Preparation method and application of gradient polymerization solid-state battery electrode

Abstract

A preparation method and application of gradient polymerization solid-state battery electrodes, belonging to the field of chemical power supply technology. Specifically comprising the following steps: NASICON type inorganic solid electrolyte Na3Zr2Si2PO 12 The electrode is prepared in a gradient distribution in the electrode material, and an electrolyte precursor solution containing a cyclic ether monomer and an initiator is injected into the electrode. The NASICON type inorganic solid electrolyte Na3Zr2Si2PO4 is distributed in a gradient 12 Inhibit the action of the initiator and the cyclic ether monomer, realize the gradient polymerization of the cyclic ether polymer electrolyte in the electrode, and obtain the gradient polymerization solid-state battery electrode. The NASICON inorganic solid electrolyte Na3Zr2Si2PO 12 The amount of addition decreases gradually from the direction close to the current collector to the direction away from the current collector. The present invention provides an innovative electrode solution for the realization of high-power, high-cycle stability solid-state batteries.

Description

Technical Field

[0001] The present invention belongs to the technical field of chemical power sources, and in particular relates to a preparation method and application of a gradient-polymerized solid-state battery electrode. Background Art

[0002] Solid-state batteries, especially those prepared based on the in-situ polymerization method of electrolytes, can significantly improve battery safety and are an important direction for the development of next-generation secondary batteries. Generally, during the charge and discharge process, especially under high-rate conditions, the electrochemical reaction kinetics of the positive and negative electrodes of alkali metal ion secondary batteries based on liquid electrolytes have large gradient changes in the longitudinal direction. That is, the reaction kinetics of the active material layer close to the current collector are poor, while the reaction kinetics of the active material layer far from the current collector are high. This characteristic will significantly affect the active material utilization rate, rate performance and cycle stability of the secondary battery. Polymer electrolytes prepared based on the in-situ polymerization method often have the characteristics of high polymerization degree and relatively low ionic conductivity. The uniformity of the electrochemical reaction kinetics of the solid-state battery electrode in the longitudinal direction will be further reduced. In view of the electrode reaction kinetics characteristics of solid-state batteries, constructing a polymer electrolyte system with a gradient change in polymerization degree inside the electrode is of great significance to improving the active material utilization rate, interface stability, rate performance and cycle stability of solid-state batteries. Summary of the Invention

[0003] In order to solve the technical problems of poor electrode electrochemical reaction kinetics, low active material utilization, poor rate performance and cycle stability of in-situ polymerization solid-state batteries under high rate conditions (≥1C), the present invention provides a preparation method and application of solid-state battery electrodes with gradient polymerization characteristics, using NASICON-type inorganic solid electrolyte Na3Zr2Si2PO4 12 The strong Lewis acid-base interaction between (NZSP) and the initiator inhibits the ring-opening polymerization of cyclic ether monomers and realizes the gradient control of the polymerization degree of the polymer electrolyte.

[0004] In order to achieve the above object, the present invention adopts the following technical solutions:

[0005] A method for preparing a gradient polymerized solid-state battery electrode comprises the following steps: adding different mass fractions of NASICON inorganic solid electrolyte Na3Zr2Si2PO4 into the electrode material. 12 Prepare several portions of slurry, and then coat several portions of slurry layer by layer on the current collector to make the NASICON type inorganic solid electrolyte Na3Zr2Si2PO 12The amount of addition decreases gradually from the current collector to the current collector, and then the electrode is dried, rolled, and cut to obtain the electrode. The electrolyte precursor solution containing cyclic ether monomers and initiators is injected into the electrode to form a gradient distribution of NASICON inorganic solid electrolyte Na3Zr2Si2PO 12 The interaction between the initiator and the cyclic ether monomer is suppressed, and the gradient polymerization of the cyclic ether-based polymer electrolyte in the electrode is realized, thereby obtaining a gradient-polymerized solid-state battery electrode.

[0006] Furthermore, the NASICON type inorganic solid electrolyte Na3Zr2Si2PO 12 The mass range of the gradient distribution in the electrode material from close to the current collector to far away from the current collector is 0.1wt%-2wt%.

[0007] Furthermore, the cyclic ether monomer includes one or more combinations of tetrahydrofuran, 1,3-dioxolane, 1,3,5-trioxane, 1,3-dioxane, epoxy-terminated linear siloxane, and epoxy-terminated cage-type polysilsesquioxane.

