A manganese-based polyanion positive electrode material and its preparation method and application

Abstract

The present invention discloses a manganese-based polyanion positive electrode material and its preparation method and application, belonging to the technical field of sodium ion battery positive electrode materials. The present invention discloses a positive electrode material, the chemical formula of which is Na x Li y MnV 0.5 Ti 0.5 (PO4)3, where 3≤x≤3.5, 0≤y≤0.5, and x+y=3.5. Due to the introduction of lithium ions, the electron orbital overlap between the alkaline metal ions and the oxygen atoms is weakened, thereby making the oxygen atoms and the surrounding Mn 2+ This enhanced Mn-O bond suppresses the Mn-O bond generated by Mn during charge and discharge. 3+ (Mn 2+ Jahn-Teller distortion caused by oxidation at high potential); this manganese-based polyanion positive electrode material can significantly improve the cycle stability and rate performance of the material while ensuring the sodium storage capacity, and its sodium storage electrochemical performance is significantly better than that of pure phase materials without lithium doping.

Description

Technical Field

[0001] The present invention belongs to the technical field of sodium ion battery positive electrode materials, and specifically relates to a manganese-based polyanion positive electrode material and a preparation method and application thereof. Background Art

[0002] With the transformation of the global energy structure and the demand for sustainable development, the development of efficient, low-cost, and environmentally friendly energy storage technologies has become particularly important. Among various energy storage technologies, lithium-ion batteries have become a research hotspot in recent years due to their advantages such as high energy density, long cycle life, and rapid charge and discharge. However, due to the high cost of lithium-ion batteries and the scarcity and difficulty of domestic lithium metal resources, the research and development of a new generation of secondary batteries with higher performance, longer life, economy, and safety is imminent. Compared with lithium metal, sodium metal resources are abundant and inexpensive. At the same time, thanks to the similar chemical properties of sodium and lithium, sodium-ion batteries have become a new choice among secondary batteries.

[0003] Cathode materials play a key role in sodium-ion batteries, not only because of their high specific gravity but also, more importantly, because they determine the battery's operating voltage range. Ideal cathode materials should possess high operating voltage, large specific capacity, good electronic and ionic conductivity, structural stability, low cost, and low toxicity. Currently, the mainstream cathode materials in sodium-ion batteries include layered oxides, polyanionic compounds, Prussian blue-based materials, and other materials. Polyanionic compounds have become a research hotspot in recent years due to their excellent cycling and rate performance, stable operating voltage platform, good ionic conductivity, and very high thermal stability. Manganese, due to its multivalent nature, abundant resources, low cost, and non-toxicity, is considered one of the best cathode materials for sodium-ion batteries. The development of a new generation of manganese-based polyanionic cathode materials with high capacity, green, low toxicity, safety, and cost-effectiveness has become a research priority.

[0004] However, manganese-based polyanionic cathode materials face numerous challenges in their applications, including short cycle life due to Jahn-Teller distortion and manganese dissolution, as well as poor rate performance and energy density due to antisite defects and the low intrinsic conductivity of polyanionic cathode materials. Finding appropriate solutions to reduce the rate of defect formation and improve these issues, such as poor energy density, short cycle life, and poor rate performance, is an urgent need in this field. Summary of the Invention

[0005] The purpose of the present invention is to provide a manganese-based polyanion positive electrode material and its preparation method and application, so as to solve the technical problems of Jahn-Teller distortion and manganese element dissolution in existing manganese-based polyanion positive electrode materials, which lead to poor cycle stability of batteries.

[0006] In order to achieve the above object, the present invention adopts the following technical solutions:

[0007] The present invention discloses a manganese-based polyanion positive electrode material, the chemical formula of the manganese-based polyanion positive electrode material is Na x Li y MnV 0.5 Ti 0.5 (PO4)3;

[0008] Among them: 3≤x≤3.5, 0≤y≤0.5, x+y=3.5.

[0009] The present invention also discloses a method for preparing the above-mentioned manganese-based polyanion positive electrode material, comprising the following steps:

[0010] According to the chemical formula Na x Li y MnV 0.5 Ti 0.5 The sodium salt, lithium salt, manganese salt, vanadium salt, titanium salt and phosphate are weighed in a stoichiometric ratio in (PO4)3, and then dissolved in a solvent together with a coupling agent as a raw material, and stirred and heated to obtain a mixed solution;

[0011] The mixed solution is dried and ground in sequence to obtain a precursor powder;

[0012] The precursor powder is sintered to obtain a manganese-based polyanion positive electrode material;

[0013] The transition metal salts are manganese salts, vanadium salts and titanium salts.

