A method for preparing an electrolyte suitable for acidic, near-neutral and alkaline zinc-based energy storage devices

Abstract

The present invention discloses a method for preparing an electrolyte suitable for acidic, near-neutral, and alkaline zinc-based energy storage devices, belonging to the technical field of aqueous zinc metal secondary batteries. The present invention uses sodium 2,6-naphthalene disulfonate (26-NADS) as an additive and introduces it into acidic, near-neutral, and alkaline electrolytes respectively. 26-NADS regulates the Zn 2+ The solvation process can also form a molecular layer on the electrode surface, delaying the concentration polarization of zinc ions in acidic / near-neutral electrolytes, accelerating the deposition kinetics of zinc ions, and inhibiting the [Zn(OH)4] 2‑ The local supersaturation in alkaline electrolytes ultimately suppresses dendrites and side reactions of the Zn anode in wide pH electrolytes. In addition, the acidic / near-neutral Zn||MnO2 full battery exhibits a high charge / discharge rate at 5 A g ‑1 Cycled 13000 times at a current density of 3 A g ‑1 Current density cycle 5000 times, alkaline Zn||Ni 0.8 Co 0.1 M n0.1 O2 full cell at 3 A g ‑1 The invention has simple preparation process, significant effect, low cost and meets the requirements of environmental and economic benefits.

Description

Technical Field

[0001] The present invention relates to the technical field of aqueous zinc metal secondary batteries, and in particular to a method for preparing an electrolyte suitable for acidic, near-neutral and alkaline zinc-based energy storage devices and applications. Background Art

[0002] Aqueous zinc metal batteries have abundant resources and large volumetric capacity (5855mAh cm -3 ), suitable redox potential (-0.76V vs standard hydrogen potential) and other advantages have triggered a research boom. However, the practical application of aqueous zinc metal batteries still faces challenges such as side reactions related to water and dendrite growth. In aqueous electrolytes, due to the high polarity and small radius of water molecules, water molecules and zinc ions coordinate to form a highly directional and ordered solvation structure. During the desolvation process, the active water molecules in the solvation structure will decompose into H near the zinc negative electrode. + and OH - , a hydrogen evolution reaction occurs, and the hydrogen produced causes the battery to swell, causing safety issues and also reducing the battery's Coulombic efficiency. Therefore, water molecules exacerbate the thermodynamic instability of the zinc negative electrode, resulting in reduced cycle performance. In addition, aqueous electrolytes, as one of the important components of batteries, are mainly divided into acidic electrolytes, near-neutral electrolytes, and alkaline electrolytes based on pH value. Therefore, enhancing the stability of the zinc negative electrode is crucial to improving the electrochemical performance of aqueous zinc metal batteries in aqueous electrolytes with a wide pH range.

[0003] The strategy of introducing organic additives into electrolytes can simultaneously modify the zinc ion solvation process and the electrode / electrolyte interface, offering advantages such as ease of operation and significant results. However, recent reports on additive modification of zinc metal batteries have been limited to single acidic and alkaline electrolytes, lacking additives that can adapt to a wide range of acidic, near-neutral, and alkaline electrolytes. Therefore, there is an urgent need to explore additives that can modulate the electrode interface and solvation structure to improve the stability and electrochemical kinetics of zinc anodes across a wide pH range.

[0004] This invention introduces sodium 2,6-naphthalene disulfonate (Na2,6-Naphthalene Disulfonate) as an additive into acidic, near-neutral, and alkaline electrolytes to create a wide-pH electrolyte, improving the thermodynamic stability of the zinc negative electrode over a wide range of pH conditions. On the one hand, the Na2,6-naphthalene disulfonate modulates the solvation structure of zinc ions, accelerating the desolvation process. Its dual capture function alleviates concentration polarization at the electrode interface, inhibiting dendrite growth. On the other hand, the Na2,6-naphthalene disulfonate self-assembles through chemical adsorption to form a molecular layer, isolating water from the electrode, slowing side reactions and improving the reversibility of the zinc negative electrode's deposition / stripping properties. Summary of the Invention

[0005] The purpose of the present invention is to provide a method for preparing an electrolyte and its application that is simultaneously suitable for acidic, near-neutral and alkaline zinc-based energy storage devices. By introducing sodium 2,6-naphthalene disulfonate additive into acidic, near-neutral and alkaline electrolytes, the solvation structure of zinc ions is reconstructed, the desolvation process is accelerated, and an ordered and stable monolayer is constructed by chemical adsorption to protect the zinc negative electrode, thereby improving the electrochemical reversibility of the zinc-based energy storage device.

