SECONDARY BATTERY AND PREPARATION METHOD THEREFOR

Abstract

A secondary battery and a method for making the same are disclosed. The secondary battery includes a battery negative electrode, an electrolyte liquid, a diaphragm and a battery positive electrode. The battery negative electrode includes a negative electrode current collector, which also acts as a negative electrode active material. The electrolyte liquid includes an electrolyte and a solvent, the electrolyte being a lithium salt. The battery positive electrode includes a positive electrode current collector and a positive electrode active material layer, which includes a positive electrode active material capable of reversibly de-intercalating lithium ions.

Description

TECHNICAL FIELD

The present disclosure relates to the field of batteries, and in particular to a secondary battery and a preparation method therefor.

BACKGROUND ART

With the development of the level of modern life as well as science and technology, people are consuming and requiring more and more energy, and seeking a new type of energy has become an urgent need today. Lithium ion battery has become a preferred object as a power supply for current electronic products because of its high specific capacity, long cycle life, and high price-quality ratio. Core components of the lithium ion battery generally comprise a positive electrode, a negative electrode, and an electrolyte. A commercial lithium ion battery comprises a transition metal oxide or a polyanionic metal compound as the positive active material, graphite or carbon as the negative active material, and an ester-based electrolyte as the electrolyte. However, when graphite is used as the negative active material, graphite occupies a large part of the volume and weight of the battery, which limits the capacity and energy density of the lithium ion battery, and increases the complexity of the production procedures and the production cost.

DISCLOSURE OF THE INVENTION

In order to overcome the technical problems described above, the present disclosure provides a secondary battery and a preparation method therefor, and is intended to solve the problem that the existing lithium battery, in which graphite is used as a negative active material, has a low capacity and energy density, is produced by a complex production process, and has a high production cost.

In a first aspect, the present disclosure provides a secondary battery comprising a negative electrode, an electrolyte, a separator, and a positive electrode, wherein

the negative electrode comprises a negative current collector; the negative current collector comprises a metal or a metal alloy or a metal composite conductive material, and the negative current collector also acts as a negative active material;

the electrolyte comprises an electrolyte salt and a solvent, and the electrolyte salt is a lithium salt;

the positive electrode comprises a positive current collector and a positive active material layer, the positive active material layer comprises a positive active material capable of reversibly intercalating and de-intercalating lithium ions, and the positive current collector comprises a metal or a metal alloy or a metal composite conductive material.

Specifically, the positive active material includes one or several of, or a composite material of one of, lithium cobalt oxide, lithium nickel oxide, lithium manganese oxide, lithium iron phosphate, lithium nickel cobalt oxide binary material, spinel-structured lithium manganese, lithium nickel cobalt manganese oxide ternary material, and a layered lithium-rich high manganese material.

Specifically, the negative current collector includes one of aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese, or an alloy of any one thereof, or a composite of any one thereof.

Preferably, the negative current collector is aluminum.

Further, the structure of the negative current collector is an aluminum foil, or porous aluminum, or porous aluminum coated with a carbon material, or a multilayered composite material of aluminum.

Specifically, the positive current collector includes one of, or a composite of any one metal of, or an alloy of any one metal of, aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese.

Preferably, the positive current collector is aluminum.

Specifically, the electrolyte includes, but is not limited to, one or several of lithium hexafluorophosphate, lithium perchlorate, lithium tetrafluoroborate, lithium acetate, lithium salicylate, lithium acetoacetate, lithium carbonate, lithium trifluoromethanesulfonate, lithium lauryl sulfate, lithium citrate, lithium bis(trimethylsilyl)amide, lithium hexafluoroarsenate, and lithium bis(trifluoromethanesulfonyl)imide, and has a concentration ranging from 0.1 to 10 mol/L. Further, the concentration of the electrolyte salt is 0.5 to 2 mol/L.

Specifically, the solvent includes one or several of ester, sulfone, ether, and nitrile-based organic solvents, or ionic liquids.

Preferably, the solvent includes one or more of propylene carbonate, ethylene carbonate, butylene carbonate, diethyl carbonate, dimethyl carbonate, dipropyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, dibutyl carbonate, butyl methyl carbonate, methyl isopropyl carbonate, methyl ester, methyl formate, methyl acetate, N,N-dimethylacetamide, fluoroethylene carbonate, methyl propionate, ethyl propionate, ethyl acetate, γ-butyrolactone, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolane, 4-methyl-1,3-dioxolane, dimethoxymethane, 1,2-dimethoxy ethane, 1,2-dimethoxy propane, triethylene glycol dimethyl ether, dimethyl sulfone, dimethyl ether, ethylene sulfite, propylene sulfite, dimethyl sulfite, diethyl sulfite, and crown ether.

Further, the electrolyte also comprises an additive including one or several of ester, sulfone, ether, nitrile or alkene-based organic additives.

Preferably, the additive includes one or several of fluoroethylene carbonate, vinylene carbonate, vinyl ethylene carbonate, 1,3-propanesultone, 1,4-butanesultone, ethylene sulfate, propylene sulfate, vinylene sulfate, ethylene sulfite, propylene sulfite, dimethylsulfite, diethylsulfite, vinylene sulfite, methyl chloroformate, dimethyl sulfoxide, anisole, acetamide, diazine, pyrimidine, crown ether/12-crown-4, crown ether/18-crown-6, 4-fluoroanisole, fluorinated noncyclic ether, difluoromethyl ethylene carbonate, trifluoromethyl ethylene carbonate, chloroethylene carbonate, bromoethylene carbonate, trifluoromethyl phosphonic acid, bromobutyrolactone, ethyl fluoroacetate, phosphate, phosphite, phosphazene, ethanolamine, carbodiimide, cyclobutyl sulfone, 1,3-dioxolane, acetonitrile, a long-chain alkene, aluminum oxide, magnesium oxide, barium oxide, sodium carbonate, calcium carbonate, carbon dioxide, sulfur dioxide, and lithium carbonate.

Preferably, the additive is vinylene carbonate contained in an amount of 5 wt %.

Preferably, the positive active material layer also comprises a conductive agent and a binder, the content of the positive active material is 60 to 95 wt %, the content of the conductive agent is 0.1 to 30 wt %, and the content of the binder is 0.1 to 10 wt %.

