METAL NEGATIVE ELECTRODE, PREPARATION METHOD THEREFOR, AND SECONDARY BATTERY

Abstract

A metal negative electrode and a method of making the metal negative electrode is disclosed. The metal negative electrode includes a metal negative electrode body and a protective layer formed on a surface of one side or each of two sides of the metal negative electrode body. The protective layer includes a liquid-state or gel-state inner layer that has an ability to dissolve alkali metal and a solid-state outer layer has a high ionic conductivity. The liquid-state or gel-state inner layer includes at least one of an aromatic hydrocarbon small molecule compound or a polymer containing an aromatic hydrocarbon group that each have an ability to accept an electron, and at least one of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, or a polythioether polymer that each have an ability to complex lithium ions.

Claims

1. A metal negative electrode, comprising: a metal negative electrode body; and a protective layer formed on a surface of one side or each of two sides of the metal negative electrode body; wherein the protective layer comprises a double-layer structure, wherein the double-layer structure comprisingcomprises a liquid-state or gel-state inner layer that has an ability to dissolve alkali metal and a solid-state outer layer that has a high ionic conductivity; wherein the liquid-state or gel-state inner layer comprises at least one member selected from a first group consisting of an aromatic hydrocarbon small molecule compound and a polymer containing an aromatic hydrocarbon group , and at least one member selected from a second group consisting of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, and a polythioether polymer; wherein each member in the first group has an ability to accept an electron; and wherein each member in the second group has an ability to complex lithium ions.

2. The metal negative electrode according to claim 1, wherein the aromatic hydrocarbon small molecule compound comprises at least one member selected from a third group consisting of biphenyl, naphthalene, phenanthrene, anthracene, tetracene, and pyrene; and wherein the polymer containing an aromatic hydrocarbon group comprises at least one member selected from a fourth group consisting of biphenyl, naphthalene, phenanthrene, anthracene, tetracene, and pyrene aromatic groups.

3. The metal negative electrode according to claim 1, wherein the ether small molecule solvent comprises at least one member from a fifth group consisting of ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, and at least one member selected from a sixth group consisting of tetrahydrofuran, 1,4-dioxane, 12-crown ether-4, 15-crown ether-5, and 18-crown ether-6; wherein the amine small molecule solvent comprises at least one member selected from a seventh group consisting of ethylenediamine dimethylamine, ethylenediamine tetramethylamonium, and diethylenediaminetetramethylamonium; and wherein the thioether small molecule solvent comprises at least one member selected from an eighth group consisting of ethylene dithiol dimethyl thioether, ethylene dithiol diethyl thioether, diethylene dithiol dimethyl thioether, and tetraethylene dithiol dimethyl thioether.

4. The metal negative electrode according to claim 1, wherein the polyether polymer comprises at least one member selected from a ninth group consisting of polyethylene oxide and polypropylene oxide, wherein the polyamine polymer comprises at least one member selected from a tenth group consisting of polymethyl ethylenediamine and polymethyl methacrylate ethylenediamine, and wherein the polythioether polymer comprises at least one member selected from an eleventh group consisting of polyethylene dithiol and methyl polyethylene dithiol.

5. The metal negative electrode according to claim 1, wherein the liquid-state or gel-state inner layer further comprises at least one member selected from a twelfth group consisting of a polyfluorinated olefin polymer, a polynitrile polymer, a polyamide polymer, a polyimide polymer, and a polyamide-imide polymer.

6. The metal negative electrode according to claim 5, wherein the polyfluorinated olefin polymer comprises at least one member selected from a thirteenth group consisting of PVDF, PVDF-HFP, and PTFE; wherein the polynitrile polymer is PAN; wherein the polyamine ester polymer comprises a poly 2,4-toluene diisocyanate polyamine ester polymer; wherein the polyamide polymer comprises at least one member selected from a fourteenth group consisting of PA11 and PA66; and wherein the polyimide is polybismaleimide.

7. The metal negative electrode according to claim 1, wherein the solid-state outer layer comprises an oxide solid electrolyte or a sulfide solid electrolyte.

8. The metal negative electrode according to claim 7, wherein the oxide solid electrolyte comprises any one of a perovskite solid electrolyte, a sodium fast ionic conductor solid electrolyte, a lithium fast ionic conductor solid electrolyte, a garnet solid electrolyte, or a glass oxide solid electrolyte; and wherein the sulfide solid electrolyte comprises any one of a thio-lithium fast ionic conductor or glass sulfide solid electrolyte.

