阅读说明：本技术 聚电解质插层二氧化锰的制备方法及其应用 (Preparation method and application of polyelectrolyte intercalated manganese dioxide ) 是由 邵智鹏 傅杰财 谢二庆 张亚雄 郭洪州 延剑锋 崔晓莎 于 2021-08-18 设计创作，主要内容包括：本发明提供了聚电解质插层二氧化锰的制备方法及其应用,其中聚电解质插层的二氧化锰包括聚电解质和二氧化锰,且聚电解质通过原位电化学的方法生长于二氧化锰层间,原位电化学方法包括以下步骤：S1、将锰盐与聚电解质分散于去离子水中；S2、利用电化学方法在三电极体系中,以步骤S1得到溶液为沉积液,通过无机-有机界面反应,在集流体上,将聚电解质插入二氧化锰层间,最后通过高温干燥形成聚电解质插层的二氧化锰。本发明提供的原位电化学合成方法工艺简单、成本低、容易操作。同时,聚电解质原位插层于二氧化锰层间,大大地扩大了层状二氧化锰的层间距,从而提高了二氧化锰的结构稳定性、电化学性能以及吸附性能,应用于离子电池等。(The invention provides a preparation method and application of polyelectrolyte intercalated manganese dioxide, wherein the polyelectrolyte intercalated manganese dioxide comprises polyelectrolyte and manganese dioxide, the polyelectrolyte is grown between layers of the manganese dioxide by an in-situ electrochemical method, and the in-situ electrochemical method comprises the following steps: s1, dispersing manganese salt and polyelectrolyte in deionized water; and S2, in a three-electrode system by using an electrochemical method, taking the solution obtained in the step S1 as a deposition solution, inserting polyelectrolyte into a manganese dioxide layer on a current collector through inorganic-organic interface reaction, and finally drying at high temperature to form the polyelectrolyte intercalated manganese dioxide. The in-situ electrochemical synthesis method provided by the invention has the advantages of simple process, low cost and easiness in operation. Meanwhile, the polyelectrolyte is intercalated between manganese dioxide layers in situ, so that the interlayer spacing of the layered manganese dioxide is greatly enlarged, the structural stability, the electrochemical performance and the adsorption performance of the manganese dioxide are improved, and the method is applied to ion batteries and the like.)

1. A preparation method of polyelectrolyte intercalated manganese dioxide is characterized by comprising the following steps:

s1, dispersing manganese salt and polyelectrolyte in deionized water, and stirring to completely dissolve the manganese salt and the polyelectrolyte to form a uniform solution;

s2, inserting polyelectrolyte into the manganese dioxide layer on the current collector through inorganic-organic interface reaction by using the solution obtained in the step S1 as a deposition solution in a three-electrode system by using an in-situ electrochemical method;

and S3, drying in an oven to form the polyelectrolyte intercalated manganese dioxide.

2. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 1, characterized in that: and in the step S1, the manganese salt is one of manganese acetate, manganese nitrate, manganese chloride, manganese carbonate or manganese sulfate.

3. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 1 or 2, characterized in that: in the step S1, the polyelectrolyte is one of a polycationic electrolyte, a polyanionic electrolyte or an amphoteric polyelectrolyte.

4. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 3, characterized in that: the mass ratio of the manganese salt, the polyelectrolyte and the deionized water in the step S1 is 10:1-20: 2500.

5. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 1 or 4, characterized in that: the in-situ electrochemical method in the step S2 is one or more of a potentiostatic method, a galvanostatic method, a cyclic voltammetry method, or a galvanostatic charging and discharging method.

6. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 5, characterized in that: the potentiostatic conditions in step S2 are: the voltage is 0.8-1.2V, and the time is 10s-3600 s; the conditions of the constant current method are as follows: the current density is 5-100mA/cm²The time is 10s-3600 s; the cyclic voltammetry conditions were: the sweeping speed is 0.1-5mV/s, the voltage window is-0.4-0.5-0.8-1.2V, and the number of turns is 1-100 turns; the conditions of the constant current charge-discharge method are as follows: the current is 0.1-100mA/cm²The voltage window is-0.4-0.5-0.8-1.2V, and the number of turns is 1-100.

7. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 1 or 6, characterized in that: the three-electrode system in the step S2 includes a working electrode-current collector, a counter electrode-platinum electrode, a reference electrode-calomel electrode or a silver chloride electrode.

8. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 7, characterized in that: the current collector in the step S2 is one of carbon cloth, carbon paper, stainless steel mesh or titanium sheet.

9. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 3, characterized in that: the polycation electrolyte in the step S2 is one or more of poly (N-butyl-4-vinylpyridine bromide), poly (diallyldimethylammonium chloride), poly (ethyleneimine hydrochloride), poly (N, N '-tetramethyl-N-p-tolylethylenediamine chloride), poly (N, N' -dimethyl-3, 5-dimethylidene nitrogen hexacyclic chloride), poly (2-acryloylethylene dimethyl sulfide chloride) or poly (glycidyl tributyl phosphonium chloride).

10. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 3, characterized in that: in the step S2, the polyanionic electrolyte is one or more of sodium polyacrylate, polystyrene sulfuric acid, styrene-maleic acid copolymer, polyglutamic acid, polyvinyl phosphoric acid, and alginic acid.

11. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 3, characterized in that: in the step S2, the amphoteric polymer electrolyte is one or more of acrylic acid-vinylpyridine copolymer, protein or nucleotide.

12. The method for preparing polyelectrolyte intercalated manganese dioxide according to claim 1 or 8, characterized in that: the drying temperature in the step S3 is 60-100 ℃.

13. The method of any preceding claim, wherein the polyelectrolyte-intercalated manganese dioxide is obtained.

14. Use of the preparation method according to any of the preceding claims to obtain polyelectrolyte-intercalated manganese dioxide, characterized in that: is used for manufacturing a water system zinc ion battery device.

Technical Field

The invention relates to the technical field of preparation methods of inorganic-organic composite materials, in particular to an electrochemical preparation method of polyelectrolyte intercalated manganese dioxide and application of the polyelectrolyte intercalated manganese dioxide in a water-based zinc ion battery device.

Technical Field

With the continuous and rapid development of science and technology and industry, energy is becoming one of the most concerned topics of people at present. However, in the development process of the industrial society, the excessive consumption of fossil energy such as petroleum, natural gas, coal and the like promotes the rapid development of some novel energy sources (solar energy, wind energy, tidal energy and the like), however, the renewable energy sources belong to intermittent energy sources and have poor stability, so that the storage and the effective utilization of the energy sources are very important. Rechargeable ion batteries are just the best choice for energy storage and release.

Manganese-based composite materials have been considered as the main materials of traditional ion batteries and supercapacitors, and particularly as the anode materials of water-based zinc ion batteries with higher theoretical capacity. However, pure manganese dioxide has poor storage capacity and cycling stability and low capacity utilization, and still faces huge challenges, mainly due to phase changes caused by the intercalation/deintercalation of ions and the consequent structural collapse during cycling.

The performance of the manganese oxide-based energy storage device can be effectively improved by widening the interlayer structure of the layered manganese dioxide. While polyelectrolyte-intercalated manganese dioxide prepared by in situ electrochemical methods has long been proposed, conventional methods of preparation tend to be complex, difficult to control, and costly. The electrochemical method for preparing the polyelectrolyte intercalated manganese dioxide makes up the defects of the traditional technology, greatly improves the storage capacity and cycle life of the manganese dioxide material in the ion battery.

Disclosure of Invention

The technical problem to be solved by the invention is to provide an in-situ electrochemical preparation method of intercalation manganese dioxide of polyelectrolyte, the preparation method has simple process, easy control of reaction and lower cost, and the prepared composite material is applied to a positive electrode of a water system zinc ion battery, and has higher capacity, good cycling stability and electrical conductivity.

The technical scheme is as follows for solving the technical problem of the invention:

a preparation method of polyelectrolyte intercalated manganese dioxide comprises the following steps:

s1, dispersing manganese salt and polyelectrolyte in deionized water, and stirring to completely dissolve the manganese salt and the polyelectrolyte to form a uniform solution;

s2, inserting polyelectrolyte into the manganese dioxide layer on the current collector through inorganic-organic interface reaction by using the solution obtained in the step S1 as a deposition solution in a three-electrode system by using an in-situ electrochemical method;

and S3, drying in an oven to form the polyelectrolyte intercalated manganese dioxide.

