CN109309243A - Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery - Google Patents

Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery Download PDF

Info

Publication number
CN109309243A
CN109309243A CN201710609085.7A CN201710609085A CN109309243A CN 109309243 A CN109309243 A CN 109309243A CN 201710609085 A CN201710609085 A CN 201710609085A CN 109309243 A CN109309243 A CN 109309243A
Authority
CN
China
Prior art keywords
lithium
alloy
carbon composite
lithium alloy
skeleton carbon
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201710609085.7A
Other languages
Chinese (zh)
Inventor
康拓
陈立桅
卢威
沈炎宾
王亚龙
郭峰
刘承浩
陈鹏
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China Amperex Technology Ltd (tianjin)
Original Assignee
China Amperex Technology Ltd (tianjin)
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China Amperex Technology Ltd (tianjin) filed Critical China Amperex Technology Ltd (tianjin)
Priority to CN201710609085.7A priority Critical patent/CN109309243A/en
Priority to PCT/CN2017/105656 priority patent/WO2019019409A1/en
Publication of CN109309243A publication Critical patent/CN109309243A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • H01M10/0525Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/661Metal or alloys, e.g. alloy coatings
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/663Selection of materials containing carbon or carbonaceous materials as conductive part, e.g. graphite, carbon fibres
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/665Composites
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

The present invention provides a kind of lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery.The lithium alloy-skeleton carbon composite includes on porous carbon materials carrier and the surface for being formed in the porous carbon materials carrier and intrapore lithium alloy.According to the technique and scheme of the present invention, compound by carrying out lithium alloy with skeleton carbon carrier, lithium metal can be effectively improved to the wellability of skeleton carbon, to improve the affinity of lithium metal and skeleton carbon, increase the load lithium amount in lithium material.