9. The metal negative electrode according to claim 1, wherein the solid-state outer layer further comprises at least one member selected from a fifteenth group consisting of a polyfluorinated olefin polymer, the polynitrile polymer, the polyurethane polymer, the polyamide polymer, a polyimide polymer, and the polyamide-imide polymer.

10. The metal negative electrode according to claim 1, wherein a thickness of the solid-state outer layer is from 0.1 to 50 microns.

11. The metal negative electrode according to claim 1, wherein the metal negative electrode body comprises a lithium negative electrode, a sodium negative electrode, a potassium negative electrode, a lithium alloy negative electrode, a sodium alloy negative electrode, or a potassium alloy negative electrode.

12. The metal negative electrode according to claim 11, wherein the lithium alloy negative electrode comprises an alloy composed of lithium metal and other elements, and at least one member selected from a sixteenth group consisting of silicon, sodium, potassium, cesium, aluminum, tin, and indium.

13. A method of making a metal negative electrode, comprising: forming a protective layer on a surface of one side or each of two sides of a metal negative electrode body, wherein the protective layer comprises a double-layer structure, wherein the double-layer structure comprises a liquid-state or gel-state inner layer that has an ability to dissolve alkali metal and a solid-state outer layer that has a high ionic conductivity; wherein the liquid-state or gel-state inner layer comprises at least one member selected from a first group consisting of an aromatic hydrocarbon small molecule compound and a polymer containing an aromatic hydrocarbon group and at least one member selected from a second group consisting of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, and a polythioether polymer; wherein each member in the first group has an ability to accept an electron; and wherein each member in the second group has an ability to complex lithium ions.

14. The method according to claim 13, wherein the forming the protective layer on the surface of one side or each of two sides of the metal negative electrode body, comprises: after coating the liquid-state or gel-state inner layer , forming the solid-state outer layer on the liquid-state or gel-state inner layer.

15. The method according to claim 13, wherein the forming the protective layer on the surface of one side or each of two sides of the metal negative electrode body comprises: after compounding the metal negative electrode body with the solid-state outer layer, injecting at least one member selected from a third group consisting of the aromatic hydrocarbon small molecule compound and the polymer containing an aromatic hydrocarbon group , and at least one member selected from a fourth group consisting of the ether small molecule solvent, the amine small molecule solvent, the thioether small molecule solvent, the polyether polymer, the polyamine polymer, and the polythioether polymer into an interlayer between the metal negative electrode body and the solid-state outer layer, to form the liquid-state or gel-state inner layer.

16. The method according to claim 13, wherein the aromatic hydrocarbon small molecule compound comprises at least member selected from a fifth group consisting of one of biphenyl, naphthalene, phenanthrene, anthracene, tetracene, and pyrene; and wherein the polymer containing the aromatic hydrocarbon group comprises at least one member selected from a sixth group consisting of biphenyl, naphthalene, phenanthrene, anthracene, tetracene, and pyrene aromatic groups.

17. The method according to claim 13, wherein the ether small molecule solvent comprises at least one member selected from a seventh group consisting of ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, and tetraethylene glycol dimethyl ether, and at least one member selected from a eighth group consisting of cyclic ether such as tetrahydrofuran, 1,4-dioxane, 12-crown ether-4, 15-crown ether-5, and 18-crown ether-6; wherein the amine small molecule solvent comprises at least one member selected from a ninth group consisting of ethylenediamine dimethylamine, ethylenediamine tetramethylamonium, and diethylenediaminetetramethylamonium; wherein the thioether small molecule solvent comprises at least one member selected from a tenth group consisting of ethylene dithiol dimethyl thioether, ethylene dithiol diethyl thioether, diethylene dithiol dimethyl thioether, and tetraethylene dithiol dimethyl thioether; and wherein the polyether polymer comprises at least one member selected from an eleventh group consisting of polyethylene oxide and polypropylene oxide; wherein the polyamine polymer comprises at least one member selected from a twelfth group consisting of polymethyl ethylenediamine and polymethyl methacrylate ethylenediamine; and wherein the polythioether polymer comprises at least one member selected from a thirteenth group consisting of polyethylene dithiol and methyl polyethylene dithiol.