[0008] Furthermore, the initiator includes a combination of one or more of a sodium salt initiator, a lithium salt initiator, an aluminum salt initiator, a tin salt initiator, a zinc salt initiator, a magnesium salt initiator, and a scandium salt initiator.

[0009] Furthermore, the cyclic ether monomer accounts for 40%-80% of the volume of the electrolyte, and the selection of this numerical range is a conventional technical means in this field.

[0010] Furthermore, the concentration of the initiator in the electrolyte is 0.1-1 mol / L, and the selection of this numerical range is a conventional technical means in this field.

[0011] Furthermore, the electrode material includes an active material, a conductive agent and a binder that are uniformly mixed.

[0012] Furthermore, the electrolyte precursor solution also includes a solvent, an ionic salt and an additive, and the ionic salt is a lithium salt, a sodium salt or a potassium salt.

[0013] Furthermore, after the electrolyte precursor solution is injected into the electrode, it is left to stand at room temperature or under heating conditions, and the cyclic ether monomer undergoes ring-opening polymerization under the action of the initiator, forming a gradient-distributed NASICON-type inorganic solid electrolyte Na3Zr2Si2PO 12 The initiation effect of the initiator is suppressed to achieve the gradient polymerization of the cyclic ether-based polymer electrolyte in the electrode.

[0014] An application of a solid-state battery electrode prepared by the preparation method, wherein the solid-state battery electrode is applied to the positive electrode and / or negative electrode of a lithium-ion battery, the positive electrode and / or negative electrode of a sodium-ion battery, or the positive electrode and / or negative electrode of a potassium-ion battery.

[0015] Compared with the prior art, the present invention has the following beneficial effects:

[0016] The present invention arranges a gradient-distributed NASICON type inorganic solid electrolyte Na3Zr2Si2PO4 in the electrode material. 12 , inhibiting the ring-opening polymerization reaction of cyclic ether monomers initiated by the initiator in the electrolyte precursor solution, thereby realizing the gradient polymerization of the cyclic ether-based polymer electrolyte in the electrode. Compared with solid-state batteries prepared based on traditional in-situ polymerization methods, the cyclic ether-based polymer electrolyte in the new solid-state battery electrode shows a change in the degree of polymerization gradient in the longitudinal direction. From the surface of the current collector to the direction away from the current collector, the degree of polymerization of the cyclic ether-based polymer electrolyte increases in a gradient manner. The ionic conductivity of the cyclic ether-based polymer electrolyte inside the electrode gradually increases from the electrode surface to the current collector surface. This characteristic can reduce the concentration polarization generated by the solid-state battery electrode during high-rate charge and discharge, improve the ion transport kinetics inside the electrode, realize the full utilization of deep-layer active materials, and significantly improve the interface stability, rate characteristics and cycle stability of the solid-state battery. DETAILED DESCRIPTION

[0017] The technical solutions of the present invention will be clearly and completely described below in conjunction with the embodiments. Obviously, the described embodiments are only part of the embodiments of the invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without making creative work are within the scope of protection of the present invention.

[0018] Example 1:

[0019] A method for preparing a gradient polymerization solid-state sodium ion battery positive electrode comprises the following steps:

[0020] Step 1: 96 parts of the positive electrode active material sodium vanadium phosphate Na3V2(PO4)3, 2 parts of the conductive agent Super P, and 2 parts of the binder polyvinylidene fluoride PVDF are uniformly mixed to form a positive electrode material and divided into 4 parts. To the 4 parts of the positive electrode material, an inorganic solid electrolyte NZSP with a mass fraction of 0.1%, 0.3%, 0.6% and 1.0% of the positive electrode material is added, respectively, and wet mixing is performed to obtain 4 parts of liquid slurries with different contents of the inorganic solid electrolyte NZSP;

[0021] Step 2: Apply the four portions of liquid slurry prepared in step 1 layer by layer on the surface of the current collector, so that the amount of inorganic solid electrolyte NZSP decreases gradually from the direction close to the current collector to the direction away from the current collector, and then dry, roll-press, and cut to obtain a positive electrode sheet with a gradient distribution of NZSP;

