydrogen gas generation by slowing down the self-dissolution rate in alkaline electrolyte.
  • the shape of the negative electrode material is not particularly limited, but it is preferably in powder form, which increases the surface area and allows it to handle large current discharges.
  • the average particle size of the negative electrode material is preferably in the range of 3 to 100 ⁇ m in short axis for zinc alloys; within this range, the large surface area makes it suitable for handling large current discharges, and it is easy to mix uniformly with the electrolyte and gelling agent, making it easy to handle when assembling the battery.
  • the negative electrode plate 14 further includes a negative electrode collector 14b.
  • the negative electrode collector 14b is provided inside and/or on the surface of the negative electrode active material layer 14a, except for the portion extending as the negative electrode current collector 15. That is, the negative electrode active material layer 14a may be provided on both sides of the negative electrode collector 14b, or the negative electrode active material layer 14a may be provided only on one side of the negative electrode collector 14b. It is preferable that a metallic negative electrode current collector 15 is further provided, which extends (for example, upward) from or connects to the negative electrode current collector 14b. It is preferable that the negative electrode current collector 15 is provided at a position that does not overlap with the positive electrode current collector 13.
  • the negative electrode current collector 15 may be made of the same material as the negative electrode collector 14b, or may be made of a different material. In any case, the negative electrode current collector 15 may be extended by adding another current collector such as a tab lead to such a tab. In any case, it is preferable that multiple negative electrode collectors 15 are joined to one negative electrode terminal 28 or to a further negative electrode collector 15 electrically connected thereto. The negative electrode terminal 28 is typically connected to the negative electrode collector 15 and protrudes from the battery container 20.
  • a metal plate having a plurality (or a large number) of openings as the negative electrode current collector 14b.
  • Preferred examples of such a negative electrode current collector 14b include expanded metal, punched metal, and metal mesh, and combinations thereof, more preferably copper expanded metal, copper punched metal, and combinations thereof, and particularly preferably copper expanded metal.
  • a mixture containing zinc oxide powder and/or zinc powder, and optionally a binder e.g. polytetrafluoroethylene particles
  • a binder e.g. polytetrafluoroethylene particles
  • the expanded metal is a mesh-shaped metal plate in which a metal plate is expanded while making staggered cuts using an expander, and the cuts are formed into a diamond or tortoiseshell shape.
  • Punched metal also known as perforated metal, is a metal plate with holes punched into it.
  • Metal mesh is a metal product with a wire mesh structure, and is different from expanded metal and punched metal.
  • the hydroxide ion conductive separator 16 is provided to isolate the positive electrode plate 12 and the negative electrode plate 14 so as to allow hydroxide ion conductivity.
  • the negative electrode plate 14 may be configured to be covered or wrapped with the hydroxide ion conductive separator 16. This makes it possible to manufacture a zinc secondary battery (particularly a stacked battery thereof) capable of preventing zinc dendrite extension extremely easily and with high productivity, without the need for a complicated sealing joint between the hydroxide ion conductive separator 16 and the battery container.
  • a simple configuration in which the hydroxide ion conductive separator 16 is arranged on one side of the positive electrode plate 12 or the negative electrode plate 14 may also be used.
  • the hydroxide ion conductive separator 16 is not particularly limited as long as it is a separator capable of isolating the positive electrode plate 12 and the negative electrode plate 14 in a hydroxide ion conductive manner, but is typically a separator that includes a hydroxide ion conductive solid electrolyte and selectively passes hydroxide ions solely by utilizing hydroxide ion conductivity.
  • a preferred hydroxide ion conductive solid electrolyte is a layered double hydroxide (LDH) and/or an LDH-like compound.
  • the hydroxide ion conductive separator 16 is preferably an LDH separator.
  • an "LDH separator” is defined as a separator that includes an LDH and/or an LDH-like compound and selectively passes hydroxide ions solely by utilizing the hydroxide ion conductivity of the LDH and/or the LDH-like compound.
  • an "LDH-like compound” is a hydroxide and/or oxide of a layered crystal structure that may not be called an LDH but has hydroxide ion conductivity, and can be considered an equivalent of an LDH.
  • LDH separator is preferably composited with a porous substrate.
  • the LDH separator preferably further comprises a porous substrate, and is composited with the porous substrate in a form in which the pores of the porous substrate are filled with LDH and/or LDH-like compounds. That is, in a preferred LDH separator, the pores of the porous substrate are blocked with LDH and/or LDH-like compounds so as to exhibit hydroxide ion conductivity and gas impermeability (and therefore function as an LDH separator exhibiting hydroxide ion conductivity).
  • the porous substrate is preferably made of a polymeric material, and it is particularly preferred that the LDH and/or LDH-like compounds are incorporated throughout the entire thickness of the porous substrate made of a polymeric material.
  • LDH separators such as those disclosed in Patent Documents 3 to 9 can be used.
  • the thickness of the LDH separator is preferably 5 to 100 ⁇ m, more preferably 5 to 80 ⁇ m, even more preferably 5 to 60 ⁇ m, and particularly preferably 5 to 40 ⁇ m.
  • the positive electrode plate 12, the positive electrode current collector 13, the negative electrode plate 14, the negative electrode current collector 15 and the hydroxide ion conductive separator 16 are each arranged vertically, and the positive electrode terminal 26 and the negative electrode terminal 28 are provided on the top cover 20a of the battery container 20. Therefore, in the case of a multi-layer cell, it is preferable that the cell is multi-layered in the horizontal direction. It is also preferable that the positive electrode current collector 13 and the negative electrode current collector 15 extend upward.
  • the zinc secondary battery 10 may further include a liquid-retaining member 17 in contact with the positive electrode plate 12 and/or the negative electrode plate 14.
  • a liquid-retaining member 17 in contact with the positive electrode plate 12 and/or the negative electrode plate 14.
  • the positive electrode plate 12 and/or the negative electrode plate 14 is covered or wrapped with the liquid-retaining member 17.
  • a simple configuration in which the liquid-retaining member 17 is arranged on one side of the positive electrode plate 12 or the negative electrode plate 14 may also be used.
  • the electrolyte 18 can be evenly present between the positive electrode plate 12 and/or the negative electrode plate 14 and the hydroxide ion conductive separator 16, and hydroxide ions can be efficiently exchanged between the positive electrode plate 12 and/or the negative electrode plate 14 and the hydroxide ion conductive separator 16.
  • the liquid-retaining member 17 is not particularly limited as long as it is a member capable of retaining the electrolyte 18, but is preferably a sheet-like member.
  • Preferred examples of the liquid-retaining member 17 include nonwoven fabric, water-absorbent resin, liquid-retaining resin, porous sheet, and various spacers, but nonwoven fabric is particularly preferred because it allows the production of a negative electrode structure with good performance at low cost.