[0006] To achieve the above object, the present invention adopts the following technical solutions:

[0007] The present invention provides a method for preparing an electrolyte suitable for acidic, near-neutral, and alkaline zinc-based energy storage devices, and the preparation steps are as follows:

[0008] (1) Dissolve a soluble acidic salt in deionized water to prepare an acidic salt solution with a concentration of 2-5 mol L -1 , adding a certain amount of sodium 2,6-naphthalene disulfonate to prepare an acidic electrolyte, wherein the pH range of the acidic electrolyte is 1-4;

[0009] (2) Alternatively, a soluble acidic salt is dissolved in deionized water to prepare a near-neutral salt solution having a concentration of 0.1-1 mol L -1 , adding a certain amount of sodium 2,6-naphthalene disulfonate to prepare a near-neutral electrolyte, wherein the pH range of the near-neutral electrolyte is 5-7;

[0010] (3) Alternatively, a soluble alkaline salt is dissolved in deionized water to prepare an alkaline salt solution having a concentration of 1-10 mol L -1 , adding a certain amount of sodium 2,6-naphthalene disulfonate to prepare an alkaline electrolyte, wherein the pH range of the alkaline electrolyte is 13-14;

[0011] (4) Preparation of acidic / near-neutral full batteries: zinc metal is used as the negative electrode, carbon material / manganese-based compound is used as the positive electrode material, and glass fiber is used as the separator. The acidic electrolyte prepared in step (1) or the near-neutral electrolyte prepared in step (2) is added dropwise to assemble button batteries (CR2032 type) or soft-pack batteries, and their zinc storage performance is tested;

[0012] (5) Preparation of alkaline full battery: zinc metal is used as the negative electrode, manganese-based / nickel-based compound is used as the positive electrode material, glass fiber is used as the separator, and the alkaline electrolyte prepared in step (3) is added dropwise to assemble into a button cell (CR2032 type) or a soft pack battery, and its zinc storage performance is tested.

[0013] Furthermore, the soluble acidic salts described in step (1) and step (2) include but are not limited to zinc sulfate, zinc nitrate, zinc trifluoromethanesulfonate, zinc acetate, zinc chloride, and zinc perchlorate; the soluble alkaline salts described in step (3) include but are not limited to potassium hydroxide and sodium hydroxide.

[0014] Furthermore, the concentration of the sodium 2,6-naphthalene disulfonate additive in the electrolyte is 1-100 mmol L -1 .

[0015] Furthermore, zinc metal includes but is not limited to zinc foil and zinc powder.

[0016] Furthermore, the manganese-based compound positive electrode material is prepared by the following method, wherein the method for preparing the manganese-based compound is an electrodeposition method: using lithium manganate leachate as a deposition solution, using three electrodes for deposition, wherein silver / silver chloride is a reference electrode, a platinum electrode is a working electrode, and a carbon cloth is a counter electrode, using an electrochemical time-transient test, setting the voltage to 1V and the deposition time to 300s, manganese dioxide is deposited on the carbon cloth, and finally using a muffle furnace, setting it to 350°C for calcination for 2h to obtain a manganese dioxide composite positive electrode sheet, wherein the mass loading of the positive electrode material of the manganese-based compound active substance is 1.0 to 10.0 mg cm -2 .

[0017] Furthermore, the carbon material nickel-based positive electrode material is prepared by the following method: using commercially available carbon / nickel-containing active material, the mass ratio of carbon / nickel-containing active material: conductive agent: binder is 8:1:1, adding an appropriate amount of solvent to mix and prepare a slurry, coating the slurry on the current collector, and drying at 80°C for 10 hours to obtain a carbon material / nickel-based positive electrode sheet, wherein the mass loading of the carbon / nickel-containing active material positive electrode material is 1.0-10.0 mg cm -2 .

[0018] The application of the above-mentioned method for preparing the electrolyte for the zinc-based energy storage device of the present invention is characterized in that the method for assembling a button battery is as follows: zinc metal is used as the negative electrode, the positive electrode material prepared by the above-mentioned method for preparing the electrolyte for the zinc-based energy storage device is used as the positive electrode, glass fiber is used as the separator, and 80 μL of the electrolyte prepared by the above-mentioned method for preparing the electrolyte for the zinc-based energy storage device is added dropwise to assemble the button battery.