And in the step S1, the manganese salt is one of manganese acetate, manganese nitrate, manganese chloride, manganese carbonate or manganese sulfate.

In the step S1, the polyelectrolyte is one of a polycationic electrolyte, a polyanionic electrolyte or an amphoteric polyelectrolyte.

The mass ratio of the manganese salt, the polyelectrolyte and the deionized water in the step S1 is 10:1-20: 2500.

The in-situ electrochemical method in the step S2 is one or more of a potentiostatic method, a galvanostatic method, a cyclic voltammetry method, or a galvanostatic charging and discharging method.

The potentiostatic conditions in step S2 are: the voltage is 0.8-1.2V, and the time is 10s-3600 s; the conditions of the constant current method are as follows: the current density is 5-100mA/cm²The time is 10s-3600 s; the cyclic voltammetry conditions were:the sweeping speed is 0.1-5mV/s, the voltage window is-0.4-0.5-0.8-1.2V, and the number of turns is 1-100 turns; the conditions of the constant current charge-discharge method are as follows: the current is 0.1-100mA/cm²The voltage window is-0.4-0.5-0.8-1.2V, and the number of turns is 1-100.

The three-electrode system in the step S2 includes a working electrode-current collector, a counter electrode-platinum electrode, a reference electrode-calomel electrode or a silver chloride electrode.

The current collector in the step S2 is one of carbon cloth, carbon paper, stainless steel mesh or titanium sheet.

The polycation electrolyte in the step S2 is one or more of poly (N-butyl-4-vinylpyridine bromide), poly (diallyldimethylammonium chloride), poly (ethyleneimine hydrochloride), poly (N, N '-tetramethyl-N-p-tolylethylenediamine chloride), poly (N, N' -dimethyl-3, 5-dimethylidene nitrogen hexacyclic chloride), poly (2-acryloylethylene dimethyl sulfide chloride) or poly (glycidyl tributyl phosphonium chloride).

In the step S2, the polyanionic electrolyte is one or more of sodium polyacrylate, polystyrene sulfuric acid, styrene-maleic acid copolymer, polyglutamic acid, polyvinyl phosphoric acid, and alginic acid.

In the step S2, the amphoteric polymer electrolyte is one or more of acrylic acid-vinylpyridine copolymer, protein or nucleotide.

The drying temperature in the step S3 is 60-100 ℃.

The polyelectrolyte intercalated manganese dioxide prepared by the preparation method of the polyelectrolyte intercalated manganese dioxide is applied to a water system zinc ion battery device, and the water system zinc ion battery can be used in the fields of electronic equipment, automobiles, aerospace, navigation and the like.

Further, the aqueous zinc ion battery can be prepared by the following method:

1. cutting a zinc sheet into a round shape by a slicer to be used as a negative electrode of the water-based zinc ion battery;

2. cutting the fiber diaphragm into a round shape by a slicer to be used as the diaphragm of the water-based zinc ion battery;

3. preparing a zinc sulfate and manganese sulfate mixed solution with a certain concentration as an electrolyte of a water-based zinc ion battery;

4. taking the polyelectrolyte intercalated manganese dioxide as the positive electrode of the water-based zinc ion battery;

5. sequentially placing a positive plate, electrolyte, a diaphragm, the electrolyte, a negative plate, a gasket (1 mm) and a spring plate into a bottom shell of the positive battery;

6. and covering the negative battery shell, and pressurizing the battery by 2Mpa by using a battery sealing machine to seal.

Compared with the prior art, the invention has the following remarkable characteristics and beneficial effects: 1. the adopted in-situ electrochemical preparation method has simple process, easy control of reaction and lower cost; 2. the polyelectrolyte intercalated manganese dioxide prepared by the method is characterized in that the polyelectrolyte in-situ intercalation is arranged between manganese dioxide layers, so that the interlayer spacing of layered manganese dioxide is greatly enlarged, the structural stability, the electrochemical performance and the adsorption performance of the manganese dioxide are improved, and the polyelectrolyte intercalated manganese dioxide is used as an anode electrode material of a water system zinc ion battery, is applied to energy storage devices such as an ion battery and a super capacitor, has higher capacity, good cycle stability and conductivity, and has good industrial prospect.