Description

Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery
Technical field
The present invention relates to energy battery field, specifically, the present invention provide a kind of lithium alloy-skeleton carbon composite and Preparation method includes the lithium alloy-skeleton carbon composite cathode and lithium battery.
Background technique
Lithium ion battery has been widely used for the every field of today's society as the representative of clean energy resource.Lithium from Sub- battery is due to characteristics such as high-energy density, environment friendly and good cyclical stabilities, by people's Favor.However, with the development of society, the energy density of traditional lithium ion battery to can no longer meet people growing Horsepower requirements.In addition, problem of environmental pollution is the maximum popular problem of today's society, the common recognition of present society is to develop clearly The clean energy replaces traditional petroleum-based energy, therefore to develop the lithium dynamical battery with higher energy density be the current energy The most important thing in field.
Since lithium anode has the specific capacity for decupling conventional graphite cathode, 3860mAh/g, and metal are reached Lithium has most negative current potential and most light density, therefore will have great raising using the energy density of the battery of cathode of lithium. In addition, lithium an- ode can provide lithium ion for anode, therefore can be with energy density higher no lithium anode such as sulphur, air Deng lithium sulphur-lithium-air battery of composition high-energy density.If the battery is commercialized, energy density can and gasoline It compares favourably, therefore environmental problem will be greatly improved.Unfortunately, lithium anode is easy to produce branch in cyclic process Crystalline substance, with the progress that battery works, the dendrite constantly grown can pierce through battery diaphragm and cause battery short circuit and release huge Heat causes a series of safety accidents such as burning, explosion.Furthermore the SEI layer on lithium metal surface in charge and discharge process is constantly grown Active material and electrolyte are consumed, the cycle life of battery is reduced.
FMC Corp. of the U.S. prepares the gold that can be applied to lithium cell cathode material using the method for melting emulsification modified again Belong to lithium particle (referring to US 8,021,496B2,102255080 A of 2013/0181160 US A1, CN).However utilize this method The lithium metal grain diameter prepared is 20-100 microns, and partial size is larger and wider distribution, can not effectively inhibit lithium The generation of dendrite.Meanwhile the material does not have the support of internal structure, and huge body can be generated in the charge and discharge process of large capacity Product variation, is unfavorable for the cycle performance of battery.Suzhou Institute of Nano-tech. and Nano-bionics, Chinese Academy of Sciences discloses one kind Lithium metal-skeleton carbon composite material and preparation method, cathode and secondary cell are (referring to PCT International Publication No. WO 2015139660A1;Chinese Patent Application No. CN 201410395114.0).Wherein, using stephanoporate framework carbon material as carrier It is mixed with molten metal lithium, prepares lithium metal-skeleton carbon composite that particle size range is 1-100 microns, safety It is substantially better than metal lithium sheet.However, the wellability of lithium metal and carbon skeleton is bad, the lithium metal prepared-skeleton carbon composite wood The load lithium amount of material is low and specific capacity is low.Furthermore Yi Cui seminar is by CVD method on electrostatic spinning carbon fiber film surface The close lithium of carbon material is improved by deposition Si or ZnO (referring to PNAS.1518188113, Nat.Commun.7:10992). However this method needs the complicated processing of CVD, is difficult to produce in enormous quantities in the short time.
Therefore, a kind of load lithium amount that can be improved skeleton carbon composite, the method tool to improve specific capacity are developed There is important meaning.
Summary of the invention
From technical problem described above, the purpose of the present invention is the lithium alloys by using melting to mix with skeleton carbon It closes, lithium alloy-skeleton carbon compound cathode is prepared by simple and fast method, which improves the parent of lithium metal and skeleton carbon And power, the load lithium amount of material is improved, and improve the specific capacity of material in turn.
The present inventor passes through thoroughgoing and painstaking research, completes the present invention.According to the technique and scheme of the present invention, by by one The method that a little specific metallic elements and molten lithium are mixed with lithium alloy reduces the surface energy of lithium metal, so that lithium metal More easily adhere in skeleton carbon, to obtain the higher lithium alloy of capacity-skeleton carbon composite.
According to an aspect of the invention, there is provided a kind of lithium alloy-skeleton carbon composite, the lithium alloy-skeleton Carbon composite includes on porous carbon materials carrier and the surface for being formed in the porous carbon materials carrier and intrapore lithium Alloy.
According to another aspect of the present invention, provide it is a kind of be used to prepare lithium alloy-skeleton carbon composite method, The method includes successively carrying out the following steps under an inert atmosphere:
(1) by heating lithium metal to 180-220 DEG C of temperature, to obtain molten lithium;
(2) under the stirring of 500-800 revolutions per seconds of revolving speed, molten lithium obtained in step (1) is warming up to 220-1000 DEG C, one or more element meltings are added and obtain the lithium alloy of molten condition, the element of addition be selected from magnesium, silicon, boron, carbon, Nitrogen, oxygen, fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, One of platinum, gold, mercury, thallium, lead, bismuth and polonium are a variety of;
(3) molten is in in described obtained in the step (2) under the stirring of 500-800 revolutions per seconds of revolving speed Porous carbon materials carrier is added in the lithium alloy of state, continues stirring 20-40 minutes, it is compound to obtain the lithium alloy-skeleton carbon Material.
According to a further aspect of the invention, a kind of cathode for lithium battery is provided, wherein the material of the cathode It is closed for the material of lithium alloy as described above-skeleton carbon composite or the cathode by being used to prepare lithium as described above The preparation of gold-skeleton carbon composite method.
According to a further aspect of the invention, a kind of lithium battery is provided, the lithium battery pack contains to be used for as described above The cathode of one-shot battery or secondary cell.
Compared with the prior art in this field, the present invention has the advantages that other specific by being added in molten lithium Metallic element prepares lithium alloy, then lithium alloy and skeleton carbon progress is compound, is capable of forming and closes with the higher lithium for carrying lithium amount Gold-skeleton carbon composite.The material can be kept substantially the original pattern of skeleton carbon (for example, spherical), partial size 5-30 Micron.In addition, surface of the lithium metal after forming alloy under its molten condition can reduce, thus more can easy and skeleton carbon materials Expect it is compound, to improve the load lithium amount in skeleton carbon.
Detailed description of the invention
Fig. 1 shows the lithium magnesium alloy-skeleton carbon composite discharge curve prepared in embodiment 1 and according to WO The comparison of lithium metal-skeleton carbon composite discharge curve of method preparation in 2015139660A1;
Fig. 2 shows that the lithium magnesium alloy-skeleton carbon composite scanning electron microscope (SEM) prepared in embodiment 1 is shone Piece and EDS elemental analysis test result, in which: A is that the SEM of material morphology schemes;B is carbon distribution in composite material EDS test chart;C is the EDS test chart of magnesium elements distribution in composite material, and the amplification factor in the above figure is 5000 times;
Fig. 3 shows the lithium magnesium alloy-skeleton carbon composite constant current charge-discharge test result prepared in embodiment 1 and root According to the ratio of lithium metal-skeleton carbon composite constant current charge-discharge test result of the method preparation in WO 2015139660A1 Compared with;
Fig. 4 shows the Li-Si alloy-skeleton carbon composite discharge curve prepared in embodiment 2 and according to WO The comparison of lithium metal-skeleton carbon composite discharge curve of method preparation in 2015139660A1;
Fig. 5 shows that the Li-Si alloy-skeleton carbon composite scanning electron microscope (SEM) prepared in embodiment 2 is shone Piece and EDS elemental analysis test result, in which: A is that the SEM of material morphology schemes;B is carbon distribution in composite material EDS test chart;C is the EDS test chart of element silicon distribution in composite material, and the amplification factor in the above figure is 5000 times; With
Fig. 6 shows the Li-Si alloy-skeleton carbon composite constant current charge-discharge test result prepared in embodiment 2 and root According to the ratio of lithium metal-skeleton carbon composite constant current charge-discharge test result of the method preparation in WO 2015139660A1 Compared with.
Specific embodiment
It should be appreciated that without departing from the scope or spirit of the present disclosure, those skilled in the art can be according to this The introduction of specification imagines other various embodiments and can modify to it.Therefore, specific embodiment below is not Restrictive meaning.
Unless otherwise specified, expression characteristic size, quantity and materialization used in specification and claims are special All numbers of property be construed as to be modified by term " about " in all cases.Therefore, unless there are opposite Illustrate, the numerical parameter otherwise listed in description above and the appended claims is approximation, those skilled in the art Member can seek the required characteristic obtained using teachings disclosed herein, suitably change these approximations.With endpoint table The use for the numberical range shown includes all numbers within the scope of this and any range within the scope of this, for example, 1 to 5 includes 1,1.1,1.3,1.5,2,2.75,3,3.80,4 and 5 etc..
According to the first aspect of the invention, a kind of lithium alloy-skeleton carbon composite, the lithium alloy-skeleton are provided Carbon composite includes on porous carbon materials carrier and the surface for being formed in the porous carbon materials carrier and intrapore lithium Alloy.
According to the technique and scheme of the present invention, the surface when lithium alloy is in molten state can be in melting lower than lithium metal Surface energy when state.