[0022] Step 3: Sodium perchlorate NaClO4, film-forming additive fluoroethylene carbonate FEC (accounting for 1 wt% of the total mass of the electrolyte precursor solution), initiator sodium hexafluorophosphate NaPF6 (concentration of 0.5 mol / L), solvent ethylene glycol dimethyl ether DME and cyclic ether monomer 1,3-dioxolane DOL (the volume ratio of DME and DOL is 1:1) are mixed uniformly to prepare an electrolyte precursor solution with a sodium salt NaClO4 concentration of 1 mol / L;

[0023] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the positive electrode sheet with gradient distribution of NZSP prepared in step 2 under vacuum;

[0024] Step 5. After standing at room temperature for 12 hours, the cyclic ether monomer DOL undergoes ring-opening polymerization under the action of the initiator NaPF6. The gradient-distributed inorganic solid electrolyte NZSP inhibits the initiation effect of the initiator NaPF6, realizing the gradient polymerization of the DOL monomer in the electrode, and obtaining a solid-state sodium ion battery positive electrode with gradient polymerization characteristics.

[0025] Example 2:

[0026] A method for preparing a gradient polymerization solid-state sodium ion battery negative electrode comprises the following steps:

[0027] Step 1: 90 parts of hard carbon (a negative electrode active material), 5 parts of Super P (a conductive agent), and 5 parts of sodium carboxymethyl cellulose (CMC) (a binder) were uniformly mixed to form a negative electrode material and divided into 4 parts. To the 4 parts of negative electrode material, an inorganic solid electrolyte NZSP (0.5%, 1.0%, 1.5%, and 2.0% by mass of the negative electrode material) was added, respectively, and wet-mixed to obtain 4 liquid slurries with different contents of the inorganic solid electrolyte NZSP.

[0028] Step 2: Apply the four portions of liquid slurry prepared in step 1 layer by layer on the surface of the current collector, so that the amount of inorganic solid electrolyte NZSP decreases gradually from the direction close to the current collector to the direction away from the current collector, and then dry, roll-press, and cut to obtain a negative electrode sheet with a gradient distribution of NZSP;

[0029] Step 3: Sodium perchlorate NaClO4, film-forming additive fluoroethylene carbonate FEC (accounting for 1 wt% of the total mass of the electrolyte precursor solution), initiator sodium hexafluorophosphate NaPF6 (concentration of 0.5 mol / L), solvent ethylene glycol dimethyl ether DME and cyclic ether monomer 1,3-dioxolane DOL (the volume ratio of DME and DOL is 1:1) are mixed uniformly to prepare an electrolyte precursor solution with a sodium salt NaClO4 concentration of 1 mol / L;

[0030] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the negative electrode sheet with gradient distribution of NZSP prepared in step 2 under vacuum;

[0031] Step 5. Let it stand at room temperature for 12 hours. The cyclic ether monomer DOL undergoes ring-opening polymerization under the action of the initiator NaPF6. The gradient-distributed inorganic solid electrolyte NZSP inhibits the initiation effect of the initiator NaPF6, realizing the gradient polymerization of the DOL monomer in the electrode, and obtaining a solid-state sodium ion battery negative electrode with gradient polymerization characteristics.

[0032] Example 3:

[0033] A button half-cell was assembled with a positive electrode sheet, a separator, and sodium metal prepared in step 2 of Example 1 with a gradient distribution of NZSP, and the electrolyte precursor solution prepared in step 3 of Example 1 was added dropwise. The mixture was allowed to stand at room temperature for 12 hours. The cyclic ether monomer DOL underwent ring-opening polymerization under the action of the initiator NaPF6. The inorganic solid electrolyte NZSP with a gradient distribution in the positive electrode sheet inhibited the initiation effect of the initiator NaPF6, achieving gradient polymerization of the DOL monomer in the positive electrode, thereby obtaining a solid-state sodium ion positive electrode half-cell with gradient polymerization characteristics. The battery had a capacity retention rate of 98% after 2500 cycles at a voltage range of 2.5-3.8V and a 1C rate. The initial reversible capacity at a 1C rate reached 95% of the reversible capacity at a 0.1C rate.