[0014] Furthermore, the sodium salt is one or more of sodium acetate trihydrate, sodium nitrate and sodium carbonate; the lithium salt is one or more of lithium acetate, lithium nitrate and lithium oxalate; the manganese salt is one or more of manganese nitrate tetrahydrate, manganese acetate and manganese acetate tetrahydrate;

[0015] The molar ratio of the coupling agent to the metal ions in the transition metal salt is 1:1.

[0016] Furthermore, the vanadium salt is one or more of ammonium metavanadate, vanadium acetylacetonate and vanadium pentoxide; the titanium salt is one or more of tetrabutyl titanate, isopropyl titanate and titanium tetrachloride; the phosphate is one or more of ammonium dihydrogen phosphate, phosphoric acid and diammonium hydrogen phosphate;

[0017] The coupling agent is one or more of citric acid monohydrate, ascorbic acid and oxalic acid.

[0018] Furthermore, the titanium salt and vanadium acetylacetonate are water-insoluble salts; when they are water-insoluble salts, anhydrous ethanol is used as the solvent.

[0019] Furthermore, the remaining vanadium salts and sodium salts, lithium salts, manganese salts, phosphates and coupling agents are all water-soluble salts;

[0020] When the salt is water-soluble, deionized water is used as the solvent.

[0021] Furthermore, the ratio of the raw material to the solvent is 1 g: (14.87-19.06) mL.

[0022] Furthermore, the temperature of the heating and mixing is 80-90°C; and the temperature of the drying is 100-120°C.

[0023] Furthermore, the process parameters of the sintering treatment are: pre-sintering at a temperature of 350-450° C. for 1-6 hours, and then sintering at a temperature of 600-700° C. for 6-20 hours.

[0024] The present invention also discloses the application of the manganese-based polyanion positive electrode material in the active material of sodium ion battery electrodes.

[0025] Compared with the prior art, the present invention has the following beneficial effects:

[0026] The present invention discloses a manganese-based polyanion positive electrode material, the chemical formula of which is Na x Li y MnV 0.5 Ti 0.5 (PO4)3, where 3≤x≤3.5, 0≤y≤0.5, and x+y=3.5. Due to the introduction of lithium ions, the electron orbital overlap between the alkaline metal ions and the oxygen atoms is weakened, thereby making the oxygen atoms and the surrounding Mn 2+ This enhanced Mn-O bond suppresses the Mn-O bond generated by the Mn during charge and discharge. 3+ (Mn 2+ Jahn-Teller distortion caused by oxidation at high potential); through this manganese-based polyanion positive electrode material, the cycle stability and rate performance of the material can be significantly improved while ensuring the sodium storage capacity, and its sodium storage electrochemical performance is significantly better than that of pure phase materials without lithium doping.

[0027] Furthermore, by replacing the material with lithium ions in different proportions at the sodium position, the defect formation rate of the manganese-based polyanion material was effectively reduced, and the distortion and dissolution of the material were suppressed to a certain extent. At the same time, through traditional carbon coating technology, the problem of poor intrinsic conductivity of the material was improved, and the sodium ion migration ability, energy density and cycle stability of the positive electrode material were significantly improved.

[0028] Furthermore, according to relevant experimental results, the Na3Li prepared by the present invention is0.5 MnV 0.5 Ti 0.5 (PO4)3 shows significant advantages in operating voltage and energy density, and can operate stably at a high voltage of 4.3V, corresponding to an energy density of 513.8Wh / kg.

[0029] The present invention also discloses a method for preparing the above-mentioned manganese-based polyanionic positive electrode material, which is synthesized through a traditional sol-gel method and sintering treatment, using common sodium salts, lithium salts, manganese salts, vanadium salts, titanium salts, phosphates and coupling agents as raw materials. No harmful waste liquid is generated during the synthesis process, and it has the advantage of low production cost; the sintering treatment temperature used in the preparation process usually does not exceed 700°C, the process is simple and easy, and is suitable for large-scale production.