According to the technique and scheme of the present invention, the lithium alloy that lithium metal is formed in the molten state with certain element-specifics has Lower surface energy, thus when lithium alloy can be effectively increased to bone by the lithium alloy and framework carbon material carrier compound tense The wellability of frame carbon improves affinity between the two, thus improve gained lithium alloy-skeleton carbon composite load lithium amount and Specific capacity.
Certain technical solutions according to the present invention, the lithium alloy by by lithium metal and selected from magnesium, silicon, boron, carbon, nitrogen, oxygen, Fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, platinum, gold, One of mercury, thallium, lead, bismuth and polonium or multiple element are formed.Preferably, the element is magnesium or silicon.
Certain technical solutions according to the present invention, lithium alloy according to the present invention include the bianry alloy of lithium, such as lithium magnesium Alloy, Li-Si alloy etc..When the lithium alloy is formed by lithium metal and another element, the weight percent of lithium in lithium alloy Than being 70%~99.9%.It, can when the percentage of lithium metal and another metallic element controls in the above range To effectively increase lithium alloy to the wellability of skeleton carbon.
Certain technical solutions according to the present invention, lithium alloy according to the present invention except above-described lithium bianry alloy with It outside, further include ternary alloy three-partalloy such as the lithium magnalium, lithium gold and silver ternary alloy three-partalloy of lithium, the quaternary alloy of lithium such as lithium magnalium tin, lithium gold Silver-colored platinum quaternary alloy, etc..When the lithium alloy is formed by lithium metal and other multiple element, in the lithium alloy, base In the total weight of the lithium alloy, the weight percent of the other multiple element is 0.1-30 weight %, preferably 10-25 weight Measure % and more preferably 10-15 weight %.When the weight percent of the other multiple element is controlled in range above When, lithium alloy can be effectively increased to the wellability of skeleton carbon.
Certain technical solutions according to the present invention, lithium alloy according to the present invention are preferably lithium magnesium alloy or Li-Si alloy.
According to the present invention, lithium alloy has the wellability of enhancing to carbon skeleton in the molten state, carries lithium amount to increase. Certain technical solutions according to the present invention, based on the lithium alloy-skeleton carbon composite total weight, the lithium alloy-bone Lithium metal content in frame carbon composite is 45-95 weight %, preferably 57-62 weight % and more preferable 59-61 weight %.
According to the present invention, lithium alloy has the wellability of enhancing to carbon skeleton in the molten state, so that lithium closes unanimous-skeleton The increase of carbon composite carries lithium amount, and then increases lithium alloy-skeleton carbon composite specific capacity.It is according to the present invention certain Technical solution, the lithium alloy-skeleton carbon composite specific capacity are 1000-2470mAh/g.Wherein, for one-shot battery For, lithium alloy-skeleton carbon composite specific capacity is preferably 1000-1200mAh/g, and for secondary cell, Lithium alloy-skeleton carbon composite specific capacity is preferably 2210-2385mAh/g and more preferable 2272-2365mAh/g.
Certain specific embodiments according to the present invention, used lithium is Battery grade lithium metal in the present invention.The electricity Pond grade lithium metal is purchased from Tianjin China Energy Lithium Co., Ltd., purity 99.9%.
Certain specific embodiments according to the present invention, it is according to the present invention for producing the side of lithium carbon composite in batches Porous carbon materials carrier employed in method is selected from one of the following or a variety of: carbon nanotube microballoon, carbon fiber microballoon, Carbonaceous mesophase spherules, acetylene black carbosphere, Ketjen black carbosphere, Super-P microballoon, porous active carbon microspheres, graphite microspheres, stone Black alkene microballoon etc..
Preferably, the porous carbon materials carrier is carbon nanotube microballoon.The carbon nanotube microballoon can be according to PCT state Preparation method disclosed in border application publication number WO 2015139660A1 and Chinese Patent Application No. CN 201410395114.0 Preparation.The carbon nanotube microballoon has tiny spherical solid aggregated structure, spherical aggregated structure, spherical aggregated structure, more Any one in hole spherical shape aggregated structure and bagel shape aggregated structure.Preferably, the carbon nanotube microballoon is average straight Diameter is 1 μm to 100 μm;And/or the conductivity of the carbon nanotube microballoon is 1 × 10-3To 103S·cm-1;And/or the carbon is received The maximum allowable stress of mitron microballoon is 20MPa;And/or the specific surface area of the carbon nanotube microballoon is 100 to 1500m2/ g;And/or the aperture of hole contained by the carbon nanotube microballoon is 1nm to 200nm.
Certain specific embodiments according to the present invention, the carbon nanotube include multi-walled carbon nanotube, double wall carbon nano-tubes Any one in pipe and single-walled carbon nanotube or two or more combinations.
According to another aspect of the present invention, it provides and a kind of is used to prepare lithium alloy-skeleton carbon composite method, institute Stating method includes successively carrying out the following steps under an inert atmosphere:
(1) by the melting temperature (180-220 DEG C) of heating lithium metal to lithium, to obtain molten lithium;
(2) under the stirring of 500-800 revolutions per seconds of revolving speed, molten lithium obtained in step (1) is warming up to 220-1000 DEG C, one or more element meltings are added and obtain the lithium alloy of molten condition, the element of addition be selected from magnesium, silicon, boron, carbon, Nitrogen, oxygen, fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, One of platinum, gold, mercury, thallium, lead, bismuth and polonium are a variety of;
(3) molten is in in described obtained in the step (2) under the stirring of 500-800 revolutions per seconds of revolving speed Porous carbon materials carrier is added in the lithium alloy of state, continues stirring 20-40 minutes, it is compound to obtain the lithium alloy-skeleton carbon Material.
According to the technique and scheme of the present invention, the lithium alloy that lithium metal is formed in the molten state with certain element-specifics has Lower surface energy, thus when lithium alloy can be effectively increased to bone by the lithium alloy and framework carbon material carrier compound tense The wellability of frame carbon improves affinity between the two, thus improve gained lithium alloy-skeleton carbon composite load lithium amount and Specific capacity.
Certain technical solutions according to the present invention, the lithium alloy by lithium metal and selected from magnesium, silicon, boron, carbon, nitrogen, oxygen, Fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, platinum, gold, One of mercury, thallium, lead, bismuth and polonium or multiple element are formed.Preferably, the element or magnesium or silicon.
Certain technical solutions according to the present invention, lithium alloy according to the present invention include the bianry alloy of lithium, such as lithium magnesium Alloy, Li-Si alloy etc..The weight percent of lithium is 70% to 99.9% in lithium alloy.When lithium metal and another described gold When belonging to the percentage control of element in the above range, lithium alloy can be effectively increased to the wellability of skeleton carbon.
Certain technical solutions according to the present invention, lithium alloy according to the present invention except above-described lithium bianry alloy with It outside, further include the ternary alloy three-partalloy such as lithium gold and silver ternary alloy three-partalloy of lithium, the quaternary alloy of lithium such as lithium Au-Ag-Pt quaternary alloy, etc. Deng.When the lithium alloy is formed by lithium metal and other multiple element, in the lithium alloy, based on the total of the lithium alloy Weight, the charged material weight percentage of the other multiple element are 0.1-30 weight %, preferably 10-25 weight % and more excellent Select 10-15 weight %.It, can be effective when the charged material weight percentage of the other multiple element is controlled in range above Increase lithium alloy to the wellability of skeleton carbon.
Certain technical solutions according to the present invention, lithium alloy according to the present invention are preferably lithium magnesium alloy or Li-Si alloy.
According to the present invention, lithium alloy has the wellability of enhancing to carbon skeleton in the molten state, carries lithium amount to increase. Certain technical solutions according to the present invention, based on the lithium alloy-skeleton carbon composite total weight, the lithium alloy-bone Lithium metal content in frame carbon composite is 45-95 weight %, preferably 57-62 weight % and more preferable 59-61 weight %.
According to the present invention, lithium alloy has the wellability of enhancing to carbon skeleton in the molten state, thus lithium alloy-skeleton The increase of carbon composite carries lithium amount, and then increases lithium alloy-skeleton carbon composite specific capacity.It is according to the present invention certain Technical solution, the lithium alloy-skeleton carbon composite specific capacity are 1000-2470mAh/g.Wherein, for one-shot battery For, lithium alloy-skeleton carbon composite specific capacity is preferably 1000-1200mAh/g, and for secondary cell, Lithium alloy-skeleton carbon composite specific capacity is preferably preferred 2210-2385mAh/g and more preferable 2272-2365mAh/ g。
Certain specific embodiments according to the present invention, used lithium is Battery grade lithium metal in the present invention.The electricity Pond grade lithium metal is purchased from Tianjin China Energy Lithium Co., Ltd., purity 99.9%.
Certain specific embodiments according to the present invention, it is according to the present invention for producing the side of lithium carbon composite in batches Porous carbon materials carrier employed in method is selected from one of the following or a variety of: carbon nanotube microballoon, carbon fiber microballoon, Carbonaceous mesophase spherules, acetylene black carbosphere, Ketjen black carbosphere, Super-P microballoon, porous active carbon microspheres, graphite microspheres, stone Black alkene microballoon etc..
Preferably, the porous carbon materials carrier is carbon nanotube microballoon.The carbon nanotube microballoon can be according to PCT state Preparation method disclosed in border application publication number WO 2015139660A1 and Chinese Patent Application No. CN 201410395114.0 Preparation.The carbon nanotube microballoon has tiny spherical solid aggregated structure, spherical aggregated structure, spherical aggregated structure, more Any one in hole spherical shape aggregated structure and bagel shape aggregated structure.Preferably, the carbon nanotube microballoon is average straight Diameter is 1 μm to 100 μm;And/or the conductivity of the carbon nanotube microballoon is 1 × 10-3To 103S·cm-1;And/or the carbon is received The maximum allowable stress of mitron microballoon is 20MPa;And/or the specific surface area of the carbon nanotube microballoon is 100 to 1500m2/ g;And/or the aperture of hole contained by the carbon nanotube microballoon is 1nm to 200nm.