[0034] Example 4:

[0035] A button half-cell was assembled with a negative electrode plate, a separator, and sodium metal prepared in step 2 of Example 2 with a gradient distribution of NZSP, and the electrolyte precursor solution prepared in step 3 of Example 2 was added dropwise. The mixture was allowed to stand at room temperature for 12 hours. The cyclic ether monomer DOL underwent ring-opening polymerization under the action of the initiator NaPF6. The inorganic solid electrolyte NZSP with a gradient distribution in the negative electrode plate inhibited the initiation effect of the initiator NaPF6, achieving gradient polymerization of the DOL monomer in the negative electrode, thereby obtaining a solid-state sodium ion negative electrode half-cell with gradient polymerization characteristics. The battery had a capacity retention rate of 97% after 2500 cycles at a voltage range of 0.1-1.5V and a rate of 1C, and the initial reversible capacity at a rate of 1C reached 96% of the reversible capacity at a rate of 0.1C.

[0036] Example 5:

[0037] The positive electrode sheet and separator with a gradient distribution of NZSP prepared in step 2 of Example 1 and the negative electrode sheet with a gradient distribution of NZSP prepared in step 2 of Example 2 were assembled into a button-type full battery, and the electrolyte precursor solution prepared in step 3 of Example 1 was added dropwise. The mixture was allowed to stand at room temperature for 12 hours. The cyclic ether monomer DOL underwent ring-opening polymerization under the action of the initiator NaPF6 to obtain a solid-state sodium ion full battery with gradient polymerization characteristics. The battery had a capacity retention rate of 95% after 2500 cycles at a 1C rate in the voltage range of 2.5-3.8 V, the initial reversible capacity at a 1C rate reached 96% of the reversible capacity at a 0.1C rate, and the initial reversible capacity at a 5C rate reached 90% of the reversible capacity at a 0.1C rate.

[0038] Example 6:

[0039] A method for preparing a gradient polymerized solid-state lithium-ion battery positive electrode comprises the following steps:

[0040] Step 1: 96 parts of lithium iron phosphate (LiFePO4), 2 parts of conductive agent Super P, and 2 parts of binder polyvinylidene fluoride (PVDF) are uniformly mixed to form a positive electrode material and divided into 4 parts. To the 4 parts of positive electrode material, an inorganic solid electrolyte NZSP accounting for 0.2%, 0.4%, 0.6%, and 0.8% of the mass fraction of the positive electrode material are added, respectively, and wet mixed to obtain 4 parts of liquid slurries with different contents of inorganic solid electrolyte NZSP;

[0041] Step 2: Apply the four portions of liquid slurry prepared in step 1 layer by layer on the surface of the current collector, so that the amount of inorganic solid electrolyte NZSP decreases gradually from the direction close to the current collector to the direction away from the current collector, and then dry, roll-press, and cut to obtain a positive electrode sheet with a gradient distribution of NZSP;

[0042] Step 3: The lithium salt lithium bis(trifluoromethylsulfonyl)imide LiTFSI, the film-forming additive fluoroethylene carbonate FEC (accounting for 2% of the total mass of the electrolyte), the initiator lithium difluorooxalatoborate LiODFB (concentration of 0.5 mol / L), the solvent ethylene glycol dimethyl ether DME and the cyclic ether monomer 1,3,5-trioxane TXE (the volume ratio of TXE to DME is 1:1) are mixed to prepare an electrolyte precursor solution with a lithium salt LiTFSI concentration of 1 mol / L;

[0043] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the positive electrode sheet with gradient distribution of NZSP prepared in step 2 under vacuum;

[0044] Step 5. The mixture was allowed to stand at 60°C for 12 hours. The cyclic ether monomer TXE underwent ring-opening polymerization under the action of the initiator LiODFB. The gradient-distributed inorganic solid electrolyte NZSP inhibited the initiation effect of the initiator LiODFB, achieving gradient polymerization of the TXE monomer in the electrode, and obtaining a solid-state lithium-ion battery positive electrode with gradient polymerization characteristics.