In a second aspect, the present disclosure also provides a method for preparing the secondary battery described above, comprising:

preparing a negative electrode of the battery, wherein a metal or a metal alloy or a metal composite conductive material is cut into a desired size, washed, and then used as a battery negative electrode, the metal or metal alloy or metal composite conductive material acting as both a negative current collector and a negative active material;

preparing an electrolyte, wherein a certain amount of a lithium salt as an electrolyte salt is weighed out, added to a corresponding solvent, and fully stirred and dissolved to provide an electrolyte;

preparing a separator, wherein a porous polymer film, an inorganic porous film or a glass fiber-based film is cut into a desired size and washed clean;

preparing a battery positive electrode, wherein a positive active material, a conductive agent and a binder are weighed out in a certain ratio, added to a suitable solvent and sufficiently grinded into a uniform slurry; a metal or a metal alloy or a metal composite conductive material is taken and used as a positive current collector after its surface is washed; and then the slurry is uniformly applied to the surface of the positive current collector, and after the slurry is completely dried to form a positive active material layer, the positive current collector with the positive active material layer is cut to provide a battery positive electrode with a desired size; and

assembling the battery negative electrode, the electrolyte, the separator, and the battery positive electrode sequentially to provide a secondary battery.

Compared with the related art, the present disclosure has the following advantageous effects: due to the elimination of the conventional negative active material, the weight, volume and manufacturing cost of the battery are effectively reduced, and the production procedures are simplified; the capacity of the battery is effectively enhanced by using a negative current collector composed of a metal or a metal alloy or a metal composite also as a negative active material simultaneously; with the reduced weight and volume of the battery and the enhanced capacity of the battery, the energy density of the battery is remarkably increased, and the battery has a good charging and discharging cycle performance.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic structural diagram of the secondary battery provided in an embodiment of the present disclosure.

DETAILED DESCRIPTION OF EMBODIMENTS

The present disclosure will be further described in detail below with reference to the accompanying drawing and specific embodiments. The following description is illustrative of a preferred embodiment of the present disclosure. It should be noted that a number of improvements and modifications may be made by those skilled in the art without departing from the principle of the embodiments of the present disclosure, and such improvements and modifications are also considered within the scope of the present disclosure.

FIG. 1 is a schematic structural diagram of a secondary battery provided in an embodiment of the present disclosure. Referring to FIG. 1, a secondary battery provided in an embodiment of the present disclosure comprises a battery negative electrode 1, an electrolyte 2, a separator 3, a battery positive electrode (comprising a positive active material layer 4 and a positive current collector 5); wherein the battery negative electrode 1 comprises a negative current collector, the negative current collector comprises a metal or a metal alloy or a metal composite conductive material, and the negative current collector also acts as a negative active material; the electrolyte 2 comprises an electrolyte salt and a solvent, and the electrolyte salt is a lithium salt; the battery positive electrode comprises a positive current collector 5 and a positive active material layer 4, the positive current collector comprises metal or metal alloy or metal composite conductive material, and the positive active material layer comprises a positive active material capable of reversibly intercalating and de-intercalating lithium ions.

The working mechanism of the battery provided in the embodiment of the present disclosure is as follows: the secondary battery provided in the embodiment of the present disclosure does not contain a negative active material. During the charging process, lithium ions are de-intercalated from the positive active material and undergoes an alloying reaction with the metal or metal alloy or their composite material which acts as both negative electrode and negative current collector to form a lithium-metal alloy; during the discharging process, the lithium ions are de-intercalated from the lithium-metal alloy on the negative electrode and then intercalated into the positive active material so that the charging and discharging process is achieved. The main difference between the conventional lithium ion battery (i.e., comparative example) and the battery provided in the present application lies in the reactions that occur at the negative electrodes are different, namely, the reaction occurring in the conventional lithium ion battery is an intercalation-de-intercalation reaction of lithium ions, while the negative electrode of the secondary battery of the present disclosure undergoes alloying-dealloying reactions of lithium ions.

The battery provided in the embodiment of the present disclosure does not need conventional negative active material, so that the volume and the cost are reduced; meanwhile, the alloying reaction of the metal with the lithium ions provides a higher battery capacity. The energy density of the battery is remarkably increased by decreasing the weight and volume of the battery and enhancing the battery capacity, and the production cost can be reduced and the production procedures are simplified.

Specifically, in the embodiment of the present disclosure, the positive active material includes, but is not limited to, one or several or a composite material of lithium cobalt oxide (LiCoO₂), lithium nickel oxide (LiNiO₂), lithium manganese oxide (LiMn₂O₄), lithium iron phosphate (LiFePO₄), lithium nickel cobalt oxide binary material (LiNi_1-xCoxO₂), a spinel structure (LiMn_2-xMxO₄, M═Ni, Co, Cr or so forth), lithium nickel cobalt manganese oxide ternary material [Li(Ni,Co,Mn)O₂], a layered lithium-rich high manganese material [Li₂MnO₃—Li(NiCoMn)O₂], Li₃M₂(PO₄)₃ (M═V, Fe, Ti, or so forth) of a NASCION (Na Super Ionic Conductor) structure, etc.

Specifically, in the embodiment of the present disclosure, the negative current collector includes, but is not limited to, one of, or an alloy or metal composite of any one of, aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese.

Specifically, in the embodiment of the present disclosure, the positive current collector includes, but is not limited to, one of, or an alloy or metal composite of any one of, aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese.

Preferably, in the embodiment of the present disclosure, the negative current collector is aluminum.

Preferably, in the embodiment of the present disclosure, the positive current collector is aluminum.

In the present embodiment of the present disclosure, the solvent in the electrolyte is not particularly limited as long as the solvent can dissociate the electrolyte salt into cations and anions, and the cations and anions can freely migrate. For example, the solvent in the embodiment of the present disclosure is an ester, sulfone, ether, or nitrile-based organic solvent or ionic liquid. The solvent includes, but is not limited to, one or more of propylene carbonate, ethylene carbonate, butylene carbonate, diethyl carbonate, dimethyl carbonate, dipropyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, dibutyl carbonate, butyl methyl carbonate, methyl isopropyl carbonate, methyl ester, methyl formate, methyl acetate, N,N-dimethylacetamide, fluoroethylene carbonate, methyl propionate, ethyl propionate, ethyl acetate, γ-butyrolactone, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolane, 4-methyl-1,3-dioxolane, dimethoxymethane, 1,2-dimethoxy ethane, 1,2-dimethoxy propane, triethylene glycol dimethyl ether, dimethyl sulfone, dimethyl ether, ethylene sulfite, propylene sulfite, dimethyl sulfite, diethyl sulfite, and crown ether.