Certain specific embodiments according to the present invention, the carbon nanotube include multi-walled carbon nanotube, double wall carbon nano-tubes Any one in pipe and single-walled carbon nanotube or two or more combinations.
According to a further aspect of the invention, a kind of cathode for lithium battery is provided, wherein the material of the cathode is The material of lithium alloy-skeleton carbon composite as described above or the cathode by being used to prepare lithium alloy-as described above It is prepared by the method for skeleton carbon composite.
According to a further aspect of the invention, a kind of lithium battery is provided, the lithium battery pack is used for one containing as described above The cathode of primary cell or secondary cell.Preferably, the one-shot battery is lithium thermal cell, and the secondary cell is lithium metal-oxygen Compound battery, lithium metal-polymer battery or rechargeable lithium ion batteries.
Following detailed description is intended to illustratively and in non-limiting manner illustrate the disclosure.
Specific embodiment 1 is a kind of lithium alloy-skeleton carbon composite, the lithium alloy-skeleton carbon composite packet It includes porous carbon materials carrier and is formed on the surface of the porous carbon materials carrier and intrapore lithium alloy.
Specific embodiment 2 is the lithium alloy according to specific embodiment 1-skeleton carbon composite, wherein described Lithium alloy by lithium metal and selected from magnesium, silicon, boron, carbon, nitrogen, oxygen, fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, One of rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, platinum, gold, mercury, thallium, lead, bismuth and polonium or multiple element are formed.
Specific embodiment 3 is the lithium alloy according to specific embodiment 2-skeleton carbon composite, wherein working as institute When stating lithium alloy and being formed by lithium metal and another element, the weight percent of lithium is 70%~99.9% in lithium alloy.
Specific embodiment 4 is the lithium alloy according to specific embodiment 2-skeleton carbon composite, wherein working as institute When stating lithium alloy and being formed by lithium metal and other multiple element, in the lithium alloy, based on the total weight of the lithium alloy, institute The weight percent for stating other multiple element is 0.1-30 weight %.
Specific embodiment 5 is the lithium alloy according to specific embodiment 2-skeleton carbon composite, wherein described Lithium alloy is lithium magnesium alloy, Li-Si alloy, lithium-aluminium alloy, lithium boron alloy and other polynary derivatives.
Specific embodiment 6 is the lithium alloy according to specific embodiment 1-skeleton carbon composite, wherein being based on The lithium alloy-skeleton carbon composite total weight, the lithium metal content in the lithium alloy-skeleton carbon composite are 45-95 weight %.
Specific embodiment 7 is the lithium alloy according to specific embodiment 1-skeleton carbon composite, wherein described Lithium alloy-skeleton carbon composite specific capacity is 1000-2470mAh/g.
Specific embodiment 8 is the lithium alloy according to specific embodiment 1-skeleton carbon composite, wherein described Porous carbon materials carrier is selected from one of the following or a variety of: carbon nanotube microballoon, carbon fiber microballoon, mesocarbon are micro- Ball, acetylene black carbosphere, Ketjen black carbosphere, Super-P microballoon, porous active carbon microspheres, graphite microspheres and graphene microballoon.
Specific embodiment 9 is the lithium alloy according to specific embodiment 1-skeleton carbon composite, wherein described Porous carbon materials carrier is carbon nanotube microballoon.
Specific embodiment 10 is the lithium alloy according to specific embodiment 9-skeleton carbon composite, wherein described Carbon nanotube microballoon has tiny spherical solid aggregated structure, spherical aggregated structure, spherical aggregated structure, porous spherical aggregation Any one in structure and bagel shape aggregated structure.
Specific embodiment 11 is the lithium alloy according to specific embodiment 9-skeleton carbon composite, in which:
The average diameter of the carbon nanotube microballoon is 1 μm to 100 μm;And/or
The conductivity of the carbon nanotube microballoon is 1 × 10-3To 103S·cm-1;And/or
The maximum allowable stress of the carbon nanotube microballoon is 20MPa;And/or
The specific surface area of the carbon nanotube microballoon is 100 to 1500m2/g;And/or
The aperture of hole contained by the carbon nanotube microballoon is 1nm to 200nm.
Specific embodiment 12 is the lithium alloy according to specific embodiment 9-skeleton carbon composite, wherein described Carbon nanotube includes any one or two or more groups in multi-walled carbon nanotube, double-walled carbon nano-tube and single-walled carbon nanotube It closes.
Specific embodiment 13 be it is a kind of be used to prepare lithium alloy-skeleton carbon composite method, the method includes The following steps are successively carried out under an inert atmosphere:
(1) by heating lithium metal to 180-220 DEG C of temperature, to obtain molten lithium;
(2) under the stirring of 500-800 revolutions per seconds of revolving speed, molten lithium obtained in step (1) is warming up to 220-1000 DEG C, one or more element meltings are added and obtain the lithium alloy of molten condition, the element of addition be selected from magnesium, silicon, boron, carbon, Nitrogen, oxygen, fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, One of platinum, gold, mercury, thallium, lead, bismuth and polonium are a variety of;
(3) molten is in in described obtained in the step (2) under the stirring of 500-800 revolutions per seconds of revolving speed Porous carbon materials carrier is added in the lithium alloy of state, continues stirring 20-40 minutes, it is compound to obtain the lithium alloy-skeleton carbon Material.
Specific embodiment 14 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein when the lithium alloy is formed by lithium metal and another element, the weight percent of lithium in the lithium alloy Than being 70% to 99.9%.
Specific embodiment 15 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein when forming the lithium alloy by lithium metal and other multiple element, it is described based on the total weight of the lithium alloy In addition the charged material weight percentage of multiple element is 0.1-30 weight %.
Specific embodiment 16 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein the lithium alloy is lithium magnesium alloy, Li-Si alloy, lithium-aluminium alloy, lithium boron alloy and other polynary derivatives.
Specific embodiment 17 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein based on the lithium alloy-skeleton carbon composite total weight, in the lithium alloy-skeleton carbon composite Lithium metal content is 45-95 weight %.
Specific embodiment 18 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein the lithium alloy-skeleton carbon composite specific capacity is 1000-2470mAh/g.
Specific embodiment 19 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein the porous carbon materials carrier is selected from one of the following or a variety of: carbon nanotube microballoon, carbon fiber are micro- Ball, carbonaceous mesophase spherules, acetylene black carbosphere, Ketjen black carbosphere, Super-P microballoon, porous active carbon microspheres, graphite microspheres With graphene microballoon.
Specific embodiment 20 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 13 Method, wherein the porous carbon materials carrier is carbon nanotube microballoon.
Specific embodiment 21 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 20 Method, wherein the carbon nanotube microballoon has tiny spherical solid aggregated structure, spherical aggregated structure, spherical aggregation knot Any one in structure, porous spherical aggregated structure and bagel shape aggregated structure.
Specific embodiment 22 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 20 Method, in which:
The average diameter of the carbon nanotube microballoon is 1 μm to 100 μm;And/or
The conductivity of the carbon nanotube microballoon is 1 × 10-3To 103S·cm-1;And/or
The maximum allowable stress of the carbon nanotube microballoon is 20MPa;And/or
The specific surface area of the carbon nanotube microballoon is 100 to 1500m2/g;And/or
The aperture of hole contained by the carbon nanotube microballoon is 1nm to 200nm.
Specific embodiment 23 is that lithium alloy-skeleton carbon composite is used to prepare according to specific embodiment 20 Method, wherein the carbon nanotube includes any one in multi-walled carbon nanotube, double-walled carbon nano-tube and single-walled carbon nanotube Or two or more combination.
Specific embodiment 24 is a kind of cathode for lithium battery, wherein the material of the cathode is according to specific implementation The material of lithium alloy described in any one of mode 1 to 12-skeleton carbon composite or the cathode is by according to specific implementation The preparation of lithium alloy-skeleton carbon composite method is used to prepare described in any one of mode 13 to 23.
Specific embodiment 25 is a kind of lithium battery, and the lithium battery pack according to specific embodiment 24 containing being used for The cathode of lithium battery.
Specific embodiment 26 is the lithium battery according to specific embodiment 25, and the lithium battery includes secondary electricity Pond (such as lithium metal-oxide cell, lithium metal-polymer battery or rechargeable lithium ion batteries) and one-shot battery (such as lithium heat Battery).
The present invention is described in more detail below with reference to embodiment.It may be noted that these descriptions and embodiment are all In order to be easy to understand the present invention, rather than limitation of the present invention.Protection scope of the present invention is with appended claims It is quasi-.
Embodiment
In the present invention, mentioned " % " is " weight % ", and mentioned " part " is " parts by weight ".
Test method
In this disclosure, to obtained various lithium alloys-skeleton carbon composite about load lithium amount, specific capacity, shape Looks are tested with lithium plating lithium cycle performance etc. is pulled out, and specific test method is described as follows.
Carry lithium amount
It lithium alloy-skeleton carbon composite or lithium metal-skeleton carbon composite and is pressed prepared by weighing m grams It makes on the foam copper that diameter is 1.5cm, as cathode.The cathode and the metal lithium sheet as anode are assembled into simulation electricity Pond, wherein used electrolyte is LiPF6It is dissolved in ethylene carbonate (EC), the dimethyl carbonate of volume ratio 1: 1: 1 (DMC) and solution obtained in the mixed solvent of methyl ethyl carbonate (EMC).The simulated battery is continued with the electric current of 0.1mA Electric discharge, until voltage value is that 1V stops electric discharge, the capacity of process electric discharge is Q (current potential of capacity is coulomb).According to following public affairs Formula calculates the load lithium amount in lithium carbon composite:
Pattern