[0045] Example 7:

[0046] A method for preparing a gradient polymerized solid-state lithium-ion battery negative electrode comprises the following steps:

[0047] Step 1: 90 parts of negative electrode active material graphite, 5 parts of conductive agent Super P, and 5 parts of binder sodium carboxymethyl cellulose CMC are uniformly mixed to form a negative electrode material and divided into 4 parts. Inorganic solid electrolyte NZSP accounting for 0.5%, 1.0%, 1.5% and 2.0% of the mass fraction of the negative electrode material are added to the 4 parts of negative electrode material, respectively, and wet mixed to obtain 4 parts of liquid slurries with different contents of inorganic solid electrolyte NZSP;

[0048] Step 2: Apply the four portions of liquid slurry prepared in step 1 layer by layer on the surface of the current collector, so that the amount of inorganic solid electrolyte NZSP decreases gradually from the direction close to the current collector to the direction away from the current collector, and then dry, roll-press, and cut to obtain a negative electrode sheet with a gradient distribution of NZSP;

[0049] Step 3: The lithium salt lithium bis(trifluoromethylsulfonyl)imide LiTFSI, the film-forming additive fluoroethylene carbonate FEC (accounting for 2% of the total mass of the electrolyte), the initiator lithium difluorooxalatoborate LiODFB (concentration of 0.5 mol / L), the solvent ethylene glycol dimethyl ether DME and the cyclic ether monomer 1,3,5-trioxane TXE (the volume ratio of TXE to DME is 1:1) are mixed to prepare an electrolyte precursor solution with a lithium salt LiTFSI concentration of 1 mol / L;

[0050] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the negative electrode sheet with gradient distribution of NZSP prepared in step 2 under vacuum;

[0051] Step 5. The mixture was allowed to stand at 60°C for 12 hours. The cyclic ether monomer TXE underwent ring-opening polymerization under the action of the initiator LiODFB. The gradient-distributed inorganic solid electrolyte NZSP inhibited the initiation effect of the initiator LiODFB, achieving gradient polymerization of the TXE monomer in the electrode, and obtaining a solid-state lithium-ion battery negative electrode with gradient polymerization characteristics.

[0052] Example 8:

[0053] A button half-cell was assembled with the NZSP prepared in step 2 of Example 6 with a gradient distribution of the positive electrode sheet, a separator, and lithium metal, and the electrolyte precursor solution prepared in step 3 of Example 6 was added dropwise. The mixture was allowed to stand at 60°C for 12 hours. The cyclic ether monomer TXE underwent ring-opening polymerization under the action of the initiator LiODFB. The gradient-distributed inorganic solid electrolyte NZSP inhibited the initiation effect of the initiator LiODFB, achieving gradient polymerization of the TXE monomer in the electrode, thereby obtaining a solid-state lithium-ion positive electrode half-cell with gradient polymerization characteristics. The battery had a capacity retention rate of 98% after 5000 cycles at a 2C rate in the voltage range of 2.5-4.0 V, and the initial reversible capacity at a 2C rate reached 98% of the reversible capacity at a 0.1C rate.

[0054] Example 9:

[0055] A button half-cell was assembled with the negative electrode sheet, separator, and lithium metal prepared in step 2 of Example 7 with a gradient distribution of NZSP, and the electrolyte precursor solution prepared in step 3 of Example 7 was added dropwise. The mixture was allowed to stand at 60°C for 12 hours. The cyclic ether monomer TXE underwent ring-opening polymerization under the action of the initiator LiODFB. The gradient-distributed inorganic solid electrolyte NZSP inhibited the initiation effect of the initiator LiODFB, achieving gradient polymerization of the TXE monomer in the electrode, thereby obtaining a solid-state lithium-ion negative electrode half-cell with gradient polymerization characteristics. The battery had a capacity retention rate of 95% after 5000 cycles at a voltage range of 0.05-1.5V and a 2C rate. The initial reversible capacity at a 2C rate reached 97% of the reversible capacity at a 0.1C rate.

[0056] Example 10:

[0057] The positive electrode sheet and separator with a gradient distribution of NZSP prepared in step 2 of Example 6 and the negative electrode sheet with a gradient distribution of NZSP prepared in step 2 of Example 7 were assembled into a button-type full battery, and the electrolyte precursor solution prepared in step 3 of Example 6 was added dropwise. The mixture was allowed to stand at 60°C for 12 hours. The cyclic ether monomer TXE underwent ring-opening polymerization under the action of the initiator LiODFB. The inorganic solid electrolyte NZSP with a gradient distribution inhibited the initiation effect of the initiator LiODFB, thereby achieving gradient polymerization of the TXE monomer in the electrode, thereby obtaining a solid-state lithium-ion full battery with gradient polymerization characteristics. The battery had a capacity retention rate of 95% after 5000 cycles at a 2C rate in the voltage range of 2.5-4.0V. The initial reversible capacity at a 2C rate reached 95% of the reversible capacity at a 0.1C rate, and the initial reversible capacity at a 5C rate reached 85% of the reversible capacity at a 0.1C rate.