[0019] The application of the above-mentioned method for preparing an electrolyte for a zinc-based energy storage device of the present invention is characterized in that the soft-pack battery assembly method is as follows: the outer packaging body aluminum-plastic film has a size of 11 cm×11 cm, the single piece area of ​​the zinc metal negative electrode is 9 cm×9 cm, the single piece area of ​​the manganese-based / nickel-based compound positive electrode sheet is 8 cm×8 cm, and the single piece area of ​​the glass fiber separator is 10 cm×10 cm. The negative electrode, separator, and positive electrode are stacked in this order, and the electrolyte prepared by the above-mentioned method for preparing an electrolyte for a zinc-based energy storage device is introduced to assemble a soft-pack battery.

[0020] Specifically, the present invention provides a method for preparing an electrolyte suitable for acidic, near-neutral, and alkaline zinc-based energy storage devices, and the preparation steps are as follows:

[0021] (1) Dissolve a soluble acidic salt in deionized water to prepare an acidic salt solution with a concentration of 2-5 mol L -1 , add sodium 2,6-naphthalene disulfonate to prepare an acidic electrolyte with a pH range of 1-4;

[0022] (2) Alternatively, a soluble acidic salt is dissolved in deionized water to prepare a near-neutral salt solution having a concentration of 0.1-1 mol L -1 , add sodium 2,6-naphthalene disulfonate to prepare a nearly neutral electrolyte with a pH range of 5-7;

[0023] (3) Alternatively, a soluble alkaline salt is dissolved in deionized water to prepare an alkaline salt solution having a concentration of 1-10 mol L -1 , add sodium 2,6-naphthalene disulfonate to prepare an alkaline electrolyte with a pH range of 13-14;

[0024] (4) Preparation of acidic / near-neutral full batteries: Zinc metal is used as the negative electrode, carbon material / manganese-based compound is used as the positive electrode material, and glass fiber is used as the separator. The acidic electrolyte prepared in step (1) or the near-neutral electrolyte prepared in step (2) is added dropwise to assemble button batteries (CR2032 type) or soft-pack batteries, and their zinc storage performance is tested.

[0025] (5) Preparation of alkaline full battery: zinc metal is used as the negative electrode, manganese-based / nickel-based compound is used as the positive electrode material, glass fiber is used as the separator, and the alkaline electrolyte prepared in step (3) is added dropwise to assemble into a button cell (CR2032 type) or a soft pack battery, and its zinc storage performance is tested.

[0026] The soluble acidic salts described in steps (1)-(2) above include but are not limited to zinc sulfate, zinc nitrate, zinc trifluoromethanesulfonate, zinc acetate, zinc chloride, and zinc perchlorate; the soluble alkaline salts described in step (3) above include but are not limited to potassium hydroxide and sodium hydroxide.

[0027] The optimal concentration of the sodium 2,6-naphthalene disulfonate additive in steps (1) to (3) is 1-100 mmol L -1 It can use the double-end capture function to regulate the concentration polarization at the interface, reconstruct the solvation process, accelerate the desolvation process, and inhibit dendrite growth; it uses chemical adsorption to construct a molecular layer on the surface to isolate water and slow down side reactions.

[0028] The zinc metal used in the preparation of the zinc-based energy storage device in steps (4) and (5) above includes but is not limited to zinc foil and zinc powder.

[0029] The method for preparing the manganese-based compound positive electrode material in step (4) above is an electrodeposition method: lithium manganate leaching solution is used as the deposition solution, and deposition is performed using three electrodes, wherein silver / silver chloride is used as the reference electrode, a platinum electrode is used as the working electrode, and a carbon cloth is used as the counter electrode. Using an electrochemical time-transient test, the voltage is set to 1V and the deposition time is set to 300s to deposit manganese dioxide on the carbon cloth. Finally, a muffle furnace is used and calcined at 350°C for 2h to obtain a manganese dioxide composite positive electrode sheet, wherein the mass loading of the positive electrode material containing the manganese active substance is 1.0 to 10.0 mg cm -2 .