By scanning electron microscope (SEM), (cold field emission of the model S4800 of Hitachi, Japan production scans electricity Sub- microscope) observation lithium metal-porous carbon composite pattern, and pass through the grain of scanning electron micrograph statistics particle Diameter distribution.In addition, carrying out EDS element point to lithium metal-porous carbon composite using the scanning electron microscope (SEM) Analysis.
Pull out lithium plating lithium circulation
It lithium alloy-skeleton carbon composite or lithium metal-skeleton carbon composite and is pressed prepared by weighing m grams It makes on the foam copper that diameter is 1.5cm, as cathode.The cathode and the metal lithium sheet as anode are assembled into simulation electricity Pond, wherein used electrolyte is LiPF6It is dissolved in ethylene carbonate (EC), the dimethyl carbonate of volume ratio 1: 1: 1 (DMC) and solution obtained in the mixed solvent of methyl ethyl carbonate (EMC).Obtained simulated battery is (deep in cell tester The cell tester of the model CT-3008 of Zhen Shi new Weir Co., Ltd production) on shelve 360 minutes, wherein with 1mA electric current Constant-current charge (plating lithium) 1 hour, then with 1mA electric current constant-current discharge (pulling out lithium) 1 hour, cycle charging discharge process 200 times.
Embodiment 1
According to PCT International Publication No. WO 2015139660A1 and Chinese Patent Application No. CN 201410395114.0 Disclosed in preparation method prepare carbon nanotube microballoon.Obtained carbon nanotube microballoon has spherical aggregated structure, wherein institute The average diameter for stating carbon nanotube microballoon is 5 μm, conductivity 10Scm-1, maximum allowable stress is 20MPa, specific surface area For 255m2/ g, and the aperture of hole contained by the carbon nanotube microballoon is 20nm to 100nm.
Under an inert atmosphere, by 9g heating lithium metal to 220 DEG C so that it is melted.To in 800 revolutions per seconds of revolving speed 1g magnesium metal is added in the lithium of melting under stirring, continues stirring 20 minutes, the lithium of the content of magnesium of 10 weight % is obtained after cooling Magnesium alloy.The lithium magnesium alloy of 10g is heated to its molten condition, and under the stirring in 800 revolutions per seconds of revolving speed Carbon nanotube microballoon obtained in 5g above step is added in the lithium magnesium alloy of melting, continues stirring 40 minutes, it is cooling to product After obtain lithium magnesium alloy-skeleton carbon composite.According to the above-described method for carrying lithium amount that calculates by calculating the lithium Magnesium alloy-skeleton carbon composite load lithium amount is 64 weight %.
Respectively, according to the method in WO 2015139660A1, by 10g heating lithium metal to 180 DEG C so that its melt, And carbon nanotube microballoon obtained in 5g above step is added into the lithium of melting, continues stirring 40 minutes, it is cooling to product After obtain lithium-skeleton carbon composite.According to the above-described method for carrying lithium amount that calculates by calculating the lithium-skeleton carbon The load lithium amount of composite material is that load lithium amount is 53 weight %.
Method described in lithium cycle performance etc. is plated with lithium is pulled out about pattern according in the above Test Methods section, it is right Lithium magnesium alloy-skeleton carbon composite pattern derived above is tested with lithium plating lithium cycle performance is pulled out, and to above Obtained lithium-skeleton carbon composite pulls out lithium plating lithium cycle performance and is tested.Fig. 1 shows the lithium magnesium prepared in embodiment 1 Alloy-skeleton carbon composite discharge curve and lithium metal-skeleton carbon according to the method preparation in WO 2015139660A1 The comparison of the discharge curve of composite material.Due to the lithium magnesium alloy that the lithium metal and magnesium metal of molten state are mixed to form reduce it is molten Melt state metallic lithium surface energy, so that molten metal lithium is easier to enter the inside of framework carbon material, therefore lithium magnesium alloy-skeleton Carbon compound cathode has higher specific capacity than lithium metal-framework carbon material.Fig. 2 shows the lithium magnesium alloy-prepared in embodiment 1 Scanning electron microscope (SEM) photo and EDS elemental analysis test result of skeleton carbon composite, in which: A is material shape The SEM of looks schemes;B is the EDS test chart of carbon distribution in composite material;C is the EDS test chart of Mg distribution in composite material, And the amplification factor in the above figure is 5000 times.By Fig. 2 (A) it is found that obtained lithium magnesium alloy-skeleton carbon/carbon composite material base The spherical form of the porous carbon materials carrier as carrier is maintained in sheet.In addition, from the comparison of Fig. 2 (B) and (C) it is found that gold The distribution and carbon for belonging to magnesium are distributed to coincide substantially, illustrates that magnesium metal is evenly distributed in the surface and hole of skeleton carbon.Fig. 3 is shown Lithium magnesium alloy-skeleton carbon composite constant current charge-discharge test result for being prepared in embodiment 1 with according to WO The comparison of lithium metal-skeleton carbon composite constant current charge-discharge test result of method preparation in 2015139660A1.From The figure can be seen that lithium magnesium alloy-skeleton carbon composite polarizing voltage very little when starting, and show that material has big ratio table Area can greatly reduce current density, effectively inhibit the generation of Li dendrite.And due to the presence of magnesium in alloy, in material Inside plays the role of promoting lithium metal deposition, therefore the material is than the gold according to the method preparation in WO 2015139660A1 Belong to lithium-skeleton carbon composite and is provided with outstanding cyclical stability.
Embodiment 2
According to PCT International Publication No. WO 2015139660A1 and Chinese Patent Application No. CN 201410395114.0 Disclosed in preparation method prepare carbon nanotube microballoon.Obtained carbon nanotube microballoon has spherical aggregated structure, wherein institute The average diameter for stating carbon nanotube microballoon is 5 μm, conductivity 10Scm-1, maximum allowable stress is 20MPa, specific surface area For 255m2/ g, and the aperture of hole contained by the carbon nanotube microballoon is 20nm to 100nm.
Under an inert atmosphere, by 9g heating lithium metal to 220 DEG C so that it is melted.To in 500 revolutions per seconds of revolving speed 1g metallic silicon is added in the lithium of melting under stirring, is warming up to 600 DEG C, continues stirring 20 minutes, obtains 10 weight % after cooling Silicone content Li-Si alloy.The Li-Si alloy of 10g is heated to its molten condition, and at 500 revolutions per seconds Carbon nanotube microballoon obtained in 5g above step is added in the Li-Si alloy of melting under the stirring of revolving speed, continues 40 points of stirring Clock obtains Li-Si alloy-skeleton carbon composite after product is cooling.Passed through according to the above-described method for carrying lithium amount that calculates The Li-Si alloy-skeleton carbon composite load lithium amount known to calculating is 57 weight %.
Respectively, according to the method in W02015139660A1, by 10g heating lithium metal to 180 DEG C so that its melt, and And carbon nanotube microballoon obtained in 5g above step is added into the lithium of melting, continue stirring 40 minutes, after product is cooling Obtain lithium-skeleton carbon composite.It is multiple by calculating the lithium-skeleton carbon according to the above-described method for calculating load lithium amount The load lithium amount of condensation material is that load lithium amount is 53 weight %.
Method described in lithium cycle performance etc. is plated with lithium is pulled out about pattern according in the above Test Methods section, it is right Li-Si alloy derived above-skeleton carbon composite pattern is tested with lithium plating lithium cycle performance is pulled out, and to above Obtained lithium-skeleton carbon composite pulls out lithium plating lithium cycle performance and is tested.Fig. 4 shows the lithium silicon prepared in embodiment 2 Alloy-skeleton carbon composite discharge curve and lithium metal-skeleton carbon according to the method preparation in WO 2015139660A1 The comparison of the discharge curve of composite material.Since the Li-Si alloy that the lithium metal and silicon of molten state are mixed to form reduces molten state Metallic lithium surface energy, so that molten metal lithium is easier to enter the inside of framework carbon material, therefore Li-Si alloy-skeleton carbon is multiple Closing cathode has higher specific capacity than lithium metal-framework carbon material.Fig. 5 shows the Li-Si alloy-skeleton prepared in embodiment 2 Scanning electron microscope (SEM) photo and EDS elemental analysis test result of carbon composite, in which: A is material morphology SEM figure;B is the EDS test chart of carbon distribution in composite material;C is the EDS test chart of Si Elemental redistribution in composite material, And the amplification factor in the above figure is 5000 times.By Fig. 5 (A) it is found that obtained Li-Si alloy-skeleton carbon/carbon composite material base The spherical form of the porous carbon materials carrier as carrier is maintained in sheet.In addition, from the comparison of Fig. 5 (B) and (C) it is found that gold The distribution and carbon for belonging to silicon are distributed to coincide substantially, illustrates that metallic silicon is evenly distributed in the surface and hole of skeleton carbon.Fig. 6 is shown The Li-Si alloy prepared in embodiment 2-skeleton carbon composite constant current charge-discharge test result with according to WO The comparison of lithium metal-skeleton carbon composite constant current charge-discharge test result of method preparation in 2015139660A1.From The figure can be seen that Li-Si alloy-skeleton carbon composite polarizing voltage very little when starting, and show that material has big ratio table Area can greatly reduce current density, effectively inhibit the generation of Li dendrite.And due to the presence of Silicon In Alloys, in material Inside plays the role of promoting lithium metal deposition, therefore the material is than the gold according to the method preparation in WO 2015139660A1 Belong to lithium-skeleton carbon composite and is provided with outstanding cyclical stability.
Although specific embodiment has been shown and described in the present invention, those skilled in the art be will be understood that, can To replace shown and described specific embodiment with various substitutions and/or equivalent embodiments, without departing from this hair Bright range.The application is intended to include any improvement or change to the specific embodiment discussed in the present invention.Therefore, this hair It is bright to be limited solely by claim and its equivalent.
It will be appreciated by those skilled in the art that in the case without departing from the scope of the present invention, can carry out a variety of modifications and Change.Such modifications and changes are intended to fall within the scope of the present invention as defined in the appended claims.