[0030] Furthermore, the present invention also proposes an effective improvement method for the problems of anti-site defects, poor sodium storage performance and short cycle life of manganese-based polyanion positive electrode materials; that is, lithium ion substitution at the sodium site can effectively reduce the defect formation rate, optimize the sodium ion migration path, and improve the Mn 3+ distortion and dissolution phenomena, thereby greatly improving the cycle performance and rate performance of the material.

[0031] The present invention also discloses the application of the above-mentioned manganese-based polyanion positive electrode material in the active material of sodium ion battery electrodes. Due to the introduction of lithium ions, the material structure degradation and antisite defect phenomenon caused by manganese are improved, and the cycle stability and rate performance of the material are improved. In addition, the lithium-doped manganese-based polyanion positive electrode material uses green, economical and environmentally friendly manganese as the main transition metal. Therefore, the lithium-doped manganese-based polyanion positive electrode material with excellent electrochemical performance prepared by this patent has obvious advantages when used as an active material for sodium ion battery electrodes. BRIEF DESCRIPTION OF THE DRAWINGS

[0032] Figure 1 XRD patterns of the positive electrode materials prepared in Example 1, Example 3, Example 5 and Comparative Example 1;

[0033] Figure 2 This is the SEM image of the positive electrode material prepared in Example 5;

[0034] Figure 3 The manganese-based polyanion positive electrode material prepared in Example 1 was -1 The charge and discharge curves of the first three cycles under the current density;

[0035] Figure 4 The manganese-based polyanion positive electrode material prepared in Example 1 was -1 Cycling stability diagram for the first 60 cycles at the current density;

[0036] Figure 5 The manganese-based polyanion positive electrode material prepared in Example 3 was -1 The charge and discharge curves of the first three cycles under the current density;

[0037] Figure 6 The manganese-based polyanion positive electrode material prepared in Example 3 was -1 Cycling stability diagram for the first 60 cycles at the current density;

[0038] Figure 7 The manganese-based polyanion positive electrode material prepared in Example 5 was -1 The charge and discharge curves of the first three cycles under the current density;

[0039] Figure 8 A comparison chart of the capacity cycle retention rate of the manganese-based polyanion positive electrode material prepared in Example 5;

[0040] Figure 9 This is a comparison chart of the rate performance of the manganese-based polyanion positive electrode material prepared in Example 5 and the positive electrode material of Comparative Example 1. DETAILED DESCRIPTION

[0041] To facilitate understanding of the features and effects of the present invention by those skilled in the art, the following provides a general description and definition of the terms and expressions used in the specification and claims. Unless otherwise indicated, all technical and scientific terms used herein have the ordinary meanings as understood by those skilled in the art regarding the present invention. In the event of conflict, the definitions in this specification shall prevail.

[0042] The theories or mechanisms described and disclosed herein, whether correct or incorrect, should not limit the scope of the present invention in any way, that is, the present invention can be implemented without being limited by any specific theory or mechanism.

[0043] All features, such as values, amounts, contents, and concentrations, described herein as numerical ranges or percentage ranges are provided for simplicity and convenience only. Accordingly, the description of numerical ranges or percentage ranges should be considered to include and specifically disclose all possible subranges and individual values ​​within the range (including integers and fractions).

[0044] In this document, unless otherwise specified, “include,” “including,” “contains,” “has” or similar terms cover the meanings of “consisting of” and “mainly consisting of,” for example, “A includes a” covers the meanings of “A includes a and other” and “A only includes a.”

[0045] In this document, for the sake of brevity, not all possible combinations of the various technical features in each embodiment or example are described. Therefore, as long as there are no contradictions in the combination of these technical features, the various technical features in each embodiment or example can be combined in any way, and all possible combinations should be considered to be within the scope of this specification.

[0046] Below in conjunction with specific embodiment, further set forth the present invention.Should be understood that these embodiments are only used to illustrate the present invention and are not used in limiting the scope of the present invention.In addition, should be understood that after reading the content taught by the present invention, those skilled in the art can make various changes or modifications to the present invention, and these equivalent forms fall equally within the scope limited by the appended claims of the application.