[0030] The preparation method of the carbon material / nickel-based positive electrode material in the above steps (4) and (5) is as follows: using commercially available carbon / nickel-containing active material, the mass ratio of carbon / nickel-containing active material: conductive agent: binder is 8:1:1, adding an appropriate amount of solvent to mix and prepare a slurry, coating the slurry on the current collector, and drying at 80°C for 10 hours to obtain a carbon material / nickel-based positive electrode sheet, wherein the mass loading of the carbon / nickel-containing active material is 1.0 to 10.0 mg cm -2 .

[0031] The method for assembling a button battery in steps (4) and (5) above is as follows: zinc metal is used as the negative electrode, the electrode sheet prepared above is used as the positive electrode, glass fiber is used as the separator, and 80 μL of the aqueous electrolyte prepared by the above preparation method is added dropwise to assemble a button battery.

[0032] The method for assembling a soft-pack battery in steps (4) and (5) above is as follows: the size of the aluminum-plastic film of the outer packaging body is 11 cm×11 cm, the single-piece area of ​​the zinc metal negative electrode is 9 cm×9 cm, the single-piece area of ​​the manganese-based / nickel-based compound positive electrode sheet is 8 cm×8 cm, and the single-piece area of ​​the glass fiber separator is 10 cm×10 cm. The negative electrode, separator, and positive electrode are stacked in sequence, and the aqueous electrolyte prepared by any of the preparation methods described in steps (1) to (3) above is introduced to assemble a soft-pack battery.

[0033] Compared with the existing technology, the present invention has the following specific advantages:

[0034] (1) Electrolyte additives are the most promising modification method to improve the performance of zinc-based energy storage devices. They are simple to operate and have obvious effects.

[0035] (2) Sodium 2,6-naphthalene disulfonate as an additive has low cost, high safety, is non-toxic and harmless, and has environmental and economic benefits.

[0036] (3) The present invention introduces sodium 2,6-naphthalene disulfonate additives into acidic, near-neutral and alkaline electrolytes to reconstruct the solvation structure of zinc ions, accelerate the desolvation process, and simultaneously construct an ordered and stable monolayer to protect the zinc negative electrode through chemical adsorption, thereby improving the electrochemical reversibility of zinc-based energy storage devices.

[0037] (4) The sodium 2,6-naphthalene disulfonate additive is effective and practical. The full battery assembled with a wide pH electrolyte containing sodium 2,6-naphthalene disulfonate has the advantages of long cycle life and stability. -1 Cycling 13000 times at the current density, the near-neutral Zn||MnO2 full battery is -1 Current density cycle 5000 times, alkaline Zn||Ni 0.8 Co 0.1 Mn 0.1 O2 full battery at 3Ag -1 The current density was cycled for 500 cycles. BRIEF DESCRIPTION OF THE DRAWINGS

[0038] Figure 1 This is a calculated diagram of the adsorption energy of water and sodium 2,6-naphthalene disulfonate on the Zn(002) crystal plane in the electrolyte obtained in Example 1.

[0039] Figure 2 This is a SEM image of the zinc negative electrode after the acidic electrolyte obtained in Example 1 is assembled into a battery and cycled.

[0040] Figure 3 This is an AFM image of the zinc negative electrode after the acidic electrolyte obtained in Example 1 was assembled into a battery and cycled.

[0041] Figure 4 The acidic electrolyte obtained in Example 1 was assembled into a symmetrical battery at 4 mA cm -2 Cycling performance diagram at current density of .

[0042] Figure 5 The near-neutral electrolyte obtained in Example 1 was assembled into a symmetrical cell at 4 mA cm -2 Cycling performance diagram at current density of .

[0043] Figure 6 The alkaline electrolyte obtained in Example 1 was assembled into a symmetrical battery at 0.5 mA cm -2 Cycling performance diagram at current density of .

[0044] Figure 7 The Zn||MnO2 full battery assembled with the acidic electrolyte obtained in Example 1 was used in 5Ag -1 Cycling performance diagram at different current densities.

[0045] Figure 8 The Zn||MnO2 full battery assembled with the near-neutral electrolyte obtained in Example 1 was tested at 3A g -1 Cycling performance diagram at different current densities.

[0046] Figure 9 The alkaline electrolyte obtained in Example 1 is assembled into Zn||Ni 0.8 Co 0.1 Mn 0.1 O2 full battery at 3A g -1 Cycling performance diagram at different current densities.