18. The method according to claim 13, wherein the liquid-state or gel-state inner layer further comprises at least one member selected from a fourteenth group consisting of a polyfluorinated olefin polymer, a polynitrile polymer, a polyamide polymer, a polyimide polymer, and a polyamide-imide polymer.

19. The method according to claim 14, wherein the coating the liquid-state or gel-state inner layer is performed in a manner that comprises at least one member selected from a fifteenth group consisting of drop coating, brush coating, roll coating, spraying, scrape coating, dip coating, and spin coating; and wherein the coating is performed in a dry room or a protective atmosphere.

20. A secondary battery, comprising; a positive electrode; a negative electrode; a diaphragm; and an electrolyte; wherein the negative electrode comprises a metal negative electrode, wherein the metal negative electrode comprises a metal negative electrode body and a protective layer formed on a surface of one side or each of two sides of the metal negative electrode body; and wherein the protective layer comprises a double-layer structure, wherein the double-layer structure comprises a liquid-state or gel-state inner layer that has an ability to dissolve alkali metal and a solid-state outer layer that has a high ionic conductivity; and wherein the liquid-state or gel-state inner layer comprises at least one member selected from a first group consisting of an aromatic hydrocarbon small molecule compound and a polymer containing an aromatic hydrocarbon , and at least one member selected from a second group consisting of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, and a polythioether polymer; wherein each member in the first group has an ability to dissolve alkali metal; and wherein each member in the second group has an ability to complex lithium ions.

21. A terminal, comprising: a housing; a circuit mainboard accommodated in the housing; and a display apparatus mounted on the housing and connected to the circuit mainboard; a secondary battery; wherein the secondary battery is configured to supply power to the circuit mainboard and the display apparatus; wherein the secondary battery comprises a positive electrode, a negative electrode, a diaphragm, and an electrolyte; wherein the negative electrode comprises the metal negative electrode, wherein the metal negative electrode comprises a metal negative electrode body and a protective layer formed on a surface of one side or each of two sides of the metal negative electrode body; wherein the protective layer comprises a double-layer structure, wherein the double-layer structure comprises a liquid-state or gel-state inner layer that has an ability to dissolve alkali metal and a solid-state outer layer that has a high ionic conductivity; wherein the liquid-state or gel-state inner layer comprises at least one member from a first group consisting of an aromatic hydrocarbon small molecule compound and a polymer containing an aromatic hydrocarbon group , and at least one member selected from a second group consisting of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, and a polythioether polymer; and wherein each member in the first group has an ability to dissolve alkali metal; and wherein each member in the second group has an ability to complex lithium ions.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0025] FIG. 1 is a schematic diagram of a structure of a lithium ion secondary battery in the conventional technology;

[0026] FIG. 2 is a schematic diagram of a structure of a metal negative electrode according to an embodiment of this application;

[0027] FIG. 3 is a scanning electron microscope (SEM) photograph of a lithium negative electrode after 100 cycles in Embodiment 1 of this application;

[0028] FIG. 4 is a scanning electron microscope (SEM) photograph of a lithium negative electrode after 100 cycles in Comparative example 1 of this application; and

[0029] FIG. 5 is a diagram of cyclic curves of batteries according to Embodiments 1 to 5 and Comparative examples 1 and 2 of this application.

DESCRIPTION OF EMBODIMENTS

[0030] The following uses an alkali metal battery as an example to describe a system or a scenario in which embodiments of this application are implemented. Core components of the alkali metal battery are mainly a positive electrode, a metal negative electrode, an electrolyte, and a diaphragm. FIG. 1 is a schematic diagram of a structure of a lithium metal battery in an alkali metal battery in the conventional technology. During charging, lithium ions are removed from a lattice of a positive electrode material, and are deposited into a lithium metal negative electrode after passing through an electrolyte. During discharging, lithium ions are removed from the lithium metal negative electrode and inserted into the lattice of the positive electrode material after passing through the electrolyte. In a charging and discharging cycle process, an interface protective film is unstable, and freshly deposited lithium metal is exposed and directly contacts the electrolyte, causing a serious side reaction and inducing lithium dendrite formation, thereby reducing coulombic efficiency and causing safety problems. In embodiments of this application, a double-layer structure with an inner protective layer and an outer protective layer is formed on a surface of one side or each of two sides of a metal negative electrode body in an existing alkali metal negative electrode, so as to effectively resolve the foregoing problem in the conventional technology.