[0047] The following examples were prepared using conventional instruments and equipment in the art. Experimental methods in the following examples, where specific conditions are not specified, were generally performed under conventional conditions or according to the conditions recommended by the manufacturer. The various raw materials used in the following examples, unless otherwise specified, were conventional commercially available products, with specifications conventional in the art. In the present specification and the following examples, unless otherwise specified, "%" indicates percentage by weight, "part" indicates parts by weight, and "ratio" indicates weight ratio.

[0048] Example 1

[0049] A manganese-based polyanion cathode material (Na 3.4 Li 0.1 MnV 0.5 Ti 0.5 The preparation method of (PO4)3) comprises the following steps:

[0050] According to the chemical formula Na 3.4 Li 0.1 MnV 0.5 Ti 0.5 The stoichiometric ratio in (PO4)3 was 0.568 g of isopropyl titanate was dissolved in 30 mL of anhydrous ethanol and stirred for 30 min to obtain a solution containing isopropyl titanate; 1.44 g of sodium carbonate, 0.041 g of lithium oxalate, 1 g of manganese nitrate tetrahydrate, 0.364 g of vanadium pentoxide, 1.41 g of ascorbic acid and 1.18 g of phosphoric acid were dissolved in 70 mL of deionized water and stirred for 30 min to obtain a solution containing sodium carbonate, lithium oxalate, manganese nitrate tetrahydrate, vanadium pentoxide, phosphoric acid and ascorbic acid;

[0051] Under high-speed stirring (600 rpm), a solution containing isopropyl titanate was added dropwise to a solution containing sodium carbonate, lithium oxalate, manganese nitrate tetrahydrate, vanadium pentoxide, phosphoric acid, and ascorbic acid to form a mixed solution. The mixed solution was stirred and heated at 80°C to obtain a mixed gel.

[0052] The mixed gel was transferred to a constant temperature forced air oven at 100°C for drying, and then ground to obtain a precursor powder;

[0053] The precursor powder was transferred to a tube furnace and pre-calcined at 350°C for 3 hours and calcined at 650°C for 12 hours under the protection of an argon atmosphere. The obtained product was ground again to obtain a manganese-based polyanion positive electrode material.

[0054] Example 2

[0055] A manganese-based polyanion cathode material (Na 3.3 Li 0.2 MnV 0.5 Ti 0.5 The preparation method of (PO4)3) comprises the following steps:

[0056] According to the chemical formula Na 3.3 Li 0.2 MnV 0.5 Ti 0.5 (PO4)3, 0.681g of tetrabutyl titanate was dissolved in 30mL of anhydrous ethanol and stirred for 30min to obtain a solution containing tetrabutyl titanate; 1.8g of sodium acetate trihydrate, 0.056g of lithium nitrate, 0.692g of manganese acetate, 0.234g of ammonium metavanadate, 1.68g of citric acid monohydrate and 1.38g of ammonium dihydrogen phosphate were dissolved in 70mL of deionized water and stirred for 30min to obtain a solution containing sodium acetate trihydrate, lithium nitrate, manganese acetate, ammonium metavanadate, ammonium dihydrogen phosphate and citric acid monohydrate;

[0057] Under high-speed stirring (600 rpm), a solution containing tetrabutyl titanate was dropwise added to a solution containing sodium acetate trihydrate, lithium nitrate, manganese acetate, ammonium metavanadate, ammonium dihydrogen phosphate, and citric acid monohydrate to form a mixed solution. The mixed solution was stirred and heated at 80° C. to obtain a mixed gel.

[0058] The mixed gel was transferred to a constant temperature forced air oven at 100°C for drying, and then ground to obtain a precursor powder;

[0059] The precursor powder was transferred to a tube furnace and pre-calcined at 350°C for 3 hours and calcined at 650°C for 12 hours under the protection of an argon atmosphere. The obtained product was ground again to obtain a manganese-based polyanion positive electrode material.