Further, in order to prevent damage of the negative current collector caused by the volume change during charging and discharging so that the structure and function of the negative current collector are stabilized and the service life and performance of the negative current collector are improved so as to improve the cycle efficiency of the secondary battery, the electrolyte in the embodiment of the present disclosure also comprises an additive, including, but not limited to, one or several of fluoroethylene carbonate, vinylene carbonate, vinyl ethylene carbonate, 1,3-propanesultone, 1,4-butanesultone, ethylene sulfate, propylene sulfate, vinylene sulfate, ethylene sulfite, propylene sulfite, dimethylsulfite, diethylsulfite, vinylene sulfite, methyl chloroformate, dimethyl sulfoxide, anisole, acetamide, diazine, pyrimidine, crown ether/12-crown-4, crown ether/18-crown-6,4-fluoroanisole, fluorinated noncyclic ether, difluoromethyl ethylene carbonate, trifluoromethyl ethylene carbonate, chloroethylene carbonate, bromoethylene carbonate, trifluoromethyl phosphonic acid, bromobutyrolactone, ethyl fluoroacetate, phosphate, phosphite, phosphazene, ethanolamine, carbodiimide, cyclobutyl sulfone, 1,3-dioxolane, acetonitrile, a long-chain alkene, aluminum oxide, magnesium oxide, barium oxide, sodium carbonate, calcium carbonate, carbon dioxide, sulfur dioxide, and lithium carbonate. Moreover, the content of the additive is from 0.1 to 20 wt %, and further from 1 to 5 wt %. The additive added in the electrolyte can form a stable solid electrolyte salt membrane on the surface of the negative current collector, so that the negative current collector is not damaged when reacting as an active material and can maintain its function and shape and increase the number of times of cycles of the battery.

Preferably, the additive is vinylene carbonate in an amount of 5 wt %.

Further, the positive active material layer also comprises a conductive agent and a binder, the content of the positive active material is 60 to 95 wt %, the content of the conductive agent is 0.1 to 30 wt %, and the content of the binder is 0.1 to 10 wt %. Moreover, the conductive agent and the binder are not particularly limited, and those commonly used in the art are applicable. The conductive agent is one or more of conductive carbon black, Super P conductive carbon spheres, conductive graphite KS6, carbon nanotube, conductive carbon fiber, graphene, and reduced graphene oxide. The binder is one or more of polyvinylidene fluoride, polytetrafluoroethylene, polyvinyl alcohol, carboxymethyl cellulose, SBR rubber, and polyolefins.

Further, more preferably, the negative current collector is aluminum foil, or porous aluminum, or porous aluminum coated with carbon material, or a multilayered composite material of aluminum. The use of the porous aluminum foil results in a more sufficient alloying reaction between the lithium ions de-intercalated from the positive active material with the aluminum metal to enhance the capacity of the battery; the use of the porous aluminum structure coated with carbon material is advantageous to maintaining the structural stability of aluminum due to the protection effect of the coated carbon layer to further improve the cycle stability of the battery, while enhancing the capacity of the battery; and the use of the multilayered composite material of aluminum is also advantageous to the inhibition and amelioration of the volume expansion effect of the aluminum foil to improve the cycle performance of the battery.

Specifically, the component of the separator used in the secondary battery provided in the embodiment of the present disclosure is an insulating, porous polymer film or inorganic porous film, including one or more of a porous polypropylene film, a porous polyethylene film, a porous composite polymer film, a glass fiber-based film, or a porous ceramic separator. The function of the separator is to physically insulate the positive and negative electrodes of the battery to prevent short circuit while allowing ions in the electrolyte to pass freely there through.

In a second aspect, an embodiment of the present disclosure also provides a method for preparing the secondary battery described above, comprising:

Step 101 of preparing a battery negative electrode, wherein a metal or a metal alloy or a metal composite conductive material is cut into a desired size, then a surface of the cut metal conductive material is washed, the washed metal conductive material is used as a negative current collector, and the negative current collector is used as the battery negative electrode;

Step 102 of preparing an electrolyte, wherein a certain amount of electrolyte salt is weighed out, added to a corresponding solvent, and fully stirred and dissolved;

Step 103 of preparing a separator, wherein a porous polymer film, an inorganic porous film or a glass fiber-based film is cut into a desired size and washed clean;

Step 104 of preparing a battery positive electrode, wherein a positive active material, a conductive agent and a binder are weighed out in a certain ratio, added to a suitable solvent and sufficiently grinded into a uniform slurry to form a positive active material layer; a metal or a metal alloy or a metal composite conductive material is used as a positive current collector with its surface washed; and then the positive active material positive active material layer is uniformly applied to the surface of the positive current collector, and after the positive active material layer is completely dried, the positive current collector with the positive active material layer is cut to provide the battery positive electrode with a desired size;

Step 105 of assembling with the battery negative electrode, the electrolyte, the separator, and the battery positive electrode.

Specifically, in the embodiment of the present disclosure, the metal conductive material in the Step 101 is one of aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese, or an alloy of any one thereof, or a composite of any one thereof.

In the embodiment of the present disclosure, the electrolyte salt in the Step 102 is a lithium salt, and the solvent includes an ester, sulfone, ether, or nitrile-based organic solvent. The preparation of the electrolyte also comprises: adding an additive to the solvent and stirring the same. Preferably, the solvent includes, but is not limited to, one or more of ethylene carbonate, diethyl carbonate, dimethyl carbonate, and ethyl methyl carbonate; the additive is one or several of vinylene carbonate, ethylene sulfite, propylene sulfite, ethylene sulfate, cyclobutyl sulfone, 1,3-dioxolane, acetonitrile, or a long-chain alkene.

Preferably, in the embodiment of the present disclosure, the positive active material in the Step 104 is selected from one or several of lithium cobalt oxide, lithium manganese oxide, lithium titanate, lithium nickel cobalt manganese oxide, or lithium iron phosphate. The metal conductive material includes, but is not limited to, one of aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese, or an alloy of any one thereof, or a composite of any one thereof.