Drawings

FIG. 1 is a scanning comparison of polyelectrolyte intercalated manganese dioxide and manganese dioxide as provided in example 1 of the present invention;

FIG. 2 is a comparison XRD plot of polyelectrolyte intercalated manganese dioxide and manganese dioxide as provided in example 1 of the present invention;

fig. 3 is a charge/discharge curve of the aqueous zinc-ion battery provided in example 1 of the present invention at a current density of 0.1A/g.

Detailed Description

The invention is further described below with reference to the figures and examples.

Example 1

A preparation method of polyelectrolyte intercalated manganese dioxide comprises the following specific steps:

s1, dispersing 0.237g of manganese sulfate and 0.095g of poly (diallyldimethylammonium chloride) into 250ml of deionized water, and then forming a uniform solution under ultrasound;

s2, in a three-electrode system, taking carbon cloth as a working electrode, a platinum electrode as a counter electrode and a calomel electrode as a reference electrode, taking the solution obtained in the step S1 as a deposition solution, adopting a potentiostatic method, wherein the voltage is 1V and the deposition time is 600S, and inserting poly (diallyl dimethyl ammonium chloride) between manganese dioxide layers on the carbon cloth through an inorganic-organic interface reaction;

and S3, drying in an oven at 80 ℃ to form poly (diallyl dimethyl ammonium chloride) intercalated manganese dioxide.

Characterization of structure and morphology of poly (diallyldimethylammonium chloride) intercalated manganese dioxide: (1) the morphological structure of the material is characterized by using a field emission scanning electron microscope (FESEM, Tescan Lyra 3), as shown in fig. 1, the morphology of manganese dioxide (a) and manganese dioxide (b) intercalated by poly (diallyldimethylammonium chloride) is compared, and it can be seen that the manganese dioxide intercalated by poly (diallyldimethylammonium chloride) has a larger pore structure, which is more beneficial to the back-and-forth transmission of ions and improves the dynamics of the battery. (2) Phase structure and crystal information of the material were studied by x-ray diffraction (XRD, Rigaku D-max 2400), and comparison of manganese dioxide XRD of manganese dioxide and poly (diallyldimethylammonium chloride) intercalation is shown in fig. 2, which shows that poly (diallyldimethylammonium chloride) intercalation manganese dioxide has (00 l, l = 1-3) planes, corresponding to 0.97nm spacing, indicating that the poly (diallyldimethylammonium chloride) intercalation manganese dioxide interlayer spacing is greatly increased.

Preparation of an aqueous zinc ion battery:

s1, cutting a zinc sheet into a round shape by using a slicing machine to be used as a negative electrode of the water-based zinc ion battery;

s2, cutting the diaphragm into a round shape by using a slicer;

s3, preparing a certain mixed solution of 2M zinc sulfate and 0.2M manganese sulfate as an electrolyte of the water-based zinc ion battery;

s4, taking the manganese dioxide of the poly (diallyl dimethyl ammonium chloride) intercalation as the anode of the water-based zinc ion battery;

s5, sequentially placing the positive plate, the electrolyte, the diaphragm, the electrolyte, the negative plate, the gasket (1 mm) and the elastic sheet into a bottom shell of the positive battery;

s6, covering the negative battery shell, and sealing the battery by pressurizing the battery to 2Mpa by using a battery sealing machine.

Testing of electrochemical performance of aqueous zinc ion battery:

electrochemical performance tests are carried out on the water-based zinc ion battery by adopting an electrochemical workstation (CHI660E, Chenhua), and as shown in a charge-discharge curve of the battery in fig. 3 under the current density of 0.1A/g, the discharge capacity can reach up to 321.6mAh/g, and higher specific capacity is shown.

Example 2

A preparation method of polyelectrolyte intercalated manganese dioxide comprises the following specific steps:

s1, dispersing 0.5g of manganese acetate and 0.1g of poly (diallyldimethylammonium chloride) in 250ml of deionized water, and then forming a uniform solution under ultrasound;

s2, in a three-electrode system, taking carbon cloth as a working electrode, a platinum electrode as an electrode and a calomel electrode as a reference electrode, taking the solution obtained in the step S1 as a deposition solution, adopting a cyclic voltammetry and constant current charging and discharging method, firstly preparing by using the cyclic voltammetry, wherein the conditions are as follows: the sweeping speed is 5mV/s, the voltage window is 0-1.2V, and the number of turns is 1 turn; then preparing by using a constant current charge-discharge method under the conditions that: the current is 5mA/cm²Inserting poly (diallyl dimethyl ammonium chloride) between manganese dioxide layers on carbon cloth through inorganic-organic interface reaction, wherein the voltage window is 0-1.2V, and the number of turns is 50;

and S3, drying in an oven at 90 ℃ to form poly (diallyl dimethyl ammonium chloride) intercalated manganese dioxide.