[0060] Example 3

[0061] A manganese-based polyanion cathode material (Na 3.2 Li 0.3 MnV 0.5 Ti 0.5The preparation method of (PO4)3) comprises the following steps:

[0062] According to the chemical formula Na 3.2 Li 0.3 MnV 0.5 Ti 0.5 The stoichiometric ratio in (PO4)3 was 0.697 g of vanadium acetylacetonate was dissolved in 30 mL of anhydrous ethanol and stirred for 30 min to obtain a solution containing vanadium acetylacetonate; 1.09 g of sodium nitrate, 0.079 g of lithium acetate, 0.692 g of manganese acetate, 0.379 g of titanium tetrachloride, 0.72 g of oxalic acid and 1.59 g of diammonium hydrogen phosphate were dissolved in 70 mL of deionized water and stirred for 30 min to obtain a solution containing sodium nitrate, lithium acetate, manganese acetate, titanium tetrachloride, diammonium hydrogen phosphate and oxalic acid;

[0063] Under high-speed stirring (600 rpm), a solution containing vanadium acetylacetonate was added dropwise to a solution containing sodium nitrate, lithium acetate, manganese acetate, titanium tetrachloride, diammonium hydrogen phosphate, and polyvinyl pyrrolidone to form a mixed solution. The mixed solution was stirred and heated at 80° C. to obtain a mixed gel.

[0064] The mixed gel was transferred to a constant temperature forced air oven at 100°C for drying, and then ground to obtain a precursor powder;

[0065] The precursor powder was transferred to a tube furnace and pre-calcined at 350°C for 3 hours and calcined at 650°C for 12 hours under the protection of an argon atmosphere. The obtained product was ground again to obtain a manganese-based polyanion positive electrode material.

[0066] Example 4

[0067] A manganese-based polyanion cathode material (Na 3.1 Li 0.4 MnV 0.5 Ti 0.5 The preparation method of (PO4)3) comprises the following steps:

[0068] According to the chemical formula Na 3.1 Li 0.4 MnV 0.5 Ti 0.5(PO4)3 in the stoichiometric ratio, weigh 0.681g of tetrabutyl titanate and dissolve it in 30mL of anhydrous ethanol, stir for 30min to obtain a solution containing tetrabutyl titanate; weigh 1.687g of sodium acetate trihydrate, 0.106g of lithium acetate, 0.98g of manganese acetate tetrahydrate, 0.234g of ammonium metavanadate, 1.41g of ascorbic acid and 1.38g of ammonium dihydrogen phosphate and dissolve them in 70mL of deionized water, stir for 30min to obtain a solution containing sodium acetate trihydrate, lithium acetate, manganese nitrate tetrahydrate, ammonium metavanadate, citric acid monohydrate and ammonium dihydrogen phosphate;

[0069] Under high-speed stirring (600 rpm), a solution containing tetrabutyl titanate was added dropwise to a solution containing sodium acetate trihydrate, lithium acetate, manganese nitrate tetrahydrate, ammonium metavanadate, citric acid monohydrate, and ammonium dihydrogen phosphate to form a mixed solution. The mixed solution was stirred and heated at 80°C to obtain a mixed gel.

[0070] The mixed gel was transferred to a constant temperature forced air oven at 100°C for drying, and then ground to obtain a precursor powder;

[0071] The precursor powder was transferred to a tube furnace and pre-calcined at 350°C for 3 hours and calcined at 650°C for 12 hours under the protection of an argon atmosphere. The obtained product was ground again to obtain a manganese-based polyanion positive electrode material.

[0072] Example 5

[0073] A manganese-based polyanion cathode material (Na3Li 0.5 MnV 0.5 Ti 0.5 The preparation method of (PO4)3) comprises the following steps:

[0074] According to the chemical formula Na3Li 0.5 MnV 0.5 Ti 0.5 (PO4)3 in the stoichiometric ratio, weigh 0.681g of tetrabutyl titanate and dissolve it in 30mL of anhydrous ethanol, stir for 30min to obtain a solution containing tetrabutyl titanate; weigh 1.633g of sodium acetate trihydrate, 0.138g of lithium nitrate, 0.98g of manganese acetate tetrahydrate, 0.234g of ammonium metavanadate, 1.68g of citric acid monohydrate and 1.38g of ammonium dihydrogen phosphate and dissolve them in 70mL of deionized water, stir for 30min to obtain a solution containing sodium acetate trihydrate, lithium nitrate, manganese nitrate tetrahydrate, ammonium metavanadate, citric acid monohydrate and ammonium dihydrogen phosphate;

[0075] Under high-speed stirring (600 rpm), a solution containing tetrabutyl titanate was added dropwise to a solution containing sodium acetate trihydrate, lithium nitrate, manganese nitrate tetrahydrate, ammonium metavanadate, citric acid monohydrate, and ammonium dihydrogen phosphate to form a mixed solution. The mixed solution was stirred and heated at 80°C to obtain a mixed gel.