Preferably, in the embodiment of the present disclosure, the Step 105 of assembling with the battery negative electrode, the electrolyte, the separator, and the battery positive electrode specifically comprises: stacking the prepared negative electrode, separator, and battery positive electrode closely successively under an inert gas or anhydrous and anaerobic condition, adding the electrolyte to completely impregnate the separator, and then packaging them into a battery case to complete the assembly of the battery.

It should be noted that although the operations of the preparation method of the present disclosure have been described in the above steps 101-104 in a specific order, this does not require or imply that these operations must be performed in the specific order. The preparations in the steps 101-104 can be performed simultaneously or in any sequence.

The method for preparing a secondary battery is based on the same inventive concept with the secondary battery described previously, and a secondary battery obtained by the method for preparing a secondary battery has all the effects of the secondary battery described previously and therefore will not be described in detail here.

The above-mentioned method for preparing a secondary battery will be further described below by way of specific examples. However, it should be understood that these examples are only used for a more detailed description, and should not be construed as limiting the present disclosure in any way.

Example 1

Preparation of negative electrode of a battery: an aluminum foil with a thickness of 0.02 mm was taken, cut into a disc with a diameter of 12 mm, washed with ethyl alcohol, and dried by airing so as to be used as a negative current collector.

Preparation of a separator: a glass fiber paper was cut into a disc with a diameter of 16 mm, and dried by baking so as to be used as a separator.

Preparation of an electrolyte: 1.5 g of lithium hexafluorophosphate (at a concentration of 1 mol/L) was weighed out and added to a mixed solvent composed of 3.2 mL of ethylene carbonate, 3.2 mL of dimethyl carbonate and 3.2 mL of ethyl methyl carbonate, to which 5% by weight of vinylene carbonate (0.545 g) was added as an additive, and was stirred sufficiently until the lithium hexafluorophosphate was completely dissolved so as to be used as an electrolyte.

Preparation of positive electrode of a battery: 0.4 g of lithium cobalt oxide, 0.05 g of carbon black, and 0.05 g of polyvinylidene fluoride were added to 2 mL of a N-methylpyrrolidone solution, and grinded sufficiently to provide a uniform slurry; and then the slurry was uniformly applied to the surface of an aluminum foil and dried in vacuum. The dried electrode sheet was cut into a disc with a diameter of 10 mm, and compacted so as to be used as a positive electrode.

The assembly of a battery: in a glove box under the protection of inert gas, the above prepared negative current collector, separator and battery positive electrode were stacked closely in this order, to which the electrolyte was added dropwise to completely impregnate the separator, and then the above stacked parts were packaged in a button battery case to complete the assembly of the battery.

Comparative Example

Preparation of negative electrode of a battery: 0.4 g of graphite, 0.05 g of carbon black, and 0.05 g of polyvinylidene fluoride were added to 2 mL of a N-methylpyrrolidone solution, and grinded sufficiently to provide a uniform slurry; and then the slurry was uniformly applied to the surface of an aluminum foil and dried in vacuum. The dried electrode sheet was cut into a disc with a diameter of 10 mm, and compacted so as to be used as a negative electrode.

Preparation of a separator: polymeric polyethylene was cut into a disc with a diameter of 16 mm, and dried by baking so as to be used as a separator.

Preparation of an electrolyte: 0.75 g of lithium hexafluorophosphate was weighed out and added to 2.5 mL of ethylene carbonate and 2.5 mL of dimethyl carbonate, and was stirred sufficiently until the lithium hexafluorophosphate was completely dissolved so as to be used as an electrolyte.

Preparation of positive electrode of a battery: 0.4 g of lithium cobalt oxide as a positive electrode material, 0.05 g of carbon black, and 0.05 g of polyvinylidene fluoride were added to 2 mL of a N-methylpyrrolidone solution, and grinded sufficiently to provide a uniform slurry; and then the slurry was uniformly applied to the surface of an aluminum foil and dried in vacuum. The dried electrode sheet was cut into a disc with a diameter of 10 mm, and compacted so as to be used as a battery positive electrode.

The assembly of a battery: in a glove box under the protection of inert gas, the above prepared negative current collector, separator and battery positive electrode were stacked closely successively, to which the electrolyte was added dropwise to completely impregnate the separator, and then the above stacked parts were packaged in a button battery case to complete the assembly of the battery.

Battery Performance Testing

Charging-discharging Test: the secondary battery prepared in the embodiment of the above method for preparing a secondary battery was charged with a constant current of 100 mA/g of the positive active material until its voltage reached 4.2 V, and then discharged at the same current until its voltage reached 3 V, its battery capacity and energy density were measured, and its cycle stability was tested and expressed by the number of cycles, which refers to the number of times of charges and discharges of the battery when the battery capacity decays to 85%.

The electrochemical performance of the secondary battery provided in Example 1 of the present disclosure was tested, and compared with the performance of the conventional lithium ion battery mentioned in the Background Art, and the results and comparison were shown in Table 1.

TABLE 1
Comparison of Electrochemical Performance Parameters of Example 1 and the Conventional Lithium Ion Battery in the Background Art
	Posi-	Posi-	Nega-	Nega-	Electrochemical
	tive	tive	tive	tive	Performance
	current	active	current	active	Electrolyte	Working	Energy
	collec-	mate-	collec-	mate-	Electrolyte		Concen-	Voltage	Density		Working
No.	tor	rial	tor	rial	salt	Solvent	tration	(V)	(Wh/kg)	Cost	Mechanism
Example 1	Al foil	lithium	Al foil (acting as both	LiPF6	ethylene carbonate +	1M	3.6 V	263	low	Negative
		cobalt	the current collector		dimethyl					electrode:Al +
		oxide	and the negative		carbonate +					Li+ + e−↔AlLi;
			active material)		ethyl methyl					Positive
					carbonate					electrode:LiCoO2 ↔
					(1:1:1) + 5%					Li1−xCoO2 +
					vinylene					xLi+ + xe−
					carbonate as an
					additive
conven-	Al foil	lithium	Al foil	graphite	LiPF6	ethylene	1M	3.7 V	170	high	Negative
tional		con-				carbonate:ethyl					electrode:6C +
lithium		taining				methyl					Li+ + e−   LiC6;
ion battery		com-				carbonate:dimethyl					Positive
		pound				carbonate = 1:1:1					electrode:LiCoO2
											Li1−xCoO2 + Li+ + e−

As can be seen from Table 1, the secondary battery of Example 1 of the present disclosure contains no graphite in the negative electrode, has reduced raw material cost and process cost, and has a further increased energy density, as compared with the conventional lithium ion battery.