  • the liquid-retaining member 17 or nonwoven fabric preferably has a thickness of 10 to 200 ⁇ m, more preferably 20 to 200 ⁇ m, even more preferably 20 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m, and most preferably 20 to 60 ⁇ m. If the thickness is within the above range, a sufficient amount of electrolyte 18 can be retained in the liquid-retaining member 17 while keeping the overall size of the positive electrode structure and/or negative electrode structure compact and without waste.
  • the outer edges of the plates are closed (except for the edges from which the positive electrode current collector 13 and the negative electrode current collector 15 extend).
  • the closed edge of the outer edge of the liquid-retaining member 17 and/or the hydroxide ion conductive separator 16 is realized by folding the liquid-retaining member 17 and/or the hydroxide ion conductive separator 16, or by sealing the liquid-retaining members 17 together and/or the hydroxide ion conductive separators 16 together.
  • sealing methods include adhesives, heat welding, ultrasonic welding, adhesive tape, sealing tape, and combinations thereof.
  • the LDH separator including the porous substrate made of a polymer material has the advantage of being flexible and therefore easy to bend, it is preferable to form the LDH separator into a long shape and fold it to form a state in which one side of the outer edge is closed.
  • Thermal welding and ultrasonic welding may be performed using a commercially available heat sealer, etc., but in the case of sealing between LDH separators, it is preferable to perform thermal welding and ultrasonic welding by sandwiching the outer periphery of the liquid-retaining member 17 between the LDH separators that constitute the outer periphery, since this allows for more effective sealing.
  • the adhesive, adhesive tape, and sealing tape may be commercially available products, but it is preferable to use those that contain a resin that is resistant to alkali in order to prevent deterioration in an alkaline electrolyte.
  • examples of preferred adhesives include epoxy resin adhesives, natural resin adhesives, modified olefin resin adhesives, and modified silicone resin adhesives, and among these, epoxy resin adhesives are more preferred because they are particularly excellent in alkali resistance.
  • An example of a product of an epoxy resin adhesive is the epoxy adhesive Hysol (registered trademark) (manufactured by Henkel).
  • the outer edge of one side that is the upper end of the hydroxide ion conductive separator 16 is open.
  • This open-top configuration makes it possible to deal with problems that occur when a nickel-zinc battery or the like is overcharged. That is, when a nickel-zinc battery or the like is overcharged, oxygen (O 2 ) may be generated at the positive electrode plate 12, but the LDH separator has such a high density that it allows only hydroxide ions to pass through, and therefore does not allow O 2 to pass through.
  • the open-top electrode laminate 11 can be used in a sealed zinc secondary battery to improve overcharge resistance.
  • the vent hole may be opened after sealing the outer edge of one side serving as the upper end of the LDH separator, or a part of the outer edge may be left unsealed so that a vent hole is formed during sealing.
  • the battery container 20 is preferably made of resin.
  • the resin constituting the battery container 20 is preferably a resin that is resistant to alkali metal hydroxides such as potassium hydroxide, more preferably a polyolefin resin, ABS resin, or modified polyphenylene ether, and even more preferably ABS resin or modified polyphenylene ether.
  • the battery container 20 has a top lid 20a.
  • the battery container 20 (e.g., top lid 20a) may have a pressure relief valve for releasing gas.
  • a group of containers in which two or more battery containers 20 are arranged may be housed within an outer frame to form a battery module.
  • Examples 1 to 9 Preparation of nickel-zinc secondary battery The following positive electrode plate, positive electrode current collector, negative electrode plate, negative electrode current collector, LDH separator, nonwoven fabric, battery container, and electrolyte were prepared. Various electrolytes were prepared by changing the type and concentration of alkali metal hydroxide. Positive electrode plate: The pores of the nickel foam are filled with a positive electrode paste containing nickel hydroxide and a binder and then dried (there is an uncoated area near one end of the nickel foam where the positive electrode paste is not applied).
  • Positive electrode current collecting member The uncoated portion of the foamed nickel that constitutes the positive electrode plate is compressed by a roll press to form a tab, and a tab lead (made of pure nickel, thickness: 100 ⁇ m) is ultrasonically welded to this tab to extend it.
  • Negative electrode plate A negative electrode paste containing ZnO powder, metallic Zn powder, polytetrafluoroethylene (PTFE) and propylene glycol is pressed onto a current collector (copper expanded metal) (there is an uncoated area near one end of the copper expanded metal where the negative electrode paste is not applied).
  • Negative electrode current collecting member A tab lead (made of copper, thickness: 100 ⁇ m) was connected to the uncoated part of the copper expanded metal by ultrasonic welding.
  • LDH separator Ni-Al-Ti-LDH (layered double hydroxide) is precipitated in the pores and on the surface of a polyethylene microporous membrane by hydrothermal synthesis and roll-pressed; thickness: 20 ⁇ m
  • Non-woven fabric polypropylene, thickness 100 ⁇ m
  • Battery container box-shaped case made of modified polyphenylene ether resin (equipped with a pressure relief valve that allows gas generated inside the case to be released), internal dimensions: length 190 mm, width 24 mm, height 165 mm, external dimensions: length 200 mm, width 30 mm, height 170 mm (not including the height of the positive and negative terminals)
  • Electrolyte 0.4 mol/L of ZnO dissolved in an aqueous solution of an alkali metal hydroxide having the composition shown in Table 1
  • the positive electrode plate was wrapped in nonwoven fabric so that it covered both sides, with the nonwoven fabric slightly protruding from the remaining three sides except for the side from which the positive electrode current collector extends. The excess parts of the nonwoven fabric protruding from the three sides of the positive electrode plate were heat-sealed with a heat seal bar to obtain a positive electrode structure.
  • the negative electrode plate was also wrapped in nonwoven fabric and LDH separator in that order from both sides, with the nonwoven fabric and LDH separator slightly protruding from the remaining three sides except for the side from which the negative electrode current collector extends. The excess parts of the nonwoven fabric and LDH separator protruding from the three sides of the negative electrode plate were heat-sealed with a heat seal bar to obtain a negative electrode structure. In this way, multiple positive electrode structures and multiple negative electrode structures were prepared.
  • An electrode laminate was produced by stacking 12 positive electrode structures and 13 negative electrode structures alternately.
  • the multiple positive electrode current collectors 13 and the multiple negative electrode current collectors 15 are designed to extend from different positions from each other when viewed in a plan view, so that the multiple positive electrode current collectors 13 are stacked on top of each other, while the multiple negative electrode current collectors 15 are stacked on top of each other at a different position.
  • the overlapping portions of the multiple positive electrode current collectors 13 were joined together to the positive electrode terminal 26 by laser welding.
  • the overlapping portions of the multiple negative electrode current collectors 15 were joined together to the negative electrode terminal 28 by laser welding.
  • the electrode laminate 11 was placed in a box-shaped battery container 20, and the electrolyte 18 was poured in to impregnate the electrode stack 11, and the top lid 20a was closed and sealed. In this way, a nickel-zinc secondary battery was produced.