[0076] The mixed gel was transferred to a constant temperature forced air oven at 100°C for drying, and then ground to obtain a precursor powder;

[0077] The precursor powder was transferred to a tube furnace and pre-calcined at 350°C for 3 hours and calcined at 650°C for 12 hours under the protection of an argon atmosphere. The obtained product was ground again to obtain a manganese-based polyanion positive electrode material.

[0078] Comparative Example 1

[0079] The difference from Example 3 is that the amount of salt added is different and no lithium salt is added. The other steps and parameters are the same as those in Example 3 to obtain a pure phase manganese-based polyanion sodium ion battery positive electrode material (Na 3.5 MnV 0.5 Ti 0.5 (PO4)3), the steps are as follows:

[0080] Weigh 0.681 g of tetrabutyl titanate and dissolve it in 30 mL of anhydrous ethanol, stirring for 30 min. Weigh 1.905 g of sodium acetate trihydrate, 0.98 g of manganese acetate tetrahydrate, 0.234 g of ammonium metavanadate, 1.68 g of citric acid monohydrate, and 1.38 g of ammonium dihydrogen phosphate and dissolve them in 70 mL of deionized water, stirring for 30 min.

[0081] Under high-speed stirring (600 rpm), a solution containing tetrabutyl titanate was added dropwise to a solution containing sodium acetate trihydrate, manganese nitrate tetrahydrate, ammonium metavanadate, citric acid monohydrate, and ammonium dihydrogen phosphate to form a mixed solution, and the mixed solution was heated and stirred at 80°C until a gel was formed;

[0082] The gel was transferred into a constant temperature forced air oven at 100° C. for drying, and then the thoroughly dried sample was ground to obtain the precursor powder;

[0083] The precursor powder was transferred to a tube furnace and pre-calcined at 350°C for 3 hours and calcined at 650°C for 12 hours under the protection of an argon atmosphere. The product was ground again to obtain a pure phase manganese-based polyanion positive electrode material.

[0084] Application Example 1

[0085] A method for preparing a button battery using the lithium-doped manganese-based polyanion material obtained in Example 1 as a positive electrode material comprises the following steps:

[0086] The manganese-based polyanion positive electrode material (Na 3.4 Li 0.1 MnV 0.5 Ti 0.5 (PO4)3), conductive carbon black and binder polyvinylidene fluoride, weighed 0.7g, 0.2g, and 0.1g respectively according to the mass ratio of 7:2:1, mixed, and evenly dispersed in N-methylpyrrolidone solvent, and then the obtained mixed slurry was evenly coated on aluminum foil and dried at 80°C for 6h to obtain a positive electrode sheet;

[0087] Sodium metal and glass fiber (Whatman, GF / D) were used as the counter electrode and separator, respectively. The negative electrode shell, spring, gasket, counter electrode, separator, positive electrode sheet, and positive electrode shell were placed in a CR2032 button battery in this order. An electrolyte with a concentration of 1 mol / L containing sodium hexafluorophosphate as the solute, propylene carbonate as the solvent, and 5% fluoroethylene carbonate as the additive was added. After packaging, a sodium ion button battery was obtained.

[0088] Application Example 2

[0089] The preparation method of a button battery using the lithium-doped manganese-based polyanion material obtained in Example 2 as the positive electrode material comprises the following steps:

[0090] The manganese-based polyanion positive electrode material (Na 3.2 Li 0.3 MnV 0.5 Ti 0.5 (PO4)3), conductive carbon black and binder polyvinylidene fluoride, weighed 0.7g, 0.2g, and 0.1g respectively according to the mass ratio of 7:2:1, mixed, and evenly dispersed in N-methylpyrrolidone solvent, and then the obtained mixed slurry was evenly coated on aluminum foil and dried at 80°C for 6h to obtain a positive electrode sheet;

[0091] Sodium metal and glass fiber (Whatman, GF / D) were used as the counter electrode and separator, respectively. The negative electrode shell, spring, gasket, counter electrode, separator, positive electrode sheet, and positive electrode shell were placed in a CR2032 button battery in this order. An electrolyte with a concentration of 1 mol / L containing sodium hexafluorophosphate as the solute, propylene carbonate as the solvent, and 5% fluoroethylene carbonate as the additive was added. After packaging, a sodium ion button battery was obtained.