Claims (10)

1. a kind of lithium alloy-skeleton carbon composite, the lithium alloy-skeleton carbon composite include porous carbon materials carrier with And it is formed on the surface of the porous carbon materials carrier and intrapore lithium alloy.
2. lithium alloy according to claim 1-skeleton carbon composite, wherein the lithium alloy is by lithium metal and is selected from Magnesium, silicon, boron, carbon, nitrogen, oxygen, fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, One of antimony, tellurium, iodine, iridium, platinum, gold, mercury, thallium, lead, bismuth and polonium or multiple element are formed.
3. lithium alloy according to claim 2-skeleton carbon composite, wherein when the lithium alloy by lithium metal in addition When a kind of formation of element, the weight percent of lithium is 70% to 99.9% in the lithium alloy.
4. lithium alloy according to claim 2-skeleton carbon composite, wherein when the lithium alloy by lithium metal in addition When multiple element formation, in the lithium alloy, based on the total weight of the lithium alloy, the weight hundred of the other multiple element Score is 0.1-30 weight %.
5. lithium alloy according to claim 2-skeleton carbon composite, wherein the lithium alloy is lithium magnesium alloy, lithium silicon Alloy, lithium-aluminium alloy, lithium boron alloy and other polynary derivatives.
6. lithium alloy according to claim 1-skeleton carbon composite, wherein compound based on the lithium alloy-skeleton carbon The total weight of material, the lithium metal content in the lithium alloy-skeleton carbon composite are 45-95 weight %.
7. lithium alloy according to claim 1-skeleton carbon composite, wherein the lithium alloy-skeleton carbon composite Specific capacity be 1000-2470mAh/g.
8. a kind of be used to prepare lithium alloy-skeleton carbon composite method, the method includes under an inert atmosphere successively into Row the following steps:
(1) by heating lithium metal to 180-220 DEG C of temperature, to obtain molten lithium;
(2) under the stirring of 500-800 revolutions per seconds of revolving speed, molten lithium obtained in step (1) is warming up to 220-1000 DEG C, One or more element meltings are added and obtain the lithium alloy of molten condition, the element of addition be selected from magnesium, silicon, boron, carbon, nitrogen, Oxygen, fluorine, aluminium, phosphorus, sulphur, chlorine, calcium, zinc, gallium, germanium, arsenic, selenium, bromine, ruthenium, rhodium, palladium, silver, cadmium, indium, tin, antimony, tellurium, iodine, iridium, platinum, One of gold, mercury, thallium, lead, bismuth and polonium are a variety of;With
(3) in described in a molten state obtained in the step (2) under the stirring of 500-800 revolutions per seconds of revolving speed Porous carbon materials carrier is added in lithium alloy, continues stirring 20-40 minutes, to obtain the lithium alloy-skeleton carbon composite.
9. a kind of cathode for lithium battery, wherein the material of the cathode is according to any one of claims 1 to 7 The material of lithium alloy-skeleton carbon composite or the cathode is used to prepare lithium alloy-by according to claim 8 It is prepared by the method for skeleton carbon composite.
10. a kind of lithium battery, the lithium battery pack is containing according to claim 9 for primary or serondary lithium battery negative Pole.
CN201710609085.7A 2017-07-26 2017-07-26 Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery Pending CN109309243A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201710609085.7A CN109309243A (en) 2017-07-26 2017-07-26 Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery
PCT/CN2017/105656 WO2019019409A1 (en) 2017-07-26 2017-10-11 Lithium alloy-skeletal carbon composite material and preparation method therefor, negative electrode and secondary battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710609085.7A CN109309243A (en) 2017-07-26 2017-07-26 Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery

Publications (1)

Publication Number Publication Date
CN109309243A true CN109309243A (en) 2019-02-05

Family

ID=65041010

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710609085.7A Pending CN109309243A (en) 2017-07-26 2017-07-26 Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery

Country Status (2)

Country Link
CN (1) CN109309243A (en)
WO (1) WO2019019409A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110416526A (en) * 2019-08-14 2019-11-05 戴嘉 A kind of lithium cell cathode material and preparation method thereof
CN110797524A (en) * 2019-11-08 2020-02-14 宁波致轻电池有限公司 Multi-element lithium-magnesium alloy cathode material for secondary battery and adaptive electrolyte thereof
CN111180698A (en) * 2019-12-31 2020-05-19 中国科学院宁波材料技术与工程研究所 Metal lithium composite negative electrode, preparation method thereof and lithium metal secondary battery
CN111211292A (en) * 2019-11-22 2020-05-29 中国科学院大连化学物理研究所 Three-dimensional graphene composite lithium alloy cathode, preparation method thereof and application of three-dimensional graphene composite lithium alloy cathode in lithium ion battery
CN112928238A (en) * 2019-12-06 2021-06-08 北京航空航天大学 Ultrathin metal lithium electrode, preparation thereof and application of ultrathin metal lithium electrode as negative electrode of secondary lithium battery
WO2021179219A1 (en) * 2020-03-11 2021-09-16 宁德新能源科技有限公司 Anode plate and manufacturing method therefor, battery using anode plate, and electronic apparatus
CN113644263A (en) * 2021-07-26 2021-11-12 西北工业大学 Preparation method and application of flexible carbon nanofiber framework coated with ultra-uniform lithium-philic sites