[0047] Figure 10 The Zn||MnO2 soft pack full battery assembled with the acidic electrolyte obtained in Example 1 was 0.1Ag -1 Cycling performance diagram at different current densities.

[0048] Figure 11 This is a diagram of Zn||MnO2 soft-pack full batteries assembled with the acidic electrolyte obtained in Example 1 and used in series for charging a mobile phone. DETAILED DESCRIPTION

[0049] Example 1

[0050] A certain mass of zinc sulfate solid (2.904 g) and sodium 2,6-naphthalene disulfonate powder (2.5 mg) were weighed, 5 ml of deionized water was added, and the mixture was ultrasonically treated until transparent and clear to prepare an acidic electrolyte containing sodium 2,6-naphthalene disulfonate with a pH of 3.64; a certain mass of zinc sulfate solid (0.436 g) and sodium 2,6-naphthalene disulfonate powder (2.5 mg) were weighed, 5 ml of deionized water was added, and the mixture was ultrasonically treated until transparent and clear to prepare a near-neutral electrolyte containing sodium 2,6-naphthalene disulfonate with a pH of 5.98; a certain mass of potassium hydroxide solid (0.280 g) and sodium 2,6-naphthalene disulfonate powder (2.5 mg) were weighed, 5 ml of deionized water was added, and the mixture was ultrasonically treated until transparent and clear to prepare an alkaline electrolyte containing sodium 2,6-naphthalene disulfonate with a pH of 13.26;

[0051] Attachment Figure 1 This is a calculation diagram of the adsorption energy of water and sodium 2,6-naphthalene disulfonate on the Zn(002) crystal surface. As can be seen from the figure, the adsorption energy of sodium 2,6-naphthalene disulfonate formed by dissolving sodium 2,6-naphthalene disulfonate in deionized water on Zn(002) (-6.71eV) is stronger than the adsorption energy of water on Zn(002) (-0.29eV). Therefore, sodium 2,6-naphthalene disulfonate is adsorbed on the surface of the zinc negative electrode before water to form a monolayer, isolating water from the electrode contact and improving the stability of the zinc negative electrode. Figure 2 This is a SEM image of the zinc negative electrode after the acidic electrolyte is assembled into a battery cycle. It can be seen from the figure that the electrolyte introduced with sodium 2,6-naphthalene disulfonate effectively protects the zinc negative electrode and inhibits dendrite growth and side reactions. Figure 3 The AFM images also show that the zinc ions are deposited evenly and the zinc negative electrode is flat without large protrusions. Therefore, using acidic, near-neutral and alkaline electrolytes containing sodium 2,6-naphthalene disulfonate, the zinc||zinc symmetric battery has a cycle life of 7200 hours ( Figure 4 ), 500 hours( Figure 5 ) and 220 hours ( Figure 6 In addition, a Zn||MnO2 full battery was assembled with zinc metal sheet as negative electrode, Whatman GF / A as separator, and acidic electrolyte containing sodium 2,6-naphthalene disulfonate at 5Ag -1 Cycle 13000 times at current density ( Figure 7 ), near neutral electrolyte assembled Zn||MnO2 full battery in 3Ag -1 Current density cycle 5000 times ( Figure 8 ), alkaline electrolyte assembly Zn||Ni 0.8 Co 0.1 Mn 0.1 O2 full battery at 3Ag -1 Cycle 500 times at current density ( Figure 9 ). In addition, a zinc sulfate electrolyte containing sodium 2,6-naphthalene disulfonate was used to organize a soft pack battery. -1 After 100 cycles at the current density, the capacity is 190mAh ( Figure 10 ), connecting soft pack batteries in series can charge mobile phones ( Figure 11 These results demonstrate the applicability, effectiveness, and practicality of sodium 2,6-naphthalene disulfonate in acidic, near-neutral, and alkaline electrolytes.