Examples 2-18

Examples 2-18 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the material selected for the negative current collector is different. See Table 2 for details.

TABLE 2
Comparison of Performance of Batteries with
Different Negative Current Collectors
	Electrochemical Performance
			Number of times
		Specific	of cycles (times)	Energy
	Negative current	Capacity	when the capacity	Density
No.	collector	(mAh/g)	decays to 90%	(Wh/kg)
Example 1	aluminum foil	170	250	263
Example 2	magnesium foil	150	30	232
Example 3	lithium foil	170	250	263
Example 4	vanadium foil	140	50	217
Example 5	copper foil	120	100	186
Example 6	iron foil	120	100	186
Example 7	tin foil	150	150	232
Example 8	zinc foil	170	200	263
Example 9	nickel foil	140	150	217
Example 10	titanium foil	150	200	232
Example 11	manganese foil	120	150	186
Example 12	aluminum-tin	170	220	263
	alloy
Example 13	aluminum-	170	220	263
	titanium alloy
Example 14	iron-tin alloy	140	180	217
Example 15	porous aluminum	170	150	263
Example 16	porous aluminum	170	500	263
	@ C
Example 17	porous aluminum	170	500	263
	@ graphene
Example 18	multilayered	170	500	263
	aluminum com-
	posite material

As can be seen from Table 2, when aluminum foil and the related composite materials thereof are selected as the negative current collector, the battery has a higher specific capacity, better cycle performance, higher energy density, and lower cost.

Examples 19-29

Examples 19-29 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the material selected for the positive active material is different. See Table 3 for details.

TABLE 3
Comparison of Performance of Batteries with Different Positive Active Materials
	Electrochemical Performance
			Number of times
		Specific	of cycles (times)	Energy
		Capacity	when the capacity	Density
No.	Positive active material	(mAh/g)	decays to 90%	(Wh/kg)
Example 1	lithium cobalt oxide	170	250	263
Example 19	lithium nickel oxide	150	250	232
Example 20	layered lithium manganese oxide	120	250	186
Example 21	lithium iron phosphate	120	500	186
Example 22	Spinel-type lithium manganese oxide	100	200	155
Example 23	lithium nickel cobalt oxide binary material	150	250	232
Example 24	lithium nickel cobalt manganese oxide ternary	170	250	263
	material
Example 25	layered lithium-rich high manganese material	250	250	387
Example 26	lithium cobalt oxide + lithium iron phosphate	150	300	232
Example 27	lithium manganese oxide + lithium nickel cobalt	150	250	232
	manganese oxide ternary material
Example 28	lithium cobalt oxide @ graphene	170	400	263
Example 29	lithium iron phosphate @ C	120	700	186

Examples 30-45

Examples 30-45 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the electrolyte salt is different. See Table 4 for details.

TABLE 4
Comparison of Performance of Batteries with Different Electrolyte Salts
	Electrochemical Performance
			Number of times
		Specific	of cycles (times)	Energy
		Capacity	when the capacity	Density
No.	Electrolyte Salt	(mAh/g)	decays to 90%	(Wh/kg)
Example 1	lithium hexafluorophosphate	170	250	263
Example 30	lithium perchlorate	160	240	248
Example 31	lithium acetate	100	150	155
Example 32	lithium tetrafluoroborate	150	220	232
Example 33	lithium salicylate	100	100	155
Example 34	lithium acetoacetate	80	120	124
Example 35	lithium carbonate	80	120	124
Example 36	lithium trifluoromethanesulfonate	120	150	186
Example 37	lithium citrate	80	150	124
Example 38	lithium lauryl sulfate	130	180	201
Example 39	lithium bis(trimethylsilyl)amide	150	180	232
Example 40	lithium hexafluoroarsenate	140	200	217
Example 41	lithium bis(trifluoromethanesulfonyl)imide	160	150	248
Example 42	lithium hexafluorophosphate + lithium carbonate	160	300	248
Example 43	lithium tetrafluoroborate + lithium citrate	140	180	217
Example 44	lithium trifluoromethanesulfonate + lithium	140	250	217
	bis(trimethylsilyl)amide
Example 45	lithium hexafluorophosphate + lithium	140	200	217
	perchlorate + lithium tetrafluoroborate

As can be seen from Table 4, when the electrolyte salt is LiPF₆, the battery has higher specific capacity, better cycle stability, and higher energy density.

Example 46-50

Examples 46-50 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the concentration of the electrolyte salt is different. See Table 5 for details.

TABLE 5
Comparison of Performance of Batteries with
Different Electrolyte Salt Concentrations
	Electrochemical Performance
			Number of times
	Electrolyte	Specific	of cycles (times)	Energy
	Salt	Capacity	when the capacity	Density
No.	Concentration	(mAh/g)	decays to 90%	(Wn/kg)
Example 46	0.1M	120	250	186
Example 47	0.5M	140	250	217
Example 1	1M	170	250	263
Example 48	2M	170	180	263
Example 49	3M	170	100	263
Example 50	4M	170	50	263

As can be seen from Table 5, when the concentration of the electrolyte salt is 1 M (mol/L), the specific capacity, energy density and cycle performance of the battery are all higher.

Examples 51-94

Examples 51-94 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the type of the solvent in the electrolyte is different. See Table 6 for details.