[0058] Comparative Example 1:

[0059] A method for preparing a solid-state sodium ion battery positive electrode comprises the following steps:

[0060] Step 1: Wet-mix 96 parts of the positive electrode active material sodium vanadium phosphate Na3V2(PO4)3, 2 parts of the conductive agent Super P, and 2 parts of the binder polyvinylidene fluoride PVDF to obtain a positive electrode slurry;

[0061] Step 2: coating the positive electrode slurry prepared in step 1 on the surface of the current collector, and then drying, rolling, and cutting to obtain positive electrode sheets;

[0062] Step 3: Sodium perchlorate NaClO4, film-forming additive fluoroethylene carbonate FEC (accounting for 1 wt% of the total mass of the electrolyte precursor solution), initiator sodium hexafluorophosphate NaPF6 (concentration of 0.5 mol / L), solvent ethylene glycol dimethyl ether DME and cyclic ether monomer 1,3-dioxolane DOL (the volume ratio of DME and DOL is 1:1) are mixed uniformly to prepare an electrolyte precursor solution with a sodium salt NaClO4 concentration of 1 mol / L;

[0063] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the positive electrode sheet prepared in step 2 under vacuum;

[0064] Step 5: Let it stand at room temperature for 12 hours, and the cyclic ether monomer DOL undergoes ring-opening polymerization under the action of the initiator NaPF6 to obtain a solid-state sodium ion battery positive electrode.

[0065] Comparative Example 2:

[0066] A method for preparing a solid-state sodium ion battery negative electrode comprises the following steps:

[0067] Step 1: Wet-mix 90 parts of negative electrode active material hard carbon, 5 parts of conductive agent Super P, and 5 parts of binder sodium carboxymethyl cellulose CMC to obtain a negative electrode slurry;

[0068] Step 2: coating the negative electrode slurry prepared in step 1 on the surface of the current collector, and then drying, rolling, and cutting to obtain negative electrode sheets;

[0069] Step 3: Sodium perchlorate NaClO4, film-forming additive fluoroethylene carbonate FEC (accounting for 1 wt% of the total mass of the electrolyte precursor solution), initiator sodium hexafluorophosphate NaPF6 (concentration of 0.5 mol / L), solvent ethylene glycol dimethyl ether DME and cyclic ether monomer 1,3-dioxolane DOL (the volume ratio of DME and DOL is 1:1) are mixed uniformly to prepare an electrolyte precursor solution with a sodium salt NaClO4 concentration of 1 mol / L;

[0070] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the negative electrode sheet prepared in step 2 under vacuum;

[0071] Step 5: Let it stand at room temperature for 12 hours, and the cyclic ether monomer DOL undergoes ring-opening polymerization under the action of the initiator NaPF6 to obtain a solid-state sodium ion battery negative electrode.

[0072] Comparative Example 3:

[0073] The positive electrode sheet, separator, and sodium metal prepared in Comparative Example 1 were assembled into a button half-cell, and the electrolyte precursor solution prepared in Comparative Example 1 was added dropwise. The cells were allowed to stand at room temperature for 12 hours to obtain a solid-state sodium ion positive electrode half-cell. The cell retained 50% of its capacity after 2500 cycles at a 1C rate in the voltage range of 2.5-3.8 V. The initial reversible capacity at a 1C rate was only 75% of the reversible capacity at a 0.1C rate.

[0074] Comparative Example 4:

[0075] The negative electrode sheet, separator, and sodium metal prepared in Comparative Example 2 were assembled into a button half-cell, and the electrolyte precursor solution prepared in Comparative Example 2 was added dropwise. The cells were allowed to stand at room temperature for 12 hours to obtain a solid-state sodium ion negative electrode half-cell. The cell retained 55% of its capacity after 2500 cycles at a rate of 1C in the voltage range of 0.1-1.5V. The initial reversible capacity at a rate of 1C was only 65% of the reversible capacity at a rate of 0.1C.