[0092] Application Example 3

[0093] The preparation method of a button battery using the lithium-doped manganese-based polyanion material obtained in Example 3 as the positive electrode material comprises the following steps:

[0094] The manganese-based polyanion positive electrode material (Na3Li 0.5 MnV 0.5 Ti 0.5 (PO4)3), conductive carbon black and binder polyvinylidene fluoride, weighed 0.7g, 0.2g, and 0.1g respectively according to the mass ratio of 7:2:1, mixed, and evenly dispersed in N-methylpyrrolidone solvent, and then the obtained mixed slurry was evenly coated on aluminum foil and dried at 80°C for 6h to obtain a positive electrode sheet;

[0095] Sodium metal and glass fiber (Whatman, GF / D) were used as the counter electrode and separator, respectively. The negative electrode shell, shrapnel, gasket, counter electrode, separator, positive electrode sheet, and positive electrode shell were placed in a CR2032 button battery in this order. An electrolyte with a concentration of 1 mol / L containing sodium hexafluorophosphate as the solute, propylene carbonate as the solvent, and 5% fluoroethylene carbonate as the additive was added. After packaging, a sodium ion button battery was obtained.

[0096] Application Example 4

[0097] The obtained pure-phase manganese-based polyanion positive electrode material was used in the same manner as in Application Example 3 to prepare a sodium ion button battery using the pure-phase manganese-based polyanion positive electrode material as the positive electrode material.

[0098] Figure 1 The XRD patterns of the positive electrode materials prepared in Example 1, Example 3, Example 5 and Comparative Example 1 show that all four materials have obvious diffraction peaks and no impurity peaks appear, indicating that the four materials have high crystallinity and phase purity.

[0099] Figure 2 This is the SEM image of Example 5. It can be seen from the figure that the material is a nanoscale block particle with good crystallinity. At the same time, amorphous carbon is tightly wrapped on the surface of the particle and has good conductivity.

[0100] Figure 3 The manganese-based polyanion positive electrode material prepared in Example 1 was -1 The charge-discharge curves of the first three cycles under the current density show that the sodium-ion battery works stably in the voltage window of 1.5~4.3V, and the first cycle discharge capacity is about 113.75mAh g -1 , the charge and discharge curves of the first three cycles almost coincide, indicating its good charge and discharge reversibility.

[0101] Figure 4 The manganese-based polyanion positive electrode material prepared in Example 1 was -1The cycling stability diagram for the first 60 cycles under current density shows that the material described in Example 1 has good cycling stability at 100 mA g -1 The capacity retention rate was 83.6% after 60 cycles at a current density of 1.5 GHz.

[0102] Figure 5 The manganese-based polyanion positive electrode material prepared in Example 3 was -1 The charge-discharge curves of the first three cycles under the current density show that the sodium-ion battery works stably in the voltage window of 1.5~4.3V, and the first cycle discharge capacity is about 110.12mAh g -1 , the charge and discharge curves of the first three cycles almost coincide, indicating its good charge and discharge reversibility.

[0103] Figure 6 The manganese-based polyanion positive electrode material prepared in Example 3 was -1 The cyclic stability diagram of the first 60 cycles under current density shows that the material described in Example 2 has a high stability at 100 mA g -1 The capacity retention rate was 67.7% after 60 cycles at a current density of .

[0104] Figure 7 The manganese-based polyanion positive electrode material prepared in Example 5 was -1 The charge-discharge curves of the first three cycles under the current density show that the sodium ion battery works stably in the voltage window of 1.5~4.3V, and the first cycle discharge capacity is about 98.8mAh g -1 , the charge and discharge curves of the first three cycles almost coincide, indicating its good charge and discharge reversibility.

[0105] Figure 8 The capacity cycle retention rate comparison chart of the manganese-based polyanion positive electrode material prepared in Example 5 shows that at 100 mA g -1 The capacity retention curve after 130 cycles at a current density of , from which we can see that the Na prepared in Example 5 3.5 MnV 0.5 Ti 0.5 (PO4)3 material has good cycle stability at 100mA g -1 The capacity retention rate was 82.8% after 130 cycles at a current density of 1.5, while the Na prepared in Comparative Example 1 had a 3.5 MnV 0.5 Ti 0.5 Under the same test conditions, the capacity retention rate of (PO4)3 material is only 49.5%.