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PCT/JP2023/040402 2023-02-24 2023-11-09 亜鉛二次電池 Ceased WO2024176531A1 (ja)

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DE112023004935.1T DE112023004935T5 (de) 2023-02-24 2023-11-09 Zink-Sekundärbatterie
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5673866A (en) * 1979-11-19 1981-06-18 Matsushita Electric Ind Co Ltd Alkaline battery
JPS6050865A (ja) * 1983-08-31 1985-03-20 Toshiba Corp アルカリ電池
JP2020087554A (ja) * 2018-11-19 2020-06-04 日立化成株式会社 亜鉛電池用電解液及び亜鉛電池
WO2020255856A1 (ja) * 2019-06-19 2020-12-24 日本碍子株式会社 水酸化物イオン伝導セパレータ及び亜鉛二次電池

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5673866A (en) * 1979-11-19 1981-06-18 Matsushita Electric Ind Co Ltd Alkaline battery
JPS6050865A (ja) * 1983-08-31 1985-03-20 Toshiba Corp アルカリ電池
JP2020087554A (ja) * 2018-11-19 2020-06-04 日立化成株式会社 亜鉛電池用電解液及び亜鉛電池
WO2020255856A1 (ja) * 2019-06-19 2020-12-24 日本碍子株式会社 水酸化物イオン伝導セパレータ及び亜鉛二次電池

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US20250372725A1 (en) 2025-12-04

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