Preparation of an aqueous zinc ion battery:

s1, cutting a zinc sheet into a round shape by using a slicing machine to be used as a negative electrode of the water-based zinc ion battery;

s2, cutting the diaphragm into a round shape by using a slicer;

s3, preparing a certain mixed solution of 2M zinc sulfate and 0.2M manganese sulfate as an electrolyte of the water-based zinc ion battery;

s4, taking the manganese dioxide of the poly (diallyl dimethyl ammonium chloride) intercalation as the anode of the water-based zinc ion battery;

s5, sequentially placing the positive plate, the electrolyte, the diaphragm, the electrolyte, the negative plate, the gasket (1 mm) and the elastic sheet into a bottom shell of the positive battery;

s6, covering the negative battery shell, and sealing the battery by pressurizing the battery to 2Mpa by using a battery sealing machine.

Example 3

A preparation method of polyelectrolyte intercalated manganese dioxide comprises the following specific steps:

s1, dispersing 0.2g of manganese nitrate and 0.04g of poly (diallyldimethylammonium chloride) in 250ml of deionized water, and then forming a uniform solution under ultrasound;

s2, in a three-electrode system, carbon paper is used as a working electrode, a platinum electrode is used as an electrode, a calomel electrode is used as a reference electrode, the solution obtained in the step S1 is used as a deposition solution, a cyclic voltammetry method and a potentiostatic method are adopted, and the preparation is firstly carried out by using the cyclic voltammetry method, wherein the conditions are as follows: the sweeping speed is 5mV/s, the voltage window is-0.4-1.2V, and the number of turns is 1 turn; then the preparation is carried out by a potentiostatic method, and the conditions are as follows: the voltage is 1V, the deposition time is 1200s, and poly (diallyl dimethyl ammonium chloride) is inserted between manganese dioxide layers on carbon paper through inorganic-organic interface reaction;

and S3, drying in an oven at 80 ℃ to form poly (diallyl dimethyl ammonium chloride) intercalated manganese dioxide.

Preparation of an aqueous zinc ion battery:

s1, cutting a zinc sheet into a round shape by using a slicing machine to be used as a negative electrode of the water-based zinc ion battery;

s2, cutting the diaphragm into a round shape by using a slicer;

s3, preparing a certain mixed solution of 2M zinc sulfate and 0.2M manganese sulfate as an electrolyte of the water-based zinc ion battery;

s4, taking the manganese dioxide of the poly (diallyl dimethyl ammonium chloride) intercalation as the anode of the water-based zinc ion battery;

s5, sequentially placing the positive plate, the electrolyte, the diaphragm, the electrolyte, the negative plate, the gasket (1 mm) and the elastic sheet into a bottom shell of the positive battery;

s6, covering the negative battery shell, and sealing the battery by using a battery sealing machine to pressurize the battery to 2 Mpa.

Example 4

A preparation method of polyelectrolyte intercalated manganese dioxide comprises the following specific steps:

s1, dispersing 0.6g of manganese acetate and 0.1g of sodium polyacrylate in 250ml of deionized water, and then forming a uniform solution under ultrasound;

s2, in a three-electrode system, taking a stainless steel net as a working electrode, a platinum electrode as an electrode and a calomel electrode as a reference electrode, taking the solution obtained in the step S1 as a deposition solution, and firstly preparing by using a cyclic voltammetry method and a potentiostatic method, wherein the conditions are as follows: the sweeping speed is 5mV/s, the voltage window is-0.4-1.2V, and the number of turns is 5 turns; then preparing by using a constant current charge-discharge method under the conditions that: the current density is 0.5mA/cm²The voltage window is-0.4-1.2V, the number of turns is 50, and sodium polyacrylate is inserted between manganese dioxide layers on a stainless steel net through inorganic-organic interface reaction;

and S3, drying in an oven at 80 ℃ to form the sodium polyacrylate intercalated manganese dioxide.