TABLE 6
Comparison of Performance of Batteries with
Different Solvents in the Electrolytes
	Electrochemical Performance
		Number of times
		of cycles (times)	Energy
		when the capacity	Density
No.	Solvent of the electrolyte	decays to 90%	(Wh/kg)
Example 51	propylene carbonate	100	100
Example 52	ethylene carbonate	50	60
Example 53	diethyl carbonate	150	140
Example 54	dimethyl carbonate	150	140
Example 55	ethyl methyl carbonate	150	140
Example 56	methyl formate	100	60
Example 57	methyl acetate	100	80
Example 58	N,N-dimethylacetamide	120	50
	(DMA)
Example 59	fluoroethylene carbonate	150	120
	(FEC)
Example 60	methyl propionate (MP)	100	80
Example 61	ethyl propionate (EP)	100	80
Example 62	ethyl acetate (EA)	100	80
Example 63	γ-butyrolactone (GBL)	80	60
Example 64	tetrahydrofuran (THF)	50	120
Example 65	triethylene glycol dimethyl	80	140
	ether (DG)
Example 66	propylene sulfite (PS)	100	160
Example 67	dimethyl sulfone (MSM)	80	150
Example 68	dimethyl ether (DME)	50	100
Example 69	ethylene sulfite (ES)	60	160
Example 70	dipropyl carbonate	150	140
Example 71	butylene carbonate	150	140
Example 72	methyl propyl carbonate	180	140
Example 73	dibutyl carbonate	180	140
Example 74	methyl butyl carbonate	160	140
Example 75	methyl isopropyl carbonate	120	120
Example 76	methyl ester	80	100
Example 77	2-methyltetrahydrofuran	60	80
Example 78	1,3-dioxolane	60	60
Example 79	4-methyl-1,3-dioxolane	50	60
Example 80	dimethoxymethane	50	80
Example 81	1,2-dimethoxypropane	80	80
Example 82	dimethyl sulfite	120	140
Example 83	diethyl sulfite	120	140
Example 84	crown ether	80	80
Example 85	dimethoxymethane +	50	80
	1,2-dimethoxypropane
	(v/v 1:1)
Example 86	methyl isopropyl car-	100	140
	bonate + methyl butyl
	carbonate (v/v 1:1)
Example 87	ethylene carbonate +	180	200
	propylene carbonate
	(v/v 1:1)
Example 88	ethylene carbonate +	200	240
	ethyl methyl carbonate
	(v/v 1:1)
Example 89	ethylene carbonate +	200	240
	dimethyl carbonate
	(v/v 1:1)
Example 90	ethylene carbonate +	160	180
	dimethyl ether (v/v 1:1)
Example 91	ethylene carbonate +	150	180
	dimethylsulfoxide (v/v 1:1)
Example 92	triethylene glycol dimethyl	100	80
	ether + sulfolane (v/v 1:1)
Example 93	ethylene carbonate +	220	240
	ethyl methyl carbonate +
	propylene carbonate
	(v/v/v 1:1:1)
Example 94	ethyl methyl carbonate +	150	180
	tetrahydrofuran + di-
	methoxymethane + 1,2-
	dimethoxypropane
	(v/v/v 1:1:1)
Example 1	ethylene carbonate +	250	263
	ethyl methyl carbonate +
	dimethyl carbonate
	(v/v/v 1:1:1)

Examples 95-145

Examples 95-145 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the type of the additive in the electrolyte is different. See Table 7 for details.

TABLE 7
Comparison of Performance of Batteries with Different Additives in the Electrolytes
	Electrochemical Performance
		Number of times
		of cycles (times)	Energy
		when the capacity	Density
No.	Additive in the Electrolyte	decays to 90%	(Wh/kg)
Example 1	vinylene carbonate (5 wt %)	250	263
Example 95	vinylene sulfite (5 wt %)	220	263
Example 96	propylene sulfite (5 wt %)	200	256
Example 97	ethylene sulfate (5 wt %)	220	240
Example 98	ethylene sulfite (5 wt %)	230	240
Example 99	acetonitrile (5 wt %)	200	240
Example 100	long-chain alkene (5 wt %)	180	240
Example 101	vinyl ethylene carbonate (5 wt %)	220	240
Example 102	1,3-propanesultone (5 wt %)	160	240
Example 103	1,4-butanesultone (5 wt %)	160	245
Example 104	propylene sulfate (5 wt %)	220	256
Example 105	1,3-dioxolane (5 wt %)	160	213
Example 106	dimethylsulfite (5 wt %)	200	240
Example 107	diethylsulfite (5 wt %)	200	240
Example 108	methyl chloroformate (5 wt %)	180	235
Example 109	dimethyl sulfoxide (5 wt %)	180	230
Example 110	anisole (5 wt %)	160	230
Example 111	acetamide (5 wt %)	160	230
Example 112	diazine (5 wt %)	140	205
Example 113	pyrimidine (5 wt %)	140	230
Example 114	crown ether/12-crown-4 (5 wt %)	140	220
Example 115	crown ether/18-crown-6 (5 wt %)	140	220
Example 116	4-fluoroanisole (5 wt %)	160	260
Example 117	fluorinated noncyclic ether (5 wt %)	140	230
Example 118	difluoromethyl ethylene carbonate (5 wt %)	140	230
Example 119	trifluoromethyl ethylene carbonate (5 wt %)	140	240
Example 120	chloroethylene carbonate (5 wt %)	140	240
Example 121	bromoethylene carbonate (5 wt %)	140	240
Example 122	trifluoromethyl phosphonic acid (5 wt %)	150	240
Example 123	bromobutyrolactone (5 wt %)	150	230
Example 124	fluoroacetoxyethane (5 wt %)	180	230
Example 125	phosphate (5 wt %)	150	220
Example 126	phosphite (5 wt %)	150	220
Example 127	phosphazene (5 wt %)	200	220
Example 128	ethanolamine (5 wt %)	200	230
Example 129	carbodiimide (5wt %)	180	225
Example 130	cyclobutyl sulfone (5 wt %)	220	230
Example 131	aluminum oxide (5 wt %)	200	240
Example 132	magnesium oxide (5 wt %)	200	240
Example 133	barium oxide (5 wt %)	200	240
Example 134	sodium carbonate (5 wt %)	200	240
Example 135	calcium carbonate (5 wt %)	200	256
Example 136	carbon dioxide (5 wt %)	180	255
Example 137	sulfur dioxide (5 wt %)	180	253
Example 138	lithium carbonate (5 wt %)	240	253
Example 139	fluoroethylene carbonate (5 wt %)	120	260
Example 140	vinylene carbonate (2.5 wt %) +	160	260
	vinylene sulfite (2.5 wt %)
Example 141	ethanolamine (2.5 wt %) + vinyl	150	240
	ethylene carbonate (2.5 wt %)
Example 142	dimethylsulfoxide (2.5 wt %) +	150	225
	diazine (2.5 wt %)
Example 143	propylene sulfite (2.5 wt %) +	180	240
	aluminum oxide (2.5 wt %)
Example 144	lithium carbonate (2.5 wt %) +	220	256
	barium carbonate (2.5 wt %)

Examples 145-151

Examples 145-151 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the content of the additive in the electrolyte is different. See Table 8 for details.