[0031] The following describes embodiments of this application with reference to accompanying drawings in embodiments of this application.

[0032] Referring to FIG. 2, an embodiment of this application provides a schematic diagram of a metal negative electrode. As shown in FIG. 2(a), the metal negative electrode includes a metal negative electrode body 10 and an inner protective layer 11 and an outer protective layer 12 that are formed on a surface of one side of the metal negative electrode body 10. As shown in FIG. 2(b), the metal negative electrode includes a metal negative electrode body 10 and an inner protective layer 11 and an outer protective layer 12 that are formed on surfaces of two sides of the metal negative electrode body 10. The one side or the two sides of the metal negative electrode body 10 is or are one side or two sides facing an electrolyte in a secondary battery.

[0033] The inner protective layer 11 is a liquid-state or gel-state inner layer that has an ability to dissolve alkali metal, and contains at least one of an aromatic hydrocarbon small molecule compound and a polymer containing an aromatic hydrocarbon group that have an ability to accept an electron, and at least one of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, and a polythioether polymer that have an ability to complex lithium ions. The liquid-state or gel-state inner layer can dissolve alkali metal in a physical manner by using a synergistic effect of the foregoing substances, so as to resolve a dendrite problem in a charging or discharging process of this type of metal negative electrode.

[0034] In addition, the outer protective layer 12 is a solid-state outer layer with a high ionic conductivity, and includes an oxide solid electrolyte or a sulfide solid electrolyte. Specifically, the oxide solid electrolyte includes a perovskite solid electrolyte, a sodium fast ionic conductor solid electrolyte (that is, a NASICON solid electrolyte), a lithium fast ionic conductor solid electrolyte (that is, a LISICON solid electrolyte), a garnet solid electrolyte, a glass oxide solid electrolyte, or the like. The sulfide solid electrolyte includes a thio-lithium fast ionic conductor solid electrolyte (that is, a thio-LISICON solid electrolyte), a glass sulfide solid electrolyte, or a compound of the foregoing inorganic solid electrolytes.

[0035] In an implementation of this application, the metal negative electrode body 10 may be a lithium negative electrode, a sodium negative electrode, a potassium negative electrode, or an alloy that includes lithium metal, sodium metal, and potassium metal. Specifically, the lithium metal alloy is an alloy composed of lithium metal and at least one of other elements such as silicon, sodium, cesium, aluminum, potassium, tin, and indium. The sodium metal alloy is an alloy composed of sodium metal and at least one of other elements such as silicon, lithium, potassium, cesium, aluminum, tin, and indium. The potassium metal alloy is an alloy composed of potassium metal and at least one of other elements such as silicon, sodium, cesium, aluminum, tin, lithium, and indium.

[0036] Specifically, for example, the metal negative electrode body 10 is a lithium negative electrode. In this embodiment of this application, the inner protective layer 11 contains an aromatic hydrocarbon small molecule compound that has an ability to accept an electron and an ether, amine, or thioether small molecule solvent that has an ability to complex lithium ions. These small molecule solvents have a relatively high solubility to alkali metal by using a synergistic effect, and a battery short-circuit risk caused by continuous growth of lithium dendrites on a surface of the lithium negative electrode when a lithium metal secondary battery is in a repeated charging or discharging process can be reduced in theory. In addition, even in an extreme condition, before a part of freshly generated lithium dendrites are fully dissolved, the lithium dendrites disengage from contact with a lithium negative electrode body during a discharging process. However, because the liquid-state or gel layer after the lithium metal is dissolved has a high electronic conductivity, the part of lithium dendrites disengaged from the lithium negative electrode body can still participate in electrode reaction until being fully consumed. A mixture of the foregoing small molecule solvents may be mixed with polymers other than aromatics, polyether, polyamine, and polythioether, such as PVDF-HFP, to form a gel for coating on a surface of the metal negative electrode body. An oxide solid electrolyte, such as a garnet solid electrolyte, may be selected for the outer protective layer 12.

[0037] In another embodiment of this application, the inner protective layer 11 may also include a gel formed by an aromatic hydrocarbon small molecule compound and a polyether polymer. An oxide solid electrolyte, such as a garnet solid electrolyte, may be selected for the outer protective layer 12.

[0038] In another embodiment of this application, the inner protective layer 11 may also include a gel formed by an ether small molecule compound and a polymer containing an aromatic group. An oxide solid electrolyte, such as a Nasicon solid electrolyte, may be selected for the outer protective layer 12.