Preparation of an aqueous zinc ion battery:

s1, cutting a zinc sheet into a round shape by using a slicing machine to be used as a negative electrode of the water-based zinc ion battery;

s2, cutting the diaphragm into a round shape by using a slicer;

s3, preparing a certain mixed solution of 2M zinc sulfate and 0.2M manganese sulfate as an electrolyte of the water-based zinc ion battery;

s4, taking the manganese dioxide of the sodium polyacrylate intercalation as the anode of the water-system zinc ion battery;

s5, sequentially placing the positive plate, the electrolyte, the diaphragm, the electrolyte, the negative plate, the gasket (1 mm) and the elastic sheet into a bottom shell of the positive battery;

s6, covering the negative battery shell, and sealing the battery by using a battery sealing machine to pressurize the battery to 2 Mpa.

Example 5

A preparation method of polyelectrolyte intercalated manganese dioxide comprises the following specific steps:

s1, dispersing 0.3g of manganese sulfate and 0.06g of polyglutamic acid in 250ml of deionized water, and then forming a uniform solution under ultrasonic waves;

s2, in a three-electrode system, taking a titanium sheet as a working electrode, a platinum electrode as an electrode and a calomel electrode as a reference electrode, taking the solution obtained in the step S1 as a deposition solution, and firstly preparing by using a cyclic voltammetry method and a potentiostatic method, wherein the conditions are as follows: sweeping speed is 0.1mV/s, voltage window is-0.4-1.2V, the number of turns is 100 turns, and polyglutamic acid is inserted between manganese dioxide layers on a titanium sheet through inorganic-organic interface reaction;

and S3, drying in an oven at 80 ℃ to form the polyglutamic acid intercalated manganese dioxide.

Preparation of an aqueous zinc ion battery:

s1, cutting a zinc sheet into a round shape by using a slicing machine to be used as a negative electrode of the water-based zinc ion battery;

s2, cutting the diaphragm into a round shape by using a slicer;

s3, preparing a certain mixed solution of 2M zinc sulfate and 0.2M manganese sulfate as an electrolyte of the water-based zinc ion battery;

s4, taking the manganese dioxide of the polyglutamic acid intercalation as the anode of the water-system zinc ion battery;

s5, sequentially placing the positive plate, the electrolyte, the diaphragm, the electrolyte, the negative plate, the gasket (1 mm) and the elastic sheet into a bottom shell of the positive battery;

s6, covering the negative battery shell, and sealing the battery by using a battery sealing machine to pressurize the battery to 2 Mpa.

Example 6

A preparation method of polyelectrolyte intercalated manganese dioxide comprises the following specific steps:

s1, dispersing 0.5g of manganese nitrate and 0.06g of nucleotide in 250ml of deionized water, and then forming a uniform solution under ultrasound;

s2, in a three-electrode system, taking carbon cloth as a working electrode, a platinum electrode as an electrode and a calomel electrode as a reference electrode, taking the solution obtained in the step S1 as a deposition solution, and firstly preparing by using a cyclic voltammetry method and a potentiostatic method, wherein the conditions are as follows: the sweeping speed is 5mV/s, the voltage window is 0.5-0.8V, and the number of turns is 50; then the preparation is carried out by a potentiostatic method, and the conditions are as follows: the voltage is 1V, the deposition time is 1200s, and nucleotide is inserted between manganese dioxide layers on carbon cloth through inorganic-organic interface reaction;

and S3, drying in an oven at 100 ℃ to form the manganese dioxide with the nucleotide intercalation.

Preparation of an aqueous zinc ion battery:

s1, cutting a zinc sheet into a round shape by using a slicing machine to be used as a negative electrode of the water-based zinc ion battery;

s2, cutting the diaphragm into a round shape by using a slicer;

s3, preparing a certain mixed solution of 2M zinc sulfate and 0.2M manganese sulfate as an electrolyte of the water-based zinc ion battery;

s4, taking the manganese dioxide of the nucleotide intercalation as the anode of the water-based zinc ion battery;

s5, sequentially placing the positive plate, the electrolyte, the diaphragm, the electrolyte, the negative plate, the gasket (1 mm) and the elastic sheet into a bottom shell of the positive battery;

s6, covering the negative battery shell, and sealing the battery by using a battery sealing machine to pressurize the battery to 2 Mpa.