[0076] Comparative Example 5:

[0077] The positive electrode sheet and separator prepared in Comparative Example 1 and the negative electrode sheet prepared in Comparative Example 2 were assembled into a button-type full battery, and the electrolyte precursor solution prepared in Comparative Example 1 was added dropwise. The battery was allowed to stand at room temperature for 12 hours to obtain a solid-state sodium ion full battery. The battery had a capacity retention rate of 45% after 2500 cycles at a 1C rate in the voltage range of 2.5-3.8V. The initial reversible capacity at a 1C rate was only 72% of the reversible capacity at a 0.1C rate, and the initial reversible capacity at a 5C rate was only 30% of the reversible capacity at a 0.1C rate.

[0078] Comparative Example 6:

[0079] A method for preparing a positive electrode of a solid-state lithium-ion battery comprises the following steps:

[0080] Step 1: Wet-mix 96 parts of positive electrode active material lithium iron phosphate LiFePO4, 2 parts of conductive agent Super P, and 2 parts of binder polyvinylidene fluoride PVDF to obtain a positive electrode slurry;

[0081] Step 2: coating the positive electrode slurry prepared in step 1 on the surface of the current collector, and then drying, rolling, and cutting to obtain positive electrode sheets;

[0082] Step 3: The lithium salt lithium bis(trifluoromethylsulfonyl)imide LiTFSI, the film-forming additive fluoroethylene carbonate FEC (accounting for 2% of the total mass of the electrolyte), the initiator lithium difluorooxalatoborate LiODFB (concentration of 0.5 mol / L), the solvent ethylene glycol dimethyl ether DME and the cyclic ether monomer 1,3,5-trioxane TXE (the volume ratio of TXE to DME is 1:1) are mixed to prepare an electrolyte precursor solution with a lithium salt LiTFSI concentration of 1 mol / L;

[0083] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the positive electrode sheet prepared in step 2 under vacuum;

[0084] Step 5: Standing at 60° C. for 12 hours, the cyclic ether monomer TXE undergoes ring-opening polymerization under the action of the initiator LiODFB to obtain a solid-state lithium-ion battery positive electrode.

[0085] Comparative Example 7:

[0086] A method for preparing a solid-state lithium-ion battery negative electrode comprises the following steps:

[0087] Step 1: Wet-mix 90 parts of negative electrode active material graphite, 5 parts of conductive agent Super P, and 5 parts of binder sodium carboxymethyl cellulose CMC to obtain a negative electrode slurry;

[0088] Step 2: coating the negative electrode slurry prepared in step 1 on the surface of the current collector, and then drying, rolling, and cutting to obtain negative electrode sheets;

[0089] Step 3: The lithium salt lithium bis(trifluoromethylsulfonyl)imide LiTFSI, the film-forming additive fluoroethylene carbonate FEC (accounting for 2% of the total mass of the electrolyte), the initiator lithium difluorooxalatoborate LiODFB (concentration of 0.5 mol / L), the solvent ethylene glycol dimethyl ether DME and the cyclic ether monomer 1,3,5-trioxane TXE (the volume ratio of TXE to DME is 1:1) are mixed to prepare an electrolyte precursor solution with a lithium salt LiTFSI concentration of 1 mol / L;

[0090] Step 4: injecting the electrolyte precursor solution prepared in step 3 into the negative electrode sheet prepared in step 2 under vacuum;

[0091] Step 5: Standing at 60° C. for 12 hours, the cyclic ether monomer TXE undergoes ring-opening polymerization under the action of the initiator LiODFB to obtain a solid-state lithium-ion battery negative electrode.

[0092] Comparative Example 8:

[0093] The positive electrode sheet, separator and lithium metal prepared in Comparative Example 6 were assembled into a button half-cell, and the electrolyte precursor solution prepared in Comparative Example 6 was added dropwise. The cells were left at 60°C for 12 hours to obtain a solid-state lithium-ion positive electrode half-cell. The battery retained 60% of its capacity after 5000 cycles at a 2C rate in the voltage range of 2.5-4.0V. The initial reversible capacity at a 2C rate was only 65% of the reversible capacity at a 0.1C rate.

[0094] Comparative Example 9:

[0095] The negative electrode sheet, separator and lithium metal prepared in Comparative Example 7 were assembled into a button half-cell, and the electrolyte precursor solution prepared in Comparative Example 7 was added dropwise. The cells were left at 60°C for 12 hours to obtain a solid-state lithium-ion negative electrode half-cell. The battery retained 55% of its capacity after 5000 cycles at a 2C rate in the voltage range of 0.05-1.5V. The initial reversible capacity at a 2C rate was only 60% of the reversible capacity at a 0.1C rate.