TABLE 8
Comparison of Performance of Batteries
with Different Amounts of Additives
	Electrochemical Performance
	Content of	Number of times of cycles	Energy
	the Additive in	(times) when the capacity	Density
No.	the electrolyte	decays to 90%	(Wh/kg)
Example 145	0.1	wt %	50	300
Example 146	1	wt %	120	250
Example 147	2	wt %	200	255
Example 148	3	wt %	220	263
Example 149	5	wt %	250	263
Example 1	10	wt %	180	263
Example 150	15	wt %	100	255
Example 151	20	wt %	50	250

As can be seen from Table 8, the cycle stability of the battery is best when the content of the additive is 5 wt %.

Examples 152-153

Examples 152-153 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the type of the separator is different. See Table 9 for details.

TABLE 9
Comparison of Performance of Batteries with Different Separators
	Electrochemical Performance
		Number of times of cycles	Energy
		(times) when the capacity	Density
No.	Separator	decays to 90%	(Wh/kg)
Example 1	glass fiber paper	250	263
Example 152	porous polymer	250	263
	separator
Example 153	inorganic porous	250	263
	film

It can be seen from Table 9 that the conventional separators can be selected and used as the separator, all of which enable the secondary battery of the present disclosure to obtain better cycle performance and higher energy density.

Examples 154-159

Examples 154-159 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the active material, the conductive agent, and the binder in the positive electrode material are different in type and percentage by weight. See Table 10 for details.

TABLE 10
Comparison of Performance of Batteries with Different Amounts
of Positive Active Materials, Conductive Agents, and Binders
	Electrochemical Performance
	Number of times
	Positive Electrode Material	of cycles (times)	Energy
	Active Material	Conductive Agent	Binder	when the capacity	Density
No.	(percentage by weight)	(percentage by weight)	(percentage by weight)	decays to 90%	(Wh/kg)
Example 1	lithium cobalt oxide	acetylene black	polyvinylidene fluoride	250	263
	(80%)	(10%)	(10%)
Example 154	lithium cobalt oxide	conductive carbon spheres	polytetrafluoroethylene	220	250
	(90%)	(0.1%)	(9.9%)
Example 155	lithium cobalt oxide	conductive graphite	polyvinyl alcohol	220	250
	(60%)	(30%)	(10%)
Example 156	lithium cobalt oxide	carbon nanotube	polypropylene	180	250
	(90%)	(9.9%)	(0.1%)
Example 157	lithium cobalt oxide	graphene (5%)	carboxymethyl cellulose +	200	260
	(90%)		SBR (5%)
Example 158	lithium cobalt oxide	conductive carbon fiber	polyvinylidene fluoride	200	260
	(90%)	(5%)	(5%)
Example 159	lithium cobalt oxide	acetylene black + carbon	polyvinylidene fluoride	200	260
	(90%)	nanotube (5%)	(5%)

Examples 160-172

Examples 160-172 are the same as Example 1 in the steps of the process for preparing a secondary battery, except that the type of the positive current collector is different. See Table 11 for details.

TABLE 11
Comparison of Performance of Batteries with
Different Positive Current Collectors
	Electrochemical Performance
			Number of times
	Positive	Specific	of cycles (times)	Energy
	current	Capacity	when the capacity	Density
No.	collector	(mAh/g)	decays to 90%	(Wh/kg)
Example 1	aluminum foil	170	250	263
Example 160	magnesium foil	170	250	263
Example 161	lithium foil	170	250	263
Example 162	vanadium foil	170	250	263
Example 163	copper foil	170	250	263
Example 164	iron foil	170	250	263
Example 165	tin foil	170	250	263
Example 166	zinc foil	170	250	263
Example 167	nickel foil	170	250	263
Example 168	titanium foil	170	250	263
Example 169	manganese foil	170	250	263
Example 170	copper-zinc	170	250	263
	alloy
Example 171	tin-iron alloy	170	250	263
Example 172	nickel-zinc	170	250	263
	alloy

Claims

1. A secondary battery comprising a battery negative electrode, an electrolyte, a separator, and a battery positive electrode, wherein the battery negative electrode comprises a negative current collector; the negative current collector is made of a metal or a metal alloy or a metal composite conductive material, and the negative current collector also acts as a negative active material;the electrolyte comprises an electrolyte salt and a solvent, and the electrolyte salt is a lithium salt;the battery positive electrode comprises a positive current collector and a positive active material layer, wherein the positive active material layer comprises a positive active material capable of reversibly de-intercalating and intercalating lithium ions, and the positive current collector is made of a metal or a metal alloy or a metal composite conductive material;wherein a structure of the negative current collector is a porous aluminum coated with a carbon material.

2. The secondary battery according to claim 1, wherein the negative current collector comprises one of aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium, and manganese, or an alloy of any one thereof, or a composite of at least two selected from the above materials.

3. The secondary battery according to claim 1, wherein the positive active material comprises one or more selected from the group consisting of lithium cobalt oxide, lithium nickel oxide, lithium manganese oxide, lithium iron phosphate, lithium nickel cobalt oxide binary material, spinel-structured oxide, lithium nickel cobalt manganese oxide ternary material, and a layered lithium-rich high-manganese material, or comprises a composite material of one selected from the above group.

4. The secondary battery according to claim 1, wherein the positive current collector comprises one selected from the group consisting of aluminum, magnesium, lithium, vanadium, copper, iron, tin, zinc, nickel, titanium and manganese, or a composite of one selected from the above group, or an alloy of one selected from the above group.