[0052] Example 2

[0053] Weigh a certain amount of zinc chloride solid (1.36 g) and sodium 2,6-naphthalene disulfonate powder (25 mg), add 5 ml of deionized water, and ultrasonicate until transparent and clear to prepare an acidic electrolyte containing sodium 2,6-naphthalene disulfonate; measure a certain amount of concentrated sulfuric acid (270 μL) and dilute to 0.1 mol L -1 , introduce sodium 2,6-naphthalene disulfonate powder (25 mg), ultrasonicate until transparent and clear, to prepare a near-neutral electrolyte containing sodium 2,6-naphthalene disulfonate; weigh a certain mass of potassium hydroxide solid (0.840 g) and sodium 2,6-naphthalene disulfonate powder (25 mg), add 5 ml of deionized water, ultrasonicate until transparent and clear, to prepare an alkaline electrolyte containing sodium 2,6-naphthalene disulfonate;

[0054] The above-mentioned acidic, near-neutral and alkaline electrolytes are introduced respectively. The size of the aluminum-plastic film of the outer packaging body is 11cm×11cm, the single-piece area of ​​the zinc metal negative electrode is 9cm×9cm, the single-piece area of ​​the MnO2 positive electrode sheet is 8cm×8cm, and the single-piece area of ​​the glass fiber separator is 10cm×10cm. The negative electrode, separator, and positive electrode are stacked in sequence to assemble acidic, near-neutral and alkaline electrolyte soft-pack batteries respectively.

[0055] Example 3

[0056] Weigh a certain mass of zinc acetate solid (4.575 g) and sodium 2,6-naphthalene disulfonate powder (25 mg), add 5 ml of deionized water, and sonicate until transparent and clear to prepare an acidic electrolyte containing sodium 2,6-naphthalene disulfonate; weigh a certain mass of zinc acetate (0.915 mg) and sodium 2,6-naphthalene disulfonate powder (25 mg), add 5 ml of deionized water, and sonicate until transparent and clear to prepare a nearly neutral electrolyte containing sodium 2,6-naphthalene disulfonate; weigh a certain mass of potassium hydroxide solid (0.840 g) and sodium 2,6-naphthalene disulfonate powder (25 mg), add 5 ml of deionized water, and sonicate until transparent and clear to prepare an alkaline electrolyte containing sodium 2,6-naphthalene disulfonate;

[0057] The above-mentioned acidic, near-neutral and alkaline electrolytes were introduced respectively, and the respective Zn||Zn symmetric batteries and Zn||MnO2 full batteries were assembled to test their cycle performance.

[0058] Example 4

[0059] Weigh a certain mass of zinc trifluoromethanesulfonate (5.445 g) and sodium 2,6-naphthalene disulfonate powder (50 mg), add 5 ml of deionized water, and sonicate until transparent and clear to prepare an acidic electrolyte containing sodium 2,6-naphthalene disulfonate; weigh a certain mass of potassium sulfate (0.435 mg) and sodium 2,6-naphthalene disulfonate powder (50 mg), add 5 ml of deionized water, and sonicate until transparent and clear to prepare a nearly neutral electrolyte containing sodium 2,6-naphthalene disulfonate; weigh a certain mass of sodium hydroxide solid (0.600 g) and sodium 2,6-naphthalene disulfonate powder (50 mg), add 5 ml of deionized water, and sonicate until transparent and clear to prepare an alkaline electrolyte containing sodium 2,6-naphthalene disulfonate;

[0060] The above-mentioned acidic, near-neutral and alkaline electrolytes were introduced respectively, and Zn||Zn symmetrical batteries and Zn||AC (activated carbon) capacitors were assembled respectively, and their cycle performance was tested.

[0061] The above description is only a preferred embodiment of the present invention. All equivalent changes and modifications made according to the scope of the patent application of the present invention should fall within the scope of the present invention.

Claims

1. A method for preparing an electrolyte suitable for acidic, near-neutral, and alkaline zinc-based energy storage devices, the preparation steps of which are as follows: (1) Dissolve a soluble acidic salt in deionized water to prepare an acidic salt solution with a concentration of 2-5 mol L -1 , adding a certain amount of sodium 2,6-naphthalene disulfonate to prepare an acidic electrolyte, wherein the pH range of the acidic electrolyte is 1-4; (2) Alternatively, a soluble acidic salt is dissolved in deionized water to prepare a near-neutral salt solution having a concentration of 0.1-1 mol L -1 , adding a certain amount of sodium 2,6-naphthalene disulfonate to prepare a near-neutral electrolyte, wherein the pH range of the near-neutral electrolyte is 5-7; (3) Alternatively, a soluble alkaline salt is dissolved in deionized water to prepare an alkaline salt solution having a concentration of 1-10 mol L -1 , adding a certain amount of sodium 2,6-naphthalene disulfonate to prepare an alkaline electrolyte, wherein the pH range of the alkaline electrolyte is 13-14; (4) Preparation of acidic / near-neutral full battery: zinc metal is used as the negative electrode, carbon material / manganese-based compound is used as the positive electrode material, and glass fiber is used as the separator. The acidic electrolyte prepared in step (1) or the near-neutral electrolyte prepared in step (2) is added dropwise to assemble into a CR2032 button cell or soft pack cell, and its zinc storage performance is tested; (5) Preparation of alkaline full battery: Use zinc metal as the negative electrode, manganese-based / nickel-based compound as the positive electrode material, glass fiber as the separator, add the alkaline electrolyte prepared in step (3) to assemble into CR2032 button battery or soft pack battery, and test its zinc storage performance.