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108923036A (en) * 2018-07-17 2018-11-30 浙江大学山东工业技术研究院 The preparation method of carbon-lithium composite powder and preparation method thereof, lithium metal electrode for secondary battery
US20240088364A1 (en) * 2022-08-31 2024-03-14 Lg Energy Solution, Ltd. Negative Electrode for a Lithium Secondary Battery, a Method for Preparing the Same and a Lithium Secondary Battery Comprising the Same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105374991A (en) * 2014-08-13 2016-03-02 中国科学院苏州纳米技术与纳米仿生研究所 Metal lithium-framework carbon composite material and preparation method thereof, negative electrode and secondary battery
CN106784770A (en) * 2017-02-28 2017-05-31 南开大学 The lithium magnesium alloy of content of magnesium high is the lithium-sulfur rechargeable battery of negative pole

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20120024653A (en) * 2009-05-28 2012-03-14 닛산 지도우샤 가부시키가이샤 Negative electrode for lithium ion secondary battery and battery using same
GB2500611A (en) * 2012-03-26 2013-10-02 Cambridge Entpr Ltd Powder comprising carbon nanostructures and method of preparation
JP5993337B2 (en) * 2012-07-03 2016-09-14 Jfeケミカル株式会社 Negative electrode material for lithium ion secondary battery, method for producing the same, negative electrode for lithium ion secondary battery using the same, and lithium ion secondary battery
KR101994877B1 (en) * 2015-06-26 2019-07-01 주식회사 엘지화학 Lithium sulfur battery and method for manufacturaing the same
CN106711456B (en) * 2015-11-12 2019-12-06 中国科学院苏州纳米技术与纳米仿生研究所 passivated metal lithium-carbon framework composite material, preparation method and application thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105374991A (en) * 2014-08-13 2016-03-02 中国科学院苏州纳米技术与纳米仿生研究所 Metal lithium-framework carbon composite material and preparation method thereof, negative electrode and secondary battery
CN106784770A (en) * 2017-02-28 2017-05-31 南开大学 The lithium magnesium alloy of content of magnesium high is the lithium-sulfur rechargeable battery of negative pole

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110416526A (en) * 2019-08-14 2019-11-05 戴嘉 A kind of lithium cell cathode material and preparation method thereof
CN110416526B (en) * 2019-08-14 2020-11-06 乐清市然景电气有限公司 Lithium battery negative electrode material and preparation method thereof
CN111916692A (en) * 2019-08-14 2020-11-10 邵峥业 Preparation method of lithium battery negative electrode material
CN111916691A (en) * 2019-08-14 2020-11-10 邵峥业 Preparation method of lithium battery negative electrode material
CN110797524A (en) * 2019-11-08 2020-02-14 宁波致轻电池有限公司 Multi-element lithium-magnesium alloy cathode material for secondary battery and adaptive electrolyte thereof
CN111211292A (en) * 2019-11-22 2020-05-29 中国科学院大连化学物理研究所 Three-dimensional graphene composite lithium alloy cathode, preparation method thereof and application of three-dimensional graphene composite lithium alloy cathode in lithium ion battery
CN112928238A (en) * 2019-12-06 2021-06-08 北京航空航天大学 Ultrathin metal lithium electrode, preparation thereof and application of ultrathin metal lithium electrode as negative electrode of secondary lithium battery
CN112928238B (en) * 2019-12-06 2022-06-21 北京航空航天大学 Ultrathin metal lithium electrode, preparation thereof and application of ultrathin metal lithium electrode as negative electrode of secondary lithium battery
CN111180698A (en) * 2019-12-31 2020-05-19 中国科学院宁波材料技术与工程研究所 Metal lithium composite negative electrode, preparation method thereof and lithium metal secondary battery
WO2021179219A1 (en) * 2020-03-11 2021-09-16 宁德新能源科技有限公司 Anode plate and manufacturing method therefor, battery using anode plate, and electronic apparatus
CN113644263A (en) * 2021-07-26 2021-11-12 西北工业大学 Preparation method and application of flexible carbon nanofiber framework coated with ultra-uniform lithium-philic sites

Also Published As

Publication number Publication date
WO2019019409A1 (en) 2019-01-31

Similar Documents

Publication Publication Date Title
CN109309243A (en) Lithium alloy-skeleton carbon composite material and preparation method, cathode and lithium battery
CN102237519B (en) Fluorine-free preparation method for three-dimensional porous silica powder anode material of lithium ion battery
CN104347857B (en) Negative electrode of lithium ionic secondary battery and preparation method thereof, cathode pole piece of lithium ion secondary battery and lithium rechargeable battery
US9012087B2 (en) Device and electrode having nanoporous graphite with lithiated sulfur for advanced rechargeable batteries
CN104051733B (en) Two selenizing vanadium/C-base composte material, preparation method and lithium ion battery negative electrode
CN107425185B (en) Preparation method of carbon nanotube-loaded molybdenum carbide material and application of carbon nanotube-loaded molybdenum carbide material in lithium-sulfur battery positive electrode material
CN107946576B (en) High-rate graphite negative electrode material, preparation method thereof and lithium ion battery
US20040229041A1 (en) Graphite granules and their method of fabrication
CN109103425A (en) Negative electrode material, cathode and the battery with the cathode
CN106784707A (en) A kind of preparation method of nano-silicone wire/carbon composite lithium ion battery cathode material
JP6003996B2 (en) Electrode active material, method for producing electrode active material, electrode, battery, and method of using clathrate compound
CN107895779B (en) High-capacity potassium ion battery negative electrode material and preparation method and application thereof
CN110474049B (en) Preparation method of antimony sulfide nanorod negative electrode of lithium ion battery
CN112018346A (en) Phosphorus-doped CoSe2Mxene composite material and preparation method thereof
CN106450246A (en) Porous silicon-carbon composite material for lithium ion battery and preparation method of material
CN106410164A (en) High-performance composite material and preparation method and application thereof
CN104638253A (en) Preparation method of Si and C-RG core-shell composite material used as cathode of lithium ion battery
CN108899495B (en) Silicon-oxygen-carbon based negative electrode material of lithium ion battery and preparation method thereof
KR20220078683A (en) Anode material, manufacturing method and use thereof, and lithium ion battery
CN111342014A (en) Silicon-carbon negative electrode material of lithium ion battery and preparation method thereof
CN109473665A (en) A kind of nano silica-base material and its preparation method and application
CN110085823B (en) Nano composite negative electrode material and preparation method and application thereof
CN110444738A (en) A method of preparing lithium ion battery micropore carbon adsorption stibnite composite negative pole
Yu et al. Lithiophilic ZnO confined in microscale carbon cubes as a stable host for lithium metal anodes
CN106941171B (en) Lithium battery cathode composite material based on nano silicon carbon and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20190205