[0039] In another embodiment of this application, the inner protective layer 11 may also include a mixed liquid formed by an ether small molecule compound and an aromatic hydrocarbon small molecule compound. An oxide solid electrolyte, such as a ceramic sulfide solid electrolyte of Thio-Nasicon, may be selected for the outer protective layer 12.

[0040] In an embodiment, the metal negative electrode body in this application includes a lithium negative electrode, a sodium negative electrode, a potassium negative electrode, a lithium alloy negative electrode, a sodium alloy negative electrode, or a potassium alloy negative electrode. The lithium alloy negative electrode is an alloy composed of lithium metal and other elements, and the other elements include at least one of silicon, sodium, potassium, cesium, aluminum, tin, and indium.

[0041] Correspondingly, an embodiment of this application further provides a preparation method for the foregoing metal negative electrode, including: coating the surface of the metal negative electrode body with the liquid-state or gel-state inner layer that has an ability to receive an electron. After the metal negative electrode is coated with the liquid-state or gel-state inner layer, the solid-state outer layer is formed on the liquid-state or gel-state inner layer, for example, the liquid-state or gel-state inner layer is fitted to the solid-state outer layer. In an embodiment, after the metal negative electrode is fitted to the solid-state outer layer, the liquid-state or gel-state inner layer is injected into an interlayer between the metal negative electrode body and an inorganic solid electrolyte membrane. The liquid-state or gel-state inner layer includes at least one of an aromatic hydrocarbon small molecule compound and a polymer containing an aromatic hydrocarbon group that have an ability to accept an electron, and at least one of an ether small molecule solvent, an amine small molecule solvent, a thioether small molecule solvent, a polyether polymer, a polyamine polymer, and a polythioether polymer that have an ability to complex lithium ions.

[0042] In an embodiment, the aromatic hydrocarbon small molecule compound includes at least one of biphenyl, naphthalene, phenanthrene, anthracene, tetracene, and pyrene. The polymer containing an aromatic hydrocarbon group includes at least one of biphenyl, naphthalene, phenanthrene, anthracene, tetracene, and pyrene aromatic groups.

[0043] The ether small molecule solvent includes at least one of chain ether such as ethylene glycol dimethyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, and tetraethylene glycol dimethyl ether, and at least one of cyclic ether such as tetrahydrofuran, 1,4-dioxane, 12-crown ether-4, 15-crown ether-5, and 18-crown ether-6. The amine small molecule solvent includes at least one of ethylenediamine dimethylamine, ethylenediamine tetramethylamonium, and diethylenediaminetetramethylamonium. The thioether small molecule solvent includes at least one of ethylene dithiol dimethyl thioether, ethylene dithiol diethyl thioether, diethylene dithiol dimethyl thioether, and tetraethylene dithiol dimethyl thioether. The polyether polymer includes at least one of polyethylene oxide and polypropylene oxide. The polyamine polymer includes at least one of polymethyl ethylenediamine and polymethyl methacrylate ethylenediamine. The polythioether polymer includes at least one of polyethylene dithiol and methyl polyethylene dithiol.

[0044] In an embodiment, the liquid-state or gel-state inner layer that has an ability to dissolve alkali metal may include another polymer different from aromatics, polyether, polyamine, and polythioether. For example, the liquid-state or gel-state inner layer that has an ability to dissolve alkali metal further includes at least one of a polyfluorinated olefin polymer, a polynitrile polymer such as PAN, a polyamide polymer, a polyimide polymer, and a polyamide-imide polymer. The polyfluorinated olefin polymer includes one or more of PVDF, PVDF-HFP, and PTFE. The polyamine ester polymer includes a poly 2,4-toluene diisocyanate polyamine ester polymer. The polyamide polymer includes one or more of polymers such as PA11 and PA66.

[0045] In an implementation of this application, a coating manner includes at least one of drop coating, brush coating, roll coating, spraying, scrape coating, dip coating, and spin coating, and the coating operation is performed in a dry environment and a protective atmosphere. A coating time is 1 min-24 h, and a coating temperature is -10° C.-50° C.

[0046] The preparation method for a metal negative electrode according to this embodiment of this application has a simple process, and mass production is possible.