[0096] Comparative Example 10:

[0097] The positive electrode sheet and separator prepared in Comparative Example 6 and the negative electrode sheet prepared in Comparative Example 7 were assembled into a button-type full battery, and the electrolyte precursor solution prepared in Comparative Example 6 was added dropwise. The battery was left at 60°C for 12 hours to obtain a solid-state lithium-ion full battery. The battery had a capacity retention rate of 40% after 5000 cycles at a 2C rate in the voltage range of 2.5-4.0V. The initial reversible capacity at a 2C rate was only 55% of the reversible capacity at a 0.1C rate, and the initial reversible capacity at a 5C rate was only 25% of the reversible capacity at a 0.1C rate.

[0098] In summary, compared with the traditional solid-state batteries prepared in Comparative Examples 5 and 10, the solid-state batteries with gradient polymerization characteristics prepared in Examples 5 and 10 show excellent electrochemical performance, and the discharge specific capacity and cycle stability at the same rate are significantly improved, which fully demonstrates the superiority of solid-state batteries with gradient polymerization characteristics.

[0099] In addition, it should be understood that although this specification is described in terms of implementation methods, not every implementation method contains only one independent technical solution. This narrative method of the specification is only for the sake of clarity. Those skilled in the art should regard the specification as a whole. The technical solutions in each embodiment can also be appropriately combined to form other implementation methods that can be understood by those skilled in the art.

Claims

1. A method for preparing a gradient polymerized solid-state battery electrode, characterized in that: The following steps are involved: Different mass fractions of Na3Zr2Si2PO4 were added to the electrode material. 12 Prepare several slurries, and then coat several slurries layer by layer on the current collector to make Na3Zr2Si2PO 12 The amount of addition decreases gradually from the current collector to the current collector, and then the electrode is dried, rolled, and cut to obtain the electrode. The electrolyte precursor solution containing cyclic ether monomers and initiators is injected into the electrode to form a gradient distribution of Na3Zr2Si2PO 12 Inhibiting the interaction between the initiator and the cyclic ether monomer, achieving gradient polymerization of the cyclic ether-based polymer electrolyte in the electrode, and obtaining a gradient polymerized solid-state battery electrode; The Na3Zr2Si2PO 12 The mass range of the gradient distribution in the electrode material from close to the current collector to far away from the current collector is 0.1wt%-2wt%.

2. The preparation method according to claim 1, wherein: The cyclic ether monomer includes one or more of tetrahydrofuran, 1,3-dioxolane, 1,3,5-trioxane, 1,3-dioxane, epoxy-terminated chain siloxane and epoxy-terminated cage-type polysilsesquioxane.

3. The preparation method according to claim 1, wherein: The initiator includes one or more combinations of sodium salt initiator, lithium salt initiator, aluminum salt initiator, tin salt initiator, zinc salt initiator, magnesium salt initiator, and scandium salt initiator.

4. The preparation method according to claim 1, wherein: The cyclic ether monomer accounts for 40%-80% of the volume of the electrolyte precursor solution.

5. The preparation method according to claim 1, wherein: The concentration of the initiator in the electrolyte precursor solution is 0.1-1 mol / L.

6. The preparation method according to claim 1, wherein: The electrode material includes an active material, a conductive agent and a binder that are uniformly mixed.

7. The preparation method according to claim 1, wherein: The electrolyte precursor solution further includes a solvent, an ionic salt and an additive, and the ionic salt is a lithium salt, a sodium salt or a potassium salt.

8. The preparation method according to claim 1, wherein: After the electrolyte precursor solution is injected into the electrode, it is left to stand at room temperature or under heating conditions. The cyclic ether monomer undergoes ring-opening polymerization under the action of the initiator, and a gradient distribution of Na3Zr2Si2PO 12 The initiation effect of the initiator is suppressed to achieve the gradient polymerization of the cyclic ether-based polymer electrolyte in the electrode.

9. An application of a solid-state battery electrode prepared by the preparation method according to any one of claims 1 to 8, characterized in that: The solid-state battery electrode is applied to the positive electrode and / or negative electrode of a lithium-ion battery, the positive electrode and / or negative electrode of a sodium-ion battery, or the positive electrode and / or negative electrode of a potassium-ion battery.