2. The method for preparing an electrolyte for a zinc-based energy storage device according to claim 1, wherein: The soluble acidic salts described in step (1) and step (2) include but are not limited to zinc sulfate, zinc nitrate, zinc trifluoromethanesulfonate, zinc acetate, zinc chloride, and zinc perchlorate; the soluble alkaline salts described in step (3) include but are not limited to potassium hydroxide and sodium hydroxide.

3. The method for preparing an electrolyte for a zinc-based energy storage device according to claim 1, wherein: The concentration of sodium 2,6-naphthalene disulfonate additive in the electrolyte is 1-100 mmol L -1 .

4. The method for preparing an electrolyte for a zinc-based energy storage device according to claim 1, wherein: Zinc metal includes but is not limited to zinc foil and zinc powder.

5. The method for preparing an electrolyte for a zinc-based energy storage device according to claim 1, wherein: The manganese-based compound positive electrode material was prepared by the following method. The method for preparing the manganese-based compound is an electrodeposition method: lithium manganate leaching solution is used as a deposition solution, and three electrodes are used for deposition, wherein silver / silver chloride is used as a reference electrode, a platinum electrode is used as a working electrode, and a carbon cloth is used as a counter electrode. By using an electrochemical time-transient test, the voltage is set to 1 V and the deposition time is set to 300 s to deposit manganese dioxide on the carbon cloth. Finally, a muffle furnace is used and calcined at 350°C for 2 h to obtain a manganese dioxide composite positive electrode sheet, wherein the mass loading of the positive electrode material of the manganese-based compound active substance is 1.0~10.0 mg cm -2 .

6. The method for preparing an electrolyte for a zinc-based energy storage device according to claim 1, wherein: The carbon material nickel-based positive electrode material was prepared by the following method: using commercially available carbon / nickel-containing active material, the mass ratio of carbon / nickel-containing active material: conductive agent: binder was 8:1:1, adding an appropriate amount of solvent to mix and prepare a slurry, coating the slurry on a current collector, and drying at 80°C for 10 h to obtain a carbon material / nickel-based positive electrode sheet, wherein the mass loading of the carbon / nickel-containing active material positive electrode material was 1.0~10.0 mg cm -2 .

7. Application of the method for preparing an electrolyte for a zinc-based energy storage device according to any one of claims 1 to 6, characterized in that: The method for assembling a button battery is as follows: zinc metal is used as the negative electrode, the positive electrode material prepared by the method for preparing the electrolyte for a zinc-based energy storage device according to any one of claims 5-6 is used as the positive electrode, glass fiber is used as the separator, and 80 μL of the electrolyte prepared by the method for preparing the electrolyte for a zinc-based energy storage device according to any one of claims 1-3 is added dropwise to assemble the button battery.

8. Application of the method for preparing an electrolyte for a zinc-based energy storage device according to any one of claims 1 to 6, characterized in that: The method for assembling a soft-pack battery is as follows: the size of the aluminum-plastic film of the outer packaging body is 11 cm×11 cm, the single-piece area of ​​the zinc metal negative electrode is 9 cm×9 cm, the single-piece area of ​​the manganese-based / nickel-based compound positive electrode sheet is 8 cm×8 cm, and the single-piece area of ​​the glass fiber separator is 10 cm×10 cm. The negative electrode, the separator, and the positive electrode are stacked in sequence, and the electrolyte prepared by the electrolyte preparation method for the zinc-based energy storage device according to any one of claims 1-3 is introduced to assemble a soft-pack battery.

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