[0047] An embodiment of this application further provides a secondary battery, where the secondary battery includes a positive electrode plate, a negative electrode plate, a diaphragm, and an electrolyte. The negative electrode plate includes the foregoing metal negative electrode according to the embodiment of this application. The metal negative electrode may be a lithium negative electrode, a sodium negative electrode, a potassium negative electrode, a magnesium negative electrode, a zinc negative electrode, or an aluminum negative electrode. Correspondingly, the secondary battery may be a lithium secondary battery, a sodium secondary battery, a potassium secondary battery, or the like. The secondary battery is of high cycle performance and high safety.

[0048] In this embodiment of this application, the electrolyte includes a solvent and metal salt. Specifically, the solvent includes one or more of a carbonic ester solvent, an ether solvent, and a carboxylic ester solvent. The carbonic ester solvent includes a cyclic carbonate or a chain carbonate. The cyclic carbonate may be specifically one or more of ethylene carbonate (EC), propylene carbonate (PC), gamma butyrolactone (GBL), butyl carbonate (BC), fluoroethylene carbonate (FEC), and vinylene carbonate (VC). The chain carbonate may be specifically one or more of dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), and dipropyl carbonate (DPC). The ether solvent includes cyclic ether or chain ether. The cyclic ether may be specifically one or more of 1,3-dioxolane (DOL), 1,4-dioxane (DX), crown ether, tetrahydrofuran (THF), 2-methyltetrahydrofuran (2-CH.sub.3-THF), and 2-trifluoromethyltetrahydrofuran (2-CF.sub.3-THF). The chain ether may be specifically one or more of dimethoxymethane (DMM), 1,2-dimethoxyethane (DME), and diethylene glycol dimethyl ether (TEGDME). The carboxylic ester solvent may be specifically one or more of methyl acetate (MA), ethyl acetate (EA), propyl acetate (EP), butyl acetate, propyl propionate (PP), and butyl propionate. An anion of the metal salt includes but is not limited to one or more of a hexafluorophosphate anion (PF.sub.6.sup.-), a hexafluoroarsenic anion (AsF.sub.6.sup.-), a perchlorate anion (ClO.sub.4.sup.-), a tetrafluoroborate anion (BF.sub.4.sup.-), a dioxalate borate anion (B (C.sub.2O.sub.4).sub.2.sup.-, BOB.sup.-), a difluoroethylene borate anion (BF.sub.2C.sub.2O.sub.4.sup.-, DFOB.sup.-), a difluoride sulfonimide anion (FSI.sup.-), and a bistrifluorosulfonimide anion (TFSI.sup.-).

[0049] As shown in FIG. 5, an embodiment of this application further provides a terminal 200. The terminal 200 may be an electronic product such as a mobile phone, a tablet computer, an intelligent wearable product, or an electric vehicle. Specifically, for example, the terminal is a mobile phone 200 and includes a housing 100 assembled outside the terminal, and a circuit board and a battery (not shown in the figure) that are located inside the housing 100. The battery is the secondary battery provided in the foregoing embodiment of this application. The housing 100 may include a display screen assembled on a front side of the terminal and a rear cover assembled on a rear side, and the battery may be fixed inside the rear cover to supply power to the terminal 200.

[0050] The following further describes embodiments of this application by using a plurality of embodiments.

Embodiment 1

[0051] Preparation of a lithium metal battery includes: [0052] (1) Preparation of a protective lithium negative electrode: In an environment without water or oxygen, dissolve 0.07 g lithium metal and 1.54 g biphenyl in an ethylene glycol dimethyl ether solution to form a homogeneous solution, and dissolve 0.01 g PVDF-HFP in a heated condition to form a gel after cooling. Then, coat a surface of an unprotected lithium metal negative electrode body with the foregoing homogeneous slurry, and compound it with a 50 .Math.m LLZO ceramic plate to obtain a lithium metal negative electrode plate with a double-layer protective structure that contains a 10 .Math.m gel protective layer. [0053] (2) Lithium cobalt oxide/lithium (LiCoO.sub.2/Li) battery assembly: Assemble the foregoing prepared protective lithium negative electrode, a lithium cobalt oxide positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L LiPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3) on a positive electrode end to soak a positive electrode plate, the diaphragm, and an outer surface of a composite lithium metal negative electrode LLZO ceramic plate.