[0106] Figure 9The figure shows the rate performance comparison of the manganese-based polyanion positive electrode material prepared in Example 5 and the positive electrode material of Comparative Example 1. It can be seen from the figure that the rate performance of the material is greatly improved by replacing the sodium position with lithium ions. At a current density of 20C, the Na prepared in Example 5 3.5 MnV 0.5 Ti 0.5 The discharge capacity of (PO4)3 material is about 52.83 mAhg -1 , while the Na prepared in Comparative Example 1 3.5 MnV 0.5 Ti 0.5 The discharge capacity of (PO4)3 material is only 7.28 mAh g -1 .

[0107] The above content is only for explaining the technical idea of ​​the present invention and cannot be used to limit the protection scope of the present invention. Any changes made on the basis of the technical solution in accordance with the technical idea proposed by the present invention shall fall within the protection scope of the claims of the present invention.

Claims

1. A manganese-based polyanion positive electrode material, characterized in that: The chemical formula of the manganese-based polyanion positive electrode material is Na x Li y MnV 0.5 Ti 0.5 (PO4)3; Among them: 3≤x≤3.5, 0≤y≤0.5, x+y=3.

5.

2. The method for preparing a manganese-based polyanion positive electrode material according to claim 1, characterized in that: The following steps are involved: According to the chemical formula Na x Li y MnV 0.5 Ti 0.5 The sodium salt, lithium salt, manganese salt, vanadium salt, titanium salt and phosphate are weighed in a stoichiometric ratio in (PO4)3, and then dissolved in a solvent together with a coupling agent as a raw material, and stirred and heated to obtain a mixed solution; The mixed solution is dried and ground in sequence to obtain a precursor powder; The precursor powder is sintered to obtain a manganese-based polyanion positive electrode material; The transition metal salts are manganese salts, vanadium salts and titanium salts.

3. The method for preparing a manganese-based polyanion positive electrode material according to claim 2, characterized in that: The sodium salt is one or more of sodium acetate trihydrate, sodium nitrate and sodium carbonate; the lithium salt is one or more of lithium acetate, lithium nitrate and lithium oxalate; the manganese salt is one or more of manganese nitrate tetrahydrate, manganese acetate and manganese acetate tetrahydrate; The molar ratio of the coupling agent to the metal ions in the transition metal salt is 1:

1.

4. The method for preparing a manganese-based polyanion positive electrode material according to claim 3, characterized in that: The vanadium salt is one or more of ammonium metavanadate, vanadium acetylacetonate and vanadium pentoxide; the titanium salt is one or more of tetrabutyl titanate, isopropyl titanate and titanium tetrachloride; the phosphate is one or more of ammonium dihydrogen phosphate, phosphoric acid and diammonium hydrogen phosphate; The coupling agent is one or more of citric acid monohydrate, ascorbic acid and oxalic acid.

5. The method for preparing a manganese-based polyanion positive electrode material according to claim 4, characterized in that: The titanium salt and vanadium acetylacetonate are water-insoluble salts; when they are water-insoluble salts, anhydrous ethanol is used as the solvent.

6. The method for preparing a manganese-based polyanion positive electrode material according to claim 5, characterized in that: The remaining vanadium salts and sodium salts, lithium salts, manganese salts, phosphates and coupling agents are all water-soluble salts; When the salt is water-soluble, deionized water is used as the solvent.

7. The method for preparing a manganese-based polyanion positive electrode material according to claim 2, characterized in that: The usage ratio of the raw material to the solvent is 1 g: (14.87-19.06) mL.

8. The method for preparing a manganese-based polyanionic cathode material according to claim 2, characterized in that: The temperature of the heating and mixing is 80-90°C; the temperature of the drying is 100-120°C.

9. The method for preparing a manganese-based polyanion positive electrode material according to claim 2, characterized in that: The process parameters of the sintering treatment are: pre-sintering at a temperature of 350-450° C. for 1-6 hours, and then sintering at a temperature of 600-700° C. for 6-20 hours.

10. Use of the manganese-based polyanion cathode material according to claim 1 in active materials for sodium ion battery electrodes.

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