5. The secondary battery according to claim 1, wherein the electrolyte salt includes one or more selected from the group consisting of lithium hexafluorophosphate, lithium perchlorate, lithium tetrafluoroborate, lithium acetate, lithium salicylate, lithium acetoacetate, lithium carbonate, lithium trifluoromethanesulfonate, lithium lauryl sulfate, lithium citrate, lithium bis(trimethylsilyl)amide, lithium hexafluoroarsenate, and lithium bis(trifluoromethanesulfonyl)imide, and has a concentration ranging from 0.1 to 10 mol/L.

6. The secondary battery according to claim 5, wherein the concentration of the electrolyte salt is 0.5 to 2 mol/L.

7. The secondary battery according to claim 5, wherein the electrolyte salt is lithium hexafluorophosphate at a concentration of 1 mol/L.

8. The secondary battery according to claim 1, wherein the solvent comprises one or more selected from the group consisting of ester, sulfone, ether, and nitrile organic solvents, and ionic liquids.

9. The secondary battery according to claim 8, wherein the solvent comprises one or more selected from the group consisting of propylene carbonate, ethylene carbonate, butylene carbonate, diethyl carbonate, dimethyl carbonate, dipropyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, dibutyl carbonate, butyl methyl carbonate, methyl isopropyl carbonate, methyl ester, methyl formate, methyl acetate, N,N-dimethylacetamide, fluoroethylene carbonate, methyl propionate, ethyl propionate, ethyl acetate, γ-butyrolactone, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolane, 4-methyl-1,3-dioxolane, dimethoxymethane, 1,2-dimethoxyethane, 1,2-dimethoxy propane, triethylene glycol dimethyl ether, dimethyl sulfone, dimethyl ether, ethylene sulfite, propylene sulfite, dimethyl sulfite, diethyl sulfite, and crown ether.

10. The secondary battery according to claim 9, wherein the solvent is ethylene carbonate, ethyl methyl carbonate and dimethyl carbonate in a volume ratio of 1:1:1, or ethylene carbonate and dimethyl carbonate in a volume ratio of 1:1, or ethylene carbonate and ethyl methyl carbonate in a volume ratio of 1:1.

11. The secondary battery according to claim 1, wherein the electrolyte further comprises an additive, and the additive comprises one or more selected from the group consisting of ester, sulfone, ether, nitrile or alkene organic additives.

12. The secondary battery according to claim 11, wherein the additive comprises one or more selected from the group consisting of fluoroethylene carbonate, vinylene carbonate, vinyl ethylene carbonate, 1,3-propanesultone, 1,4-butanesultone, ethylene sulfate, propylene sulfate, vinylene sulfate, ethylene sulfite, propylene sulfite, dimethylsulfite, diethylsulfite, vinylene sulfite, methyl chloroformate, dimethyl sulfoxide, anisole, acetamide, diazine, pyrimidine, crown ether/12-crown-4, crown ether/18-crown-6, 4-fluoroanisole, fluorinated noncyclic ether, difluoromethyl ethylene carbonate, trifluoromethyl ethylene carbonate, chloroethylene carbonate, bromoethylene carbonate, trifluoromethyl phosphonic acid, bromobutyrolactone, ethyl fluoroacetate, phosphate, phosphite, phosphazene, ethanolamine, carbodiimide, cyclobutyl sulfone, 1,3-dioxolane, acetonitrile, long-chain alkene, aluminum oxide, magnesium oxide, barium oxide, sodium carbonate, calcium carbonate, carbon dioxide, sulfur dioxide, and lithium carbonate.

13. The secondary battery according to claim 11, wherein in the electrolyte, a content of the additive is 0.1 to 20 wt % by weight.

14. The secondary battery according to claim 12, wherein in the electrolyte, the additive is vinylene carbonate and wherein a content of the additive is 1 to 5 wt % by weight.

15. The secondary battery according to claim 12, wherein in the electrolyte, the additive is ethylene sulfite, propylene sulfite, or vinylene sulfite, and wherein a content of the additive is 1 to 5 wt % by weight.

16. The secondary battery according to claim 1, wherein the positive active material layer further comprises a conductive agent and a binder, wherein a content of the positive active material is 60 to 95 wt %, a content of the conductive agent is 0.1 to 30 wt %, and a content of the binder is 0.1 to 10 wt %.

17. The secondary battery according to claim 1, wherein the separator is an insulating porous polymer film or inorganic porous film, comprising one or more selected from the group consisting of a porous polypropylene film, a porous polyethylene film, a porous composite polymer film, a glass fiber-based film, and a porous ceramic separator.

18. A method for preparing a secondary battery, comprising: preparing a negative electrode, wherein a metal or a metal alloy or a metal composite conductive material is cut to be in a desired size, washed clean, and then used as the negative electrode, wherein the metal or the metal alloy or the metal composite conductive material acts as both a negative current collector and a negative active material simultaneously, wherein a structure of the negative current collector is a porous aluminum coated with a carbon material;preparing an electrolyte, wherein a certain amount of a lithium salt is weighed and added to a corresponding solvent, fully stirred and dissolved to obtain the electrolyte;preparing a separator, wherein a porous polymer film, an inorganic porous film or a glass fiber film is cut to be in a desired size and washed clean;preparing a battery positive electrode, wherein a positive active material, a conductive agent and a binder are weighed in a certain ratio, added to a suitable solvent and sufficiently grinded into a uniform slurry; a metal or a metal alloy or a metal composite conductive material, after a surface thereof is washed clean, is used as a positive current collector; and then the slurry is uniformly applied to a surface of the positive current collector, and after the slurry is completely dried to form a positive active material layer, the positive current collector with the positive active material layer is cut to act as the battery positive electrode with a desired size; andassembling the battery negative electrode, the electrolyte, the separator, and the battery positive electrode sequentially to obtain the secondary battery.

19. A secondary battery comprising a battery negative electrode, an electrolyte, a separator, and a battery positive electrode, wherein the battery negative electrode comprises a negative current collector; the negative current collector is made of a metal or a metal alloy or a metal composite conductive material, and the negative current collector also acts as a negative active material;the electrolyte comprises an electrolyte salt and a solvent, and the electrolyte salt is a lithium salt;the battery positive electrode comprises a positive current collector and a positive active material layer, wherein the positive active material layer comprises a positive active material capable of reversibly de-intercalating and intercalating lithium ions, and the positive current collector is made of a metal or a metal alloy or a metal composite conductive material;wherein a structure of the negative current collector is a multilayered composite material of aluminum.