Embodiment 2

[0054] Preparation of a lithium metal battery includes: [0055] (1) Preparation of a protective lithium negative electrode: In an environment without water or oxygen, dissolve 0.07 g lithium metal and 1.54 g biphenyl in a THF solution of polyethylene oxide (PEO) to form homogeneous slurry. Then, coat a surface of an unprotected lithium metal negative electrode body with the homogeneous slurry, and compound it with a 50 .Math.m LLZO ceramic plate after the THF is dried and removed, to obtain a lithium metal negative electrode plate with a double-layer protective structure that contains a 10 .Math.m gel protective layer. [0056] (2) Lithium cobalt oxide/lithium (LiCoO.sub.2/Li) battery assembly: Assemble the foregoing prepared protective lithium negative electrode, a lithium cobalt oxide positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L LiPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3) on a positive electrode end to soak a positive electrode plate, the diaphragm, and an outer surface of a composite lithium metal negative electrode LLZO ceramic plate.

Embodiment 3

[0057] Preparation of a lithium metal battery includes: [0058] (1) Preparation of a protective lithium negative electrode: In an environment without water or oxygen, heat and dissolve 0.07 g lithium metal and 1.8 g poly 4-vinyl biphenyl in ethylene glycol dimethyl ether to form a gel after cooling. Then, coat a surface of an unprotected lithium metal negative electrode body with the gel, and compound it with a 50 .Math.m LLZO ceramic plate, to obtain a lithium metal negative electrode plate with a double-layer protective structure that contains a 10 .Math.m gel protective layer. [0059] (2) Lithium cobalt oxide/lithium (LiCoO.sub.2/Li) battery assembly: Assemble the foregoing prepared protective lithium negative electrode, a lithium cobalt oxide positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L LiPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3) on a positive electrode end to soak a positive electrode plate, the diaphragm, and an outer surface of a composite lithium metal negative electrode LLZO ceramic plate.

Embodiment 4

[0060] Preparation of a lithium metal battery includes: [0061] (1) Preparation of a protective lithium negative electrode: In an environment without water or oxygen, dissolve 0.07 g lithium metal and 1.54 g biphenyl in an ethylene glycol dimethyl ether solution to form a homogeneous solution, and dissolve 0.01 g PVDF-HFP in a heated condition to form a gel after cooling. Then, coat a surface of an unprotected lithium metal negative electrode body with the foregoing homogeneous slurry, and compound it with a 50 .Math.m Li3PS4 solid electrolyte plate to obtain a lithium metal negative electrode plate with a double-layer protective structure that contains a 10 .Math.m gel protective layer. [0062] (2) Lithium cobalt oxide/lithium (LiCoO.sub.2/Li) battery assembly: Assemble the foregoing prepared protective lithium negative electrode, a lithium cobalt oxide positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L LiPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3) on a positive electrode end to soak a positive electrode plate, the diaphragm, and an outer surface of a composite lithium metal negative electrode Li3PS4 solid electrolyte plate.

Embodiment 5

[0063] Preparation of a sodium metal battery includes: [0064] (1) Preparation of a protective lithium negative electrode: In an environment without water or oxygen, dissolve 0.23 g sodium metal and 1.54 g biphenyl in an ethylene glycol dimethyl ether solution to form a homogeneous solution, and dissolve 0.01 g PVDF-HFP in a heated condition to form a gel after cooling. Then, coat a surface of an unprotected lithium metal negative electrode body with the foregoing homogeneous slurry, and compound it with a 50 .Math.m Na(4-x)Sn(1-x)SbxS4 solid electrolyte plate to obtain a sodium metal negative electrode plate with a double-layer protective structure that contains a 10 .Math.m gel protective layer. [0065] (2) Na2MnFe(CN).sub.6/Na battery assembly: Assemble the foregoing prepared protective lithium negative electrode, a Na2MnFe(CN).sub.6 positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L NaPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3) on a positive electrode end to soak a positive electrode plate, the diaphragm, and an outer surface of a composite sodium metal negative electrode Na(4-x)Sn(1-x)SbxS4 solid electrolyte plate.

Comparative Example 1

[0066] LiCoO.sub.2/Li battery assembly: Assemble an unprotected lithium metal negative electrode body, a lithium cobalt oxide positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L LiPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3).

Comparative Example 2

[0067] Na2MnFe(CN).sub.6/Na battery assembly: Assemble an unprotected sodium metal negative electrode body, a Na2MnFe(CN).sub.6 positive electrode, and a diaphragm into a battery, and dropwise add 50 .Math.L 1.0 mol/L NaPF.sub.6 electrolyte (a weight ratio of DMC, FEC, and VC is 45:52:3).

[0068] To strongly support the beneficial effects of the technical solutions in this embodiment, the following tests are provided.

[0069] 1. Charging and discharging tests are performed on the batteries assembled in Embodiments 1 to 5 and Comparative examples 1 and 2 according to a 0.1 C/0.2 C charging and discharging system. A voltage range of the lithium metal battery is 3.0 V-4.5 V, a voltage range of the sodium metal battery is 2.5 V-4.0 V, and test results of capacity retention ratios after 100 weeks are shown in Table 1 and FIG. 5.

TABLE-US-00001 Performance test results of batteries assembled by using different lithium negative electrodes Serial number Lithium negative electrode type Capacity retention ratio after 100 weeks Embodiment 1 LLZO/Liquid metal A protects a lithium metal negative electrode 90.8% Embodiment 2 LLZO/Liquid metal gel B protects a lithium metal negative electrode 88.3% Embodiment 3 LLZO/Liquid metal gel C protects a lithium metal negative electrode 80.9% Embodiment 4 Li3PS4/Liquid metal A protects a lithium metal negative electrode 80.9% Embodiment 5 Na(4-x)Sn(1-x)SbxS4/Liquid metal D protects a sodium metal negative electrode 85.6% Comparative example 1 Unprotected lithium metal negative electrode 68.4% Comparative example 2 Unprotected sodium metal negative electrode 69.5%

[0070] It can be learned from the test results in Table 1 and FIG. 5 that capacity retention ratios of the lithium cobalt oxide/lithium batteries in Embodiments 1 to 4 and the sodium metal battery in Embodiment 5 after 100 weeks are much higher than capacity retention ratios of the lithium cobalt oxide/lithium battery in Comparative example 1 and the sodium metal battery in Comparative example 2 after 100 weeks. This indicates that battery cycle performance can be significantly improved by using an alkali metal negative electrode with double protection from liquid metal and a solid electrolyte. On the one hand, a double-layer protective layer isolates the alkali metal negative electrode from contacting a carbonic ester electrolyte, and avoids a loss of active lithium/sodium due to continuous side reaction between alkali metal and the electrolyte. On the other hand, due to good wettability of a liquid metal inner layer, continuous and stable interface contact between a solid electrolyte layer and a metal negative electrode can be kept, so as to ensure that lithium metal deposition is as homogeneous as possible. In addition, for dendrites growing in extreme cases, a good conductivity of the liquid metal and a solubility of the alkali metal can fundamentally solve a metal negative electrode pulverization problem and a possible safety risk caused by dendrites. The batteries obtained after a 100-week cyclic test in Embodiment 1 and Comparative example 1 are disassembled, and negative electrode surface appearances of the batteries are shown in FIG. 3 (Embodiment 1) and FIG. 4 (Comparative example 1). It can be clearly seen from the figures that, after being protected by a liquid metal layer that has an ability to dissolve an alkali metal dendrite, a surface of a lithium metal negative electrode is still relatively flat after a 100-week cycle (FIG. 3), and a surface of a lithium negative electrode that is exposed to an electrolyte for cycle (FIG. 4) is relatively rough, which proves that a large quantity of dendrites appear. This is exactly consistent with an expected effect.

[0071] An effect of Embodiment 1 is better than those of Embodiments 2 to 4, which proves that both a composition of a liquid metal inner layer and a chemical structure of a solid electrolyte protective layer have great impact on a protection effect. When the inner layer contains at least one of an aromatic hydrocarbon small molecule compound that has a relatively strong solubility to alkali metal and a polymer containing an aromatic hydrocarbon group, and a mixture composed of at least one of an ether small molecule solvent and a polyether polymer, a battery cycle capacity retention ratio is the highest. This indirectly proves that a liquid metal inner layer with an alkali metal dissolution effect is necessary for improving cycle life of an alkali metal battery.

[0072] The foregoing descriptions are merely specific implementations of this application, but are not intended to limit the protection scope of this application. Any variation or replacement readily figured out by a person skilled in the art within the technical scope disclosed in the present invention shall fall within the protection scope of this application. Therefore, the protection scope of this application shall be subject to the protection scope of the claims.